WO2013081463A2 - Influenza a virus specific antibodies - Google Patents
Influenza a virus specific antibodies Download PDFInfo
- Publication number
- WO2013081463A2 WO2013081463A2 PCT/NL2012/050851 NL2012050851W WO2013081463A2 WO 2013081463 A2 WO2013081463 A2 WO 2013081463A2 NL 2012050851 W NL2012050851 W NL 2012050851W WO 2013081463 A2 WO2013081463 A2 WO 2013081463A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- antibody
- influenza
- sequence
- virus
- functional equivalent
- Prior art date
Links
- 241000712431 Influenza A virus Species 0.000 title claims abstract description 189
- 206010022000 influenza Diseases 0.000 claims abstract description 127
- 230000000069 prophylactic effect Effects 0.000 claims abstract description 29
- 239000003814 drug Substances 0.000 claims abstract description 22
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 21
- 208000024891 symptom Diseases 0.000 claims abstract description 10
- 238000003745 diagnosis Methods 0.000 claims abstract description 6
- 230000027455 binding Effects 0.000 claims description 162
- 108060003951 Immunoglobulin Proteins 0.000 claims description 122
- 102000018358 immunoglobulin Human genes 0.000 claims description 122
- 230000003472 neutralizing effect Effects 0.000 claims description 122
- 102100035360 Cerebellar degeneration-related antigen 1 Human genes 0.000 claims description 117
- 101710154606 Hemagglutinin Proteins 0.000 claims description 113
- 101710093908 Outer capsid protein VP4 Proteins 0.000 claims description 113
- 101710135467 Outer capsid protein sigma-1 Proteins 0.000 claims description 113
- 101710176177 Protein A56 Proteins 0.000 claims description 113
- 101100112922 Candida albicans CDR3 gene Proteins 0.000 claims description 101
- 102100035361 Cerebellar degeneration-related protein 2 Human genes 0.000 claims description 98
- 101000737796 Homo sapiens Cerebellar degeneration-related protein 2 Proteins 0.000 claims description 98
- 239000000185 hemagglutinin Substances 0.000 claims description 80
- 150000007523 nucleic acids Chemical class 0.000 claims description 72
- 108020004707 nucleic acids Proteins 0.000 claims description 60
- 102000039446 nucleic acids Human genes 0.000 claims description 60
- 101000737793 Homo sapiens Cerebellar degeneration-related antigen 1 Proteins 0.000 claims description 59
- 241000700605 Viruses Species 0.000 claims description 53
- 238000000338 in vitro Methods 0.000 claims description 49
- 208000037797 influenza A Diseases 0.000 claims description 49
- 239000013598 vector Substances 0.000 claims description 35
- 150000001413 amino acids Chemical group 0.000 claims description 31
- 238000000034 method Methods 0.000 claims description 31
- 208000015181 infectious disease Diseases 0.000 claims description 23
- 238000006386 neutralization reaction Methods 0.000 claims description 17
- 206010069767 H1N1 influenza Diseases 0.000 claims description 14
- 201000010740 swine influenza Diseases 0.000 claims description 14
- 239000008194 pharmaceutical composition Substances 0.000 claims description 13
- 125000003729 nucleotide group Chemical group 0.000 claims description 12
- 206010064097 avian influenza Diseases 0.000 claims description 11
- 239000002773 nucleotide Substances 0.000 claims description 11
- 239000003085 diluting agent Substances 0.000 claims description 4
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000003306 harvesting Methods 0.000 claims description 2
- 210000004027 cell Anatomy 0.000 description 149
- 241000712461 unidentified influenza virus Species 0.000 description 82
- 241000282414 Homo sapiens Species 0.000 description 54
- 235000001014 amino acid Nutrition 0.000 description 32
- 241000699670 Mus sp. Species 0.000 description 31
- 241000282898 Sus scrofa Species 0.000 description 30
- 241000282412 Homo Species 0.000 description 29
- 101100271175 Oryza sativa subsp. japonica AT10 gene Proteins 0.000 description 26
- 102000004169 proteins and genes Human genes 0.000 description 21
- 108090000623 proteins and genes Proteins 0.000 description 21
- 235000018102 proteins Nutrition 0.000 description 20
- 210000003719 b-lymphocyte Anatomy 0.000 description 18
- 230000037396 body weight Effects 0.000 description 18
- 239000000872 buffer Substances 0.000 description 17
- 241000272525 Anas platyrhynchos Species 0.000 description 16
- 238000003556 assay Methods 0.000 description 15
- 230000000694 effects Effects 0.000 description 15
- 238000002474 experimental method Methods 0.000 description 15
- 230000001681 protective effect Effects 0.000 description 15
- 239000000523 sample Substances 0.000 description 15
- 239000000203 mixture Substances 0.000 description 14
- 238000002198 surface plasmon resonance spectroscopy Methods 0.000 description 14
- 238000011282 treatment Methods 0.000 description 14
- 239000000427 antigen Substances 0.000 description 13
- 102000036639 antigens Human genes 0.000 description 13
- 108091007433 antigens Proteins 0.000 description 13
- 241001122767 Theaceae Species 0.000 description 12
- 238000001727 in vivo Methods 0.000 description 12
- 238000007056 transamidation reaction Methods 0.000 description 12
- 241000271566 Aves Species 0.000 description 11
- 238000006467 substitution reaction Methods 0.000 description 11
- 238000004458 analytical method Methods 0.000 description 10
- 238000011534 incubation Methods 0.000 description 10
- 238000002965 ELISA Methods 0.000 description 9
- 241000287828 Gallus gallus Species 0.000 description 9
- 231100000111 LD50 Toxicity 0.000 description 9
- 235000013330 chicken meat Nutrition 0.000 description 9
- 239000012634 fragment Substances 0.000 description 9
- 230000003993 interaction Effects 0.000 description 9
- 230000001717 pathogenic effect Effects 0.000 description 9
- 229960004641 rituximab Drugs 0.000 description 9
- 241000282326 Felis catus Species 0.000 description 8
- 108091028043 Nucleic acid sequence Proteins 0.000 description 8
- 125000003275 alpha amino acid group Chemical group 0.000 description 8
- 230000001225 therapeutic effect Effects 0.000 description 8
- 108700042778 Antimicrobial Peptides Proteins 0.000 description 7
- 102000044503 Antimicrobial Peptides Human genes 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 7
- 102000012745 Immunoglobulin Subunits Human genes 0.000 description 7
- 108010079585 Immunoglobulin Subunits Proteins 0.000 description 7
- 108010006232 Neuraminidase Proteins 0.000 description 7
- 102000005348 Neuraminidase Human genes 0.000 description 7
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 7
- 235000018417 cysteine Nutrition 0.000 description 7
- 231100000517 death Toxicity 0.000 description 7
- 230000034994 death Effects 0.000 description 7
- 238000005516 engineering process Methods 0.000 description 7
- 230000009385 viral infection Effects 0.000 description 7
- FWBHETKCLVMNFS-UHFFFAOYSA-N 4',6-Diamino-2-phenylindol Chemical compound C1=CC(C(=N)N)=CC=C1C1=CC2=CC=C(C(N)=N)C=C2N1 FWBHETKCLVMNFS-UHFFFAOYSA-N 0.000 description 6
- 208000031648 Body Weight Changes Diseases 0.000 description 6
- 108020004414 DNA Proteins 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 101900159346 Influenza A virus Hemagglutinin Proteins 0.000 description 6
- 241001465754 Metazoa Species 0.000 description 6
- 102000004142 Trypsin Human genes 0.000 description 6
- 108090000631 Trypsin Proteins 0.000 description 6
- 230000004579 body weight change Effects 0.000 description 6
- 230000008878 coupling Effects 0.000 description 6
- 238000010168 coupling process Methods 0.000 description 6
- 238000005859 coupling reaction Methods 0.000 description 6
- VHJLVAABSRFDPM-QWWZWVQMSA-N dithiothreitol Chemical compound SC[C@@H](O)[C@H](O)CS VHJLVAABSRFDPM-QWWZWVQMSA-N 0.000 description 6
- 230000004927 fusion Effects 0.000 description 6
- 239000013642 negative control Substances 0.000 description 6
- 230000009257 reactivity Effects 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 239000012588 trypsin Substances 0.000 description 6
- 241000272517 Anseriformes Species 0.000 description 5
- 102000007999 Nuclear Proteins Human genes 0.000 description 5
- 108010089610 Nuclear Proteins Proteins 0.000 description 5
- 230000000903 blocking effect Effects 0.000 description 5
- 150000001945 cysteines Chemical class 0.000 description 5
- 229940072221 immunoglobulins Drugs 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000006228 supernatant Substances 0.000 description 5
- 230000003612 virological effect Effects 0.000 description 5
- 102100026596 Bcl-2-like protein 1 Human genes 0.000 description 4
- 108010054477 Immunoglobulin Fab Fragments Proteins 0.000 description 4
- 102000001706 Immunoglobulin Fab Fragments Human genes 0.000 description 4
- 241000286209 Phasianidae Species 0.000 description 4
- 206010035664 Pneumonia Diseases 0.000 description 4
- 229920001213 Polysorbate 20 Polymers 0.000 description 4
- 210000000628 antibody-producing cell Anatomy 0.000 description 4
- 239000003443 antiviral agent Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 230000005540 biological transmission Effects 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 description 4
- 238000010494 dissociation reaction Methods 0.000 description 4
- 230000005593 dissociations Effects 0.000 description 4
- 230000002458 infectious effect Effects 0.000 description 4
- 230000001404 mediated effect Effects 0.000 description 4
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 4
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 4
- 239000003910 polypeptide antibiotic agent Substances 0.000 description 4
- 108090000765 processed proteins & peptides Proteins 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 230000004083 survival effect Effects 0.000 description 4
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 3
- UAIUNKRWKOVEES-UHFFFAOYSA-N 3,3',5,5'-tetramethylbenzidine Chemical compound CC1=C(N)C(C)=CC(C=2C=C(C)C(N)=C(C)C=2)=C1 UAIUNKRWKOVEES-UHFFFAOYSA-N 0.000 description 3
- 239000012114 Alexa Fluor 647 Substances 0.000 description 3
- 208000002979 Influenza in Birds Diseases 0.000 description 3
- 241000699666 Mus <mouse, genus> Species 0.000 description 3
- 208000009620 Orthomyxoviridae Infections Diseases 0.000 description 3
- 241000508269 Psidium Species 0.000 description 3
- 108010003723 Single-Domain Antibodies Proteins 0.000 description 3
- 230000010530 Virus Neutralization Effects 0.000 description 3
- 230000000890 antigenic effect Effects 0.000 description 3
- 210000004899 c-terminal region Anatomy 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 239000012228 culture supernatant Substances 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 230000002068 genetic effect Effects 0.000 description 3
- 150000002333 glycines Chemical class 0.000 description 3
- 230000036541 health Effects 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 230000008105 immune reaction Effects 0.000 description 3
- 208000037798 influenza B Diseases 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 238000002955 isolation Methods 0.000 description 3
- 238000011068 loading method Methods 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 210000001806 memory b lymphocyte Anatomy 0.000 description 3
- 239000003068 molecular probe Substances 0.000 description 3
- 230000035772 mutation Effects 0.000 description 3
- -1 penciclovar Chemical compound 0.000 description 3
- 230000003389 potentiating effect Effects 0.000 description 3
- 244000144977 poultry Species 0.000 description 3
- 235000013594 poultry meat Nutrition 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 230000004044 response Effects 0.000 description 3
- 238000002560 therapeutic procedure Methods 0.000 description 3
- NFGXHKASABOEEW-UHFFFAOYSA-N 1-methylethyl 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate Chemical compound COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C NFGXHKASABOEEW-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- IGAZHQIYONOHQN-UHFFFAOYSA-N Alexa Fluor 555 Chemical compound C=12C=CC(=N)C(S(O)(=O)=O)=C2OC2=C(S(O)(=O)=O)C(N)=CC=C2C=1C1=CC=C(C(O)=O)C=C1C(O)=O IGAZHQIYONOHQN-UHFFFAOYSA-N 0.000 description 2
- 102100021631 B-cell lymphoma 6 protein Human genes 0.000 description 2
- 101000741307 Bothrops atrox Batroxicidin Proteins 0.000 description 2
- 101000741308 Bothrops lutzi Lutzicidin Proteins 0.000 description 2
- 241000282472 Canis lupus familiaris Species 0.000 description 2
- 241000283707 Capra Species 0.000 description 2
- 208000017667 Chronic Disease Diseases 0.000 description 2
- 101000741306 Crotalus durissus cascavella Cathelicidin-related peptide isoform 3 Proteins 0.000 description 2
- 101000741303 Crotalus durissus terrificus Crotalicidin Proteins 0.000 description 2
- 239000006144 Dulbecco’s modified Eagle's medium Substances 0.000 description 2
- 241000283086 Equidae Species 0.000 description 2
- 238000012413 Fluorescence activated cell sorting analysis Methods 0.000 description 2
- 206010019233 Headaches Diseases 0.000 description 2
- 101000971234 Homo sapiens B-cell lymphoma 6 protein Proteins 0.000 description 2
- 206010061218 Inflammation Diseases 0.000 description 2
- 102100034349 Integrase Human genes 0.000 description 2
- 102000015696 Interleukins Human genes 0.000 description 2
- 108010063738 Interleukins Proteins 0.000 description 2
- 101000741319 Lachesis muta rhombeata Lachesicidin Proteins 0.000 description 2
- 241000124008 Mammalia Species 0.000 description 2
- 101100381525 Mus musculus Bcl6 gene Proteins 0.000 description 2
- 241000282339 Mustela Species 0.000 description 2
- 208000000112 Myalgia Diseases 0.000 description 2
- 101000933753 Ophiophagus hannah Cathelicidin-related peptide Oh-Cath Proteins 0.000 description 2
- 241000283973 Oryctolagus cuniculus Species 0.000 description 2
- QSLJIVKCVHQPLV-PEMPUTJUSA-N Oxandrin Chemical compound C([C@@H]1CC2)C(=O)OC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@](C)(O)[C@@]2(C)CC1 QSLJIVKCVHQPLV-PEMPUTJUSA-N 0.000 description 2
- 108091093037 Peptide nucleic acid Proteins 0.000 description 2
- 101000932958 Pseudonaja textilis Cathelicidin-related peptide Pt_CRAMP1 Proteins 0.000 description 2
- 101000741290 Pseudonaja textilis Cathelicidin-related peptide Pt_CRAMP2 Proteins 0.000 description 2
- 206010037660 Pyrexia Diseases 0.000 description 2
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 210000001744 T-lymphocyte Anatomy 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 208000036142 Viral infection Diseases 0.000 description 2
- 150000001345 alkine derivatives Chemical class 0.000 description 2
- 125000000539 amino acid group Chemical group 0.000 description 2
- 238000000540 analysis of variance Methods 0.000 description 2
- 239000012491 analyte Substances 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 238000012412 chemical coupling Methods 0.000 description 2
- 238000010367 cloning Methods 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000001010 compromised effect Effects 0.000 description 2
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 239000000539 dimer Substances 0.000 description 2
- 231100000673 dose–response relationship Toxicity 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 241001493065 dsRNA viruses Species 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 238000002523 gelfiltration Methods 0.000 description 2
- 210000004602 germ cell Anatomy 0.000 description 2
- 231100000869 headache Toxicity 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 239000000833 heterodimer Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 230000036039 immunity Effects 0.000 description 2
- 230000016784 immunoglobulin production Effects 0.000 description 2
- 230000004054 inflammatory process Effects 0.000 description 2
- 229960003971 influenza vaccine Drugs 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 108010045069 keyhole-limpet hemocyanin Proteins 0.000 description 2
- 231100000518 lethal Toxicity 0.000 description 2
- 230000001665 lethal effect Effects 0.000 description 2
- 231100000350 mutagenesis Toxicity 0.000 description 2
- 229960001084 peramivir Drugs 0.000 description 2
- XRQDFNLINLXZLB-CKIKVBCHSA-N peramivir Chemical compound CCC(CC)[C@H](NC(C)=O)[C@@H]1[C@H](O)[C@@H](C(O)=O)C[C@H]1NC(N)=N XRQDFNLINLXZLB-CKIKVBCHSA-N 0.000 description 2
- 108010062940 pexiganan Proteins 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920001184 polypeptide Polymers 0.000 description 2
- 102000004196 processed proteins & peptides Human genes 0.000 description 2
- 238000011321 prophylaxis Methods 0.000 description 2
- 230000001177 retroviral effect Effects 0.000 description 2
- 230000001932 seasonal effect Effects 0.000 description 2
- 230000003248 secreting effect Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 150000003568 thioethers Chemical class 0.000 description 2
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 2
- 229960005486 vaccine Drugs 0.000 description 2
- 210000002845 virion Anatomy 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- IVLXQGJVBGMLRR-UHFFFAOYSA-N 2-aminoacetic acid;hydron;chloride Chemical compound Cl.NCC(O)=O IVLXQGJVBGMLRR-UHFFFAOYSA-N 0.000 description 1
- UZOVYGYOLBIAJR-UHFFFAOYSA-N 4-isocyanato-4'-methyldiphenylmethane Chemical compound C1=CC(C)=CC=C1CC1=CC=C(N=C=O)C=C1 UZOVYGYOLBIAJR-UHFFFAOYSA-N 0.000 description 1
- 108010009551 Alamethicin Proteins 0.000 description 1
- 239000012099 Alexa Fluor family Substances 0.000 description 1
- 101800002011 Amphipathic peptide Proteins 0.000 description 1
- 102100022005 B-lymphocyte antigen CD20 Human genes 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 102000017420 CD3 protein, epsilon/gamma/delta subunit Human genes 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 241000282465 Canis Species 0.000 description 1
- 102000053642 Catalytic RNA Human genes 0.000 description 1
- 108090000994 Catalytic RNA Proteins 0.000 description 1
- 108050004290 Cecropin Proteins 0.000 description 1
- 108020004705 Codon Proteins 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- 206010010741 Conjunctivitis Diseases 0.000 description 1
- 206010011224 Cough Diseases 0.000 description 1
- 241000699802 Cricetulus griseus Species 0.000 description 1
- 102000016928 DNA-directed DNA polymerase Human genes 0.000 description 1
- 108010014303 DNA-directed DNA polymerase Proteins 0.000 description 1
- 108010002069 Defensins Proteins 0.000 description 1
- 102000000541 Defensins Human genes 0.000 description 1
- 241000271559 Dromaiidae Species 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 101710091045 Envelope protein Proteins 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Natural products NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 108090000288 Glycoproteins Proteins 0.000 description 1
- 102000003886 Glycoproteins Human genes 0.000 description 1
- 101000897405 Homo sapiens B-lymphocyte antigen CD20 Proteins 0.000 description 1
- 101001014213 Homo sapiens Morphogenetic neuropeptide Proteins 0.000 description 1
- 101710107979 Hydramacin-1 Proteins 0.000 description 1
- XQFRJNBWHJMXHO-RRKCRQDMSA-N IDUR Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(I)=C1 XQFRJNBWHJMXHO-RRKCRQDMSA-N 0.000 description 1
- 206010061598 Immunodeficiency Diseases 0.000 description 1
- 108010067060 Immunoglobulin Variable Region Proteins 0.000 description 1
- 102000017727 Immunoglobulin Variable Region Human genes 0.000 description 1
- 241000134304 Influenza A virus H3N2 Species 0.000 description 1
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical class OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 1
- QNRRHYPPQFELSF-CNYIRLTGSA-N Laninamivir Chemical compound OC[C@@H](O)[C@@H](OC)[C@@H]1OC(C(O)=O)=C[C@H](N=C(N)N)[C@H]1NC(C)=O QNRRHYPPQFELSF-CNYIRLTGSA-N 0.000 description 1
- 229940127388 M2 Protein Inhibitors Drugs 0.000 description 1
- 108010013610 MSI 594 Proteins 0.000 description 1
- 108060003100 Magainin Proteins 0.000 description 1
- 108010036176 Melitten Proteins 0.000 description 1
- 101000931108 Mus musculus DNA (cytosine-5)-methyltransferase 1 Proteins 0.000 description 1
- MQUQNUAYKLCRME-INIZCTEOSA-N N-tosyl-L-phenylalanyl chloromethyl ketone Chemical compound C1=CC(C)=CC=C1S(=O)(=O)N[C@H](C(=O)CCl)CC1=CC=CC=C1 MQUQNUAYKLCRME-INIZCTEOSA-N 0.000 description 1
- 241000272458 Numididae Species 0.000 description 1
- 206010068319 Oropharyngeal pain Diseases 0.000 description 1
- 241000712464 Orthomyxoviridae Species 0.000 description 1
- 108010058846 Ovalbumin Proteins 0.000 description 1
- 101800004819 PGLa Proteins 0.000 description 1
- 241000845082 Panama Species 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 201000007100 Pharyngitis Diseases 0.000 description 1
- 241000283216 Phocidae Species 0.000 description 1
- 206010035226 Plasma cell myeloma Diseases 0.000 description 1
- 206010036790 Productive cough Diseases 0.000 description 1
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Chemical class OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 101710188315 Protein X Proteins 0.000 description 1
- 108010092799 RNA-directed DNA polymerase Proteins 0.000 description 1
- 206010057190 Respiratory tract infections Diseases 0.000 description 1
- IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical compound N1=C(C(=O)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 IWUCXVSUMQZMFG-AFCXAGJDSA-N 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 108010071390 Serum Albumin Proteins 0.000 description 1
- 102000007562 Serum Albumin Human genes 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- 239000012505 Superdex™ Substances 0.000 description 1
- 108010078233 Thymalfasin Proteins 0.000 description 1
- 206010046306 Upper respiratory tract infection Diseases 0.000 description 1
- 229960004150 aciclovir Drugs 0.000 description 1
- MKUXAQIIEYXACX-UHFFFAOYSA-N aciclovir Chemical compound N1C(N)=NC(=O)C2=C1N(COCCO)C=N2 MKUXAQIIEYXACX-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- LGHSQOCGTJHDIL-UTXLBGCNSA-N alamethicin Chemical compound N([C@@H](C)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@H](C(=O)NC(C)(C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)NC(C)(C)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](C(C)C)C(=O)NC(C)(C)C(=O)NC(C)(C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](CO)CC=1C=CC=CC=1)C(C)C)C(=O)C(C)(C)NC(=O)[C@@H]1CCCN1C(=O)C(C)(C)NC(C)=O LGHSQOCGTJHDIL-UTXLBGCNSA-N 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229960003805 amantadine Drugs 0.000 description 1
- DKNWSYNQZKUICI-UHFFFAOYSA-N amantadine Chemical compound C1C(C2)CC3CC2CC1(N)C3 DKNWSYNQZKUICI-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000000840 anti-viral effect Effects 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 239000000611 antibody drug conjugate Substances 0.000 description 1
- 229940049595 antibody-drug conjugate Drugs 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- HQMRIBYCTLBDAK-UHFFFAOYSA-M bis(2-methylpropyl)alumanylium;chloride Chemical compound CC(C)C[Al](Cl)CC(C)C HQMRIBYCTLBDAK-UHFFFAOYSA-M 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 208000030303 breathing problems Diseases 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 108060001132 cathelicidin Proteins 0.000 description 1
- POIUWJQBRNEFGX-XAMSXPGMSA-N cathelicidin Chemical compound C([C@@H](C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(O)=O)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CC(C)C)C1=CC=CC=C1 POIUWJQBRNEFGX-XAMSXPGMSA-N 0.000 description 1
- 102000014509 cathelicidin Human genes 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 239000013553 cell monolayer Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000013599 cloning vector Substances 0.000 description 1
- 239000002299 complementary DNA Substances 0.000 description 1
- 238000004590 computer program Methods 0.000 description 1
- 230000009260 cross reactivity Effects 0.000 description 1
- 210000004748 cultured cell Anatomy 0.000 description 1
- 229940127089 cytotoxic agent Drugs 0.000 description 1
- 239000002254 cytotoxic agent Substances 0.000 description 1
- 231100000599 cytotoxic agent Toxicity 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 239000012636 effector Substances 0.000 description 1
- 230000002121 endocytic effect Effects 0.000 description 1
- 210000001163 endosome Anatomy 0.000 description 1
- 239000006167 equilibration buffer Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 206010016256 fatigue Diseases 0.000 description 1
- MHMNJMPURVTYEJ-UHFFFAOYSA-N fluorescein-5-isothiocyanate Chemical compound O1C(=O)C2=CC(N=C=S)=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 MHMNJMPURVTYEJ-UHFFFAOYSA-N 0.000 description 1
- 238000001943 fluorescence-activated cell sorting Methods 0.000 description 1
- 238000001641 gel filtration chromatography Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 229960004716 idoxuridine Drugs 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 230000002519 immonomodulatory effect Effects 0.000 description 1
- 230000002163 immunogen Effects 0.000 description 1
- 230000009851 immunogenic response Effects 0.000 description 1
- 230000005847 immunogenicity Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- USSYUMHVHQSYNA-SLDJZXPVSA-N indolicidin Chemical compound CC[C@H](C)[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(N)=O)CC1=CNC2=CC=CC=C12 USSYUMHVHQSYNA-SLDJZXPVSA-N 0.000 description 1
- 230000015788 innate immune response Effects 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 229960001627 lamivudine Drugs 0.000 description 1
- JTEGQNOMFQHVDC-NKWVEPMBSA-N lamivudine Chemical compound O=C1N=C(N)C=CN1[C@H]1O[C@@H](CO)SC1 JTEGQNOMFQHVDC-NKWVEPMBSA-N 0.000 description 1
- 229950004244 laninamivir Drugs 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 231100000225 lethality Toxicity 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- VDXZNPDIRNWWCW-UHFFFAOYSA-N melitten Chemical compound NCC(=O)NC(C(C)CC)C(=O)NCC(=O)NC(C)C(=O)NC(C(C)C)C(=O)NC(CC(C)C)C(=O)NC(CCCCN)C(=O)NC(C(C)C)C(=O)NC(CC(C)C)C(=O)NC(C(C)O)C(=O)NC(C(C)O)C(=O)NCC(=O)NC(CC(C)C)C(=O)N1CCCC1C(=O)NC(C)C(=O)NC(CC(C)C)C(=O)NC(C(C)CC)C(=O)NC(CO)C(=O)NC(C(=O)NC(C(C)CC)C(=O)NC(CCCCN)C(=O)NC(CCCNC(N)=N)C(=O)NC(CCCCN)C(=O)NC(CCCNC(N)=N)C(=O)NC(CCC(N)=O)C(=O)NC(CCC(N)=O)C(N)=O)CC1=CNC2=CC=CC=C12 VDXZNPDIRNWWCW-UHFFFAOYSA-N 0.000 description 1
- 230000001576 membenolytic effect Effects 0.000 description 1
- 244000000010 microbial pathogen Species 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000003032 molecular docking Methods 0.000 description 1
- 238000010172 mouse model Methods 0.000 description 1
- 229940126619 mouse monoclonal antibody Drugs 0.000 description 1
- 238000002887 multiple sequence alignment Methods 0.000 description 1
- 208000013465 muscle pain Diseases 0.000 description 1
- 238000002703 mutagenesis Methods 0.000 description 1
- 201000000050 myeloid neoplasm Diseases 0.000 description 1
- JCJAEDXFONBNIP-PTPTXAFISA-N n-[4-[2-[(2r,3r,4r,5s,6r)-3-acetamido-5-[(2s,3r,4r,5r,6r)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]phenyl]-2,2,2-trifluoroacetamide Chemical compound O([C@H]1[C@@H](CO)O[C@H]([C@@H]([C@H]1O)O)O[C@H]1[C@H](O)[C@H]([C@@H](O[C@@H]1CO)OCCC=1C=CC(NC(=O)C(F)(F)F)=CC=1)NC(=O)C)[C@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O JCJAEDXFONBNIP-PTPTXAFISA-N 0.000 description 1
- 201000009240 nasopharyngitis Diseases 0.000 description 1
- 230000009871 nonspecific binding Effects 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- VSZGPKBBMSAYNT-RRFJBIMHSA-N oseltamivir Chemical compound CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1 VSZGPKBBMSAYNT-RRFJBIMHSA-N 0.000 description 1
- 229960003752 oseltamivir Drugs 0.000 description 1
- 229940092253 ovalbumin Drugs 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- KGZGFSNZWHMDGZ-KAYYGGFYSA-N pexiganan Chemical compound C([C@H](NC(=O)[C@H](CCCCN)NC(=O)CNC(=O)[C@@H](NC(=O)CN)[C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(N)=O)C1=CC=CC=C1 KGZGFSNZWHMDGZ-KAYYGGFYSA-N 0.000 description 1
- 229950001731 pexiganan Drugs 0.000 description 1
- 239000013641 positive control Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 238000000159 protein binding assay Methods 0.000 description 1
- 238000002708 random mutagenesis Methods 0.000 description 1
- 239000011535 reaction buffer Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 239000012557 regeneration buffer Substances 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
- 208000020029 respiratory tract infectious disease Diseases 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229960000329 ribavirin Drugs 0.000 description 1
- HZCAHMRRMINHDJ-DBRKOABJSA-N ribavirin Natural products O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1N=CN=C1 HZCAHMRRMINHDJ-DBRKOABJSA-N 0.000 description 1
- 108091092562 ribozyme Proteins 0.000 description 1
- 108700022109 ropocamptide Proteins 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000013207 serial dilution Methods 0.000 description 1
- 125000005629 sialic acid group Chemical group 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000002741 site-directed mutagenesis Methods 0.000 description 1
- 230000000392 somatic effect Effects 0.000 description 1
- 210000003802 sputum Anatomy 0.000 description 1
- 208000024794 sputum Diseases 0.000 description 1
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- NZVYCXVTEHPMHE-ZSUJOUNUSA-N thymalfasin Chemical compound CC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O NZVYCXVTEHPMHE-ZSUJOUNUSA-N 0.000 description 1
- 229960004231 thymalfasin Drugs 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 238000001890 transfection Methods 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 239000004474 valine Substances 0.000 description 1
- 230000007482 viral spreading Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229960001028 zanamivir Drugs 0.000 description 1
- ARAIBEBZBOPLMB-UFGQHTETSA-N zanamivir Chemical compound CC(=O)N[C@@H]1[C@@H](N=C(N)N)C=C(C(O)=O)O[C@H]1[C@H](O)[C@H](O)CO ARAIBEBZBOPLMB-UFGQHTETSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/08—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from viruses
- C07K16/10—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from viruses from RNA viruses
- C07K16/1018—Orthomyxoviridae, e.g. influenza virus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P21/00—Preparation of peptides or proteins
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/569—Immunoassay; Biospecific binding assay; Materials therefor for microorganisms, e.g. protozoa, bacteria, viruses
- G01N33/56983—Viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/21—Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/31—Immunoglobulins specific features characterized by aspects of specificity or valency multispecific
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/33—Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
- C07K2317/565—Complementarity determining region [CDR]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
- C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/005—Assays involving biological materials from specific organisms or of a specific nature from viruses
- G01N2333/08—RNA viruses
- G01N2333/11—Orthomyxoviridae, e.g. influenza virus
Definitions
- the invention relates to the fields of biology, immunology and medicine.
- the invention relates to influenza A virus specific antibodies.
- Influenza is an infectious disease of birds and mammals that can be caused by three types of influenza viruses, types A, B and C.
- Influenza viruses are RNA viruses belonging to the family of Orthomyxoviridae.
- Influenza viruses are RNA viruses consisting of seven negative single-stranded RNA-segments encoding nine proteins (influenza Q, or eight negative single-stranded RNA-segments encoding eleven proteins (influenza A and B).
- Influenza viruses infect millions of people every year. Symptoms of influenza include symptoms comparable with the common cold, such as fever, headache, chills, muscle pains and soar throat. However, influenza can also lead to life-threatening complications, such as pneumonia, and death, in high- risk groups such as young children, the elderly, and immune compromised or chronically ill individuals.
- influenza A virus can be subdivided into different types based on envelope protein expression.
- HA hemagglutinin
- N1-N9 9 neuraminidase serotypes
- H1N1 hemagglutinin
- HA hemagglutinin
- NA neuraminidase
- H1N1 neuraminidase
- HA consists of two subunits, HAl and HA2, linked by disulphide bonds.
- HA must be cleaved by host proteases to yield the two polypeptides HAl and HA2 in order to be infectious.
- the major part of HAl forms the globular head region of HA and HA2 mainly forms the stem region of HA.
- HA is needed for host cell entry. Following cleavage, the exposed N-terminus of the HA2 polypeptide acts to mediate fusion of the viral membrane with the host cell membrane, allowing the virus to infect the host cell. NA is needed for the release of new virions. NA catalyses the hydrolysis of terminal sialic acid residues of glycoproteins of the host cell, thereby preventing binding of HA to these proteins. NA thus facilitates release of the virus from a cell and consequently spreading of the virus.
- figure 1 a schematic representation of an influenza virus is shown.
- Influenza virus infections are most prevalent in winter. In annual influenza epidemics 5- 15% of the population are affected with upper respiratory tract infections. Hospitalization and deaths mainly occur in high-risk groups (very young children, elderly, immuno compromised and chronically ill individuals). Annual epidemics are thought to result in between three and five million cases of severe illness and between 250 000 and 500 000 deaths every year around the world, The estimated costs of influenza epidemics to the US economy are 71-167 billion per year, resulting from health care costs and lost productivity. Seasonal influenza vaccines need to be developed each year as a result of antigenic drift of influenza virus.
- influenza genome may induce amino acid substitution(s) that cause antigenic changes in the HA and NA protein, resulting in the escape of immunity of a host. So, even though influenza strains may have high homology, a specific vaccine may not protect against different strains from the same influenza A subtype. In addition, because the newly developed influenza vaccines are based on a prediction of the dominant subtypes for the coming year, the vaccines not always protect against the influenza subtype that actually arises.
- a process called antigenic shift results in the formation of new virus subtypes through combination of HA and NA from different influenza virus subtypes.
- Mutations and genetic mixing of human and avian and/or swine influenza can lead to a pandemic.
- a pandemic can start when three conditions have been met, namely emergence of a disease new to a population, agents that infect humans, causing serious illness, and agents that spread easily and sustainably among humans.
- pandemic influenza outbreaks have occurred, such as the 1889 Asiatic pandemic (H2N8), the 1918 Spanish Flu pandemic (H1N1), the 1957 Asian Flue pandemic (H2N2), the 1968 Hong Kong Flu (H3N2) and the 2009 pandemic (H1N1). These pandemics were responsible for the death of millions of people.
- Antiviral drugs can be effective for the prevention and treatment of influenza. Two classes of antiviral drugs are available: M2 protein inhibitors and Neuramidase inhibitors. However, the number of influenza strains that show resistance against those inhibitors is increasing.
- An alternative approach to prevent and treat influenza infection is the administration of antibodies directed against the influenza proteins.
- Broadly cross- neutralizing antibodies have been described for influenza viruses belonging to phylogenetic group 1 (Throsby et al. PLoS ONE, 2008 & Sui et al. Nature structural & molecular biology, 2009). These antibodies recognize a conserved region in the stem of the HA protein and are capable of treating influenza infection in mice.
- a mouse monoclonal antibody (mAb) has been described that recognizes a conserved epitope in the region containing the receptor binding domain of the HA1 subunit. This antibody neutralizes H1N1, H2N2 and H3N2 influenza viruses (Yoshida et al. PLoS Pathogen. 2009).
- escape mutants have been reported to arise.
- This antibody is a mouse antibody which has the disadvantage of possible side effects when used in humans.
- WO 2009/115972 discloses a human monoclonal antibody having neutralizing activity against H1N1 and H3N2.
- neutralizing activity against both H1N1 and H3N2 is inefficient, with IC50 values of around 10 g/ml.
- FI6 a human antibody, FI6, is described that neutralizes H5N1 (group 1) and H7N1 (group 2) pseudotyped influenza viruses and H1N1 and H3N2 infectious viruses. Again, neutralizing activity against both infectious viruses is inefficient, with IC50 values between 2 and 12.5 Human antibodies disclosed in
- WO 2010/130636 have H3 and H7 cross-binding activity.
- H3 and H7 are both group 2 influenza viruses. Some of these antibodies are, in addition, capable of binding Hi (group 1). However, none of these antibodies was capable of neutralizing influenza viruses of both group 1 and group 2. As a result, a cocktail of antibodies is necessary for the neutralization of both group 1 and group 2 influenza subtypes.
- the H3N2 neutralizing activity of antibodies capable of neutralizing both H3 and H7 influenza virus subtypes is above 1 ig/ml. It is for instance shown in the Examples and Table 7 that antibody CR8020, described in WO 2010/130636, has an inefficient neutralizing activity against H3N2 A/swine/Neth/St. Oedenrode/96, with an IC50 value of more than 15 pg/ml. For these reasons, there is a need for additional influenza A virus antibodies and therapies against influenza A virus infection.
- antibodies are provided that have a high influenza virus neutralizing activity.
- antibodies are provided which are capable of neutralizing at least two influenza virus subtypes.
- the present invention provides such antibodies specific for multiple influenza A virus subtypes. As demonstrated in the Examples, antibodies are provided that are capable of binding at least two influenza A virus subtypes, preferably both group 1 and group 2 influenza A virus subtypes. Furthermore, antibodies are provided that have a high influenza A virus neutralizing capacity.
- the invention provides in one embodiment an isolated, synthetic or recombinant antibody or functional part thereof or immunoglobulin chain or functional equivalent thereof, having an in vitro H3N2 influenza A virus neutralizing activity with an IC50 value of less than 1 ⁇ /ml, preferably of less than 0.7 ⁇ g/ml, more preferably of equal to or less than 0.3 more preferably of less than 0.2 g/ml, which antibody or functional part or immunoglobulin chain or functional equivalent is capable of specifically binding at least one other influenza A virus subtype.
- Said H3N2 influenza A virus preferably comprises a H3N2 A/Ned/177/2008, H3N2 HKX-31 or H3N2 A/swine/Neth/St.Oedenrode/96 strain, most preferably a H3N2 A/Ned/177/2008 strain.
- H3N2 influenza virus is one of the influenza viruses capable of infecting humans. H3N2 can be transferred from human to other humans. Antibodies capable of neutralizing H3N2 influenza virus are therefore particularly important for application in humans.
- the invention provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, having an in vitro H7N1 influenza A virus neutralizing activity with an IC50 value of less than 5,0 g/ml, preferably of less than 4.0 ⁇ /ml, more preferably of less than 1.0 ⁇ 3 ⁇ 4/ ⁇ 1, more preferably equal to or less than about 0.6
- Said H7N1 influenza A virus preferably comprises a H7N1
- said antibody or functional part or immunoglobulin chain or functional equivalent is also capable of specifically binding at least one other influenza A virus subtype, so that protection against multiple strains can be obtained.
- the invention provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, having an in vitro H7N7 influenza A virus neutralizing activity with an IC50 value of less than 0.5 ⁇ ml, preferably equal to or less than about 0.4 ⁇ g/ml, more preferably equal to or less than about 0.2 ⁇ /ml, most preferably equal to or less than about 0.1 ⁇ g/ml.
- Said H7N7 influenza A virus preferably comprises a H7N7 A/ck/Neth/621557/03 strain.
- said antibody or functional part or immunoglobulin chain or functional equivalent is also capable of specifically binding at least one other influenza A virus subtype, so that protection against multiple strains can be obtained.
- H7N7 influenza virus is one of the influenza viruses capable of infecting humans following bird to human transmission. Antibodies capable of neutralizing H7N7 influenza virus are therefore particularly important for application in humans,
- the invention provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, having an in vitro H1N1 influenza A virus neutralizing activity with an IC50 value of less than 5.0 ⁇ /ml, preferably of less than 4.0 ug/ml, more preferably of less than 3.0 ⁇ g/ml, more preferably equal to or less than about 2.7 ⁇ g/ml.
- Said H1N1 influenza A virus preferably comprises a H1N1
- H1N1 influenza virus is one of the influenza viruses capable of infecting humans following human to human transmission. Antibodies capable of neutralizing H1N1 influenza virus are therefore particularly important for
- the invention provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, having an in vitro H5N1 influenza A virus neutralizing activity with an IC50 value of ' less than 5.0 g ml, preferably of less than 4.0 ⁇ g/ml, more preferably of less than 3.0 more preferably of less than 2.0 ⁇ ig/ml, more preferably equal to or less than about 1.3 ⁇ g/ml.
- Said H5N1 influenza A virus preferably comprises a H5N1 A/turkey/Turkey/05 strain.
- said antibody or functional part or immunoglobulin chain or functional equivalent is also capable of specifically binding at least one other influenza A virus subtype, so that protection against multiple strains can be obtained.
- H5N1 influenza virus is one of the influenza viruses capable of infecting humans following human to human transmission. Antibodies capable of neutralizing H5N1 influenza virus are therefore particularly important for application in humans.
- a “functional part of an antibody” is defined herein as a part that has at least one shared property as said antibody in kind, not necessarily in amount. Said functional part is capable of binding the same antigen as said antibody, albeit not necessarily to the same extent.
- a functional part of an antibody preferably comprises a single domain antibody, a single chain antibody, a nanobody, an unibody, a single chain variable fragment (scFv), a Fab fragment or a F(ab')2 fragment.
- a functional part of an antibody is also produced by altering an antibody such that at least one property - preferably an antigen-binding property - of the resulting compound is essentially the same in kind, not necessarily in amount. This is done in many ways, for instance through conservative amino acid substitution, whereby an amino acid residue is substituted by another residue with generally similar properties (size, hydrophobicity, etc), such that the overall functioning is not seriously affected.
- a "functional equivalent of an immunoglobulin chain” is defined herein as an artificial binding compound, comprising at least one CDR sequence of an immunoglobulin chain.
- Neutralizing activity as used herein is defined as the inhibition or reduction of an influenza virus' capacity of infecting a host cell. Neutralizing activity can be measured by any method known in the art. One of such methods is detailed in the Examples of this application and involves the prevention of influenza infection of cultured cells by monoclonal antibodies. In this method, influenza virus is mixed with an antibody and after 1 hour of incubation added to cells. After 24 hours influenza infection of the cells can be measured by the detection of expression of the nuclear protein of influenza in the target cells. Potent antibodies will prevent or reduce influenza infection and subsequent influenza nuclear protein expression in the target cell. "IC50" is a term well known in the art and refers herein to the concentration of influenza A neutralizing antibody necessary to inhibit or reduce influenza A virus infectivity of host cells by half.
- a "group 2 subtype influenza A virus” is an influenza A virus having a HA serotype of group 2 influenza A viruses.
- viruses having a H3, H4, H7, H10, H14 and H15 serotype are the group 2 influenza A viruses.
- a "group 1 subtype influenza A virus” is an influenza A virus having a HA serotype of group 1 influenza A viruses.
- viruses having a HI, H2, H5, H6, H8, H9, Hl l, H12, H13 and H16 serotype are the group 1 influenza A viruses.
- binding refers to the interaction between an antibody and its epitope, indicating that said antibody preferentially binds to said epitope.
- the antibody may non-specifically bind to other antigens or amino acid sequences, the binding affinity of said antibody for its epitope is significantly higher than the non-specific binding affinity of said antibody for any other antigen or amino acid sequence.
- An 'influenza A virus subtype refers to different influenza
- a viruses for example H1N1, H1N2, H1N7, H2N2, H3N2, H3N8, H4N8, H5N1, H5N2, H5N9, H6N2, H6N5, H7N2, H7N3, H7N7, H8N4, H9N2, H10N7, H11N6, H12N5 or H13N6.
- An "influenza A virus strain” as used herein refers to different influenza A viruses belonging to the same subtype, for example H3N2 A/Ned/177/2008, H3N2 A/Wyoming/03/2003 and H3N2 A/Panama/2007/99.
- antibody Isolated, synthetic or recombinant antibodies or functional parts thereof or immunoglobulin chains or functional equivalents thereof according to the present invention are herein also referred to as "antibody according to the invention".
- Preferred influenza A neutralizing antibodies according to the invention are AT10_0Q4, AT10J302 and AT10J3Q1, because these antibodies have been demonstrated to have particularly desired cross-binding and/or neutralizing characteristics.
- AT10__004, AT10 pain002 and AT10_001 have heavy chain sequences of SEQ ID NO's:31, 33 and 34 as depicted in table 1, respectively, and light chain sequences of SEQ ID NO's:36, 38 and 39 as depicted in table 1, respectively.
- the heavy and light chain CDR sequences of these preferred antibodies are also depicted in table 1.
- SEQ ID NO's: l, 3 and 4 are the heavy chain CDR1 sequences of antibodies AT10_004, AT10J)02 and AT10 abuse001 respectively
- SEQ ID NO's:6, 8 and 9 are the heavy chain CDR2 sequences of these antibodies
- SEQ ID NQ's: l l, 13 and 14 are the heavy chain CDR3 sequences of these antibodies.
- SEQ ID NO's: 16, 18 and 19 are the light chain CDR1 sequences of antibodies AT10_004, AT10_0Q2 and AT10_001 respectively
- SEQ ID NO's:21, 23 and 24 are the light chain CDR2 sequences of these antibodies
- SEQ ID NO's:26, 28 and 29 are the light chain CDR3 sequences of these antibodies.
- Antibody AT10_.0O4 is a preferred antibody because it is capable of specifically binding both group 1 and group 2 influenza A viruses. As shown in the Examples, antibody AT1Q_004 has cross-binding activity to at least HI, H3 and H7 subtype influenza A viruses. AT10_004 is capable of binding to a wide variety of recombinant HA subtypes and influenza A viruses.
- Antibody AT10_004 is furthermore preferred because, in addition to recognizing HA of human influenza viruses and human influenza virus infected cells, it is also capable of recognizing cells infected with several influenza viruses infecting non-human animals, namely cells infected with turkey H5N1
- Antibody AT10J304 is also preferred because it has a high neutralizing activity for H3N2 viruses, having an in vitro H3N2 A/Ned/177/2008 neutralizing activity with an IC50 value of about 0.17 ⁇ g/ml, and having an in vitro H3N2 A/swine/Neth/St. Oedenrode/96 neutralizing activity with an IC50 value of about 2.3 ⁇ ig/ml, and even having an in vitro H3N2 HKX-31 neutralizing activity with an IC50 value of about 0.017 AT10J304 also has protective activity against H3N2 virus (influenza A/HKx-31) in vivo. Antibody AT10_ .
- H7N1 furthermore has a particularly high neutralizing activity for H7N1 viruses, having an in vitro H7N1 A/ck/Italy/1067/99 neutralizing activity with an IC50 value of about 0.6 ⁇ %/ ⁇ , As shown in Table 7, the protective effect of antibody AT10_ 0Q4 against H7N1
- a ck/Italy/1067/99 is even higher, meaning that a lower IC50 value is obtained, as compared to the protective effect of antibody AT10_004 against
- Antibody AT10J)04 furthermore has a particularly high neutralizing activity for H7N7 viruses, having an in vitro
- Antibody AT10_004 is further preferred because it binds to an epitope in the conserved stem region of the HA protein. Because limited variation is present in this region, an antibody of which the epitope is located in the stem region is capable of binding to a broad range of influenza viruses.
- One embodiment therefore provides an antibody or functional part or immunoglobulin chain or functional equivalent which has heavy chain CDRl, CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences of antibody AT10J304, comprising the sequence of SEQ ID NO: l, SEQ ID NO:6, SEQ ID NO: l l, SEQ ID NO: 16, SEQ ID NO:21 and SEQ ID NO:26, or sequences that are at least 70% identical thereto.
- an antibody or functional part or immunoglobulin chain or functional equivalent comprises heavy chain CDRl, CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences of antibody AT10_002, comprising the sequence of SEQ ID NO:3, SEQ ID NO:8, SEQ ID NO: 13, SEQ ID NO: 18, SEQ ID NO:23 and SEQ ID NO:28 or sequences that are at least 70% identical thereto.
- Antibody AT10_002 is a preferred antibody because it has cross- binding activity to at least H3 and H7 subtype influenza A viruses. AT10_002 is capable of binding to a wide variety of recombinant HA subtypes and influenza A viruses. It is capable of binding at least human influenza H3N2
- Antibody AT10 gar002 is furthermore preferred because, in addition to recognizing HA of human influenza viruses and human influenza virus infected cells, it is also capable of recognizing cells infected with several influenza viruses infecting non-human animals, namely cells infected with swine H3N2
- antibody AT10_002 neutralizes at least one H3 subtype influenza A virus.
- Antibody AT10_002 is further preferred because it has a high neutralizing activity for H3N2 viruses, having an in vitro H3N2 A/Ned/177/2008 neutralizing activity with an IC50 value of about 0.18 ⁇ ig/ml, and having an in vitro
- AT10_002 also has protective activity against H3N2 virus (influenza A/HKx-31) in vivo. As demonstrated in the Example antibody
- Antibody AT10J302 provides the best protective activity of the antibodies tested and is therefore particularly preferred.
- Antibody AT10_002 furthermore has a particularly high neutralizing activity for H7N1 viruses, having an in vitro H7N1
- Antibody AT10_002 furthermore has a particularly high neutralizing activity for H7N7 viruses, having an in vitro H7N7 A/ck/Neth/621557/03 neutralizing activity with an IC50 value of about 0.1
- Antibody AT10_002 is further preferred because it binds to an epitope in the conserved stem region of the HA protein. Because limited variation is present in this region, an antibody of which the epitope is located in the stem region is capable of binding to a broad range of influenza viruses.
- an antibody or functional part or immunoglobulin chain or functional equivalent comprises heavy chain CDR1, CDR2 and CDR3 sequences and light chain CDR1, CDR2 and CDR3 sequences of antibody AT10_001, comprising the sequence of SEQ ID NO:4, SEQ ID NO:9, SEQ ID NO: 14, SEQ ID NO: 19, SEQ ID NO:24 and SEQ ID NO:29 or sequences that are at least 70% identical thereto.
- Antibody AT10_001 is a preferred antibody because it has cross- binding activity to at least H3 and H7 subtype influenza A viruses. AT10_001 is capable of binding to a wide variety of recombinant HA subtypes and influenza A viruses.
- Antibody AT10_001 is furthermore preferred because, in addition to recognizing HA of human influenza viruses and human influenza virus infected cells, it is also capable of recognizing cells infected with several influenza viruses infecting non-human animals, such as cells infected with chicken H7N1 (A/Ch/Italy/1067/1999) and chicken H7N7
- antibody AT10J301 neutralizes at least one H3 subtype influenza A virus.
- Antibody AT10_001 is further preferred because it has a high neutralizing activity for H3N2 viruses, having an in vitro H3N2 A Ned/177/2008 neutralizing activity with an IC50 value of about 0.64 and having an in vitro H3N2 HKX-31 neutralizing activity with an IC50 value of about 2.1 ⁇ g/ml.
- AT10_001 also has protective activity against H3N2 virus (influenza A HKx-31) in vivo.
- Antibody AT10_001 furthermore has a particularly high neutralizing activity for H7N7 viruses, having an in vitro H7N7 A ck/Neth/621557/03 neutralizing activity with an IC50 value of about 0.4
- Antibody AT10_001 is further preferred because binds to an epitope in the conserved stem region of the HA protein. Because limited variation is present in this region, an antibody of which the epitope is located in the stem region is capable of binding to a broad range of influenza viruses.
- an influenza A neutralizing antibody comprises heavy chain CDR1, CDR2 and CDR3 sequences and light chain CDR1, CDR2 and CDR3 sequences that are at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99% identical to the sequences depicted in table 1.
- AT10_004", "AT10_002” and “AT10_001” as used herein encompass all antibodies and functional equivalents with the indicated heavy chain and light chain sequences, for instance isolated and/or purified or recombinantly produced.
- a heavy chain of an antibody is the larger of the two types of chains making up an immunoglobulin molecule.
- a heavy chain comprises constant domains and a variable domain, which variable domain is involved in antigen binding.
- a light chain of an antibody is the smaller of the two types of chains making up an immunoglobulin molecule.
- a light chain comprises a constant domain and a variable domain. The variable domain is often, together with the variable domain of the heavy chain, involved in antigen binding.
- Complementary-determining regions are the hypervariable regions present in heavy chain variable domains and light chain variable domains. In case of whole antibodies, the CDRs of a heavy chain and the connected light chain of an antibody together form the antigen-binding site.
- an immunoglobulin chain or functional equivalent thereof comprising at least one CDR sequence of an immunoglobulin variable domain depicted in table 1 which is specific for and capable of neutralizing influenza A virus.
- an isolated, recombinant or synthetic immunoglobulin chain or functional equivalent thereof comprising at least one CDR sequence of an immunoglobulin variable region depicted in table 1.
- antibodies are provided which comprises at least two CDR's, more preferably at least three CDR's, of the same antibody indicated in table 1.
- At least two or three CDR's of AT10_004, or AT10_003, or AT10_002 or AT10_001 or AT10_005, are jointly present in one antibody or functional part according to the invention.
- a human antibody is provided because the use of a human antibody diminishes the chance of side-effects due to an immunological reaction in a human individual.
- said at least one CDR sequence is optimized, preferably in order to improve binding efficacy or stability. This is for instance done by mutagenesis experiments where after the stability and/or binding efficacy of the resulting compounds are preferably tested and an improved influenza A neutralizing antibody is selected.
- a skilled person is well capable of generating variants comprising at least one altered CDR sequence according to the invention. For instance, conservative amino acid substitution is applied. It is also possible to alter at least one CDR sequence depicted in table 1 in order to generate a variant antibody, or a functional part thereof, with at least one altered property as compared to the original antibody.
- an antibody or functional part is provided comprising a CDR sequence which is at least 70% identical to a CDR sequence as depicted in table 1, so that the favourable binding and neutralizing characteristics of an influenza A neutralizing antibody according to the invention are at least in part maintained or even improved.
- a CDR sequence as depicted in table 1 is preferably altered such that the resulting antibody or functional part comprises at least one improved property, such as for instance an improved binding affinity, selectivity and/or stability, as compared to the original antibody.
- Variant antibodies or functional parts thereof comprising an amino acid sequence which is at least 70% identical to a CDR sequence as depicted in table 1 are therefore also within the scope of the present invention.
- Various methods are available in the art for altering an amino acid sequence, For instance, a heavy chain or light chain sequence with a desired CDR sequence is artificially synthesized.
- a nucleic acid molecule encoding a CDR sequence according to the invention is mutated, for instance using random - or site-directed - mutagenesis.
- framework sequences are for instance optimized by mutating a nucleic acid molecule encoding such framework sequence where after the characteristics of the resulting antibody - or functional part - are preferably tested. This way, it is possible to obtain improved antibodies or functional parts.
- human germline sequences are used for framework regions in antibodies or functional parts thereof or immunoglobulin chains or functional equivalents according to the invention, The use of germline sequences preferably minimizes the risk of
- immunogenicity of said antibodies or functional parts, immunoglobulin chains or functional equivalents because these sequences are less likely to contain somatic alterations which are unique to individuals from which the framework regions are derived, and may cause an immunogenic response when applied to another human individual.
- the invention thus provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof comprising:
- a heavy chain CDR1 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO'si l, 3 and 4, and/or
- a heavy chain CDR2 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's:6, 8 and 9, and/or - a heavy chain CDR3 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's: l l, 13 and 14, and/or
- a light chain CDR1 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's: 16, 18 and 19, and/or
- a light chain CDR2 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's:21, 23 and 24, and/or
- a light chain CDR3 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's:26, 28 and 29.
- said antibody or functional part or immunoglobulin chain or functional equivalent comprises heavy chain CDR1, CDR2 and/or CDR3 sequences and/or light chain CDR1, CDR2 and/or CDR3 sequences that are at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, most preferably 100% identical to these sequences.
- an antibody according to the invention comprises heavy chain CDR1, CDR2 and CDR3 sequences and light chain CDR1, CDR2 and CDR3 sequences of antibody AT10_003, which has a heavy chain sequence of SEQ ID NO: 32 as depicted in table 1, and a light chain sequence of SEQ ID NO: 37 as depicted in table 1.
- SEQ ID NO:2 is the heavy chain CDR1 sequence
- SEQ ID NO:7 is the heavy chain CDR2 sequence
- SEQ ID NO: 12 is the heavy chain CDR3 sequence
- SEQ ID NO: 17 is the light chain CDR1 sequence
- SEQ ID NO:22 is the light chain CDR2 sequence
- SEQ ID NO:27 is the light chain CDR3 sequence of antibody AT10_003.
- Antibody AT10_003 is a preferred antibody because it is capable of specifically binding both group 1 and group 2 influenza A viruses.
- Antibody AT1CL0Q3 has cross- binding activity to at least H3, H5 and H7 subtype influenza A viruses.
- AT10_003 is capable of binding to a wide variety of recombinant HA subtypes and influenza A viruses. It is capable of binding at least human influenza H1N1 (A/Hawaii/31/2007) infected cells and human influenza H3N2 (A/Netherlands/ 177/2008) infected cells, and HA of human influenza H3N2 (A/Wyoming/03/2003, A/Aichi/2/1968 and
- H5N1 A/Vietnam/1203/2004 and A/Thailand/Vietnam
- H7N7 A/Netherlands/219/2003
- H9N2 A/Hong
- Antibody AT10_003 is furthermore preferred because, in addition to recognizing HA of human influenza viruses and human influenza virus infected cells, it is also capable of recognizing cells infected with several influenza viruses infecting non-human animals, such as cells infected with chicken H7N7
- AT10_003 encompass all antibodies and functional equivalents with the AT10_003heavy chain and light chain sequences depicted in table 1, for instance isolated and/or purified or recombinantly produced.
- an immunoglobulin chain or functional equivalent thereof comprising at least one CDR sequence of an immunoglobulin variable domain depicted in table 1 which is specific for influenza A virus and of generating variants comprising at least one altered CDR sequence according to the invention.
- the invention therefore provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof comprising:
- heavy chain CDRl sequence comprising a sequence which is at least 70% identical to SEQ ID NO:2, and/or
- heavy chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 7, and/or
- a heavy chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 12, and/or
- a light chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:22, and/or
- said antibody or functional part or immunoglobulin chain or functional equivalent comprises heavy chain CDRl, CDR2 and/or CDR3 sequences and/or light chain CDRl, CDR2 and/or CDR3 sequences that are at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, most preferably 100% identical to these sequences.
- an antibody according to the invention comprises at least one of heavy chain CDRl , CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences of antibody AT10__005, which has a heavy chain sequence of SEQ ID NO:35 as depicted in table 1, and a light chain sequence of SEQ ID NO:40 as depicted in table 1.
- SEQ ID NO:5 is the heavy chain CDRl sequence, SEQ ID NO:
- SEQ ID NO: 10 is the heavy chain CDR2 sequence
- SEQ ID NO: 15 is the heavy chain CDR3 sequence
- SEQ ID NO:20 is the light chain CDRl sequence
- SEQ ID NO:25 is the light chain CDR2 sequence
- SEQ ID NO: 30 is the light chain CDR3 sequence of antibody AT10_005.
- Antibody AT10_005 is a preferred antibody because it has cross- binding activity to at least HI, H5 and H9 subtype influenza A viruses.
- AT1Q_005 is capable of binding to a wide variety of recombinant HA subtypes and influenza A viruses.
- HlNl A/Neth/602/2009 infected cells
- HA of human influenza HlNl A/California/07/2009, and A/New Caledonia/20/1999
- H5N1 A/Vietnam/1203/2004
- H9N2 A/Hong
- Antibody AT10_005 is furthermore preferred because, in addition to recognizing HA of human influenza viruses and human influenza virus infected cells, it is also capable of recognizing cells infected with several influenza viruses infecting non-human animals, such as cells infected with turkey H5N1
- Antibody AT10 gar005 is also preferred because it has a high neutralizing activity for HlNl viruses, having an in vitro HlNl A/Haw aii/31/2007 neutralizing activity with an IC50 value of about 0.24 ⁇ /ml, and having an in vitro HlNl A/Neth/602/2009 (swine origin) neutralizing activity with an IC50 value of about 2.7 AT10_005 also has protective activity against HlNl in vivo.
- Antibody AT10_005 furthermore has a particularly high neutralizing activity for H5N1 viruses, having an in vitro H5N1 A/turkey/Turkey/05 neutralizing activity with an IC50 value of about 1,3 g/ml.
- Antibody AT10_005 is further preferred because it binds to an epitope in the conserved stem region of the HA protein. Because limited variation is present in this region, an antibody of which the epitope is located in the stem region is capable of binding to a broad range of influenza viruses.
- the term "AT10_005" as used herein encompass all antibodies and functional equivalents with the indicated heavy chain and light chain sequences, for instance isolated and/or purified or
- a skilled person is well capable of producing an immunoglobulin chain or functional equivalent thereof comprising at least one CDR sequence of an immunoglobulin variable domain depicted in table 1 which is specific for influenza A virus and of generating variants comprising at least one altered CDR sequence according to the invention.
- the invention therefore provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof comprising: - a heavy chain CDRl sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 5, and/or
- heavy chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 10, and/or
- heavy chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 15, and/or
- a light chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 25, and/or
- said antibody or functional part or immunoglobulin chain or functional equivalent comprises heavy chain CDRl, CDR2 and/or CDR3 sequences and/or light chain CDRl, CDR2 and/or CDR3 sequences that are at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, most preferably 100% identical to these sequences,
- an antibody according to the invention comprises both the heavy and light chain CDR sequences of one of the above mentioned antibodies.
- antibodies which have heavy chain CDRl, CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences of antibody AT10_003 comprising the sequence of SEQ ID NO:2, SEQ ID NO:7, SEQ ID NO: 12, SEQ ID NO: 17, SEQ ID NO:22 and SEQ ID NO:27, or sequences that are at least 70% identical thereto.
- antibodies which have heavy chain CDR1, CDR2 and CDR3 sequences and light chain CDR1, CDR2 and CDR3 sequences of antibody AT10_002 comprising the sequence of SEQ ID NQ:3, SEQ ID NO:8,
- SEQ ID NO: 13 SEQ ID NO: 18, SEQ ID NO:23 and SEQ ID NO:28, or sequences that are at least 70% identical thereto.
- antibodies which have heavy chain CDR1, CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences of antibody AT10_001 comprising the sequence of SEQ ID NO:4, SEQ ID NO:9,
- SEQ ID NO: 14 SEQ ID NO: 19, SEQ ID NO:24 and SEQ ID NO:29, or sequences that are at least 70% identical thereto.
- antibodies which have heavy chain CDRl, CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences of antibody AT10_005 comprising the sequence of SEQ ID NO:5, SEQ ID NO: 10,
- SEQ ID NO: 15 SEQ ID NO:20, SEQ ID NO:25 and SEQ ID NO:30, or sequences that are at least 70% identical thereto.
- antibodies also encompasses functional parts, immunoglobulin chains or functional equivalents thereof,
- said antibody or functional part or immunoglobulin chain or functional equivalent comprises heavy chain CDRl, CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences that are at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%), more preferably at least 91%, more preferably at least
- an antibody according to the invention comprises a heavy chain sequence and/or light chain sequence, or a sequence which has at least 70% sequence identity thereto, as depicted in table 1. Also provided is therefore an antibody or functional part or immunoglobulin chain or functional equivalent, having a heavy chain sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's:31-35 and/or having a light chain sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's: 36-40, or sequences that are at least at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more
- an antibody according to the invention comprises a heavy chain sequence which is at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90% identical to a sequence selected from the group consisting of SEQ ID NO's:31-35 and/or a light chain sequence which is at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90% identical to a sequence selected from the group consisting of SEQ ID NO's: 36-40.
- an antibody according to the invention comprises a heavy chain sequence which is at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical to a sequence selected from the group consisting of SEQ ID NO's:31-35 and/or a light chain sequence which is at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, most preferably 100% identical to a sequence selected from the group consisting of SEQ ID NO's:36-40.
- an antibody or functional part or immunoglobulin chain or functional equivalent according to the invention preferably comprises a heavy chain as well as a light chain which resemble the heavy and the light chain of the same antibody depicted in table 1.
- an antibody according to the invention comprises a heavy chain sequence of a given antibody, preferably antibody AT10_004, comprising the sequence of SEQ ID NO: 31.
- a light chain sequence of the same antibody preferably AT10_004, comprising the sequence of SEQ ID NO:36, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
- an antibody according to the invention or functional part thereof comprises a heavy chain sequence of antibody AT10_003, comprising the sequence of SEQ ID NO:32 and a light chain sequence of antibody AT10_003, comprising the sequence of SEQ ID NO:37 or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto,
- an antibody according to the invention or functional part thereof comprises a heavy chain sequence of antibody AT10_002, comprising the sequence of SEQ ID NO:33 and the light chain sequence of antibody AT10J302, comprising the sequence of SEQ ID NO:38, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
- an antibody according to the invention or functional part thereof comprises a heavy chain sequence of antibody AT10_001, comprising the sequence of SEQ ID NO:34 and the light chain sequence of antibody AT10_001, comprising the sequence of SEQ ID NO:39, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
- an antibody according to the invention or functional part thereof comprises a heavy chain sequence of antibody AT10_005, comprising the sequence of SEQ ID NO:35, and the light chain sequence of antibody AT10_005, comprising the sequence of SEQ ID NO:40, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
- the invention provides antibodies having an in vitro H3N2 influenza A virus neutralizing activity with an IC50 value of less than 1
- An advantage of such antibodies is that a low dosis of said antibody is needed in order to obtain neutralizing capacity. Therefore, less of said influenza A neutralizing antibody has to be administered to an individual for treatment and/or prevention of an influenza A infection. It is favourable to use an amount as low as possible to achieve a desired effect from both a health care point of view and from an economical point of view. It is preferred to administer to a subject as less as possible of a therapeutic antibody, because this reduces the chance of undesired effects, such as immunological reactions to the antibody. Furthermore, if a lower amount of antibody is used, the cost of treatment of an individual to prevent of counteract influenza infection is reduced.
- antibody AT10_ 001 has an in vitro H3N2 A/Ned/177/2008 virus
- an antibody according to the invention has an in vitro H3N2 influenza A virus
- AT10_004 have in vivo H3N2 neutralizing activity. These antibodies were shown to protect mice against influenza A virus H3N2 HKx-31. All mice receiving antibody AT10_001, AT10_002 or AT10_004 treatment survived a challenge with H3N2 virus, whereas all control mice receiving treatment with a control antibody lost more than 25% of their body weight and had to be removed from the study.
- an antibody according to the invention therefore has in vivo H3N2 neutralization activity, for instance as measured by protective activity against influenza H3N2 infection in a mouse model as described in the Example.
- an influenza A neutralizing antibody according to the invention has said in vitro neutralizing activity as determined in a neutralization assay as described in the examples.
- an influenza A neutralizing antibody according to the invention neutralizes at least one H3N2 influenza virus strain with the indicated neutralizing activity, more preferably at least two, more preferably at least three, more preferably at least four, more preferably at least five different H3N2 influenza virus strains.
- an influenza A neutralizing antibody according to the invention neutralizes at least H3N2 A/Ned/177/2008 influenza virus strain, and/or H3N2 HKx-31, and/or H3N2
- Antibodies provided by the invention are capable of binding at least two different influenza subtypes.
- an antibody is provided that is capable of binding H3N2 and at least one other group 2 influenza A virus subtype.
- an antibody is provided that is capable of binding H1N1 and at least one other group 1 influenza A virus subtype.
- An advantage of such antibodies is that they thus have cross-binding activity, i.e. are capable of binding at least two different influenza A virus subtypes.
- an influenza A neutralizing antibody is provided that is further capable of neutralizing said at least one other group subtype influenza A virus.
- Such antibodies have cross-neutralizing activity, i.e. have neutralizing activity for at least two different influenza A virus subtypes.
- Such antibodies have the advantage that the use of a single antibody allows neutralization of multiple influenza subtypes. Such antibodies thus have broad neutralizing activity.
- an influenza A neutralizing antibody is provided that is capable of binding at least one group 2 subtype influenza A virus and at least one group 1 subtype influenza A virus. In a more preferred embodiment, an influenza A neutralizing antibody is provided that is further capable of neutralizing said at least one group 2 and/or said at least one group 1. subtype influenza A virus.
- An influenza A neutralizing antibody according to the invention capable of specifically binding at least two group 2 influenza A virus subtypes, or at least one group 1 and one group 2 influenza A virus subtype is preferably capable of binding to an epitope within a hemagglutinin protein of an influenza A virus protein that is shared between influenza subtypes.
- said epitope is located in a conserved region of the hemagglutinin protein of influenza A virus.
- H3, H4, H7, H10, H14 and H15 are currently known influenza viruses from group 2.
- Said at least two group 2 subtype influenza A virus subtypes are thus preferably selected from the group consisting of H3, H4, H7, H10, H14 and H15 containing influenza A virus subtypes.
- an antibody according to the invention capable of binding and/or neutralizing a H3N2 influenza A virus and capable of binding a H4, H7, H10, H14 or H15 containing influenza A virus.
- such antibody is capable of binding a H7 containing influenza A virus subtype.
- H7 containing influenza viruses frequently infect poultry. Because humans are in direct contact with infected poultry, there is considerable risk of infection of humans with H7 influenza viruses and mixing of avian H7 and human influenza viruses. Infection of humans with H7 containing influenza virus resulting in death has been reported. Therefore, in a preferred embodiment, the invention provides an influenza A neutralizing antibody capable of binding a H3 and a H7 subtype influenza A virus. Preferably, said antibody is further capable of neutralizing both H3 and H7 subtype influenza A virus.
- HI, H2, H5, H6, H8, H9, Hl l, H12, H13 and H16 are currently known influenza viruses from group 1.
- the above mentioned at least one group 1 subtype influenza A virus is therefore preferably selected from the group consisting of HI, H2, H5, H6, H8, H9, Hl l, H12, H13 and H16 containing influenza A virus subtypes.
- an antibody according to the invention capable of binding and/or neutralizing a H3N2 influenza A virus and capable of binding a HI, H2, H5, H6, H8, H9, Hl l, H12, H13 or H16 containing influenza A virus.
- said at least one group 1 subtype influenza A virus is selected from the group consisting of HI and H5 containing influenza A virus subtypes.
- H1N1 is one of the influenza A viruses capable of infecting humans and generally the seasonal influenza epidemic comprises at least one H1N1 influenza virus.
- H5 containing viruses such as H5N1, H5N3, H5N4 and H5N9, mainly infect birds.
- H5 influenza subtypes can be transferred from birds to human. Infection of humans with H5 influenza subtypes is particularly dangerous because of a risk of life-threatening complications, such as pneumonia, and of death.
- the invention provides an influenza A neutralizing antibody capable of binding and/or neutralizing a H3, a H7 and a HI subtype influenza A virus.
- antibodies according to the invention are capable of binding at least one influenza virus which infects non-human animals, including, but not limited to birds such as chickens, ducks, geese, turkeys, and pheasants, and swine, ferrets, rabbits, cats, dogs and horses.
- Such antibodies can be used to counteract influenza virus infection in said non-human animals, for instance, but not limited to, animals that are kept as livestock or pet.
- humans are in direct contact with such animals, there is considerable risk of infection of humans with influenza viruses that have infected said animals.
- an antibody according to the invention is provided which is capable of binding an influenza A virus subtype that infects non- human animals.
- said antibody is capable of binding an avian and/or swine influenza A virus subtype.
- avian and/or swine influenza A virus subtype include, but are not limited to, H4, H10, H15, H5 and H7 containing influenza viruses such as H4N6, H10N3, H15N8, H7N1, H7N7 and/or H5N1.
- an antibody according to the invention is provided which is capable of binding a H7 subtype influenza A virus. More preferably, an antibody is provided which is capable of neutralizing a H7 subtype influenza A virus.
- such antibody has an in vitro H7N7 (such as A/Ch/Neth/621557/03) and/or H7N1 (such as A/Ch/Italy/1067/99) influenza A virus neutralizing activity.
- said antibody has an in vitro H7N1 and/or H7N7 influenza A virus neutralizing activity with an IC50 value of less than 10 ⁇ /ml, more preferably of less than 5 g/ml, more preferably of less than 4 more preferably of less than 2 ⁇ /ml, more preferably of les more preferably of less than 0.8 ng/ml, more preferably of less than 0.6 eferably of less than 0.5 ⁇ ig/ml, more preferably of less than 0.4 ng/ml, more preferably of less than 0.3 ⁇ g/ml, more preferably of less than 0.2 ⁇ /ml.
- influenza A neutralizing antibody according to the invention has said in vitro neutralizing activity as determined in a neutralization assay as described in the examples.
- an influenza A neutralizing antibody according to the invention neutralizes at least one H7N1 and/or H7N7 influenza virus strain with the indicated neutralizing activity, more preferably at least two, more preferably at least three, more preferably at least four, more preferably at least five different H7N1 and/or H7N7 influenza virvis strains.
- an influenza A neutralizing antibody according to the invention neutralizes at least H7N7 (A/Ch/Neth/621557/03) and/or H7N1 (A Ch/Italy/1067/99).
- a particularly preferred antibody of the invention capable of binding H7 subtype influenza A viruses is AT10_004, which has a heavy chain sequence of SEQ ID NO:31 as depicted in table 1, and a light chain sequence of SEQ ID NO:36 as depicted in table 1.
- Another particularly preferred antibody of the invention capable of binding H7 subtype influenza A viruses is AT10_002, which has a heavy chain sequence of SEQ ID NO:33 as depicted in table 1, and a light chain sequence of SEQ ID NO:38 as depicted in table 1.
- Another particularly preferred antibody of the invention capable of binding H7 subtype influenza A viruses is AT10_001, which has a heavy chain sequence of SEQ ID NO:34 as depicted in table 1, and a light chain sequence of SEQ ID NO:39 as depicted in table 1.
- SEQ ID NO: l is the heavy chain CDRl sequence
- SEQ ID NO:6 is the heavy chain CDR2 sequence
- SEQ ID NO: 11 is the heavy chain CDR3 sequence
- SEQ ID NO: 16 is the light chain CDRl sequence
- SEQ ID NO:21 is the light chain CDR2 sequence
- SEQ ID NO: 26 is the light chain CDR3 sequence of antibody AT10_004.
- SEQ ID NO:3 is the heavy chain CDRl sequence
- SEQ ID NO:8 is the heavy chain CDR2 sequence
- SEQ ID NO: 131 is the heavy chain CDR3 sequence
- SEQ ID NO: 18 is the light chain CDRl sequence
- SEQ ID NO:23 is the light chain CDR2 sequence
- SEQ ID NO:28 is the light chain CDR3 sequence of antibody AT10_002.
- SEQ ID NO:4 is the heavy chain CDRl sequence
- SEQ ID NO:9 is the heavy chain CDR2 sequence
- SEQ ID NO: 14 is the heavy chain CDR3 sequence
- SEQ ID NO: 19 is the light chain CDRl sequence
- SEQ ID NO:24 is the light chain CDR2 sequence
- SEQ ID NO:29 is the light chain CDR3 sequence of antibody AT10_001.
- heavy chain CDR1 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 1, and
- heavy chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:6, and
- heavy chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 11, and
- the invention further provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof comprising:
- a heavy chain CDR1 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:3, and
- heavy chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:8, and
- a heavy chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 13, and
- the invention further provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof comprising: - a heavy chain CDR1 sequence comprising a sequence which is at least 70% identical to SEQ ID NQ:4, and
- heavy chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:9
- said antibody or functional part or immunoglobulin chain or functional equivalent comprises heavy chain CDR1, CDR2 and/or CDR3 sequences and/or light chain CDR1, CDR2 and/or CDR3 sequences that are at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, most preferably 100% identical to these sequences.
- H5 influenza subtypes can infect humans.
- an antibody according to the invention is provided which is capable of binding a H5 subtype influenza A virus. More preferably, an antibody is provided which is capable of neutralizing a H5 subtype influenza A virus.
- an antibody has an in vitro H5N1 (such as A/Turkey/Turkey/04) influenza A virus neutralizing activity.
- said antibody has an in vitro H5N1 influenza A virus neutralizing activity with an IC50 value of less than 10 ng/ml, more preferably of less than 5 more preferably of less than 4 more preferably of less than 3 more preferably of less than 1 ⁇ /ml, more preferably of less than 0.8 ⁇ g/ml, more preferably of less than 0.6 ⁇ /ml, more preferably of less than 0.5 ⁇ g/ml, more preferably of less than 0.4 ⁇ 3 ⁇ 4/ ⁇ 1, more preferably of less than 0.3 ⁇ g/ml, more preferably of less than 0.2 ⁇ /ml.
- an IC50 value of less than 10 ng/ml, more preferably of less than 5 more preferably of less than 4 more preferably of less than 3 more preferably of less than 1 ⁇ /ml, more preferably of less than 0.8 ⁇ g/ml, more preferably of less than 0.6 ⁇ /ml, more preferably of less than 0.5 ⁇ g/m
- influenza A neutralizing antibody according to the invention has said in vitro neutralizing activity as determined in a neutralization assay as described in the examples.
- an influenza A neutralizing antibody according to the invention is provided that neutralizes at least one H5N1 influenza virus strain with the indicated neutralizing activity, more preferably at least two, more preferably at least three, more preferably at least four, more preferably at least five different
- H5N1 influenza virus strains In a preferred embodiment, an influenza A neutralizing antibody according to the invention neutralizes at least H5N1 (A/Turkey/Turkey/04)).
- a particularly preferred antibody according to the invention capable of binding a H5 subtype influenza A virus is AT10_003
- Another particularly preferred antibody according to the invention capable of binding a H5 subtype influenza A virus is AT10_005.
- Antibodies or functional parts having sequences that are at least 70% identical to the CDR sequences of AT10_003 or AT10_005 are therefore preferred for counteracting a H5 subtype influenza A virus.
- An antibody according to the invention is preferably a human antibody.
- the use of human antibodies for prophylaxis and therapy in humans diminishes the chance of side-effects due to an immunological reaction in a human individual against non-human sequences.
- an antibody according to the invention is a humanized antibody. Humanized antibodies are made by incorporating non- human hypervariable domains into human antibodies and therefore immunogenic properties are diminished as compared to fully non-human antibodies.
- an antibody according to the invention is a chimeric antibody. In a chimeric antibody, sequences of interest, such as for instance a binding site of interest, are included into an antibody according to the invention.
- Binding affinity generally refers to the strength of the total sum of the noncovalent interactions between a single binding site of a molecule (e.g., an antibody) and its binding partner (e.g., an antigen). Unless indicated otherwise, as used herein, "binding affinity” refers to intrinsic binding affinity which reflects a 1: 1 interaction between members of a binding pair (e.g., antibody and antigen).
- the affinity can generally be represented by the equilibrium dissociation constant (Kp), which is calculated as the k a to kd ratio, , see, e.g., Chen, Y., et ah, (1999) J, Mol Biol 293: 865-881.
- Kp equilibrium dissociation constant
- Affinity can be measured by common methods known in the art, such as for instance a surface plasmon resonance (SPR) assay such as BiaCore or IBIS-iSPR instrument at IBIS Technologies BV (Hengelo, the
- an antibody according to the invention has a binding affinity for an epitope on the influenza HA protein characterized by a dissociation constant (KD) of at most 100 nM, more preferably at most 50 nM, more preferably at most 25 nM, more preferably at most 10 nM, more preferably at most 5 nM, more preferably at most 2 nM, more preferably at most 1 nM, more preferably at most 0.5 nM, more preferably at most 0.3 nM, more preferably at most 0. 1 nM.
- KD dissociation constant
- the invention further provides an isolated, synthetic or recombinant nucleic acid molecule with a length of at least 15 nucleotides, or a functional equivalent thereof, encoding at least one CDR sequence of an antibody or functional part or immunoglobulin chain or functional equivalent according to the invention.
- a nucleic acid according to the invention has a length of at least 30 nucleotides, more preferably at least 50 nucleotides, more preferably at least 75 nucleotides.
- a nucleic acid according to the invention is for instance isolated from a B-cell which is capable of producing an antibody according to the invention.
- a nucleic acid encoding an antibody according to the invention is provided.
- nucleic acid molecule or functional equivalent thereof As used herein "an isolated, synthetic or recombinant nucleic acid molecule with a length of at least 15 nucleotides, or a functional equivalent thereof, encoding at least one CDR sequence of an antibody or functional part thereof or immunoglobulin chain or functional equivalent thereof according to the invention" is herein also referred to as "a nucleic acid molecule or functional equivalent thereof according to the invention.
- a nucleic acid molecule or nucleic acid sequence of the invention preferably comprises a chain of nucleotides, more preferably DNA and/or RNA.
- a nucleic acid molecule or nucleic acid sequence of the invention comprises other kinds of nucleic acid structures such as for instance a DNA/RNA helix, peptide nucleic acid (PNA), locked nucleic acid (LNA) and/or a ribozyme.
- PNA peptide nucleic acid
- LNA locked nucleic acid
- ribozyme a nucleic acid sequence
- nucleic acid molecule also encompasses a chain comprising non-natural nucleotides, modified nucleotides and/or non-nucleotide building blocks which exhibit the same function as natural nucleotides.
- Nucleic acid sequences encoding preferred heavy chain and light chain CDR's of antibodies AT1Q_004, AT10J)03, AT10_002, AT10J)01 and AT10_005 are depicted in table 1.
- Nucleic acid molecules encoding a heavy or light chain CDR of an antibody according to the invention which differ from the CDR nucleic acid sequences depicted in table 1 but have nucleic acid codons encoding for the same amino acids of said heavy or light chain CDR are also encompassed by the invention.
- Nucleic acid molecules encoding a heavy or light chain CDR of an antibody depicted in table 1 which has been altered, for instance through conservative amino acid substitution, whereby an amino acid residue is substituted by another residue with generally similar properties (size, hydrophobicity, etc), are also encompassed by the invention, as long as the resulting CDR has at least 70% sequence identity with a CDR depicted in table 1.
- a preferred nucleic acid molecule according to the invention comprises: a heavy chain CDR1 encoding sequence which has at least 70% sequence identity to a sequence which is selected from the group consisting of SEQ ID NO's:41-45, and/or a heavy chain CDR2 encoding sequence which has at least 70% sequence identity to a sequence which is selected from the group consisting of SEQ ID NO's:46-50, and/or
- a heavy chain CDR3 encoding sequence which has at least 70% sequence identity to a sequence which is selected from the group consisting of SEQ ID NO's:51-55, and/or
- a light chain CDR1 encoding sequence which has at least 70% sequence identity to a sequence which is selected from the group consisting of SEQ ID NO's: 56-60, and/or
- a light chain CDR3 encoding sequence which has at least 70% sequence identity to a sequence which is selected from the group consisting of SEQ ID NO's:66-70.
- a nucleic acid molecule according to the invention preferably comprises a sequence which has at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 90%, most preferably at least 95% sequence, most preferably 100% identity to said sequences.
- said nucleic acid molecule comprises at least one CDR encoding sequence.
- nucleic acid molecule or functional equivalent thereof comprising a sequence which has at least 70% sequence identity, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 90%, most preferably at least 95%, most preferably 100%o sequence identity to a nucleic acid molecule selected from SEQ ID NO's:41-70, said nucleic acid molecule or functional equivalent having at least 15 nucleotides.
- a nucleic acid molecule or functional equivalent thereof according to the present invention preferably encodes a region which has at least 70% sequence identity to a heavy chain and/or a light chain as depicted in table 1.
- a preferred nucleic acid molecule or a functional equivalent comprises a sequence which has at least 70% sequence identity to a sequence selected from the group consisting of SEQ ID NO's:71-75 and/or a sequence which has at least 70% sequence identity to a sequence selected from the group consisting of SEQ ID NO's:76-80.
- a nucleic acid molecule or a functional equivalent according to the invention comprises a heavy chain encoding sequence as well as a light chain encoding sequence which resemble the heavy and the light chain encoding sequences of the same antibody depicted in table 1.
- a nucleic acid or functional equivalent according to the invention comprises a heavy chain encoding sequence of antibody AT10J304, comprising the sequence of SEQ ID NO:71 and a light chain encoding sequence of antibody AT10cali004, comprising the sequence of SEQ ID NO:76 or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
- a nucleic acid or functional equivalent according to the invention comprises a heavy chain encoding sequence of antibody AT10 hug003, comprising the sequence of SEQ ID NO: 72 and a light chain encoding sequence of antibody AT10_003, comprising the sequence of SEQ ID NO:77, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
- a nucleic acid or functional equivalent according to the invention comprises a heavy chain encoding sequence of antibody AT10_002, comprising the sequence of SEQ ID NO:73 and a light chain encoding sequence of antibody AT10 cramp002, comprising the sequence of SEQ ID NO:78, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
- a nucleic acid or functional equivalent according to the invention comprises a heavy chain encoding sequence of antibody AT10_001, comprising the sequence of SEQ ID NO: 74 and a light chain encoding sequence of antibody ATI 0_001, comprising the sequence of SEQ ID NO:79, or sequences that are at least 70%, preferably at least 75%), more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
- a nucleic acid or functional equivalent according to the invention comprises a heavy chain encoding sequence of antibody AT10_005, comprising the sequence of SEQ ID NO: 75 and a light chain encoding sequence of antibody AT10_005, comprising the sequence of SEQ ID NO:80, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
- the percentage of identity of an amino acid or nucleic acid sequence is defined herein as the percentage of residues in a candidate amino acid or nucleic acid sequence that is identical with the residues in a reference sequence after aligning the two sequences and introducing gaps, if necessary, to achieve the maximum percent identity. Methods and computer programs for the alignment are well known in the art.
- a vector comprising a nucleic acid molecule or sequence or functional equivalent according to the invention As used herein "a vector comprising a nucleic acid sequence or molecule or functional equivalent according to the invention” is also referred to as "a vector according to the invention”. Methods for constructing a vector with a nucleic acid or functional equivalent according to the invention are well known in the art.
- Non-limiting examples of vectors suitable for generating a vector of the invention are retroviral and lentiviral vectors. Such vector is suitable for a variety of applications.
- a vector of the invention comprising a therapeutically beneficial nucleic acid sequence is suitable for prophylactic or therapeutic applications against influenza.
- Administration of such vector to an individual, preferably a human, in need thereof results in expression of said prophylactic or therapeutic nucleic acid sequence in vivo resulting in at least partial treatment or prophylaxis against influenza.
- Said vector can also be used in applications involving in vitro expression of a nucleic acid molecule of interest, for instance for (commercial) production of antibodies or functional equivalents according to the invention.
- an isolated or recombinant cell comprising a nucleic acid molecule or functional equivalent a vector according to the invention.
- a nucleic acid molecule or vector according to the invention is particularly useful for generating antibodies or functional parts, or immunoglobulin chains or functional equivalents, which are specific for influenza A virus HA protein. This is for instance done by introducing such nucleic acid molecule or vector into a cell so that the cell's micleic acid translation machinery will produce the encoded antibodies or functional parts, immunoglobulin chains or functional equivalents.
- This is for instance done by introducing such nucleic acid molecule or vector into a cell so that the cell's micleic acid translation machinery will produce the encoded antibodies or functional parts, immunoglobulin chains or functional equivalents.
- a nucleic acid molecule or vector encoding a heavy and/or light chain according to the invention is expressed in so called producer cells, such as for instance cells of a Chinese hamster ovary (CHO), NSO (a mouse myeloma) or 293(T) cell line, some of which are adapted to commercial antibody production. Proliferation of said producer cells results in a producer cell line capable of producing antibodies according to the invention.
- said producer cell line is suitable for producing antibodies for use in humans.
- said producer cell line is preferably free of pathogenic agents such as pathogenic micro-organisms.
- antibodies consisting of human sequences are generated using at least one nucleic acid molecule or vector according to the invention.
- An isolated or recombinant antibody producing cell capable of producing an antibody according to the invention is therefore also provided.
- An antibody producing cell is defined herein as a cell which is capable of producing and/or secreting antibodies or functional equivalents thereof, and/or which is capable of developing into a cell which is capable of producing and/or secreting antibodies or functional equivalents thereof.
- An antibody producing cell according to the invention is preferably a producer cell which is adapted to commercial antibody production.
- said producer cell is suitable for producing antibodies for use in humans.
- a method for producing an antibody according to the invention comprising providing a cell, preferably an antibody producing cell, with a nucleic acid molecule or functional equivalent or a vector according to the invention, and allowing said cell to translate said nucleic acid molecule or functional equivalent or vector, thereby producing antibodies according to the invention.
- a method according to the invention preferably further comprises a step of harvesting, purifying and/or isolating antibodies according to the invention. Obtained antibodies according to the invention are preferably used in human therapy, optionally after additional purifying, isolation or processing steps.
- an antibody according to the invention is coupled to another moiety to form an antibody-drug conjugate.
- An antibody according to the invention is for instance coupled to an antiviral agent, such as acyclovir, penciclovar, lamivudine, ribavirin, zanamivir, laninamivir, peramivir, idoxuridine, oseltamivir, amantadine, remantidine, maxamine, peramivir, or thymalfasin.
- an antiviral agent refers to any substance that reduces or blocks the function, or growth, of a virus and/or causes destruction of a virus.
- a moiety that is coupled to an antibody according to the invention is an antimicrobial peptide.
- antimicrobial peptide refers to small amphipathic peptides of variable length (typically 6 to 100 amino acids), sequence and structure with activity against microorganisms such as for instance bacteria, protozoa, yeast, fungi and/or virusses.
- Antimicrobial peptides usually act through relatively non- specific mechanisms resulting in membranolytic activity but several antimicrobial peptides can also stimulate the innate immune response.
- said antimicrobial peptide has anti-viral activity.
- Non-limiting examples of suitable antimicrobial peptides are magainins, PGLa, cathelicidins (such as LL-37 and cathelicidin-related antimicrobial peptide (CRAMP)), alamethicin, mellitin and cecropin, hydramacin-1, pexiganan, MSI-78, MSI-843, MSI-594, polyphemusin, human antimicrobial peptide, defensins, protegrins and indolicidin.
- a moiety that is coupled to an antibody according to the invention is an immunomodulatory molecule such as an CDS antibody.
- Such CD3 antibody is capable of binding T cells and, if coupled to an antibody according to the invention, targeting T cells to influenza A virus infected cells.
- Said other moiety for example a cytotoxic agent, is preferably coupled to an antibody according to the invention via a linker such as for instance an acid-labile hydrazone linker, or via a peptide linker like citruline-valine, or through a thioether linkage, or by sortase catalized transamidation, which is described in detail in WO 2010/087994.
- a linker such as for instance an acid-labile hydrazone linker, or via a peptide linker like citruline-valine, or through a thioether linkage, or by sortase catalized transamidation, which is described in detail in WO 2010/087994.
- Sortase catalized transamidation involves engineering of a sortase recognition site (LPETGG) on the heavy chain of an antibody, preferably on the C- terminal part of the heavy chain, and on the moiety to be coupled to said antibody.
- the antibody and the moiety further typically contain a GGGGS sequence and a tag for purification purposes, such as a HIS tag.
- sortase mediated transamidation is performed followed by click chemistry linkage.
- click chemistry linkage typically involves chemical coupling of, for instance, an alkyne-containing reagent and, for instance, an azide- containing reagent which are added by sortase through addition of glycines to the sortase motif on the heavy chain of the antibody and to a sortase motif on the moiety (such as a protein, peptide or antibody) to be coupled to the antibody.
- the invention therefore provides an antibody according to the invention wherein a sortase recognition site (LPETGG) is engineered on the heavy chain of the antibody, preferably on the C-terminal part of the heavy chain, the antibody preferably further containing a GGGGS sequence and a purification tag, such as a HIS tag.
- LPETGG sortase recognition site
- an antibody according to the invention is coupled to another moiety via a thioether linkage.
- one or more cysteines are preferably incorporated into an antibody according to the invention.
- Cysteines contain a thiol group and, therefore, incorporation of one or more cysteines into an antibody according to the invention, or replacement of one or more amino acids by one or more cysteines of an antibody according to the invention, enable coupling of said antibody to another moiety.
- Said one or more cysteines are preferably introduced into an antibody according to the invention at a position where it does not significantly influence folding of said antibody, and does not significantly alter antigen binding or effector function.
- the invention therefore also provides an antibody according to the invention wherein at least one amino acid other than cysteine has been replaced by a cysteine.
- Influenza specific antibodies described herein have different (cross-) binding and neutralizing capacities.
- An antibody according to the invention such as AT10_001, AT10_002, AT10_003, AT10_004 or AT10_005 can be advantageously used in combination with another antibody according to the invention. Such combination provides an even stronger anti-influenza effect.
- an antibody according to the invention is combined with another antibody according to the invention that is capable of binding and/or neutralizing at least one other influenza A subtype.
- Combination of antibodies according to the invention which bind and/or neutralize different influenza A virus subtypes enables counteracting a wider range of influenza A subtypes in a single treatment. Such combination is thus useful in counteracting a broad range of influenza viruses.
- an antibody according to the invention provides a stronger response against an influenza A virus and/or provides a response against a wide range of influenza subtypes.
- the invention provides an influenza A virus bispecific antibody with specificity for at least two different influenza A virus subtypes, preferably at least three influenza A virus subtypes, more preferably at least four influenza A subtypes.
- an “influenza A virus bispecific antibody” as used herein is defined as an antibody capable of simultaneously binding at least two different influenza A virus subtypes, such as two, three or four subtypes, and is also referred to as an "influenza A virus bispecific antibody according to the invention” or a “bispecific antibody according to the invention".
- the term “influenza A virus bispecific antibody” also encompasses functional parts of such influenza A virus bispecific antibody which has retained its capability of binding at least two different influenza A virus subtypes simultaneously, such as bispecific single chain variable fragments (scFv), bispecific Fab fragments and bispecific F(ab')2 fragments.
- a pharmaceutical composition comprising an influenza A virus bispecific antibody according to the invention.
- a bispecific antibody according to the invention comprises two non-identical heavy chain-light chain combinations, thus having two antigen-binding regions which recognize two different influenza A virus subtypes, preferably two different HA subtypes.
- an influenza A virus bispecific antibody comprises a heavy and light chain of an antibody according to the invention as depicted in table 1 and a heavy and light chain of another antibody according to the invention as depicted in table 1.
- Bispecific single chain variable fragments scFv
- bispecific Fab fragments and bispecific F(ab')2 fragments comprise for instance a scFv or Fab or F(ab')2 fragment of an antibody according to the invention and a scFv or Fab or F(ab')2 fragment of another antibody according to the invention.
- an influenza A virus bispecific antibody according to the invention comprises a heavy and light chain of two antibodies selected from the group consisting of AT10_001, ⁇ 10_002, AT10_003, AT10_Q04 and AT10_005 as depicted in table 1, or a scFv or Fab fragment thereof.
- said bispecific antibody comprises a heavy and light chain of antibody AT10_003 or AT10_005, preferably of antibody AT10_005, and a heavy and light chain of an antibody selected from the group consisting of AT10J301, AT10_002 and AT10_004.
- two antibodies according to the invention are coupled to each other or an antibody according to the invention is coupled to a known influenza specific antibody.
- sortase catalized transamidation involves engineering of a sortase recognition site (LPETGG) on the heavy chains of both antibodies to be coupled, preferably on the C-terminal part of the heavy chains.
- the antibodies further typically contain a GGGGS sequence and a purification tag, such as a HIS tag.
- sortase mediated transamidation is preferably performed followed by click chemistry linkage to couple both antibodies via their heavy chains.
- click chemistry linkage involves chemical coupling of, for instance, an alkyne-containing reagent and, for instance, an azide-containing reagent which are added by sortase through addition of glycines to the sortase motif on the heavy chain of a first antibody and to the heavy chain of a second antibody that is to be coupled to the first antibody.
- click chemistry linkage involves chemical coupling of, for instance, an alkyne-containing reagent and, for instance, an azide-containing reagent which are added by sortase through addition of glycines to the sortase motif on the heavy chain of a first antibody and to the heavy chain of a second antibody that is to be coupled to the first antibody.
- One embodiment of the invention therefore provides a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent thereof, comprising:
- At least two antibodies according to the invention are coupled to each other by sortase catalized transamidation, whereby said at least two antibodies are preferably selected from the group consisting of AT10_001, AT10_002, ⁇ 0_003, AT10_004 and AT10_005 as depicted in Table 1.
- One preferred embodiment of the invention therefore provides a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent thereof, comprising:
- a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention comprises the heavy chain CDR1, CDR2 and CDR3 and light chain CDR1, CDR2 and CDR3 sequences of at least two antibodies according to the invention.
- a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent thereof comprising:
- a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention comprises the heavy chain sequence and the light chain sequence of at least two antibodies according to the invention, or sequences that are at least 70% identical thereto.
- the invention thus also provides a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent thereof, comprising:
- Such multimeric antibody, multimeric immunoglobulin or functional equivalent is typically a hetero multimeric complex, comprising at least one heavy chain of one antibody and at least one heavy chain of another antibody.
- the heavy chain of one kind of antibody is paired with the heavy chain of another kind of antibody.
- said hetero multimeric complex comprises two paired heavy chains of one kind of antibody, coupled to two paired heavy chains of another kind of antibody.
- the corresponding light chains of said antibodies are also bound to said paired heavy chains, thus forming two coupled antibodies.
- the term "dimeric antibody” refers to two antibodies that are coupled to each other (wherein each antibody contains two heavy chains and two light chains).
- multimeric antibody refers to at least two, such as for instance two, three, four or five, antibodies that are coupled to each other.
- multimeric immunoglobulin refers to at least two immunoglobulin chains (such as for instance single domain antibodies, single chain antibodies, nanobodies, unibodies or single chain variable fragments (scFv)) that are coupled to each other.
- antibody AT10_003 or AT10_005 is coupled to an antibody selected from the group consisting of AT10_001, AT10_002 and AT10_004 by sortase catalized transamidation.
- Such combination of antibodies is preferred because antibodies AT10_003 and AT10_005 have specificity against at least influenza A virus subtypes HI and H5 and antibodies AT10_001, AT10_002 and AT10_004 have specificity against at least influenza A virus subtypes H3 and H7 and are capable of neutralizing at least H3N2 with high neutralizing capacity. Therefore, such combinations provide activity against a broad range of influenza A virus subtypes.
- antibody AT10_005 is coupled to antibody AT10J)01, ⁇ 0_002 or AT10_004 by sortase catalized transamidation, because antibody AT10_005 is capable of neutralizing at least ⁇ 1 influenza A virus with high neutralizing capacity.
- the invention therefore in one embodiment provides an influenza A virus bispecific antibody according to the invention comprising at least part of the sequence, preferably the heavy and/or light chain, of antibody AT10_003 or antibody AT10_005 as depicted in table 1, preferably of antibody AT10_005, and comprising at least part of the sequence, preferably the heavy and/or light chain, of antibody AT10_001, AT10_002 or AT1Q_004 as depicted in table 1, whereby said part of the sequence preferably comprises at least 70% of the sequence of said antibody, more preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 90%, more preferably at least 95%, more preferably at least 95% of the sequence of said antibody.
- an influenza A virus bispecific antibody according to the invention comprising essentially the whole sequence of antibody AT10_003 or antibody AT10J305 as depicted in table 1, preferably antibody AT10_005, and comprising essentially the whole sequence of antibody AT10_001, AT10_002 or AT10_004 as depicted in table 1 is provided.
- an influenza A virus bispecific antibody according to the invention comprises the heavy chain and the light chain of antibody AT10_003 or of antibody AT10_005 and the heavy chain and the light chain of antibody AT10_001, of antibody AT10_Q02 or of antibody AT10J304.
- said antibodies are coupled by sortase catalized transamidation as herein described.
- antibody AT10J303 is coupled to an antibody selected from the group consisting of ATIOJXU, AT10_002, AT10_004 and AT10_005 by sortase catalized transamidation.
- Such combination of antibodies is preferred because the AT10_003 epitope is located on the HA1 subunit of the HA protein, whereas the binding epitope of antibodies AT10_001, AT10_002, AT10_004 and AT10_005 is, at least partly, located on the HA2 subunit of the protein. Therefore, such combinations target different epitopes within the HA protein and therefore such combination provides a strong response against influenza A virus.
- the invention therefore in one embodiment provides an influenza A virus bispecific antibody according to the invention comprising at least part of the sequence, preferably the heavy and/or light chain, of antibody AT10_003 as depicted in table 1 and comprising at least part of the sequence, preferably the heavy and/or light chain, of antibody AT10_001, AT10_002, AT10 discomfort004 or AT10J)Q5 as depicted in table 1, whereby said part of the sequence preferably comprises at least 70% of the sequence of said antibody, more preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 90%, more preferably at least 95%, more preferably at least 95% of the sequence of said antibody.
- an influenza A virus bispecific antibody comprising essentially the whole sequence of antibody AT10_003 as depicted in table 1, and comprising essentially the whole sequence of antibody AT10_001, AT10_002, AT10_004 or AT10_005 as depicted in table 1 is provided.
- said antibodies are coupled by sortase catalized transamidation as herein described.
- Yet another embodiment of the invention provides a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent thereof, comprising:
- said multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention comprises:
- said multimeric antibody, multimeric immunoglobulin or functional equivalent comprises:
- the heavy chain sequence and the light chain sequence of antibody AT10_002 or sequences that are at least 70%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto; and
- a multimeric antibody or immunoglobulin based on antibodies AT10_002 and AT10_005 provide excellent influenza neutralizing activity, both in vitro and in vivo. Since AT10_002 is capable of neutralizing H3N2 and AT10_005 is capable of neutralizing H1N1, a multimeric antibody or
- immunoglobulin based on antibodies AT10_002 and AT10_005 is particularly suitable for neutralizing both H3N2 and H1N1. Further provided is therefore a method for neutralizing a H1N1 influenza A virus and/or an H3N2 influenza A virus, comprising contacting said H1N1 influenza A virus and/or said H3N2 influenza A virus with a multimeric antibody, multimeric immunoglobulin or functional equivalent comprising at least two, preferably three, different heavy chain CDR sequences and at least two, preferably three, different light chain CDR sequences of antibodies AT10_002 and AT10_005, resulting in neutralization of said virus.
- a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention is a dimeric antibody or dimeric immunoglobulin.
- the invention also encompasses other multimeric antibodies or immunoglobulims, such as for instance trimeric, tetrameric or pentameric antibodies or immunoglobulins.
- an isolated or recombinant cell or a pharmaceutical composition comprising a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention, as well as a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention for use as a medicament and/or prophylactic agent.
- multimeric antibodies or immunoglobulins are particularly suitable for treating and/or preventing and/or alleviating the symptoms of an influenza A infection.
- the invention therefore also provides a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention for use as a medicament and/or prophylactic agent for at least in part treating and/or preventing and/or alleviating the symptoms of an influenza A infection, as well as a method for at least in part treating and/or preventing an influenza A virus infection, comprising administering to an individual in need thereof a therapeutically effective amount of a multimeric antibody, multimeric
- immunoglobulin or functional equivalent according to the invention and/or a cell or pharmaceutical composition comprising a multimeric antibody, multimeric
- a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention is also suitable for use in diagnosis of an influenza A virus. This is for instance done by contacting a sample with a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention and subsequently determining whether influenza A virus is bound to said multimeric antibody, multimeric immunoglobulin or functional equivalent.
- the invention therefore also provides a method for determining whether an influenza A virus is present in a sample comprising:
- a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent thereby determining whether an influenza A virus is present in said sample.
- a major advantage of a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention over a mixture of separately produced antibodies is the fact that for pharmaceutical uses, only one registration procedure is required for a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention, whereas a mixture of antibodies requires multiple registration procedures, usually one procedure for each individual antibody and one separate procedure for such mixture as a whole.
- the use of a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention is therefore more time and cost effective.
- Antibodies according to the invention are capable of counteracting influenza A viruses.
- Antibodies according to the invention are therefore particularly suitable for use as a medicine or prophylactic agent.
- antibodies according to the invention are used which consist of human sequences, in order to reduce the chance of adverse side effects when human individuals are treated, Such human sequences can be isolated from a human or synthetically or recombinantly produced based on the sequence of human antibodies.
- an antibody according to the invention for use as a medicament and/or prophylactic agent.
- a nucleic acid molecule or functional equivalent thereof according to the invention or a vector according to the invention comprising such nucleic acid or functional equivalent for use as a medicament and/or prophylactic agent.
- nucleic acid or functional equivalent according to the invention When a nucleic acid or functional equivalent according to the invention is administered, it will be translated in situ by the host's machinery into an antibody according to the invention.
- Produced antibodies according to the invention are capable of preventing and/or counteracting an influenza A infection.
- Antibodies according to the invention are particularly suitable for use as a medicament because they are (heterosubtype) cross-binding antibodies, capable of binding several influenza A virus subtypes.
- said antibody comprises antibody AT10_004, AT10_003, AT10_002, AT10_001, AT10_005 or a functional part thereof.
- antibody AT10_004 comprising a heavy chain sequence of SEQ ID NO:31 and a light chain sequence of SEQ ID NO:36, for use as a medicament and/or prophylactic agent.
- antibody AT10_003 comprising a heavy chain sequence of SEQ ID NO:32 and a light chain sequence of SEQ ID NO:37, for use as a medicament and/or prophylactic agent.
- antibody AT10 thread002 comprising a heavy chain sequence of SEQ ID NO:33 and a light chain sequence of SEQ ID NO:38, for use as a medicament and/or prophylactic agent.
- antibody AT10_001 comprising a heavy chain sequence of SEQ ID NO:34 and a light chain sequence of SEQ ID NO: 39, for use as a medicament and/or prophylactic agent.
- antibody AT10_005 comprising a heavy chain sequence of SEQ ID NO:35 and a light chain sequence of SEQ ID NO:40, for use as a medicament and/or prophylactic agent.
- said antibody according to the invention for use as a medicament and/or prophylactic agent is selected from the group consisting of
- these antibodies are particularly effective in counteracting influenza.
- the invention provides AT10_002 for use as a medicament and/or prophylactic agent, because this antibody is very effective in counteracting influenza.
- An antibody according to the invention, or a nucleic acid molecule or functional equivalent thereof according to the invention is preferably used for at least in part treating and/or preventing an influenza A virus infection.
- at least in part treating an influenza A virus infection includes counteracting an influenza A virus infection, alleviating symptoms resulting from an influenza A virus infection and/or counteracting inflammation resulting from an influenza A virus infection.
- symptoms resulting from an influenza A virus infection include, but are not limited to, fever, respiratory symptoms such as cough, sore throat, runny or stuffy nose, breathing problems and pneumonia, muscle aches, headache, fatigue and conjunctivitis.
- Preferred antibodies are antibodies AT1CL004, AT10_003, AT10_002, AT10_001 and AT10_005, which have heavy chain and light chain sequences as depicted in table 1.
- the invention further provides a pharmaceutical composition comprising an antibody according to the invention, and/or a bispecific antibody according to the invention, and a pharmaceutical acceptable carrier, diluent and/or excipient.
- a pharmaceutical composition comprising a nucleic acid molecule or functional equivalent according to the invention, or a vector according to the invention comprising such nucleic acid or functional equivalent, and a pharmaceutical acceptable carrier, diluent and/or excipient.
- suitable carriers for instance comprise keyhole limpet haemocyanin (KLH), serum albumin (e.g. BSA or RSA) and ovalbumin.
- said suitable carrier comprises a solution, like for example saline.
- a pharmaceutical composition according to the invention is preferably suitable for human use.
- the invention further provides a method for at least in part treating and/or preventing an influenza A virus infection, comprising administering to an individual in need thereof a therapeutically effective amount of an antibody according to the invention, and/or a bispecific antibody according to the invention, and/or a nucleic acid molecule or functional equivalent thereof according to the invention, and/or a vector according to the invention, and/or a pharmaceutical composition according to the invention.
- an "individual” is a human or an animal, preferably an animal that can be infected by influenza virus, such as birds and mammals.
- Individuals include, but are not limited to, chickens, ducks, geese, turkeys, swans, emus, guinea fowls and pheasants, humans, pigs, ferrets, seals, rabbits, cats, dogs and horses.
- an individual is a human.
- an antibody, a nucleic acid molecule or functional equivalent thereof, a vector, and/or a pharmaceutical composition according to the invention is preferably administered to an individual before an influenza A virus infection has taken place.
- an antibody, a nucleic acid molecule or functional equivalent thereof, a vector, and/or a pharmaceutical composition according to the invention is administered when an individual is already infected. In that case, an influenza A virus infection is counteracted, symptoms resulting from an influenza A virus infection are alleviated and/or inflammation resulting from an influenza A virus infection is counteracted.
- Said antibody or functional equivalent is particularly suitable for administered to individuals with an increased risk of complications, such as hospitalized individuals, for instance infants, individuals with compromised immunity and/or elderly people.
- An antibody, a nucleic acid molecule or functional equivalent thereof, a vector, and/or a pharmaceutical composition according to the invention is preferably administered via one or more injections. Typical doses of administration of an antibody according to the invention or combinations of at least two thereof are between 0.1 and 10 mg per kg body weight.
- antibodies according to the invention are preferably combined with a pharmaceutically acceptable carrier, diluent and/or excipient.
- An antibody according to the invention is also particularly suitable for diagnostic uses. For instance, if an individual, preferably a human, is suspected of suffering from an influenza A virus infection, a sample, such as a saliva, sputum, blood, or tissue sample, can be obtained from said individual. Subsequently, said sample can be tested for the presence of influenza A virus, using an antibody according to the invention. Preferably, said sample is mixed with an antibody according to the invention, which will specifically bind to a HA protein of influenza A virus. The presence of HA proteins of influenza A virus in a sample is indicative for the presence of an influenza A virus infection.
- HA proteins of influenza A virus and/or influenza A virus comprising a HA protein bound to an antibody according to the invention can be isolated from the sample and/or detected using any method known in the art, for example, but not limited to, isolation using magnetic beads, streptavidin- coated beads, or isolation through the use of secondary antibodies immobilized on a column.
- an antibody according to the invention is labeled in order to be able to detect said antibody, for instance, but not limited to, fluorescently labeled, or radioactively labeled.
- an antibody according to the invention is detected using a labeled secondary antibody which is directed against said antibody. If binding of said antibody is detected, HA protein of influenza A virus is present, which is indicative for the presence of an influenza A virus infection.
- the invention thus provides an antibody according to the invention for use in diagnosis of an influenza A virus infection.
- the invention thus further provides a method for determining whether an influenza A virus is present in a sample comprising:
- a method for determining whether an individual is suffering from an influenza A virus infection comprising:
- said individual is suffering from an influenza A virus infection.
- said individual is a human.
- the invention provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, capable of interacting with amino acids at positions A38, A40, A41, A42, A291, A292, A293, A318, B18, B19, B20, B21, B38, B41, B42, B45, B46, B48, B49, B52, B53, and B56 of influenza A virus group 1 hemagglutinin (H1/H5). These are hemagglutinin amino acids that interact with antibody AT10_005. Antibodies, immunoglobulins or functional parts or functional equivalents thereof, capable of specifically interacting with said hemagglutinin amino acids, are therefore herewith provided.
- Yet another embodiment provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, capable of interacting with amino acids at positions A21, A324, A325, A327, B12, B14, B15, B16, B17, B18, B19, B25, B26, B30, B31, B32, B33, B34, B35, B36, B38, B146, B150, B153, and B154 of influenza A virus group 2 hemagglutinin (H3/H7). These are hemagglutinin amino acids that interact with antibody AT10_004. Antibodies, immunoglobulins or functional parts or functional equivalents thereof, capable of specifically interacting with said hemagglutinin amino acids, are therefore herewith provided.
- Yet another embodiment provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, capable of interacting with amino acids at positions A38, A48, A275, A276, A277, A278, A289, A291, A318, B19, B20, B21, B36, B38, B39, B41, B42, B45, B46, B48, B49, B50, B52, B53, B56, B57, B58, B150 of influenza A virus group 2 hemagglutinin (H3/H7). These are hemagglutinin amino acids that interact with antibody AT10_002. Antibodies, immunoglobulins or functional parts or functional equivalents thereof, capable of specifically interacting with said hemagglutinin amino acids, are therefore herewith provided.
- Yet another embodiment provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, capable of competing with AT10_001 or AT10_002 or AT10_003 or AT10_004 or AT10_005 for at least part of the same epitope on influenza A virus hemagglutinin, said antibody, immunoglobulin, functional part or equivalent having at least the same affinity for said influenza A virus hemagglutinin (typically having the same or a lower Km value as compared to AT10_001 or AT10_002 or AT10_003 or AT1CL004 or AT10_005), resulting in a decreased binding between said influenza A virus hemagglutinin and AT10J)G1 or AT10_002 or AT10 compress003 or AT10_004 or AT10_005.
- Said epitope preferably comprises the amino acids at positions A38, A40, A41, A42, A291, A292, A293, A318, B18, B 19, B20, B21, B38, B41, B42, B45, B46, B48, B49, B52, B53 and B56 of influenza A virus hemagglutinin.
- said epitope comprises the amino acids at positions A21, A324, A325, A327, B12, B14, B15, B16, B17, B18, B19, B25, B26, B30, B31, B32, B33, B34, B35, B36, B38, B146, B150, B153, B154 of influenza A virus hemagglutinin.
- said epitope comprises A38, A48, A275, A276, A277, A278,
- FIG. 1 Schematic representation of an influenza virus (Subbarao K. and Joseph T. Nature Reviews Immunology 2007: 7, 267-278).
- FIG. 1 Cell sorting of H3 and H7 binding B cells following incubation of Alexa Fluor 647 labeled Influenza H3 (A/Wyoming/03/2003) and H7 (A/Netherlands/219/2003) HA proteins with Bcl6 and Bcl-xL transduced polyclonal cultured B cells.
- Figure 3. Antibody binding to HA transfected 293T cells. 293T cells were transfected with DNA encoding for the HA of HI (A/New Caledonia/20/199), H3
- MDCK-SIAT cells were infected with Influenza HlNl (A Hawaii/31/2007) and H3N2 (A/Netherlands/177/2008) and incubated with mAb. Antibody binding was detected with anti-human IgG-PE, Figure 5. Antibody binding to virus infected cells. MDCK cells were infected with Influenza HlNl (A/Neth/602/2009), H3N2 (A/Swine/St. Oedenrode/1996), high pathogenic H5N1 (A/Turkey/Turkey/2004), high pathogenic H7N7
- FIG. 6 Antibody competition assay. Labeled antibodies AT10_001, AT10_002 and AT10_004 were tested for binding to H3N2 (A Netherlands/177/2008) infected MDCK- SIAT cells in the presence of non-labeled competitor antibody (A). Labeled AT10_004 was also tested for binding to HlNl (A/Hawaii/31/2007) infected MDCK-SIAT cells in the presence of non-labeled competitor antibody (B). Rituximab (Ritux, CD20 antibody) was used as a negative control. Figure 7. Binding of AT 10 antibodies to different HA conformations by in vitro pH- shift experiment.
- 293T cells were transfected with DNA encoding for the HA of H3 (A/Wisconsin/67/2005), detached from the plastic with Trypsin-EDTA and treated with either 500 mM Dithiothreitol (DTT), PBS pH5, or left untreated. Cells were subsequently incubated with recombinant AT10_001, AT10_002, AT1Q_003 or AT10J304. Antibody binding was detected using anti-human-IgG-PE.
- FIG. Survival (A) and body weight change (B) of C57B1/6J mice challenged intranasally with increasing amounts of influenza A/HKx-31 (H3N2).
- FIG. 9 Survival (A) and body weight change (B,C,D) of mice intravenously injected with 1 or 5 mg/kg antibody AT10_001, AT10_002 or AT10_004 one day before intranasal challenge with 10 Lethal Dose 50 (20,000 TCID50) of influenza A/HKx-31 (H3N2).
- FIG. 10 Survival (A) and body weight change (B) of mice intravenously injected with 15 mg/kg antibody AT10_002 one day before intranasal challenge or 2, 3 or 4 days post intranasal challenge with 10 Lethal Dose 50 (20,000 TCID50) of influenza A/HKx-31 (H3N2)
- FIG. 11 SPR plot showing the dual specificity of BiFlu for H3 and HI and the presence of both kappa and lambda light chain on BiFlu.
- Antibodies AT10_002 (lambda light chain), AT10_005 (kappa light chain) and BiFlu (contains AT10_002 and AT10_005) were captured on an anti-IgG (A) or anti-lambda (B) coated sensor chip.
- A anti-IgG
- B anti-lambda
- captured antibodies were tested for their ability to bind hemagglutinin H3 and HI and light chain antibodies directed against kappa and/or lambda.
- An increase in the SPR shift indicates proteins binding to the captured antibodies.
- MDCK-SIAT cells were infected with Influenza H1N1 (A/Haw aii/31/2007) and H3N2 (A/Netherlands/177/2008) and incubated with several concentrations of AT10_002, AT10_005 or BiFlu mAb.
- AT10_002/AT10_005 mix (1 mg/kg for each antibody) or 2 mg/kg BiFlu one day before intranasal challenge with 10 Lethal Dose 50 of H1N1 Influenza A PR/8/34.
- Human memory B cells were immortalized using the BCL6 / Bcl-xL technology described by Kwakkenbos et al. (Generation of stable monoclonal antibody-producing B cell receptor- positive human memory B cells by genetic programming. Nature Medicine (2010) vol. 16 (1) pp. 123-8 and patent application WO 2007/067046).
- human memory B cells from Influenza vaccinated donors were transduced with a retroviral vector containing BCL6 and Bcl-xL.
- Transduced B cells can be maintained in culture with CD40Ligand expressing L-cells and interleukin (IL)-21 (R&D systems).
- HA binding B cells were sorted single cell per well by FACSAria ( Figure 2) and maintained in culture for 2 to 3 weeks before the supernatant of the B cell clones were screened for HA binding by ELISA or binding to H3N2 (A Netherlands/177/2008) infected cells and/or H7 (A/Netherlands/219/2003) transfected HEK cells.
- ii) Cells were seeded in small pools, e.g. 40 cells per well and maintained in culture for 2-3 weeks. The supernatant of these pools was screened for binding to H7 transfected HEK cells. The B cells of the double positive tested wells were seeded 1 cell per well. The culture supernatant of these monoclonal B cell lines was used to screen for HA binding by ELISA.
- 293T cells were transfected with different full length HA constructs. Using Fugene (Roche) 293T cells were transfected with DNA encoding the HA of HI (A/New
- AT10_003 and AT10J304 showed binding to all human group 2 HA proteins.
- AT10_001, AT1CLQ03 and AT10_004 also showed reactivity to Swine H4N6
- AT10_002 and AT10_003 recognized Duck H10N3 (A duck/Hong Kong/786/1979) and Duck H15N8 (A/duck/AUS/341/1983), AT10_004 also showed some activity to H15N8 (A/duck/AUS/341/1983).
- AT10_003 recognized the group 1 HA molecules from H9N2 (A/Hong Kong/1073/1999) and H5N1
- AT10_004 also showed binding to the HAs of HlNl (A/California/07/2009) and H9N2 (A/Hong Kong/1073/1999).
- AT10_005 bound exclusively to the group 1 HA proteins tested.
- MDCK-SIAT cells were grown in a T175 culture flask to 80- 100% confluency in DMEM/FCS/PS/G418.
- the cell layer was washed 2x with 10 ml PBS after which 15 ml of Optimem/PS/G418/Trypsin was added.
- 0.5 ml of 100.000 TCID50 Influenza virus H lNl or H3N2 was added to the flask and cells were cultured at 37°C. After 24-48 hr the cells were washed 2x with 10 ml PBS and detached from the plastic using Trypsin-EDTA. Cells were counted and frozen at - 15Q°C until use.
- the infected cells were defrosted and incubated with IgG
- Antibodies AT10_002 and AT10_004 recognized all three group 2 Influenza infected cell batches, AT10_004 also showed some reactivity to H5N1 (A/Turkey/Turkey/2004) Influenza. AT10_003 only showed some low binding to H3N2 (A/Swine/St.Oedenrode/1996) and H7N7
- AT10_005 bound to group 1 Influenza infected cells and not to group 2 Influenza infected cells.
- an in vitro neutralization assay was performed.
- the assay was performed on MDCK-SIAT cells (Journal of Virology Aug. 2003; pp. 8418-25).
- MDCK- SIAT cells were grown in DMEM/8%FCS/PS/G418 in an 96 well plate (CellCarrier Plate, PerkinElmer) to 80- 100% confluency.
- Neutralization assays are performed in Optimem/PS/G418/Trypsin medium without FCS or BSA. Fifty ⁇ of recombinant mAb was mixed with 50 ⁇ of virus suspension (100TCID50/50 ⁇ ) of H3N2
- IC50 values were calculated in Prism, values are from 1 representative experiment, assay points performed in quadruplicate.
- AT10_001, AT10_002 and AT10_004 showed potent inhibition of H3N2 (A Ned/177/2008) and H3N2 HKX-31 Influenza virus infection in vitro. Neutralization of H1N1 (A/Hawaii/31/2007) was not observed for AT10_001, AT10_002, AT10J)03 and AT10_004.
- A/ck/Neth/621557/03 H7N7; van der Goot et al. 2005
- A/ek/Italy/1067/99 H7N1
- a turkey/Turkey/05 H5N1; Londt et al. 2008
- A/Neth/602/2009 swine-origin H1N1; Munster et al. 2009
- Madin-Darby canine kidney (MDCK) cells were cultured in Optimem (Gibco BRL Life Technologies) containing 5% FBS (Integro) and 1% Pen Streptomycine (Gibco BRL Life Technologies).
- mAbs were seeded at a density of 3 x 10 4 cells per well in 96-well plates and incubated O/N at 37°C.
- Three-fold serial dilutions of the mAbs were made in PBS starting with a concentration of 15 ⁇ g/ml, Rituximab mAb was taken along as negative control.
- Virus dilutions were prepared in virus infection medium consisting of Optimem supplemented with antibiotics and, in case of LPAI viruses, 1 ⁇ g/ml trypsin/TPCK (Sigma). Each mAb dilution was mixed with an equal volume of virus followed by 1 hour incubation at 37°C.
- the mAb/virus mixture (-100-1000 TCID50) was inoculated onto the cell monolayers.
- Cells were incubated for 24-32 hours at 37°C, after which they were washed twice with PBS, fixed with 4% formalin for 20 min and then washed again with PBS.
- Cells incubated with medium only were included as negative control and cells incubated with virus only as positive control.
- the assay was performed in quadruplicate. Cells were stained with 1 hour with DAPI and an antibody against the nuclear protein of the Influenza virus (NP-100-1000 TCID50) was inoculated onto the cell monolayers.
- Cells were incubated for 24-32 hours at 37°C, after which they were washed twice with PBS, fixed with 4% formalin for 20 min and then washed again with PBS.
- Cells incubated with medium only were included as negative control and cells incubated with virus only as positive control.
- the assay was performed in quadruplicate. Cells were
- AT10_005 prevents infection with group 1 Influenza A viruses but has no effect on group 2 viruses.
- Antibody CR8020 (WO 2010 130636) does not show any neutralizing capacity for H3N2 A/Swine/Neth/St. Oedenrode/96 and H7N1 A/ck/Italy/1067/99 at 15 ⁇ g/ml while AT10_002 and AT10_004 show IC50 values below 4 ⁇ 3 ⁇ 4/ ⁇ 1.
- Antibody AT10_001 and AT10_003 were labeled with Alexa Fluor 555 (Molecular Probes) and antibody AT10J302 and AT10_004 were labeled with Alexa Fluor 647 (Molecular Probes). Labeled antibodies were tested for binding to H3N2
- AT10J302 and AT10_004 all bind to a similar region on the HA protein as they all block each other's binding (Figure 6A).
- Antibody competition was also performed on H1N1 infected cells (A/Haw aii/31/2007).
- AT10_004-Alexa-647 antibody binding was blocked by unlabeled AT10_0Q4 and AT10_005 ( Figure 6B).
- the AT10_005 antibody recognize the stem region of the group 1 HA molecules.
- AT10_004 competes with AT10_005 for binding it is likely that AT10_004 also recognizes the HA stem region.
- AT10_001, AT10_002 and AT10_004 all bind to a similar region on the HA protein (figure 6A) AT10_001 and AT10_002 therefore also have their binding epitope on the stem region.
- HA1 subunit specific ELISA was done.
- Recombinant HA of full length H3 (A/Aichi/2/1968, full length) and H3 HAl subunit (A/Aichi/2/1968, HA1 subunit, Met-1 - Arg 345) were coated to ELISA plates at 1 ⁇ g/ml. After coating, the plates were washed lx with PBS and 300 ⁇ blocking buffer, PBS/4%Protivar, was added and incubated 1 hr at RT. The plates were then washed 3x with PBST
- HA- driven fusion of the viral and the endosomal membrane Upon endocytic uptake of virions, the acidic environment of the endosome triggers HA- driven fusion of the viral and the endosomal membrane. This fusion is mediated by a conformational change of the HA protein (triggered by the low pH) from a precision state to a post-fusion state.
- AT10_001, AT10 abuse002, AT10_003 and AT10_004 all bind the trypsin treated cells. Binding of AT10_001, AT10_002 and AT10_004 is lost upon treatment of the transfected cells with pH5 buffer, indicating that these antibodies recognize the pre- fusion but not the post-fusion conformation of the HA protein. Treatment of the cells with DTT, which induces dissociation of the HAl subunit from the HA2 subunit, has no effect on binding of these antibodies indicating that the binding epitope is located on the HA2 subunit.
- AT10_003 recognizes both the pre-fusion and post-fusion conformation but binding is lost upon DTT treatment, indicating that the binding epitope is only available when is the HAl subunit is present. Prophylactic and therapeutic efficacy of AT10 antibodies in vivo
- the AT10 antibodies were tested in a mouse influenza challenge model to determine their efficacy.
- Male C57B1/6J mice (4 per group) were intranasally challenged with increasing amounts of influenza A/HKx-31 (H3N2) and body weight changes were monitored twice a day for 14 days to determine the viral dose response. Twenty-five percent bodyweight loss was used as humane endpoint; mice loosing more than 25% of their body weight were removed from the study. In the highest dose group (20000 TCID50) all animals lost 25% of their bodyweight within 8 days while in the 2000 TCID50 group only 50% of the mice reached this bodyweight loss (Figure 8). Based on these results a viral dose of 10 LD50 (20,000 TCID50) was used in subsequent antibody experiments.
- mice were tested for prophylactic efficacy in the influenza model.
- Mice were intravenously injected with 1 or 5 mg/kg antibody one day before challenge with 10 LD50 influenza A HKx31.
- a dose dependent effect could be seen, e.g. mice that received a dose of 1 mg/kg antibody lost more body weight than the mice that received 5 mg/kg of the same antibody ( Figures 9B,C,D).
- the antibodies can be ranked for activity as follows; AT10_002 > AT10_004 > AT10_001.
- mice were intravenously injected with 15 mg/kg antibody two, three, or four days post challenge with 10 LD50 influenza A/HKx31.
- mice were injected with 15 mg/kg AT10J302 or a negative control antibody (Rituximab, 15 mg/kg) one day before 10 LD50 influenza A/HKx31 challenge.
- Bodyweight was monitored for 10 days after which the experiment was terminated. The results are shown in Figure 10.
- AT10_002 administration of AT10_002 at days two or three post Influenza challenge prevented lethal bodyweight loss in all the mice, showing the therapeutic effect of the AT10_002 antibody.
- a tag (named ST) containing a sortase recognition site plus a His6 tag, with sequence GGGGSLPETGGGHHHHHH, is attached to the C-terminus of the heavy chain of the antibodies via genetic fusion.
- the sortase reaction was performed by mixing 10.0 mg AT10-002 ST antibody in 2000 ⁇ reaction buffer (25 mM Trie, pH 7.5, 150 mM NaCl, 10 mM CaCl 2 ) containing 60 ⁇ sortase and 500 ⁇ GGG-Dibenzo-azacyclo-octyn (DIBAC). Similarly, 10.0 mg AT10-005 ST antibody was mixed with 2000 ⁇ sortase-buffer containing 90 ⁇ sortase and 1 mM GGG-azide.
- 2000 ⁇ reaction buffer 25 mM Trie, pH 7.5, 150 mM NaCl, 10 mM CaCl 2
- DIBAC GGG-Dibenzo-azacyclo-octyn
- the purified antibodies were subjected to click-chemistry coupling.
- 3.0 mg AT10- 002-DIBAC was mixed with 2.9 mg ATl0-005-azide and incubated at 25° C in 3.0 ml coupling buffer (25 mM Tris, pH 7.5, 150 mM NaCl). After 16 h the sample was subjected to gel filtration (as above) in PBS (Fresenius Kabi, Bad Homburg,
- one SPR analysis cycle consists of one or more incubation steps in which analytes are flushed over a coated sensor. This is followed by a regeneration step in which any bound analyte is removed from the sensor. Multiple cycles can be performed in one experiment.
- an isotype-specific antibody i.e. anti-human IgG, anti-human kappa light chain or anti-human lambda light chain
- Obtained data was analyzed using Sprint software (version 1.6.8.0, IBIS Technologies BV, Enschede, The Netherlands).
- the SPR sensor was coated by immobilization of isotype specific antibodies anti- human IgG (Jackson Immunoresearch, West Grove, PA, USA), anti-human kappa light chain (Dako, Glostrup, Denmark) and anti-human lambda light chain (Dako, Glostrup, Denmark) on an amine-specific EasySpot gold-film gel-type SPR-chip (Ssens BV, Enschede, The Netherlands) by spotting them on the sensor surface using a continuous flow microspotter device (Wasatch Microfluidics, Salt Lake City, UT, USA) in coupling buffer (10 mM NaAc, pH 4.5, 0.03 % Tween20).
- the sensor After spotting for 45 minutes the sensor is deactivated with 0. 1 M ethanolamine, pH 8.5 and washed three times with system buffer (PBS + 0.03 % Tween20 + 0.05 % NaN3). Before starting the analysis, the coupled sensor was incubated for two minutes with regeneration buffer (10 mM glycine-HCl, pH 2), followed by three wash steps with system buffer. Then the coated SPR chip is injected either with AT10_002, AT10_005 (2 ⁇ g/ml in system buffer) or BiFlu (4 ⁇ /ml in system buffer) and incubated for 30 min.
- system buffer PBS + 0.03 % Tween20 + 0.05 % NaN3
- non-captured IgG is removed by a 5 minute incubation with system buffer.
- the sensor is injected with influenza H3-hemagglutinin protein (H3N2, Wyoming, 03/2003, Sino Biological inc., Beijing, P.R. China, 0.25 to 2.0 in system buffer and incubated for 30 min to measure association.
- influenza H3-hemagglutinin protein H3N2, Wyoming, 03/2003, Sino Biological inc., Beijing, P.R. China, 0.25 to 2.0 in system buffer and incubated for 30 min to measure association.
- To measure complex dissociation the sensor is washed with system buffer and incubated for 40 min.
- the injection of H3 is followed by injections with influenza Hl-hemagglutinin (H1N1, New Caledonia, 20/1999, Sin Biological inc., Beijing, P.R. China, 1.0 ug/ml) and anti- human light chain antibody (anti-kappa or anti-lambda) in a similar fashion
- BiFlu When the single antibodies and BiFlu are captured on anti-human IgG ( Figure 11A) and on anti-lambda light chain (Figure l lB), BiFlu binds both HI and H3 with the same affinity as the single antibodies. Furthermore, the results demonstrate that BiFlu is heterodimer with two different light chains. The two monomeric antibodies (AT10__002 and AT10_005) bind only one analyte and have one type of light chain. Altogether, the SPR analysis demonstrates that BiFlu is a heterodimer of AT10_002 and AT10_005, which binds H3 and HI with equal affinity as the single antibodies.
- BiFlu and AT10_005 showed concentration dependent binding to H1N1 infected cells while AT10_002 did not bind to these cells.
- H3N2 infected cells were bound by BiFlu and AT10_002 but not by AT10_005 antibodies.
- the BiFlu antibodies show similar binding affinity (as shown by MFI of the APC signal) as the relevant single control antibody. Together these results show that BiFlu antibodies have the combined binding properties of AT10_002 and AT10_005.
- concentration depicted for BiFlu has been adjusted to represent the same available binding opportunities (e.g. concentration shown is half of the actual concentration BiFlu as BiFlu has the double molecular weight compared to the single antibodies).
- BiFlu neutralizes HlNl and H3N2 as well as its relevant single components.
- AT10_002/AT10__005 mix and a negative control antibody were tested for prophylactic efficacy in the influenza model.
- mice were intravenously injected with 1 mg/kg AT10_002, 1 mg/kg AT10_005, a mix of AT10_002 and AT10_005 1 mg/kg each, 2 mg/kg BiFlu or 1 mg/kg Rituximab antibody one day before viral challenge. All control mice (Rituximab) lost 25% bodyweight within 8 days and were removed from the study. In the HlNl challenge model AT10_005 antibody showed a protective effect e.g. none of the mice had to be removed from the study. In addition, the mice that received the BiFlu preparation and the AT10J)02/AT10J)05 antibody mix were also protected (Figure 14).
- the first step to build a 3D model of the antibody is to select the best 3D template. This is done by using a global alignment (Needleman and Wunsch) of the query sequence against a databank of all sequences of antibodies present in the protein database (PDB). Then one structure is chosen amongst the structure with the highest percentage of identity in the sequence.
- a global alignment Needleman and Wunsch
- the next step is to highlight the regions where substitutions occurred and modify the sequence and the structure in such a way that the final model resembles the antibody to analyse.
- Two techniques are applied: 1) Substitution of amino acid, this method keeps the main chain in place and only replaces the side chain. 2) Grafting of loop, this method modifies the main chain and is necessary when there are insertion or deletion in a loop, when the sequence is too far or when substitutions may affect the main chain conformation, e.g. substitution of Glycine or Proline.
- the docking procedure was to: (i) analyse the stem of haemagglutinin to restrict the area where actual binding were tested, (ii) manual positioning of the antibody in the remaining area of point (i), (iii) evaluation of the quality of the complex by checking the structure for short contacts, hydrogen bond capable groups missing hydrogen bonds in the complex, size of the contact area, ⁇ 10_005:
- the amino acids of influenza A virus group 1 haemagglutinin (H1/H5) in contact with AT10_005 are: A38, A40, A41, A42, A291, A292, A293, A318, B18, B19, B20, B21, B38, B41, B42, B45, B46, B48, B49, B52, B53, B56.
- the amino acids of influenza A virus group 2 haemagglutinin (H3/H7) in contact with AT10_004 are: A21, A324, A325, A327, B12, B14, B15, B16, B17, B18, B19, B25, B26, B30, B31, B32, B33, B34, B35, B36, B38, B146, B150, B153, B154.
- the amino acids of influenza A virus group 2 haemagglutinin (H3/H7) in contact with AT10_002 are: A38, A48, A275, A276, A277, A278, A289, A291, A318, B19, B20, B21, B36, B38, B39, B41, B42, B45, B46, B48, B49, B50, B52, B53, B56, B57, B58, B15Q.
- Amino acid numbering for the HA molecule was done according to: Wilson et al. 1981 Nature 289, 366-373 and Nobusawa et al. 1991 Virology 182, 475-485.
- AT10_005 interacts with the conserved hydrophobic pocket demonstrated by the crystal of the complex of CR6261 or F10 antibodies with haemagglutinin. The interaction is mainly hydrophobic as for all antibodies binding this pocket.
- AT10J304 interacts with the same beta strand as CR8020 in its crystal complex with haemagglutinin but AT10_004 binds in a stronger way by, among other interactions, continuing the beta sheet of haemagglutinin. This interaction is mediated via the main chain and thus it allows cross-reactivity between HI and H3 even in the absence of conservation (because the main chain is conserved between amino acids).
- AT10_002 interacts with the conserved hydrophobic patch in a new way since except for the CDR3 of VH, all interactions come from the VL domain.
- Londt BZ Nunez A, Banks J, Nili H, Johnson LK, Alexander DJ: Pathogenesis of highly pathogenic avian influenza A/turkey/Turkey/1/2005 H5N1 in Pekin ducks (Anas platyrhynchos) infected experimentally. Avian Pathol 2008, 37:619-627. van der Goot JA, Koch G, de Jong MC, van Boven M: Quantification of the effect of vaccination on transmission of avian influenza (H7N7) in chickens. Proc Natl Acad Sci U S A 2005, 102: 18141- 18146.
- Needleman SB, Wunsch CD A general method applicable to the search for
- Wilson IA, Skehel JJ, Wiley DC Structure of the haemagglutinin membrane glycoprotein of influenza virus at 3 A resolution. Nature. 1981 Jan 29;289(5796):366- 73.
- Heavy chain CDR2 act ate tat cac agt ggc age acc tac tac aac ccg tec etc aag agt
- H3N2 A/Aichi/2/1968 HAl subunit 0.010 -0.006 1.277 0.096 -0.007
- TCID50 tested Virus 1 AT10_001 AT10_002 AT10_003 AT10_004 AT10_005 CR8020
- Table 8 Selection of sequences to replace segments where substitutions occur between the target sequence (AT10_002) and the template (2XZA and 3TNN). The numbering follows the rules of Rabat.
- VL 29-38 3TNML, 3KDML, 3TNNL, 2JB5L, 2JB6A
- Table 10 Selection of sequences to replace segments where substitutions occur between the target sequence (AT10_OOI and the template (3QOT). The numbering follows the rules of Kabat.
- VH 28-31 3NPSB, 2JB5H, 2JB6B, 1 ZIB
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Virology (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Genetics & Genomics (AREA)
- Biomedical Technology (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Communicable Diseases (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Biophysics (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Physics & Mathematics (AREA)
- General Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Tropical Medicine & Parasitology (AREA)
- Cell Biology (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Analytical Chemistry (AREA)
- Food Science & Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
Abstract
The invention relates to isolated, synthetic or recombinant antibodies and functional parts thereof specific for multiple influenza A virus subtypes. The invention further relates to the use of such antibodies for diagnosis of an influenza A virus infection and as a medicament and/or prophylactic agent for at least in part treating or alleviating symptoms of an influenza A virus infection.
Description
Title: INFLUENZA A VIRUS SPECIFIC ANTIBODIES
The invention relates to the fields of biology, immunology and medicine. In particular, the invention relates to influenza A virus specific antibodies.
Influenza is an infectious disease of birds and mammals that can be caused by three types of influenza viruses, types A, B and C. Influenza viruses are RNA viruses belonging to the family of Orthomyxoviridae. Influenza viruses are RNA viruses consisting of seven negative single-stranded RNA-segments encoding nine proteins (influenza Q, or eight negative single-stranded RNA-segments encoding eleven proteins (influenza A and B). Influenza viruses infect millions of people every year. Symptoms of influenza include symptoms comparable with the common cold, such as fever, headache, chills, muscle pains and soar throat. However, influenza can also lead to life-threatening complications, such as pneumonia, and death, in high- risk groups such as young children, the elderly, and immune compromised or chronically ill individuals.
The influenza A virus can be subdivided into different types based on envelope protein expression. Currently 16 hemagglutinin (HA) serotypes (H1-H16) and 9 neuraminidase (NA) serotypes (N1-N9) have been identified, which are used to classify influenza viruses (e.g. H1N1). HA consists of two subunits, HAl and HA2, linked by disulphide bonds. HA must be cleaved by host proteases to yield the two polypeptides HAl and HA2 in order to be infectious. The major part of HAl forms the globular head region of HA and HA2 mainly forms the stem region of HA. The globular head region differs considerable between different HA subtypes, whereas the stem region is more conserved. HA is needed for host cell entry. Following cleavage, the exposed N-terminus of the HA2 polypeptide acts to mediate fusion of the viral membrane with the host cell membrane, allowing the virus to infect the host cell. NA is needed for the release of new virions. NA catalyses the hydrolysis of terminal sialic acid residues of glycoproteins of the host cell, thereby preventing binding of HA to these proteins. NA thus facilitates release of the virus from a cell and consequently
spreading of the virus. In figure 1 a schematic representation of an influenza virus is shown.
Influenza virus infections are most prevalent in winter. In annual influenza epidemics 5- 15% of the population are affected with upper respiratory tract infections. Hospitalization and deaths mainly occur in high-risk groups (very young children, elderly, immuno compromised and chronically ill individuals). Annual epidemics are thought to result in between three and five million cases of severe illness and between 250 000 and 500 000 deaths every year around the world, The estimated costs of influenza epidemics to the US economy are 71-167 billion per year, resulting from health care costs and lost productivity. Seasonal influenza vaccines need to be developed each year as a result of antigenic drift of influenza virus.
Mutations in the influenza genome may induce amino acid substitution(s) that cause antigenic changes in the HA and NA protein, resulting in the escape of immunity of a host. So, even though influenza strains may have high homology, a specific vaccine may not protect against different strains from the same influenza A subtype. In addition, because the newly developed influenza vaccines are based on a prediction of the dominant subtypes for the coming year, the vaccines not always protect against the influenza subtype that actually arises.
Additionally, a process called antigenic shift results in the formation of new virus subtypes through combination of HA and NA from different influenza virus subtypes. Mutations and genetic mixing of human and avian and/or swine influenza can lead to a pandemic. According to the World Health Organization (WHO), a pandemic can start when three conditions have been met, namely emergence of a disease new to a population, agents that infect humans, causing serious illness, and agents that spread easily and sustainably among humans. In the past, several pandemic influenza outbreaks have occurred, such as the 1889 Asiatic pandemic (H2N8), the 1918 Spanish Flu pandemic (H1N1), the 1957 Asian Flue pandemic (H2N2), the 1968 Hong Kong Flu (H3N2) and the 2009 pandemic (H1N1). These pandemics were responsible for the death of millions of people.
Antiviral drugs can be effective for the prevention and treatment of influenza. Two classes of antiviral drugs are available: M2 protein inhibitors and Neuramidase inhibitors. However, the number of influenza strains that show resistance against those inhibitors is increasing.
An alternative approach to prevent and treat influenza infection is the administration of antibodies directed against the influenza proteins. Broadly cross- neutralizing antibodies have been described for influenza viruses belonging to phylogenetic group 1 (Throsby et al. PLoS ONE, 2008 & Sui et al. Nature structural & molecular biology, 2009). These antibodies recognize a conserved region in the stem of the HA protein and are capable of treating influenza infection in mice. A mouse monoclonal antibody (mAb) has been described that recognizes a conserved epitope in the region containing the receptor binding domain of the HA1 subunit. This antibody neutralizes H1N1, H2N2 and H3N2 influenza viruses (Yoshida et al. PLoS Pathogen. 2009). However, escape mutants have been reported to arise. This antibody is a mouse antibody which has the disadvantage of possible side effects when used in humans.
WO 2009/115972 discloses a human monoclonal antibody having neutralizing activity against H1N1 and H3N2. However, neutralizing activity against both H1N1 and H3N2 is inefficient, with IC50 values of around 10 g/ml. In WO 2010/010466 a human antibody, FI6, is described that neutralizes H5N1 (group 1) and H7N1 (group 2) pseudotyped influenza viruses and H1N1 and H3N2 infectious viruses. Again, neutralizing activity against both infectious viruses is inefficient, with IC50 values between 2 and 12.5
Human antibodies disclosed in
WO 2010/130636 have H3 and H7 cross-binding activity. H3 and H7 are both group 2 influenza viruses. Some of these antibodies are, in addition, capable of binding Hi (group 1). However, none of these antibodies was capable of neutralizing influenza viruses of both group 1 and group 2. As a result, a cocktail of antibodies is necessary for the neutralization of both group 1 and group 2 influenza subtypes. Furthermore, the H3N2 neutralizing activity of antibodies capable of neutralizing both H3 and H7 influenza virus subtypes is above 1 ig/ml. It is for instance shown in the Examples and Table 7 that antibody CR8020, described in WO 2010/130636, has an inefficient neutralizing activity against H3N2 A/swine/Neth/St. Oedenrode/96, with an IC50 value of more than 15 pg/ml.
For these reasons, there is a need for additional influenza A virus antibodies and therapies against influenza A virus infection.
It is an object of the present invention to provide additional antibodies specific for multiple influenza A virus subtypes, or functional equivalents of such antibodies and compositions comprising such antibodies. Preferably antibodies are provided that have a high influenza virus neutralizing activity. Furthermore, preferably antibodies are provided which are capable of neutralizing at least two influenza virus subtypes.
The present invention provides such antibodies specific for multiple influenza A virus subtypes. As demonstrated in the Examples, antibodies are provided that are capable of binding at least two influenza A virus subtypes, preferably both group 1 and group 2 influenza A virus subtypes. Furthermore, antibodies are provided that have a high influenza A virus neutralizing capacity.
The invention provides in one embodiment an isolated, synthetic or recombinant antibody or functional part thereof or immunoglobulin chain or functional equivalent thereof, having an in vitro H3N2 influenza A virus neutralizing activity with an IC50 value of less than 1 μ /ml, preferably of less than 0.7 μg/ml, more preferably of equal to or less than 0.3
more preferably of less than 0.2 g/ml, which antibody or functional part or immunoglobulin chain or functional equivalent is capable of specifically binding at least one other influenza A virus subtype. Said H3N2 influenza A virus preferably comprises a H3N2 A/Ned/177/2008, H3N2 HKX-31 or H3N2 A/swine/Neth/St.Oedenrode/96 strain, most preferably a H3N2 A/Ned/177/2008 strain.
H3N2 influenza virus is one of the influenza viruses capable of infecting humans. H3N2 can be transferred from human to other humans. Antibodies capable of neutralizing H3N2 influenza virus are therefore particularly important for application in humans.
In another preferred embodiment the invention provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin
chain or functional equivalent thereof, having an in vitro H7N1 influenza A virus neutralizing activity with an IC50 value of less than 5,0 g/ml, preferably of less than 4.0 μ /ml, more preferably of less than 1.0 μ¾/πι1, more preferably equal to or less than about 0.6
Said H7N1 influenza A virus preferably comprises a H7N1
A/ck/Italy/1067/99 strain. In a particularly preferred embodiment said antibody or functional part or immunoglobulin chain or functional equivalent is also capable of specifically binding at least one other influenza A virus subtype, so that protection against multiple strains can be obtained. Although to date, no cases have been reported of transmission of H7N1 from birds to humans, mutations may occur making this virus infectious for humans.
In another preferred embodiment the invention provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, having an in vitro H7N7 influenza A virus neutralizing activity with an IC50 value of less than 0.5 μ ml, preferably equal to or less than about 0.4 μg/ml, more preferably equal to or less than about 0.2 μ /ml, most preferably equal to or less than about 0.1 μg/ml. Said H7N7 influenza A virus preferably comprises a H7N7 A/ck/Neth/621557/03 strain. In a particularly preferred embodiment said antibody or functional part or immunoglobulin chain or functional equivalent is also capable of specifically binding at least one other influenza A virus subtype, so that protection against multiple strains can be obtained. H7N7 influenza virus is one of the influenza viruses capable of infecting humans following bird to human transmission. Antibodies capable of neutralizing H7N7 influenza virus are therefore particularly important for application in humans,
In another preferred embodiment the invention provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, having an in vitro H1N1 influenza A virus neutralizing activity with an IC50 value of less than 5.0 μ /ml, preferably of less than 4.0 ug/ml, more preferably of less than 3.0 μg/ml, more preferably equal to or less than about 2.7 μg/ml. Said H1N1 influenza A virus preferably comprises a H1N1
A/Neth/602/2009 strain or, most preferably, a H1N1 A/Haw aii/31/2007 strain. In a particularly preferred embodiment said antibody or functional part or
immunoglobulin chain or functional equivalent is also capable of specifically binding at least one other influenza A virus subtype, so that protection against multiple strains can be obtained. H1N1 influenza virus is one of the influenza viruses capable of infecting humans following human to human transmission. Antibodies capable of neutralizing H1N1 influenza virus are therefore particularly important for
application in humans.
In another preferred embodiment the invention provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, having an in vitro H5N1 influenza A virus neutralizing activity with an IC50 value of' less than 5.0 g ml, preferably of less than 4.0 μg/ml, more preferably of less than 3.0
more preferably of less than 2.0 ^ig/ml, more preferably equal to or less than about 1.3 μg/ml. Said H5N1 influenza A virus preferably comprises a H5N1 A/turkey/Turkey/05 strain. In a particularly preferred embodiment said antibody or functional part or immunoglobulin chain or functional equivalent is also capable of specifically binding at least one other influenza A virus subtype, so that protection against multiple strains can be obtained. H5N1 influenza virus is one of the influenza viruses capable of infecting humans following human to human transmission. Antibodies capable of neutralizing H5N1 influenza virus are therefore particularly important for application in humans.
A "functional part of an antibody" is defined herein as a part that has at least one shared property as said antibody in kind, not necessarily in amount. Said functional part is capable of binding the same antigen as said antibody, albeit not necessarily to the same extent. A functional part of an antibody preferably comprises a single domain antibody, a single chain antibody, a nanobody, an unibody, a single chain variable fragment (scFv), a Fab fragment or a F(ab')2 fragment.
A functional part of an antibody is also produced by altering an antibody such that at least one property - preferably an antigen-binding property - of the resulting compound is essentially the same in kind, not necessarily in amount. This is done in many ways, for instance through conservative amino acid substitution, whereby an amino acid residue is substituted by another residue with generally
similar properties (size, hydrophobicity, etc), such that the overall functioning is not seriously affected.
A "functional equivalent of an immunoglobulin chain" is defined herein as an artificial binding compound, comprising at least one CDR sequence of an immunoglobulin chain.
"Neutralizing activity" as used herein is defined as the inhibition or reduction of an influenza virus' capacity of infecting a host cell. Neutralizing activity can be measured by any method known in the art. One of such methods is detailed in the Examples of this application and involves the prevention of influenza infection of cultured cells by monoclonal antibodies. In this method, influenza virus is mixed with an antibody and after 1 hour of incubation added to cells. After 24 hours influenza infection of the cells can be measured by the detection of expression of the nuclear protein of influenza in the target cells. Potent antibodies will prevent or reduce influenza infection and subsequent influenza nuclear protein expression in the target cell. "IC50" is a term well known in the art and refers herein to the concentration of influenza A neutralizing antibody necessary to inhibit or reduce influenza A virus infectivity of host cells by half.
A "group 2 subtype influenza A virus" is an influenza A virus having a HA serotype of group 2 influenza A viruses. Currently, viruses having a H3, H4, H7, H10, H14 and H15 serotype are the group 2 influenza A viruses. A "group 1 subtype influenza A virus" is an influenza A virus having a HA serotype of group 1 influenza A viruses. Currently, viruses having a HI, H2, H5, H6, H8, H9, Hl l, H12, H13 and H16 serotype are the group 1 influenza A viruses.
As used herein "specifically binding" refers to the interaction between an antibody and its epitope, indicating that said antibody preferentially binds to said epitope. Thus, although the antibody may non-specifically bind to other antigens or amino acid sequences, the binding affinity of said antibody for its epitope is significantly higher than the non-specific binding affinity of said antibody for any other antigen or amino acid sequence.
An 'influenza A virus subtype" as used herein refers to different influenza
A viruses, for example H1N1, H1N2, H1N7, H2N2, H3N2, H3N8, H4N8, H5N1, H5N2, H5N9, H6N2, H6N5, H7N2, H7N3, H7N7, H8N4, H9N2, H10N7, H11N6, H12N5 or H13N6.
An "influenza A virus strain" as used herein refers to different influenza A viruses belonging to the same subtype, for example H3N2 A/Ned/177/2008, H3N2 A/Wyoming/03/2003 and H3N2 A/Panama/2007/99.
Isolated, synthetic or recombinant antibodies or functional parts thereof or immunoglobulin chains or functional equivalents thereof according to the present invention are herein also referred to as "antibody according to the invention".
Preferred influenza A neutralizing antibodies according to the invention are AT10_0Q4, AT10J302 and AT10J3Q1, because these antibodies have been demonstrated to have particularly desired cross-binding and/or neutralizing characteristics. AT10__004, AT10„002 and AT10_001 have heavy chain sequences of SEQ ID NO's:31, 33 and 34 as depicted in table 1, respectively, and light chain sequences of SEQ ID NO's:36, 38 and 39 as depicted in table 1, respectively. The heavy and light chain CDR sequences of these preferred antibodies are also depicted in table 1. SEQ ID NO's: l, 3 and 4 are the heavy chain CDR1 sequences of antibodies AT10_004, AT10J)02 and AT10„001 respectively, SEQ ID NO's:6, 8 and 9 are the heavy chain CDR2 sequences of these antibodies, and SEQ ID NQ's: l l, 13 and 14 are the heavy chain CDR3 sequences of these antibodies. SEQ ID NO's: 16, 18 and 19 are the light chain CDR1 sequences of antibodies AT10_004, AT10_0Q2 and AT10_001 respectively, SEQ ID NO's:21, 23 and 24 are the light chain CDR2 sequences of these antibodies, and SEQ ID NO's:26, 28 and 29 are the light chain CDR3 sequences of these antibodies.
Antibody AT10_.0O4 is a preferred antibody because it is capable of specifically binding both group 1 and group 2 influenza A viruses. As shown in the Examples, antibody AT1Q_004 has cross-binding activity to at least HI, H3 and H7 subtype influenza A viruses. AT10_004 is capable of binding to a wide variety of recombinant HA subtypes and influenza A viruses. It is capable of binding at least human influenza HlNl (A/Haw aii/31/2007) infected cells and human influenza H3N2 (A/Netherlands/177/2008) infected cells and HA of human influenza HlNl (A/New Caledonia/20/1999), H3N2 (A/Wyoming/03/2003, A Aichi/2/1968 and
A Wisconsin/67/2005), H7N7 (A/Netherlands/219/2003) and H9N2 (A/Hong
Kong/1073/1999). Antibody AT10_004 is furthermore preferred because, in addition to recognizing HA of human influenza viruses and human influenza virus infected cells,
it is also capable of recognizing cells infected with several influenza viruses infecting non-human animals, namely cells infected with turkey H5N1
(A/Turkey/Turkey/2004), swine H3N2 (A/swine/St.oedenrode/1996), chicken H7N1 (A/Ch/Italy/1067/1999) and chicken H7N7 (A/Ch/Neth/621557/2003) and binding to HA of swine H4N6 (A/Swine/Ontario/01911- 1/1999) and HA of duck H15N8
(A duck/AUS/341- 1983). Antibody AT10J304 is also preferred because it has a high neutralizing activity for H3N2 viruses, having an in vitro H3N2 A/Ned/177/2008 neutralizing activity with an IC50 value of about 0.17 μg/ml, and having an in vitro H3N2 A/swine/Neth/St. Oedenrode/96 neutralizing activity with an IC50 value of about 2.3 ^ig/ml, and even having an in vitro H3N2 HKX-31 neutralizing activity with an IC50 value of about 0.017
AT10J304 also has protective activity against H3N2 virus (influenza A/HKx-31) in vivo. Antibody AT10_.004 furthermore has a particularly high neutralizing activity for H7N1 viruses, having an in vitro H7N1 A/ck/Italy/1067/99 neutralizing activity with an IC50 value of about 0.6 μ%/ναΙ, As shown in Table 7, the protective effect of antibody AT10_ 0Q4 against H7N1
A ck/Italy/1067/99 is even higher, meaning that a lower IC50 value is obtained, as compared to the protective effect of antibody AT10_004 against
H3N2 A/swine/Neth/St. Oedenrode/96. Antibody AT10J)04 furthermore has a particularly high neutralizing activity for H7N7 viruses, having an in vitro
H7N7 A/ck/Neth/621557/03 neutralizing activity with an IC50 value of about 0.2 μg/ml. Antibody AT10_004 is further preferred because it binds to an epitope in the conserved stem region of the HA protein. Because limited variation is present in this region, an antibody of which the epitope is located in the stem region is capable of binding to a broad range of influenza viruses. One embodiment therefore provides an antibody or functional part or immunoglobulin chain or functional equivalent which has heavy chain CDRl, CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences of antibody AT10J304, comprising the sequence of SEQ ID NO: l, SEQ ID NO:6, SEQ ID NO: l l, SEQ ID NO: 16, SEQ ID NO:21 and SEQ ID NO:26, or sequences that are at least 70% identical thereto.
In another embodiment an antibody or functional part or immunoglobulin chain or functional equivalent is provided that comprises heavy chain CDRl, CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences of antibody AT10_002, comprising the sequence of SEQ ID NO:3, SEQ ID NO:8, SEQ ID NO: 13,
SEQ ID NO: 18, SEQ ID NO:23 and SEQ ID NO:28 or sequences that are at least 70% identical thereto. Antibody AT10_002 is a preferred antibody because it has cross- binding activity to at least H3 and H7 subtype influenza A viruses. AT10_002 is capable of binding to a wide variety of recombinant HA subtypes and influenza A viruses. It is capable of binding at least human influenza H3N2
(A/Netherlands/ 177/2008) infected cells, and HA of human influenza H3N2
(A/Wyoming/03/2003, A/Aichi/2/1968 and A/Wisconsin/67/2005) and H7N7
(A/Netherlands/219/2003). Antibody AT10„002 is furthermore preferred because, in addition to recognizing HA of human influenza viruses and human influenza virus infected cells, it is also capable of recognizing cells infected with several influenza viruses infecting non-human animals, namely cells infected with swine H3N2
(A/swine/St.oedenrode/1996), chicken H7N1 (A/Ch/Italy/1067/1999) and chicken H7N7 (A/Ch/Neth/621557/2003) and binding to HA of duck H10N3 (A/duck/Hong
Kong/786/1979) and HA of duck H15N8 (A/duck/AUS/341-1983). Furthermore, antibody AT10_002 neutralizes at least one H3 subtype influenza A virus. Antibody AT10_002 is further preferred because it has a high neutralizing activity for H3N2 viruses, having an in vitro H3N2 A/Ned/177/2008 neutralizing activity with an IC50 value of about 0.18 ^ig/ml, and having an in vitro
H3N2 A swine/Neth/St. Oedenrode/96 neutralizing activity with an IC50 value of about 0.3
and having an in vitro H3N2 HKX-31 neutralizing activity with an IC50 value of about 0.25 ng/ml. AT10_002 also has protective activity against H3N2 virus (influenza A/HKx-31) in vivo. As demonstrated in the Example antibody
AT10J302 provides the best protective activity of the antibodies tested and is therefore particularly preferred. Antibody AT10_002 furthermore has a particularly high neutralizing activity for H7N1 viruses, having an in vitro H7N1
A ck/Italy/1067/99 neutralizing activity with an IC50 value of about 3.6 μg/ml.
Antibody AT10_002 furthermore has a particularly high neutralizing activity for H7N7 viruses, having an in vitro H7N7 A/ck/Neth/621557/03 neutralizing activity with an IC50 value of about 0.1
Antibody AT10_002 is further preferred because it binds to an epitope in the conserved stem region of the HA protein. Because limited variation is present in this region, an antibody of which the epitope is located in the stem region is capable of binding to a broad range of influenza viruses.
In another embodiment an antibody or functional part or immunoglobulin chain or functional equivalent is provided that comprises heavy chain CDR1, CDR2 and CDR3 sequences and light chain CDR1, CDR2 and CDR3 sequences of antibody AT10_001, comprising the sequence of SEQ ID NO:4, SEQ ID NO:9, SEQ ID NO: 14, SEQ ID NO: 19, SEQ ID NO:24 and SEQ ID NO:29 or sequences that are at least 70% identical thereto. Antibody AT10_001 is a preferred antibody because it has cross- binding activity to at least H3 and H7 subtype influenza A viruses. AT10_001 is capable of binding to a wide variety of recombinant HA subtypes and influenza A viruses. It is capable of binding at least human influenza H1N1 (A/Neth/602/2009) infected cells, human influenza H3N2 (A/Netherlands/177/2008) infected cells and HA of human influenza H3N2 (A Wyoming/03/2003, A/Aichi/2/1968 and
A/Wisconsin/67/2005) and H7N7 (A/Netherlands/219/2003). Antibody AT10_001 is furthermore preferred because, in addition to recognizing HA of human influenza viruses and human influenza virus infected cells, it is also capable of recognizing cells infected with several influenza viruses infecting non-human animals, such as cells infected with chicken H7N1 (A/Ch/Italy/1067/1999) and chicken H7N7
(A/Ch/Neth/621557/2003) and binding to HA of swine H4N6 (A/Swine/Ontario/01911- 1/1999). Furthermore, antibody AT10J301 neutralizes at least one H3 subtype influenza A virus. Antibody AT10_001 is further preferred because it has a high neutralizing activity for H3N2 viruses, having an in vitro H3N2 A Ned/177/2008 neutralizing activity with an IC50 value of about 0.64
and having an in vitro H3N2 HKX-31 neutralizing activity with an IC50 value of about 2.1 μg/ml. AT10_001 also has protective activity against H3N2 virus (influenza A HKx-31) in vivo.
Antibody AT10_001 furthermore has a particularly high neutralizing activity for H7N7 viruses, having an in vitro H7N7 A ck/Neth/621557/03 neutralizing activity with an IC50 value of about 0.4
Antibody AT10_001 is further preferred because binds to an epitope in the conserved stem region of the HA protein. Because limited variation is present in this region, an antibody of which the epitope is located in the stem region is capable of binding to a broad range of influenza viruses.
Preferably, an influenza A neutralizing antibody according to the invention comprises heavy chain CDR1, CDR2 and CDR3 sequences and light chain CDR1, CDR2 and CDR3 sequences that are at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%,
more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99% identical to the sequences depicted in table 1.
The terms «AT10_004", "AT10_002" and "AT10_001" as used herein encompass all antibodies and functional equivalents with the indicated heavy chain and light chain sequences, for instance isolated and/or purified or recombinantly produced.
As is well known by the skilled person, a heavy chain of an antibody is the larger of the two types of chains making up an immunoglobulin molecule. A heavy chain comprises constant domains and a variable domain, which variable domain is involved in antigen binding. A light chain of an antibody is the smaller of the two types of chains making up an immunoglobulin molecule. A light chain comprises a constant domain and a variable domain. The variable domain is often, together with the variable domain of the heavy chain, involved in antigen binding.
Complementary-determining regions (CDRs) are the hypervariable regions present in heavy chain variable domains and light chain variable domains. In case of whole antibodies, the CDRs of a heavy chain and the connected light chain of an antibody together form the antigen-binding site.
Based on the antibodies depicted in table 1, it is possible to produce an immunoglobulin chain or functional equivalent thereof comprising at least one CDR sequence of an immunoglobulin variable domain depicted in table 1 which is specific for and capable of neutralizing influenza A virus. Further provided is thus an isolated, recombinant or synthetic immunoglobulin chain or functional equivalent thereof comprising at least one CDR sequence of an immunoglobulin variable region depicted in table 1. Preferably, antibodies are provided which comprises at least two CDR's, more preferably at least three CDR's, of the same antibody indicated in table 1.
Hence, preferably at least two or three CDR's of AT10_004, or AT10_003, or AT10_002 or AT10_001 or AT10_005, are jointly present in one antibody or functional part according to the invention. In a preferred embodiment, a human antibody is provided because the use of a human antibody diminishes the chance of side-effects due to an
immunological reaction in a human individual. Optionally, said at least one CDR sequence is optimized, preferably in order to improve binding efficacy or stability. This is for instance done by mutagenesis experiments where after the stability and/or binding efficacy of the resulting compounds are preferably tested and an improved influenza A neutralizing antibody is selected.
A skilled person is well capable of generating variants comprising at least one altered CDR sequence according to the invention. For instance, conservative amino acid substitution is applied. It is also possible to alter at least one CDR sequence depicted in table 1 in order to generate a variant antibody, or a functional part thereof, with at least one altered property as compared to the original antibody. Preferably, an antibody or functional part is provided comprising a CDR sequence which is at least 70% identical to a CDR sequence as depicted in table 1, so that the favourable binding and neutralizing characteristics of an influenza A neutralizing antibody according to the invention are at least in part maintained or even improved. A CDR sequence as depicted in table 1 is preferably altered such that the resulting antibody or functional part comprises at least one improved property, such as for instance an improved binding affinity, selectivity and/or stability, as compared to the original antibody. Variant antibodies or functional parts thereof comprising an amino acid sequence which is at least 70% identical to a CDR sequence as depicted in table 1 are therefore also within the scope of the present invention. Various methods are available in the art for altering an amino acid sequence, For instance, a heavy chain or light chain sequence with a desired CDR sequence is artificially synthesized.
Preferably, a nucleic acid molecule encoding a CDR sequence according to the invention is mutated, for instance using random - or site-directed - mutagenesis.
Besides optimizing CDR sequences in order to improve binding efficacy or stability, it is often advantageous to optimize at least one sequence in at least one of the framework regions. This is preferably done in order to improve binding efficacy or stability. Framework sequences are for instance optimized by mutating a nucleic acid molecule encoding such framework sequence where after the characteristics of the resulting antibody - or functional part - are preferably tested. This way, it is possible to obtain improved antibodies or functional parts. In a preferred embodiment, human germline sequences are used for framework regions in antibodies or functional parts thereof or immunoglobulin chains or functional equivalents according to the
invention, The use of germline sequences preferably minimizes the risk of
immunogenicity of said antibodies or functional parts, immunoglobulin chains or functional equivalents, because these sequences are less likely to contain somatic alterations which are unique to individuals from which the framework regions are derived, and may cause an immunogenic response when applied to another human individual.
The invention thus provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof comprising:
- a heavy chain CDR1 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO'si l, 3 and 4, and/or
- a heavy chain CDR2 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's:6, 8 and 9, and/or - a heavy chain CDR3 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's: l l, 13 and 14, and/or
- a light chain CDR1 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's: 16, 18 and 19, and/or
- a light chain CDR2 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's:21, 23 and 24, and/or
- a light chain CDR3 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's:26, 28 and 29.
Preferably, said antibody or functional part or immunoglobulin chain or functional equivalent comprises heavy chain CDR1, CDR2 and/or CDR3 sequences and/or light chain CDR1, CDR2 and/or CDR3 sequences that are at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, most preferably 100% identical to these sequences.
In another embodiment an antibody according to the invention comprises heavy chain CDR1, CDR2 and CDR3 sequences and light chain CDR1, CDR2 and CDR3 sequences of antibody AT10_003, which has a heavy chain sequence of SEQ ID NO: 32 as depicted in table 1, and a light chain sequence of SEQ ID NO: 37 as depicted in table 1. SEQ ID NO:2 is the heavy chain CDR1 sequence, SEQ ID NO:7 is the heavy chain CDR2 sequence, SEQ ID NO: 12 is the heavy chain CDR3 sequence, SEQ ID NO: 17 is the light chain CDR1 sequence, SEQ ID NO:22 is the light chain CDR2 sequence, and SEQ ID NO:27 is the light chain CDR3 sequence of antibody AT10_003. Antibody AT10_003 is a preferred antibody because it is capable of specifically binding both group 1 and group 2 influenza A viruses. Antibody AT1CL0Q3 has cross- binding activity to at least H3, H5 and H7 subtype influenza A viruses. AT10_003 is capable of binding to a wide variety of recombinant HA subtypes and influenza A viruses. It is capable of binding at least human influenza H1N1 (A/Hawaii/31/2007) infected cells and human influenza H3N2 (A/Netherlands/ 177/2008) infected cells, and HA of human influenza H3N2 (A/Wyoming/03/2003, A/Aichi/2/1968 and
A/Wisconsin/67/2005), H5N1 (A/Vietnam/1203/2004 and A/Thailand/Vietnam
Consensus/2004), H7N7 (A/Netherlands/219/2003) and H9N2 (A/Hong
Kong/1073/1999). Antibody AT10_003 is furthermore preferred because, in addition to recognizing HA of human influenza viruses and human influenza virus infected cells, it is also capable of recognizing cells infected with several influenza viruses infecting non-human animals, such as cells infected with chicken H7N7
(A/Ch/Neth/621557/2003) and swine H3N2 (A/swine/St.oedenrode/1996), and it is capable of binding to HA of swine H4N6 (A/Swine/Ontario/01911- 1/1999), HA of duck H10N3 (A/duck/Hong Kong/786/1979) and HA of duck H15N8 (A/duck/AUS/341/1983). The term "AT10_003" as used herein encompass all antibodies and functional equivalents with the AT10_003heavy chain and light chain sequences depicted in table 1, for instance isolated and/or purified or recombinantly produced.
As described above, a skilled person is well capable of producing an immunoglobulin chain or functional equivalent thereof comprising at least one CDR sequence of an immunoglobulin variable domain depicted in table 1 which is specific for influenza A virus and of generating variants comprising at least one altered CDR sequence according to the invention.
The invention therefore provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof comprising:
- a heavy chain CDRl sequence comprising a sequence which is at least 70% identical to SEQ ID NO:2, and/or
- a heavy chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 7, and/or
- a heavy chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 12, and/or
- a light chain CDRl sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 17, and/or
- a light chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:22, and/or
- a light chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:27. Preferably, said antibody or functional part or immunoglobulin chain or functional equivalent comprises heavy chain CDRl, CDR2 and/or CDR3 sequences and/or light chain CDRl, CDR2 and/or CDR3 sequences that are at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, most preferably 100% identical to these sequences.
In another embodiment an antibody according to the invention comprises at least one of heavy chain CDRl , CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences of antibody AT10__005, which has a heavy chain sequence of SEQ ID NO:35 as depicted in table 1, and a light chain sequence of SEQ ID NO:40 as depicted in table 1. SEQ ID NO:5 is the heavy chain CDRl sequence, SEQ ID
NO: 10 is the heavy chain CDR2 sequence, SEQ ID NO: 15 is the heavy chain CDR3 sequence, SEQ ID NO:20 is the light chain CDRl sequence, SEQ ID NO:25 is the light chain CDR2 sequence, and SEQ ID NO: 30 is the light chain CDR3 sequence of
antibody AT10_005. Antibody AT10_005 is a preferred antibody because it has cross- binding activity to at least HI, H5 and H9 subtype influenza A viruses. AT1Q_005 is capable of binding to a wide variety of recombinant HA subtypes and influenza A viruses. It is capable of binding at least human influenza HlNl (A/Neth/602/2009) infected cells, and HA of human influenza HlNl (A/California/07/2009, and A/New Caledonia/20/1999), H5N1 (A/Vietnam/1203/2004), and H9N2 (A/Hong
Kong/1073/1999). Antibody AT10_005 is furthermore preferred because, in addition to recognizing HA of human influenza viruses and human influenza virus infected cells, it is also capable of recognizing cells infected with several influenza viruses infecting non-human animals, such as cells infected with turkey H5N1
(A/Turkey/Turkey/2004). Antibody AT10„005 is also preferred because it has a high neutralizing activity for HlNl viruses, having an in vitro HlNl A/Haw aii/31/2007 neutralizing activity with an IC50 value of about 0.24 μ /ml, and having an in vitro HlNl A/Neth/602/2009 (swine origin) neutralizing activity with an IC50 value of about 2.7
AT10_005 also has protective activity against HlNl in vivo. Antibody AT10_005 furthermore has a particularly high neutralizing activity for H5N1 viruses, having an in vitro H5N1 A/turkey/Turkey/05 neutralizing activity with an IC50 value of about 1,3 g/ml. Antibody AT10_005 is further preferred because it binds to an epitope in the conserved stem region of the HA protein. Because limited variation is present in this region, an antibody of which the epitope is located in the stem region is capable of binding to a broad range of influenza viruses. The term "AT10_005" as used herein encompass all antibodies and functional equivalents with the indicated heavy chain and light chain sequences, for instance isolated and/or purified or
recombinantly produced.
As described above, a skilled person is well capable of producing an immunoglobulin chain or functional equivalent thereof comprising at least one CDR sequence of an immunoglobulin variable domain depicted in table 1 which is specific for influenza A virus and of generating variants comprising at least one altered CDR sequence according to the invention.
The invention therefore provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof comprising:
- a heavy chain CDRl sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 5, and/or
- a heavy chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 10, and/or
- a heavy chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 15, and/or
- a light chain CDRl sequence comprising a sequence which is at least 70% identical to SEQ ID NO:20, and/or
- a light chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 25, and/or
- a light chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:30. Preferably, said antibody or functional part or immunoglobulin chain or functional equivalent comprises heavy chain CDRl, CDR2 and/or CDR3 sequences and/or light chain CDRl, CDR2 and/or CDR3 sequences that are at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, most preferably 100% identical to these sequences,
In a preferred embodiment an antibody according to the invention comprises both the heavy and light chain CDR sequences of one of the above mentioned antibodies. Provided are thus antibodies which have heavy chain CDRl, CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences of antibody AT10_004, comprising the sequence of SEQ ID NO: l, SEQ ID NO:6, SEQ ID NO: 11, SEQ ID NO: 16, SEQ ID NO:21 and SEQ ID NO:26, or sequences that are at least 70% identical thereto.
In another embodiment antibodies which have heavy chain CDRl, CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences of antibody AT10_003 are provided, comprising the sequence of SEQ ID NO:2, SEQ ID NO:7,
SEQ ID NO: 12, SEQ ID NO: 17, SEQ ID NO:22 and SEQ ID NO:27, or sequences that are at least 70% identical thereto.
In another embodiment antibodies which have heavy chain CDR1, CDR2 and CDR3 sequences and light chain CDR1, CDR2 and CDR3 sequences of antibody AT10_002 are provided, comprising the sequence of SEQ ID NQ:3, SEQ ID NO:8,
SEQ ID NO: 13, SEQ ID NO: 18, SEQ ID NO:23 and SEQ ID NO:28, or sequences that are at least 70% identical thereto.
In another embodiment antibodies which have heavy chain CDR1, CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences of antibody AT10_001 are provided, comprising the sequence of SEQ ID NO:4, SEQ ID NO:9,
SEQ ID NO: 14, SEQ ID NO: 19, SEQ ID NO:24 and SEQ ID NO:29, or sequences that are at least 70% identical thereto.
In another embodiment antibodies which have heavy chain CDRl, CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences of antibody AT10_005 are provided, comprising the sequence of SEQ ID NO:5, SEQ ID NO: 10,
SEQ ID NO: 15, SEQ ID NO:20, SEQ ID NO:25 and SEQ ID NO:30, or sequences that are at least 70% identical thereto.
As described herein before, the term "antibodies" also encompasses functional parts, immunoglobulin chains or functional equivalents thereof,
Preferably, said antibody or functional part or immunoglobulin chain or functional equivalent comprises heavy chain CDRl, CDR2 and CDR3 sequences and light chain CDRl, CDR2 and CDR3 sequences that are at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%), more preferably at least 91%, more preferably at least
92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, most preferably 100% identical to the above mentioned CDR sequences.
In a preferred embodiment, an antibody according to the invention comprises a heavy chain sequence and/or light chain sequence, or a sequence which has at least 70% sequence identity thereto, as depicted in table 1. Also provided is
therefore an antibody or functional part or immunoglobulin chain or functional equivalent, having a heavy chain sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's:31-35 and/or having a light chain sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's: 36-40, or sequences that are at least at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, most preferably 100% identical to any one of these heavy chain or light chain sequences.
Preferably, an antibody according to the invention comprises a heavy chain sequence which is at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90% identical to a sequence selected from the group consisting of SEQ ID NO's:31-35 and/or a light chain sequence which is at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90% identical to a sequence selected from the group consisting of SEQ ID NO's: 36-40. Most preferably, an antibody according to the invention comprises a heavy chain sequence which is at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical to a sequence selected from the group consisting of SEQ ID NO's:31-35 and/or a light chain sequence which is at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, most preferably 100% identical to a sequence selected from the group consisting of SEQ ID NO's:36-40. The higher the identity, the more closely an antibody resembles an antibody depicted in table 1.
An antibody or functional part or immunoglobulin chain or functional equivalent according to the invention preferably comprises a heavy chain as well as a light chain which resemble the heavy and the light chain of the same antibody depicted in table 1. Thus, in a preferred embodiment an antibody according to the invention comprises a heavy chain sequence of a given antibody, preferably antibody AT10_004, comprising the sequence of SEQ ID NO: 31. and a light chain sequence of the same antibody, preferably AT10_004, comprising the sequence of SEQ ID NO:36, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
In another embodiment an antibody according to the invention or functional part thereof comprises a heavy chain sequence of antibody AT10_003, comprising the sequence of SEQ ID NO:32 and a light chain sequence of antibody AT10_003, comprising the sequence of SEQ ID NO:37 or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto,
In another embodiment an antibody according to the invention or functional part thereof comprises a heavy chain sequence of antibody AT10_002, comprising the sequence of SEQ ID NO:33 and the light chain sequence of antibody AT10J302, comprising the sequence of SEQ ID NO:38, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more
preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
In another embodiment an antibody according to the invention or functional part thereof comprises a heavy chain sequence of antibody AT10_001, comprising the sequence of SEQ ID NO:34 and the light chain sequence of antibody AT10_001, comprising the sequence of SEQ ID NO:39, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
In another embodiment an antibody according to the invention or functional part thereof comprises a heavy chain sequence of antibody AT10_005, comprising the sequence of SEQ ID NO:35, and the light chain sequence of antibody AT10_005, comprising the sequence of SEQ ID NO:40, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
The invention provides antibodies having an in vitro H3N2 influenza A virus neutralizing activity with an IC50 value of less than 1
An advantage of such antibodies is that a low dosis of said antibody is needed in order to obtain neutralizing capacity. Therefore, less of said influenza A neutralizing antibody has to be administered to an individual for treatment and/or prevention of an influenza A infection. It is favourable to use an amount as low as possible to achieve a desired
effect from both a health care point of view and from an economical point of view. It is preferred to administer to a subject as less as possible of a therapeutic antibody, because this reduces the chance of undesired effects, such as immunological reactions to the antibody. Furthermore, if a lower amount of antibody is used, the cost of treatment of an individual to prevent of counteract influenza infection is reduced.
Generally, the higher the neutralizing activity of an antibody, the lower the amount of antibody necessary for treatment of an individual. As shown in the examples, antibody AT10_ 001 has an in vitro H3N2 A/Ned/177/2008 virus
neutralizing activity with an IC50 value of about 0.64 μg/ml, antibody ATI 0_004 has an in vitro H3N2 A/Ned/177/2008 virus neutralizing activity with an IC50 value of about 0.17 μg/ml, and antibody AT10_002 has an in vitro H3N2 A/Ned/177/2008 virus neutralizing activity with an IC50 value of about 0.18 μg/ml. Therefore, preferably an antibody according to the invention has an in vitro H3N2 influenza A virus
neutralizing activity with an IC50 value of less than 0.8 /ml, more preferably of less than 0.6 g/ml, more preferably of less than 0.5 μg/ml, more preferably of less than 0,4 μg/ml, more preferably of less than 0.3 μ /ml, more preferably of less than 0.2
The example further demonstrates that antibodies AT10_001, AT10_002 and
AT10_004 have in vivo H3N2 neutralizing activity. These antibodies were shown to protect mice against influenza A virus H3N2 HKx-31. All mice receiving antibody AT10_001, AT10_002 or AT10_004 treatment survived a challenge with H3N2 virus, whereas all control mice receiving treatment with a control antibody lost more than 25% of their body weight and had to be removed from the study. In a preferred embodiment, an antibody according to the invention therefore has in vivo H3N2 neutralization activity, for instance as measured by protective activity against influenza H3N2 infection in a mouse model as described in the Example.
Preferably an influenza A neutralizing antibody according to the invention has said in vitro neutralizing activity as determined in a neutralization assay as described in the examples.
Several strains of influenza A virus of the same subtype exist. Different strains of the same influenza A virus subtype may have differences in host infectivity. Therefore, in a preferred embodiment, an influenza A neutralizing antibody according to the invention neutralizes at least one H3N2 influenza virus strain with the indicated neutralizing activity, more preferably at least two, more preferably at least
three, more preferably at least four, more preferably at least five different H3N2 influenza virus strains. In a preferred embodiment, an influenza A neutralizing antibody according to the invention neutralizes at least H3N2 A/Ned/177/2008 influenza virus strain, and/or H3N2 HKx-31, and/or H3N2
A/swine/Neth/St. Oedenrode/96.
Antibodies provided by the invention are capable of binding at least two different influenza subtypes. In one embodiment, an antibody is provided that is capable of binding H3N2 and at least one other group 2 influenza A virus subtype. In another embodiment, an antibody is provided that is capable of binding H1N1 and at least one other group 1 influenza A virus subtype. An advantage of such antibodies is that they thus have cross-binding activity, i.e. are capable of binding at least two different influenza A virus subtypes. In a preferred embodiment, an influenza A neutralizing antibody is provided that is further capable of neutralizing said at least one other group subtype influenza A virus. Such antibodies have cross-neutralizing activity, i.e. have neutralizing activity for at least two different influenza A virus subtypes. Such antibodies have the advantage that the use of a single antibody allows neutralization of multiple influenza subtypes. Such antibodies thus have broad neutralizing activity.
In another preferred embodiment, an influenza A neutralizing antibody is provided that is capable of binding at least one group 2 subtype influenza A virus and at least one group 1 subtype influenza A virus. In a more preferred embodiment, an influenza A neutralizing antibody is provided that is further capable of neutralizing said at least one group 2 and/or said at least one group 1. subtype influenza A virus.
An influenza A neutralizing antibody according to the invention capable of specifically binding at least two group 2 influenza A virus subtypes, or at least one group 1 and one group 2 influenza A virus subtype, is preferably capable of binding to an epitope within a hemagglutinin protein of an influenza A virus protein that is shared between influenza subtypes. Preferably, said epitope is located in a conserved region of the hemagglutinin protein of influenza A virus. As described above, H3, H4, H7, H10, H14 and H15 are currently known influenza viruses from group 2. Said at
least two group 2 subtype influenza A virus subtypes are thus preferably selected from the group consisting of H3, H4, H7, H10, H14 and H15 containing influenza A virus subtypes. Provided is in one embodiment an antibody according to the invention capable of binding and/or neutralizing a H3N2 influenza A virus and capable of binding a H4, H7, H10, H14 or H15 containing influenza A virus. Preferably, such antibody is capable of binding a H7 containing influenza A virus subtype. H7 containing influenza viruses frequently infect poultry. Because humans are in direct contact with infected poultry, there is considerable risk of infection of humans with H7 influenza viruses and mixing of avian H7 and human influenza viruses. Infection of humans with H7 containing influenza virus resulting in death has been reported. Therefore, in a preferred embodiment, the invention provides an influenza A neutralizing antibody capable of binding a H3 and a H7 subtype influenza A virus. Preferably, said antibody is further capable of neutralizing both H3 and H7 subtype influenza A virus.
As described above, HI, H2, H5, H6, H8, H9, Hl l, H12, H13 and H16 are currently known influenza viruses from group 1. The above mentioned at least one group 1 subtype influenza A virus is therefore preferably selected from the group consisting of HI, H2, H5, H6, H8, H9, Hl l, H12, H13 and H16 containing influenza A virus subtypes. Provided is therefore in one embodiment an antibody according to the invention capable of binding and/or neutralizing a H3N2 influenza A virus and capable of binding a HI, H2, H5, H6, H8, H9, Hl l, H12, H13 or H16 containing influenza A virus. Preferably said at least one group 1 subtype influenza A virus is selected from the group consisting of HI and H5 containing influenza A virus subtypes. H1N1 is one of the influenza A viruses capable of infecting humans and generally the seasonal influenza epidemic comprises at least one H1N1 influenza virus. H5 containing viruses, such as H5N1, H5N3, H5N4 and H5N9, mainly infect birds. However, some of H5 influenza subtypes can be transferred from birds to human. Infection of humans with H5 influenza subtypes is particularly dangerous because of a risk of life-threatening complications, such as pneumonia, and of death.
In a particularly preferred embodiment, the invention provides an influenza A neutralizing antibody capable of binding and/or neutralizing a H3, a H7 and a HI subtype influenza A virus.
In one embodiment, antibodies according to the invention are capable of binding at least one influenza virus which infects non-human animals, including, but not limited to birds such as chickens, ducks, geese, turkeys, and pheasants, and swine, ferrets, rabbits, cats, dogs and horses. Such antibodies can be used to counteract influenza virus infection in said non-human animals, for instance, but not limited to, animals that are kept as livestock or pet. Furthermore, because humans are in direct contact with such animals, there is considerable risk of infection of humans with influenza viruses that have infected said animals. Another risk is the mixing of influenza viruses capable of infecting non-human animals and influenza viruses capable of infecting humans resulting in new, potentially highly pathogenic, influenza viruses. Therefore, preferably an antibody according to the invention is provided which is capable of binding an influenza A virus subtype that infects non- human animals. In a preferred embodiment, said antibody is capable of binding an avian and/or swine influenza A virus subtype. Examples of such avian and/or swine influenza A virus subtype include, but are not limited to, H4, H10, H15, H5 and H7 containing influenza viruses such as H4N6, H10N3, H15N8, H7N1, H7N7 and/or H5N1.
As indicated above, H7 containing influenza viruses frequently infect poultry and there is a considerable risk of infection of humans with H7 influenza viruses and mixing of avian H7 and human influenza viruses. Therefore, in one embodiment an antibody according to the invention is provided which is capable of binding a H7 subtype influenza A virus. More preferably, an antibody is provided which is capable of neutralizing a H7 subtype influenza A virus. For example, such antibody has an in vitro H7N7 (such as A/Ch/Neth/621557/03) and/or H7N1 (such as A/Ch/Italy/1067/99) influenza A virus neutralizing activity. Preferably, said antibody has an in vitro H7N1 and/or H7N7 influenza A virus neutralizing activity with an IC50 value of less than 10 μ /ml, more preferably of less than 5 g/ml, more preferably of less than 4
more preferably of less than 2 μ /ml, more preferably of les more preferably of less than 0.8 ng/ml, more preferably of less than 0.6
eferably of less than 0.5 ^ig/ml, more preferably of less than 0.4 ng/ml, more preferably of less than 0.3 μg/ml, more preferably of less than 0.2 μ /ml. Preferably such influenza A neutralizing
antibody according to the invention has said in vitro neutralizing activity as determined in a neutralization assay as described in the examples. In a preferred embodiment, an influenza A neutralizing antibody according to the invention neutralizes at least one H7N1 and/or H7N7 influenza virus strain with the indicated neutralizing activity, more preferably at least two, more preferably at least three, more preferably at least four, more preferably at least five different H7N1 and/or H7N7 influenza virvis strains. In a preferred embodiment, an influenza A neutralizing antibody according to the invention neutralizes at least H7N7 (A/Ch/Neth/621557/03) and/or H7N1 (A Ch/Italy/1067/99).
A particularly preferred antibody of the invention capable of binding H7 subtype influenza A viruses is AT10_004, which has a heavy chain sequence of SEQ ID NO:31 as depicted in table 1, and a light chain sequence of SEQ ID NO:36 as depicted in table 1. Another particularly preferred antibody of the invention capable of binding H7 subtype influenza A viruses is AT10_002, which has a heavy chain sequence of SEQ ID NO:33 as depicted in table 1, and a light chain sequence of SEQ ID NO:38 as depicted in table 1. Another particularly preferred antibody of the invention capable of binding H7 subtype influenza A viruses is AT10_001, which has a heavy chain sequence of SEQ ID NO:34 as depicted in table 1, and a light chain sequence of SEQ ID NO:39 as depicted in table 1.
The heavy and light chain CDR sequences of these preferred antibodies are also depicted in table 1. SEQ ID NO: l is the heavy chain CDRl sequence, SEQ ID NO:6 is the heavy chain CDR2 sequence, SEQ ID NO: 11 is the heavy chain CDR3 sequence, SEQ ID NO: 16 is the light chain CDRl sequence, SEQ ID NO:21 is the light chain CDR2 sequence, and SEQ ID NO: 26 is the light chain CDR3 sequence of antibody AT10_004. SEQ ID NO:3 is the heavy chain CDRl sequence, SEQ ID NO:8 is the heavy chain CDR2 sequence, SEQ ID NO: 131 is the heavy chain CDR3 sequence, SEQ ID NO: 18 is the light chain CDRl sequence, SEQ ID NO:23 is the light chain CDR2 sequence, and SEQ ID NO:28 is the light chain CDR3 sequence of antibody AT10_002. SEQ ID NO:4 is the heavy chain CDRl sequence, SEQ ID NO:9 is the heavy chain CDR2 sequence, SEQ ID NO: 14 is the heavy chain CDR3 sequence, SEQ ID NO: 19 is the light chain CDRl sequence, SEQ ID NO:24 is the light chain CDR2 sequence, and SEQ ID NO:29 is the light chain CDR3 sequence of antibody AT10_001.
The invention thus provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof comprising:
- a heavy chain CDR1 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 1, and
- a heavy chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:6, and
- a heavy chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 11, and
- a light chain CDR1 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 16, and
- a light chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:21, and
- a light chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:26.
The invention further provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof comprising:
- a heavy chain CDR1 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:3, and
- a heavy chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:8, and
- a heavy chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 13, and
- a light chain CDR1 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 18, and
- a light chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:23, and
- a light chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:28.
The invention further provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof comprising:
- a heavy chain CDR1 sequence comprising a sequence which is at least 70% identical to SEQ ID NQ:4, and
- a heavy chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:9, and
- a heavy chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 14, and
- a light chain CDR1 sequence comprising a sequence which is at least 70% identical to SEQ ID NO: 19, and
- a light chain CDR2 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:24, and
- a light chain CDR3 sequence comprising a sequence which is at least 70% identical to SEQ ID NO:29.
Preferably, said antibody or functional part or immunoglobulin chain or functional equivalent comprises heavy chain CDR1, CDR2 and/or CDR3 sequences and/or light chain CDR1, CDR2 and/or CDR3 sequences that are at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, most preferably 100% identical to these sequences.
As described above, some H5 influenza subtypes can infect humans.
Infection of humans with H5 influenza subtypes is particularly dangerous because of a risk of life -threatening complications, such as pneumonia, and of death. Therefore, in one embodiment an antibody according to the invention is provided which is capable of binding a H5 subtype influenza A virus. More preferably, an antibody is provided which is capable of neutralizing a H5 subtype influenza A virus. For example such antibody has an in vitro H5N1 (such as A/Turkey/Turkey/04) influenza A virus neutralizing activity. Preferably, said antibody has an in vitro H5N1 influenza A virus neutralizing activity with an IC50 value of less than 10 ng/ml, more preferably of less than 5
more preferably of less than 4 more preferably
of less than 3
more preferably of less than 1 μ /ml, more preferably of less than 0.8 μg/ml, more preferably of less than 0.6 μ /ml, more preferably of less than 0.5 μg/ml, more preferably of less than 0.4 μ¾/πι1, more preferably of less than 0.3 μg/ml, more preferably of less than 0.2 μ /ml. Preferably such influenza A neutralizing antibody according to the invention has said in vitro neutralizing activity as determined in a neutralization assay as described in the examples. In a preferred embodiment, an influenza A neutralizing antibody according to the invention is provided that neutralizes at least one H5N1 influenza virus strain with the indicated neutralizing activity, more preferably at least two, more preferably at least three, more preferably at least four, more preferably at least five different
H5N1 influenza virus strains. In a preferred embodiment, an influenza A neutralizing antibody according to the invention neutralizes at least H5N1 (A/Turkey/Turkey/04)). A particularly preferred antibody according to the invention capable of binding a H5 subtype influenza A virus is AT10_003, Another particularly preferred antibody according to the invention capable of binding a H5 subtype influenza A virus is AT10_005. Antibodies or functional parts having sequences that are at least 70% identical to the CDR sequences of AT10_003 or AT10_005 are therefore preferred for counteracting a H5 subtype influenza A virus.
An antibody according to the invention is preferably a human antibody. The use of human antibodies for prophylaxis and therapy in humans diminishes the chance of side-effects due to an immunological reaction in a human individual against non-human sequences. In another embodiment an antibody according to the invention is a humanized antibody. Humanized antibodies are made by incorporating non- human hypervariable domains into human antibodies and therefore immunogenic properties are diminished as compared to fully non-human antibodies. In another embodiment an antibody according to the invention is a chimeric antibody. In a chimeric antibody, sequences of interest, such as for instance a binding site of interest, are included into an antibody according to the invention.
Preferred antibodies according to the invention have a high binding affinity for the hemagglutinin protein. Measurement of the affinity constant and
specificity of binding between antigen and antibody is preferred in determining the efficacy of prophylactic, therapeutic, diagnostic and research methods using anti- influenza A antibodies of the invention. "Binding affinity" generally refers to the strength of the total sum of the noncovalent interactions between a single binding site of a molecule (e.g., an antibody) and its binding partner (e.g., an antigen). Unless indicated otherwise, as used herein, "binding affinity" refers to intrinsic binding affinity which reflects a 1: 1 interaction between members of a binding pair (e.g., antibody and antigen). The affinity can generally be represented by the equilibrium dissociation constant (Kp), which is calculated as the ka to kd ratio, , see, e.g., Chen, Y., et ah, (1999) J, Mol Biol 293: 865-881. Affinity can be measured by common methods known in the art, such as for instance a surface plasmon resonance (SPR) assay such as BiaCore or IBIS-iSPR instrument at IBIS Technologies BV (Hengelo, the
Netherlands) or solution phase assays, such as Kinexa. Preferably an antibody according to the invention has a binding affinity for an epitope on the influenza HA protein characterized by a dissociation constant (KD) of at most 100 nM, more preferably at most 50 nM, more preferably at most 25 nM, more preferably at most 10 nM, more preferably at most 5 nM, more preferably at most 2 nM, more preferably at most 1 nM, more preferably at most 0.5 nM, more preferably at most 0.3 nM, more preferably at most 0. 1 nM.
The invention further provides an isolated, synthetic or recombinant nucleic acid molecule with a length of at least 15 nucleotides, or a functional equivalent thereof, encoding at least one CDR sequence of an antibody or functional part or immunoglobulin chain or functional equivalent according to the invention. Preferably a nucleic acid according to the invention has a length of at least 30 nucleotides, more preferably at least 50 nucleotides, more preferably at least 75 nucleotides. A nucleic acid according to the invention is for instance isolated from a B-cell which is capable of producing an antibody according to the invention. In a preferred embodiment a nucleic acid encoding an antibody according to the invention is provided.
As used herein "an isolated, synthetic or recombinant nucleic acid molecule with a length of at least 15 nucleotides, or a functional equivalent thereof, encoding at least one CDR sequence of an antibody or functional part thereof or immunoglobulin
chain or functional equivalent thereof according to the invention" is herein also referred to as "a nucleic acid molecule or functional equivalent thereof according to the invention".
As used herein, a nucleic acid molecule or nucleic acid sequence of the invention preferably comprises a chain of nucleotides, more preferably DNA and/or RNA. In other embodiments a nucleic acid molecule or nucleic acid sequence of the invention comprises other kinds of nucleic acid structures such as for instance a DNA/RNA helix, peptide nucleic acid (PNA), locked nucleic acid (LNA) and/or a ribozyme. Such other nucleic acid structures are referred to as functional equivalents of a nucleic acid sequence. The term "functional equivalent of a nucleic acid molecule" also encompasses a chain comprising non-natural nucleotides, modified nucleotides and/or non-nucleotide building blocks which exhibit the same function as natural nucleotides.
Nucleic acid sequences encoding preferred heavy chain and light chain CDR's of antibodies AT1Q_004, AT10J)03, AT10_002, AT10J)01 and AT10_005 are depicted in table 1. Nucleic acid molecules encoding a heavy or light chain CDR of an antibody according to the invention which differ from the CDR nucleic acid sequences depicted in table 1 but have nucleic acid codons encoding for the same amino acids of said heavy or light chain CDR are also encompassed by the invention. Nucleic acid molecules encoding a heavy or light chain CDR of an antibody depicted in table 1 which has been altered, for instance through conservative amino acid substitution, whereby an amino acid residue is substituted by another residue with generally similar properties (size, hydrophobicity, etc), are also encompassed by the invention, as long as the resulting CDR has at least 70% sequence identity with a CDR depicted in table 1.
A preferred nucleic acid molecule according to the invention comprises: a heavy chain CDR1 encoding sequence which has at least 70% sequence identity to a sequence which is selected from the group consisting of SEQ ID NO's:41-45, and/or
a heavy chain CDR2 encoding sequence which has at least 70% sequence identity to a sequence which is selected from the group consisting of SEQ ID NO's:46-50, and/or
a heavy chain CDR3 encoding sequence which has at least 70% sequence identity to a sequence which is selected from the group consisting of SEQ ID NO's:51-55, and/or
a light chain CDR1 encoding sequence which has at least 70% sequence identity to a sequence which is selected from the group consisting of SEQ ID NO's: 56-60, and/or
- a light chain CDR2 encoding sequence which has at least 70% sequence identity to a sequence which is selected from the group consisting of SEQ ID NO's:61-65, and/or
a light chain CDR3 encoding sequence which has at least 70% sequence identity to a sequence which is selected from the group consisting of SEQ ID NO's:66-70.
A nucleic acid molecule according to the invention preferably comprises a sequence which has at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 90%, most preferably at least 95% sequence, most preferably 100% identity to said sequences. Preferably, said nucleic acid molecule comprises at least one CDR encoding sequence. Further provided is a nucleic acid molecule or functional equivalent thereof comprising a sequence which has at least 70% sequence identity, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 90%, most preferably at least 95%, most preferably 100%o sequence identity to a nucleic acid molecule selected from SEQ ID NO's:41-70, said nucleic acid molecule or functional equivalent having at least 15 nucleotides.
A nucleic acid molecule or functional equivalent thereof according to the present invention preferably encodes a region which has at least 70% sequence identity to a heavy chain and/or a light chain as depicted in table 1. Thus, a preferred nucleic acid molecule or a functional equivalent comprises a sequence which has at least 70% sequence identity to a sequence selected from the group consisting of SEQ ID NO's:71-75 and/or a sequence which has at least 70% sequence identity to a sequence selected from the group consisting of SEQ ID NO's:76-80. More preferably, a
nucleic acid molecule or a functional equivalent according to the invention comprises a heavy chain encoding sequence as well as a light chain encoding sequence which resemble the heavy and the light chain encoding sequences of the same antibody depicted in table 1. Thus, in a preferred embodiment a nucleic acid or functional equivalent according to the invention comprises a heavy chain encoding sequence of antibody AT10J304, comprising the sequence of SEQ ID NO:71 and a light chain encoding sequence of antibody AT10„004, comprising the sequence of SEQ ID NO:76 or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
In another embodiment a nucleic acid or functional equivalent according to the invention comprises a heavy chain encoding sequence of antibody AT10„003, comprising the sequence of SEQ ID NO: 72 and a light chain encoding sequence of antibody AT10_003, comprising the sequence of SEQ ID NO:77, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
In another embodiment a nucleic acid or functional equivalent according to the invention comprises a heavy chain encoding sequence of antibody AT10_002, comprising the sequence of SEQ ID NO:73 and a light chain encoding sequence of antibody AT10„002, comprising the sequence of SEQ ID NO:78, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least
93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
In another embodiment a nucleic acid or functional equivalent according to the invention comprises a heavy chain encoding sequence of antibody AT10_001, comprising the sequence of SEQ ID NO: 74 and a light chain encoding sequence of antibody ATI 0_001, comprising the sequence of SEQ ID NO:79, or sequences that are at least 70%, preferably at least 75%), more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
In another embodiment a nucleic acid or functional equivalent according to the invention comprises a heavy chain encoding sequence of antibody AT10_005, comprising the sequence of SEQ ID NO: 75 and a light chain encoding sequence of antibody AT10_005, comprising the sequence of SEQ ID NO:80, or sequences that are at least 70%, preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto.
The percentage of identity of an amino acid or nucleic acid sequence, or the term "% sequence identity", is defined herein as the percentage of residues in a candidate amino acid or nucleic acid sequence that is identical with the residues in a reference sequence after aligning the two sequences and introducing gaps, if necessary, to achieve the maximum percent identity. Methods and computer programs for the alignment are well known in the art.
Further provided is a vector comprising a nucleic acid molecule or sequence or functional equivalent according to the invention. As used herein "a vector comprising a nucleic acid sequence or molecule or functional equivalent according to the invention" is also referred to as "a vector according to the invention". Methods for constructing a vector with a nucleic acid or functional equivalent according to the invention are well known in the art. Non-limiting examples of vectors suitable for generating a vector of the invention are retroviral and lentiviral vectors. Such vector is suitable for a variety of applications. For instance, a vector of the invention comprising a therapeutically beneficial nucleic acid sequence is suitable for prophylactic or therapeutic applications against influenza. Administration of such vector to an individual, preferably a human, in need thereof results in expression of said prophylactic or therapeutic nucleic acid sequence in vivo resulting in at least partial treatment or prophylaxis against influenza. Said vector can also be used in applications involving in vitro expression of a nucleic acid molecule of interest, for instance for (commercial) production of antibodies or functional equivalents according to the invention. Also provided is therefore an isolated or recombinant cell comprising a nucleic acid molecule or functional equivalent a vector according to the invention.
A nucleic acid molecule or vector according to the invention is particularly useful for generating antibodies or functional parts, or immunoglobulin chains or functional equivalents, which are specific for influenza A virus HA protein. This is for instance done by introducing such nucleic acid molecule or vector into a cell so that the cell's micleic acid translation machinery will produce the encoded antibodies or functional parts, immunoglobulin chains or functional equivalents. In one
embodiment, a nucleic acid molecule or vector encoding a heavy and/or light chain according to the invention is expressed in so called producer cells, such as for instance cells of a Chinese hamster ovary (CHO), NSO (a mouse myeloma) or 293(T) cell line, some of which are adapted to commercial antibody production. Proliferation of said producer cells results in a producer cell line capable of producing antibodies according to the invention. Preferably, said producer cell line is suitable for producing antibodies for use in humans. Hence, said producer cell line is preferably free of pathogenic agents such as pathogenic micro-organisms. Most preferably, antibodies
consisting of human sequences are generated using at least one nucleic acid molecule or vector according to the invention.
An isolated or recombinant antibody producing cell capable of producing an antibody according to the invention is therefore also provided. An antibody producing cell is defined herein as a cell which is capable of producing and/or secreting antibodies or functional equivalents thereof, and/or which is capable of developing into a cell which is capable of producing and/or secreting antibodies or functional equivalents thereof. An antibody producing cell according to the invention is preferably a producer cell which is adapted to commercial antibody production.
Preferably, said producer cell is suitable for producing antibodies for use in humans. A method for producing an antibody according to the invention is also provided, said method comprising providing a cell, preferably an antibody producing cell, with a nucleic acid molecule or functional equivalent or a vector according to the invention, and allowing said cell to translate said nucleic acid molecule or functional equivalent or vector, thereby producing antibodies according to the invention. A method according to the invention preferably further comprises a step of harvesting, purifying and/or isolating antibodies according to the invention. Obtained antibodies according to the invention are preferably used in human therapy, optionally after additional purifying, isolation or processing steps.
In one embodiment, an antibody according to the invention is coupled to another moiety to form an antibody-drug conjugate. An antibody according to the invention is for instance coupled to an antiviral agent, such as acyclovir, penciclovar, lamivudine, ribavirin, zanamivir, laninamivir, peramivir, idoxuridine, oseltamivir, amantadine, remantidine, maxamine, peramivir, or thymalfasin. The term "antiviral agent" as used herein refers to any substance that reduces or blocks the function, or growth, of a virus and/or causes destruction of a virus. In another embodiment, a moiety that is coupled to an antibody according to the invention is an antimicrobial peptide. The term "antimicrobial peptide" as used herein refers to small amphipathic peptides of variable length (typically 6 to 100 amino acids), sequence and structure with activity against microorganisms such as for instance bacteria, protozoa, yeast, fungi and/or virusses. Antimicrobial peptides usually act through relatively non-
specific mechanisms resulting in membranolytic activity but several antimicrobial peptides can also stimulate the innate immune response. In a preferred embodiment, said antimicrobial peptide has anti-viral activity. Non-limiting examples of suitable antimicrobial peptides are magainins, PGLa, cathelicidins (such as LL-37 and cathelicidin-related antimicrobial peptide (CRAMP)), alamethicin, mellitin and cecropin, hydramacin-1, pexiganan, MSI-78, MSI-843, MSI-594, polyphemusin, human antimicrobial peptide, defensins, protegrins and indolicidin. In yet another embodiment, a moiety that is coupled to an antibody according to the invention is an immunomodulatory molecule such as an CDS antibody. Such CD3 antibody is capable of binding T cells and, if coupled to an antibody according to the invention, targeting T cells to influenza A virus infected cells.
Said other moiety, for example a cytotoxic agent, is preferably coupled to an antibody according to the invention via a linker such as for instance an acid-labile hydrazone linker, or via a peptide linker like citruline-valine, or through a thioether linkage, or by sortase catalized transamidation, which is described in detail in WO 2010/087994.
Sortase catalized transamidation involves engineering of a sortase recognition site (LPETGG) on the heavy chain of an antibody, preferably on the C- terminal part of the heavy chain, and on the moiety to be coupled to said antibody. The antibody and the moiety further typically contain a GGGGS sequence and a tag for purification purposes, such as a HIS tag. Subsequently sortase mediated transamidation is performed followed by click chemistry linkage. In a sortase catalized transaminidation, "click chemistry linkage" typically involves chemical coupling of, for instance, an alkyne-containing reagent and, for instance, an azide- containing reagent which are added by sortase through addition of glycines to the sortase motif on the heavy chain of the antibody and to a sortase motif on the moiety (such as a protein, peptide or antibody) to be coupled to the antibody. In one embodiment, the invention therefore provides an antibody according to the invention wherein a sortase recognition site (LPETGG) is engineered on the heavy chain of the antibody, preferably on the C-terminal part of the heavy chain, the antibody preferably further containing a GGGGS sequence and a purification tag, such as a HIS tag.
In another embodiment an antibody according to the invention is coupled to another moiety via a thioether linkage. In such case, one or more cysteines are preferably incorporated into an antibody according to the invention. Cysteines contain a thiol group and, therefore, incorporation of one or more cysteines into an antibody according to the invention, or replacement of one or more amino acids by one or more cysteines of an antibody according to the invention, enable coupling of said antibody to another moiety. Said one or more cysteines are preferably introduced into an antibody according to the invention at a position where it does not significantly influence folding of said antibody, and does not significantly alter antigen binding or effector function. The invention therefore also provides an antibody according to the invention wherein at least one amino acid other than cysteine has been replaced by a cysteine.
Influenza specific antibodies described herein have different (cross-) binding and neutralizing capacities. An antibody according to the invention, such as AT10_001, AT10_002, AT10_003, AT10_004 or AT10_005 can be advantageously used in combination with another antibody according to the invention. Such combination provides an even stronger anti-influenza effect. In one embodiment an antibody according to the invention is combined with another antibody according to the invention that is capable of binding and/or neutralizing at least one other influenza A subtype. Combination of antibodies according to the invention which bind and/or neutralize different influenza A virus subtypes enables counteracting a wider range of influenza A subtypes in a single treatment. Such combination is thus useful in counteracting a broad range of influenza viruses. Furthermore, it is also
advantageous to combine an antibody according to the invention with a known antibody capable of binding and/or neutralizing an influenza A virus subtype. Such combination for instance provides a stronger response against an influenza A virus and/or provides a response against a wide range of influenza subtypes. Yet another example is a combination of an antibody according to the invention and a known antibody specific for influenza B. In another embodiment, the invention provides an influenza A virus bispecific antibody with specificity for at least two different influenza A virus subtypes, preferably at least three influenza A virus subtypes, more preferably at least four influenza A subtypes. An "influenza A virus bispecific
antibody" as used herein is defined as an antibody capable of simultaneously binding at least two different influenza A virus subtypes, such as two, three or four subtypes, and is also referred to as an "influenza A virus bispecific antibody according to the invention" or a "bispecific antibody according to the invention". The term "influenza A virus bispecific antibody" also encompasses functional parts of such influenza A virus bispecific antibody which has retained its capability of binding at least two different influenza A virus subtypes simultaneously, such as bispecific single chain variable fragments (scFv), bispecific Fab fragments and bispecific F(ab')2 fragments. Also provided is a pharmaceutical composition comprising an influenza A virus bispecific antibody according to the invention.
In one embodiment, a bispecific antibody according to the invention comprises two non-identical heavy chain-light chain combinations, thus having two antigen-binding regions which recognize two different influenza A virus subtypes, preferably two different HA subtypes. For instance, in one embodiment, an influenza A virus bispecific antibody comprises a heavy and light chain of an antibody according to the invention as depicted in table 1 and a heavy and light chain of another antibody according to the invention as depicted in table 1. Bispecific single chain variable fragments (scFv), bispecific Fab fragments and bispecific F(ab')2 fragments comprise for instance a scFv or Fab or F(ab')2 fragment of an antibody according to the invention and a scFv or Fab or F(ab')2 fragment of another antibody according to the invention. In a preferred embodiment, an influenza A virus bispecific antibody according to the invention comprises a heavy and light chain of two antibodies selected from the group consisting of AT10_001, ΑΤ10_002, AT10_003, AT10_Q04 and AT10_005 as depicted in table 1, or a scFv or Fab fragment thereof. Preferably said bispecific antibody comprises a heavy and light chain of antibody AT10_003 or AT10_005, preferably of antibody AT10_005, and a heavy and light chain of an antibody selected from the group consisting of AT10J301, AT10_002 and AT10_004.
In another embodiment, two antibodies according to the invention are coupled to each other or an antibody according to the invention is coupled to a known influenza specific antibody. This is in a preferred embodiment done by sortase catalized transamidation, which is described herein before and in detail in WO 2010/087994. For this purpose, sortase catalized transamidation involves engineering
of a sortase recognition site (LPETGG) on the heavy chains of both antibodies to be coupled, preferably on the C-terminal part of the heavy chains. The antibodies further typically contain a GGGGS sequence and a purification tag, such as a HIS tag. Thus, if two antibodies according to the invention are coupled, both said antibodies are preferably engineered as described herein before and in detail in WO 2010/087994. Subsequently sortase mediated transamidation is preferably performed followed by click chemistry linkage to couple both antibodies via their heavy chains. As herein explained before, "click chemistry linkage" involves chemical coupling of, for instance, an alkyne-containing reagent and, for instance, an azide-containing reagent which are added by sortase through addition of glycines to the sortase motif on the heavy chain of a first antibody and to the heavy chain of a second antibody that is to be coupled to the first antibody. One embodiment of the invention therefore provides a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent thereof, comprising:
i) at least two, preferably three, different heavy chain CDR sequences and at least two, preferably three, different light chain CDR sequences of an antibody selected from the group consisting of AT10_001 and AT10_002 and AT10_003 and AT10_004 and AT10_005; and
ii) at least two, preferably three, different heavy chain CDR sequences and at least two, preferably three, different light chain CDR sequences of another antibody. Said other antibody is preferably another influenza specific antibody, although this is not necessary. In a particularly preferred embodiment, at least two antibodies according to the invention are coupled to each other by sortase catalized transamidation, whereby said at least two antibodies are preferably selected from the group consisting of AT10_001, AT10_002, ΑΊΊ0_003, AT10_004 and AT10_005 as depicted in Table 1.
One preferred embodiment of the invention therefore provides a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent thereof, comprising:
i) at least two different heavy chain CDR sequences and at least two different light chain CDR sequences of an antibody selected from the group consisting of AT10_001 and AT10„002 and AT10_003 and AT10_004 and AT10_005; and
ii) at least two different heavy chain CDR sequences and at least two different light
chain CDR sequences of an antibody selected from the group consisting of AT10_001 and ATKL002 and AT10_Q03 and AT1Q_004 and AT1Q_005,
wherein said antibody selected in i) is different from said antibody selected in ii). Preferably, a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention comprises the heavy chain CDR1, CDR2 and CDR3 and light chain CDR1, CDR2 and CDR3 sequences of at least two antibodies according to the invention. Further provided is therefore a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent thereof, comprising:
i) heavy chain CDR1, CDR2 and CDR3 and light chain CDR1, CDR2 and CDR3 sequences of an antibody selected from the group consisting of AT10J301 and AT10_002 and AT10_003 and AT10„004 and AT10J)05; and
ii) heavy chain CDR1, CDR2 and CDR3 and light chain CDR1, CDR2 and CDR3 sequences of an antibody selected from the group consisting of AT10_001 and
AT10_002 and AT10_003 and AT10_004 and AT10_005,
wherein said antibody selected in i) is different from said antibody selected in ii).
In one embodiment a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention comprises the heavy chain sequence and the light chain sequence of at least two antibodies according to the invention, or sequences that are at least 70% identical thereto. The invention thus also provides a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent thereof, comprising:
i) the heavy chain sequence and the light chain sequence of an antibody selected from the group consisting of AT10_001 and AT10_002 and AT10_003 and AT10_004 and AT10_005, or a sequence that is at least 70%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto; and
ii) the heavy chain sequence and the light chain sequence of an antibody selected from the group consisting of AT10_001 and AT10_002 and AT10_Q03 and AT10.004 and AT10_005, or a sequence that is at least 70%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto,
wherein said antibody selected in i) is different from said antibody selected in ii).
Such multimeric antibody, multimeric immunoglobulin or functional equivalent is typically a hetero multimeric complex, comprising at least one heavy chain of one antibody and at least one heavy chain of another antibody. In one embodiment, the heavy chain of one kind of antibody is paired with the heavy chain of another kind of antibody. In a preferred embodiment, said hetero multimeric complex comprises two paired heavy chains of one kind of antibody, coupled to two paired heavy chains of another kind of antibody. Preferably, the corresponding light chains of said antibodies are also bound to said paired heavy chains, thus forming two coupled antibodies. As used herein, the term "dimeric antibody" refers to two antibodies that are coupled to each other (wherein each antibody contains two heavy chains and two light chains). The term "multimeric antibody" refers to at least two, such as for instance two, three, four or five, antibodies that are coupled to each other. The term "multimeric immunoglobulin" refers to at least two immunoglobulin chains (such as for instance single domain antibodies, single chain antibodies, nanobodies, unibodies or single chain variable fragments (scFv)) that are coupled to each other.
In one embodiment, antibody AT10_003 or AT10_005 is coupled to an antibody selected from the group consisting of AT10_001, AT10_002 and AT10_004 by sortase catalized transamidation. Such combination of antibodies is preferred because antibodies AT10_003 and AT10_005 have specificity against at least influenza A virus subtypes HI and H5 and antibodies AT10_001, AT10_002 and AT10_004 have specificity against at least influenza A virus subtypes H3 and H7 and
are capable of neutralizing at least H3N2 with high neutralizing capacity. Therefore, such combinations provide activity against a broad range of influenza A virus subtypes. Preferably, antibody AT10_005 is coupled to antibody AT10J)01, ΑΤΊ0_002 or AT10_004 by sortase catalized transamidation, because antibody AT10_005 is capable of neutralizing at least ΗΓΝ1 influenza A virus with high neutralizing capacity. The invention therefore in one embodiment provides an influenza A virus bispecific antibody according to the invention comprising at least part of the sequence, preferably the heavy and/or light chain, of antibody AT10_003 or antibody AT10_005 as depicted in table 1, preferably of antibody AT10_005, and comprising at least part of the sequence, preferably the heavy and/or light chain, of antibody AT10_001, AT10_002 or AT1Q_004 as depicted in table 1, whereby said part of the sequence preferably comprises at least 70% of the sequence of said antibody, more preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 90%, more preferably at least 95%, more preferably at least 95% of the sequence of said antibody. In a particularly preferred embodiment, an influenza A virus bispecific antibody according to the invention comprising essentially the whole sequence of antibody AT10_003 or antibody AT10J305 as depicted in table 1, preferably antibody AT10_005, and comprising essentially the whole sequence of antibody AT10_001, AT10_002 or AT10_004 as depicted in table 1 is provided. For instance, preferably an influenza A virus bispecific antibody according to the invention comprises the heavy chain and the light chain of antibody AT10_003 or of antibody AT10_005 and the heavy chain and the light chain of antibody AT10_001, of antibody AT10_Q02 or of antibody AT10J304. Preferably said antibodies are coupled by sortase catalized transamidation as herein described.
In another embodiment, antibody AT10J303 is coupled to an antibody selected from the group consisting of ATIOJXU, AT10_002, AT10_004 and AT10_005 by sortase catalized transamidation. Such combination of antibodies is preferred because the AT10_003 epitope is located on the HA1 subunit of the HA protein, whereas the binding epitope of antibodies AT10_001, AT10_002, AT10_004 and AT10_005 is, at least partly, located on the HA2 subunit of the protein. Therefore, such combinations target different epitopes within the HA protein and therefore such combination provides a strong response against influenza A virus. The invention therefore in one embodiment provides an influenza A virus bispecific antibody
according to the invention comprising at least part of the sequence, preferably the heavy and/or light chain, of antibody AT10_003 as depicted in table 1 and comprising at least part of the sequence, preferably the heavy and/or light chain, of antibody AT10_001, AT10_002, AT10„004 or AT10J)Q5 as depicted in table 1, whereby said part of the sequence preferably comprises at least 70% of the sequence of said antibody, more preferably at least 75%, more preferably at least 80%, more preferably at least 85%, more preferably at least 90%, more preferably at least 95%, more preferably at least 95% of the sequence of said antibody. In a particularly preferred embodiment, an influenza A virus bispecific antibody according to the invention comprising essentially the whole sequence of antibody AT10_003 as depicted in table 1, and comprising essentially the whole sequence of antibody AT10_001, AT10_002, AT10_004 or AT10_005 as depicted in table 1 is provided. Preferably said antibodies are coupled by sortase catalized transamidation as herein described. Yet another embodiment of the invention provides a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent thereof, comprising:
i) at least two different heavy chain CDR sequences and at least two different light chain CDR sequences of antibody AT10J302; and
ii) at least two different heavy chain CDR sequences and at least two different light chain CDR sequences of antibody AT10_005,
Preferably, said multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention comprises:
i) heavy chain CDR1, CDR2 and CDR3 and light chain CDR1, CDR2 and CDR3 sequences of antibody AT10__002; and
ii) heavy chain CDR1, CDR2 and CDR3 and light chain CDR1, CDR2 and CDR3 sequences of antibody AT10_005.
In a particularly preferred embodiment, said multimeric antibody, multimeric immunoglobulin or functional equivalent comprises:
i) the heavy chain sequence and the light chain sequence of antibody AT10_002, or sequences that are at least 70%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%,
more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99%, identical thereto; and
ii) the heavy chain sequence and the light chain sequence of antibody A 1Q_005, or sequences that are at least 70%, more preferably at least 80%, more preferably at least 85%, more preferably at least 86%, more preferably at least 87%, more preferably at least 88%, more preferably at least 89%, more preferably at least 90%, more preferably at least 91%, more preferably at least 92%, more preferably at least 93%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, more preferably at least 99% identical thereto.
As shown in the Examples, a multimeric antibody or immunoglobulin based on antibodies AT10_002 and AT10_005 provide excellent influenza neutralizing activity, both in vitro and in vivo. Since AT10_002 is capable of neutralizing H3N2 and AT10_005 is capable of neutralizing H1N1, a multimeric antibody or
immunoglobulin based on antibodies AT10_002 and AT10_005 is particularly suitable for neutralizing both H3N2 and H1N1. Further provided is therefore a method for neutralizing a H1N1 influenza A virus and/or an H3N2 influenza A virus, comprising contacting said H1N1 influenza A virus and/or said H3N2 influenza A virus with a multimeric antibody, multimeric immunoglobulin or functional equivalent comprising at least two, preferably three, different heavy chain CDR sequences and at least two, preferably three, different light chain CDR sequences of antibodies AT10_002 and AT10_005, resulting in neutralization of said virus.
In one embodiment, a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention is a dimeric antibody or dimeric immunoglobulin. However, the invention also encompasses other multimeric antibodies or immunoglobulims, such as for instance trimeric, tetrameric or pentameric antibodies or immunoglobulins.
Further provided is an isolated or recombinant cell or a pharmaceutical composition comprising a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention, as well as a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention for use as a medicament and/or prophylactic agent. As shown in the Examples, such multimeric antibodies or immunoglobulins are particularly suitable for treating and/or preventing and/or alleviating the symptoms of an influenza A infection. The invention therefore also provides a synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention for use as a medicament and/or prophylactic agent for at least in part treating and/or preventing and/or alleviating the symptoms of an influenza A infection, as well as a method for at least in part treating and/or preventing an influenza A virus infection, comprising administering to an individual in need thereof a therapeutically effective amount of a multimeric antibody, multimeric
immunoglobulin or functional equivalent according to the invention and/or a cell or pharmaceutical composition comprising a multimeric antibody, multimeric
immunoglobulin or functional equivalent according to the invention.
A multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention is also suitable for use in diagnosis of an influenza A virus. This is for instance done by contacting a sample with a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention and subsequently determining whether influenza A virus is bound to said multimeric antibody, multimeric immunoglobulin or functional equivalent. The invention therefore also provides a method for determining whether an influenza A virus is present in a sample comprising:
- contacting said sample with a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention,
- allowing said multimeric antibody, multimeric immunoglobulin or functional equivalent to bind said influenza A virus, if present, and
- determining whether influenza A virus is bound to said multimeric antibody, multimeric immunoglobulin or functional equivalent, thereby determining whether an influenza A virus is present in said sample.
A synthetic or recombinant multimeric antibody, multimeric
immunoglobulin or functional equivalent according to the invention for use in diagnosis of an influenza A infection is also provided herewith. A major advantage of a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention over a mixture of separately produced antibodies is the fact that for pharmaceutical uses, only one registration procedure is required for a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention, whereas a mixture of antibodies requires multiple registration procedures, usually one procedure for each individual antibody and one separate procedure for such mixture as a whole. The use of a multimeric antibody, multimeric immunoglobulin or functional equivalent according to the invention is therefore more time and cost effective. Antibodies according to the invention are capable of counteracting influenza A viruses. Antibodies according to the invention are therefore particularly suitable for use as a medicine or prophylactic agent. Preferably, antibodies according to the invention are used which consist of human sequences, in order to reduce the chance of adverse side effects when human individuals are treated, Such human sequences can be isolated from a human or synthetically or recombinantly produced based on the sequence of human antibodies. Provided is therefore an antibody according to the invention for use as a medicament and/or prophylactic agent. Also provided is a nucleic acid molecule or functional equivalent thereof according to the invention or a vector according to the invention comprising such nucleic acid or functional equivalent for use as a medicament and/or prophylactic agent. When a nucleic acid or functional equivalent according to the invention is administered, it will be translated in situ by the host's machinery into an antibody according to the invention. Produced antibodies according to the invention are capable of preventing and/or counteracting an influenza A infection. Antibodies according to the invention are particularly suitable for use as a medicament because they are (heterosubtype) cross-binding antibodies, capable of binding several influenza A virus subtypes. In a particularly preferred embodiment said antibody comprises antibody AT10_004, AT10_003, AT10_002, AT10_001, AT10_005 or a functional part thereof. Provided is
thus antibody AT10_004, comprising a heavy chain sequence of SEQ ID NO:31 and a light chain sequence of SEQ ID NO:36, for use as a medicament and/or prophylactic agent. Also provided is antibody AT10_003, comprising a heavy chain sequence of SEQ ID NO:32 and a light chain sequence of SEQ ID NO:37, for use as a medicament and/or prophylactic agent. Also provided is antibody AT10„002, comprising a heavy chain sequence of SEQ ID NO:33 and a light chain sequence of SEQ ID NO:38, for use as a medicament and/or prophylactic agent. Also provided is antibody AT10_001, comprising a heavy chain sequence of SEQ ID NO:34 and a light chain sequence of SEQ ID NO: 39, for use as a medicament and/or prophylactic agent. Also provided is antibody AT10_005, comprising a heavy chain sequence of SEQ ID NO:35 and a light chain sequence of SEQ ID NO:40, for use as a medicament and/or prophylactic agent.
More preferably, said antibody according to the invention for use as a medicament and/or prophylactic agent is selected from the group consisting of
AT10_002 and AT10_004 and AT10_001 and AT10_005. As shown in the Examples, these antibodies are particularly effective in counteracting influenza. Most preferably, the invention provides AT10_002 for use as a medicament and/or prophylactic agent, because this antibody is very effective in counteracting influenza.
An antibody according to the invention, or a nucleic acid molecule or functional equivalent thereof according to the invention is preferably used for at least in part treating and/or preventing an influenza A virus infection. As used herein "at least in part treating an influenza A virus infection" includes counteracting an influenza A virus infection, alleviating symptoms resulting from an influenza A virus infection and/or counteracting inflammation resulting from an influenza A virus infection. Examples of symptoms resulting from an influenza A virus infection include, but are not limited to, fever, respiratory symptoms such as cough, sore throat, runny or stuffy nose, breathing problems and pneumonia, muscle aches, headache, fatigue and conjunctivitis. Also provided is therefore an antibody according to the invention, or a nucleic acid molecule or functional equivalent thereof according to the invention, or a vector according to the invention, for use in a method of at least in part treating and/or preventing an influenza A virus infection. Further provided is a use of an antibody or functional part or immunoglobulin chain or functional equivalent or a nucleic acid molecule or functional equivalent according to the invention or a vector
according to the invention for the preparation of a medicament and/or prophylactic agent for at least in part treating and/or preventing an influenza A virus infection. Preferred antibodies are antibodies AT1CL004, AT10_003, AT10_002, AT10_001 and AT10_005, which have heavy chain and light chain sequences as depicted in table 1.
The invention further provides a pharmaceutical composition comprising an antibody according to the invention, and/or a bispecific antibody according to the invention, and a pharmaceutical acceptable carrier, diluent and/or excipient. Also provided is a pharmaceutical composition comprising a nucleic acid molecule or functional equivalent according to the invention, or a vector according to the invention comprising such nucleic acid or functional equivalent, and a pharmaceutical acceptable carrier, diluent and/or excipient. Examples of suitable carriers for instance comprise keyhole limpet haemocyanin (KLH), serum albumin (e.g. BSA or RSA) and ovalbumin. In one preferred embodiment said suitable carrier comprises a solution, like for example saline. A pharmaceutical composition according to the invention is preferably suitable for human use.
The invention further provides a method for at least in part treating and/or preventing an influenza A virus infection, comprising administering to an individual in need thereof a therapeutically effective amount of an antibody according to the invention, and/or a bispecific antibody according to the invention, and/or a nucleic acid molecule or functional equivalent thereof according to the invention, and/or a vector according to the invention, and/or a pharmaceutical composition according to the invention. As used herein, an "individual" is a human or an animal, preferably an animal that can be infected by influenza virus, such as birds and mammals. Individuals include, but are not limited to, chickens, ducks, geese, turkeys, swans, emus, guinea fowls and pheasants, humans, pigs, ferrets, seals, rabbits, cats, dogs and horses. In a preferred embodiment of the invention an individual is a human.
In order to at least in part treat or prevent a influenza A virus infection, an antibody, a nucleic acid molecule or functional equivalent thereof, a vector, and/or a pharmaceutical composition according to the invention is preferably administered to an individual before an influenza A virus infection has taken place. Alternatively, an
antibody, a nucleic acid molecule or functional equivalent thereof, a vector, and/or a pharmaceutical composition according to the invention is administered when an individual is already infected. In that case, an influenza A virus infection is counteracted, symptoms resulting from an influenza A virus infection are alleviated and/or inflammation resulting from an influenza A virus infection is counteracted. Said antibody or functional equivalent is particularly suitable for administered to individuals with an increased risk of complications, such as hospitalized individuals, for instance infants, individuals with compromised immunity and/or elderly people. An antibody, a nucleic acid molecule or functional equivalent thereof, a vector, and/or a pharmaceutical composition according to the invention is preferably administered via one or more injections. Typical doses of administration of an antibody according to the invention or combinations of at least two thereof are between 0.1 and 10 mg per kg body weight. For prophylactic or therapeutic application antibodies according to the invention are preferably combined with a pharmaceutically acceptable carrier, diluent and/or excipient.
An antibody according to the invention is also particularly suitable for diagnostic uses. For instance, if an individual, preferably a human, is suspected of suffering from an influenza A virus infection, a sample, such as a saliva, sputum, blood, or tissue sample, can be obtained from said individual. Subsequently, said sample can be tested for the presence of influenza A virus, using an antibody according to the invention. Preferably, said sample is mixed with an antibody according to the invention, which will specifically bind to a HA protein of influenza A virus. The presence of HA proteins of influenza A virus in a sample is indicative for the presence of an influenza A virus infection. HA proteins of influenza A virus and/or influenza A virus comprising a HA protein bound to an antibody according to the invention can be isolated from the sample and/or detected using any method known in the art, for example, but not limited to, isolation using magnetic beads, streptavidin- coated beads, or isolation through the use of secondary antibodies immobilized on a column. Alternatively, or additionally, an antibody according to the invention is labeled in order to be able to detect said antibody, for instance, but not limited to, fluorescently labeled, or radioactively labeled. Alternatively, an antibody according to the invention is detected using a labeled secondary antibody which is directed against
said antibody. If binding of said antibody is detected, HA protein of influenza A virus is present, which is indicative for the presence of an influenza A virus infection. The invention thus provides an antibody according to the invention for use in diagnosis of an influenza A virus infection.
The invention thus further provides a method for determining whether an influenza A virus is present in a sample comprising:
- contacting said sample with an antibody according to the invention,
- allowing said antibody to bind said influenza A virus, if present, and
- determining whether influenza A virus is bound to said antibody thereby
determining whether an influenza A virus is present.
In a preferred embodiment it is determined whether an individual is suffering from an influenza A virus infection. Provided is therefore a method for determining whether an individual is suffering from an influenza A virus infection comprising:
- contacting a sample from said individual with an antibody according to the invention,
- allowing said antibody to bind said influenza A virus, if present, and
- determining whether influenza A virus is bound to said antibody thereby
determining whether said individual is suffering from an influenza A virus infection. Preferably said individual is a human.
In yet another embodiment, the invention provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, capable of interacting with amino acids at positions A38, A40, A41, A42, A291, A292, A293, A318, B18, B19, B20, B21, B38, B41, B42, B45, B46, B48, B49, B52, B53, and B56 of influenza A virus group 1 hemagglutinin (H1/H5). These are hemagglutinin amino acids that interact with antibody AT10_005. Antibodies, immunoglobulins or functional parts or functional equivalents thereof, capable of specifically interacting with said hemagglutinin amino acids, are therefore herewith provided.
Yet another embodiment provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof,
capable of interacting with amino acids at positions A21, A324, A325, A327, B12, B14, B15, B16, B17, B18, B19, B25, B26, B30, B31, B32, B33, B34, B35, B36, B38, B146, B150, B153, and B154 of influenza A virus group 2 hemagglutinin (H3/H7). These are hemagglutinin amino acids that interact with antibody AT10_004. Antibodies, immunoglobulins or functional parts or functional equivalents thereof, capable of specifically interacting with said hemagglutinin amino acids, are therefore herewith provided.
Yet another embodiment provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, capable of interacting with amino acids at positions A38, A48, A275, A276, A277, A278, A289, A291, A318, B19, B20, B21, B36, B38, B39, B41, B42, B45, B46, B48, B49, B50, B52, B53, B56, B57, B58, B150 of influenza A virus group 2 hemagglutinin (H3/H7). These are hemagglutinin amino acids that interact with antibody AT10_002. Antibodies, immunoglobulins or functional parts or functional equivalents thereof, capable of specifically interacting with said hemagglutinin amino acids, are therefore herewith provided.
The above mentioned amino acid numbering for hemagglutinin is according to Wilson et al. 1981 Nature 289, 366-373 and Nobusawa et al. 1991 Virology 182, 475-485.
Yet another embodiment provides an isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, capable of competing with AT10_001 or AT10_002 or AT10_003 or AT10_004 or AT10_005 for at least part of the same epitope on influenza A virus hemagglutinin, said antibody, immunoglobulin, functional part or equivalent having at least the same affinity for said influenza A virus hemagglutinin (typically having the same or a lower Km value as compared to AT10_001 or AT10_002 or AT10_003 or AT1CL004 or AT10_005), resulting in a decreased binding between said influenza A virus hemagglutinin and AT10J)G1 or AT10_002 or AT10„003 or AT10_004 or AT10_005. Said epitope preferably comprises the amino acids at positions A38, A40, A41, A42, A291, A292, A293, A318, B18, B 19, B20, B21, B38, B41, B42, B45, B46, B48, B49,
B52, B53 and B56 of influenza A virus hemagglutinin. In another preferred embodiment said epitope comprises the amino acids at positions A21, A324, A325, A327, B12, B14, B15, B16, B17, B18, B19, B25, B26, B30, B31, B32, B33, B34, B35, B36, B38, B146, B150, B153, B154 of influenza A virus hemagglutinin. In yet another preferred embodiment said epitope comprises A38, A48, A275, A276, A277, A278,
A289, A291, A318, B19, B20, B21, B36, B38, B39, B41, B42, B45, B46, B48, B49, B50, B52, B53, B56, B57, B58, B150 of influenza A virus hemagglutinin.
The invention is further explained in the following examples. These examples do not limit the scope of the invention, but merely serve to clarify the invention.
Brief description of the drawings
Figure 1. Schematic representation of an influenza virus (Subbarao K. and Joseph T. Nature Reviews Immunology 2007: 7, 267-278).
Figure 2. Cell sorting of H3 and H7 binding B cells following incubation of Alexa Fluor 647 labeled Influenza H3 (A/Wyoming/03/2003) and H7 (A/Netherlands/219/2003) HA proteins with Bcl6 and Bcl-xL transduced polyclonal cultured B cells. Figure 3. Antibody binding to HA transfected 293T cells. 293T cells were transfected with DNA encoding for the HA of HI (A/New Caledonia/20/199), H3
(A Wisconsin/67/2005), H5 (A/Thailand/Vietnam Consensus/2004) and H7
(A/Netherlands/219/2003) and incubated with mAb. Antibody binding was detected with anti-human IgG-PE.
Figure 4. Antibody binding to virus infected cells. MDCK-SIAT cells were infected with Influenza HlNl (A Hawaii/31/2007) and H3N2 (A/Netherlands/177/2008) and incubated with mAb. Antibody binding was detected with anti-human IgG-PE, Figure 5. Antibody binding to virus infected cells. MDCK cells were infected with Influenza HlNl (A/Neth/602/2009), H3N2 (A/Swine/St. Oedenrode/1996), high pathogenic H5N1 (A/Turkey/Turkey/2004), high pathogenic H7N7
(A/Ch/Neth/621557/03) and low pathogenic H7N1 (A/Ch/Italy/1067/1999)
and incubated with mAb. Antibody binding was detected with anti-human IgG-PE.
Figure 6. Antibody competition assay. Labeled antibodies AT10_001, AT10_002 and AT10_004 were tested for binding to H3N2 (A Netherlands/177/2008) infected MDCK- SIAT cells in the presence of non-labeled competitor antibody (A). Labeled AT10_004 was also tested for binding to HlNl (A/Hawaii/31/2007) infected MDCK-SIAT cells in the presence of non-labeled competitor antibody (B). Rituximab (Ritux, CD20 antibody) was used as a negative control.
Figure 7. Binding of AT 10 antibodies to different HA conformations by in vitro pH- shift experiment. 293T cells were transfected with DNA encoding for the HA of H3 (A/Wisconsin/67/2005), detached from the plastic with Trypsin-EDTA and treated with either 500 mM Dithiothreitol (DTT), PBS pH5, or left untreated. Cells were subsequently incubated with recombinant AT10_001, AT10_002, AT1Q_003 or AT10J304. Antibody binding was detected using anti-human-IgG-PE.
Figure 8. Survival (A) and body weight change (B) of C57B1/6J mice challenged intranasally with increasing amounts of influenza A/HKx-31 (H3N2).
Figure 9. Survival (A) and body weight change (B,C,D) of mice intravenously injected with 1 or 5 mg/kg antibody AT10_001, AT10_002 or AT10_004 one day before intranasal challenge with 10 Lethal Dose 50 (20,000 TCID50) of influenza A/HKx-31 (H3N2).
Figure 10. Survival (A) and body weight change (B) of mice intravenously injected with 15 mg/kg antibody AT10_002 one day before intranasal challenge or 2, 3 or 4 days post intranasal challenge with 10 Lethal Dose 50 (20,000 TCID50) of influenza A/HKx-31 (H3N2)
Figure 11. SPR plot showing the dual specificity of BiFlu for H3 and HI and the presence of both kappa and lambda light chain on BiFlu. Antibodies AT10_002 (lambda light chain), AT10_005 (kappa light chain) and BiFlu (contains AT10_002 and AT10_005) were captured on an anti-IgG (A) or anti-lambda (B) coated sensor chip. In subsequent incubation cycles captured antibodies were tested for their ability to bind hemagglutinin H3 and HI and light chain antibodies directed against kappa and/or lambda. An increase in the SPR shift indicates proteins binding to the captured antibodies.
Figure 12. Antibody binding to virus infected cells. MDCK-SIAT cells were infected with Influenza H1N1 (A/Haw aii/31/2007) and H3N2 (A/Netherlands/177/2008) and incubated with several concentrations of AT10_002, AT10_005 or BiFlu mAb.
Antibody binding was detected with anti-human IgG-PE.
Figure 13. Neutralization curves of antibodies AT10_002, AT10_005 and BiFlu for Influenza H1N1 (A/Hawaii/31/2007) (A) and H3N2 (A/Netherlands/177/2008) (B). Each virus was incubated with different amounts of antibody and then added to a confluent monolayer of MDCK-SIAT cells. Following an 24hr incubation period cells were washed, fixed and, stained for DAPI and Influenza nuclear protein. The percentage of infected cells (relative to the no antibody control) is shown for each concentration of the antibody tested. Figure 14. Survival (A) and body weight change (B) of mice intravenously injected with 1 mg/kg antibody AT 10_002, AT10J)05 or Rituximab, 2mg/kg
AT10_002/AT10_005 mix (1 mg/kg for each antibody) or 2 mg/kg BiFlu one day before intranasal challenge with 10 Lethal Dose 50 of H1N1 Influenza A PR/8/34.
Examples
Generation of immortalized B cells
Human memory B cells were immortalized using the BCL6 / Bcl-xL technology described by Kwakkenbos et al. (Generation of stable monoclonal antibody-producing B cell receptor- positive human memory B cells by genetic programming. Nature Medicine (2010) vol. 16 (1) pp. 123-8 and patent application WO 2007/067046). In brief, human memory B cells from Influenza vaccinated donors were transduced with a retroviral vector containing BCL6 and Bcl-xL. Transduced B cells can be maintained in culture with CD40Ligand expressing L-cells and interleukin (IL)-21 (R&D systems).
Selection of heterosubtypic mabs
To identify B cells that secrete heterosubtypic cross-binding mAbs two approaches were used.
i) The Influenza H3 (A/Wyoming/03/2003) and H7 (A/Netherlands/219/2003) HA proteins (Protein Sciences) were labeled with Alexa Fluor 647 (Molecular Probes) and incubated with Bcl6 and Bcl-xL transduced polyclonal cultured B cells. HA binding B cells were sorted single cell per well by FACSAria (Figure 2) and maintained in culture for 2 to 3 weeks before the supernatant of the B cell clones were screened for HA binding by ELISA or binding to H3N2 (A Netherlands/177/2008) infected cells and/or H7 (A/Netherlands/219/2003) transfected HEK cells.
ii) Cells were seeded in small pools, e.g. 40 cells per well and maintained in culture for 2-3 weeks. The supernatant of these pools was screened for binding to H7 transfected HEK cells. The B cells of the double positive tested wells were seeded 1 cell per well. The culture supernatant of these monoclonal B cell lines was used to screen for HA binding by ELISA.
B cells that showed reactivity to more than 1 HA type were further cultured and characterized for HA recognition by ELISA (Table 2) and binding to HA expressing HEK cells (Figure 3).
HA ELISA
The B cell supernatant of cross-reactive B cell clones was tested for binding to different HA antigens by ELISA. Recombinant HA of HI (A/New Caledonia/20/1999), H3 (A/Wyoming/03/2003), H5 (A/Vietnam/1203/2004) and H7
(A/Netherlands/219/2003) (Protein Sciences) were coated to ELISA plates at 1 ^ig/ml. After coating, the plates were washed lx with PBS and 350 μΐ blocking buffer, PBS/4%Protivar, was added and incubated 1 hr at RT. The plates were then washed 3x with PBST (PBS/0.05%Tween20) and the antibodies/culture supernatants were added to the wells. Incubation was allowed to proceed for 1 hr at RT, then the plates were washed 3x with PBST. Samples were then incubated with a goat anti-human IgG-HRP antibody (Jackson) for 1 hr at RT. Bound antibodies were detected using TMB (3,3', 5,5' tetramethyl benzidine) substrate buffer, the reaction was stopped using H2SO4. OD 450nm was measured on an Envision (PerkinElmer). AT10_001 and AT10J302 recognized both H3 and H7 proteins but not the HA proteins of HI and H5. AT10_003 recognized H3, H5 and H7 protein while AT10J304 recognized HI, H3 and H7 proteins (Table 2).
Antibody binding HA transfected 293T cells
To test heterosubtypic binding of the AT10 mAbs to cell surface expressed HA, 293T cells were transfected with different full length HA constructs. Using Fugene (Roche) 293T cells were transfected with DNA encoding the HA of HI (A/New
Caledonia/20/1999), H3 (A/Wisconsin/67/2005), H5 (A/Thailand/Vietnam
Consensus/2004) and H7 (A/Netherlands/219/2003). The transfected cells were incubated with B cell supernatant containing IgG antibodies for 30 minutes at 4°C and then washed 2x with 150 μΐ PBS/2%FCS. Antibody binding was detected with anti-human IgG-PE (Southern Biotech) and analyzed on a FACScanto (Becton, Dickinson and Company) (Figure 3). As a control untransfected 293T cells were used. AT10_001 and AT10_002 recognized both H3 and H7 cell surface expressed proteins but not the HA proteins of HI and H5. AT10_003 recognized H3, H5 and H7 protein while AT10_004 recognized the HI, H3 and H7 HA proteins.
Cloning of selected antibodies.
We isolated total RNA with the RNeasy® mini kit (Qiagen), generated cDNA, performed PCR and cloned the heavy and light chain variable regions into the pCR2.1 TA cloning vector (Invitrogen). To rule out reverse transcriptase or DNA polymerase induced mutations, we performed several independent cloning experiments. To produce recombinant mAb we cloned the heavy and light variable regions in frame with human IgGl and Kappa constant regions into a pcDNA3.1 (Invitrogen) based vector and transiently transfected 293T cells. We purified recombinant mAb from the culture supernatant with an AKTA (GB healthcare).
Cross binding specificity of AT10 antibodies
Eleven different recombinant HA proteins (Sino Biological Inc and Protein Sciences) were used to test the potential of the antibodies to bind different HA subtypes.
Reactivity to these HA proteins (table 3) was tested in an ELISA, as described above. None of the mAbs showed reactivity with Influenza B. AT10_001, AT10_002,
AT10_003 and AT10J304 showed binding to all human group 2 HA proteins.
AT10_001, AT1CLQ03 and AT10_004 also showed reactivity to Swine H4N6
(A/Swine/Ontario/01911- 1/1999). AT10_002 and AT10_003 recognized Duck H10N3 (A duck/Hong Kong/786/1979) and Duck H15N8 (A/duck/AUS/341/1983), AT10_004 also showed some activity to H15N8 (A/duck/AUS/341/1983). AT10_003 recognized the group 1 HA molecules from H9N2 (A/Hong Kong/1073/1999) and H5N1
(A/Vietnam/1203/2004) while AT10_004 also showed binding to the HAs of HlNl (A/California/07/2009) and H9N2 (A/Hong Kong/1073/1999). AT10_005 bound exclusively to the group 1 HA proteins tested.
Antibody binding to virus infected cells
To test the binding capacity of the AT10 antibodies AT10_001, AT10J)02, AT10_003 and AT10_004 to virus infected cells we performed FACS analysis on Influenza HlNl (A Hawaii/31/2007) and H3N2 (A Netherlands/177/2008) infected cells (both virus strains were obtained from the Department of Medical Microbiology, AMC,
Amsterdam). MDCK-SIAT cells were grown in a T175 culture flask to 80- 100% confluency in DMEM/FCS/PS/G418. The cell layer was washed 2x with 10 ml PBS after which 15 ml of Optimem/PS/G418/Trypsin was added. Subsequently 0.5 ml of
100.000 TCID50 Influenza virus (H lNl or H3N2) was added to the flask and cells were cultured at 37°C. After 24-48 hr the cells were washed 2x with 10 ml PBS and detached from the plastic using Trypsin-EDTA. Cells were counted and frozen at - 15Q°C until use. The infected cells were defrosted and incubated with IgG
antibodies/B cell supernatant for 30 minutes at 4°C and then washed 2x with 150 μΐ PBS/2%FCS. Antibody binding was detected with anti-human IgG-PE and analyzed on a FACScanto (Becton, Dickinson and Company). As a control non-infected cells were used (Figure 4). All mAbs showed binding to H3N2 infected cells but not to non- infected cells. Antibodies AT10_004 and AT10_003 also showed some binding to H lNl infected cells,
Similar experiments were performed for the AT10 antibodies AT10_001, AT10_002, AT10_003, AT10_004 and AT10_ 005 with Influenza HlNl (A/Neth/602/2009), H3N2 (A/Swine/St. Oedenrode/1996), high pathogenic H5N1 (A/Turkey/Turkey/2004), high pathogenic H7N7 (A/Ch/Neth/621557/03) and low pathogenic H7N1
(A/Ch/Italy/1067/1999) infected cells (Central Veterinary Institue, Lelystad). MDCK cells were infected with virus as described above, only the cells were fixated with 4% paraformaldehyde for 20 minutes at 4°C, washed lx with PBS and then frozen. As a control non-infected cells were used. FACS staining and analysis was done a described above (Figure 5 and Table 4). AT10_001 recognized both H7 viruses but failed to recognize H3N2 (A/Swine/St. Oedenrode/1996) infected cells. AT10_001 showed some reactivity to HlNl (A/Neth/602/2009). Antibodies AT10_002 and AT10_004 recognized all three group 2 Influenza infected cell batches, AT10_004 also showed some reactivity to H5N1 (A/Turkey/Turkey/2004) Influenza. AT10_003 only showed some low binding to H3N2 (A/Swine/St.Oedenrode/1996) and H7N7
(A/Ch/Neth/621557/2003) infected cells. AT10_005 bound to group 1 Influenza infected cells and not to group 2 Influenza infected cells.
Virus neutralization
To determine whether the obtained antibodies were capable of blocking Influenza A virus infection, an in vitro neutralization assay was performed. The assay was performed on MDCK-SIAT cells (Journal of Virology Aug. 2003; pp. 8418-25). MDCK- SIAT cells were grown in DMEM/8%FCS/PS/G418 in an 96 well plate (CellCarrier
Plate, PerkinElmer) to 80- 100% confluency. Neutralization assays are performed in Optimem/PS/G418/Trypsin medium without FCS or BSA. Fifty μΐ of recombinant mAb was mixed with 50 μΐ of virus suspension (100TCID50/50 μΐ) of H3N2
(A/Ned/177/2008) or H1N1 (A/Hawaii/31/2007) Influenza and incubated for 1 hr at 37°C. The suspension was then transferred in multiply into 96-well plates containing MDCK- SI AT cells in 100 μΐ Optimem/PS/G418/Trypsin. Prior to use the MDCK-SIAT cells were washed twice with 150 μΐ PBS. The plates were then centrifuged for 15 minutes at RT at 2500 rpm and placed at 37°C/5% C02. After 24 hr cells were washed twice with PBS, fixed with Formalin (37% formaldehyde in water) for 10 minutes at RT, washed twice with 150 μΐ PBS and stained with DAPI and an antibody against the nuclear protein of the Influenza virus (NP-FITC, Abeam) at RT. After 30 minutes cells were washed twice with 150 μΐ PBS and 100 μΐ of PBS/50%Glycerol was added to the wells. Viral infection of the MDCK-SIAT cells was measured and analyzed on the Operetta (PerkinElmer) using an 20x objective. To quantify neutralizing capacity of the mAbs the number of infected cells was counted (positive for DAPI and NP-FITC) (Table 5). IC50 values were calculated in Prism, values are from 1 representative experiment, assay points performed in quadruplicate. AT10_001, AT10_002 and AT10_004 showed potent inhibition of H3N2 (A Ned/177/2008) and H3N2 HKX-31 Influenza virus infection in vitro. Neutralization of H1N1 (A/Hawaii/31/2007) was not observed for AT10_001, AT10_002, AT10J)03 and AT10_004.
To determine whether the obtained AT10 antibodies were capable of blocking multiple Influenza A virus strains, additional in vitro neutralization assays were performed. Influenza viruses A/swine/Neth/St. Oedenrode/96 (H3N2; de Jong et al. 1999),
A/ck/Neth/621557/03 (H7N7; van der Goot et al. 2005), A/ek/Italy/1067/99 (H7N1), A turkey/Turkey/05 (H5N1; Londt et al. 2008) and A/Neth/602/2009 (swine-origin H1N1; Munster et al. 2009) were used in this assay. Madin-Darby canine kidney (MDCK) cells were cultured in Optimem (Gibco BRL Life Technologies) containing 5% FBS (Integro) and 1% Pen Streptomycine (Gibco BRL Life Technologies).
Cells were seeded at a density of 3 x 104 cells per well in 96-well plates and incubated O/N at 37°C. Three-fold serial dilutions of the mAbs were made in PBS starting with a concentration of 15 μg/ml, Rituximab mAb was taken along as negative control.
Virus dilutions were prepared in virus infection medium consisting of Optimem supplemented with antibiotics and, in case of LPAI viruses, 1 μg/ml trypsin/TPCK (Sigma). Each mAb dilution was mixed with an equal volume of virus followed by 1 hour incubation at 37°C. After washing of the cells with PBS, the mAb/virus mixture (-100-1000 TCID50) was inoculated onto the cell monolayers. Cells were incubated for 24-32 hours at 37°C, after which they were washed twice with PBS, fixed with 4% formalin for 20 min and then washed again with PBS. Cells incubated with medium only were included as negative control and cells incubated with virus only as positive control. The assay was performed in quadruplicate. Cells were stained with 1 hour with DAPI and an antibody against the nuclear protein of the Influenza virus (NP-
FITC, Abeam or HB65 followed by Goat-anti-mouse IgG Alexa-647, Invitrogen) at RT. Cells were washed twice with 150 μΐ PBS after staining and 100 μΐ of
PBS/50%Glycerol was added to the wells. Viral infection of the MDCK cells was measured and analysed on the Operetta (PerkinElmer) using an lOx objective. To quantify neutralizing capacity of the mAbs the number of infected cells was counted (positive for DAPI and NP-FITC/HB65-Alexa-647). IC50 values were calculated in Prism, values are from 1 representative experiment. The results are shown in Table 7. AT10_002 and AT10_004 showed potent inhibition of the group 2 influenza virus infection in vitro but did not prevent infection with group 1 viruses. Antibody
AT10_005 prevents infection with group 1 Influenza A viruses but has no effect on group 2 viruses. Antibody CR8020 (WO 2010 130636) does not show any neutralizing capacity for H3N2 A/Swine/Neth/St. Oedenrode/96 and H7N1 A/ck/Italy/1067/99 at 15 μg/ml while AT10_002 and AT10_004 show IC50 values below 4 μ¾/ιη1.
Antibody competition
Antibody AT10_001 and AT10_003 were labeled with Alexa Fluor 555 (Molecular Probes) and antibody AT10J302 and AT10_004 were labeled with Alexa Fluor 647 (Molecular Probes). Labeled antibodies were tested for binding to H3N2
(A Netherlands/177/2008) infected MDCK-SIAT cells to determine if they maintained their binding capacity. For competition experiments H3N2 (A/Netherlands/177/2008) infected cells were incubated with increasing amounts of non-labeled competitor antibody for 10 minutes at 4°C before the addition of Alexa Fluor-labeled antibody.
Cell-antibody mix was incubated for another 15 minutes at 4°C and washed 2x with PBS/2%FCS before analysis on the Guava easyCyte 8 (Millipore). AT10_QQ1,
AT10J302 and AT10_004 all bind to a similar region on the HA protein as they all block each other's binding (Figure 6A). Antibody competition was also performed on H1N1 infected cells (A/Haw aii/31/2007). AT10_004-Alexa-647 antibody binding was blocked by unlabeled AT10_0Q4 and AT10_005 (Figure 6B). The AT10_005 antibody recognize the stem region of the group 1 HA molecules. As AT10_004 competes with AT10_005 for binding it is likely that AT10_004 also recognizes the HA stem region. Because AT10_001, AT10_002 and AT10_004 all bind to a similar region on the HA protein (figure 6A) AT10_001 and AT10_002 therefore also have their binding epitope on the stem region.
HA1 subunit ELISA
To test whether the HA1 subunit is essential for the binding of the antibodies to the HA protein an HA1 subunit specific ELISA was done. Recombinant HA of full length H3 (A/Aichi/2/1968, full length) and H3 HAl subunit (A/Aichi/2/1968, HA1 subunit, Met-1 - Arg 345) were coated to ELISA plates at 1 μg/ml. After coating, the plates were washed lx with PBS and 300 μΐ blocking buffer, PBS/4%Protivar, was added and incubated 1 hr at RT. The plates were then washed 3x with PBST
(PBS/0.05%Tween20) and the recombinant antibodies were added to the wells.
Incubation was allowed to proceed for 1 hr at RT, then the plates were washed 3x with PBST. Samples were then incubated with a goat anti-human IgG-HRP antibody (Jackson) for 1 hr at RT. Bound antibodies were detected using TMB substrate buffer, the reaction was stopped using H2SO4. OD 450nm was measured on an Envision (PerkinElmer) (Table 6). AT10_001, ΑΊΊ0_002 and AT10_004 recognized full-length H3 HA protein but not the HAl subunit of this protein indicating their binding epitope is, at least partly, located on the HA2 subunit of the protein. AT10_003 recognized both the full-length HA protein and the HAl subunit indicating that the AT10J303 epitope is located on the HAl subunit of the HA protein.
Binding of AT10 antibodies to different HA conformations
Upon endocytic uptake of virions, the acidic environment of the endosome triggers HA- driven fusion of the viral and the endosomal membrane. This fusion is mediated
by a conformational change of the HA protein (triggered by the low pH) from a precision state to a post-fusion state. We performed an in vitro pH-shift experiment to test to which conformational configuration of HA the antibodies can bind.
Using Fugene (Roche) 293T cells were transfected with DNA encoding the HA of H3 (A/Wisconsin/67/2005). 48 hours post transfection the cells were harvested using trypsin-EDTA and stored at - 150°C until further use. For the pH-shift experiment, cells were washed 2x with PBS and then incubated for 30 minutes at room
temperature with 10 pg/ml trypsin-EDTA in PBS. Cells were washed 2x with PBS and a fraction was set aside as trypsin condition. Remaining cells were split to two tubes and treated with either 500 mM Dithiothreitol (DTT) for 20 minutes at room temperature or incubated for 5 minutes at 37°C with PBS pH5. Cells were washed 2x with PBS and incubated with recombinant AT10_001, AT10_002, AT10_003 or AT10_004. Antibody binding was detected using anti-human-IgG-PE (southern Biotech) antibody and analyzed on a Guava easyCyte 8 (Millipore) (Figure 7).
AT10_001, AT10„002, AT10_003 and AT10_004 all bind the trypsin treated cells. Binding of AT10_001, AT10_002 and AT10_004 is lost upon treatment of the transfected cells with pH5 buffer, indicating that these antibodies recognize the pre- fusion but not the post-fusion conformation of the HA protein. Treatment of the cells with DTT, which induces dissociation of the HAl subunit from the HA2 subunit, has no effect on binding of these antibodies indicating that the binding epitope is located on the HA2 subunit. AT10_003 recognizes both the pre-fusion and post-fusion conformation but binding is lost upon DTT treatment, indicating that the binding epitope is only available when is the HAl subunit is present. Prophylactic and therapeutic efficacy of AT10 antibodies in vivo
The AT10 antibodies were tested in a mouse influenza challenge model to determine their efficacy. Male C57B1/6J mice (4 per group) were intranasally challenged with increasing amounts of influenza A/HKx-31 (H3N2) and body weight changes were monitored twice a day for 14 days to determine the viral dose response. Twenty-five percent bodyweight loss was used as humane endpoint; mice loosing more than 25% of their body weight were removed from the study. In the highest dose group (20000 TCID50) all animals lost 25% of their bodyweight within 8 days while in the 2000 TCID50 group only 50% of the mice reached this bodyweight loss (Figure 8). Based on
these results a viral dose of 10 LD50 (20,000 TCID50) was used in subsequent antibody experiments.
Antibodies AT10J301, AT10_002, AT10J)04 and a negative control antibody
(Rituximab) were tested for prophylactic efficacy in the influenza model. Mice were intravenously injected with 1 or 5 mg/kg antibody one day before challenge with 10 LD50 influenza A HKx31. Bodyweight was monitored for 10 days after which the experiment was terminated. All control mice lost 25% bodyweight within 8 days and were removed from the study, however none of the mice that received prophylactic AT10 antibody had to be removed from the study demonstrating a protective effect of the antibodies (P=<Q.000.1, Mantel-Cox, Figure 9A). For all AT10 antibody groups a dose dependent effect could be seen, e.g. mice that received a dose of 1 mg/kg antibody lost more body weight than the mice that received 5 mg/kg of the same antibody (Figures 9B,C,D). Treatment with AT10_002 at lmg/kg is significantly more protective than treatment with 1 mg/kg of AT10_001 from day 4 post infection to the end of the experiment (P=<0.05, 2 way ANOVA). There is no significant difference in weight loss between the groups of mice that received AT10_002 at lmg/kg and mice that received AT10_004 at 1 mg/kg although a trend towards a better protective activity of AT10J302 can clearly be seen. Based on the weight loss graphs the antibodies can be ranked for activity as follows; AT10_002 > AT10_004 > AT10_001.
The AT10 antibody that showed the best protective activity in the prophylactic Influenza experiment, AT10_002, was tested for therapeutic efficacy in the influenza model. Mice were intravenously injected with 15 mg/kg antibody two, three, or four days post challenge with 10 LD50 influenza A/HKx31. As controls, mice were injected with 15 mg/kg AT10J302 or a negative control antibody (Rituximab, 15 mg/kg) one day before 10 LD50 influenza A/HKx31 challenge. Bodyweight was monitored for 10 days after which the experiment was terminated. The results are shown in Figure 10. All control mice that received Rituximab lost 25% bodyweight within 8.5 days and were removed from the study, none of the mice that received prophylactic AT10_002 antibody (day - 1) showed loss of bodyweight and had to be removed from the study, confirming the protective effect of the AT10J302 antibodies. Intravenous
administration of AT10_002 at days two or three post Influenza challenge prevented
lethal bodyweight loss in all the mice, showing the therapeutic effect of the AT10_002 antibody. Treatment of Influenza challenged mice with AT10_002 antibodies four days post infection protected 40% of the mice against lethal bodyweight loss. These findings show that AT10_002 antibodies can be used to prevent lethality up to several days after an Influenza infection.
Generation of pan-specific anti-Influenza A IgG multimeric antibody
To generate a multimeric antibody complex that recognises most Influenza A viruses we coupled AT10_Q02 and AT10_005 together (BiFlu) using the sortase technology, described in detail in WO 2010/087994.
To be able to link AT10_002 and AT10_005 a tag (named ST) containing a sortase recognition site plus a His6 tag, with sequence GGGGSLPETGGGHHHHHH, is attached to the C-terminus of the heavy chain of the antibodies via genetic fusion.
The sortase reaction was performed by mixing 10.0 mg AT10-002 ST antibody in 2000 μΐ reaction buffer (25 mM Trie, pH 7.5, 150 mM NaCl, 10 mM CaCl2) containing 60 μΜ sortase and 500 μΜ GGG-Dibenzo-azacyclo-octyn (DIBAC). Similarly, 10.0 mg AT10-005 ST antibody was mixed with 2000 μΐ sortase-buffer containing 90 μΜ sortase and 1 mM GGG-azide.
Both samples were incubated 16 h at 37 °C. After incubation sortase was de-activated by the addition of 50 mM EDTA. Before loading the sample on a gel filtration column, the reaction mixture was centrifuged (3 min, 13.200 rpm) to pellet any aggregates. Gel filtration chromatography of the two sortase-tagged antibodies was performed on a HiLoad Superdex 200 16/60 column (GE Healthcare, Piscataway, NJ, United States) in coupling buffer (25 mM Tris, pH 7.5 + 150 mM NaCl). Before loading samples, the column was equilibrated with 1.0 CV (column volumes) coupling buffer. After loading, the column was run with 1.5 CV equilibration buffer.
Next, the purified antibodies were subjected to click-chemistry coupling. 3.0 mg AT10- 002-DIBAC was mixed with 2.9 mg ATl0-005-azide and incubated at 25° C in 3.0 ml coupling buffer (25 mM Tris, pH 7.5, 150 mM NaCl). After 16 h the sample was subjected to gel filtration (as above) in PBS (Fresenius Kabi, Bad Homburg,
Germany). Fractions containing the IgG dimers were collected, pooled and
concentrated with 50 kDa cut-off membranes AMICON centrifugal filter devices (Millipore, Billerica, MA, United States).
Qualitative SPR analysis of the BiFlu preparation
Surface plasma resonance (SPR) analysis was performed on the BiFlu preparation to determine if dimeric BiFlu was formed (e.g. dimers consisting of both AT10_002 (lambda light chain) and AT10_005 (kappa light chain)) and if the preparation consists of AT10_002 AT10_005 heterodimers
SPR analysis was performed on an IBIS MX96 SPR imaging system (IBIS
Technologies BV., Enschede, The Netherlands) as described (Lokate et αί.,2007, J.
Am. Chem. Soc. 129: 14013- 140318). In short, one SPR analysis cycle consists of one or more incubation steps in which analytes are flushed over a coated sensor. This is followed by a regeneration step in which any bound analyte is removed from the sensor. Multiple cycles can be performed in one experiment. In our SPR capture- binding assay the antibodies of interest are first captured on an isotype-specific antibody (i.e. anti-human IgG, anti-human kappa light chain or anti-human lambda light chain), which is immobilized on the SPR sensor and then incubated with analytes. Obtained data was analyzed using Sprint software (version 1.6.8.0, IBIS Technologies BV, Enschede, The Netherlands).
The SPR sensor was coated by immobilization of isotype specific antibodies anti- human IgG (Jackson Immunoresearch, West Grove, PA, USA), anti-human kappa light chain (Dako, Glostrup, Denmark) and anti-human lambda light chain (Dako, Glostrup, Denmark) on an amine-specific EasySpot gold-film gel-type SPR-chip (Ssens BV, Enschede, The Netherlands) by spotting them on the sensor surface using a continuous flow microspotter device (Wasatch Microfluidics, Salt Lake City, UT, USA) in coupling buffer (10 mM NaAc, pH 4.5, 0.03 % Tween20).
After spotting for 45 minutes the sensor is deactivated with 0. 1 M ethanolamine, pH 8.5 and washed three times with system buffer (PBS + 0.03 % Tween20 + 0.05 % NaN3). Before starting the analysis, the coupled sensor was incubated for two minutes with regeneration buffer (10 mM glycine-HCl, pH 2), followed by three wash steps with system buffer.
Then the coated SPR chip is injected either with AT10_002, AT10_005 (2 μg/ml in system buffer) or BiFlu (4 μ /ml in system buffer) and incubated for 30 min.
Subsequently, non-captured IgG is removed by a 5 minute incubation with system buffer. Next, the sensor is injected with influenza H3-hemagglutinin protein (H3N2, Wyoming, 03/2003, Sino Biological inc., Beijing, P.R. China, 0.25 to 2.0
in system buffer and incubated for 30 min to measure association. To measure complex dissociation the sensor is washed with system buffer and incubated for 40 min. The injection of H3 is followed by injections with influenza Hl-hemagglutinin (H1N1, New Caledonia, 20/1999, Sin Biological inc., Beijing, P.R. China, 1.0 ug/ml) and anti- human light chain antibody (anti-kappa or anti-lambda) in a similar fashion as described above.
When the single antibodies and BiFlu are captured on anti-human IgG (Figure 11A) and on anti-lambda light chain (Figure l lB), BiFlu binds both HI and H3 with the same affinity as the single antibodies. Furthermore, the results demonstrate that BiFlu is heterodimer with two different light chains. The two monomeric antibodies (AT10__002 and AT10_005) bind only one analyte and have one type of light chain. Altogether, the SPR analysis demonstrates that BiFlu is a heterodimer of AT10_002 and AT10_005, which binds H3 and HI with equal affinity as the single antibodies.
Antibody binding to virus infected cells
To test if the binding capacity of the Bi Tu antibodies is maintained and if the BiFlu has the combined binding properties of AT10_002 and AT10_005 we performed FACS analysis on Influenza H1N1 (A/Hawaii/31/2007) and H3N2 (A/Netherlands/177/2008) infected cells. Influenza A infected MDCK-SIAT cells were generated as described above. The infected cells were defrosted and incubated with different concentrations of AT10_002, AT10_005 or BiFlu antibodies for 30 minutes at 4°C and then washed 2x with 150 μΐ IMDM/2%FCS. Antibody binding was detected with anti-human IgG-APC and analyzed on a Guava easyCyte 8HT (Millepore). The results are shown in Figure 12. BiFlu and AT10_005 showed concentration dependent binding to H1N1 infected cells while AT10_002 did not bind to these cells. H3N2 infected cells were bound by BiFlu and AT10_002 but not by AT10_005 antibodies. For both virus subtypes the BiFlu antibodies show similar binding affinity (as shown by MFI of the APC signal) as
the relevant single control antibody. Together these results show that BiFlu antibodies have the combined binding properties of AT10_002 and AT10_005.
Virus neutralization
To determine whether BiFlu is also capable of blocking Influenza A virus infection, an in vitro neutralization assay was performed. The assay was performed on MDCK- SIAT cells as described above. To quantify neutralizing capacity of the mAbs the number of infected cells was counted (positive for DAPI and NP-FITC). Shown in Figure 13 are the neutralization curves for HlNl (A/Haw aii/31/2007) and H3N2 (A/Ned/ 177/2008) neutralization for AT1Q_Q02, AT10J)05 and BiFlu. The
concentration depicted for BiFlu has been adjusted to represent the same available binding opportunities (e.g. concentration shown is half of the actual concentration BiFlu as BiFlu has the double molecular weight compared to the single antibodies). BiFlu neutralizes HlNl and H3N2 as well as its relevant single components.
Prophylactic efficacy of BiFlu antibodies in vivo (Figure 14)
Antibodies AT10_002, AT10_005, BiFlu (AT10_002 - AT10_005 dimer),
AT10_002/AT10__005 mix and a negative control antibody (Rituximab) were tested for prophylactic efficacy in the influenza model. Male C57B1/6J mice (6 per group) were intranasally challenged with 10 LD50 influenza A/HKx31 or 10 LD50 HlNl Influenza A/PR/8/34 and body weight changes were monitored for 10 days. Twenty-five percent bodyweight loss was used as humane endpoint; mice loosing more than 25% of their body weight were removed from the study.
Mice were intravenously injected with 1 mg/kg AT10_002, 1 mg/kg AT10_005, a mix of AT10_002 and AT10_005 1 mg/kg each, 2 mg/kg BiFlu or 1 mg/kg Rituximab antibody one day before viral challenge. All control mice (Rituximab) lost 25% bodyweight within 8 days and were removed from the study. In the HlNl challenge model AT10_005 antibody showed a protective effect e.g. none of the mice had to be removed from the study. In addition, the mice that received the BiFlu preparation and the AT10J)02/AT10J)05 antibody mix were also protected (Figure 14). No statistical difference in bodyweight loss is observed between the groups of mix that received the AT10_002/AT10_005 antibody mix and the BiFlu group (P>0.05, 2 way ANOVA). Similar results were obtained in the H3N2 in vivo model. AT10„002
antibody, the antibody mix (A 10_002/AT10_005) and BiFlu showed protection in the H3N2 model. Together these data show that the BiFlu antibody complex retains its functionality in vivo and has similar protective activity as a mix of its single components.
Protein modelling to determine the amino acids involved in the antibody hemagglutinin interaction. (Table 8, 9 and 10)
The multiple sequence alignments were done by ClustalQ and further processed by showalign, part of EMBOSS. All the structural work was done with Pymol.
Minimisation was done using the software NAMD with the force field CHARMM.
The first step to build a 3D model of the antibody is to select the best 3D template. This is done by using a global alignment (Needleman and Wunsch) of the query sequence against a databank of all sequences of antibodies present in the protein database (PDB). Then one structure is chosen amongst the structure with the highest percentage of identity in the sequence.
The next step is to highlight the regions where substitutions occurred and modify the sequence and the structure in such a way that the final model resembles the antibody to analyse. Two techniques are applied: 1) Substitution of amino acid, this method keeps the main chain in place and only replaces the side chain. 2) Grafting of loop, this method modifies the main chain and is necessary when there are insertion or deletion in a loop, when the sequence is too far or when substitutions may affect the main chain conformation, e.g. substitution of Glycine or Proline.
To generate the complex antibody-haemagglutinin with the antibodies AT10_005 and AT10_004 the structure of experimentally determined complexes were used as template. The model of the antibody is superimposed on the antibody of the crystal determined structure, the haemagglutinin is kept intact. For AT10_002 the docking procedure was to: (i) analyse the stem of haemagglutinin to restrict the area where actual binding were tested, (ii) manual positioning of the antibody in the remaining area of point (i), (iii) evaluation of the quality of the complex by checking the structure for short contacts, hydrogen bond capable groups missing hydrogen bonds in the complex, size of the contact area,
ΑΤ10_005:
The amino acids of influenza A virus group 1 haemagglutinin (H1/H5) in contact with AT10_005 are: A38, A40, A41, A42, A291, A292, A293, A318, B18, B19, B20, B21, B38, B41, B42, B45, B46, B48, B49, B52, B53, B56.
AT10_004:
The amino acids of influenza A virus group 2 haemagglutinin (H3/H7) in contact with AT10_004 are: A21, A324, A325, A327, B12, B14, B15, B16, B17, B18, B19, B25, B26, B30, B31, B32, B33, B34, B35, B36, B38, B146, B150, B153, B154.
AT10_002:
The amino acids of influenza A virus group 2 haemagglutinin (H3/H7) in contact with AT10_002 are: A38, A48, A275, A276, A277, A278, A289, A291, A318, B19, B20, B21, B36, B38, B39, B41, B42, B45, B46, B48, B49, B50, B52, B53, B56, B57, B58, B15Q.
Amino acid numbering for the HA molecule was done according to: Wilson et al. 1981 Nature 289, 366-373 and Nobusawa et al. 1991 Virology 182, 475-485.
Interactions antibody-haemagglutinin
AT10_005 interacts with the conserved hydrophobic pocket demonstrated by the crystal of the complex of CR6261 or F10 antibodies with haemagglutinin. The interaction is mainly hydrophobic as for all antibodies binding this pocket.
AT10J304 interacts with the same beta strand as CR8020 in its crystal complex with haemagglutinin but AT10_004 binds in a stronger way by, among other interactions, continuing the beta sheet of haemagglutinin. This interaction is mediated via the main chain and thus it allows cross-reactivity between HI and H3 even in the absence of conservation (because the main chain is conserved between amino acids).
AT10_002 interacts with the conserved hydrophobic patch in a new way since except for the CDR3 of VH, all interactions come from the VL domain.
References
Chen, Y., et al., (1999) J, Mol Biol 293:865-881 de Jong JC, van Nieuwstadt AP, Kimman TG, Loeffen WL, Bestebroer TM, Bijlsma K, Verweij C, Osterhaus AD, Class EC: Antigenic drift in swine influenza H3
haemagglutinins with implications for vaccination policy. Vaccine 1999, 17: 1321-1328.
Kabat,E.A., Wu,T.T., Perry,H., Gottesman,K. and Foeller,C. (1991) Sequences of Proteins of Immunological Interest, Fifth Edition. NIH Publication No. 91.-3242
Kwakkenbos et al. (Generation of stable monoclonal antibody-producing B cell receptor- positive human memory B cells by genetic programming. Nature Medicine (2010) vol. 16 (1) pp. 123-8
Lokate et ai.,2007, J. Am. Chem. Soc. 129: 14013-140318
Londt BZ, Nunez A, Banks J, Nili H, Johnson LK, Alexander DJ: Pathogenesis of highly pathogenic avian influenza A/turkey/Turkey/1/2005 H5N1 in Pekin ducks (Anas platyrhynchos) infected experimentally. Avian Pathol 2008, 37:619-627. van der Goot JA, Koch G, de Jong MC, van Boven M: Quantification of the effect of vaccination on transmission of avian influenza (H7N7) in chickens. Proc Natl Acad Sci U S A 2005, 102: 18141- 18146.
Munster VJ, de Wit E, van den Brand JM, Herfst S, Schrauwen EJ, Bestebroer TM, van de Vijver D, Boucher CA, Koopmans M, Rimmelzwaan GF: Pathogenesis and transmission of swine-origin 2009 A(H1N1) influenza virus in ferrets. Science 2009, 325:481-483.
Needleman SB, Wunsch CD: A general method applicable to the search for
similarities in the amino acid sequence of two proteins. J Mol Biol. 1970
Mar;48(3):443-53.
Nobusawa E, Aoyama T, Kato H, Suzuki Y, Tateno Y, Nakajima K: Comparison of complete amino acid sequences and receptor-binding properties among 13 serotypes of hemagglutinins of influenza A viruses. Virology. 1991 Jun;182(2):475-85.
Subbarao K. and Joseph T. Nature Reviews Immunology 2007: 7, 267-278
Sui J, Hwang WC, Perez S, Wei G, Aird D, Chen LM, Santelli E, Stec B, Cadwell G, Ali M, Wan H, Murakami A, Yammanuru A, Han T, Cox NJ, Bankston LA, Donis RO, Liddington RC, Marasco WA: Structural and functional bases for broad-spectrum neutralization of avian and human influenza A viruses. Nat Struct Mol Biol. 2009 Mar; 16(3):265-73. Epub 2009 Feb 22. Throsby M, van den Brink E, Jongeneelen M, Boon LL, Alard P, Cornelissen L,
Bakker A, Cox F, van Deventer E, Guan Y, Cinatl J, ter Meulen J, Lasters I, Carsetti R, Peiris M, de Kruif J, Goudsmit J: Heterosubtypic neutralizing monoclonal antibodies cross-protective against H5N1 and H1N1 recovered from human IgM+ memory B cells. PLoS One. 2008;3(12):e3942. Epub 2008 Dec 16.
Wilson IA, Skehel JJ, Wiley DC: Structure of the haemagglutinin membrane glycoprotein of influenza virus at 3 A resolution. Nature. 1981 Jan 29;289(5796):366- 73. Yoshida R, Igarashi M, Ozaki H, Kishida N, Tomabechi D, Kida H, Ito K, Takada A: Cross-protective potential of a novel monoclonal antibody directed against antigenic site B of the hemagglutinin of influenza A viruses. PLoS Pathog. 2009
Mar;5(3):el000350. Epub 2009 Mar 20.
WO 2007/067046
WO 2009/115972
WO 2010/130636 5 WO 2010/087994 WO 2007/067046
Table 1. Preferred influenza A virus specific antibodies according to the invention
SEQ Antibody Identity Sequence
ID NO
1 AT10-004 Heavy chain CDR1 RHGIS
2 AT10-003 Heavy chain CDR1 ELSIH
3 AT10-002 Heavy chain CDR1 SSNYY
4 ATlO-001 Heavy chain CDR1 TYAMS
5 AT10-005 Heavy chain CDR1 NYAIS
6 AT10-004 Heavy chain CDR2 WISAYTGDTDYAQKFQG
7 AT10-003 Heavy chain CDR2 SFDPEDGETIYAQKFQG
8 AT10-002 Heavy chain CDR2 TIYHSGSTYYNPSLKS
9 ATlO-001 Heavy chain CDR2 GISGSGESTYYADSVKG
10 AT10-005 Heavy chain CDR2 GIIPIFGTTNYAQKFQG
11 AT 10-004 Heavy chain CDR3 LRLQGE VPPSQSNWFDP
12 AT10-003 Heavy chain CDR3 GWGAVTSPFDF
13 AT10-002 Heavy chain CDR3 GGGFGWSQTYFGY
14 ATlO-001 Heavy chain CDR3 QGDHIAWLLRGINFDY
15 AT10-005 Heavy chain CDR3 HGGVYYYGSASSGWFDP
16 AT10-004 Light chain CDR1 RASQSVSRYLA
17 AT10-003 Light chain CDR1 RSSQSLLHSNGHIYFD
18 AT10-002 Light chain CDR1 TGTS SDVGAYNYVS
19 ATlO-001 Light chain CDR1 RASQSVSSSYLA
20 AT10-005 Light chain CDR1 RASQSVSSSYLA
21 AT10-004 Light chain CDR2 DASNRAT
22 AT10-003 Light chain CDR2 LVSKRAS
23 AT10-002 Light chain CDR2 DVTYRPS
24 ATlO-001 Light chain CDR2 GASTRAT
25 AT10-005 Light chain CDR2 GASTRAT
26 AT10-004 Light chain CDR3 QQRSNWLK
27 AT10-003 Light chain CDR3 MQALETP
28 AT10-002 Light chain CDR3 SSQSRSST
29 ATlO-001 Light chain CDR3 QNYGSPF
30 AT10-005 Light chain CDR3 QQYGSLP
31 AT10-004 Heavy chain QVQLVQSGAEWKPGASVIWSCKASGYTFTRHGISWVEQAPGQGLEWMGWISAYTGDTDYAQK
QGRVTMTTDTSTNTAYMELRSLRSDDAAVYYCARLRLQGEVWPPSQSNWFDPWGQGTLVTVSS
32 AT10-003 Heavy chain QVHLVQSGAEVRKPGASVKVSCKVSGYTLNELSIHWLRQAPGRGLEWMGSFDPEDGETIYAQKF
QGRVTMTGDTSTDTAYLELTSLRSEDTALYYCARGWGAVTSPFDFWGQGTLVTVSS
33 AT10-002 Heavy chain QLQLQESGPRLVEPSETLSLTCSVSGVSISSSNYYWGWIRQPPGKGLEWIGTrYHSGSTYYNPSLK
RLIISVDTSKNQFYLQLTSLTAADSAVYYCATGGGFGWSQTYFGYWGQGTLVTASS
34 ATlO-001 Heavy chain EVQLLESGGGLVQPGGSLRLSCAASGFSFSTYAMSWVRQAPGKGLEWVSGISGSGESTYYADSVK
GRFTVSRDNSKNTLYLQMNSLRAEDTAVYYCAKQGDHIAWLLRGINFDYWGQGVLVTVSS
35 AT10-005 Heavy chain QVQLVQSGAEVKKPGSSVKVSCKASGGAFSNY SV^vTRQAPGQGLEWMGGIIPIFGTTNYAQKFQ
GRVTITADKFTTIAYMELRSLRSEDTAVYYCARHGGVYYYGSASSGWFDPWGQGTLVTVSS
36 AT10-004 Light chain EIVLTQSPATLSLYPGERATLSCRASQSVSRYLAWYQQKPGQAPRLLIYDASNRATGIPARFSGSGS
GTDFTLTISSLEPEDFAVYYCCDR3 QQRSNWLKITFGQGTRLEIKGTV
37 AT10-003 Light chain DIVMTQSPLSLPVTPGEPASISCRSSQSLLHSNGHIYFDWYLQKPGQSPQLL 7LVSKRASGVPDR
SGSGSGTDFTLKISRA^AEDVGVYYCMQALETPFTFGPGTKVHIKRTV
38 AT10-002 Light chain QSALTQPASVSGSPGQSITISCTGTSSDVGAYNYVSWYQHHPGKAPKLMIYDVTYRPSG\¾TRFSG
KSGNTASLTISGLQAEDEADYYCSSQSRSSTLVIFGGGTKLTVLGQPK
39 ATlO-001 Light chain EIVLTQSPGTLSLSPGERATLSCRASQSVSSSYLAWYQQKPGQAPRLLIYGASTRATGIPDRFSGRG
GTDFTLTISSLEPEDFA\^YYCQNYGSPFLFTFGPGTKVDIKRTV
40 AT10-005 Light chain EIVLTQSPGTLSLSPGERATLSCRASQSVSSSYLAWYQQKPGQAPRLLIFGASTRATGIPDRFSGSG
GTDFTLTISRLEPEDFAVFYCQQYGSLPLTFGGGTKVEIKGTV
41 AT10-004 Heavy chain CDRl agg cat ggt ate age
42 AT10-003 Heavy chain CDRl gaa tta tec att cac
43 AT10-002 Heavy chain CDRl agt agt aat tat tac
44 ATlO-001 Heavy chain CDRl acc tat gec atg age
45 AT10-005 Heavy chain CDRl aac tat get ate age
46 AT10-004 Heavy chain CDR2 tgg ate age get tac act ggt gac aca gac tat gca cag aaa ttc cag ggg
47 AT10-003 Heavy chain CDR2 agt ttt gat cct gaa gat ggt gaa aca ate tac gcg cag aag ttc cag ggc
48 AT10-002 Heavy chain CDR2 act ate tat cac agt ggc age acc tac tac aac ccg tec etc aag agt
49 ATlO-001 Heavy chain CDR2 ggt att agt ggt agt ggt gag age aca tac tac gca gac tec gtg aag ggc
50 AT10-005 Heavy chain CDR2 ggg ate ate cct ate ttt gga aca aca aac tac gca cag aag ttc cag ggc
51 AT10-004 Heavy chain CDR3 ctt cgt ttg cag ggt gaa gtg gtg gtc cct cct agt caa tec aat tgg ttc gac ccc
52 AT10-003 Heavy chain CDR3 ggt tgg ggg gcg gtg act tea ccc ttt gac ttc
53 AT10-002 Heavy chain CDR3 ggg ggg ggg ttt ggc tgg tct caa acc tac ttt ggc tac
54 ATlO-001 Heavy chain CDR3 caa ggg gat cat att gec tgg tta tta agg ggg att aac ttt gac tac
55 AT10-005 Heavy chain CDR3 cat ggg gga gtg tat tat tat ggg teg gcg agt teg gga tgg ttc gac ccc
56 AT10-004 Light chain CDRl agg gee agt cag agt gtt age agg tac tta gec
57 AT10-003 Light chain CDR1 agg tct agt cag age etc ctg cat agt aat ggg cac ate tat tte gat
58 AT10-002 Light chain CDR1 act gga acc age agt gac gtt ggt get tat aac tat gtt tct
59 ATlO-001 Light chain CDR1 agg gcc agt cag agt gtt age age agt tac tta gcc
60 AT10-005 Light chain CDR1 agg gcc agt cag agt gtt agt age age tac tta
61 AT10-004 Light chain CDR2 gat gea tec aac agg gcc act
62 AT10-003 Light chain CDR2 ttg gtt tct aag egg gcc tec
63 AT10-002 Light chain CDR2 gat gtc act tat egg ecc tea
64 ATlO-001 Light chain CDR2 ggt gea tec acc agg gcc act
65 AT10-005 Light chain CDR2 ggt gea tec acc agg gcc act
66 AT10-004 Light chain CDR3 cag cag cgt age aac tgg ctt aag
67 AT10-003 Light chain CDR3 atg caa get eta gaa act cca
68 AT10-002 Light chain CDR3 agt tea cag tea cgc age age act
69 ATlO-001 Light chain CDR3 cag aac tat ggt agt cca ttt
70 AT10-005 Light chain CDR3 cag cag tat ggt age tta cct
71 AT10-004 Heavy chain cag gtt cag ctg gtg cag tct gga get gag gtg agg aag cct ggg gcc tea gtg aag gtc tec tgc aag get tec ggt tac acg ttt acc agg cat ggt ate age tgg gtg cga cag gcc cct gga caa ggg ctt gag tgg atg gga tgg ate age get ta act ggt gac aca gac tat gea cag aaa tte cag ggg cga gtc acc atg acc aca gat aca tec acg aac aca gcc tac atg gaa ctg agg age ctg aga tct gac gac gcg gcc gta tat tac tgt gcg aga ctt cgt ttg cag ggt gaa gtg gtg gt cct cct agt caa tec aat tgg tte gac ecc tgg ggc cag gga acc ctg gtc acc gtc tec tea
72 AT10-003 Heavy chain cag gtc cac ctg gta cag tct ggg get gag gtg agg aag cct ggg gcc tea gtg aag gtc tec tgc aaa gtt tec gga ta aca etc aat gaa tta tec att cac tgg ctg cga cag get ect gga aga ggg ctt gag tgg atg gga agt ttt gat cct gaa gat ggt gaa aca ate tac gcg cag aag tte cag ggc aga gtc acc atg acc ggg gac aca tct aca gac aca gcc tac ctg gag ctg acc age ctg aga tct gag gac acg gcc etc tat tac tgt gea aga ggt tgg ggg gcg gtg act tea ecc ttt gac tte tgg ggc cag gga aca ctg gtc acc gtc tec tea
73 AT10-002 Heavy chain cag ctg cag ctg cag gag teg ggc cca cga ctg gtg aag ecc teg gag acc ctg tec etc acc tgc tct gtc tec ggt gtc tec ate age agt agt aat tat tac tgg ggc tgg ate cgc cag ecc cca ggg aag ggg ctg gag tgg att ggg act ate tat cac agt ggc age acc tac tac aac ccg tec etc aag agt cga etc ate ate tec gtc gac acg tec aag aat cag tte tac ctg cag ttg acc tct ctg acc gcc gea gac teg get gtc tat tac tgt gcg acc ggg ggg ggg ttt ggc tgg tct caa acc tac ttt ggc tac tgg ggc cag gga acc ctg gtc acc gcc tec tea
74 ATlO-001 Heavy chain gag gtg cag ctg ttg gag tct ggg gga ggc ttg gta cag cct ggg ggg tec ctg aga etc tec tgt gea gcc tec gga tte age ttt age acc tat gcc atg age tgg gtc cgc cag get cca gga aag ggg ctg gag tgg gtc tea ggt att agt ggt ag ggt gag age aca tac tac gea gac tec gtg aag ggc egg tte acc gtc tec aga gac aat tec aag aac acc ctg tat ct caa atg aac age ctg aga gcc gag gac acg gcc gtc tat tac tgt gcg aaa caa ggg gat cat att gee tgg tta tta agg ggg att aac ttt gac tac tgg ggc cag gga gtc ctt gtc acc gtc tec tea
75 AT10-005 Heavy chain cag gtg cag ctg gtg cag tct ggg get gaa gtg aag aag cct ggg tec teg gtg aag gtc tec tgc aag get tct gga gg
Table 2. Recombinant human HA recognition by B cells that secrete heterosubt pic cross-binding mAbs.
Table 3. Recombinant human, swine and duck infecting Influenza HA protein recognition by heterosubtypic cross-binding mAbs.
Table 4. Antibody binding to virus infected MDCK cells.
Table 5. In vitro influenza A virus neutralization of virus infected MDCK-SIAT cells by recombinant antibodies.
ND = Not done
IC50 values displayed in μ g/ml
Table 6. Recombinant HA and HAl subunit recognition by recombinant antibodies.
ATlO-001 AT10-002 AT10-003 AT10-004 AT10 005
H3IN2 A/Aichi/2/1968 Full length 0.953 0.920 1.319 0.491 -0.003
H3N2 A/Aichi/2/1968 HAl subunit 0.010 -0.006 1.277 0.096 -0.007
Table 7
Table 7. In vitro influenza A neutralization of virus infected MDCK cells by recombinant antibodies
TCID50 tested Virus 1 AT10_001 AT10_002 AT10_003 AT10_004 AT10_005 CR8020
917 H1N1 A/Neth/602/2009 (swine-origin) I >15 >15 >15 >15 2.7 >15
41 H5N1 A/turkey/Turkey/05 I >15 >15 >15 >15 1.3 >15
355 H3N2 A/swine/Neth/St. Oedenrode/96 1 14 0.3 >15 2.3 >15 >15
100 H7N1 A/ck/ltaly/1067/99 >15 3.6 >15 0.6 >15 >15
40 H7N7 A/ck/Neth/621557/03 0.4 0.1 >15 0.2 >15 0.6
IC50 values displayed in igjm\
Table 8
Table 8. Selection of sequences to replace segments where substitutions occur between the target sequence (AT10_002) and the template (2XZA and 3TNN). The numbering follows the rules of Rabat.
AT10_002 3D template:
VH 2XZA 77.2% identity
VL 3TNN 85.6% identity
Region Amino Acids Alignment {PDB nr)
VH ' 2 2J6EH, 3Q6GH, 3TJEH, 3THMH, 2XZAH
¥ 10 2XZAH, 2XZAH, 3B2UH, 3B2VH, 2J6EH
23-33 3B2UH, 3B2VH, 2J6EH, 1MCOH, 2VXQH
' 50 2XZAH, 2XZCH, 2VXQH 3B2UH, 3B2VH
67-68 2XZAH, 2XZCH, 2J6EH, 2J1XD, 2E SB
79-82c 1U6AH, 3HJ1H, 2XZAH, 2XZCH, 2J6EH
" 87 3G01H, 2XZAH, 2XZCH, 3B2UH, 3B2VH
94-102 1BZ7B, 1R24B, 1XIWD, 31VKH, 4D EH
109-111 3B2UH, 3B2VH, 2jiXD, 2YK1H, 2YKLH
VL 29-38 3TNML, 3KDML, 3TNNL, 2JB5L, 2JB6A
50-60 3 DML, 20LDA, 20MBA, 20MNA, 1NL0L
91-97 1JVKA, 1LGVA, 1LHZA, 20LOA, 20MBA
107 UVKA, 1LGVA, 1LHZA, 2JB5L, 2JB6A
Table 9
Table 9. Selection of sequences to replace segments where substitutions occur between the target sequence (AT10_004) and the template (3SDY). The numbering follows the rules of Kabat.
AT10_004 3D template:
VH 3SDYH 77.3% identity
VL 3EYQ 96.3% identity
Region Amino Acids Alignment {PDB nr}
VH 5 2XQBH, 4FQJH, 4FQKE, 3!YWH,3N9GH
12-13 3IYWH, 3N9GH, 3QEHA, 2CMRH, 3LMJH
31-37 3GRWH, 2XQBH, 3SDYH, 4FQJH, 4FQKE
43 4FQJH, 4FQKE, 2XQBH, 3SDYH, 3S 5H
54-58 3SDYH, 4FQJH, 4FQKE, 1RMFH, 2XQBH
65 2D7TH, 2XQBH, 3SDYH, 4FQJH, 4FQ E
76 3C0SH, 3C09H, 3LMJH, 3LQAH, 3NTCH
82 2XQBH, 4FQJH, 4FQKE, 1HZHH, 1N0XH
87 2XQBH, 3SDYH, 2D7TH, 1WT5A, liQDB
95-103 3BN9D, 3 LXH, 3MLYH, 3MLZH, I XTB
VL CDR3 2XQY
Table 10
Table 10. Selection of sequences to replace segments where substitutions occur between the target sequence (AT10_OOI and the template (3QOT). The numbering follows the rules of Kabat.
AT10_005 3D template:
VH 3QOTH 83.3% identity
VL 4FQL 93.5% identity
Region Amino Acids Alignment {PDB nr)
VH 28-31 3NPSB, 2JB5H, 2JB6B, 1 ZIB
57 3MA9H, 3NPSB, 2CMRH, 1RHHB
73-82A 3PP3H, 3PP4H, 3HC4H, 3HC0H, 3HC3H
95-102 4FQ.IH, 3P30H, 2FB4H, 21G2H, 3NPSB, 3MLWH
VL CDR3 1DN0
Claims
1. An isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, having an in vitro H3N2 influenza A virus neutralizing activity with an IC50 value of less than 1
preferably of less than 0.7 μg/ml, more preferably of equal to or less than 
more preferably of less than 0.2 
which antibody or functional part or immunoglobulin chain or functional equivalent is capable of specifically binding at least one other influenza A virus subtype.
2. An antibody or functional part or immunoglobulin chain or functional equivalent according to claim 1, wherein said at least one other influenza A virus subtype is a group 2 influenza A virus subtype.
3. An antibody or functional part or immunoglobulin chain or functional equivalent according to claim 1, wherein said at least one other influenza A virus subtype is a group 1 influenza A virus subtype.
4. An isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, comprising:
- a heavy chain CDRl sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's: l-5, and/or
- a heavy chain CDR2 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's:6- 10, and/or
- a heavy chain CDR3 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's: l l- 15, and/or
- a light chain CDRl sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's: 16-20, and/or
- a light chain CDR2 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's:21-25, and/or - a light chain CDR3 sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's:26-30.
5. An antibody or functional part or immunoglobulin chain or functional equivalent according to claim 4, having a heavy chain sequence comprising a sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's:31-35 and/or having a light chain sequence which is at least 70% identical to a sequence selected from the group consisting of SEQ ID NO's:36-40.
6. An isolated, synthetic or recombinant nucleic acid molecule with a length of at least 15 nucleotides, or a functional equivalent thereof, encoding at least one CDR sequence of an antibody or functional part thereof or immunoglobulin chain or functional equivalent according to claim 4 or 5.
7. A nucleic acid molecule or a functional equivalent according to claim 6, comprising a sequence which has at least 70% sequence identity to a sequence selected from the group consisting of:
- SEQ ID NO's:41-45, and
- SEQ ID NO's: 46-50, and
- SEQ ID NO's:51-55, and
- SEQ ID NO's:56-60, and
- SEQ ID NO's:61-65, and
- SEQ ID NO's:66-70.
8. A nucleic acid molecule or a functional equivalent according to claim 6 or 7, comprising a sequence which has at least 70% sequence identity to a sequence selected from the group consisting of SEQ ID NO's:71-75 and/or comprising a sequence which has at least 70% sequence identity to a sequence selected from the group consisting of SEQ ID NO's: 76-80.
9. A vector comprising a nucleic acid molecule or functional equivalent according to any one of claims 6-8.
10. An isolated or recombinant cell comprising a nucleic acid molecule or functional equivalent according to any one of claims 6-8, and/or a vector according to claim 9.
11. A pharmaceutical composition comprising an antibody or functional part or immunoglobulin chain or functional equivalent or a nucleic acid molecule or functional equivalent or a vector according to any one of claims 1-9 and a
pharmaceutical acceptable carrier, diluent and/or excipient.
12. An antibody or functional part or immunoglobulin chain or functional equivalent or a nucleic acid molecule or functional equivalent thereof or a vector according to any one of claims 1-9, for use as a medicament and/or prophylactic agent.
13. An antibody or functional part or immunoglobulin chain or functional equivalent, or a nucleic acid molecule or functional equivalent, or a vector according to any one of claims 1-9, for use as a medicament and/or prophylactic agent for at least in part treating and/or preventing an influenza A virus infection.
14. A method for producing an antibody or functional part or immunoglobulin chain or functional equivalent according to any one of claims 1-5, comprising providing a cell with a nucleic acid molecule or functional equivalent or a vector according to any one of claims 6-9, and allowing said cell to translate said nucleic acid molecule or functional equivalent or vector, thereby producing said antibody or functional part or immunoglobulin chain or functional equivalent according to any one of claims 1-5, preferably further comprising harvesting, purifying and/or isolating said antibody or functional part or immunoglobulin chain or functional equivalent according to any one of claims 1-5.
15. An antibody or functional part or immunoglobulin chain or functional equivalent according to any one of claims 1-5 for use in diagnosis of an influenza A virus infection.
16. A method for determining whether an influenza A virus is present in a sample comprising:
- contacting said sample with an antibody or functional part or immunoglobulin chain or functional equivalent according to any one of claims 1-5, - allowing said antibody or functional part or immunoglobulin chain or functional equivalent to bind said influenza A virus, if present, and
- determining whether influenza A virus is bound to said antibody or functional part or immunoglobulin chain or functional equivalent, thereby determining whether an influenza A virus is present in said sample.
17. An isolated, synthetic or recombinant antibody or functional part thereof, immunoglobulin chain or functional equivalent thereof, having an in vitro H7N1 influenza A virus neutralizing activity with an IC50 value of less than 5.0 μδ/ηαΐ, preferably of less than 4.0 
more preferably of less than 1.0 μ /ml, more preferably equal to or less than about 0.6 
18. An isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, having an in vitro H7N7 influenza A virus neutralizing activity with an IC50 value of less than 0.5 
preferably equal to or less than about 0.4 
more preferably equal to or less than about 0.2 
most preferably equal to or less than about 0.1.
19. An isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, having an in vitro H1N1 influenza A virus neutralizing activity with an IC50 value of less than 5.0 μg/ml, preferably of less than 4.0 μ /ml, more preferably of less than 3.0 μ /ml, more preferably equal to or less than about 2.7 μ /ml.
20. An isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, having an in vitro H5N1 influenza A virus neutralizing activity with an IC50 value of less than 5.0 μg/ml, preferably of less than 4.0 μ /ml, more preferably of less than 3.0 μ§/ηύ, more preferably of less than 2.0 μg/ml, more preferably equal to or less than about 1.3 μg/ \.
21. An antibody or functional part or immunoglobulin chain or functional equivalent according to any one of claims 17-20, which is capable of specifically binding at least one other influenza A virus subtype.
22. A synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent thereof, comprising:
i) at least two different heavy chain CDR sequences and at least two different light chain CDR sequences of an antibody selected from the group consisting of AT10__001 and AT10_002 and AT10_003 and AT10_004 and AT10_005; and
ii) at least two different heavy chain CDR sequences and at least two different light chain CDR sequences of an antibody selected from the group consisting of AT10_001 and AT10_002 and AT10_003 and AT10_004 and AT10_005,
wherein said antibody selected in i) is different from said antibody selected in ii).
23. A multimeric antibody, multimeric immunoglobulin or functional equivalent according to claim 22, comprising:
i) heavy chain CDR1, CDR2 and CDR3 and light chain CDR1, CDR2 and CDR3 sequences of an antibody selected from the group consisting of AT10_001 and ΑΤ10_002 and AT10_003 and AT10_004 and AT1CL005; and
ii) heavy chain CDR1, CDR2 and CDR3 and light chain CDR1, CDR2 and CDR3 sequences of an antibody selected from the group consisting of AT10_001 and AT10_002 and AT10_003 and AT10_004 and AT10_005,
wherein said antibody selected in i) is different from said antibody selected in ii).
24. A multimeric antibody, multimeric immunoglobulin or functional equivalent according to claim 22 or 23, comprising:
i) the heavy chain sequence and the light chain sequence of an antibody selected from the group consisting of AT10_001 and AT10_002 and AT10_003 and AT10_004 and AT10_005, or a sequences that is at least 70% identical thereto; and
ii) the heavy chain sequence and the light chain sequence of an antibody selected from the group consisting of AT10_001 and AT10_002 and AT10_003 and AT10_004 and AT10_005, or a sequence that is at least 70% identical thereto,
wherein said antibody selected in i) is different from said antibody selected in ii).
25. A multimeric antibody, multimeric immunoglobulin or functional equivalent according to claim 22, comprising:
i) at least two different heavy chain CDR sequences and at least two different light chain CDR sequences of antibody AT10_0Q2; and
ii) at least two different heavy chain CDR sequences and at least two different light chain CDR sequences of antibody AT10_Q05.
26. A multimeric antibody, multimeric immunoglobulin or functional equivalent according to claim 22 or 23, comprising:
i) heavy chain CDR1, CDR2 and CDR3 and light chain CDR1, CDR2 and CDR3 sequences of antibody AT10_002; and
ii) heavy chain CDR1, CDR2 and CDR3 and light chain CDR1, CDR2 and CDR3 sequences of antibody AT1Q_005.
27. A multimeric antibody, multimeric immunoglobulin or functional equivalent according to any one of claims 22-26, comprising:
i) the heavy chain sequence and the light chain sequence of antibody AT10_002, or sequences that are at least 70% identical thereto; and
ii) the heavy chain sequence and the light chain sequence of antibody AT10_005, or sequences that are at least 70% identical thereto.
28. A multimeric antibody, multimeric immunoglobulin or functional equivalent according to any one of claims 22-27, which is a dimeric antibody.
29. An isolated or recombinant cell or a pharmaceutical composition comprising a multimeric antibody, multimeric immunoglobulin or functional equivalent according to any one of claims 22-28.
30. A synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent according to any one of claims 22-28 for use as a medicament and/or prophylactic agent.
31. A synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent according to any one of claims 22-28 for use as a medicament and/or prophylactic agent for at least in part treating and/or preventing and/or alleviating the symptoms of an influenza A infection.
32. A synthetic or recombinant multimeric antibody, multimeric immunoglobulin or functional equivalent according to any one of claims 22-28 for use in diagnosis of an influenza A infection.
33. A method for at least in part treating and/or preventing an influenza A virus infection, comprising administering to an individual in need thereof a therapeutically effective amount of a multimeric antibody, multimeric immunoglobulin or functional equivalent according to any one of claims 22-28 and/or a cell or pharmaceutical composition according to claim 29.
34. A method for neutralizing a H1N1 influenza A virus and/or an H3N2 influenza A virus, comprising contacting said H1N1 influenza A virus and/or said H3N2 influenza A virus with a multimeric antibody, multimeric immunoglobulin or functional equivalent according to any one of claims 22-28, resulting in neutralization of said virus.
35. A method for determining whether an influenza A virus is present in a sample comprising:
- contacting said sample with a multimeric antibody, multimeric immunoglobulin or functional equivalent according to any one of claims 22-28,
- allowing said multimeric antibody, multimeric immunoglobulin or functional equivalent to bind said influenza A virus, if present, and
- determining whether influenza A virus is bound to said multimeric antibody, multimeric immunoglobulin or functional equivalent, thereby determining whether an influenza A virus is present in said sample.
36. An isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, capable of interacting with amino acids at positions A38, A40, A41, A42, A291, A292, A293, A318, B18, B19, B20, B21, B38, B41, B42, B45, B46, B48, B49, B52, B53, and B56 of influenza A virus group 1 hemagglutinin (H1/H5).
37. An isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, capable of interacting with amino acids at positions A21, A324, A325, A327, B12, B14, B15, B16, B17, B18, B19, B25, B26, B30, B31, B32, B33, B34, B35, B36, B38, B146, B150, B153, and B154 of influenza A virus group 2 hemagglutinin (H3/H7).
38. An isolated, synthetic or recombinant antibody or functional part thereof, or immunoglobulin chain or functional equivalent thereof, capable of interacting with amino acids at positions A38, A48, A275, A276, A277, A278, A289, A291, A318, B19, B20, B21, B36, B38, B39, B41, B42, B45, B46, B48, B49, B50, B52, B53, B56, B57, B58, B150 of influenza A virus group 2 hemagglutinin (H3/H7).
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SG11201402780UA SG11201402780UA (en) | 2011-12-02 | 2012-12-03 | Influenza a virus specific antibodies |
| EP12798020.9A EP2785737A2 (en) | 2011-12-02 | 2012-12-03 | Influenza a virus specific antibodies |
| AU2012346669A AU2012346669B2 (en) | 2011-12-02 | 2012-12-03 | Influenza A virus specific antibodies |
| KR1020147018417A KR20140112495A (en) | 2011-12-02 | 2012-12-03 | Influenza a virus specific antibodies |
| JP2014544698A JP6325451B2 (en) | 2011-12-02 | 2012-12-03 | Antibodies specific for influenza A |
| US14/362,210 US9718874B2 (en) | 2011-12-02 | 2012-12-03 | Influenza A virus specific antibodies |
| CA2892992A CA2892992A1 (en) | 2011-12-02 | 2012-12-03 | Influenza a virus specific antibodies |
| US15/645,399 US20170313766A1 (en) | 2011-12-02 | 2017-07-10 | Influenza a virus specific antibodies |
| AU2017216562A AU2017216562A1 (en) | 2011-12-02 | 2017-08-18 | Influenza A virus specific antibodies |
| AU2021245146A AU2021245146A1 (en) | 2011-12-02 | 2021-10-05 | Influenza A virus specific antibodies |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11191783.7 | 2011-12-02 | ||
| EP11191783 | 2011-12-02 |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US14/362,210 A-371-Of-International US9718874B2 (en) | 2011-12-02 | 2012-12-03 | Influenza A virus specific antibodies |
| US15/645,399 Continuation US20170313766A1 (en) | 2011-12-02 | 2017-07-10 | Influenza a virus specific antibodies |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2013081463A2 true WO2013081463A2 (en) | 2013-06-06 |
| WO2013081463A3 WO2013081463A3 (en) | 2013-11-14 |
Family
ID=47297373
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/NL2012/050851 WO2013081463A2 (en) | 2011-12-02 | 2012-12-03 | Influenza a virus specific antibodies |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US9718874B2 (en) |
| EP (1) | EP2785737A2 (en) |
| JP (1) | JP6325451B2 (en) |
| KR (1) | KR20140112495A (en) |
| AU (3) | AU2012346669B2 (en) |
| CA (1) | CA2892992A1 (en) |
| SG (1) | SG11201402780UA (en) |
| WO (1) | WO2013081463A2 (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8877200B2 (en) | 2012-05-10 | 2014-11-04 | Visterra, Inc. | HA binding agents |
| WO2015093949A2 (en) | 2013-12-17 | 2015-06-25 | Aimm Therapeutics B.V. | Means and methods for counteracting myeloproliferative or lymphoproliferative disorders |
| WO2015115892A1 (en) | 2014-01-31 | 2015-08-06 | Aimm Therapeutics B.V. | Means and methods for producing stable antibodies |
| KR20150118400A (en) * | 2014-04-14 | 2015-10-22 | 아이디바이오 주식회사 | Novel virus vaccine to form cross-protection against multiple subtypes of influenza viruses |
| WO2016209079A1 (en) | 2015-06-24 | 2016-12-29 | Aimm Therapeutics B.V. | Aml antigens and uses thereof |
| CN106928350A (en) * | 2015-12-30 | 2017-07-07 | 中国科学院天津工业生物技术研究所 | A kind of Antibody of Influenza, its preparation method and application |
| US9822339B2 (en) | 2005-12-09 | 2017-11-21 | Academisch Medisch Centrum Bij De Universiteit Van Amsterdam | Means and methods for influencing the stability of antibody producing cells |
| US9969795B2 (en) | 2010-12-02 | 2018-05-15 | Aimm Therapeutics B.V. | Means and methods for producing high affinity antibodies |
| US10077427B2 (en) | 2005-12-09 | 2018-09-18 | Academisch Medisch Centrum Bij De Universiteit Van Amsterdam | Means and methods for influencing the stability of cells |
| US10344076B2 (en) | 2009-07-15 | 2019-07-09 | Aimm Therapeutics B.V. | Means and methods for producing high affinity antibodies |
| WO2019147867A1 (en) | 2018-01-26 | 2019-08-01 | Regeneron Pharmaceuticals, Inc. | Human antibodies to influenza hemagglutinin |
| US10392432B2 (en) | 2014-12-19 | 2019-08-27 | Regeneron Pharmaceuticals, Inc. | Human antibodies to influenza hemagglutinin |
| US10513553B2 (en) | 2015-11-13 | 2019-12-24 | Visterra, Inc. | Compositions and methods for treating and preventing influenza |
| WO2021141492A1 (en) | 2020-01-10 | 2021-07-15 | Kling Biotherapeutics B.V. | Epithelial cadherin-specific antibodies |
| US11230593B2 (en) | 2019-03-25 | 2022-01-25 | Visterra, Inc. | Compositions and methods for treating and preventing influenza |
| JP2022119757A (en) * | 2013-10-02 | 2022-08-17 | メディミューン，エルエルシー | Neutralizing anti-influenza A antibodies and uses thereof |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11781112B2 (en) | 2016-03-06 | 2023-10-10 | Kareem Thomas Robinson | Method of generating antigen-specific immunological memory in a subject that rejects classical vaccines |
| US10738338B2 (en) | 2016-10-18 | 2020-08-11 | The Research Foundation for the State University | Method and composition for biocatalytic protein-oligonucleotide conjugation and protein-oligonucleotide conjugate |
| WO2019067884A1 (en) * | 2017-09-28 | 2019-04-04 | The Children's Medical Center Corporation | Molecular grafting of complex, broadly neutralizing antibody epitopes |
| CN111298101B (en) * | 2020-02-21 | 2023-05-30 | 佛山科学技术学院 | Application of antibacterial peptide PG-1 in inhibiting avian influenza virus |
| US20240018218A1 (en) * | 2020-09-08 | 2024-01-18 | Novelgen Co., Ltd. | Antiviral composition against influenza a virus |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007067046A1 (en) | 2005-12-09 | 2007-06-14 | Academisch Medisch Centrum Bij De Universiteit Van Amsterdam | Means and methods for influencing the stability of antibody producing cells |
| WO2009115972A1 (en) | 2008-03-17 | 2009-09-24 | Pomona Biotechnologies Llc | Monoclonal antibodies capable of reacting with a plurality of influenza virus a subtypes |
| WO2010010466A2 (en) | 2008-07-25 | 2010-01-28 | Institute For Research In Biomedicine | Neutralizing anti-influenza a virus antibodies and uses thereof |
| WO2010087994A2 (en) | 2009-01-30 | 2010-08-05 | Whitehead Institute For Biomedical Research | Methods for ligation and uses thereof |
| WO2010130636A1 (en) | 2009-05-11 | 2010-11-18 | Crucell Holland B.V. | Human binding molecules capable of neutralizing influenza virus h3n2 and uses thereof |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4656478B2 (en) | 2000-02-22 | 2011-03-23 | 株式会社医学生物学研究所 | Antibody library |
| WO2003083061A2 (en) | 2002-03-26 | 2003-10-09 | Centocor, Inc. | Anti-tnf antibodies, compositions, methods and uses |
| EP2450377A1 (en) * | 2006-09-07 | 2012-05-09 | Crucell Holland B.V. | Human binding molecules capable of neutralizing influenza virus H5N1 and uses thereof |
| NO347649B1 (en) | 2006-12-14 | 2024-02-12 | Regeneron Pharma | Human antibody or antibody fragment that specifically binds human delta-like ligand 4 (hDII4), nucleic acid molecule that codes for such and vector and host-vector systems, as well as method for production, composition and use. |
| US8871207B2 (en) | 2008-07-25 | 2014-10-28 | Humabs, LLC | Neutralizing anti-influenza A virus antibodies and uses thereof |
| WO2010138564A1 (en) | 2009-05-26 | 2010-12-02 | Mount Sinai School Of Medicine Of New York University | Monoclonal antibodies against influenza virus generated by cyclical administration and uses thereof |
| CN102791734B (en) | 2010-03-08 | 2014-10-15 | 赛特瑞恩股份有限公司 | Human monoclonal antibodies derived from human B cells and having neutralizing activity against influenza a viruses |
| CN102958539B (en) | 2010-03-26 | 2015-07-01 | 泼莫纳搜索有限公司 | Full-length immunoglobulins of the IgG isotvpe capable of recognizing a heterosubtvpe neutralizing epitope on the hemagglutinin stem region and their use as anti-influenza medicament |
-
2012
- 2012-12-03 US US14/362,210 patent/US9718874B2/en active Active - Reinstated
- 2012-12-03 KR KR1020147018417A patent/KR20140112495A/en active IP Right Grant
- 2012-12-03 AU AU2012346669A patent/AU2012346669B2/en active Active
- 2012-12-03 WO PCT/NL2012/050851 patent/WO2013081463A2/en active Application Filing
- 2012-12-03 CA CA2892992A patent/CA2892992A1/en not_active Abandoned
- 2012-12-03 JP JP2014544698A patent/JP6325451B2/en active Active
- 2012-12-03 EP EP12798020.9A patent/EP2785737A2/en not_active Withdrawn
- 2012-12-03 SG SG11201402780UA patent/SG11201402780UA/en unknown
-
2017
- 2017-07-10 US US15/645,399 patent/US20170313766A1/en not_active Abandoned
- 2017-08-18 AU AU2017216562A patent/AU2017216562A1/en not_active Abandoned
-
2021
- 2021-10-05 AU AU2021245146A patent/AU2021245146A1/en active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007067046A1 (en) | 2005-12-09 | 2007-06-14 | Academisch Medisch Centrum Bij De Universiteit Van Amsterdam | Means and methods for influencing the stability of antibody producing cells |
| WO2009115972A1 (en) | 2008-03-17 | 2009-09-24 | Pomona Biotechnologies Llc | Monoclonal antibodies capable of reacting with a plurality of influenza virus a subtypes |
| WO2010010466A2 (en) | 2008-07-25 | 2010-01-28 | Institute For Research In Biomedicine | Neutralizing anti-influenza a virus antibodies and uses thereof |
| WO2010087994A2 (en) | 2009-01-30 | 2010-08-05 | Whitehead Institute For Biomedical Research | Methods for ligation and uses thereof |
| WO2010130636A1 (en) | 2009-05-11 | 2010-11-18 | Crucell Holland B.V. | Human binding molecules capable of neutralizing influenza virus h3n2 and uses thereof |
Non-Patent Citations (22)
| Title |
|---|
| CHEN, Y. ET AL., J. MOL BIOL, vol. 293, 1999, pages 865 - 881 |
| CHEN, Y. ET AL., MOL BIOL, vol. 293, 1999, pages 865 - 881 |
| DE JONG JC; VAN NIEUWSTADT AP; KIMMAN TG; LOEFFEN WL; BESTEBROER TM; BIJLSMA K; VERWEIJ C; OSTERHAUS AD: "Class EC: Antigenic drift in swine influenza H3 haemagglutinins with implications for vaccination policy", VACCINE, vol. 17, 1999, pages 1321 - 1328, XP004158259, DOI: doi:10.1016/S0264-410X(98)00392-2 |
| JOURNAL OF VIROLOGY, August 2003 (2003-08-01), pages 8418 - 25 |
| KABAT,E.A.; WU,T.T.; PERRY,H.; GOTTESMAN,K.; FOELLER,C.: "Sequences of Proteins of Immunological Interest", 1991, NIH PUBLICATION |
| KWAKKENBOS ET AL.: "Generation of stable monoclonal antibody-producing B cell receptor- positive human memory B cells by genetic programming", NATURE MEDICINE, vol. 16, no. 1, 2010, pages 123 - 8 |
| LOKATE ET AL., J. AM. CHEM. SOC., vol. 129, 2007, pages 14013 - 140318 |
| LONDT BZ; NUNEZ A; BANKS J; NILI H; JOHNSON LK; ALEXANDER DJ: "Pathogenesis of highly pathogenic avian influenza A/turkey/Turkey/1/2005 H5N1 in Pekin ducks (Anas platyrhynchos) infected experimentally", AVIAN PATHOL, vol. 37, 2008, pages 619 - 627 |
| MUNSTER VJ; DE WIT E; VAN DEN BRAND JM; HERFST S; SCHRAUWEN EJ; BESTEBROER TM; VAN DE VIJVER D; BOUCHER CA; KOOPMANS M; RIMMELZWAA: "Pathogenesis and transmission of swine-origin 2009 A(H1N1) influenza virus in ferrets", SCIENCE, vol. 325, 2009, pages 481 - 483 |
| NEEDLEMAN SB; WUNSCH CD: "A general method applicable to the search for similarities in the amino acid sequence of two proteins", J MOL BIOL., vol. 48, no. 3, March 1970 (1970-03-01), pages 443 - 53, XP024011703, DOI: doi:10.1016/0022-2836(70)90057-4 |
| NOBUSAWA E; AOYAMA T; KATO H; SUZUKI Y; TATENO Y; NAKAJIMA K: "Comparison of complete amino acid sequences and receptor-binding properties among 13 serotypes of hemagglutinins of influenza A viruses", VIROLOGY, vol. 182, no. 2, June 1991 (1991-06-01), pages 475 - 85, XP023051404, DOI: doi:10.1016/0042-6822(91)90588-3 |
| NOBUSAWA ET AL., VIROLOGY, vol. 182, 1991, pages 475 - 485 |
| SUBBARAO K.; JOSEPH T., NATURE REVIEWS IMMUNOLOGY, vol. 7, 2007, pages 267 - 278 |
| SUI ET AL., NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2009 |
| SUI J; HWANG WC; PEREZ S; WEI G; AIRD D; CHEN LM; SANTELLI E; STEC B; CADWELL G; ALI M: "Structural and functional bases for broad-spectrum neutralization of avian and human influenza A viruses", NAT STRUCT MOL BIOL., vol. 16, no. 3, 22 February 2009 (2009-02-22), pages 265 - 73, XP002538005, DOI: doi:10.1038/nsmb.1566 |
| THROSBY ET AL., PLOS ONE, 2008 |
| THROSBY M; VAN DEN BRINK E; JONGENEELEN M; POON LL; ALARD P; CORNELISSEN L; BAKKER A; COX F; VAN DEVENTER E; GUAN Y: "Heterosubtypic neutralizing monoclonal antibodies cross-protective against H5Nl and H1N1 recovered from human IgM+ memory B cells", PLOS ONE, vol. 3, no. 12, 16 December 2008 (2008-12-16), pages E3942, XP002762305, DOI: doi:10.1371/journal.pone.0003942 |
| VAN DER GOOT JA; KOCH G; DE JONG MC; VAN BOVEN M: "Quantification of the effect of vaccination on transmission of avian influenza (H7N7) in chickens", PROC NATL ACAD SCI USA, vol. 102, 2005, pages 18141 - 18146 |
| WILSON ET AL., NATURE, vol. 289, 1981, pages 366 - 373 |
| WILSON IA; SKEHEL JJ; WILEY DC: "Structure of the haemagglutinin membrane glycoprotein of influenza virus at 3 A resolution", NATURE, vol. 289, no. 5796, 29 January 1981 (1981-01-29), pages 366 - 73, XP002689324, DOI: doi:10.1038/289366a0 |
| YOSHIDA ET AL., PLOS PATHOGEN, 2009 |
| YOSHIDA R; IGARASHI M; OZAKI H; KISHIDA N; TOMABECHI D; KIDA H; ITO K; TAKADA A: "Cross-protective potential of a novel monoclonal antibody directed against antigenic site B of the hemagglutinin of influenza A viruses", PLOS PATHOG., vol. 5, no. 3, 20 March 2009 (2009-03-20), pages E1000350, XP002541080, DOI: doi:10.1371/journal.ppat.1000350 |
Cited By (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9822339B2 (en) | 2005-12-09 | 2017-11-21 | Academisch Medisch Centrum Bij De Universiteit Van Amsterdam | Means and methods for influencing the stability of antibody producing cells |
| US10774308B2 (en) | 2005-12-09 | 2020-09-15 | Academisch Medisch Centrum Bij De Universiteit Van Amsterdam | Means and methods for influencing the stability of cells |
| US10273454B2 (en) | 2005-12-09 | 2019-04-30 | Academisch Medisch Centrum Bij De Universiteit Van Amsterdam | Means and methods for influencing the stability of antibody producing cells |
| US10077427B2 (en) | 2005-12-09 | 2018-09-18 | Academisch Medisch Centrum Bij De Universiteit Van Amsterdam | Means and methods for influencing the stability of cells |
| US10344076B2 (en) | 2009-07-15 | 2019-07-09 | Aimm Therapeutics B.V. | Means and methods for producing high affinity antibodies |
| US9969795B2 (en) | 2010-12-02 | 2018-05-15 | Aimm Therapeutics B.V. | Means and methods for producing high affinity antibodies |
| US9969794B2 (en) | 2012-05-10 | 2018-05-15 | Visterra, Inc. | HA binding agents |
| US12024552B2 (en) | 2012-05-10 | 2024-07-02 | Visterra, Inc. | Ha binding agents |
| US10800835B2 (en) | 2012-05-10 | 2020-10-13 | Visterra, Inc. | HA binding agents |
| US8877200B2 (en) | 2012-05-10 | 2014-11-04 | Visterra, Inc. | HA binding agents |
| US9096657B2 (en) | 2012-05-10 | 2015-08-04 | Visterra, Inc. | HA binding agents |
| JP2022119757A (en) * | 2013-10-02 | 2022-08-17 | メディミューン，エルエルシー | Neutralizing anti-influenza A antibodies and uses thereof |
| WO2015093949A2 (en) | 2013-12-17 | 2015-06-25 | Aimm Therapeutics B.V. | Means and methods for counteracting myeloproliferative or lymphoproliferative disorders |
| US10611829B2 (en) | 2014-01-31 | 2020-04-07 | Aimm Therapeutics B.V. | Means and methods for producing stable antibodies |
| WO2015115892A1 (en) | 2014-01-31 | 2015-08-06 | Aimm Therapeutics B.V. | Means and methods for producing stable antibodies |
| KR101582490B1 (en) | 2014-04-14 | 2016-01-19 | 아이디바이오 주식회사 | Novel virus vaccine to form cross-protection against multiple subtypes of influenza viruses |
| KR20150118400A (en) * | 2014-04-14 | 2015-10-22 | 아이디바이오 주식회사 | Novel virus vaccine to form cross-protection against multiple subtypes of influenza viruses |
| US10392432B2 (en) | 2014-12-19 | 2019-08-27 | Regeneron Pharmaceuticals, Inc. | Human antibodies to influenza hemagglutinin |
| US10689436B2 (en) | 2014-12-19 | 2020-06-23 | Regeneron Pharmaceuticals, Inc. | Human antibodies to influenza hemagglutinin |
| US11453714B2 (en) | 2014-12-19 | 2022-09-27 | Regeneron Pharmaceuticals, Inc. | Human antibodies to influenza hemagglutinin |
| WO2016209079A1 (en) | 2015-06-24 | 2016-12-29 | Aimm Therapeutics B.V. | Aml antigens and uses thereof |
| US10513553B2 (en) | 2015-11-13 | 2019-12-24 | Visterra, Inc. | Compositions and methods for treating and preventing influenza |
| CN106928350B (en) * | 2015-12-30 | 2020-11-03 | 中国科学院天津工业生物技术研究所 | Influenza virus antibody, preparation method and application thereof |
| CN106928350A (en) * | 2015-12-30 | 2017-07-07 | 中国科学院天津工业生物技术研究所 | A kind of Antibody of Influenza, its preparation method and application |
| WO2019147867A1 (en) | 2018-01-26 | 2019-08-01 | Regeneron Pharmaceuticals, Inc. | Human antibodies to influenza hemagglutinin |
| US11780907B2 (en) | 2018-01-26 | 2023-10-10 | Regeneron Pharmaceuticals, Inc. | Human antibodies to influenza hemagglutinin |
| US11230593B2 (en) | 2019-03-25 | 2022-01-25 | Visterra, Inc. | Compositions and methods for treating and preventing influenza |
| WO2021141492A1 (en) | 2020-01-10 | 2021-07-15 | Kling Biotherapeutics B.V. | Epithelial cadherin-specific antibodies |
Also Published As
| Publication number | Publication date |
|---|---|
| US20150010566A1 (en) | 2015-01-08 |
| US9718874B2 (en) | 2017-08-01 |
| AU2012346669A1 (en) | 2014-07-24 |
| AU2012346669B2 (en) | 2017-08-31 |
| AU2017216562A1 (en) | 2017-09-07 |
| AU2021245146A1 (en) | 2021-10-21 |
| US20170313766A1 (en) | 2017-11-02 |
| EP2785737A2 (en) | 2014-10-08 |
| SG11201402780UA (en) | 2014-10-30 |
| JP2015506668A (en) | 2015-03-05 |
| JP6325451B2 (en) | 2018-05-16 |
| KR20140112495A (en) | 2014-09-23 |
| WO2013081463A3 (en) | 2013-11-14 |
| CA2892992A1 (en) | 2013-06-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2012346669B2 (en) | Influenza A virus specific antibodies | |
| US11136379B2 (en) | Binding molecules directed against influenza hemagglutinin and uses thereof | |
| Kallewaard et al. | Structure and function analysis of an antibody recognizing all influenza A subtypes | |
| US10703802B2 (en) | Composition comprising at least two influenza A virus-neutralizing-binding molecules | |
| Ekiert et al. | Cross-neutralization of influenza A viruses mediated by a single antibody loop | |
| EP2793945B1 (en) | Antibodies useful in passive influenza immunization | |
| Xiao et al. | Light chain modulates heavy chain conformation to change protection profile of monoclonal antibodies against influenza A viruses | |
| Paul | Characterization and Optimization of Interaction of Monoclonal Antibodies with Influenza a Hemagglutinin | |
| Wyrzucki | Characterization of influenza a neutralizing, heterosubtypic antibodies isolated with a newly developed antigen | |
| NZ626716B2 (en) | Antibodies useful in passive influenza immunization |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 12798020 Country of ref document: EP Kind code of ref document: A2 |
|
| ENP | Entry into the national phase |
Ref document number: 2014544698 Country of ref document: JP Kind code of ref document: A |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 14362210 Country of ref document: US |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2012798020 Country of ref document: EP |
|
| ENP | Entry into the national phase |
Ref document number: 20147018417 Country of ref document: KR Kind code of ref document: A |
|
| ENP | Entry into the national phase |
Ref document number: 2012346669 Country of ref document: AU Date of ref document: 20121203 Kind code of ref document: A |
|
| ENP | Entry into the national phase |
Ref document number: 2892992 Country of ref document: CA |