NZ738043B2 - Nanoparticle compositions for sustained therapy - Google Patents
Nanoparticle compositions for sustained therapy Download PDFInfo
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- NZ738043B2 NZ738043B2 NZ738043A NZ73804316A NZ738043B2 NZ 738043 B2 NZ738043 B2 NZ 738043B2 NZ 738043 A NZ738043 A NZ 738043A NZ 73804316 A NZ73804316 A NZ 73804316A NZ 738043 B2 NZ738043 B2 NZ 738043B2
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- dra
- drb3
- relevant antigen
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- drb1
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Abstract
This disclosure provides compositions and methods for promoting the formation, expansion and recruitment of TR1 cells and/or B cells in an antigen-specific manner and treating diseases and disorders in a subject in need thereof. In particular, the invention provides a complex comprising a nanoparticle coupled via a less than 5 kDa PEG linker with maleimide end to a plurality of antigen relevant MHC class II complexes, where the 1nm-100nm nanoparticle core comprises iron oxide and where the pMHCII density per nanoparticle is 0.4 - 50 pMHC/100nm^2 and where the pMHCII complexes are from a list.
Claims (25)
1. A complex comprising a nanoparticle core coupled, through a polyethylene glycol (PEG) linker, to a plurality of autoimmune disease or inflammation-relevant antigen-MHC class II (pMHCII) complexes, wherein the nanoparticle core comprises iron oxide, has a diameter from 1 nm to 100 nm, and the pMHCIIs are coupled to a maleimide functionalized end of the PEG linker, wherein a non-maleimide functionalized end of the polyethylene glycol of the PEG linker ses one or more of a C1-C3 alkoxy group, C(O)R-, -R10C(O)NHR-, - R10OC(O)R-, or -R10C(O)OR-, wherein each R is independently H or C1-C6 alkyl and wherein each R10 is independently a bond or C1-C6 alkyl, wherein the PEG linker is less than 5 kilodaltons in molecular weight, and n the pMHCII density per nanoparticle is from 0.4 pMHC/100 nm2 to 12 pMHC/100 nm2 of the surface area of the nanoparticle, and n the valency of the ity of pMHCII complexes per nanoparticle core is from 10:1 to 100:1, and wherein the pMHCII complexes comprise HLA-DRB1/DRA, HLA-DRB3/DRA, HLA-DRB4/DRA, B5/DRA, HLA-DQA1/HLA-DQB1, or HLA-DPB1/HLADPA1.
2. The complex of claim 1, wherein the nanoparticle core further comprises an outer layer comprising a radable sugar or other r on the nanoparticle core.
3. The complex of claim 1 or 2, wherein the nanoparticle core ses a diameter from 5 nm to 50 nm.
4. The complex of any one of claims 1 to 3, wherein the autoimmune disease, or mation-relevant antigen is one or more of the group consisting of: an asthma-relevant antigen, a diabetes-relevant antigen, a pre-diabetes relevant n, a multiple sclerosisrelevant antigen, an allergic asthma-relevant antigen, a primary biliary cirrhosis-relevant antigen, a cirrhosis-relevant antigen, a Neuromyelitis optica spectrum disorder (Devic’s disease, NMO)-relevant antigen, an mune encephalitis-relevant antigen, an antigen relevant to autoantibody-mediated neurological syndromes, a Stiff Man syndrome-relevant n, a paraneoplastic disease-relevant antigen, antigens relevant to other es of the central and peripheral nervous systems, a Pemphigus vulgaris-relevant antigen, inflammatory bowel disease (IBD)-relevant antigen, Crohn’s disease-relevant antigen, Ulcerative Colitis- relevant antigen, an arthritis-relevant antigen, a Rheumatoid Arthritis-relevant antigen, a systemic lupus erythematosus (SLE)-relevant antigen, a Celiac Disease nt antigen, a psoriasis-relevant n, an Alopecia Areata-relevant antigen, an Acquired Thrombocytopenic a-relevant antigen, an autoimmune cardiomyopathy-relevant antigen, an idiopathic dilated cardiomyopathy (IDCM)-relevant antigen, a Myasthenia Gravis-relevant antigen, an Uveitis-relevant antigen, an Ankylosing Spondylitis-relevant antigen, a Grave’s Disease-relevant antigen, a Hashimoto’s thyroiditis-relevant antigen, an Immune Mediated Myopathies-relevant antigen, an anti-phospholipid syndrome (ANCA+)- relevant antigen, an atherosclerosis-relevant antigen, a scleroderma-relevant antigen, an autoimmune hepatitis-relevant antigen, a dermatomyositis-relevant antigen, a chronic obstructive pulmonary disease-relevant antigen, a spinal cord -relevant antigen, a traumatic injury-relevant antigen, a tobacco-induced lung destruction-relevant antigen, a Chronic Obstructive ary e (COPD)-relevant n, a lung emphysemarelevant antigen, a sing cholangitis-relevant antigen, a peripheral neuropathy-relevant antigen, a narcolepsy-relevant antigen, a Goodpasture Syndrome-relevant antigen, a Kawasaki´s Disease-relevant antigen, an autoimmune uveitis-relevant antigen, a colitisrelevant n, an emphysema-relevant antigen, a gus-relevant antigen, a pemphigus folliaceus-relevant antigen, an arthritis-relevant antigen, a Sjogren’s Syndrome-relevant n, an ssociated vasculitis-relevant antigen, a primary sclerosing cholangitisrelevant antigen, an adipose tissue inflammation/diabetes type II-relevant antigen, and an obesity associated adipose tissue inflammation/insulin resistance-relevant antigen.
5. The complex of any one of claims 1 to 4, wherein the pMHCII complex is covalently coupled to the nanoparticle core by the linker.
6. The complex of any one of claims 1 to 5, wherein the autoimmune disease- or inflammation-relevant antigen is a Celiac e-relevant antigen and the pMHC x is selected from the group of: aGlia57HLA-DQA1*0501/HLA-DQB1*0201, aGlia62HLADQA1 *0501/HLA-DQB1*0201, aGlia217HLA-DQA1*0501/HLA-DQB1*0302, or aGlia217HLA-DQA1*03/HLA-DQB1*0302.
7. The x of any one of claims 1 to 5, wherein the autoimmune disease- or inflammation-relevant antigen is a y biliary gitis-relevant antigen and pMHC complex is selected from the group of: PDC-E2122HLA-DRB4*0101/DRA, PDC-E2249- 262-HLA-DRB4*0101/DRA, PDC-E2249HLA-DRB1*0801/DRA, PDC-E2629HLA- DRB1*0801/DRA, PDC-E272HLA-DRB3*0202/DRA, PDC-E2353HLADRB3 *0202/DRA, PDC-E2422HLA-DRB3*0202/DRA, PDC-E2629HLADRB4 *0101/DRA, PDC-E280HLA-DRB5*0101/DRA, PDC-E2353HLADRB5 *0101/DRA, or PDC-E2535HLA- DRB5*0101/DRA.
8. The complex of any one of claims 1 to 5, wherein the autoimmune disease- or inflammation-relevant antigen is an autoimmune hepatitis-relevant antigen and the pMHC complex is selected from the group of: CYP2D6193HLA-DRB1*0301/DRA, CYP2D676HLA-DRB1*0301/DRA, CYP2D6293HLA-DRB1*0301/DRA, CYP2D6313HLA-DRB1*0301/DRA, CYP2D6393HLA-DRB1*0301/DRA, 199HLA-DRB1*0401/DRA, CYP2D6450HLA-DRB1*0401/DRA, CYP2D6301HLA-DRB1*0401/DRA, CYP2D6452HLA-DRB1*0701/DRA, CYP2D659HLA-DRB1*0701/DRA, CYP2D6130HLA-DRB1*0701/DRA, CYP2D6193HLA-DRB1*0701/DRA, CYP2D6305HLA-DRB1*0701/DRA, 131HLA-DRB3*0202/DRA, CYP2D6216HLA-DRB3*0202/DRA, 238HLA-DRB3*0202/DRA, 199HLA-DRB4*0101/DRA, CYP2D6235HLA-DRB4*0101/DRA, CYP2D6293HLA-DRB4*0101/DRA, CYP2D6238HLA-DRB5*0101/DRA, CYP2D6381HLA-DRB5*0101/DRA, CYP2D6429HLA-DRB5*0101/DRA, SLA334HLA-DRB1*0301/DRA, SLA196- A-DRB1*0301/DRA, SLA115HLA-DRB1*0301/DRA, SLA373HLADRB1 *0301/DRA, SLA186HLA-DRB1*0301/DRA, SLA317HLADRB1 *0401/DRA, SLA171HLA-DRB1*0401/DRA, SLA417HLADRB1 *0401/DRA, SLA359HLA-DRB1*0701/DRA, SLA215HLADRB1 *0701/DRA, SLA111HLA- DRB1*0701/DRA, SLA110HLADRB3 *0202/DRA, SLA299HLA-DRB3*0202/DRA, SLA342HLADRB3 *0202/DRA, SLA49HLA-DRB4*0101/DRA, SLA119HLADRB4 *0101/DRA, SLA260HLA-DRB4*0101/DRA, SLA26HLADRB5 DRA, SLA86HLA-DRB5*0101/DRA, and SLA331HLADRB5 *0101/DRA.
9. A composition comprising a plurality of complexes of any one of claims 1 to 8 and a pharmaceutically acceptable r.
10. The complex of any one of claims 1 to 5 or the composition of claim 10 for use in the treatment of pre-diabetes, multiple sclerosis, allergic asthma, y biliary cirrhosis, cirrhosis, yelitis optica spectrum disorder (Devic’s e, NMO), autoimmune encephalitis, autoantibody-mediated neurological syndromes, a Stiff Man syndrome, oplastic disease, other diseases of the l and peripheral nervous systems, Pemphigus vulgaris, inflammatory bowel disease, Crohn’s disease, Ulcerative Colitis, arthritis, toid Arthritis, systemic lupus erythematosus (SLE), Celiac Disease, psoriasis, Alopecia , Acquired ocytopenic Purpura, autoimmune cardiomyopathy, idiopathic d cardiomyopathy (IDCM), Myasthenia Gravis, Uveitis, Ankylosing Spondylitis, Grave’s Disease, Hashimoto’s thyroiditis, Immune Mediated Myopathies, anti-phospholipid syndrome (ANCA+), sclerosis, scleroderma, mune hepatitis, dermatomyositis, chronic obstructive pulmonary disease, a spinal cord injury, tic injury, tobacco-induced lung destruction, Chronic Obstructive Pulmonary Disease (COPD), lung emphysema, sclerosing cholangitis, peripheral athy, narcolepsy, Goodpasture Syndrome, Kawasaki´s Disease, autoimmune uveitis, colitis, emphysema, pemphigus, pemphigus folliaceus, Sjogren’s Syndrome, ssociated vasculitis, primary sclerosing cholangitis-relevant antigen, adipose tissue inflammation/diabetes type II, or obesity associated adipose tissue inflammation/insulin resistance.
11. Use of the complex of any one of claims 1 to 5 for the manufacture of a medicament for the ent of pre-diabetes, multiple sclerosis, allergic asthma, primary biliary cirrhosis, cirrhosis, Neuromyelitis optica spectrum disorder (Devic’s disease, NMO), autoimmune encephalitis, autoantibody-mediated neurological syndromes, a Stiff Man syndrome, paraneoplastic disease, other diseases of the central and peripheral nervous systems, Pemphigus vulgaris, inflammatory bowel disease, Crohn’s disease, Ulcerative Colitis, arthritis, Rheumatoid Arthritis, systemic lupus erythematosus (SLE), Celiac Disease, psoriasis, Alopecia Areata, Acquired Thrombocytopenic a, autoimmune cardiomyopathy, idiopathic dilated cardiomyopathy (IDCM), Myasthenia Gravis, Uveitis, Ankylosing Spondylitis, s Disease, Hashimoto’s thyroiditis, Immune Mediated hies, anti-phospholipid syndrome (ANCA+), atherosclerosis, scleroderma, autoimmune hepatitis, dermatomyositis, chronic obstructive pulmonary disease, a spinal cord injury, traumatic , tobacco-induced lung destruction, c Obstructive Pulmonary Disease (COPD), lung emphysema, sclerosing cholangitis, peripheral neuropathy, narcolepsy, Goodpasture Syndrome, Kawasaki´s Disease, autoimmune uveitis, colitis, emphysema, gus, pemphigus ceus, Sjogren’s Syndrome, ANCA-associated vasculitis, primary sclerosing gitis-relevant antigen, adipose tissue mation/diabetes type II, or obesity associated adipose tissue inflammation/insulin resistance.
12. The complex of any one of claims 1 to 5, wherein the autoimmune disease- or inflammation-relevant antigen is a type I diabetes-relevant antigen and the pMHC complex is selected from the group of: PPI76-90(K88S)-HLA-DRB1*0401/DRA, IGRP13HLADRB1 *0301/DRA, GAD555HLA-DRB1*0401/DRA, GAD555-567(557I)-HLADRB1 *0401/DRA, IGRP23HLA-DRB1*0401/DRA, B24-C36-HLA-DRB1*0301/DRA, or PPI76HLA-DRB1*0401/DRA.
13. The complex of any one of claims 1 to 5, wherein the autoimmune disease- or inflammation-relevant n is a multiple sclerosis-relevant antigen and the pMHC complex is selected from the group of: MBP86HLA-DRB1*1501/DRA, 101-HLADRB5 *0101/DRA, MOG38HLA-DRB4*0101/DRA, MOG97-109(E107S)-HLADRB1 *0401/DRA, MOG203HLA-DRB3*0101/DRA, PLP54HLA-DRB3*0101/DRA, PLP94HLA-DRB1*0301/DRA, PLP250HLA-DRB4*0101/DRA, MPB13HLADRB5 *0101/DRA, MPB83HLA-DRB5*0101/DRA, MPB111HLA-DRB5*0101/DRA, MPB146HLA-DRB5*0101/DRA, MOG223HLA-DRB3*0202/DRA, MOG6HLADRB5 DRA, PLP88HLA-DRB3*0202/DRA, or PLP139HLADRB5 *0101/DRA.
14. The complex of any one of claims 1 to 5, wherein the autoimmune disease- or inflammation-relevant antigen is a gus foliaceus and/or pemphigus vulgaris-relevant antigen and the pMHC complex is ed from the group of: DG1216HLADRB1 *0101/DRA, DG1216HLA-DRB1*0102/DRA, 111-HLA-DRB1*0402/DRA, HLA-DRB1*0402/DRA, DG3251HLA-DRB1*0401/DRA, DG3441HLADRB1 *0402/DRA, DG3351HLA-DRB3*0202/DRA, DG3453HLA-DRB3*0202/DRA, DG3540HLA-DRB3*0202/DRA, DG3280HLA-DRB4*0101/DRA, DG3326HLADRB4 *0101/DRA, DG3367HLA-DRB4*0101/DRA, DG313HLA-DRB5*0101/DRA, DG3323HLA-DRB5*0101/DRA, DG3438HLA-DRB5*0101/DRA, DG148HLADRB3 *0202/DRA, DG1206HLA-DRB3*0202/DRA, DG1363HLA-DRB3*0202/DRA, DG13HLA-DRB4*0101/DRA, DG1192HLA-DRB4*0101/DRA, DG1326HLADRB4 *0101/DRA, DG11HLA-DRB5*0101/DRA, 49-HLA-DRB5*0101/DRA, or DG1325HLA-DRB5*0101/DRA.
15. The complex of any one of claims 1 to 5, wherein the autoimmune disease- or inflammation-relevant antigen is a neuromyelitis optica spectrum disorder-relevant antigen and the pMHC complex is selected from the group of: AQP4129HLA-DRB1*0101/DRA, AQP4284HLA-DRB1*0301/DRA, AQP463HLA-DRB1*0301/DRA, AQP4129HLADRB1 *0401/DRA, or AQP439HLA-DRB1*1501/DRA.
16. The complex of any one of claims 1 to 5, wherein the autoimmune disease- or inflammation-relevant antigen is an allergic asthma-relevant antigen and the pMHC complex is selected from the group of: DERP30–HLA-DRB1*0101/DRA, DERP30 -HLADRB1 *1501/DRA, DERP1171-185 – HLA-DRB1*1501/DRA, DERP124 –HLADPB1 *0401/DRA, DERP40 -HLA-DRB1*0101/DRA; DERP40-HLADRB1 *1501/DRA, or 107-121–HLA-DRB1*0301/DRA.
17. The complex of any one of claims 1 to 5, n the autoimmune disease- or inflammation-relevant antigen is a COPD and/or emphysema-relevant antigen and the pMHC x is selected from the group of: elastin89HLA-DRB3*0101/DRA, n698 HLA-DRB5*0101/DRA, elastin8HLA-DRB5*0101/DRA, elastin94HLADRB5 *0101/DRA, elastin13HLA-DRB4*0101/DRA, n695HLADRB4 *0101/DRA, elastin563HLA-DRB4*0101/DRA, elastin558HLADRB4 *0101/DRA, elastin698HLA-DRB5*0101/DRA, elastin566HLADRB3 *0202/DRA, or elastin645HLA-DRB3*0202/DRA.
18. The complex of any one of claims 1 to 5, wherein the autoimmune disease- or mation-relevant antigen is a psoriasis-relevant antigen and the pMHC complex is selected from the group of: 4HLA-DRB3*0101/DRA, Cap1834HLADRB3 *0101/DRA, Cap1847HLA-DRB3*0101/DRA, Cap18151HLA - DRB4*0101/DRA, Cap18149HLA-DRB5*0101/DRA, Cap18152HLADRB5 *0101/DRA, Cap18131HLA-DRB5*0101/DRA, Cap1824HLADRB3 *0202/DRA, ADMTSL5245HLA-DRB3*0101/DRA, ADMTSL5267HLADRB3 *0101/DRA, ADMTSL5372HLA-DRB3*0101/DRA, 5289HLADRB4 *0101/DRA, ADMTSL5396HLA-DRB4*0101/DRA, ADMTSL5433HLADRB4 *0101/DRA, ADMTSL5142HLA-DRB5*0101/DRA, ADMTSL5236HLADRB5 DRA, ADMTSL5301HLA-DRB5*0101/DRA, ADMTSL5203HLADRB3 *0202/DRA, ADMTSL5404HLA-DRB3*0202/DRA, or ADMTSL5433HLADRB3 *0202/DRA.
19. The complex of any one of claims 1 to 5, wherein the autoimmune disease- or inflammation-relevant antigen is a uveitis-relevant n and the pMHC complex is selected from the group of: arrestin199HLA-DRB3*0101/DRA, arrestin77HLADRB3 *0101/DRA, arrestin250HLA-DRB3*0101/DRA, arrestin172HLADRB4 *0101/DRA, arrestin354HLA-DRB4*0101/DRA, arrestin239HLADRB4 *0101/DRA, arrestin102HLA-DRB5*0101/DRA, in59HLA-DRB5*0101, arrestin280HLA-DRB5*0101, arrestin291HLA-DRB1*0301/DRA, arrestin195HLADRB3 *0202/DRA, arrestin199HLA-DRB3*0202/DRA, or arrestin200HLADRB3 *0202/DRA.
20. The complex of any one of claims 1 to 5, wherein the autoimmune disease- or inflammation-relevant antigen is a Sjögren Syndrome-relevant antigen and the pMHC x is selected from the group of: 7HLA-DRB1*0301/DRA, RO60523 HLA-DRB1*0301/DRA, RO60243HLA-DRB1*0301/DRA, RO60484HLADRB3 *0101/DRA, RO60347HLA-DRB3*0101/DRA, RO60369HLADRB3 *0101/DRA, RO60426HLA-DRB4*0101/DRA, RO60267HLADRB4 *0101/DRA, RO60178HLA-DRB4*0101/DRA, RO60358HLADRB5 *0101/DRA, RO60358HLA-DRB4*0101/DRA, RO60221HLADRB5 *0101/DRA, RO60221HLA-DRB4*0101/DRA, RO60318HLADRB5 *0101/DRA, RO60318HLA-DRB4*0101/DRA, RO60407HLADRB4 *0101/DRA, RO60407HLA-DQA1*0501/HLA-DQB1*0201, RO60459HLADRB4 DRA, RO60459HLA-DQA1*0501/HLA-DQB1*0201, RO60318HLADQA1 HLA-DQB1*0201, RO6051HLA-DRB3*0202/DRA, RO60312HLADRB3 DRA, RO60347HLA-DRB3*0202/DRA, LA241HLA-DRB1*0301/DRA, LA101HLA-DRB1*0301/DRA, LA153HLA-DRB1*0301/DRA, LA178HLADRB3 *0101/DRA, LA19HLA-DRB3*0101/DRA, LA37HLA-DRB3*0101/DRA, LA133- 147-HLA-DRB4*0101/DRA, LA50HLA-DRB4*0101/DRA, 6-HLA- DRB4*0101/DRA, LA153HLA-DRB5*0101/DRA, LA83HLA-DRB5*0101/DRA, LA136HLA-DRB5*0101/DRA, LA297HLA-DQA1*0501/HLA-DQB1*0201, LA59 HLA-DQA1*0501/HLA-DQB1*0201, LA59HLA-DRB4*0101/DRA, LA151HLADQA1 *0501/HLA-DQB1*0201, LA151HLA-DRB4*0101/DRA, LA297HLADRB4 *0101/DRA, LA50HLA-DRB3*0202/DRA, LA86HLA-DRB3*0202/DRA, or LA154HLA-DRB3*0202/DRA.
21. The complex of any one of claims 1 to 5, wherein the autoimmune disease- or inflammation-relevant antigen is a derma-relevant antigen and the pMHC complex is selected from the group of: TOP1346HLA-DRB3*0101/DRA, TOP1420HLADRB3 *0101/DRA, TOP1750HLA-DRB3*0101/DRA, TOP1419HLADRB4 *0101/DRA, TOP1591HLA-DRB4*0101/DRA, TOP1695HLADRB4 *0101/DRA, TOP1305HLA-DRB5*0101/DRA, TOP1346HLADRB5 *0101/DRA, TOP1419HLA-DRB5*0101/DRA, TOP1420HLADRB3 *0202/DRA, TOP1425HLA-DRB3*0202/DRA, 4HLADRB3 *0202/DRA, CENP-C297HLA-DRB3*0101/DRA, CENP-C857HLADRB3 *0101/DRA, CENP-C887HLA-DRB3*0101/DRA, CENP-C212HLADRB4 *0101/DRA, CENP-C643HLA-DRB4*0101/DRA, CENP-C832HLADRB4 *0101/DRA, CENP-C167HLA-DRB5*0101/DRA, CENP-C246HLADRB5 *0101/DRA, CENP-C846HLA-DRB5*0101/DRA, CENP-C149HLADRB3 DRA, CENP-C833HLA-DRB3*0202/DRA, or CENP-C847HLADRB3 *0202/DRA.
22. The complex of any one of claims 1 to 5, wherein the mune disease- or inflammation-relevant antigen is an anti-phospholipid syndrome-relevant antigen and the pMHC complex is ed from the group of: APOH235HLA-DRB3*0101/DRA, 6HLA-DRB3*0101/DRA, APOH237HLA-DRB3*0101/DRA, APOH295 HLA-DRB3*0101/DRA, APOH28HLA-DRB4*0101/DRA, APOH173HLADRB4 *0101/DRA, APOH264HLA-DRB4*0101/DRA, 5HLADRB4 *0101/DRA, APOH49HLA-DRB5*0101/DRA, APOH269HLADRB5 *0101/DRA, APOH295HLA-DRB5*0101/DRA, APOH321HLADRB3 *0202/DRA, APOH322HLA-DRB3*0202/DRA, or APOH324HLADRB3
23. The complex of any one of claims 1 to 5, wherein the autoimmune e- or inflammation-relevant antigen is an ANCA-associated vasculitis-relevant n and the pMHC complex is selected from the group of: MPO506HLA-DRB3*0101/DRA, MPO302- 316-HLA-DRB3*0101/DRA, MPO7HLA-DRB3*0101/DRA, MPO689HLA- DRB4*0101/DRA, MPO248HLA-DRB4*0101/DRA, MPO444HLADRB4 *0101/DRA, MPO513HLA-DRB5*0101/DRA, MPO97HLA-DRB5*0101/DRA, MPO616HLA-DRB5*0101/DRA, MPO462HLA-DRB3*0202/DRA, MPO617HLA- DRB3*0202/DRA, MPO714HLA-DRB3*0202/DRA, PRTN344HLADRB3 *0101/DRA, PRTN3234HLA-DRB3*0101/DRA, PRTN359HLA DRB3*0101/DRA, PRTN359HLA-DRB5*0101/DRA, PRTN3117HLADRB4 *0101/DRA, PRTN3164HLA-DRB4*0101/DRA, PRTN371HLADRB4 *0101/DRA, PRTN3241HLA-DRB5*0101/DRA, PRTN3183HLADRB5 *0101/DRA, PRTN362HLA-DRB3*0202/DRA, PRTN3118HLADRB3 *0202/DRA, or 39HLA-DRB3*0202/DRA.
24. The complex of any one of claims 1 to 5, wherein the autoimmune disease- or mation-relevant antigen is a Stiff man syndrome-relevant antigen and the pMHC complex is selected from the group of: GAD212HLA-DRB1*0801/DRA, GAD555 HLA-DRB1*0801/DRA, or GAD297HLA-DRB1*0301/DRA.
25. The x of any one of claims 1 to 5, wherein the autoimmune disease- or inflammation-relevant antigen is an inflammatory bowel disease(IBD)-relevant antigen, a Crohn’s disease-relevant antigen, an ulcerative colitis-relevant antigen, and/or a colitisrelevant antigen, and the pMHC complex is selected from the group of: bacteroides integrase antigen183-197 - HLA-DRB3*0101/DRA, bacteroides integrase antigen146-160 - HLADRB3 *0101/DRA, bacteroides integrase antigen175-189 - HLA-DRB3*0101/DRA, bacteroides integrase antigen1-15 - HLA-DRB5*0101/DRA, bacteroides integrase antigen183-197 - HLADRB5 *0101/DRA, bacteroides integrase antigen183-197 - B3*0101/DRA, bacteroides integrase antigen30-44 - HLA-DRB5*0101/DRA, oides integrase antigen70-84 - HLA-DRB4*0101/DRA, bacteroides integrase n337-351 - HLA-DRB4*0101/DRA, oides integrase antigen171-185 - HLA-DRB4*0101/DRA, bacteroides integrase antigen4 HLA-DRB3*0202/DRA, bacteroides integrase antigen171-185 - HLA-DRB3*0202/DRA, bacteroides integrase antigen256-270 - HLA-DRB3*0202/DRA, Fla-X366-380 - HLADRB3 *0101/DRA, Fla-2/Fla-X164-178 - HLA-DRB3*0101/DRA, Fla-2/Fla-X261-275 - HLADRB5 *0101/DRA, Fla-X1-15 - HLA-DRB5*0101/DRA, Fla-X51-65 - HLADRB4 *0101/DRA, Fla-2/Fla-X269-283 - HLA-DRB4*0101/DRA, Fla-2/Fla-X4-18 - HLA- DRB3*0202/DRA, Fla-X261-275 - HLA-DRB3*0202/DRA, Fla-2/Fla-X271-285 - HLADRB3 *0202/DRA, -92 - HLA-DRB3*0101/DRA, YIDX78-92 - HLADRB4 *0101/DRA, YIDX93-107 - HLA-DRB3*0101/DRA, -112 - HLADRB5 *0101/DRA, YIDX23-37 - HLA-DRB5*0101/DRA, YIDX78-92 - HLADRB4 *0101/DRA, YIDX195-209 - HLA-DRB4*0101/DRA, YIDX22-36 - HLA- DRB3*0202/DRA, -94 - HLA-DRB3*0202/DRA, or YIDX101-115 - HLADRB3 *0202/DRA. None set by MYN MigrationNone set by MYN Unmarked set by MYN None set by MYN MigrationNone set by MYN Unmarked set by MYN 6% 1A .11ngI//WI//’ gum zig?? x {xxx/”fl, “‘“‘“‘-- “xv“ \\\\\».\\\\\\\V~é~\sx\\w\\H *\.\\\'".\\\
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562157933P | 2015-05-06 | 2015-05-06 | |
| US201562273953P | 2015-12-31 | 2015-12-31 | |
| US201662296032P | 2016-02-16 | 2016-02-16 | |
| PCT/IB2016/000691 WO2016198932A2 (en) | 2015-05-06 | 2016-05-06 | Nanoparticle compositions for sustained therapy |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NZ738043A NZ738043A (en) | 2024-11-29 |
| NZ738043B2 true NZ738043B2 (en) | 2025-03-04 |
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