WO2007019620A1 - Engineered antibodies with new world primate framework regions - Google Patents

Engineered antibodies with new world primate framework regions Download PDF

Info

Publication number
WO2007019620A1
WO2007019620A1 PCT/AU2006/001165 AU2006001165W WO2007019620A1 WO 2007019620 A1 WO2007019620 A1 WO 2007019620A1 AU 2006001165 W AU2006001165 W AU 2006001165W WO 2007019620 A1 WO2007019620 A1 WO 2007019620A1
Authority
WO
WIPO (PCT)
Prior art keywords
antigen
antibody
binding portion
new world
sequence
Prior art date
Application number
PCT/AU2006/001165
Other languages
French (fr)
Other versions
WO2007019620A8 (en
Inventor
Philip Anthony Jennings
Anthony Gerard Doyle
Adam William Clarke
Robert Daniel Gay
Original Assignee
Arana Therapeutics Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from AU2005904406A external-priority patent/AU2005904406A0/en
Application filed by Arana Therapeutics Limited filed Critical Arana Therapeutics Limited
Priority to EP06774812A priority Critical patent/EP1945668A4/en
Priority to BRPI0614430-6A priority patent/BRPI0614430A2/en
Priority to CA002619244A priority patent/CA2619244A1/en
Priority to JP2008526322A priority patent/JP2009504685A/en
Priority to AU2006281980A priority patent/AU2006281980A1/en
Publication of WO2007019620A1 publication Critical patent/WO2007019620A1/en
Priority to US11/832,553 priority patent/US20080095767A1/en
Publication of WO2007019620A8 publication Critical patent/WO2007019620A8/en
Priority to NO20080799A priority patent/NO20080799L/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/24—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
    • C07K16/241—Tumor Necrosis Factors
    • 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
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/06—Antipsoriatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
    • 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
    • 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

Definitions

  • the present invention relates to an antibody or antigen-binding portion thereof having a variable region comprising at least two complementarity determining regions (CDRs) and at least three framework regions.
  • the framework regions are, or are derived from New World primate framework regions, and al least one of the CDRs is either a modified New World primate CDR or a non-New World primate CDR.
  • Antibodies play an important role in the immune system of a mammal. They arc produced by plasma cells which have developed from precursor B cells. Antibodies consist of two identical light polypeptide chains and two identical heavy polypeptide chains which ares joined by disulfide bridges. The light chains are referred to as cither kappa or lambda light chains and the heavy chains as gamma, mu, delta, alpha or cpsilon. Each chain consists of a constant and variable region. The variable region gives the antibody its specificity. Within each variable region are regions of hypervariability or complementarity determining regions (CDRs) which are flanked by more conserved regions referred to as framework regions. Within each variable region arc tlirce CDRs and four framework regions.
  • CDRs complementarity determining regions
  • Antibodies arc bifunctional molecules, the N-lerminal variable segments from the heavy and light chains associate together in a specific manner to generate a three-dimensional structure with affinity for a particular epitope on the surface of an antigen.
  • the constant region segments are responsible for prolonged scrum half-life and the effector functions of the antibody and relate to complement binding, stimulation of phagocytosis, antibody- dependent cellular cytotoxicity and triggering of granulocyte granule release.
  • the development of hybridoma teclinology has facilitated the production of monoclonal antibodies of a particular specificity. Typically, such hybridomas are murine hybridomas.
  • Human/mouse chimeric antibodies have been created in which antibody variable region sequences from the mouse genome arc combined with antibody constant region sequences from the human genome.
  • the chimeric antibodies exhibit the binding characteristics of the parental mouse antibody, and the effector functions associated with the human constant region.
  • the antibodies are produced by expression in a host cell, including for example Chinese Hamster Ovary (CHO), NSO myeloma cells, COS cells and SP2 cells.
  • CHO Chinese Hamster Ovary
  • NSO myeloma cells including for example Chinese Hamster Ovary (CHO), NSO myeloma cells, COS cells and SP2 cells.
  • Such chimeric antibodies have been used in human therapy, however antibodies to these chimeric antibodies have been produced by the human recipient. Such a ⁇ ti-chimeric antibodies are detrimental to continued therapy with chimeric antibodies.
  • human monoclonal antibodies are expected to be an improvement over mouse monoclonal antibodies for in vivo human therapy. From work done with antibodies from Old World primates (rhesus monkeys and chimpanzees) it has been postulated that these non-human primate antibodies will be tolerated in humans because they are structurally similar to human antibodies (Ehrlich PH el td,, Clin Chetn., 1988, 34:9 1681-1688).
  • EP 0605 442 discloses chimeric antibodies which bind human antigens. These antibodies comprise the whole variable region from an Old World monkey and the constant region of a human or chimpanzee antibody.
  • One of the advantages suggested in this reference for these constructs is the ability to raise antibodies in Old World monkeys to human antigens which are less immunogenic in humans compared with antibodies raised in a mouse host
  • New World primates comprise at least 53 species commonly divided into two families, the Caltithricidae and Cehidae.
  • the Callithricidae consist of marmosets and tarnarins.
  • the Cehidae includes the squirrel monkey, titi monkey, spider monkey, woolly monkey, capuchin, uakaris, sakis, night or owl monkey and tlie howler monkey.
  • Evolutionarily distant primates such as New World primates, are not only sufficiently different from humans to allow antibodies against human antigens to be generated, but are sufficiently similar to humans to have antibodies similar to human antibodies so that the host does not generate an anti-antibody immune response when such primate-derived antibodies are introduced into a human.
  • Domain antibodies are functional binding units which can be created using antibody frameworks and correspond to the variable regions of either the heavy (VH) or light (VL) chains of antibodies. Domain antibodies have a molecular weight of approximately 13 kDa, or less than one tenth the size of a full antibody.
  • Immunoglobulin light chains arc referred to as cither kappa or lambda light chains and the heavy chains as gamma, mu, delta, alpha or cpsilon.
  • the variable region gives the antibody its specificity.
  • regions of hypcrvariability otherwise known as complementarity determining regions (CDRs) which arc flanked by more conserved regions referred to as framework regions.
  • CDRs complementarity determining regions
  • framework regions Within each light and heavy chain variable region arc three CDRs and four framework regions.
  • domain antibodies are well expressed in bacterial, yeast and mammalian systems. Their small size allows for higher molar quantities per gram of product, thus providing a significant increase in potency.
  • domain antibodies can be used as a building block to create therapeutic products such as multiple targeting dAbs in which a construct containing two or more variable omainss bind to two or more therapeutic targets, or dAbs targeted for pulmonary or oral administration.
  • the present inventors have found (hat New World primates provide a source of antibody sequences which are predicted to have low immunogcnicity in humans.
  • New world primates were chosen as a repository of immunoglobulin sequences that, existed at the branch point of New World and Old World Primates.
  • the key idea was that, tins repository might thus yield immunoglobulin sequences primordial to later divergences in immunoglobulin sequences as found in Old World Primates, Such primordial sequences would have co-existed with the T cell repertoire, as it subsequently evolved on the path to man, for the 35 million years ago (M YA) estimated to be the branch point of Old and New World Primates (Schneider H et at, Mo! Phylogenet Evol. 7 1993 Sep;2(3):225-42.). This represents a protracted period of selection for immunological tolerance and thus such primordial sequences were predicted, by the inventors, to be free of certain helper T cell epitopes that, would have evolved more recently.
  • the present, invention provides an antibody or antigen-binding portion thereof having a variable region comprising at. least two complementarity dcte ⁇ nining regions (CDRs) and at least three framework regions, wherein the framework regions are, or are derived from New World primate framework regions, and wherein at least one of the CDRs is a non-New World primaLe CDR.
  • CDRs complementarity dcte ⁇ nining regions
  • the invention provides a pharmaceutical composition comprising an effective amount of the antibody or antigen-binding portion thereof according to the present invention, together with a one or more pharmaceutically acceptable excipie ⁇ t(s) or dilucnt(s).
  • the invention provides for the use of an antibody or antigen-binding portion thereof of the present invention in a diagnostic application for detecting an antigen associated with a particular disease or disorder.
  • the present invention provides a method for treating a disease or disorder characterised by human TNF- ⁇ activity in a human subject, comprising administering to the subject in need thereof an effective amount of the antibody or antigen binding portion thereof as described herein (or a pharmaceutical composition thereof) in which the antibody or antigen- binding portion thereof binds TNF- ⁇ ,
  • the use of the antibodies, and antigen binding portions thereof, and pharmaceutical compositions thereof as described herein in the manufacture of a medicament Particularly, the manufacture of a medicament for use in the treatment or diagnosis of diseases or disorders as described herein.
  • the present invention provides a designed New World primate antibody or antigen-binding portion thereof which binds a cell surface antigen or a cytokine wherein the antibody or antigen-binding thereof comprises a variable region comprising at least two complementarity determining regions (CDRs) and at least three framework regions, wherein the CDRs are selected such that the antibody or antigen-binding portion binds to the cell surface antigen or to the cytokine.
  • CDRs complementarity determining regions
  • the antibodies and antigen binding portions thereof as described herein may be used without limitation in the pharmaceutical compositions described herein and incorporated in the kits described herein.
  • the antibodies and antigen binding portions thereof, as well as the pharmaceutical compositions and kits, as described herein may be used in the methods of treatment and diagnosis disclosed herein, unless otherwise noted or clearly indicated by the context.
  • Figure 1 demonstrates the binding of AB138 to rat MOG present in rat spinal cord lysate (lane 2) and not to CHOKlSV lysate (laiic 3). Lane 1 contains molecular weight markers.
  • Figure 2 demonstrates the lack of non-specific binding of an anti-TNF ⁇ monoclonal antibody Io the same sample of rat MOG present in rat spinal cord lysate (lane 2) and CHOKlSV lysate (lane 3). Lane 1 contains molecular weight markers.
  • Figure 3 is an alignment of the donor and acceptor V H amino acid sequences
  • Figure 4 is an alignment of the donor and acceptor V L amino acid sequences
  • Figure 5 Binding of anLibodics AB 164, AB 103 and AB 197 to TNF- ⁇ by ELISA.
  • Figure 6 Neutralisation by AB 164, AB 197, AB 103 of TNF- ⁇ -induced L-929 cell cytotoxicity
  • the present invention provides an antibody or antigen-binding portion thereof having a variable region comprising at least two complementarity determining regions (CIDRs) and at least three framework regions, wherein the framework regions are, or are derived from New World primate framework regions, and wherein at least one of the CDRs is a non-New World primate CDR.
  • CIDRs complementarity determining regions
  • the invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising an effective amount of the antibody or antigen-binding portion thereof according to the present invention, together with a one or more pharmaceutically acceptable excipicnt(s) or diluent(s).
  • the invention provides for the use of an antibody or antigen-binding portion thereof of the present invention in a diagnostic application for detecting an antigen associated with a particular disease or disorder
  • the present invention provides a method for treating a disease or disorder characterised by human TNF- ⁇ activity in a human subject, comprising administering to the subject in need thereof an effective amount of the antibody or antigen binding portion thereof as described herein (or a pharmaceutical composition thereof ) in which the antibody or antigen-binding portion thereof binds TNF- ⁇ .
  • the variable region comprises three CDRs and four framework regions. It is also preferred that the antibody has low predicted immiinogeniciiy in humans.
  • variable region of the antibody or antigen-binding portion thereof may comprise a combination of CDRs from differing sources.
  • variable region comprises CDRs selected from the group consisting of at least one murine CDR sequence (preferably either mouse or rat), at least one human CDR sequence, at least one synthetic CDR sequence, at least one rabbit CDR sequence, at least one modified New World primate CDR sequence and combinations of two or mo ⁇ e of the forgoing, at least one human CDR and at least one murine CDR, at least one human CDR and at least One synthetic CDR 7 at least one human CDR and at least one rabbit CDR, at least one human CDR and at least one New World primate CDR, at least one murine CDR and at least one synthetic CDR, at least one murine CDR and at least one rabbit CDR, al leasL one murine CDR and at least one New World primate CDR, at least one synthetic CDR and at least one rabbit CDR, at least one synthetic CDR and at least one New World primate CDR, and at least one rabbit CDR and at least, one New World primate CDR.
  • at least one murine CDR sequence preferably either mouse or
  • variable region comprises 3 murine CDR sequences, in particular 3 mouse CDR sequences. In an alternative embodiment the variable region comprises 3 human CDR sequences.
  • variable region comprises 4 New World primate framework regions or 4 framework regions in which the regions are derived from New World primate framework regions.
  • the antigen-binding portion is a domain antibody.
  • the antibody or antigen-binding portion further comprises a human or non- human Old World primate constant region sequence or a combination thereof.
  • non-human Old World primates include, but are not limited to, chimpanzees, baboons, orang utans, macaques and gorillas.
  • the dAb may be multimerised, as for example, hetero- or homodimers (e.g., VH/VH, VJ/VL or V ⁇ /VL), hetero- or liomotrimcrs (e.g., V H /V H /V H , V 1 ZVLZVL, V H /V H /VL or V H /V ⁇ ZV L ), hetero- or hornotetramcrs (e.g., VH/VH/VH/VH, VLZVLZVLZVL, V H /VH/VH,VL, VHWVI/VL or VH/VLZVL/VL), or higher order hetero- or homomultimers.
  • Multimerisation can increase the strength of antigen binding, wherein the strength of binding is related to the sum of the binding affinities of the multiple binding sites.
  • the invention provides a domain antibody wherein the domain antibody is linked to at least one further domain antibody.
  • Each dAb may bind to the same or different antigens.
  • the dAb multimers may further comprise one or more dAbs which are linked and wherein each dAb binds to a different antigen, multi-specific ligands including so-called "dual- specific ligands".
  • the dual specific ligands may comprise a pair of V H domains or a pair of VL domains.
  • dual-specific ligands are described in WO 2004/003019 (PCT/GB2003/002804) in the name of Domantis I ,td, incorporated by reference herein in its entirety.
  • the New World primate framework region sequence is preferably from a New World primate selected from the group consisting of marmosets, tamari ⁇ s, squirrel monkey, titi monkey, spider monkey, woolly monkey, capuchin, uakaris, sakis, night or owl monkey and the howler monkey, most preferably a marmoset
  • the antigen to which the chimeric antibody or antigen-binding portion thereof binds is peptide, protein, carbohydrate, glycoprotein, lipid or glycolipid in nature, selected from a tumour-associated antigen including carcinoembryonic antigen, EpCAM, I-ewis-Y, Lewis-Y/b, PMSA, CD20, CD30, CD33, CD38, CD52, CD154, EGF-R, Her-2, TRAIL and VEGF receptors, an antigen involved in an immune or inflammatory disease or disorder including CD3, CD4, CD25, CD40, CD49d, MHC class I, MMC class ⁇ , GM- CSF, intcrfcron- ⁇ , IL-I , IL-12, IL-13, IL-23, TNF- ⁇ , and IgE, an antigen expressed on a host cell including glycoprotein Ilb/IIIa, P-glycoprotein, purinergic receptors and adhesion receptors including CDl Ia 1 CDlIb, CDl
  • anti-CD4 by acting wilh complement, or killer cells (eg. NK cells) or is active as a cytotoxic agent or to cause Fe-reccptor binding by a phagocyte or neutralizes biological activity of its target.
  • wilh complement or killer cells (eg. NK cells) or is active as a cytotoxic agent or to cause Fe-reccptor binding by a phagocyte or neutralizes biological activity of its target.
  • NK cells eg. NK cells
  • the sequence of at least one framework region is modified to increase binding or potency or to decrease predicted,immunogenicity in humans.
  • An increase in binding or potency or a decrease in predicted immunogenicity in humans of an antibody or antigen-binding portion of the invention is relative to an antibody or antigen binding portion in which the framework region is unmodifiedi
  • sequence of one or more of lhe CDRs are modified to increase binding or potency or to decrease predicted immunogenicity in humans.
  • An increase in binding or potency or a decrease in predicted immunogenicity in humans of an antibody or antigen-binding portion of the invention is relative to an antibody or antigen binding portion in which the framework region is unmodified.
  • an increase in binding is demonstrated by a decrease in K D (K rt yK w ) for the antibody or antigen binding portion thereof.
  • An increase in potency is demonstrated in biological assays.
  • assays that can be used to measure the potency of the antibody or antigen-binding portion thereof include the TNF ⁇ -induccd L929 cytotoxicity neutralisation assay, IL- 12-induced human PHA-activated peripheral blood mononuclear cell (PBMC) proliferation assay, and RANKL mediated osteoclast differentiation of mouse splenocytes (Stem, Proc. Natl. Acad. ScI USA 87:6808 - 6812 (1990); Kong, Y-Y. et al.
  • antibody as used herein, is entended to refer to immunoglobulin molecules comprised of four polypeptide chains, two heavy (H) chains and two light (L) chains inter- connected by disulfide bonds.
  • Each heavy chain is comprised of a heavy chain variable region (HCVR or YH) and a heavy chain constant region.
  • the heavy chain constant region comprises three domains. CHI, C II 2 and C ⁇ 3.
  • Each light chain is comprised of a light chain variable region (LCVR or VL) and a light chain constant region.
  • the light chain constant region is comprised of one domain, CL.
  • V H and V L regions can be further subdivided into regions of hypervariability, termed complementarity determining regions (CDR), interspersed with regions that are more conserved, termed framework regions (FR).
  • CDR complementarity determining regions
  • FR framework regions
  • Each VH and V L is composed of three CDRs and four FRs, arranged from amino-terminus to carboxy-te ⁇ minus in the following order: FRl, CDRl, FR2, CDR2, FR3, CDR3, FR4.
  • antigen-binding portion of an antibody refers to one or more components or derivatives of an immunoglobulin that exhibit the ability to bind to an antigen. It has been shown that the antigen-binding function of an antibody can be performed by fragments of a full length antibody.
  • binding fragments encompassed within the term "antigen-binding portion" of an antibody include (i) a Fab fragment, a monovalent fragment consisting of the V L , V H , C L and C H 1 domains; (ii) a F(ab') 2 fragment, a bivalent fragment comprising two Fab fragments linked by a disulfide bridge at the hinge region; (iii) a Fd fragment consisting of the V H and C H 1 domains; (iv) a Fv fragment consisting of the V L and V H domains of a single arm of an antibody; (v) a dAb fragment (Ward et at, 1989, Nature 341 :544-54 ⁇ ) which consists of a single V H domain, or a VL domain (van den BeukenT et al, 2001, J.
  • Single chain Pvs are also intended to be encompassed within the term "antigen-binding portion" of an antibody.
  • Other forms of single chain Fvs and related molecules such as diabodies or triabodies arc also encompassed.
  • Diabodies are bivalent antibodies in which V H and V L domains are expressed on a single polypeptide chain, but using a linker that is loo short to allow for pairing between the two domains on the same chain, thereby forcing Lhe domains to pair with complementary domains of another chain and creating two antigen binding sites (sec e.g., Holliger, P., et al, 1993, Proc. Natl. Acad. Sci. USA, 90:6444-6448; Poljak, R.J., et al., 1994, Structure, 2:1121-1123).
  • the antibody or antigen-binding portion thereof according to the present invention has predicted low irnmunogenicily in a human host.
  • low immun ⁇ gei ⁇ icily it is meant that the antibody does not raise an antibody response in at least the majority of individuals receiving the antibody of sufficient magnitude to reduce the effectiveness of continued administration of the antibody for a sufficient lime to achieve therapeutic efficacy.
  • the level of immunogenicity in humans may predicted using (lie MHC class II binding prediction program Propred (http://www.imlech.res.in/raghava/propred) using a 1 % threshold value analysis of all alleles.
  • Other programs which may be used include: Rankpep (http://bio.dfci.harvard.edu/Tools/rankpep.html)
  • Epibase ⁇ lgonomics proprietary software: algonomics.com
  • Reduced immunogenicity molecules will contain no or a reduced numbers of peptides predicted to bind to MHC class II alleles that are highly expressed in the target population, relative to the starting donor molecule (Flower DR, Doytchinova IA. (2004) and the prediction of immunogenicity, Drug Discov Today, 9(2): 82- 90).
  • Functional analysis of MHC class II binding can be performed by generating overlapping peptides corresponding to the protein of interest and testing these for their ability to evoke T cell activation (T cell proliferation assay) or displace a reporter peptide, a known MHC class n-bindiug peptide (Hammer J et al, 1994, J. Exp. Med., 180:2353).
  • the term "derived from” as used herein in relation to New World primate framework regions means that the sequence of the New World primate framework region is altered from the native sequence. Typically the changes will be made to increase binding such as described in US Patent No. 5,585,089 and US 20030039649 or to reduce predicted immunogenicity in humans: The term “derived from” does not include changes which result in the total sequence of the framework regions present in the variable region being identical to a human framework sequences.
  • One database which may be used for comparison is htt ⁇ ://www,ncbi.nlm.nih.gov/.
  • the present invention provides a designed New World primate antibody or antigen-binding portion thereof which binds a cell surface antigen or a cytokine wherein Lhe antibody or antigen-binding thereof comprises a variable region comprising at least two complementarity detennining regions (CDRs) and al least three framework regions, wherein the CDRs are selected such that the antibody or antigen-binding portion binds to the cell surface antigen or to the cytokine.
  • CDRs complementarity detennining regions
  • the term "designed" means the New World primate CDRs have been selected using the epitope imprinting methods described in Hoogenb ⁇ jom et ah, PCT Publication No.
  • the antibody libraries used in this method are preferably scFv libraries prepared and screened as described in McCafferty et al,, PCT Publication No, WO 92/01047, McCafferty et «/., 1990, Nature, 348:552-554; and Griffiths etah, 1993, EMBO J, 12:725-734 which are hereby incorporated by reference in their entirety,
  • , and V H segments of the preferred VL/VH pair(s) can be randomly mutated, preferably within the CDR3 region of VH and/or VL, in a process analogous to the in vivo somatic mutation process responsible for affinity maturation of antibodies during a natural immune response.
  • This in vitro affinity maturation can be accomplished by amplifying Vn and VL regions using PCR primers complimentary to the VH CDR3 or V L CDR3, respectively, which primers have been "spiked” with a random mixture of the four nucleotide bases at certain positions such that the resultant I 5 CR products encode VH and V L segments into which random mutations have been introduced into the V H and/or VL CDR3 regions.
  • These randomly mutated VH and VL segments can be rescreened for binding to the antigen and sequences that exhibit high affinity and a low off rate for antigen binding can be selected.
  • nucleic acid encoding the selected antibody can be recovered from the display package (c.g., from the phage genome) and subcloned into other expression vectors by standard recombinant DNA techniques. If desired, the nucleic acid can be further manipulated to create other antibody forms of the invention (e.g., linked to nucleic acid encoding additional immunoglobulin domains, such as additional constant regions).
  • the DNA encoding the antibody is cloned into a recombinant expression vector and introduced into a mammalian host cells.
  • cell surface antigens which may be targeted and antibodies which may be used in the imprinting include but arc not limited to
  • cytokines which may be targeted and antibodies which may be used in the imprinting include bul are not limited to
  • the present invention is further based on a method for amplification of New World primate immunoglobulin genes, for example by polymerase chain reaction (PCR) from nucleic acid extracted from New World primate lymphocytes using primers specific for heavy and light chain variable region gene families.
  • PCR polymerase chain reaction
  • the amplified variable region is then cloned into an expression vector containing a human or primate constant region gene for the production of New World primate chimeric recombinant antibody.
  • Standard recombinant DNA methodologies are used to obtain antibody heavy and light chain genes, incorporate these genes into recombinant expression vectors and introduce the vectors into host cells, such as those described in Sambrook, Fritsch and Maniatis (cds), Molecular Cloning; a laboratory manual, second edition, Cold Spring Harbor, N.Y (1989).
  • Suitable expression vectors will be familiar to those skilled in the ait.
  • the New World primate lymphocytes producing the immunoglobulins are typically immortalised by fusion with a myeloma cell line to generate a hybridoma.
  • Preferred mammalian host cells for expressing the recombinant antibodies of the invention include Chinese Hamster Ovary (CHO), NSO myeloma cells, COS cells and SP2 cells.
  • the present invention also contemplates the use of non-mammalian expression systems such as those which are plant or prokaryotic (bacterial) derived. Such expression systems would be familiar to persorcs skilled in the art.
  • the repertoire of V H , VL and constant region domains can be a naturally occurring repertoire of immunoglobulin sequences or a synthetic repertoire
  • a naturally occurring repertoire is one prepared, for example, from immunoglobulin expressing cells harvested from one or more primates.
  • Such repertoires can be naive ie. prepared from newborn immunoglobulin expressing cells, or rearranged ie. prepared from, for example, adult primate B cells. If desired, clones identified from a natural repertoire, or any repertoire that bind the target antigen are then subject to mutagenesis and further screening in order to produce and select variants with improved binding characteristics.
  • Synthetic repertoires of immunoglobulin variable domains are prepared by artificially introducing diversity into a cloned variable domain.
  • affinity maturation techniques will be familiar to persons skilled in the art such as those described by R.A. Irving et id., 2001, Journal of Immunological Methods, 248, 31-45.
  • variable region, or a CDR thereof, of a New World primate antibody gene may be cloned by providing nucleic acid eg. cDNA, providing a primer complementary to the cDNA sequence encoding a 5' leader sequence of an antibody gene, contacting that cDNA and the primer to form a hybrid complex and amplifying the cDN A to produce nucleic acid encoding the variable region (or CDR region) of the New World primate antibody gene.
  • New World primate variable region sequence may be used as acceptors for the grafting of non-New World primate sequences, in particular, CDR sequences using standard recombinant techniques.
  • US Patent No. 5,585,089 describes methods for creating low imrnunogcnicity chimeric antibodies that retain the high affinity of the non-human parent antibody and contain one or more CDRs from a donor immunoglobulin and a framework region from a human immunoglobulin.
  • United Stales publication no, 20030039649 describes a hunianisation method for creating low immunogemicity chimeric antibodies containing CDR sequences from a non-human antibody and framework sequences of human antibodies based on using canonical CDR structure types of the non-human antibody in comparison to germline canonical CDR structure types of human antibodies as the basis for selecting the appropriate human framework sequences for a humanised antibody. Accordingly, these principles can be applied to the grafting of one or more non-New World primate CDRs into a New World primate acceptor variable region.
  • Tlic CDR sequences may be obtained from the genomic DNA isolated from an antibody, or from sequences present in a database e.g. The National Centre for Biotechnology Information protein and nucleotide databases, The Kabat Database of Sequences of Proteins of Immunological Interest.
  • the CDR sequence may be a genomic DNA or a cDNA.
  • Methods for grafting a replacement CDR(s) into an acceptor variable sequence will be familiar to persons skilled in the art of the present invention.
  • the CDRs will be grafted into acceptor variable region sequences for each of a variable light chain and a variable heavy chain or a single chain in the case of a domain antibody.
  • the preferred method of the present invention involves replacement of either CDR 1 or, more preferably, CDR2 in a variable region sequence via primer directed mutagenesis.
  • the method consists of annealing a synthetic oligonucleotide encoding a desired mutation to a target region where it serves as a primer for initiation of DNA synthesis in vitro, extending the oligonucleotide by a .DN A polymerase to generate a double-stranded DNA that carries the desired mutation, ang ligating and cloning the sequence into an appropriate expression vector (Sambrook, Joseph; and David W. Russell (2001). Molecular Cloning: A Laboratory Manual, 3rd ed., Cold Spring Harbor, N. Y.; Cold Spring Harbor Laboratory Press).
  • an antibody or antigen-binding portion thereof may be part of a larger immunoadhesion molecule, formed by covalent or noncovalent association of the antibody or antibody portion with one or more other proteins or peptides.
  • immunoadhesion molecules include use of the streptavidin core region to make a tetrameric scFv molecule (Kipriyanov, S. M., et al., 1995 Human Antibodies and Hybridomas, 6:93-101) and use of a cysteine residue, a marker peptide and a C-terminai polyhistidinc tag to make bivalent and biotinylated scFv molecules (Kipriyanov, S.
  • Antibody portions such as Fab and F(ab') 2 fragments, can be prepared from whole antibodies using conventional techniques, such as papain or pepsin digestion, respectively, of whole antibodies.
  • antibodies, antibody portions and immunoadhesion molecules can be obtained using standard recombinant DNA techniques, as described herein and known to the skilled artisan.
  • the constant region sequence is preferably obtained from a human or primate immunoglobulin sequence.
  • the primate sequence may be a New World primate or an Old World primate sequence. Suitable Old World primates include chimpanzee, or other hominid ape eg. gorilla or orang utan, which because of their close phylogcnctic proximity to humans, share a high degree of homology with the human constant region sequence. Sequences which encode for human or primate constant regions are available from databases including e.g. The National Centre for Biotechnology Information protein and nucleotide databases, The Kabat Database of Sequences of Proteins of Immunological Interest.
  • the antibody or antigen-binding portion according to the invention is capable of binding to a human or non-human antigen.
  • the antigen to which the chimeric antibody or antigen-binding portion thereof binds is peptide, protein, carbohydrate, glycoprotein, lipid or glycolipid in nature, selected from a tumour-associated antigen including carcinoembryonic antigen, EpCAM, Lewis-Y, Lewis- Y/b, PMSA, CD20, CD30, CD33, CD38, CD52, CD154, EGF-R, Hcr-2, TRAIL and VEGF receptors, an antigen involved in an immune or inflammatory disease or disorder including CD3, CD4, CD25, CEHO, CD49d, MHC class I, MHC class II, GM- CSF, interferon- ⁇ , IL-I, IL-12, IL-13, IL-23, TNF- ⁇ , and IgE, an antigen expressed on a liost cell including glycoprotein Ilb/IIIa, P-glycoprotein
  • anti-CD4 by acting with complement, or killer cells (eg. NK cells) or is active as a cytotoxic agent or to cause Fc-receptor binding by a phagocyte or neutralizes biological activity of its target.
  • the antigen is TNF ⁇ , most preferably human TN Fa.
  • the antibody or antigen-binding portion thereof may bind a non-human antigen.
  • the non-human antigen is selected from the group consisting of respiratory syncytial virus F protein, cytomegalovirus, snake venoms and digoxin.
  • the term "binds to” as used herein, is intended to refer to the binding of an antigen by an immunoglobulin variable region of an antibody with a dissociation constant. (Kd) of l ⁇ M or lower as measured by surface plasmon resonance analysis using, for example a BlAcoreTM surface plasmon resonance system and BI ⁇ corcTM kinetic evaluation software (eg. version 2.1).
  • the affinity or dissociation constant (Kd) for a specific binding interaction is preferably about 500 ⁇ M to about 50 pM, more preferably about.500 nM or lower, more preferably about 300 nM or lower and preferably at least, about 3 ( X) nM to about 50 pM, about 200 nM to about 50 pM, and more preferably at least, about 100 nM to about 50 pM, about 75 nM to about 50 pM, about 10 nM to about 50 pM.
  • the antibodies of the present invention are advantageous in human therapy because the likelihood of induction of a human anti-antibody response will be reduced.
  • Recombinant atibodiess produced according to the invention that bind a target antigen can be identified and isolated by screening a combinatorial immunoglobulin library (e.g., a phage display library) to isolate library members that exhibit the desired binding specificity and functional behaviour (for example neutralisation of TNF ⁇ can be measured using L929 cells).
  • a combinatorial immunoglobulin library e.g., a phage display library
  • phage display lechnique has been described extensively in the art and examples of methods and compounds for generating and screening such libraries and affinity maturing the products of them can be found in, for example, Barbas et al, 1991, Proc. Natl. Acad. Sci. USA, 88:7978-7982; Clarkson et al.,
  • Recombinant libraries expressing the antibodies of the invention can be expressed on the surface of microorganisms eg. yeast or bacteria (see PCT publications WO99/36569 and 98/49286).
  • the Selected Lymphocyte Antibody Method or SLAM as it is referred to in the state of the art, is another means of generating high affinity antibodies rapidly. Unlike phage display approaches all antibodies are fully divalent.
  • New World primates are immunised with a human antigen eg. a TNF ⁇ polypeptide. Following immunisation cells are removed and selectively proliferated in individual micro cells. Supernatants are removed from wells and tested for both binding and function. Gene sequences can be recovered for subsequent manipulations eg. humanisation, Fab fragment, scFv or dAb generation.
  • the recombinant peptide/protein library is displayed on ribosomes (for examples see Roberts, RW and Szostak, J.W.1997. Proc.Natl.Acad.Sci.USA. 94: 12297 - 123202 and PCT Publication No. WO98/31700).
  • a DNA library eg of antibodies and derivatives
  • translation of the library such that the protein and "immunised" mRNAs stay on the ribosome, affinity selection (eg by binding to RSP), mRNA isolation, reverse translation and subsequent amplification (eg by polymerase chain reaction or related technology).
  • the antibody or antigen-binding portion thereof according to the invention can be derivatised or linked to another functional molecule.
  • the antibody or antigen- binding portion can be functionally linked by chemical coupling, genetic fusion, noncovalcnt association or otherwise, to one or more other molecular entities, such as another antibody, a detectable agent, a cytotoxic agent, a pharmaceutical agent, and/or a protein or peptide that can mediate association of the antibody or antigen-binding portion thereof with another molecule (such as a streptavidin core region or a polyhistidiue tag).
  • Cytotoxic agents commonly used to generate immunotoxins include radioactive isotopes such as ' " In or 90 Y, selenium, ribonucleascs, binding domain - deleted truncated microbial toxins such as Pseudomo ⁇ as exotoxin or Diphtheria toxin, tubulin inhibitors such as calicheainicin (ozagamicin), maytansinoids (including DM-I), auristatLns, and taxoids, ribosome inactivating proteins such as ricin, ebulin I, saporiti and gelonin, and prodrugs such as melphalan.
  • radioactive isotopes such as ' " In or 90 Y, selenium, ribonucleascs, binding domain - deleted truncated microbial toxins such as Pseudomo ⁇ as exotoxin or Diphtheria toxin
  • tubulin inhibitors such as calicheainicin
  • Useful detectable agents with which an antibody or antigen-binding portion thereof may be dcrivatised include fluorescent compounds.
  • Exemplary fluorescent detectable agents include fluorescein, fluorescein isothiocyanate, rhodarnine, 5-di methyl am ine-1- napthalenesulfonyl chloride, phycoerythrin and the like.
  • An antibody may also be derivalised with detectable enzymes such as alkaline phosphatase, horseradish peroxidase, glucose oxidase and the like. When an antibody is derivatized with a detectable enzyme, it is delected by adding additional reagents that the enzyme uses to produce a detectable reaction product.
  • An antibody may also be dcrivatised with biotin, and detected through indirect measurement of avidin or strcptavidin binding.
  • the present invention also extends to PEGylatcd antibodies or antibody-binding portion which provide increased half-life and resistance to degradation without a loss in activity (e.g., reduction in binding affinity) relative to non-PEGylated antibody polypeptides.
  • the antibody or antigen-binding portion as described herein can be coupled, using methods known in the art, to polymer molecules (preferably PEG) useful for achieving the increased half-life and degradation resistance properties.
  • polymer molecules preferably PEG
  • Polymer moieties which can be utilised in the invention can be synthetic or naturally occurring and include, but are not limited to, straight or branched chain polyalkylene, polyalkenyle ⁇ e or polyoxyalkylene polymers, or a branched or unbranched polysaccharide such as a homo-or heteropolysaccharide.
  • Preferred examples of synthetic polymers which can be used in the invention include straight or branched chain poly(elhylene glycol) (PEG), poly(pxopylene glycol), or polyvinyl alcohol) and derivatives or substituted forms thereof.
  • Particularly preferred substituted polymers for linkage to antibodies as described herein include substituted PEG, including methoxy(polycthylene glycol).
  • Naturally occurring polymer moieties which can be used in addition to or in place of PEG include lactose, amylose, dextran, or glycogen, as well as derivatives thereof which would be recognised by persons skilled in the art,
  • Derivatized forms of polymer molecules include, for example, derivatives which have additional moieties or reactive groups present therein to permit interaction with amino acid residues of the antibody polypeptides described herein.
  • Such derivatives include N- hydroxylsuccinimide (NHS) active esters, succi ⁇ imidyl propionate polymers, and sulfhydryl-selective reactive agents such as maleimide, vinyl sulfone, and thiol.
  • Particularly preferred derivatized polymers include, but are not limited to PEG polymers having the formulae: PEG-O-CI F 2 CH 2 CH 2 -CO 2 -NHS; PEG-O-CH 2 -NHS; PEG-O- CH 2 CH 2 -CO 2 -NHS; PEC-S-CH 2 CH 2 -CO-NHS; PIiG-O 2 CNH-CH(R)-CO 2 -NHS; PEG- NHCO-CH 2 CH 2 -CO-NHS; and PEG-O-CI 1,-CO 1 -NUS; where R is (CH 2 ) 4 )NHCO 2 (mPEG), PEG polymers can be linear molecules, or can be branched wherein multiple PEG moieties are present in a single polymer.
  • the reactive group e.g., MAL, NHS, SPA; VS, or Thiol
  • the size of polymers useful in the invention can be in the Tange of between 500 Da to 60 kDa, for example, between 1000 Da and 60 kDa, 10 kDa and 60 kDa, 20 kDa and 60 kDa, 30 kDa and 60 kDa, 40 kDa and 60 kDa, and up to between 50 kDa and 60 kDa.
  • the polymers used in the invention, particularly PEG can be straight chain polymers or may possess a branched conformation.
  • the polymer (PEG) molecules useful in the invention can be attached to an antibody or •antigen-binding portion thereof using mehtods which are well known in the art.
  • the first step in the attachment of PEG or other polymer moieties to an antibody polypeptide monomer or multimcr of the invention is the substitution of the hydroxyl end-groups of the PEG polymer by olcctrophilc-containing functional groups.
  • PEG polymers are attached to cither cysteine or lysine residues present in the antibody polypeptide monomers or multimers.
  • the cysteine and lysine residues can be naturally occurring, or can be engineered into the antibody polypeptide molecule.
  • cysteine residues can be recombinantly engineered at the C-terminus of an antibody polypeptide, or residues at specific solvent accessible locations in an antibody polypeptide can be substituted with cysteine or lysine.
  • the antibody may be linked to one or more molecules which can increase its half-life in vivo. These molecules are linked to the antibody at a site on the antibody other than the antigen binding site, so that they do not interfere/sterically hinder the antigen-binding site- Typically, such molecules are polypeptides which occur naturally in vivo and which resist degradation or removal by endogenous mechanisms. It will be obvious to one skilled in the art that fragments or derivatives of such naturally occurring molecules may be used, and that some may not be polypeptides. Molecules which increase half life may be selected from the following:
  • proteins from the extracellular matrix eg. collagen, laminin, integrin and fibronectin;
  • proteins found in blood eg. fibrin ⁇ -2 macroglobidin, serum albumin, fibrinogen A, fibrinogen B, serum amyloid protein ⁇ , heptaglobin, protein, ubiquitin, uteroglobin, ⁇ -2 microglobulin, plasminogen, lysozyme, cystalinC, alpha-1-antitrypsin and pancreatic kypsi ⁇ inhibitor;
  • immune serum proteins eg. IgE, IgG 1 IgM;
  • transport proteins eg. retinol binding protein, oc-1 microglobulin;
  • defensins eg, beta-defensi ⁇ 1, Neutrophil defensins 1, 2 and 3;
  • proteins found at the blood brain barrier or in neural tissues eg, melanocorlin receptor, myelin, ascorbate transporters;
  • transferrin receptor specific ligand-Ncuro pharmaceutical agent fusion proteins see US5977307; brain capillary endothelial cell receptor, transferrin, transferrin receptor, insulin, insulin-like growth factor 1 (IGF 1) receplor, insulin-like growth factor 2 (IGF 2) receptor, insulin receptor;
  • IGF 1 insulin-like growth factor 1
  • IGF 2 insulin-like growth factor 2
  • Qx proLeins localised to the kidney, eg, polycystin, type IV collagen, organic anion transporter Kl, Heymann's antigen;
  • proLeins localised to the liver eg. alcohol dehydrogenase, G250;
  • blood coagulation factor X blood coagulation factor
  • proteins localised lo the lung eg. secretory component (binds IgA);
  • proteins localised to the Heart eg. HSP 27;
  • proteins localised to the skin eg, keratin;
  • bone specific proteins such as bone morphogenic proteins (BMPs) eg. BMP-2, -4, -5, -6, -7 (also referred to as osteogenic protein (OP-I) and -8 (OP-2);
  • BMPs bone morphogenic proteins
  • OP-I osteogenic protein
  • OP-2 osteogenic protein
  • tumour specific proteins eg. human trophoblast antigen, herceptin receptor, oestrogen receptor, cathepsins eg cathepsin B (found in liver and spleen);
  • disease-specific proteins eg. antigens expressed only on activated T- cells: including LAG-3 (lymphocyte activation gene); osteoprotegerin ligand (OPGL) see Nature 402, 304-309, 1999; OX40 (a member of the TNF receptor family, expressed on activated T cells and lhe only costimulatory T cell molecule known to be specifically up-regulated in human T cell leukaemia virus type-I (HTLV-I)-producing cells - see J. Immunol.
  • HTLV-I human T cell leukaemia virus type-I
  • mctalloprotcases associated with arthritis/cancers, including CG6512 Drosophila, human paraplcgin, human FtsH, human AFG3L2, murine ftsH; angiogenic growth factors, including acidic fibroblast growth factor (FGF- 1), basic fibroblast growth factor (FGF-2), Vascular endothelial growth factor/vascular permeability factor (VF-GFZVPF), transforming growth factor- ⁇ (TGF- ⁇ ), tumor necrosis factor-alpha (TNF- ⁇ ), angiogenic interieukin-3 (1L-3), interlcukin -8 (IL-8), platelet derived endothelial growth factor (PD- ECGF), placental growth factor (PlGF), midkine platelet-derived growth factor-BB (PDGF), fractalkine;
  • FGF- 1 acidic fibroblast growth factor
  • FGF-2 basic fibroblast growth factor
  • VF-GFZVPF Vascular endothelial growth factor/vascular permeability
  • stress proteins heat shock proteins
  • proteins involved in Fc transport proteins involved in Fc transport
  • vitamins eg B 12, Biotin vitamins eg B 12, Biotin.
  • the invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising an effective amount of the antibody or antigen-binding portion thereof according to the present invention, together with a one or more pharmaceutically acceptable excipient or diluent.
  • a "pharmaceutically acceptable excipient or diluent” includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorplion delaying agents, and the like that are physiologically compatible.
  • pharmaceutically acceptable carriers include one or more of water, saline, phosphate buffered saline, dextrose, glycerol, ethanol, and the like as well as combinations thereof.
  • isotonic agents for example, sugars, polyalcohols such as manitol, sorbitol, or sodium chloride in the composition.
  • the term "effective amount” refers to an amount of an antibody or antigen binding portion thereof (including pharmaceutical compositions comprising the antibody or antigen binding portion thereof) sufficient to treat or ameliorate a specified disease or disorder or one or more of its symptoms and/or to prevenl or reduce the occurrence of the disease or disorder.
  • diagnosis refers to an amount of a antibody or antigen binding portion thereof (including pharmaceutical compositions comprising the antibody or antigen binding portion thereof) sufficient to diagnose a specified disease or disorder and/or one or more of its manifestations, where diagnosis includes identification of the existence of the disease or disorder and/or detection of the extent or severity of the disease or disorder.
  • diagnosis will be carried out with reference to a baseline or background detection level observed for individuals without the disease or disorder.
  • Levels of detection above background or baseline levels are indicative of the presence and, in some cases, the severity of the condition.
  • an individual "in need thereof * may be an individual who has been diagnosed with or previously treated for the disease or disorder to be treated.
  • an individual 'in need thereof may be an individual who is suspected to have a disease or disorder, is at.
  • the antibody or antigen-binding portion thereof blocks or stimulates receptors functions or neutralizes active soluble products, such as one or more of the inierleukins, TNF or C5a. More preferably, the active soluble product is human TNF- ⁇ .
  • the composition may be in a variety of forms, including liquid, semi-solid or solid dosage forms, such as liquid solutions (eg injectable and infusible solutions), dispersions or suspensions, tablets, pills, powders, liposomes or suppositories.
  • the composition is in the form of an injectable solution for immunization.
  • the administration may be intravenous, subcutaneous, intraperitoneal, intramuscular, transdermal, intrathecal, and intra-arteriai.
  • the dosage form is in the range of from about 0.001 mg to about 10 mg/kg body weight administered daily, weekly, bi- or tii-weekly or monthly, more preferably about 0.05 to about 5 mg/kg body weight weekly.
  • composition may also be formulated as a sterile powder for the preparation of sterile injectable solutions.
  • the active compound may be prepared with a carrier that will protect the compound against rapid release, such as a controlled release formulation, including implants, transdermal patches, and microencapsulated delivery systems.
  • a carrier that will protect the compound against rapid release
  • Compatible polymers may be used such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoosters or polylaclic acid.
  • composition may also be formulated for oral administration.
  • the antibody may be enclosed in a hard or soft shell gelatin capsule, compressed into tablets, or incorporated directly into the subject's diet.
  • composition may also be formulated for rectal administration.
  • the antibody may be administered in order to bind to and identify selected cells in viir ⁇ and in vivo, Io bind to and destroy selected cells in vivo, or in order to penetrate into and destroy selected cells in vivo.
  • the antibody may be used as an immunotoxL ⁇ to deliver a cytotoxic agent eg. a toxin or chemolherapeutic agent to a particular cell type such as a tumour cell. Production of immunoloxins would be familiar to persons skilled hi the art.
  • the composition is administered to a human
  • the present invention also provides for the use of the antibody or antigen-binding portion thereof in a diagnostic application for detecting an antigen associated with a particular disease or disorder. More particularly, the invention provides for the use of the antibody or antigen-binding portion thereof in a method for diagnosing a subject having an antigen associated with a particular disease or disorder, comprising administering to said subject a diagnostically effective amount of an antibody, an antigen-binding portion thereof or pharmaceutical composition, as described herein, according to the third aspect.
  • the subject is a human.
  • the antibody or antigen-binding fragment thereof can be used to detect the presence of an antigen, or elevated levels of an antigen (e.g. TNF- ⁇ ) in a biological sample, such as serum or plasma using a convention immunoassay, such as an enzyme linked immunosorbent assay (ELISA), a radioimmunoassay (RIA) or tissue immunohistochemistry.
  • an antigen e.g. TNF- ⁇
  • a biological sample such as serum or plasma
  • ELISA enzyme linked immunosorbent assay
  • RIA radioimmunoassay
  • tissue immunohistochemistry tissue immunohistochemistry
  • the antigen to which the chimeric antibody or antigen-binding portion thereof binds is peptide, protein, carbohydrate, glycoprotein, lipid or glyculipid in nature, selected from a tumour-associated antigen including carci ⁇ oembryonic antigen, EpCAM, Lewis-Y, Lcwis-Y/b, PMSA, CD20, CD30, CD33, CD38, CD52, CD154, EGF-R 1 Her-2, TRAIL and VEGF receptors, an antigen involved in an immune or inflammatory disease or disorder including CD3, CD4, CD25, CD40, CD49d, MHC class I, MHC class II, GM- CSF, interferon- ⁇ , IL-I, IL-12, IL-13, IL-23, TNF- ⁇ , and IgE, an antigen expressed on a host cell including glycoprotein Ilb/UIa, P-glycoprotein ⁇ purinergic receptors and adhesion receptors including CD 1 1 a, CD 1 1 b
  • the anti-human TNF- ⁇ antibody or antigen binding portion thereof according to the invention may also be used in cell culture applications where it is desired to inhibit TNF- ⁇ activity.
  • the present invention also provides a method for treating a disease or disorder characterised by human TNF- ⁇ activity in a human subject, comprising administering to the subject in need thereof an antibody, an antigen-binding portion thereof or a pharmaceutical composition, as described herein, according to the present invention in which the antibody or antigen-binding portion thereof binds TNF- ⁇ .
  • disease or disorder characterised by human TNF- ⁇ activity is intended to include diseases or disorders in which the presence of TNF- ⁇ in a subject suffering from the disease or disorder has been shown to be or is suspected of being either responsible for or involved in the pathophysiology of the disease or disorder or a factor that contributes to the worsening of the disease or disorder. Accordingly, a disease or disorder in which TNF- ⁇ activity is detrimental is a disease or disorder in which inhibition of TNF- ⁇ activity is expected to alleviate symptoms and/or progression of the disease or disorder.
  • Such diseases or disorders may be evidenced, for example, by an increase in the concentration of TNF- ⁇ in a biological fluid of a subject suffering from lhe disease or disorder (c.g., an increase in the concentration of TNF- ⁇ in serum, plasma, synovial fluid etc of the subject), which can be detected, for example, using an antibody of the invention specific for TNF- ⁇ .
  • a disease or disorder characterised by human TNF- ⁇ activity is intended to include diseases or disorders in which the presence of TNF- ⁇ in a subject suffering from the disease or disorder has been shown to be, or is suspected of being, either responsible for the pathophysiology of the disease or diso ⁇ der or a factor which contributes to a worsening of lhe disease or disorder.
  • the disease or disorder characterised by human TNF- ⁇ activity is selected from the group consisting of sepsis, including septic shock, endolo ⁇ ic shock, gram negative sepsis and toxic shock syndrome; autoimmune disea.se, including rheumatoid arthritis, rheumatoid spondylitis, osteoarthritis, psoriasis and gouty arthritis, allergy, multiple sclerosis, autoimmune diabetes, autoimmune uveitis and nephrotic syndrome; infectious disease, including fever and myalgias due to infection and cachexia secondary to infection; graft versus host disease; tumour growth or metastasis; pulmonary diseases including adult respiratory distress syndrome, shock lung, chronic pulmonary inflammatory disease, pulmonary sarcoidosis, pulmonary fibrosis and silicosis; inflammatory bowel diseases including Crohn's disease and ulcerative colitis; cardiac diseases; inflammatory bone diseases, hepatitis, coagulation disturbances, burns, rep
  • Supplementary active compounds can also be incorporated into the composition.
  • the antibody or antibody-binding fragment may be co-formulated with and/or administered simultaneously, separately or sequentially with one or more additional therapeutic agents eg. antibodies that bind to other targets such as cytokines or cell surface molecules or alternatively one or more chemical agents that inhibit human TNF- ⁇ production or activity.
  • the invention provides a kit comprising a therapeutically effective emount of an antibody or antigen-binding portion of the invention, or a pharmaceutical composition comprising a therapeutically effective amount of an antibody or antigen- binding portion thereof, together with packaging and instructions for use.
  • the instructions for use include instructions for how to effectively administer a therapeutic amount of an antibody or antigen-binding portion of the invention.
  • V N chain (Accession Number: AAM54057, SF,Q ID NO: 1) of the MOG specific marmoset derived antibody was expressed with a human constant region (human IgGl heavy chain C H 1, hinge, C H 2 & C H 3 domains (such as NCBI accession number P01857) (SEQ ID NO: 2)).
  • SEQ ID NO: 2 human IgGl heavy chain C H 1, hinge, C H 2 & C H 3 domains (such as NCBI accession number P01857)
  • SEQ ID NO: 2 human constant region
  • DNA sequence optimisation tJie specific restriction enzyme sites Asc f and Tth 1 111 were included to allow for future manipulation of the V H region.
  • V L chain (Accession Number: AAM54058, SEQ IO NO: 3) of the MOG specific marmoset derived antibody was expressed with a human kappa light chain constant region (such as NCBI accession number AAA58989) (SEQ ID NO: 4).
  • DNA encoding the light chain (V L - Kappa) amino acid sequence was prepared as described above for the heavy chain.
  • specific restriction enzyme sites Bsi WI / Rsr TT were included to allow future manipulation of the VL region.
  • the resultant fragment was subcloned using Not I and BamH I sites into the pEE12.4-V L -Kappa vector downstream of the light chain expression cassette (hCMV-MIE promoter, Kozak sequence, marmoset VL, human Kappa constant region and SV40 polyA site) creating a vector expressing both the heavy and light chains of AB 138 (SEQ ID NOs: 5 and 6).
  • the supernatant was passed over a I liTrap Protein A column (Amersham Biosciences, Cat No: 17-0402-01) three times at a flow rate of 1 mL/min, The column was then washed with 20 mM sodium phosphate for 40 mins at 1 mL/mi ⁇ , The antibody was eluted with OA M citric acid pH 3,5 with fractions collected and immediately neutralised with 1 M Tris- HCl pH 9.0. Antibody samples were then desalted on a PD-IO column (Amersham Bioscicjiccs, Cat No: 17-0851-01). Analysis of the antibody by SDS-PAGE and size- exclusion HPLC confirmed the correct molecular weight, presence of assembled antibody and the concentration of antibody.
  • AB 138 The ability of AB 138 to retain binding to the antigen of M26 ⁇ rat MOG (inyclin- oligodendrocyte glycoprotein), was investigated by Western B lot. 130 mg of rat spinal cord (IMVS, Australia) was homogenized in 1.8 ml CelLytic M Cell Lysis Reagent (SIGMA, C2978) and incubated for 30 minutes at 4°C Further homogenizatlon was performed by drawing the lysate throu gh a 27gl/2 needle several times followed by centrifugation at 4°C and 13000g for 30 minutes.
  • SIGMA CelLytic M Cell Lysis Reagent
  • SDS-PAGE sample buffer 125 rnM Tris-HCl pH 6.8, 5% SDS, 0.25% bromophenol blue, 25% glycerol.
  • SDS-PAGE sample buffer 125 rnM Tris-HCl pH 6.8, 5% SDS, 0.25% bromophenol blue, 25% glycerol.
  • SDS-PAGE sample buffer 125 rnM Tris-HCl pH 6.8, 5% SDS, 0.25% bromophenol blue, 25% glycerol.
  • SlGMA CclLylic M Cell Lysis Reagent
  • rat MOG retained affinity for rat MOG present in rat spinal cord lysate and demonstrates that a marmoset human fusion antibody can retain antigen binding ability. It can be appreciated by someone skilled in the art that rat MOG could be produced using recombinant DNA technology and the ability of AB 138 to bind rat MOG determined in binding assays such as ELISA or Biacore analysis.
  • a donor sequence is defined as any immunoglobulin sequence derived from a species other then a New World primate.
  • An acceptor sequence is defined as an immunoglobulin sequence derived from a New World primate.
  • a common residue is a residue that is common (e.g. >30%) at a given amino acid position when determined by comparison with immunoglobulin sequences available for a species.
  • An uncommon residue is a residue that is uncommon (e.g. ⁇ 30%) at a given amino acid position when determined by comparison with the immunoglobulin sequences available for a species.
  • Engineering is the process of transferring structural binding features of a donor sequence into an acceptor sequence such that the structural binding features maintain their binding activity.
  • a framework amino acid is defined as an amino acid located in an antibody variable re.gio ⁇ but not located in a CDR, 2.
  • MOG myelin/oligodendrocyte glycoprotein TNF- ⁇ , tumour necrosis factor - alpha
  • V H variable heavy chain
  • V L variable light chain
  • BSA bovine serum albumin
  • substitutions of an acceptor amino acid with the corresponding donor amino acid may be made aL positions that fall into the following criteria: (i) if the donor residue is predicted capable of interacting with the antigen based on three dimensional modelling;
  • the engineered antibody is predicted to be non-immunogenic or of low immunogenicily in humans by selecting appropriate acceptor sequences based on amino acid sequence homology with equivalent human sequences and predicted low immunogenicity,
  • the engineered antibody will bind to the antigen of the donor immunoglobulin with a similar binding affinity to the donor immunoglobulin.
  • the binding affinity of the engineered antibody can be further increased by methods of affinity maturation (R. A. Irving et al Journal of Immunological Methods, 248, 31-45 (2001)).
  • the sequence of a monoclonal antibody against rat MOG was obtained from Pub Med (http://www.ncbi.nlm.Ti ih. ⁇ v/) and was used as the acceptor sequence.
  • This monoclonal antibody was derived from a common marmoset (white-tuffed-ear marmoset) (Callithrix jacchus), a New World primate.
  • the framework regions of the V H chain (Accession Number: AAM54057, SEQ ID NO: 1) and the VL chain (Accession Number: AAM54058, SEQ ID No: 3) were examined for their predicted immunogenicity in humans by the MHC class IT binding prediction program Proprcd (http://www.imtech.res.in/raghava/propred ' ) using a 1% threshold value analysis of all alleles.
  • a BLAST analysis of the sequence, excluding CDRs, of the V H chain (Accession Number: AAM54057, SEQ TD NO: 1) and the V L chain (Accession Number: ⁇ AM54O58, SEQ ID No: 3) of the MOO specific antibody identified the closest human homologue heavy chain sequence (Accession Number AAH 19337.1 ; SEQ ID NO: 9) and (he light chain sequence (Accession Number: BAC53922.1 ; SEQ ID NO: 10).
  • acceptor heavy chain variable framework region is likely to be less immunogenic than its human equivalent.
  • the acceptor heavy chain variable region had one peptide in the framework, LRPEDTAVY, which is predicted to bind MHC class 11 encoded by alleles DRBl_0101 , DRBl_0102, DRBl J)3O9, Whereas the closest human homoloque heavy chain had three peptides, in the framework, that were predicted to bind to MHC class II.
  • the MOG specific light chain variable framework region and the closest human homologue were predicted to be non-immunogenic, 6, Identification of the CDRs in the donor/acceptor variable regions
  • Table 1 Amino acid positions for the CDRs of V H and V L chains of ⁇ B164 (SEQ ID NOs: 7 and 8) and MOG-specific immunoglobulin (SEQ ID NOs: 1 and 3) 7. Alignment of donor and acceptor sequences V H chain alignment
  • the amino acid for the V L chains of AB 164 and MOG specific immunoglobulin (SEQ ID No: 8 and 3) were aligned ( Figure 4).
  • the number of residues differs by four additional amino acids located in the CDRl of AB 164. Sequence identity between the two hequences. is 62.3 %.
  • the amino acid sequences of the CDRs differ as expected given the different antigen specificities of donor and acceptor antibodies. There are 23 amino acid differences between the sequences in the framework regions.
  • Table 3 V H framework differences in the donor/acceptor sequence, their proximity to the CT)Rs and their relative common residues in the conor/acceptor species. A determination of the common residues at each position in the respective murine germline and the available marmoset V H sequences was performed. At selected positions that satisfied a particular criteria the acceptor amino acid was replaced with a donor amino acid and the number ot that criteria is given.; 1. if the donor residue is predicted capable of interacting with the antigen based on three dimensional modelling; '
  • the donor residue is determined to lie within 3.2 A of the donor CDRs based on three dimensional modelling; 3. if the donor residue is a common residue in acceptor species immunoglobulin sequences; 4. if the donor residue is uncommon in the donor germline.
  • acceptor sequence there were 8 framework amino acid substitutions in which acceptor sequence was replaced with donor sequence.
  • acceptor sequence There were four amino acids in which the acceptor sequence was substituted with the donor sequence because the donor residue was determined to lie with 3.2 A of the donor CDRs, based on three dimensional modelling, Two amino acid substitutions were made because the donor residues were predicted capable of interacting with the antigen being located on the turn of a loop that is in close proximity (though not less then 3.2 ⁇ ) with CDR-2, Further, two amino acid substitutions were made because the donor residue was found to be common in the acceptor species immunoglobulin sequences available. A further change could also be made at position 97.
  • Table 4 V L framework differences in the donor/acceptor sequence, their proximity to the CDRs and their relative common residues in the donor/acceptor species. A determination of the common residues at each position in the respective murine germline sequence and the available marmoset VL sequences was performed. At each position the criteria for selecting differences in framewoek sequence given above was applied, At a position that satisfied a particular criteria the acceptor amino acid was replaced with a donoi amino acid and the numbei of that criteria is given.;
  • the AB 164 hybridoma was generated by fusion of splenocytes from mice immunized with human TNF- ⁇ , with the myeloma cell line SP2/0-Agl4 by standard methods (Fazekas dc St. Groth, S., el al. Journal of Immunological Methods 35: 1-21 (1980); Sugasawara, R., Journal of Tissue Culture Methods 12: 93-95 (1989)).
  • Tqtal RNA was extracted from 1 x 10 7 to 1 x. 10 8 viable cells using RNeasy Mini or Midi columns (QIAgen) according to the manufacturer's instructions. Following quantitation, the tRNA was used as a template for first strand cDNA synthesis using an oligo(dT) primer and Superscript II Reverse Transcriptase (hwitrogen) according to manufacturer's instructions. Finally the tRNA was degraded using RNase H and the remaining single stranded cDNA tagged with a poly-G tail using terminal transferase and dGTP (Roche).
  • PCR reactions were performed using Hcrculase (Stratagene), a high fidelity polymerase blend. In each case an oligo (dC) was used as the forward primer with an IgGi heavy chain specific or a Kappa light chain specific reverse primer. Following 30 cycles PCR reactions were incubated in the presence of Taq polymerase to add overhanging A bases. The resulting PCR product was then cloned into pGcmT-Easy (Promcga) and transformed into competent Top 10 E coli cells (Invitrogcn). Plasmids were extracted from overnight culture of single colonies using QIAquick Miniprep columns (QIAgen) and quantified.
  • V H region (Accession Number: AAM54057, SEQ ID No: 1) of the acceptor sequence was e ⁇ pressed with a human constant region (human IgG 1 heavy chain C H I , hinge, C H 2 & C H 3 domains (such as NCBI accession number PO 1.857) (vSEQ ID No:2), The V t .
  • AB 138 SEQ ID NOs: 5 and 6
  • This antibody was used as a template into which alterations in the V H and V 1 , chains were made.
  • Vj] and VL regions from the fully murine AB 164 were expressed with the same human constant regions as described above.
  • This chimeric antibody was given the designation AB 103.
  • V 11 and V L regions from the fully murine AB 164 were back translated into DNA sequences which were optimized for mammalian cell expression using GcncOptimizer technology and synthesized de novo by assembly of synthetic oligonucleotides (OeneArt, Germany).
  • V H gene each sequence was flanked at the 5' end with a Aac I site, a Kozak sequence (GCCACC) and a human IgG gamma leader sequence (amino acid sequence M EWS WVFLFFLS VTTGVHS).
  • GCCACC Kozak sequence
  • human IgG gamma leader sequence amino acid sequence M EWS WVFLFFLS VTTGVHS
  • each sequence was flanked at the 5' end with a Bsi WI site, a Kozak sequence (GCCACC) and a human Kappa leader sequence (amino acid sequence MSVPTQVLGLLLLWLTDARC).
  • GCCACC Kozak sequence
  • MSVPTQVLGLLLLWLTDARC human Kappa leader sequence
  • the variable regions were provided cloned into a pCRScript vector (Stratagene) and were released by Asc I / Tth 1111 and Bsi WI / Rsr II digestion for the Vn and VL sequences respectively.
  • Each gene was Iigated into the prepared backbone using the LigaFast Rapid DNA Ligation System from Promcga (Cat No. M8221). Ligations were then transformed into One Shot Top 10 (chemically competent cells (fnvtrogen Cat No. C4040-03) and positive colonies identified by standard techniques.
  • ⁇ double gene vector for stable expression was prepared as outlined above (Example 1). Large quantities of the resulting vectors were prepared by midiprep of overnight cultures using QI ⁇ filter midiprep columns (QIAgen Cat No. 12243). Vectors were prepared for transfection by precipitating 20 ⁇ g in 100% ethanol with 1/10 volume of 3M sodium acetate (pH5.2) (Sigma Cat Nos. E7023-500ML and S2889 respectively). Following a wash in 70% ethanol vectors were resuspended in 40 ⁇ l of T.E. pH8.0 (Sigma Cat No. T9285-100ML) at a working concentration of 0.5 ⁇ g/ ⁇ l.
  • Table 5 Species origin of the CDRs, VD/V I , framework and the constant regions for AB138, AJJ164, AB197, AB103 Cloning of AB 197
  • VH and VL antibody sequences were determined (SEQ ID No: 11 and 12).
  • the antibody sequence was back translated into DNA sequences and synthesized de novn by assembly of synthetic oligonucleotides (Genc ⁇ rt, Germany). During synthesis the relevant restriction enzyme sites were incorporated in the sequence Lo allow cloning and the generation of a double gene vector expressing AB 197 as described previously (Example 1).
  • Hybridoma cells expressing AB 164 were cultured using standard tissue culture methods and the supernatant harvested and centrifuged at 4,000 x g for 5 minutes to pellet cell debris followed by filter sterilisation through 0.22 ⁇ m cartridge filters, Antibody Purification of AB 103, AB 197 and AB 164
  • the supernatant was passed over a HiTrap Protein ⁇ column (Amcrsham Bioscicnces, Cat No: 17-0402-01) three times at a flow rate of I mL/min.
  • the column was then washed with 20 roM sodium phosphate for 40 mins at 1 mL/min.
  • the antibody was eluted with 0.1 M citric acid pH 3.5 with fractions collected and immediately neutralised with IM Tris-HCl pH 9.0.
  • Antibody samples were then desalted on a PD- 10 column (Amersham Biosciences, Cat No: 17-0851-01). Analysis of the antibody by SDS-PAGE and size-exclusion HPLC confirmed the molecular weight, presence of assembled antibody and the concentration of antibody.
  • TNF- ⁇ (Peprotech Cat No: 300-01A) was diluted to 1 ⁇ g/mL in carbonate coating buffer (10 niM disodium phosphate, 20 mM sodium hydrogen phosphate pH 9.6). 100 ⁇ L of this solution was added to each well of a 96 well plate and incubated at 4"C overnight hi a humidified container. The plate was then washed three times with wash buffer (0.01M PBS pH 7.2, 0.05% Tween-20) and then three times with 0.01 M PBS pH 7.2.
  • carbonate coating buffer (10 niM disodium phosphate, 20 mM sodium hydrogen phosphate pH 9.6). 100 ⁇ L of this solution was added to each well of a 96 well plate and incubated at 4"C overnight hi a humidified container. The plate was then washed three times with wash buffer (0.01M PBS pH 7.2, 0.05% Tween-20) and then three times with 0.01 M PBS pH 7.2.
  • the wells were then blocked by adding 200 ⁇ L blocking buffer (1% w/v BSA in 0.01 M PBS pH 7.2) to each well and incubating the plate at 25 0 C, in a humidified container, for 1 hour.
  • the antibody was diluted in antibody diluent (1% w/v BSA, 0.05% Tween-20 in 0.01 M PBS -pH 7.2) sufficient to generate a titration curve covering the ranges 6.00 ⁇ g/mL to 0.0578 ng/mL.
  • the wells were incubated with the antibody for 1 hour at 25 0 C. The plate was then washed as previously described.
  • L929 cells (ATCC No: CCH) were cultured in RPMI 1640 (Invitrogen Cat No: 21870- 076) containing 10% foetal bovine serum, 50 ⁇ g/mL Penicillin/Streptomycin (Sigma Cat No: P0781), 2 niM L-glutamine (Invitrogen Cat No: 25030-081) and 10 ⁇ M 2- mercaptoethanol (Invitrogen Cat No: 21985-023) till the cells reached a 70% level of confluence. Fnto each well of a 96-well tissue culture plate 50 ⁇ L media was added.
  • TNF- ⁇ working solution per well 30 ng/mL was added to the first column of the plate in triplicate with serial half log dilutions performed across the plate reaching a final concentration of 9 fg/mL.
  • Actinomycin D (Sigma Cat No: A1410) at 40 ⁇ g/mL was added.

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Immunology (AREA)
  • Biophysics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Dermatology (AREA)
  • Pain & Pain Management (AREA)
  • Neurology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Diabetes (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Communicable Diseases (AREA)
  • Neurosurgery (AREA)
  • Hematology (AREA)
  • Vascular Medicine (AREA)
  • Biomedical Technology (AREA)
  • Transplantation (AREA)
  • Oncology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)

Abstract

The present invention provides an antibody or antigen-binding portion thereof having a variable region comprising at least two complementarity determining regions (CDRs) and at least three framework regions. The the framework regions are, or are derived from New World primate framework regions, and at least one of the CDRs is a non-New World primate CDR.

Description

Engineered antibodies with New World primate framework regions
FIELD OF THE INVENTION
The present invention relates to an antibody or antigen-binding portion thereof having a variable region comprising at least two complementarity determining regions (CDRs) and at least three framework regions. The framework regions are, or are derived from New World primate framework regions, and al least one of the CDRs is either a modified New World primate CDR or a non-New World primate CDR.
BACKGROUND OF THE INVENTION
Antibodies (immunoglobulins) play an important role in the immune system of a mammal. They arc produced by plasma cells which have developed from precursor B cells. Antibodies consist of two identical light polypeptide chains and two identical heavy polypeptide chains which ares joined by disulfide bridges. The light chains are referred to as cither kappa or lambda light chains and the heavy chains as gamma, mu, delta, alpha or cpsilon. Each chain consists of a constant and variable region. The variable region gives the antibody its specificity. Within each variable region are regions of hypervariability or complementarity determining regions (CDRs) which are flanked by more conserved regions referred to as framework regions. Within each variable region arc tlirce CDRs and four framework regions.
Antibodies arc bifunctional molecules, the N-lerminal variable segments from the heavy and light chains associate together in a specific manner to generate a three-dimensional structure with affinity for a particular epitope on the surface of an antigen. The constant region segments are responsible for prolonged scrum half-life and the effector functions of the antibody and relate to complement binding, stimulation of phagocytosis, antibody- dependent cellular cytotoxicity and triggering of granulocyte granule release. The development of hybridoma teclinology has facilitated the production of monoclonal antibodies of a particular specificity. Typically, such hybridomas are murine hybridomas.
Human/mouse chimeric antibodies have been created in which antibody variable region sequences from the mouse genome arc combined with antibody constant region sequences from the human genome. The chimeric antibodies exhibit the binding characteristics of the parental mouse antibody, and the effector functions associated with the human constant region. The antibodies are produced by expression in a host cell, including for example Chinese Hamster Ovary (CHO), NSO myeloma cells, COS cells and SP2 cells. Such chimeric antibodies have been used in human therapy, however antibodies to these chimeric antibodies have been produced by the human recipient. Such aπti-chimeric antibodies are detrimental to continued therapy with chimeric antibodies.
It has been suggested that human monoclonal antibodies are expected to be an improvement over mouse monoclonal antibodies for in vivo human therapy. From work done with antibodies from Old World primates (rhesus monkeys and chimpanzees) it has been postulated that these non-human primate antibodies will be tolerated in humans because they are structurally similar to human antibodies (Ehrlich PH el td,, Clin Chetn., 1988, 34:9 1681-1688). Furthermore, because human antibodies arc non-immunogenic in Rhesus monkeys (Ehrich PH et aLt Hybridoma, 1987, 6:151-60), it is likely that the converse is also applicable and primate antibodies will be uon-immunogcnic in humans. These monoclonal antibodies are secreted by hybridomas constructed by fusing lymphocytes to a human x mouse heteromyeloma.
EP 0605 442 discloses chimeric antibodies which bind human antigens. These antibodies comprise the whole variable region from an Old World monkey and the constant region of a human or chimpanzee antibody. One of the advantages suggested in this reference for these constructs is the ability to raise antibodies in Old World monkeys to human antigens which are less immunogenic in humans compared with antibodies raised in a mouse host
New World primates (infraorder- Platyrrhini) comprise at least 53 species commonly divided into two families, the Caltithricidae and Cehidae. The Callithricidae consist of marmosets and tarnarins. The Cehidae includes the squirrel monkey, titi monkey, spider monkey, woolly monkey, capuchin, uakaris, sakis, night or owl monkey and tlie howler monkey.
Evolutionarily distant primates, such as New World primates, are not only sufficiently different from humans to allow antibodies against human antigens to be generated, but are sufficiently similar to humans to have antibodies similar to human antibodies so that the host does not generate an anti-antibody immune response when such primate-derived antibodies are introduced into a human.
Previous studies have characterised the expressed immunoglobulin heavy chain repertoire of the Callithrixjacchus marmoset (von Budingen H-C et al.f Inmiunogenetics, 2001 , 53:557-563). Six IGHV subgroups were identified which showed a high degree of sequence similarity to their human IGHV counterparts. The framework regions were more conserved when compared to the complementarity determining regions (CDRs). The degree of similarity between C. jacchus and human IGHV sequences was less than between non-human Old World primates and humans. Domain antibodies
Domain antibodies (dAb) are functional binding units which can be created using antibody frameworks and correspond to the variable regions of either the heavy (VH) or light (VL) chains of antibodies. Domain antibodies have a molecular weight of approximately 13 kDa, or less than one tenth the size of a full antibody.
Immunoglobulin light chains arc referred to as cither kappa or lambda light chains and the heavy chains as gamma, mu, delta, alpha or cpsilon. The variable region gives the antibody its specificity. Within each variable region arc regions of hypcrvariability, otherwise known as complementarity determining regions (CDRs) which arc flanked by more conserved regions referred to as framework regions. Within each light and heavy chain variable region arc three CDRs and four framework regions.
In contrast to conventional antibodies, domain antibodies are well expressed in bacterial, yeast and mammalian systems. Their small size allows for higher molar quantities per gram of product, thus providing a significant increase in potency. In addition, domain antibodies can be used as a building block to create therapeutic products such as multiple targeting dAbs in which a construct containing two or more variable omainss bind to two or more therapeutic targets, or dAbs targeted for pulmonary or oral administration.
SUMMARY OF THE INVENTION
The present inventors have found (hat New World primates provide a source of antibody sequences which are predicted to have low immunogcnicity in humans.
New world primates were chosen as a repository of immunoglobulin sequences that, existed at the branch point of New World and Old World Primates. The key idea was that, tins repository might thus yield immunoglobulin sequences primordial to later divergences in immunoglobulin sequences as found in Old World Primates, Such primordial sequences would have co-existed with the T cell repertoire, as it subsequently evolved on the path to man, for the 35 million years ago (M YA) estimated to be the branch point of Old and New World Primates (Schneider H et at, Mo! Phylogenet Evol.7 1993 Sep;2(3):225-42.). This represents a protracted period of selection for immunological tolerance and thus such primordial sequences were predicted, by the inventors, to be free of certain helper T cell epitopes that, would have evolved more recently.
Accordingly in a first aspect the present, invention provides an antibody or antigen-binding portion thereof having a variable region comprising at. least two complementarity dcteπnining regions (CDRs) and at least three framework regions, wherein the framework regions are, or are derived from New World primate framework regions, and wherein at least one of the CDRs is a non-New World primaLe CDR.
In a second aspect, the invention provides a pharmaceutical composition comprising an effective amount of the antibody or antigen-binding portion thereof according to the present invention, together with a one or more pharmaceutically acceptable excipieπt(s) or dilucnt(s).
In a third aspect, the invention provides for the use of an antibody or antigen-binding portion thereof of the present invention in a diagnostic application for detecting an antigen associated with a particular disease or disorder. In. a fourth aspect, the present invention provides a method for treating a disease or disorder characterised by human TNF-α activity in a human subject, comprising administering to the subject in need thereof an effective amount of the antibody or antigen binding portion thereof as described herein (or a pharmaceutical composition thereof) in which the antibody or antigen- binding portion thereof binds TNF-α, In a further aspect of the invention is provided the use of the antibodies, and antigen binding portions thereof, and pharmaceutical compositions thereof as described herein in the manufacture of a medicament. Particularly, the manufacture of a medicament for use in the treatment or diagnosis of diseases or disorders as described herein.
In a further aspect the present invention provides a designed New World primate antibody or antigen-binding portion thereof which binds a cell surface antigen or a cytokine wherein the antibody or antigen-binding thereof comprises a variable region comprising at least two complementarity determining regions (CDRs) and at least three framework regions, wherein the CDRs are selected such that the antibody or antigen-binding portion binds to the cell surface antigen or to the cytokine. Unless otherwise noted or clearly indicated in by the context, it is intended that the antibodies and antigen binding portions thereof as described herein may be used without limitation in the pharmaceutical compositions described herein and incorporated in the kits described herein. And, further the antibodies and antigen binding portions thereof, as well as the pharmaceutical compositions and kits, as described herein may be used in the methods of treatment and diagnosis disclosed herein, unless otherwise noted or clearly indicated by the context. BRIEF DESCRIPTION OF THE FIGURES
Figure 1 demonstrates the binding of AB138 to rat MOG present in rat spinal cord lysate (lane 2) and not to CHOKlSV lysate (laiic 3). Lane 1 contains molecular weight markers.
Figure 2 demonstrates the lack of non-specific binding of an anti-TNFα monoclonal antibody Io the same sample of rat MOG present in rat spinal cord lysate (lane 2) and CHOKlSV lysate (lane 3). Lane 1 contains molecular weight markers.
Figure 3 is an alignment of the donor and acceptor VH amino acid sequences Figure 4 is an alignment of the donor and acceptor VL amino acid sequences Figure 5: Binding of anLibodics AB 164, AB 103 and AB 197 to TNF-α by ELISA. Figure 6: Neutralisation by AB 164, AB 197, AB 103 of TNF-α-induced L-929 cell cytotoxicity
DETAILED DESCRIPTION OF THE INVENTION
Tn a first aspect the present invention provides an antibody or antigen-binding portion thereof having a variable region comprising at least two complementarity determining regions (CIDRs) and at least three framework regions, wherein the framework regions are, or are derived from New World primate framework regions, and wherein at least one of the CDRs is a non-New World primate CDR.
In a second aspect, the invention provides a pharmaceutical composition comprising an effective amount of the antibody or antigen-binding portion thereof according to the present invention, together with a one or more pharmaceutically acceptable excipicnt(s) or diluent(s).
In a third aspect, the invention provides for the use of an antibody or antigen-binding portion thereof of the present invention in a diagnostic application for detecting an antigen associated with a particular disease or disorder, In a fourth aspect, the present invention provides a method for treating a disease or disorder characterised by human TNF-α activity in a human subject, comprising administering to the subject in need thereof an effective amount of the antibody or antigen binding portion thereof as described herein (or a pharmaceutical composition thereof ) in which the antibody or antigen-binding portion thereof binds TNF-α. In certain embodiments of the invention the variable region comprises three CDRs and four framework regions. It is also preferred that the antibody has low predicted immiinogeniciiy in humans.
The variable region of the antibody or antigen-binding portion thereof may comprise a combination of CDRs from differing sources. -
In certain embodiments the variable region comprises CDRs selected from the group consisting of at least one murine CDR sequence (preferably either mouse or rat), at least one human CDR sequence, at least one synthetic CDR sequence, at least one rabbit CDR sequence, at least one modified New World primate CDR sequence and combinations of two or moτe of the forgoing, at least one human CDR and at least one murine CDR, at least one human CDR and at least One synthetic CDR7 at least one human CDR and at least one rabbit CDR, at least one human CDR and at least one New World primate CDR, at least one murine CDR and at least one synthetic CDR, at least one murine CDR and at least one rabbit CDR, al leasL one murine CDR and at least one New World primate CDR, at least one synthetic CDR and at least one rabbit CDR, at least one synthetic CDR and at least one New World primate CDR, and at least one rabbit CDR and at least, one New World primate CDR.
IQ a preferred form the variable region comprises 3 murine CDR sequences, in particular 3 mouse CDR sequences. In an alternative embodiment the variable region comprises 3 human CDR sequences.
In a further preferred embodiment the variable region comprises 4 New World primate framework regions or 4 framework regions in which the regions are derived from New World primate framework regions.
In some embodiments the antigen-binding portion is a domain antibody. In particular embodiments, the antibody or antigen-binding portion further comprises a human or non- human Old World primate constant region sequence or a combination thereof.
Examples of non-human Old World primates include, but are not limited to, chimpanzees, baboons, orang utans, macaques and gorillas.
In a further embodiment of the present invention, the dAb may be multimerised, as for example, hetero- or homodimers (e.g., VH/VH, VJ/VL or VΠ/VL), hetero- or liomotrimcrs (e.g., VH/VH/VH, V1ZVLZVL, VH/VH/VL or VH/VτZVL), hetero- or hornotetramcrs (e.g., VH/VH/VH/VH, VLZVLZVLZVL, VH/VH/VH,VL, VHWVI/VL or VH/VLZVL/VL), or higher order hetero- or homomultimers. Multimerisation can increase the strength of antigen binding, wherein the strength of binding is related to the sum of the binding affinities of the multiple binding sites.
For example, the invention provides a domain antibody wherein the domain antibody is linked to at least one further domain antibody. Each dAb may bind to the same or different antigens.
The dAb multimers may further comprise one or more dAbs which are linked and wherein each dAb binds to a different antigen, multi-specific ligands including so-called "dual- specific ligands". For example, the dual specific ligands may comprise a pair of VH domains or a pair of VL domains. Such dual-specific ligands are described in WO 2004/003019 (PCT/GB2003/002804) in the name of Domantis I ,td, incorporated by reference herein in its entirety.
The New World primate framework region sequence is preferably from a New World primate selected from the group consisting of marmosets, tamariπs, squirrel monkey, titi monkey, spider monkey, woolly monkey, capuchin, uakaris, sakis, night or owl monkey and the howler monkey, most preferably a marmoset
Preferably, the antigen to which the chimeric antibody or antigen-binding portion thereof binds, is peptide, protein, carbohydrate, glycoprotein, lipid or glycolipid in nature, selected from a tumour-associated antigen including carcinoembryonic antigen, EpCAM, I-ewis-Y, Lewis-Y/b, PMSA, CD20, CD30, CD33, CD38, CD52, CD154, EGF-R, Her-2, TRAIL and VEGF receptors, an antigen involved in an immune or inflammatory disease or disorder including CD3, CD4, CD25, CD40, CD49d, MHC class I, MMC class π, GM- CSF, intcrfcron-γ, IL-I , IL-12, IL-13, IL-23, TNF-α, and IgE, an antigen expressed on a host cell including glycoprotein Ilb/IIIa, P-glycoprotein, purinergic receptors and adhesion receptors including CDl Ia1 CDlIb, CDlIc, CD18, CD56, CD58, CD62 or CD144, an antigen comprising a cytokine, chcmokiue, growth factor or other soluble physiological modulator or a receptor thereof including eotaxiu, IL-6, IL-S1 TGF-β, C3a, C5a, VEGF, NGF and their receptors, an antigen involved in central nervous system diseases or disorders including β-amyloid and prions, an antigen of non-human origin such as microbial, nanobial or viral antigens or toxins including respiratory syncitial virus protein F, anthrax toxin, ratlle snake venom and digoxin; wherein the chimeric antibody acts as an agonist or antagonist or is active to cither deplete (kill or eliminate) undesired cells (eg. anti-CD4) by acting wilh complement, or killer cells (eg. NK cells) or is active as a cytotoxic agent or to cause Fe-reccptor binding by a phagocyte or neutralizes biological activity of its target. It is also preferred that the sequence of at least one framework region is modified to increase binding or potency or to decrease predicted,immunogenicity in humans. An increase in binding or potency or a decrease in predicted immunogenicity in humans of an antibody or antigen-binding portion of the invention is relative to an antibody or antigen binding portion in which the framework region is unmodifiedi
In other embodiments the sequence of one or more of lhe CDRs are modified to increase binding or potency or to decrease predicted immunogenicity in humans, An increase in binding or potency or a decrease in predicted immunogenicity in humans of an antibody or antigen-binding portion of the invention is relative to an antibody or antigen binding portion in which the framework region is unmodified.
An increase in binding is demonstrated by a decrease in KD (KrtyKw) for the antibody or antigen binding portion thereof. An increase in potency is demonstrated in biological assays. For example, assays that can be used to measure the potency of the antibody or antigen-binding portion thereof include the TNFα-induccd L929 cytotoxicity neutralisation assay, IL- 12-induced human PHA-activated peripheral blood mononuclear cell (PBMC) proliferation assay, and RANKL mediated osteoclast differentiation of mouse splenocytes (Stem, Proc. Natl. Acad. ScI USA 87:6808 - 6812 (1990); Kong, Y-Y. et al. Nature 397:315 - 323 (1990); Matthews, N. and M. L. Neale m Lymphokines and Interferons, a Practical Approach, 1987, MJ. Clemens, A.C, Morris and AJ. H, Gearing, cds., IRL Press, p. 221)
The term "antibody" as used herein, is entended to refer to immunoglobulin molecules comprised of four polypeptide chains, two heavy (H) chains and two light (L) chains inter- connected by disulfide bonds. Each heavy chain is comprised of a heavy chain variable region (HCVR or YH) and a heavy chain constant region. The heavy chain constant region comprises three domains. CHI, CII2 and Cπ3. Each light chain is comprised of a light chain variable region (LCVR or VL) and a light chain constant region. The light chain constant region is comprised of one domain, CL. The VH and VL regions can be further subdivided into regions of hypervariability, termed complementarity determining regions (CDR), interspersed with regions that are more conserved, termed framework regions (FR). Each VH and VL is composed of three CDRs and four FRs, arranged from amino-terminus to carboxy-teτminus in the following order: FRl, CDRl, FR2, CDR2, FR3, CDR3, FR4.
The term "antigen-binding portion" of an antibody, as used herein refers to one or more components or derivatives of an immunoglobulin that exhibit the ability to bind to an antigen. It has been shown that the antigen-binding function of an antibody can be performed by fragments of a full length antibody. Examples of binding fragments encompassed within the term "antigen-binding portion" of an antibody include (i) a Fab fragment, a monovalent fragment consisting of the VL, VH, CL and CH1 domains; (ii) a F(ab')2 fragment, a bivalent fragment comprising two Fab fragments linked by a disulfide bridge at the hinge region; (iii) a Fd fragment consisting of the VH and CH1 domains; (iv) a Fv fragment consisting of the VL and VH domains of a single arm of an antibody; (v) a dAb fragment (Ward et at, 1989, Nature 341 :544-54ό) which consists of a single VH domain, or a VL domain (van den BeukenT et al, 2001, J. MoI. Bio!, 310, 591); and (vi) an isolated complementarity determining region (CDR). Furthermore, although the two domains of the Fv fragment, VL and Vn, are coded by separate genes, they can be joined, using recombinant methods, by a synthetic linker that enables them to be made as a single protein chain in which the VL and YH regions pair to form monovalent molecules (known as single chain Fv (scFv); (see eg Bird et al., 1988, Science 242:423-426 and Huston et «/., 1988 Proc. Natl. Acad, ScL USA 85:5879-5883). Such single chain Pvs are also intended to be encompassed within the term "antigen-binding portion" of an antibody. Other forms of single chain Fvs and related molecules such as diabodies or triabodies arc also encompassed. Diabodies are bivalent antibodies in which VH and VL domains are expressed on a single polypeptide chain, but using a linker that is loo short to allow for pairing between the two domains on the same chain, thereby forcing Lhe domains to pair with complementary domains of another chain and creating two antigen binding sites (sec e.g., Holliger, P., et al, 1993, Proc. Natl. Acad. Sci. USA, 90:6444-6448; Poljak, R.J., et al., 1994, Structure, 2:1121-1123).
Methods of producing antibodies according to the invention will be familiar to persons skilled in the art, see for example. US Patent No.4,816,567, US Patent No. 5,585,089 and US 20030039649 which are incorporated herein by reference in their entirety. Such methods require the use of standard recombinant techniques,
It is preferred that the antibody or antigen-binding portion thereof according to the present invention has predicted low irnmunogenicily in a human host.
By "low immunυgeiϊicily" it is meant that the antibody does not raise an antibody response in at least the majority of individuals receiving the antibody of sufficient magnitude to reduce the effectiveness of continued administration of the antibody for a sufficient lime to achieve therapeutic efficacy.
The level of immunogenicity in humans may predicted using (lie MHC class II binding prediction program Propred (http://www.imlech.res.in/raghava/propred) using a 1 % threshold value analysis of all alleles. Other programs which may be used include: Rankpep (http://bio.dfci.harvard.edu/Tools/rankpep.html) Epibase (Λlgonomics proprietary software: algonomics.com)
Reduced immunogenicity molecules will contain no or a reduced numbers of peptides predicted to bind to MHC class II alleles that are highly expressed in the target population, relative to the starting donor molecule (Flower DR, Doytchinova IA. (2004)
Figure imgf000011_0001
and the prediction of immunogenicity, Drug Discov Today, 9(2): 82- 90).
Functional analysis of MHC class II binding can be performed by generating overlapping peptides corresponding to the protein of interest and testing these for their ability to evoke T cell activation (T cell proliferation assay) or displace a reporter peptide, a known MHC class n-bindiug peptide (Hammer J et al, 1994, J. Exp. Med., 180:2353).
The term "derived from" as used herein in relation to New World primate framework regions means that the sequence of the New World primate framework region is altered from the native sequence. Typically the changes will be made to increase binding such as described in US Patent No. 5,585,089 and US 20030039649 or to reduce predicted immunogenicity in humans: The term "derived from" does not include changes which result in the total sequence of the framework regions present in the variable region being identical to a human framework sequences. One database which may be used for comparison is httρ://www,ncbi.nlm.nih.gov/.
In a further aspect the present invention provides a designed New World primate antibody or antigen-binding portion thereof which binds a cell surface antigen or a cytokine wherein Lhe antibody or antigen-binding thereof comprises a variable region comprising at least two complementarity detennining regions (CDRs) and al least three framework regions, wherein the CDRs are selected such that the antibody or antigen-binding portion binds to the cell surface antigen or to the cytokine. As used herein the term "designed" means the New World primate CDRs have been selected using the epitope imprinting methods described in Hoogenb<jom et ah, PCT Publication No. WO 93/06213 and Jespers et al, BIO/TECH N OLO GY VoI 12 1994, pp 899-903 which are hereby incorporated in their entirety. The antibody libraries used in this method are preferably scFv libraries prepared and screened as described in McCafferty et al,, PCT Publication No, WO 92/01047, McCafferty et «/., 1990, Nature, 348:552-554; and Griffiths etah, 1993, EMBO J, 12:725-734 which are hereby incorporated by reference in their entirety,
For example, once initial human Vi, and VH segments are selected, "mix and match" experiments, in which different pairs of the initially selected VL and Vn segments arc screened for hTNF-α binding, are performed to select preferred VL/VH pair combinations. Additionally, to further improve the affinity and/or lower the off rate constant for hTNF-α, binding, the V|, and VH segments of the preferred VL/VH pair(s) can be randomly mutated, preferably within the CDR3 region of VH and/or VL, in a process analogous to the in vivo somatic mutation process responsible for affinity maturation of antibodies during a natural immune response. This in vitro affinity maturation can be accomplished by amplifying Vn and VL regions using PCR primers complimentary to the VH CDR3 or VL CDR3, respectively, which primers have been "spiked" with a random mixture of the four nucleotide bases at certain positions such that the resultant I5CR products encode VH and VL segments into which random mutations have been introduced into the VH and/or VL CDR3 regions. These randomly mutated VH and VL segments can be rescreened for binding to the antigen and sequences that exhibit high affinity and a low off rate for antigen binding can be selected.
Following screening and isolation of an antibody or antigen-binding portion thereof which binds the antigen of interest from a recombinant immunoglobulin display library, nucleic acid encoding the selected antibody can be recovered from the display package (c.g., from the phage genome) and subcloned into other expression vectors by standard recombinant DNA techniques. If desired, the nucleic acid can be further manipulated to create other antibody forms of the invention (e.g., linked to nucleic acid encoding additional immunoglobulin domains, such as additional constant regions). To express a recombinant human antibody isolated by screening of a combinatorial library, the DNA encoding the antibody is cloned into a recombinant expression vector and introduced into a mammalian host cells.
Examples of cell surface antigens which may be targeted and antibodies which may be used in the imprinting include but arc not limited to
Figure imgf000013_0001
Examples of cytokines which may be targeted and antibodies which may be used in the imprinting include bul are not limited to
Figure imgf000014_0001
The present invention is further based on a method for amplification of New World primate immunoglobulin genes, for example by polymerase chain reaction (PCR) from nucleic acid extracted from New World primate lymphocytes using primers specific for heavy and light chain variable region gene families. The amplified variable region is then cloned into an expression vector containing a human or primate constant region gene for the production of New World primate chimeric recombinant antibody. Standard recombinant DNA methodologies are used to obtain antibody heavy and light chain genes, incorporate these genes into recombinant expression vectors and introduce the vectors into host cells, such as those described in Sambrook, Fritsch and Maniatis (cds), Molecular Cloning; a laboratory manual, second edition, Cold Spring Harbor, N.Y (1989).
Suitable expression vectors will be familiar to those skilled in the ait. The New World primate lymphocytes producing the immunoglobulins are typically immortalised by fusion with a myeloma cell line to generate a hybridoma.
Preferred mammalian host cells for expressing the recombinant antibodies of the invention include Chinese Hamster Ovary (CHO), NSO myeloma cells, COS cells and SP2 cells.
In addition to mammalian expression systems, the present invention also contemplates the use of non-mammalian expression systems such as those which are plant or prokaryotic (bacterial) derived. Such expression systems would be familiar to persorcs skilled in the art.
The repertoire of VH, VL and constant region domains can be a naturally occurring repertoire of immunoglobulin sequences or a synthetic repertoire, A naturally occurring repertoire is one prepared, for example, from immunoglobulin expressing cells harvested from one or more primates. Such repertoires can be naive ie. prepared from newborn immunoglobulin expressing cells, or rearranged ie. prepared from, for example, adult primate B cells. If desired, clones identified from a natural repertoire, or any repertoire that bind the target antigen are then subject to mutagenesis and further screening in order to produce and select variants with improved binding characteristics.
Synthetic repertoires of immunoglobulin variable domains are prepared by artificially introducing diversity into a cloned variable domain. Such affinity maturation techniques will be familiar to persons skilled in the art such as those described by R.A. Irving et id., 2001, Journal of Immunological Methods, 248, 31-45.
The variable region, or a CDR thereof, of a New World primate antibody gene may be cloned by providing nucleic acid eg. cDNA, providing a primer complementary to the cDNA sequence encoding a 5' leader sequence of an antibody gene, contacting that cDNA and the primer to form a hybrid complex and amplifying the cDN A to produce nucleic acid encoding the variable region (or CDR region) of the New World primate antibody gene.
In view of the teaching of the present specification, it will be appreciated by persons skilled in the art of the present invention, that New World primate variable region sequence may be used as acceptors for the grafting of non-New World primate sequences, in particular, CDR sequences using standard recombinant techniques. For example, US Patent No. 5,585,089 describes methods for creating low imrnunogcnicity chimeric antibodies that retain the high affinity of the non-human parent antibody and contain one or more CDRs from a donor immunoglobulin and a framework region from a human immunoglobulin. United Stales publication no, 20030039649 describes a hunianisation method for creating low immunogemicity chimeric antibodies containing CDR sequences from a non-human antibody and framework sequences of human antibodies based on using canonical CDR structure types of the non-human antibody in comparison to germline canonical CDR structure types of human antibodies as the basis for selecting the appropriate human framework sequences for a humanised antibody. Accordingly, these principles can be applied to the grafting of one or more non-New World primate CDRs into a New World primate acceptor variable region.
Tlic CDR sequences may be obtained from the genomic DNA isolated from an antibody, or from sequences present in a database e.g. The National Centre for Biotechnology Information protein and nucleotide databases, The Kabat Database of Sequences of Proteins of Immunological Interest. The CDR sequence may be a genomic DNA or a cDNA. Methods for grafting a replacement CDR(s) into an acceptor variable sequence will be familiar to persons skilled in the art of the present invention. Typically, the CDRs will be grafted into acceptor variable region sequences for each of a variable light chain and a variable heavy chain or a single chain in the case of a domain antibody. The preferred method of the present invention involves replacement of either CDR 1 or, more preferably, CDR2 in a variable region sequence via primer directed mutagenesis. The method consists of annealing a synthetic oligonucleotide encoding a desired mutation to a target region where it serves as a primer for initiation of DNA synthesis in vitro, extending the oligonucleotide by a .DN A polymerase to generate a double-stranded DNA that carries the desired mutation, ang ligating and cloning the sequence into an appropriate expression vector (Sambrook, Joseph; and David W. Russell (2001). Molecular Cloning: A Laboratory Manual, 3rd ed., Cold Spring Harbor, N. Y.; Cold Spring Harbor Laboratory Press).
Still further, an antibody or antigen-binding portion thereof may be part of a larger immunoadhesion molecule, formed by covalent or noncovalent association of the antibody or antibody portion with one or more other proteins or peptides. Examples of such immunoadhesion molecules include use of the streptavidin core region to make a tetrameric scFv molecule (Kipriyanov, S. M., et al., 1995 Human Antibodies and Hybridomas, 6:93-101) and use of a cysteine residue, a marker peptide and a C-terminai polyhistidinc tag to make bivalent and biotinylated scFv molecules (Kipriyanov, S. M,, et al, 1994 MoI. Immunol, 31 : 1047-1058). Antibody portions, such as Fab and F(ab')2 fragments, can be prepared from whole antibodies using conventional techniques, such as papain or pepsin digestion, respectively, of whole antibodies. Moreover, antibodies, antibody portions and immunoadhesion molecules can be obtained using standard recombinant DNA techniques, as described herein and known to the skilled artisan.
The constant region sequence (Fc portion) is preferably obtained from a human or primate immunoglobulin sequence. The primate sequence may be a New World primate or an Old World primate sequence. Suitable Old World primates include chimpanzee, or other hominid ape eg. gorilla or orang utan, which because of their close phylogcnctic proximity to humans, share a high degree of homology with the human constant region sequence. Sequences which encode for human or primate constant regions are available from databases including e.g. The National Centre for Biotechnology Information protein and nucleotide databases, The Kabat Database of Sequences of Proteins of Immunological Interest. The antibody or antigen-binding portion according to the invention is capable of binding to a human or non-human antigen. Preferably, the antigen to which the chimeric antibody or antigen-binding portion thereof binds, is peptide, protein, carbohydrate, glycoprotein, lipid or glycolipid in nature, selected from a tumour-associated antigen including carcinoembryonic antigen, EpCAM, Lewis-Y, Lewis- Y/b, PMSA, CD20, CD30, CD33, CD38, CD52, CD154, EGF-R, Hcr-2, TRAIL and VEGF receptors, an antigen involved in an immune or inflammatory disease or disorder including CD3, CD4, CD25, CEHO, CD49d, MHC class I, MHC class II, GM- CSF, interferon-γ, IL-I, IL-12, IL-13, IL-23, TNF-α, and IgE, an antigen expressed on a liost cell including glycoprotein Ilb/IIIa, P-glycoprotein, purinergic receptors and adhesion receptors including CDl Ia, CDlIb, CDlIc, CD18, CD56, CD58, CD62 or CD144, an antigen comprising a cyLokine, chemokine, growth factor or other soluble physiological modulator or a receptor thereof including eotaxin, IL-6, lL-8, TGF-β, C3a, C5a, VEGF, NGF and their receptors, an antigen involved in central nervous system diseases or disorders including β-amyloid and prions, an antigen of non-human origin such as microbial, πanobial or viral antigens or toxins including respiratory syncitial virus protein F, anthrax toxin, rattle snake venom and digoxin; wherein the chimeric antibody acts as an agonist or antagonist or is active to either deplete (kill or eliminate) undcsircd cells (eg. anti-CD4) by acting with complement, or killer cells (eg. NK cells) or is active as a cytotoxic agent or to cause Fc-receptor binding by a phagocyte or neutralizes biological activity of its target. More preferably, the antigen is TNFα, most preferably human TN Fa.
Alternatively the antibody or antigen-binding portion thereof may bind a non-human antigen. Preferably the non-human antigen is selected from the group consisting of respiratory syncytial virus F protein, cytomegalovirus, snake venoms and digoxin.
The term "binds to" as used herein, is intended to refer to the binding of an antigen by an immunoglobulin variable region of an antibody with a dissociation constant. (Kd) of lμM or lower as measured by surface plasmon resonance analysis using, for example a BlAcore™ surface plasmon resonance system and BIΛcorc™ kinetic evaluation software (eg. version 2.1). The affinity or dissociation constant (Kd) for a specific binding interaction is preferably about 500 πM to about 50 pM, more preferably about.500 nM or lower, more preferably about 300 nM or lower and preferably at least, about 3(X) nM to about 50 pM, about 200 nM to about 50 pM, and more preferably at least, about 100 nM to about 50 pM, about 75 nM to about 50 pM, about 10 nM to about 50 pM.
The antibodies of the present invention are advantageous in human therapy because the likelihood of induction of a human anti-antibody response will be reduced. Recombinant atibodiess produced according to the invention that bind a target antigen can be identified and isolated by screening a combinatorial immunoglobulin library (e.g., a phage display library) to isolate library members that exhibit the desired binding specificity and functional behaviour (for example neutralisation of TNFα can be measured using L929 cells). It will be understood that all approaches where antigen-binding portions or derivatives of antibodies are used, eg Fabs, scFv and V domains or domain antibodies, lie within the scope of the present invention. The phage display lechnique has been described extensively in the art and examples of methods and compounds for generating and screening such libraries and affinity maturing the products of them can be found in, for example, Barbas et al, 1991, Proc. Natl. Acad. Sci. USA, 88:7978-7982; Clarkson et al.,
1991, Nature, 352:624:628; Dower et al., PCT Publication no. WO 91/17271, US Patent No. 5,427,908, US Patent No. 5,580,717 and EP 527,839; Fuchs et al, 1991, Bio/Technology, 9:1370-1372; Garrad et al, 1991 Bio/Technology, 9:1373: 1377; Garrard el al, PCT Publication no. WO 92/09690; Gram et al,, 1992, Proc. Natl. Acad. Sci. USA, 89:3576-3580; Griffiths et α/., 1993 EMBO J, 12:725:734; Griffiths et al, US Patent No. 5,885,793 and EP 589,877; Hawkins et al, 1992, J MoI Biol, 226:889-896; Hay et al,
1992, Hum Antibod Hybridomas, 3:81-85; Hoogenboom et al, 199J Nuc Acid Res, 19:4133-4137; Huse et aL 1989, Science, 246:1275-1281; Knappik et al, 2000, J MoI Biol, 296:57-86; Knappik et al. PCT WO 97/08320; Ladner et al, US PatenL No. 5,223,409, No. 5,403,484, No. 5,571,698, No. 5,837,500 and EP 436,597; McCafferty et al, 1990, Nature. 348:552-554; McCafferty et al., PCT Publication no. WO 92/01047, US Patent No. 5,969,108 and EP 589,877; Salfeld et al, PCT WO 97/29131, US Provisional Application No. 60/126,603; and Winter et al. PCT WO 92/20791 and EP 368,684;
Recombinant libraries expressing the antibodies of the invention can be expressed on the surface of microorganisms eg. yeast or bacteria (see PCT publications WO99/36569 and 98/49286).
The Selected Lymphocyte Antibody Method or SLAM as it is referred to in the state of the art, is another means of generating high affinity antibodies rapidly. Unlike phage display approaches all antibodies are fully divalent. In order io generate New World primate antibodies, New World primates are immunised with a human antigen eg. a TNFα polypeptide. Following immunisation cells are removed and selectively proliferated in individual micro cells. Supernatants are removed from wells and tested for both binding and function. Gene sequences can be recovered for subsequent manipulations eg. humanisation, Fab fragment, scFv or dAb generation. Thus another example is the derivation of the ligand of the invention by Sl-AM and its derivatives (Babcook, J.S. et al 1996, Proc. Natl. Acad. Sci, USA 93; 7843-7848, US Patent 5,627,052 and PCT publication WO92/Q2551). Adaptations of SLAM, such as the use of alternatives to testing supernatants such as panning, also lie wiihin the scope of this invention.
In one expression system the recombinant peptide/protein library is displayed on ribosomes (for examples see Roberts, RW and Szostak, J.W.1997. Proc.Natl.Acad.Sci.USA. 94: 12297 - 123202 and PCT Publication No. WO98/31700). Thus another example involves the generation and in vitro transcription of a DNA library (eg of antibodies and derivatives) preferably prepared from immunised cells, but not so limited), translation of the library such that the protein and "immunised" mRNAs stay on the ribosome, affinity selection (eg by binding to RSP), mRNA isolation, reverse translation and subsequent amplification (eg by polymerase chain reaction or related technology). Additional rounds of selection and amplification can be coupled as necessary to affinity maturation through introduction of somatic mutation in this system or by other methods of affinity maturation as known in the state of the art (R.Λ. Irving et al. Journal of Immunological Methods, 248, 31-45 (2001)). Another example sees the application of emulsion compartmcntalisatioii technology to the generation of the antibodies of the invention. In emulsion compartmentalisation,,/« vitro and optical sorting methods are combined with co-compartmentalisatioπ of translated protein and its nucleotide coding sequence in aqueous phase within an oil droplet in an emulsion (see PCT publications no's WO99026711 and WO0040712). The main elements for the generation and selection of antibodies are essentially similar to the in vitro method of ribosome display.
The antibody or antigen-binding portion thereof according to the invention can be derivatised or linked to another functional molecule. For example, the antibody or antigen- binding portion can be functionally linked by chemical coupling, genetic fusion, noncovalcnt association or otherwise, to one or more other molecular entities, such as another antibody, a detectable agent, a cytotoxic agent, a pharmaceutical agent, and/or a protein or peptide that can mediate association of the antibody or antigen-binding portion thereof with another molecule (such as a streptavidin core region or a polyhistidiue tag).
Cytotoxic agents commonly used to generate immunotoxins include radioactive isotopes such as ' " In or 90Y, selenium, ribonucleascs, binding domain - deleted truncated microbial toxins such as Pseudomoπas exotoxin or Diphtheria toxin, tubulin inhibitors such as calicheainicin (ozagamicin), maytansinoids (including DM-I), auristatLns, and taxoids, ribosome inactivating proteins such as ricin, ebulin I, saporiti and gelonin, and prodrugs such as melphalan. Useful detectable agents with which an antibody or antigen-binding portion thereof may be dcrivatised include fluorescent compounds. Exemplary fluorescent detectable agents include fluorescein, fluorescein isothiocyanate, rhodarnine, 5-di methyl am ine-1- napthalenesulfonyl chloride, phycoerythrin and the like. An antibody may also be derivalised with detectable enzymes such as alkaline phosphatase, horseradish peroxidase, glucose oxidase and the like. When an antibody is derivatized with a detectable enzyme, it is delected by adding additional reagents that the enzyme uses to produce a detectable reaction product. An antibody may also be dcrivatised with biotin, and detected through indirect measurement of avidin or strcptavidin binding. The present invention also extends to PEGylatcd antibodies or antibody-binding portion which provide increased half-life and resistance to degradation without a loss in activity (e.g., reduction in binding affinity) relative to non-PEGylated antibody polypeptides.
The antibody or antigen-binding portion as described herein can be coupled, using methods known in the art, to polymer molecules (preferably PEG) useful for achieving the increased half-life and degradation resistance properties. Polymer moieties which can be utilised in the invention can be synthetic or naturally occurring and include, but are not limited to, straight or branched chain polyalkylene, polyalkenyleπe or polyoxyalkylene polymers, or a branched or unbranched polysaccharide such as a homo-or heteropolysaccharide. Preferred examples of synthetic polymers which can be used in the invention include straight or branched chain poly(elhylene glycol) (PEG), poly(pxopylene glycol), or polyvinyl alcohol) and derivatives or substituted forms thereof. Particularly preferred substituted polymers for linkage to antibodies as described herein include substituted PEG, including methoxy(polycthylene glycol). Naturally occurring polymer moieties which can be used in addition to or in place of PEG include lactose, amylose, dextran, or glycogen, as well as derivatives thereof which would be recognised by persons skilled in the art,
Derivatized forms of polymer molecules include, for example, derivatives which have additional moieties or reactive groups present therein to permit interaction with amino acid residues of the antibody polypeptides described herein. Such derivatives include N- hydroxylsuccinimide (NHS) active esters, succiπimidyl propionate polymers, and sulfhydryl-selective reactive agents such as maleimide, vinyl sulfone, and thiol.
Particularly preferred derivatized polymers include, but are not limited to PEG polymers having the formulae: PEG-O-CI F2CH2CH2-CO2-NHS; PEG-O-CH2-NHS; PEG-O- CH2CH2-CO2-NHS; PEC-S-CH2CH2-CO-NHS; PIiG-O2CNH-CH(R)-CO2-NHS; PEG- NHCO-CH2CH2-CO-NHS; and PEG-O-CI 1,-CO1-NUS; where R is (CH2)4)NHCO2(mPEG), PEG polymers can be linear molecules, or can be branched wherein multiple PEG moieties are present in a single polymer. The reactive group (e.g., MAL, NHS, SPA; VS, or Thiol) may be attached directly to the PEG polymer or may be attached to PEG via a linker molecule.
The size of polymers useful in the invention can be in the Tange of between 500 Da to 60 kDa, for example, between 1000 Da and 60 kDa, 10 kDa and 60 kDa, 20 kDa and 60 kDa, 30 kDa and 60 kDa, 40 kDa and 60 kDa, and up to between 50 kDa and 60 kDa. The polymers used in the invention, particularly PEG, can be straight chain polymers or may possess a branched conformation.
The polymer (PEG) molecules useful in the invention can be attached to an antibody or •antigen-binding portion thereof using mehtods which are well known in the art. The first step in the attachment of PEG or other polymer moieties to an antibody polypeptide monomer or multimcr of the invention is the substitution of the hydroxyl end-groups of the PEG polymer by olcctrophilc-containing functional groups. Particularly, PEG polymers are attached to cither cysteine or lysine residues present in the antibody polypeptide monomers or multimers. The cysteine and lysine residues can be naturally occurring, or can be engineered into the antibody polypeptide molecule. For example, cysteine residues can be recombinantly engineered at the C-terminus of an antibody polypeptide, or residues at specific solvent accessible locations in an antibody polypeptide can be substituted with cysteine or lysine.
The antibody may be linked to one or more molecules which can increase its half-life in vivo. These molecules are linked to the antibody at a site on the antibody other than the antigen binding site, so that they do not interfere/sterically hinder the antigen-binding site- Typically, such molecules are polypeptides which occur naturally in vivo and which resist degradation or removal by endogenous mechanisms. It will be obvious to one skilled in the art that fragments or derivatives of such naturally occurring molecules may be used, and that some may not be polypeptides. Molecules which increase half life may be selected from the following:
(a) proteins from the extracellular matrix, eg. collagen, laminin, integrin and fibronectin;
(b) proteins found in blood, eg. fibrin α-2 macroglobidin, serum albumin, fibrinogen A, fibrinogen B, serum amyloid protein Λ, heptaglobin, protein, ubiquitin, uteroglobin, β-2 microglobulin, plasminogen, lysozyme, cystalinC, alpha-1-antitrypsin and pancreatic kypsiπ inhibitor;
(c) immune serum proteins, eg. IgE, IgG1 IgM;
(d) transport proteins, eg. retinol binding protein, oc-1 microglobulin; (e) defensins, eg, beta-defensiπ 1, Neutrophil defensins 1, 2 and 3; (f) proteins found at the blood brain barrier or in neural tissues, eg, melanocorlin receptor, myelin, ascorbate transporters;
(g) transferrin receptor specific ligand-Ncuro pharmaceutical agent fusion proteins (see US5977307); brain capillary endothelial cell receptor, transferrin, transferrin receptor, insulin, insulin- like growth factor 1 (IGF 1) receplor, insulin-like growth factor 2 (IGF 2) receptor, insulin receptor;
Qx) proLeins localised to the kidney, eg, polycystin, type IV collagen, organic anion transporter Kl, Heymann's antigen;
(i) proLeins localised to the liver, eg. alcohol dehydrogenase, G250; (j) blood coagulation factor X;
(k) α-l antitrypsin; (1) HNF 1α;
(m) proteins localised lo the lung, eg. secretory component (binds IgA); (n) proteins localised to the Heart,eg. HSP 27; (o) proteins localised to the skin, eg, keratin;
(p) bone specific proteins, such as bone morphogenic proteins (BMPs) eg. BMP-2, -4, -5, -6, -7 (also referred to as osteogenic protein (OP-I) and -8 (OP-2);
(q) tumour specific proteins, eg. human trophoblast antigen, herceptin receptor, oestrogen receptor, cathepsins eg cathepsin B (found in liver and spleen); (r) disease-specific proteins, eg. antigens expressed only on activated T- cells: including LAG-3 (lymphocyte activation gene); osteoprotegerin ligand (OPGL) see Nature 402, 304-309, 1999; OX40 (a member of the TNF receptor family, expressed on activated T cells and lhe only costimulatory T cell molecule known to be specifically up-regulated in human T cell leukaemia virus type-I (HTLV-I)-producing cells - see J. Immunol. 2000 JuI l;16561);263-70; mctalloprotcases (associated with arthritis/cancers), including CG6512 Drosophila, human paraplcgin, human FtsH, human AFG3L2, murine ftsH; angiogenic growth factors, including acidic fibroblast growth factor (FGF- 1), basic fibroblast growth factor (FGF-2), Vascular endothelial growth factor/vascular permeability factor (VF-GFZVPF), transforming growth factor-α (TGF-α), tumor necrosis factor-alpha (TNF- α), angiogenic interieukin-3 (1L-3), interlcukin -8 (IL-8), platelet derived endothelial growth factor (PD- ECGF), placental growth factor (PlGF), midkine platelet-derived growth factor-BB (PDGF), fractalkine;
(s) stress proteins (heat shock proteins); (t) proteins involved in Fc transport; and (u) vitamins eg B 12, Biotin.
In another aspect, the invention provides a pharmaceutical composition comprising an effective amount of the antibody or antigen-binding portion thereof according to the present invention, together with a one or more pharmaceutically acceptable excipient or diluent.
A "pharmaceutically acceptable excipient or diluent" includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorplion delaying agents, and the like that are physiologically compatible. Examples of pharmaceutically acceptable carriers include one or more of water, saline, phosphate buffered saline, dextrose, glycerol, ethanol, and the like as well as combinations thereof. In many cases it will be preferable to include isotonic agents, for example, sugars, polyalcohols such as manitol, sorbitol, or sodium chloride in the composition. The term "effective amount" refers to an amount of an antibody or antigen binding portion thereof (including pharmaceutical compositions comprising the antibody or antigen binding portion thereof) sufficient to treat or ameliorate a specified disease or disorder or one or more of its symptoms and/or to prevenl or reduce the occurrence of the disease or disorder. The term "diagnostically effective amount" or "amounts effective for diagnosis" and cognates thereof, refers to an amount of a antibody or antigen binding portion thereof (including pharmaceutical compositions comprising the antibody or antigen binding portion thereof) sufficient to diagnose a specified disease or disorder and/or one or more of its manifestations, where diagnosis includes identification of the existence of the disease or disorder and/or detection of the extent or severity of the disease or disorder. Often, diagnosis will be carried out with reference to a baseline or background detection level observed for individuals without the disease or disorder. Levels of detection above background or baseline levels (eievated levels of detection) are indicative of the presence and, in some cases, the severity of the condition. When used with respect to methods of treatment and the use of the antibody or antigen binding portion thereof (including pharmaceutical compositions comprising the antibody or antigen binding portion thereof), an individual "in need thereof* may be an individual who has been diagnosed with or previously treated for the disease or disorder to be treated. With respect to methods of diagnosis, an individual 'in need thereof" may be an individual who is suspected to have a disease or disorder, is at. risk for a disease or disorder, or has previously been diagnosed with tine disease or disorder (e.g., diagnosis can include monitoring of the severity (e.g., progression/regression) of the disease or disorder over time and/or in conjunction with therapy). It is preferred that the antibody or antigen-binding portion thereof blocks or stimulates receptors functions or neutralizes active soluble products, such as one or more of the inierleukins, TNF or C5a. More preferably, the active soluble product is human TNF-α.
The composition may be in a variety of forms, including liquid, semi-solid or solid dosage forms, such as liquid solutions (eg injectable and infusible solutions), dispersions or suspensions, tablets, pills, powders, liposomes or suppositories. Preferably, the composition is in the form of an injectable solution for immunization. The administration may be intravenous, subcutaneous, intraperitoneal, intramuscular, transdermal, intrathecal, and intra-arteriai. Preferably the dosage form is in the range of from about 0.001 mg to about 10 mg/kg body weight administered daily, weekly, bi- or tii-weekly or monthly, more preferably about 0.05 to about 5 mg/kg body weight weekly.
The composition may also be formulated as a sterile powder for the preparation of sterile injectable solutions.
In certain embodiments, the active compound may be prepared with a carrier that will protect the compound against rapid release, such as a controlled release formulation, including implants, transdermal patches, and microencapsulated delivery systems. Compatible polymers may be used such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoosters or polylaclic acid.
The composition may also be formulated for oral administration. In this embodiment, the antibody may be enclosed in a hard or soft shell gelatin capsule, compressed into tablets, or incorporated directly into the subject's diet.
The composition may also be formulated for rectal administration.
The antibody may be administered in order to bind to and identify selected cells in viirυ and in vivo, Io bind to and destroy selected cells in vivo, or in order to penetrate into and destroy selected cells in vivo. Alternatively, the antibody may be used as an immunotoxLα to deliver a cytotoxic agent eg. a toxin or chemolherapeutic agent to a particular cell type such as a tumour cell. Production of immunoloxins would be familiar to persons skilled hi the art.
In the preferred embodiment, the composition is administered to a human, The present invention also provides for the use of the antibody or antigen-binding portion thereof in a diagnostic application for detecting an antigen associated with a particular disease or disorder. More particularly, the invention provides for the use of the antibody or antigen-binding portion thereof in a method for diagnosing a subject having an antigen associated with a particular disease or disorder, comprising administering to said subject a diagnostically effective amount of an antibody, an antigen-binding portion thereof or pharmaceutical composition, as described herein, according to the third aspect. Preferably the subject is a human.
The antibody or antigen-binding fragment thereof, preferably labelled, can be used to detect the presence of an antigen, or elevated levels of an antigen (e.g. TNF-α) in a biological sample, such as serum or plasma using a convention immunoassay, such as an enzyme linked immunosorbent assay (ELISA), a radioimmunoassay (RIA) or tissue immunohistochemistry.
Preferably, the antigen to which the chimeric antibody or antigen-binding portion thereof binds, is peptide, protein, carbohydrate, glycoprotein, lipid or glyculipid in nature, selected from a tumour-associated antigen including carciαoembryonic antigen, EpCAM, Lewis-Y, Lcwis-Y/b, PMSA, CD20, CD30, CD33, CD38, CD52, CD154, EGF-R1 Her-2, TRAIL and VEGF receptors, an antigen involved in an immune or inflammatory disease or disorder including CD3, CD4, CD25, CD40, CD49d, MHC class I, MHC class II, GM- CSF, interferon-γ, IL-I, IL-12, IL-13, IL-23, TNF-α, and IgE, an antigen expressed on a host cell including glycoprotein Ilb/UIa, P-glycoproteinτ purinergic receptors and adhesion receptors including CD 1 1 a, CD 1 1 b, CD 1 1 c, CD 18, CD56, CD58, CD62 or CD144, an antigen comprising a cytokine, chemokine, growth factor or other soluble physiological modulator or a receptor thereof including eotaxin, IL-6, IL-8, TGF-β, C3a, C5a, VEGF, NGF and their receptors, an antigen involved in central nervous system diseases or disorders including {."amyloid and prions, an antigen of non-human origin such as microbial, nanobial or viral antigens or toxins including respiratory syncitial virus protein F, anthrax toxin, rattle snake venom and digoxin; wherein the chimeric antibody acts as an agonist or antagonist or is active to either deplete (Mil or eliminate) tindcsired cells (eg. anti-CD4) by acting with complement, or killer cells (eg. NK cells) or is active as a cytotoxic agent or to cause Fc-receptor binding by a phagocyte or neutralizes biological activity of its target.
The anti-human TNF-α antibody or antigen binding portion thereof according to the invention may also be used in cell culture applications where it is desired to inhibit TNF-α activity.
The present invention also provides a method for treating a disease or disorder characterised by human TNF-α activity in a human subject, comprising administering to the subject in need thereof an antibody, an antigen-binding portion thereof or a pharmaceutical composition, as described herein, according to the present invention in which the antibody or antigen-binding portion thereof binds TNF-α.
The term "disease or disorder characterised by human TNF-α activity" as used herein is intended to include diseases or disorders in which the presence of TNF-α in a subject suffering from the disease or disorder has been shown to be or is suspected of being either responsible for or involved in the pathophysiology of the disease or disorder or a factor that contributes to the worsening of the disease or disorder. Accordingly, a disease or disorder in which TNF-α activity is detrimental is a disease or disorder in which inhibition of TNF-α activity is expected to alleviate symptoms and/or progression of the disease or disorder. Such diseases or disorders may be evidenced, for example, by an increase in the concentration of TNF-α in a biological fluid of a subject suffering from lhe disease or disorder (c.g., an increase in the concentration of TNF-α in serum, plasma, synovial fluid etc of the subject), which can be detected, for example, using an antibody of the invention specific for TNF-α.
A disease or disorder characterised by human TNF-α activity is intended to include diseases or disorders in which the presence of TNF-α in a subject suffering from the disease or disorder has been shown to be, or is suspected of being, either responsible for the pathophysiology of the disease or disoτder or a factor which contributes to a worsening of lhe disease or disorder. Preferably, the disease or disorder characterised by human TNF-α activity is selected from the group consisting of sepsis, including septic shock, endoloλic shock, gram negative sepsis and toxic shock syndrome; autoimmune disea.se, including rheumatoid arthritis, rheumatoid spondylitis, osteoarthritis, psoriasis and gouty arthritis, allergy, multiple sclerosis, autoimmune diabetes, autoimmune uveitis and nephrotic syndrome; infectious disease, including fever and myalgias due to infection and cachexia secondary to infection; graft versus host disease; tumour growth or metastasis; pulmonary diseases including adult respiratory distress syndrome, shock lung, chronic pulmonary inflammatory disease, pulmonary sarcoidosis, pulmonary fibrosis and silicosis; inflammatory bowel diseases including Crohn's disease and ulcerative colitis; cardiac diseases; inflammatory bone diseases, hepatitis, coagulation disturbances, burns, reperfusion injury, keloid formation and scar tissue formation.
Supplementary active compounds can also be incorporated into the composition. The antibody or antibody-binding fragment may be co-formulated with and/or administered simultaneously, separately or sequentially with one or more additional therapeutic agents eg. antibodies that bind to other targets such as cytokines or cell surface molecules or alternatively one or more chemical agents that inhibit human TNF-α production or activity. In another aspect, the invention provides a kit comprising a therapeutically effective emount of an antibody or antigen-binding portion of the invention, or a pharmaceutical composition comprising a therapeutically effective amount of an antibody or antigen- binding portion thereof, together with packaging and instructions for use. In certain embodiments, the instructions for use include instructions for how to effectively administer a therapeutic amount of an antibody or antigen-binding portion of the invention.
Throughout this specification the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion, of a staled element, integer or step, or group of elements, integers or steps, but not the exclusion of any other element, integer or step, or group of elements, integers or steps.
All publications mentioned in this specification arc herein incorporated by reference, Any discussion of documents, acts, materials, devices, articles or the like which has been included in the present specification is solely for the purpose of providing a context for the present invention. It is not to be taken as an admission that any or all of these matters form part of lhe prior art base or were common general knowledge in the field relevant, to the present invention as it existed in Australia or elsewhere before the priority date of each claim of this application.
In order that the nature of the present invention may be more clearly understood, preferred forms thereof will now be described with reference to the following non-limiting examples.
EXAMPLE 1
Fusion of a marmoset variable region to a human constant region Materials and methods
Gene Synthesis and Cloning The VN chain (Accession Number: AAM54057, SF,Q ID NO: 1) of the MOG specific marmoset derived antibody was expressed with a human constant region (human IgGl heavy chain CH1, hinge, CH2 & CH3 domains (such as NCBI accession number P01857) (SEQ ID NO: 2)). This was achieved by back translation of the amino acid sequence into a DNA sequence which was optimized for mammalian cell expression using GeneOptimizer technology and synthesized de nova by assembly of synthetic oligonucleotides (GeneArt, Germany). During DNA sequence optimisation tJie specific restriction enzyme sites Asc f and Tth 1 111 were included to allow for future manipulation of the VH region. Following gene synthesis the whole sequence including a Kozak sequence was cloned into the multiple cloning site of the pEE6,4 GS accessory vector (Lonza Biologies). The VL chain (Accession Number: AAM54058, SEQ IO NO: 3) of the MOG specific marmoset derived antibody was expressed with a human kappa light chain constant region (such as NCBI accession number AAA58989) (SEQ ID NO: 4). DNA encoding the light chain (VL- Kappa) amino acid sequence was prepared as described above for the heavy chain. During DNA sequence optimization and synthesis the specific restriction enzyme sites Bsi WI / Rsr TT were included to allow future manipulation of the VL region. Following gene synthesis the whole sequence including a Kozak sequence was cloned into the multiple cloning site of the pEE12.4 GS expression vector (Lonza Biologies). For stable expression the two single gene vectors (pEE6.4- VH-IgG1 and pEE12.4-VL-Kappa) were combined into a double gene vector. This was done by digesting out of the pEE6.4 backbone the heavy chain expression cassette (hCMV-MIE promoter, Kozak sequence, marmoset VH, human constant region and SV40 polyA site) using Not I and BamΑ I. The resultant fragment was subcloned using Not I and BamH I sites into the pEE12.4-VL-Kappa vector downstream of the light chain expression cassette (hCMV-MIE promoter, Kozak sequence, marmoset VL, human Kappa constant region and SV40 polyA site) creating a vector expressing both the heavy and light chains of AB 138 (SEQ ID NOs: 5 and 6).
Transfection nor each transfectioπ 175μl of Lipofectamine 2000 was added to 5mL of Oplimem I media (Invitrogen Cat Nos, 1 1668-027 and 31985-062) in a well of a 6 well plate. In a second well 70μl of the expression vector (70μg) was added to 5 mL of Optimcm I media.
Following a 5 minute room temperature incubation, the contents of the two wells were mixed together and left for a further 20 minute incubation. Following this second incubation the whole transfcction mixture was added to a T175 tissue culture flask containing the CHOKlSV cells. Cells were incubated for 72 to 96 hours and supernatants harvested. Supernatants were centrifuged at 4,0(.X) x g for 5 minutes to pellet, cell debris, and were filter sterilised through 0.22 μm cartridge filter.
Antibody Purification
The supernatant was passed over a I liTrap Protein A column (Amersham Biosciences, Cat No: 17-0402-01) three times at a flow rate of 1 mL/min, The column was then washed with 20 mM sodium phosphate for 40 mins at 1 mL/miπ, The antibody was eluted with OA M citric acid pH 3,5 with fractions collected and immediately neutralised with 1 M Tris- HCl pH 9.0. Antibody samples were then desalted on a PD-IO column (Amersham Bioscicjiccs, Cat No: 17-0851-01). Analysis of the antibody by SDS-PAGE and size- exclusion HPLC confirmed the correct molecular weight, presence of assembled antibody and the concentration of antibody.
Western Blot analysis
The ability of AB 138 to retain binding to the antigen of M26\ rat MOG (inyclin- oligodendrocyte glycoprotein), was investigated by Western B lot. 130 mg of rat spinal cord (IMVS, Australia) was homogenized in 1.8 ml CelLytic M Cell Lysis Reagent (SIGMA, C2978) and incubated for 30 minutes at 4°C Further homogenizatlon was performed by drawing the lysate throu gh a 27gl/2 needle several times followed by centrifugation at 4°C and 13000g for 30 minutes. The pellet and supernatant was diluted into SDS-PAGE sample buffer (125 rnM Tris-HCl pH 6.8, 5% SDS, 0.25% bromophenol blue, 25% glycerol). Along with this 200 μl CHOKlSV cells at 1 X 10° viable cells per ml were spun down at 13000 x g at 4°C for 1 minute and resuspended in 200 μl CclLylic M Cell Lysis Reagent (SlGMA). Following centrifu gation at 4°C and 13000 x g for 30 minutes the supernatant was mixed with the appropriate amount of SDS-PAGE sample buffer. AU samples, along with a sample of molecular weight markers, were run on a 4- 20% No vex pre-cast gel (Invitrogen, Australia) for 2 hours at 120 V. Proteins were then transferred to PVDF (BioRad, Australia) using a western blot apparatus in 1 X Tris- Glycinc Buffer with 20% methanol (BioRad, Cat 161+-0771) at 40C at 250 mA for 2 hours. The membrane was then blocked by incubation with 5 % skim milk powder in PBS for 1 h at room temperature. The membrane was then washed with 1 X PBS three times followed by an overnight incubation at 4°C with AB 138 in PBS at 10 ug/mL. After washing, the membrane was incubated with Goat Anti-human IgG (H+L) HRP conjugate (Sigma, Australia) diluted 1:5000 in 1 X PBS for 1 hour at room temperature. Following washing, bound antibody was detected using the ECL Western Blotting Analysis System, (Amersham Biosciences Cat: RPN2109). A parallel experiment was performed in winch AB138 was replaced with an isotype-matched irrelevant specificity negative control antibody (anti-TNFtx monoclonal antibody) in order to identify any non-specific binding events.
Results After successful protein expression and purification, western blot analysis was performed on AB 138 to determine if it retained binding affinity to rat MOG, AB 138 bound a protein with approximate size of 25 kDa present in the rat spinal cord cleared lysate, a protein not present in cleared CHOKlSV lysate (Figure 1). The negative control antibody did not bind to protein present in either lysate indicating the interaction between AB 138 and the protein of size 25 kDa was not due to artifact or non-specific binding events associated with the human constant τegioπ (Figure 2). This protein matches the expected size of τal MOG minus the signal sequence (24.9 kDa). This result indicates that AB138 retained affinity for rat MOG present in rat spinal cord lysate and demonstrates that a marmoset human fusion antibody can retain antigen binding ability. It can be appreciated by someone skilled in the art that rat MOG could be produced using recombinant DNA technology and the ability of AB 138 to bind rat MOG determined in binding assays such as ELISA or Biacore analysis.
EXAMPLE 2
Engineering of a monoclonal antibody 1. Terminology
A donor sequence is defined as any immunoglobulin sequence derived from a species other then a New World primate.
An acceptor sequence is defined as an immunoglobulin sequence derived from a New World primate. A common residue is a residue that is common (e.g. >30%) at a given amino acid position when determined by comparison with immunoglobulin sequences available for a species.
An uncommon residue is a residue that is uncommon (e.g. < 30%) at a given amino acid position when determined by comparison with the immunoglobulin sequences available for a species. Engineering is the process of transferring structural binding features of a donor sequence into an acceptor sequence such that the structural binding features maintain their binding activity.
A framework amino acid is defined as an amino acid located in an antibody variable re.gioπ but not located in a CDR, 2. Abbreviations
CDR complementarity determining region, MOG, myelin/oligodendrocyte glycoprotein TNF-α , tumour necrosis factor - alpha; VH, variable heavy chain; VL, variable light chain; BSA, bovine serum albumin. 3. Engineering Process
A. Pr oduction of a monoclonal antibody (other than a New World primate monoclonal antibody).
B. Selection of an acceptor immunoglobulin sequence derived from a New World primate, on the basis of high amino acid sequence homology and predicted low immunogenic! ty.
C. Identification of the CDRs for both the donor and acceptor immunoglobulin sequences according to the numbering system of Kabat (See "Sequences of Proteins of Immunological Interest" E. Kabat et al., U.S. Department of Health and Human Services, 1983).
D. Determination of differences in the framework sequence by alignment of donor and acceptor seuqneces
E. Prediction of donor immunoglobulin structure by three dimensional modelling and determination of proximity of the framework sequence differences relative to the CDRs. Optional substitution of acceptor residues with donor residues according to substitution criteria 1& 2 (below)
F. Substitution of the entire acceptor CDR sequences with entire donor CDR sequences.
G. Determination of common residues by comparison of the donor/acceptor framework amino acid sequence with the germ line and available acceptor immunoglobulin framework sequences. Optional substitution of acceptor residues with donor residues according to substitution criterion 3 & 4 (below)
H. Production of a chimeric antibody with acceptor variable regions and human constant regions I. Expression of engineered immunoglobulin protein J. Assay analysis of engineered immunoglobulin protein Substitution criteria:
In generating a engineered antibody based on differences in the framework: sequences, substitutions of an acceptor amino acid with the corresponding donor amino acid may be made aL positions that fall into the following criteria: (i) if the donor residue is predicted capable of interacting with the antigen based on three dimensional modelling;
(ii) if the donor residue is determined to lie within 3.2 A of the donor CDRs based on three dimensional modelling; (iii) if the donor residue is a common in acceptor species immunoglobulin sequences;
(iv) if the donor residue is uncommon in the donor germ line,
The engineered antibody is predicted to be non-immunogenic or of low immunogenicily in humans by selecting appropriate acceptor sequences based on amino acid sequence homology with equivalent human sequences and predicted low immunogenicity, The engineered antibody will bind to the antigen of the donor immunoglobulin with a similar binding affinity to the donor immunoglobulin. The binding affinity of the engineered antibody can be further increased by methods of affinity maturation (R. A. Irving et al Journal of Immunological Methods, 248, 31-45 (2001)). THE ENGINEERING OF MURINE ANTIBODY AB164 TO YIELD ANTIBODY AB197
4. Donor immunoglobulin sequences
Production of a murine hybridoma secreting a monoclonal antibody AB 164 against human TNF-α was produced using hydridoma technology and served as the donor immunoglobulin sequences (SEQ ID NOs: 7 and 8).
5. Selection of acceptor immunoglobulin sequences
The sequence of a monoclonal antibody against rat MOG (myelin/oligodendrocyte glycoprotein) was obtained from Pub Med (http://www.ncbi.nlm.Ti ih.κθv/) and was used as the acceptor sequence. This monoclonal antibody was derived from a common marmoset (white-tuffed-ear marmoset) (Callithrix jacchus), a New World primate. The framework regions of the VH chain (Accession Number: AAM54057, SEQ ID NO: 1) and the VL chain (Accession Number: AAM54058, SEQ ID No: 3) were examined for their predicted immunogenicity in humans by the MHC class IT binding prediction program Proprcd (http://www.imtech.res.in/raghava/propred') using a 1% threshold value analysis of all alleles. A BLAST analysis of the sequence, excluding CDRs, of the VH chain (Accession Number: AAM54057, SEQ TD NO: 1) and the VL chain (Accession Number: ΛAM54O58, SEQ ID No: 3) of the MOO specific antibody identified the closest human homologue heavy chain sequence (Accession Number AAH 19337.1 ; SEQ ID NO: 9) and (he light chain sequence (Accession Number: BAC53922.1 ; SEQ ID NO: 10). n
Notably, this prediction analysis indicates that the selected acceptor heavy chain variable framework region is likely to be less immunogenic than its human equivalent. The acceptor heavy chain variable region had one peptide in the framework, LRPEDTAVY, which is predicted to bind MHC class 11 encoded by alleles DRBl_0101 , DRBl_0102, DRBl J)3O9, Whereas the closest human homoloque heavy chain had three peptides, in the framework, that were predicted to bind to MHC class II. This included the peptide WVRQAPGQGL which is predicted to bind MItC class 11 encoded by alleles DRBJLOlOl, DRBl_0102 and DRB1_0309; the peptide VYMELTS which is predicted to bind MHC class π encoded by alleles DRB 1,0401, DRB IJM08, DRB1_0421, DRBl_042ό, DRBl_1101, DRBl-1128, DRB 1_ 1305; and the peptide LRSEDTAVY, which is predicted to bind MHC class II encoded by alleles DRB1_0M40O1l,, DRBl „0421, DRB1J)426.
The MOG specific light chain variable framework region and the closest human homologue were predicted to be non-immunogenic, 6, Identification of the CDRs in the donor/acceptor variable regions
Using Lhe rules of Kabal (See "Sequences of Proteins of Immunological Interest" E. Kabat el al., U.S. Department of Health and Human Services, 1983) the CDRs were determined for VH and VL chains of AB 164 (SEQ ID NOs: 7 and 8 respectively) and for the VH and VL chains of the marmoset MOG specific immunoglobulin (SEQ ID No: 1 and 3 respectively) (Table 1). .
Figure imgf000033_0001
Table 1: Amino acid positions for the CDRs of VH and VL chains of ΛB164 (SEQ ID NOs: 7 and 8) and MOG-specific immunoglobulin (SEQ ID NOs: 1 and 3) 7. Alignment of donor and acceptor sequences VH chain alignment
The amino acid sequences for the VH chains of AB 164 and MOG specific immunoglobulin (SEO ID NOs; 7 and 1) were aligned (Figure 3). The number of residues differs by one with an extra amino acid located in the CDR3 of the MOG specific immunoglobulin VH chain. Sequence identity between the tow sequences is 63.6 %. The amino acid sequences of the CDRs differ as expected given the different antigen specificities of donor and acceptor antibodies, '['here are 22 amino acid differences between the sequences in the framework regions. VL Chain alignment
The amino acid for the VL chains of AB 164 and MOG specific immunoglobulin (SEQ ID No: 8 and 3) were aligned (Figure 4). The number of residues differs by four additional amino acids located in the CDRl of AB 164. Sequence identity between the two hequences. is 62.3 %. The amino acid sequences of the CDRs differ as expected given the different antigen specificities of donor and acceptor antibodies. There are 23 amino acid differences between the sequences in the framework regions.
8. Predicted three-dimensional moedlling of the VH and the VL chains of AB 164
Using SWISS-PROT three-dimensional prediction modelling software and Deep View (http://swissmodel.expasy.org/ ) a three-dimensional model of the Vn and VL chains of AB 164 was determined. The CDRs were identified. The amino acid differences between the donor and acceptor sequences in the framework region, as determined by alignment described previously, were identified and a prediction made on their proximity to the CDRs (Tables 3 and 4)
9. Substitution of acceptor CDRs with donor CDRs
The CDRs of the VH and VL chains of MOG specific immunoglobulin were replaced with CDRs of the VH and VL chains of AB164 (Table 2)
Figure imgf000035_0001
Table 2: The replacement of the CDRs of the acceptor sequence (MOG specific immunoglobulin) with the CDRs of the donor .sequence (AB164)
10. Determining common residues in the murine germline and marmoset Ig sequences abd selection of engineered framework sequence VIII Chain
The murine germline alignment, of VH regions can be found at http://www.ibt.unam.inx/vir/vh mice directory.html#GL,
Marmoset VH sequences can be obtained from http:// www.ncbi.nhn nih.gov/cπtrez/qιicrv.fcgi?dh=Protein& itool-toolbar by searching for all VH amino acid sequences from Catlithrix jacchux and aligning these sequences. Using alignment tools the common residues in both lhe murine germlines and the available CalUthrixjacchus sequences were determined at each amino acid position where a difference in amino acids LQ the framework sequence between donor and acceptor sequence occurred (Table 3)
Figure imgf000036_0001
Table 3: VH framework differences in the donor/acceptor sequence, their proximity to the CT)Rs and their relative common residues in the conor/acceptor species. A determination of the common residues at each position in the respective murine germline and the available marmoset VH sequences was performed. At selected positions that satisfied a particular criteria the acceptor amino acid was replaced with a donor amino acid and the number ot that criteria is given.; 1. if the donor residue is predicted capable of interacting with the antigen based on three dimensional modelling; '
2. if the donor residue is determined to lie within 3.2 A of the donor CDRs based on three dimensional modelling; 3. if the donor residue is a common residue in acceptor species immunoglobulin sequences; 4. if the donor residue is uncommon in the donor germline.
At positions that fail the criteria the acceptor sequence was used and the criteria listed as None. Note: Uncommon residues are in shaded in grey and substitutions are in bold. *Murine germline contains no sequence data at position 113 and as such marmoset sequence was used here.
In summary, there were 8 framework amino acid substitutions in which acceptor sequence was replaced with donor sequence. There were four amino acids in which the acceptor sequence was substituted with the donor sequence because the donor residue was determined to lie with 3.2 A of the donor CDRs, based on three dimensional modelling, Two amino acid substitutions were made because the donor residues were predicted capable of interacting with the antigen being located on the turn of a loop that is in close proximity (though not less then 3.2 Λ) with CDR-2, Further, two amino acid substitutions were made because the donor residue was found to be common in the acceptor species immunoglobulin sequences available. A further change could also be made at position 97.
VL Chain
The murine germline alignment of VL regions can be found at http://www.ihLunam.mx/vir/vk mice directorv.html#GLvk Marmoset Vi, sequences can be obtained from http://www.πcbi.nlm.nih.gov/entrez/querv.fcgi?db=Protein&itool=tuolbar by searching for all amino acid sequences from Callithrix jacchus and aligning these sequences. Using alignment tools the common residues in the murine germline and the available marmoset immunoglobulin sequences were determined at each amino acid position relative to differences in amino acids in the framework sequence between donor and acceptor sequence (Table 4)
Figure imgf000038_0001
Table 4: VL framework differences in the donor/acceptor sequence, their proximity to the CDRs and their relative common residues in the donor/acceptor species. A determination of the common residues at each position in the respective murine germline sequence and the available marmoset VL sequences was performed. At each position the criteria for selecting differences in framewoek sequence given above was applied, At a position that satisfied a particular criteria the acceptor amino acid was replaced with a donoi amino acid and the numbei of that criteria is given.;
1 if the donor residue is predicted capable of interacting with the antigen based on three dimensional modelling; 2. if the donor residue is determined to He within 3.2 A of the donor CDRs based on three dimensional modelling;
3. if the donor residue is a common residue in acceptor species immunoglobulin sequences;
4. if the donor residue is uncommon in the donor gcrmline.
Ai positions that fail the criteria the acceptor sequence was used and the criteria listed as None.
Note: Uncommon residues arc in shaded in grey and substitutions are in bold. *Murine germline contains no sequence data at position 104 and beyond and as such marmoset sequence was used here.
In summary, there was 1 framework amino acid substitution in which acceptor sequence was replaced with donor sequence as the donor residue was determined to He within 3.2 A of the donor CDRs based on three dimensional modelling,
MATERIALS AND METHODS The AB 164 hybridoma was generated by fusion of splenocytes from mice immunized with human TNF-α, with the myeloma cell line SP2/0-Agl4 by standard methods (Fazekas dc St. Groth, S., el al. Journal of Immunological Methods 35: 1-21 (1980); Sugasawara, R., Journal of Tissue Culture Methods 12: 93-95 (1989)).
1 1. Sequencing of monoclonal antibody AB 164
Tqtal RNA (tRNA) was extracted from 1 x 107 to 1 x. 108 viable cells using RNeasy Mini or Midi columns (QIAgen) according to the manufacturer's instructions. Following quantitation, the tRNA was used as a template for first strand cDNA synthesis using an oligo(dT) primer and Superscript II Reverse Transcriptase (hwitrogen) according to manufacturer's instructions. Finally the tRNA was degraded using RNase H and the remaining single stranded cDNA tagged with a poly-G tail using terminal transferase and dGTP (Roche).
PCR reactions were performed using Hcrculase (Stratagene), a high fidelity polymerase blend. In each case an oligo (dC) was used as the forward primer with an IgGi heavy chain specific or a Kappa light chain specific reverse primer. Following 30 cycles PCR reactions were incubated in the presence of Taq polymerase to add overhanging A bases. The resulting PCR product was then cloned into pGcmT-Easy (Promcga) and transformed into competent Top 10 E coli cells (Invitrogcn). Plasmids were extracted from overnight culture of single colonies using QIAquick Miniprep columns (QIAgen) and quantified. 100 to 500ng were mixed in duplicate with <5.4pmol of either pUC3 forward or pUC3 reverse primer and submitted to cycle sequencing using BigDye v3.1 chemistry (AppliedBiosystcms). Elcctrophoretograms were resolved on ABI PRISM 3700 DNA Analyser and following alignment of derived sequences, manual correction of aberrant base calling was performed. Once four matching sequences (2 forward and 2 reverse) were obtained the sequence of the antibodies variable region was confirmed. These sequences were then translated into amino acid sequences for the heavy and light chains of AB 164 (SEQ ID NOS: 7 and 8) 12. Creation of AB 138 (MOG specific marmoset derived variable region - human constant region chimera) and AB 103 (anti-TNFα murine variable region - human constant region chimera)
The VH region (Accession Number: AAM54057, SEQ ID No: 1) of the acceptor sequence was eΛpressed with a human constant region (human IgG 1 heavy chain CHI , hinge, CH2 & CH3 domains (such as NCBI accession number PO 1.857) (vSEQ ID No:2), The Vt. region (Accession Number: AAM54058, SEQ ID No: 3) of the acceptor sequence was expressed with a human kappa light chain constant domain (such as NCBI accession number AAA58989) (SEQ ID No:4), The resultant chimeric antibody was designated AB 138 (SEQ ID NOs: 5 and 6), This antibody was used as a template into which alterations in the VH and V1, chains were made.
Vj] and VL regions from the fully murine AB 164 (SEQ ID No: 7 and 8) were expressed with the same human constant regions as described above. This chimeric antibody was given the designation AB 103.
Cloning of AB103
The V11 and VL regions from the fully murine AB 164 (SEQ ID No: 7 and 8) were back translated into DNA sequences which were optimized for mammalian cell expression using GcncOptimizer technology and synthesized de novo by assembly of synthetic oligonucleotides (OeneArt, Germany). For the VH gene each sequence was flanked at the 5' end with a Aac I site, a Kozak sequence (GCCACC) and a human IgG gamma leader sequence (amino acid sequence M EWS WVFLFFLS VTTGVHS). At the 3' end the DNA sequence was manipulated to introduce a Tth 1111 restriction enzyme site without compromising the required amino acid sequence. For the VL gene each sequence was flanked at the 5' end with a Bsi WI site, a Kozak sequence (GCCACC) and a human Kappa leader sequence (amino acid sequence MSVPTQVLGLLLLWLTDARC). At the 3' end DNA sequence was manipulated to introduce a Rsr II restriction enzyme site without compromising the required amino acid sequence. Following de novo gene synthesis, the variable regions were provided cloned into a pCRScript vector (Stratagene) and were released by Asc I / Tth 1111 and Bsi WI / Rsr II digestion for the Vn and VL sequences respectively. Released sequences were Iigated into single gene vector backbones derived from the vecLors created to express AB138 prepared by Asc I / Tth 1111 for PEE6,4-VH- IgGi and Bsi WI / Rsr II for pEE12.4-VL-Kappa digestion.
Each gene was Iigated into the prepared backbone using the LigaFast Rapid DNA Ligation System from Promcga (Cat No. M8221). Ligations were then transformed into One Shot Top 10 (chemically competent cells (fnvtrogen Cat No. C4040-03) and positive colonies identified by standard techniques. Λ double gene vector for stable expression was prepared as outlined above (Example 1). Large quantities of the resulting vectors were prepared by midiprep of overnight cultures using QIΛfilter midiprep columns (QIAgen Cat No. 12243). Vectors were prepared for transfection by precipitating 20μg in 100% ethanol with 1/10 volume of 3M sodium acetate (pH5.2) (Sigma Cat Nos. E7023-500ML and S2889 respectively). Following a wash in 70% ethanol vectors were resuspended in 40μl of T.E. pH8.0 (Sigma Cat No. T9285-100ML) at a working concentration of 0.5μg/μl.
13. Creation of engineered monoclonal antibody AU 197 Using the MOG specific immunoglobulin as an acceptor sequence and by replacing the CDRs and nominated residues in the Framework with those of the donor sequence (AB 164), the engineered VH and VL antibody sequences were determined. These variable region protein mequences were expressed with human constant regions (SEQ ID NOs: 2 and 4). The resultant engineered antibody was designated AB197 (SEQ ED NOs: 11 and- 12). Table 5 descirbes the species origin of the CDRs, VH/VL framework and the constant regions for each antibody.
Figure imgf000042_0001
Table 5: Species origin of the CDRs, VD/VI, framework and the constant regions for AB138, AJJ164, AB197, AB103 Cloning of AB 197
By replacing the CDRs and nominated residues in the framework of the acceptor sequence with those of the donor sequence, the engineered VH and VL antibody sequences were determined (SEQ ID No: 11 and 12). The antibody sequence was back translated into DNA sequences and synthesized de novn by assembly of synthetic oligonucleotides (GencΛrt, Germany). During synthesis the relevant restriction enzyme sites were incorporated in the sequence Lo allow cloning and the generation of a double gene vector expressing AB 197 as described previously (Example 1).
14. Expression of AB 103, AB197 and ΛB164
Transfection of AB 103 and AB197
For each transFection 175μl of Lipofcctamine 2000 was added to 5mL of Optimem 1 medi a (Invitrogen Cat Nos. 11668-027 and 31985-062) in a well of a 6 well plate, hi a second well 70μl of the expression vector (70μg) was added to 5 mL of Optimem I media. Following a 5 minute room temperature incubation, the contents of the two wells were mixed together and left for a further 20 minute incubation. Following this second incubation the whole transfection mixture was added a T 175 tissue culture flask contai ning the CHOKlSV cells. Cells were incubated for 72 to 96 hours and supernatants harvested. Supernatants were ceπtrifuged at 4,000 x g for 5 minutes to pellet cell debris, and were filter sterilised through 0.22 μm cartridge filter. Production of murine monoclonal antibody AB 164
Hybridoma cells expressing AB 164 were cultured using standard tissue culture methods and the supernatant harvested and centrifuged at 4,000 x g for 5 minutes to pellet cell debris followed by filter sterilisation through 0.22 μm cartridge filters, Antibody Purification of AB 103, AB 197 and AB 164
The supernatant was passed over a HiTrap Protein Λ column (Amcrsham Bioscicnces, Cat No: 17-0402-01) three times at a flow rate of I mL/min. The column was then washed with 20 roM sodium phosphate for 40 mins at 1 mL/min. The antibody was eluted with 0.1 M citric acid pH 3.5 with fractions collected and immediately neutralised with IM Tris-HCl pH 9.0. Antibody samples were then desalted on a PD- 10 column (Amersham Biosciences, Cat No: 17-0851-01). Analysis of the antibody by SDS-PAGE and size-exclusion HPLC confirmed the molecular weight, presence of assembled antibody and the concentration of antibody.
15. Affinity binding assays Methods
ELISA methods
TNF-α (Peprotech Cat No: 300-01A) was diluted to 1 μg/mL in carbonate coating buffer (10 niM disodium phosphate, 20 mM sodium hydrogen phosphate pH 9.6). 100 μL of this solution was added to each well of a 96 well plate and incubated at 4"C overnight hi a humidified container. The plate was then washed three times with wash buffer (0.01M PBS pH 7.2, 0.05% Tween-20) and then three times with 0.01 M PBS pH 7.2. The wells were then blocked by adding 200 μL blocking buffer (1% w/v BSA in 0.01 M PBS pH 7.2) to each well and incubating the plate at 250C, in a humidified container, for 1 hour. The antibody was diluted in antibody diluent (1% w/v BSA, 0.05% Tween-20 in 0.01 M PBS -pH 7.2) sufficient to generate a titration curve covering the ranges 6.00 μg/mL to 0.0578 ng/mL. The wells were incubated with the antibody for 1 hour at 25 0C. The plate was then washed as previously described. 100 μL of Anti-IgG K + L antibody HRP conjugate (Zymed, Cat No: 81-71200) at 1:2000 in antibody diluent was used to detect bound AB 197 and AB 103. 100 μL of Anti-murinc immunoglobulin antibody HRP conjugate (Dako, Cat No: P0260) at 1 ;2000 in antibody diluent was used to detect bound AB 164. Wells with antibody diluent only were used to measure the background absorbance. After incubaLion at 25°C, in a humidified container, for 1 hour the plate was washed again as previously described. 100 μL TMB substrate solution (Zymed, Cat Nfo: 00-2023) was added to each well and the colour allowed to develop for 4 min. 100 μL of IM HCl was added to terminate the colour development reaction and absorbance was determined at 450 nm (rcf . 620 urn)
ELISA results
ELISA was used to compare the binding of AB164, AB 197 and AB103 to TNF-α coated in the solid phase. From these results all antibodies displayed strong binding for TNF-α with all EC50 values less or equal to 0.68 μg/ml (Figure 5, Table 6). The replacement of a murine constant region (AB 164) with human IgGi constant (AB103) region did not significantly lower the binding affinity as can be seen by comparison of the binding profiles of the antibodies AB 164 and AB 103. Engineering of AB 164 to yield AB 197 did not result in any significant loss of TNF-α binding, as can be seen by comparison of the binding profiles of the antibodies AB164 and AB197. (Figure 5)
Figure imgf000044_0001
Table 6 TNF-α cytotoxicity neutralisation assay using live cells (L-929 neutralisation assay) method
L929 cells (ATCC No: CCH) were cultured in RPMI 1640 (Invitrogen Cat No: 21870- 076) containing 10% foetal bovine serum, 50 μg/mL Penicillin/Streptomycin (Sigma Cat No: P0781), 2 niM L-glutamine (Invitrogen Cat No: 25030-081) and 10 μM 2- mercaptoethanol (Invitrogen Cat No: 21985-023) till the cells reached a 70% level of confluence. Fnto each well of a 96-well tissue culture plate 50 μL media was added.
To investigate the cytotoxicity of TNF-α on L929 cells, 50 μL of TNF-α working solution per well (30 ng/mL) was added to the first column of the plate in triplicate with serial half log dilutions performed across the plate reaching a final concentration of 9 fg/mL. Control wells with 50 μL media without TNF-α were also prepared (V=tOO%). To all wells 50 μL of L929 cells at 5 X 10"5 cells/mL was added. Further control wells were also prepared containing 100 μL of media with no additional cells or TNF-α (background). To all wells Actinomycin D (Sigma Cat No: A1410) at 40 μg/mL was added.
To investigate neutralisation by engineered antibodies against TNF-α a neutralisation assay was performed, 23 μL of antibody at 10 μg/mL was added to the first column of a separate plate in triplicate and serial log dilutions were performed across the plate reaching a final concentration of 30.4 pg/mL. To these wells 50 μL of L-929 cells at 5 X 10'5 cells/mL was added. A further 25 μL of Actinomyrin-D was added to all wells.
All plates were incubated at 37 0C with 5 % CO2 for 20 hours. Following incubation 25 uL MTS/PES CellTiter 96 AQ,)CW8 One Solution Reagent (Promega Cat No: G358B) was edded to all wells and incubated for 2 hours at 37 °C. The absorbance was read at 492nm (ref. 630nm) using an ELlSA plate reader. Average absorbance of all replicate treatments was subtracted from the average absorbance of the no cell and no TNF control wells (background). From this the % Viability of L-929 cells was calculated as:
A492 experimental wells
% Viability = x100
A492 V= 100% viable
TNF-α cytotoxicity neutralisation assay using live cells (L-929 neutralisation assay) results
AB164, AB 197 and AB 103 were able Io neutralise TNF-α -induced cytotoxicity (Figure 6, Table 7),
Figure imgf000045_0001
Table 7 It will be appreciated by persons skilled in the art that numerous variations and/or modifications may be made to Lhe invention as shown in the specific embodiments without departing from the spirit or scope of the invention as broadly described. The present embodiments are, therefore, to be considered in all tcspects as illustrative and not restrictive.

Claims

CLAIMS:-
L. An antibody or antigen-binding portion thereof having a variable region comprising at least two complementarity determining regions (CDRs) and at least three framework, regions, wherein the framework regions are, or are derived from New World primate framework regions, and wherein at least one of the CDRs is a non-New World primate CDR.
2. An antibody or antigen-binding portion thereof according to claim 1 wherein the variable region comprises three CDRs and four framework regions.
3. An antibody or antigen-binding portion thereof according to claim 1 or claim 2 wherein the variable region comprises at least one murine CDR sequence.
4. An antibody or antigen-binding portion thereof according to any one of claims 1 to 3 wherein the variable region comprises at least one mouse CDR sequence.
5. An antibody or antigen-binding portion thereof according to any one of claims 1 to 4 wherein the variable region comprises at least one rat CDR sequence. 6. An antibody or antigen-binding portion thereof according to any one of claims ϊ to 5 wherein the variable region comprises at least one human CDR sequence.
7. An antibody or antigen-binding portion thereof according to any one of claims 1 to 6 wherein the variable region comprises at least one synthetic CDR sequence.
8. An antibody or antigen-binding portion thereof according to any one of claims 1 to 7 wherein the variable region comprises at least one rabbit CDR sequence.
9. An antibody or antigen-binding portion thereof according to any one of claims I to 8 wherein the variable region comprises a combination of CDRs from differing sources.
10. An antibody or antigen-binding portion thereof according to any one of clai ms 1 to 3 wherein the variable region comprises 3 murine CDR sequences,
H . An antibody or antigen-binding portion thereof according to claim 10 wherein, the 3 murine CDR sequences arc mouss eDR sequences.
12, An antibody or anligen-binding portion thereof according to any one of claims 1 to 3 wherein the variable region comprises 3 hiunan CDR sequences.
13. An antibody or antigen-binding portion thereof according to any one of claims 1 to ) 2 wherein the variable region comprises 4 New World primate framework sequences,
14. Ai- antibody or antigen-binding portion thereof according to any one of claims 1 to 12 wherein the variable region comprises 4 framework regions in which the framework regions are derived from New World priπiale framework regions.
15. An antibody or an antigen-binding portion thereof according to any one of claims 1 to 14 wherein the antigen-binding portion is a domain antibody.
16. An antibody or an antigen-binding portion thereof according to any one of claims 1 to 15 wherein the antibody or antigen-binding portion further comprises a human or non-human Old World primate constant region sequence.
17. An antibody or antigen-binding portion thereof according to any one of claims 1 to 16 wherein the New World primate framework regions are from a New World primate selected from the group consisting of marmosets, tamarins, squirrel monkey, titi monkey, spider monkey, woolly monkey, capuchin, uakaris, sakis, night or owl monkey and the howler monkey.
18. An antibody or antigen-binding portion thereof according to claim 17 wherein the New World primate is a marmoset,
19. An antibody or antigen-binding portion according to any one of claims 1 to 18 wherein the antibody or antigen-binding portion binds to an antigen that is peptide, protein, carbohydrate, glycoprotein, lipid or glycolipid in nature, selected from a tumour-associated antigen including carcinoembryoπic antigen, EpCAM, Lewis-Y, Uwis-Y/b, PMSA, CD20, CD30, CD33, CD38, CD52, CD154, EGF- R, Her-2, TRAIL and VBGF receptors, an antigen involved in an immune or inflammatory disease or disorder including CD3, CD4, CD25, CD40, CD49d,
MHC class I, MHC class IT, GM-CSF, interferon-γ, IL-I, EL-12, IL-13, JL-23, TNF-α, and IgE, an antigen expressed on a host cell Including glycoprotein Ub/Nfa, P-glycoprotein, purinergie receptors and adhesion receptors including CDI I a, CDl Ib, CDl Ic, CDl 8, CD56, CD58, CD62 or CD144, an antigen comprising a cytokine, chemokine, growth factor or other soluble physiological modulator or a receptor thereof including eotaxin, IL-6, IL-8, TGF-β, C3a, C5a, VEGF, NGF and their receptors, an antigen involved in central nervous system, diseases or disorders including β-amyloid and prions, an antigen of non-human origin szch as microbial, nanobial or viral antigens or toxins including respiratory syncitial virus protein F, anthrax toxin, rattle snake venom and digoxin; wherein the chimeric antibody acts as an agonist or antagonist or is active to either deplete (kill or eliminate) undesired cells (eg. anti-CD4) by acting with complement, or killer cells (eg. NK cells) or is active as a cytotoxic agent or to cause Fc-receptor binding by a phagocyte or neutralizes biological activity of its target.
20. An antibody or antigen-binding portion thereof according to claim 19 wherein the antigen is human TN Ha.
21. An antibody or antigen-binding portion thereof according to any one of claims 1 to 20 wherein the sequence of at least one framework region is modified to increase binding.
22. An antibody or antigen-binding portion thereof according to any one of claims 1 to 20 wherein the sequence of at least one framework region is modified to decrease predicted immunogenicity in humans.
23. A kit comprising an antibody or an antigen-binding portion thereof according to any one of claims 1 to 22, or a pharmaceutical composition thereof, packaging and instructions for use.
24. A designed New World primate antibody or antigen-binding portion thereof which binds a cell surface antigen or a cytokine wherein the aπlibody or anligeii- binding portion thereof comprises a variable region comprising at least two complementarity determining regions (CDRs) and at least three framework regions, wherein the CDRs are selected such that the antibody or antigen-binding portion binds to the cell surface antigen or to the cytokine.
25. A designed New World primate antibody or antigen-binding portion thereof as claimed in claim 24 wherein the antibody or antigen-binding portion thereof binds to a cell surface antigen selected from the group consisting of CD3, CD20,
CD33, EGF-R, Her-2 and CD25.
26. A designed New World primate antibody or antigen-binding portion thereof as claimed in claim 24 wherein flic antibody or antigen-binding portion thereof binds to TNFα or VEGF. 27. A designed New World antibody or an antigen-binding portion thereof according to any one of claims 24 to 26 wherein the antigen-binding portion is a domain antibody. the A designed New World antibody or an antigen-binding portion thereof according to any one of claims 24 to 27 wherein the antibody or antigen-binding portion further comprises a human or non-human Old World primate constant region sequence. 29. A designed New World antibody or antigen-binding portion thereof according to any one of claims 24 to 28 wherein the New World primate is selected from the group consisting of marmosets, tamarins, squirrel monkey, titi monkey, spider monkey, woolly monkey, capuchin, uakaris, sakis, night or owl monkey and the howler monkey. 30. A designed New World antibody or antigen-binding portion thereof according to claim 29 wherein the New World primate is a marmoset,
31. A designed New World antibody or antigen-binding portion thereof according to any one of claims 24 to 30 wherein the sequence of at least one framework region is modified to increase binding. 32. Λ designed New World antibody or antigen-binding portion thereof according to any one of claims 24 to 31 wherein the sequence of al least one framework region is modified to decrease predicted immunogenicity in humans.
33. A kit comprising a designed New World antibody or an antigen-binding portion thereof according to any one of claims 24 to 32, or a pharmaceutical composition thereof, packaging and instructions for use.
PCT/AU2006/001165 2005-08-15 2006-08-15 Engineered antibodies with new world primate framework regions WO2007019620A1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
EP06774812A EP1945668A4 (en) 2005-08-15 2006-08-15 Engineered antibodies with new world primate framework regions
BRPI0614430-6A BRPI0614430A2 (en) 2005-08-15 2006-08-15 antibody or an antigen binding portion thereof, and kit
CA002619244A CA2619244A1 (en) 2005-08-15 2006-08-15 Engineered antibodies with new world primate framework regions
JP2008526322A JP2009504685A (en) 2005-08-15 2006-08-15 Engineered antibodies using the New World primate framework region
AU2006281980A AU2006281980A1 (en) 2005-08-15 2006-08-15 Engineered antibodies with new world primate framework regions
US11/832,553 US20080095767A1 (en) 2005-08-15 2007-08-01 Engineered antibodies with new world primate framework regions
NO20080799A NO20080799L (en) 2005-08-15 2008-02-14 Reconstructed antibodies with New World primate framework regions

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
AU2005904406 2005-08-15
AU2005904406A AU2005904406A0 (en) 2005-08-15 New World Antibodies
US70933305P 2005-08-17 2005-08-17
US60/709,333 2005-08-17

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US11/832,553 Continuation US20080095767A1 (en) 2005-08-15 2007-08-01 Engineered antibodies with new world primate framework regions

Publications (2)

Publication Number Publication Date
WO2007019620A1 true WO2007019620A1 (en) 2007-02-22
WO2007019620A8 WO2007019620A8 (en) 2007-08-02

Family

ID=37757237

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/AU2006/001165 WO2007019620A1 (en) 2005-08-15 2006-08-15 Engineered antibodies with new world primate framework regions

Country Status (9)

Country Link
US (1) US20080095767A1 (en)
EP (1) EP1945668A4 (en)
JP (1) JP2009504685A (en)
KR (1) KR20080068004A (en)
AU (1) AU2006281980A1 (en)
CA (1) CA2619244A1 (en)
NO (1) NO20080799L (en)
RU (1) RU2008110060A (en)
WO (1) WO2007019620A1 (en)

Cited By (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7846439B2 (en) 2006-02-01 2010-12-07 Cephalon Australia Pty Ltd Domain antibody construct
JP2011530297A (en) * 2008-08-14 2011-12-22 セファロン・オーストラリア・ピーティーワイ・リミテッド Variant domain antibody
WO2012009760A1 (en) 2010-07-20 2012-01-26 Cephalon Australia Pty Ltd Anti-il-23 heterodimer specific antibodies
WO2012021934A1 (en) 2010-08-17 2012-02-23 Csl Limited Humanized anti-interleukin 3 receptor alpha chain antibodies
WO2013059886A1 (en) 2011-10-28 2013-05-02 Patrys Limited Pat-lm1 epitopes and methods for using same
EP2762496A1 (en) 2013-02-05 2014-08-06 EngMab AG Method for the selection of antibodies against BCMA
WO2014122143A1 (en) 2013-02-05 2014-08-14 Engmab Ag Method for the selection of antibodies against bcma
EP2789630A1 (en) 2013-04-09 2014-10-15 EngMab AG Bispecific antibodies against CD3e and ROR1
RU2531523C2 (en) * 2008-06-25 2014-10-20 ИЭсБиЭйТЕК, ЭН АЛЬКОН БАЙОМЕДИКАЛ РИСЕРЧ ЮНИТ ЭлЭлСи Vegf inhibiting stable and soluble antibodies
US9062101B2 (en) 2010-08-14 2015-06-23 AbbVie Deutschland GmbH & Co. KG Amyloid-beta binding proteins
WO2015089585A1 (en) 2013-12-18 2015-06-25 Csl Limited Method of treating wounds
WO2016055592A1 (en) 2014-10-09 2016-04-14 Engmab Ag Bispecific antibodies against cd3epsilon and ror1
WO2016094962A1 (en) 2014-12-19 2016-06-23 Monash University Il-21 antibodies
RU2588467C2 (en) * 2008-06-25 2016-06-27 ИЭсБиЭйТЕК, ЭН АЛЬКОН БАЙОМЕДИКАЛ РИСЕРЧ ЮНИТ ЭлЭлСи Stable and soluble antibodies inhibiting vegf
US9803008B2 (en) 2013-11-28 2017-10-31 Csl Limited Method of treating diabetic nephropathy by administering antibodies to vascular endothelial growth factor B (VEGF-B)
US9822171B2 (en) 2010-04-15 2017-11-21 AbbVie Deutschland GmbH & Co. KG Amyloid-beta binding proteins
WO2018053597A1 (en) 2016-09-23 2018-03-29 Csl Limited Coagulation factor binding proteins and uses thereof
US9951125B2 (en) 2006-11-30 2018-04-24 Abbvie Inc. Aβ conformer selective anti-Aβ globulomer monoclonal antibodies
WO2018083204A1 (en) 2016-11-02 2018-05-11 Engmab Sàrl Bispecific antibody against bcma and cd3 and an immunological drug for combined use in treating multiple myeloma
US10208109B2 (en) 2005-11-30 2019-02-19 Abbvie Inc. Monoclonal antibodies against amyloid beta protein and uses thereof
EP3495389A1 (en) 2011-09-30 2019-06-12 Teva Pharmaceuticals Australia Pty Ltd Antibodies against tl1a and uses thereof
US10464976B2 (en) 2003-01-31 2019-11-05 AbbVie Deutschland GmbH & Co. KG Amyloid β(1-42) oligomers, derivatives thereof and antibodies thereto, methods of preparation thereof and use thereof
WO2019218009A1 (en) 2018-05-16 2019-11-21 Csl Limited Soluble complement receptor type 1 variants and uses thereof
US10538581B2 (en) 2005-11-30 2020-01-21 Abbvie Inc. Anti-Aβ globulomer 4D10 antibodies
EP3670535A1 (en) 2015-08-03 2020-06-24 EngMab Sàrl Monoclonal antibodies against bcma
WO2020168555A1 (en) * 2019-02-22 2020-08-27 武汉友芝友生物制药有限公司 Cd3 antigen binding fragment and application thereof
WO2022013613A2 (en) 2020-07-17 2022-01-20 Onena Medicines S.L. Antibodies against lefty proteins
US11466073B2 (en) 2017-10-18 2022-10-11 Csl Limited Human serum albumin variants and uses thereof
EP4219552A2 (en) 2013-02-07 2023-08-02 CSL Ltd. Il-11r binding proteins and uses thereof
US11725048B2 (en) 2019-12-20 2023-08-15 Hudson Institute of Medical Research CXCL10 binding proteins and compositions thereof

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1969010A4 (en) * 2005-12-20 2009-07-22 Peptech Ltd Anti-inflammatory dab
US20080139790A1 (en) * 2006-12-08 2008-06-12 Jennings Philip A Chimeric antibodies
WO2008104386A2 (en) 2007-02-27 2008-09-04 Abbott Gmbh & Co. Kg Method for the treatment of amyloidoses
KR101852915B1 (en) 2008-04-28 2018-04-27 휴머니건, 아이엔씨. Antibodies to granulocyte-macrophage colony-stimulating factor
US20110178024A1 (en) * 2008-09-29 2011-07-21 Ben Gurion University Of The Negev Research And Development Authority Amyloid beta-peptides and methods of use thereof
US11214610B2 (en) 2010-12-01 2022-01-04 H. Lundbeck A/S High-purity production of multi-subunit proteins such as antibodies in transformed microbes such as Pichia pastoris
US9539324B2 (en) 2010-12-01 2017-01-10 Alderbio Holdings, Llc Methods of preventing inflammation and treating pain using anti-NGF compositions
US9067988B2 (en) 2010-12-01 2015-06-30 Alderbio Holdings Llc Methods of preventing or treating pain using anti-NGF antibodies
AU2011336470B8 (en) 2010-12-01 2017-09-14 Alderbio Holdings Llc Anti-NGF compositions and use thereof
US9884909B2 (en) 2010-12-01 2018-02-06 Alderbio Holdings Llc Anti-NGF compositions and use thereof
US9078878B2 (en) 2010-12-01 2015-07-14 Alderbio Holdings Llc Anti-NGF antibodies that selectively inhibit the association of NGF with TrkA, without affecting the association of NGF with p75
PT2951208T (en) 2013-02-01 2019-12-30 Univ California Anti-cd83 antibodies and use thereof
US10870704B2 (en) 2014-10-23 2020-12-22 Kira Biotech Pty Limited CD83 binding proteins and uses thereof
ES2962885T3 (en) 2015-05-15 2024-03-21 Massachusetts Gen Hospital Tumor necrosis factor receptor superfamily antagonist antibodies
KR20240052871A (en) 2016-04-27 2024-04-23 애브비 인코포레이티드 Methods of treatment of diseases in which il-13 activity is detrimental using anti-il-13 antibodies
EP3877399A4 (en) 2018-11-06 2022-10-19 Alsatech, Inc. Cell-based gene therapy for neurodegenerative diseases

Family Cites Families (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4002531A (en) * 1976-01-22 1977-01-11 Pierce Chemical Company Modifying enzymes with polyethylene glycol and product produced thereby
US4816567A (en) * 1983-04-08 1989-03-28 Genentech, Inc. Recombinant immunoglobin preparations
US5225539A (en) * 1986-03-27 1993-07-06 Medical Research Council Recombinant altered antibodies and methods of making altered antibodies
US5892019A (en) * 1987-07-15 1999-04-06 The United States Of America, As Represented By The Department Of Health And Human Services Production of a single-gene-encoded immunoglobulin
US5223409A (en) * 1988-09-02 1993-06-29 Protein Engineering Corp. Directed evolution of novel binding proteins
US5349052A (en) * 1988-10-20 1994-09-20 Royal Free Hospital School Of Medicine Process for fractionating polyethylene glycol (PEG)-protein adducts and an adduct for PEG and granulocyte-macrophage colony stimulating factor
US5530101A (en) * 1988-12-28 1996-06-25 Protein Design Labs, Inc. Humanized immunoglobulins
US5324844A (en) * 1989-04-19 1994-06-28 Enzon, Inc. Active carbonates of polyalkylene oxides for modification of polypeptides
US20030225254A1 (en) * 1989-08-07 2003-12-04 Rathjen Deborah Ann Tumour necrosis factor binding ligands
US5977307A (en) * 1989-09-07 1999-11-02 Alkermes, Inc. Transferrin receptor specific ligand-neuropharmaceutical agent fusion proteins
US5427908A (en) * 1990-05-01 1995-06-27 Affymax Technologies N.V. Recombinant library screening methods
GB9015198D0 (en) * 1990-07-10 1990-08-29 Brien Caroline J O Binding substance
CA2090126C (en) * 1990-08-02 2002-10-22 John W. Schrader Methods for the production of proteins with a desired function
DE69233628T2 (en) * 1991-07-25 2007-04-26 Biogen Idec Inc., San Diego Recombinant antibodies for human therapy
WO1993011236A1 (en) * 1991-12-02 1993-06-10 Medical Research Council Production of anti-self antibodies from antibody segment repertoires and displayed on phage
JP2002512776A (en) * 1998-04-28 2002-05-08 スミスクライン・ビーチャム・コーポレイション Monoclonal antibodies with reduced immunogenicity
US7235643B2 (en) * 2000-11-07 2007-06-26 Morphotek, Inc. Antibodies and methods for generating genetically altered antibodies with high affinity
US7754208B2 (en) * 2001-01-17 2010-07-13 Trubion Pharmaceuticals, Inc. Binding domain-immunoglobulin fusion proteins
US7070995B2 (en) * 2001-04-11 2006-07-04 City Of Hope CE7-specific redirected immune cells
US20050271663A1 (en) * 2001-06-28 2005-12-08 Domantis Limited Compositions and methods for treating inflammatory disorders
US20060073141A1 (en) * 2001-06-28 2006-04-06 Domantis Limited Compositions and methods for treating inflammatory disorders
AU2002368077B2 (en) * 2001-07-12 2010-03-04 Jefferson Foote Super humanized antibodies
US20080241166A1 (en) * 2002-06-28 2008-10-02 Domantis Limited Ligands that bind a receptor
US7696320B2 (en) * 2004-08-24 2010-04-13 Domantis Limited Ligands that have binding specificity for VEGF and/or EGFR and methods of use therefor
MXPA05008815A (en) * 2003-02-19 2006-05-25 Rinat Neuroscience Corp Methods for treating pain by administering a nerve growth factor antagonist and an nsaid and compositions containing the same.
ES2609102T3 (en) * 2003-06-27 2017-04-18 Bioren, LLC Mutagenesis by review
GB0316294D0 (en) * 2003-07-11 2003-08-13 Polytherics Ltd Conjugated biological molecules and their preparation
TW201319088A (en) * 2003-07-18 2013-05-16 Amgen Inc Specific binding agents to hepatocyte growth factor
CA2543631A1 (en) * 2003-11-07 2005-05-26 Amgen Inc. Monkey immunoglobulin sequences
ATE526037T1 (en) * 2003-12-04 2011-10-15 Vaccinex Inc METHOD FOR KILLING TUMOR CELLS BY TARGETING INTERNAL ANTIGENS EXPOSED ON APOPTOTIC TUMOR CELLS
WO2006105021A2 (en) * 2005-03-25 2006-10-05 Tolerrx, Inc. Gitr binding molecules and uses therefor
EP1969010A4 (en) * 2005-12-20 2009-07-22 Peptech Ltd Anti-inflammatory dab
CN103232540A (en) * 2006-02-01 2013-08-07 赛法隆澳大利亚控股有限公司 Domain antibody construct
US20080139790A1 (en) * 2006-12-08 2008-06-12 Jennings Philip A Chimeric antibodies

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
LANGERMANS J. ET AL.: "Reactivity of human T-lymphocyte-specific antibodies with peripheral blood mononuclear cells and spleen of Aotus azarae ssp. boliviensis (owl monkey)", J. MED. PRIMATOL., vol. 29, 2000, pages 397 - 401, XP008077203 *

Cited By (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10464976B2 (en) 2003-01-31 2019-11-05 AbbVie Deutschland GmbH & Co. KG Amyloid β(1-42) oligomers, derivatives thereof and antibodies thereto, methods of preparation thereof and use thereof
US10538581B2 (en) 2005-11-30 2020-01-21 Abbvie Inc. Anti-Aβ globulomer 4D10 antibodies
US10208109B2 (en) 2005-11-30 2019-02-19 Abbvie Inc. Monoclonal antibodies against amyloid beta protein and uses thereof
US10323084B2 (en) 2005-11-30 2019-06-18 Abbvie Inc. Monoclonal antibodies against amyloid beta protein and uses thereof
US7846439B2 (en) 2006-02-01 2010-12-07 Cephalon Australia Pty Ltd Domain antibody construct
US9951125B2 (en) 2006-11-30 2018-04-24 Abbvie Inc. Aβ conformer selective anti-Aβ globulomer monoclonal antibodies
US10590193B2 (en) 2008-06-25 2020-03-17 Novartis Ag Stable and soluble antibodies inhibiting VEGF
RU2588467C2 (en) * 2008-06-25 2016-06-27 ИЭсБиЭйТЕК, ЭН АЛЬКОН БАЙОМЕДИКАЛ РИСЕРЧ ЮНИТ ЭлЭлСи Stable and soluble antibodies inhibiting vegf
RU2531523C2 (en) * 2008-06-25 2014-10-20 ИЭсБиЭйТЕК, ЭН АЛЬКОН БАЙОМЕДИКАЛ РИСЕРЧ ЮНИТ ЭлЭлСи Vegf inhibiting stable and soluble antibodies
RU2531523C9 (en) * 2008-06-25 2015-04-10 ИЭсБиЭйТЕК, ЭН АЛЬКОН БАЙОМЕДИКАЛ РИСЕРЧ ЮНИТ ЭлЭлСи Vegf inhibiting stable and soluble antibodies
RU2648152C2 (en) * 2008-06-25 2018-03-22 ИЭсБиЭйТЕК, ЭН АЛЬКОН БАЙОМЕДИКАЛ РИСЕРЧ ЮНИТ ЭлЭлСи Stable and soluble antibodies inhibiting vegf
RU2747735C2 (en) * 2008-06-25 2021-05-13 Новартис Аг Stable and soluble antibodies inhibiting vegf
US9090684B2 (en) 2008-06-25 2015-07-28 Esbatech, An Alcon Biomedical Research Unit Llc Stable and soluble antibodies inhibiting VEGF
US9873737B2 (en) 2008-06-25 2018-01-23 Esbatech, An Alcon Biomedical Research Unit Llc Stable and soluble antibodies inhibiting VEGF
RU2696972C1 (en) * 2008-06-25 2019-08-07 ИЭсБиЭйТЕК, ЭН АЛЬКОН БАЙОМЕДИКАЛ РИСЕРЧ ЮНИТ ЭлЭлСи Stable and soluble vegf inhibiting antibodies
JP2011530297A (en) * 2008-08-14 2011-12-22 セファロン・オーストラリア・ピーティーワイ・リミテッド Variant domain antibody
US9822171B2 (en) 2010-04-15 2017-11-21 AbbVie Deutschland GmbH & Co. KG Amyloid-beta binding proteins
US9127057B2 (en) 2010-07-20 2015-09-08 Teva Pharmaceuticals Ausralia Pty Ltd Anti-IL-23 heterodimer specific antibodies
WO2012009760A1 (en) 2010-07-20 2012-01-26 Cephalon Australia Pty Ltd Anti-il-23 heterodimer specific antibodies
US9062101B2 (en) 2010-08-14 2015-06-23 AbbVie Deutschland GmbH & Co. KG Amyloid-beta binding proteins
US10047121B2 (en) 2010-08-14 2018-08-14 AbbVie Deutschland GmbH & Co. KG Amyloid-beta binding proteins
EP2778175A1 (en) 2010-08-17 2014-09-17 CSL Limited Humanized anti-interleukin 3 receptor alpha chain antibodies for use in treating acute myeloid leukemia (AML)
WO2012021934A1 (en) 2010-08-17 2012-02-23 Csl Limited Humanized anti-interleukin 3 receptor alpha chain antibodies
EP3495389A1 (en) 2011-09-30 2019-06-12 Teva Pharmaceuticals Australia Pty Ltd Antibodies against tl1a and uses thereof
WO2013059886A1 (en) 2011-10-28 2013-05-02 Patrys Limited Pat-lm1 epitopes and methods for using same
US10077315B2 (en) 2013-02-05 2018-09-18 Engmab Sàrl Bispecific antibodies against CD3 and BCMA
EP3620468A1 (en) 2013-02-05 2020-03-11 EngMab Sàrl Method for the selection of antibodies against bcma
US9963513B2 (en) 2013-02-05 2018-05-08 Engmab Sàrl Method for the selection of antibodies against BCMA
EP2762496A1 (en) 2013-02-05 2014-08-06 EngMab AG Method for the selection of antibodies against BCMA
US10851171B2 (en) 2013-02-05 2020-12-01 Engmab Sarl Method for the selection of antibodies against BCMA
WO2014122143A1 (en) 2013-02-05 2014-08-14 Engmab Ag Method for the selection of antibodies against bcma
EP4219552A2 (en) 2013-02-07 2023-08-02 CSL Ltd. Il-11r binding proteins and uses thereof
EP2789630A1 (en) 2013-04-09 2014-10-15 EngMab AG Bispecific antibodies against CD3e and ROR1
US9803008B2 (en) 2013-11-28 2017-10-31 Csl Limited Method of treating diabetic nephropathy by administering antibodies to vascular endothelial growth factor B (VEGF-B)
US11261243B2 (en) 2013-11-28 2022-03-01 Csl Limited Methods of treating diabetic nephropathy by administering an anti-vegf-b (vascular endothelial growth factor-b) antibody
US10407498B2 (en) 2013-11-28 2019-09-10 Csl Limited Method of treating diabetic nephropathy in a subject suffering from type 2 diabetes by administering an antibody which inhibits VEGF-B signaling
WO2015089585A1 (en) 2013-12-18 2015-06-25 Csl Limited Method of treating wounds
WO2016055592A1 (en) 2014-10-09 2016-04-14 Engmab Ag Bispecific antibodies against cd3epsilon and ror1
US11952421B2 (en) 2014-10-09 2024-04-09 Bristol-Myers Squibb Company Bispecific antibodies against CD3EPSILON and ROR1
WO2016094962A1 (en) 2014-12-19 2016-06-23 Monash University Il-21 antibodies
EP3670535A1 (en) 2015-08-03 2020-06-24 EngMab Sàrl Monoclonal antibodies against bcma
WO2018053597A1 (en) 2016-09-23 2018-03-29 Csl Limited Coagulation factor binding proteins and uses thereof
US11124577B2 (en) 2016-11-02 2021-09-21 Engmab Sàrl Bispecific antibody against BCMA and CD3 and an immunological drug for combined use in treating multiple myeloma
WO2018083204A1 (en) 2016-11-02 2018-05-11 Engmab Sàrl Bispecific antibody against bcma and cd3 and an immunological drug for combined use in treating multiple myeloma
EP4295918A2 (en) 2016-11-02 2023-12-27 Bristol-Myers Squibb Company Bispecific antibody against bcma and cd3 and an immunological drug for combined use in treating multiple myeloma
US11466073B2 (en) 2017-10-18 2022-10-11 Csl Limited Human serum albumin variants and uses thereof
WO2019218009A1 (en) 2018-05-16 2019-11-21 Csl Limited Soluble complement receptor type 1 variants and uses thereof
EP4410379A2 (en) 2018-05-16 2024-08-07 CSL Ltd. Soluble complement receptor type 1 variants and uses thereof
CN112703013A (en) * 2019-02-22 2021-04-23 武汉友芝友生物制药有限公司 CD3 antigen binding fragment and application thereof
CN112703013B (en) * 2019-02-22 2022-09-30 武汉友芝友生物制药股份有限公司 CD3 antigen binding fragment and application thereof
US11639388B2 (en) 2019-02-22 2023-05-02 Wuhan Yzy Biopharma Co., Ltd. CD3 antigen binding fragment and application thereof
WO2020168555A1 (en) * 2019-02-22 2020-08-27 武汉友芝友生物制药有限公司 Cd3 antigen binding fragment and application thereof
US11725048B2 (en) 2019-12-20 2023-08-15 Hudson Institute of Medical Research CXCL10 binding proteins and compositions thereof
WO2022013613A2 (en) 2020-07-17 2022-01-20 Onena Medicines S.L. Antibodies against lefty proteins

Also Published As

Publication number Publication date
KR20080068004A (en) 2008-07-22
NO20080799L (en) 2008-05-13
EP1945668A1 (en) 2008-07-23
WO2007019620A8 (en) 2007-08-02
US20080095767A1 (en) 2008-04-24
RU2008110060A (en) 2009-09-27
EP1945668A4 (en) 2009-07-22
AU2006281980A1 (en) 2007-02-22
CA2619244A1 (en) 2007-02-22
JP2009504685A (en) 2009-02-05

Similar Documents

Publication Publication Date Title
WO2007019620A1 (en) Engineered antibodies with new world primate framework regions
US20080255343A1 (en) Chimeric antibodies
AU2006281981A1 (en) Chimeric antibodies with new world primate regions
AU2007211829B2 (en) Domain antibody construct
AU2006326937B2 (en) Anti-inflammatory dAb
JP2008515420A (en) Single domain antibody against TNFR1 and method of use thereof
JP2009525031A5 (en)
MX2008002162A (en) Engineered antibodies with new world primate framework regions
NZ569405A (en) Anti-inflammatory domain antibody binding to TNF-alpha
WO2008092209A1 (en) Protein construct with improved properties
MX2008008029A (en) Anti-inflammatory dab

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200680038157.7

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 11832553

Country of ref document: US

WWE Wipo information: entry into national phase

Ref document number: 578/KOLNP/2008

Country of ref document: IN

Ref document number: 12008500361

Country of ref document: PH

WWE Wipo information: entry into national phase

Ref document number: 2006281980

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 2619244

Country of ref document: CA

Ref document number: 565905

Country of ref document: NZ

WWE Wipo information: entry into national phase

Ref document number: MX/a/2008/002162

Country of ref document: MX

WWE Wipo information: entry into national phase

Ref document number: 2008526322

Country of ref document: JP

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 2006281980

Country of ref document: AU

Date of ref document: 20060815

Kind code of ref document: A

WWP Wipo information: published in national office

Ref document number: 2006281980

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 2006774812

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: KR

Ref document number: 1020087006269

Country of ref document: KR

WWE Wipo information: entry into national phase

Ref document number: 2008110060

Country of ref document: RU

WWP Wipo information: published in national office

Ref document number: 11832553

Country of ref document: US

WWP Wipo information: published in national office

Ref document number: 2006774812

Country of ref document: EP

ENP Entry into the national phase

Ref document number: PI0614430

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20080215