Methods and materials for the induction of T cell anergy

{
  "publication_number": "US5747034A",
  "country": "US",
  "kind": "A",
  "title": "Methods and materials for the induction of T cell anergy",
  "abstract": "Anti-B7-1 antibodies or other B7-1 ligands may be used to prevent or treat a T-cell-mediated immune system disease in a patient or to induce antigen-specific tolerance. The anti-B7-1 antibodies may be used to cause T cell anergy, treat allograft transplant rejection, treat graft versus host disease, and prevent or treat rheumatoid arthritis. An immunosuppressive agent is co-administered with the antibody.",
  "claims": [
    "1. A method for treating transplant rejection in a patient, the method comprising administering to a patient in need of such treatment a therapeutically effective amount of (a) an antibody or an antigen binding fragment thereof that binds to the B7-1 antigen but not to the B7-2 and B7-3 antigens; and (b) an immunosuppressive agent in a pharmaceutically acceptable excipient.",
    "2. A method for treating graft versus host diseases (GVHD) in a patient, the method comprising administering to a patient in need of such treatment a therapeutically effective amount of (a) an antibody or an antigen binding fragment thereof that binds to the B7-1 antigen but not to the B7-2 and B7-3 antigens; and (b) an immunosuppressive agent in a pharmaceutically acceptable excipient.",
    "3. A method for treating rheumatoid arthritis in a patient, the method comprising administering to a patient in need of such treatment a therapeutically effective amount of (a) an antibody or an antigen binding fragment thereof that binds to the B7-1 antigen but not to the B7-2 and B7-3 antigens; and (b) an immunosuppressive agent in a pharmaceutically acceptable excipient.",
    "4. The method of claim 1, 2, 3, wherein the antibody binds to the B7-1 antigen is an anti-B7-1 antibody.",
    "5. The method of claim 1, 2, 3, wherein the immunosuppressive agent is selected from the group consisting of cyclosporin A, FK506, rapamycin and corticosteroids.",
    "6. Monoclonal antibody B7-24 produced by the hybridoma cell line designated ATCC HB11341.",
    "7. The method of claim 4 wherein the anti-B7-1 antibody is a monoclonal antibody.",
    "8. The method of claim 7 wherein the monoclonal antibody is a humanized monoclonal antibody.",
    "9. The method of claim 1, 2, 3, wherein said antibody is an antigen binding fragment of an anti B7-1 antibody that retains the antigen binding function of said antibody.",
    "10. The method of claim 7 wherein the monoclonal antibody is Mab B7-24 produced by the hybridoma cell line designated ATCC HB 11341.",
    "11. The hybridoma cell line ATCC HB 11341 which specifically produces monoclonal antibody B7-24.",
    "12. A composition for inducing T cell anergy comprising in combination: a) a monoclonal antibody or an antigen binding fragment thereof, said antibody or fragment capable of specifically binding to the B7-1 antigen but not to the B7-2 and B7-3 antigens on the surface of an antigen presenting cell, and b) an immunosuppressive agent; said antibody or fragment and said immunosuppressive agent each being present in an amount that is effective to induce a T cell anergy by the combination that is greater than the sum of the T cell anergies induced by the same amount of each of the components alone.",
    "13. The composition of claim 12 wherein the monoclonal antibody is B7-24 and the antigen binding fragment is a fragment of monoclonal antibody B7-24 produced by the hybridoma cell line designated ATCC HB 11341.",
    "14. The composition of claim 12 wherein the immunosuppressive agent is a member selected from the group consisting of cyclosporin A, FK506, rapamicin and corticosteroids.",
    "15. The composition of claim 12 wherein said monoclonal antibody is a humanized monoclonal antibody.",
    "16. The composition of claim 12 comprising in combination said antigen binding fragment and said immunosuppressive agent.",
    "17. The composition of claim 16 wherein said antigen binding fragment has a humanized component."
  ],
  "cpc": [
    "C07K 16/2827",
    "A61K 2039/505",
    "A61K 38/00",
    "A61K 39/395",
    "A61P 19/02",
    "A61P 29/00",
    "A61P 37/02",
    "A61P 37/06",
    "C07K 14/70532",
    "C07K 16/2878",
    "C07K 2317/24",
    "C07K 2317/73",
    "C07K 2319/30",
    "C12N 2799/026",
    "Y10S 530/809"
  ],
  "assignees": [
    "CHIRON CORP"
  ],
  "filing_date": "1994-02-18",
  "publication_date": "1998-05-05",
  "grant_date": "1998-05-05",
  "priority_date": "1992-07-09",
  "application_number": "US-20071694-A",
  "family_id": "22742885",
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  ]
}