Anti-vista antibodies and fragments, uses thereof, and methods of identifying same
US-2017233479-A1 · Aug 17, 2017 · US
US11603403B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11603403-B2 |
| Application number | US-201715489245-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 17, 2017 |
| Priority date | Apr 15, 2016 |
| Publication date | Mar 14, 2023 |
| Grant date | Mar 14, 2023 |
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The invention provides agonistic anti-human VISTA antibodies and antibody fragments. These agonist antibodies and antibody fragments may be used to potentiate or enhance or mimic VISTA's suppressive effects on T cell immunity and thereby suppress T cell immunity. These agonist antibodies and antibody fragments are especially useful in the treatment of autoimmunity, allergy, inflammatory conditions, GVHD, sepsis and transplant recipients. Screening assays for identifying these agonists are also provided.
Opening claim text (preview).
The invention claimed is: 1. A method of treating or preventing graft versus host disease comprising administering to a patient in need thereof a therapeutically or prophylactically effective amount of a full length isolated antibody comprising an antigen binding region that specifically binds to human V-domain Ig Suppressor of T cell Activation (human VISTA), wherein the antibody agonizes or promotes one or more of the effects of VISTA on immunity, wherein said antibody is an agonistic anti-human VISTA antibody comprising a light chain which comprises the light chain CDR 1, CDR2 and CDR3 polypeptides of SEQ ID NO.: 743, 744 and 745 respectively, and comprising a heavy chain comprising the heavy chain CDR 1, CDR2 and CDR3 polypeptides of SEQ ID NO.: 740, 741 and 742 respectively, which full length antibody comprises a human IgG2 constant region or human IgG2 Fc region. 2. The method of claim 1 , wherein the light chain of said antibody comprises a V L polypeptide which possesses at least 90% sequence identity to the V L polypeptide of SEQ ID NO:748. 3. The method of claim 2 , wherein the heavy chain of said antibody comprises a V H polypeptide which possesses at least 90% sequence identity to the V H polypeptide of SEQ ID NO:746. 4. The method of claim 1 , wherein the light chain of said antibody comprises a V L polypeptide which possesses at least 95% sequence identity to the V L polypeptide of SEQ ID NO:748. 5. The method of claim 4 , wherein the heavy chain of said antibody comprises a V H polypeptide which possesses at least 95% sequence identity to the V H polypeptide of SEQ ID NO:746. 6. The method of claim 1 , wherein the light chain of said antibody comprises a V L polypeptide is identical to the V L polypeptide of SEQ ID NO:748. 7. The method of claim 6 , wherein the heavy chain of said antibody comprises a V H polypeptide which is identical to the V H polypeptide of SEQ ID NO:746. 8. The method of claim 1 , wherein the heavy chain of said antibody comprises a V H polypeptide which possesses at least 90% sequence identity to the V H polypeptide of SEQ ID NO:746. 9. The method of claim 1 , wherein the heavy chain of said antibody comprises a V H polypeptide which possesses at least 95% sequence identity to the V H polypeptide of SEQ ID NO:746. 10. The method of claim 1 , wherein the heavy chain of said antibody comprises a V H polypeptide which is identical to the V H polypeptide of SEQ ID NO:746. 11. The method of claim 1 , wherein said antibody is administered in combination with another immunosuppressant drug.
Medicinal preparations containing antigens or antibodies (materials for immunoassay G01N33/53) · CPC title
Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof {(enzyme inhibitors A61K38/005)} · CPC title
Receptors; Cell surface antigens; Cell surface determinants {(tumour specific antigens C07K14/4748)} · CPC title
against immunoglobulins · CPC title
Hybrid immunoglobulins (hybrids of an immunoglobulin with a peptide not being an immunoglobulin C07K19/00) · CPC title
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