Interferon receptor 1 antibodies and their uses

US9453077B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9453077-B2
Application numberUS-201313890494-A
CountryUS
Kind codeB2
Filing dateMay 9, 2013
Priority dateJun 21, 2004
Publication dateSep 27, 2016
Grant dateSep 27, 2016

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The present invention provides isolated human monoclonal antibodies that bind to IFNAR-1 and that are capable of inhibiting the biological activity of Type I interferons. Immunoconjugates, bispecific molecules and pharmaceutical compositions comprising the antibodies of the invention are also provided. The invention also provides methods for inhibiting Type I interferon-mediated disorders using the antibodies of the invention, including methods for treating autoimmune disorders, transplant rejection or Graft Versus Host Disease using the antibodies of the invention.

First claim

Opening claim text (preview).

What is claimed is: 1. An isolated monoclonal antibody, or antigen-binding portion thereof, which specifically binds to human interferon alpha receptor 1 (IFNAR-1), wherein the antibody or antigen-binding portion thereof is selected from the group consisting of: (a) an antibody, or antigen-binding portion thereof, comprising: a heavy chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 1; a heavy chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO:5; a heavy chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO:9; a light chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 13; a light chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO: 17; and a light chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO:21; (b) an antibody, or antigen-binding portion thereof, comprising: a heavy chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO:2; a heavy chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO:6; a heavy chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO: 10; a light chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 14; a light chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO: 18; and a light chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO:22; and (c) an antibody, or antigen-binding portion thereof, comprising: a heavy chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO:4; a heavy chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO:8; a heavy chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO: 12; a light chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 16; a light chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO:20; and a light chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO:24. 2. An isolated monoclonal antibody, or antigen-binding portion thereof, which specifically binds to human interferon alpha receptor 1 (IFNAR-1), wherein the antibody or antigen-binding portion thereof is selected from the group consisting of: (a) an antibody, or antigen-binding portion thereof, comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO:25 and a light chain variable region comprising the amino acid sequence of SEQ ID NO:29; (b) an antibody, or antigen-binding portion thereof, comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO:26 and a light chain variable region comprising the amino acid sequence of SEQ ID NO:30; and (c) an antibody, or antigen-binding portion thereof, comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO:28 and a light chain variable region comprising the amino acid sequence of SEQ ID NO:32. 3. A composition comprising the antibody, or antigen-binding portion thereof, of claim 1 , and a pharmaceutically acceptable carrier. 4. An immunoconjugate comprising the antibody, or antigen-binding portion thereof, of claim 1 , linked to a therapeutic agent. 5. The immunoconjugate of claim 4 , further comprising a pharmaceutically acceptable carrier. 6. The immunoconjugate of claim 4 , wherein the therapeutic agent is a cytotoxin or a radioactive isotope. 7. A method for preparing an anti-IFNAR-1 antibody comprising: (a) providing: (i) a heavy chain variable region antibody sequence comprising a CDR1 sequence that is selected from the group consisting of SEQ ID NOs: 1, 2, and 4, a CDR2 sequence that is selected from the group consisting of SEQ ID NOs: 5, 6, and 8; and a CDR3 sequence that is selected from the group consisting of SEQ ID NOs: 9, 10, and 12; or (ii) a light chain variable region antibody sequence comprising a CDR1 sequence that is selected from the group consisting of SEQ ID NOs: 13, 14, and 16, a CDR2 sequence that is selected from the group consisting of SEQ ID NOs: 17, 18, and 20 and a CDR3 sequence that is selected from the group consisting of SEQ ID NOs: 21, 22, and 24; (b) altering at least one amino acid residue within at least one variable region antibody sequence, said sequence being selected from the heavy chain variable region antibody sequence and the light chain variable region antibody sequence, to create at least one altered antibody sequence; and (c) expressing the altered antibody sequence as a protein. 8. An isolated nucleic acid encoding a heavy chain variable region and a light chain variable region of an anti-IFNAR-1 antibody, or antigen-binding portion thereof, said variable regions comprising: (a) a heavy chain variable region comprising amino acids having the sequence set forth in SEQ ID NO:25; and a light chain variable region comprising amino acids having the sequence set forth in SEQ ID NO:29; (b) a heavy chain variable region comprising amino acids having the sequence set forth in SEQ ID NO:26; and a light chain variable region comprising amino acids having the sequence set forth in SEQ ID NO:30; or (c) a heavy chain variable region comprising amino acids having the sequence set forth in SEQ ID NO:28; and a light chain variable region comprising amino acids having the sequence set forth in SEQ ID NO:32. 9. An isolated nucleic acid encoding a heavy chain variable region of an anti-IFNAR-1 monoclonal antibody, or antigen-binding portion thereof, comprising amino acids having the sequence set forth in SEQ ID NO:25, SEQ ID NO:26, or SEQ ID NO:28. 10. An isolated nucleic acid encoding a light chain variable region of an anti-IFNAR-1 monoclonal antibody, or antigen-binding portion thereof, comprising amino acids having the sequence set forth in SEQ ID NO:29, SEQ ID NO:30, or SEQ ID NO:32. 11. An isolated nucleic acid encoding a heavy chain variable region of an anti-IFNAR-1 monoclonal antibody, or antigen-binding portion thereof, said nucleic acid comprising nucleotides having the sequence set forth in SEQ ID NO:33, SEQ ID NO:34, SEQ ID NO:35 or SEQ ID NO:36. 12. An isolated nucleic acid encoding a light chain variable region of an anti-IFNAR-1 monoclonal antibody, or antigen-binding portion thereof, said nucleic acid comprising nucleotides having the sequence set forth in SEQ ID NO:37, SEQ ID NO:38, or SEQ ID NO:40. 13. An expression vector comprising the nucleic acid of claim 8 . 14. A host cell expressing a polypeptide encoded by the nucleic acid of claim 8 . 15. A transgenic mouse comprising the host cell of claim 14 , wherein the mouse expresses a polypeptide encoded by the nucleic acid.

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Classifications

  • for HIV · CPC title

  • Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

  • for hyperglycaemia, e.g. antidiabetics · CPC title

  • Drugs for immunological or allergic disorders · CPC title

  • of the thyroid hormones, e.g. T3, T4 · CPC title

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What does patent US9453077B2 cover?
The present invention provides isolated human monoclonal antibodies that bind to IFNAR-1 and that are capable of inhibiting the biological activity of Type I interferons. Immunoconjugates, bispecific molecules and pharmaceutical compositions comprising the antibodies of the invention are also provided. The invention also provides methods for inhibiting Type I interferon-mediated disorders using…
Who is the assignee on this patent?
Medarex Inc, Squibb & Sons Llc
What technology area does this patent fall under?
Primary CPC classification C07K16/2866. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 27 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).