Anti-IL13 antibodies and uses thereof
View Patent ↗The present invention relates to anti-IL13 antibodies that bind specifically and with high affinity to both glycosylated and non-glycosylated human IL13, does not bind mouse IL13, and neutralize human IL13 activity at an approximate molar ratio of 1:2 (MAb:IL13). The invention also relates to the use of these antibodies in the treatment of IL13-mediated diseases, such as allergic disease, including asthma, allergic asthma, non-allergic (intrinsic) asthma, allergic rhinitis, atopic dermatitis, allergic conjunctivitis, eczema, urticaria, food allergies, chronic obstructive pulmonary disease, ulcerative colitis, RSV infection, uveitis, scleroderma, and osteoporosis.
1. A method for treating atopic dermatitis in a patient, comprising administering to a patient in need thereof an effective amount of a monoclonal anti-interleukin-13 (“IL-13”) antibody that specifically binds human IL-13, wherein the anti-IL-13 antibody comprises a heavy chain variable region and a light chain variable region comprising the complementarity determining regions of an antibody produced by the hybridoma designated with American Type Culture Collection (“ATCC”) accession number PTA-5657.
2. A method for treating atopic dermatitis in a patient, comprising administering to a patient in need thereof an effective amount of a monoclonal anti-IL-13 antibody that specifically binds human IL-13, wherein the anti-IL-13 antibody comprises a heavy chain variable region comprising complementarity determining regions CDRH1, CDRH2 and CDRH3 having the amino acid sequences of SEQ ID NO: 117, SEQ ID NO: 123, and SEQ ID NO: 135, respectively; and wherein the anti-IL-13 antibody comprises a light chain variable region comprising complementarity determining regions CDRL1, CDRL2 and CDRL3 having the amino acid sequences of SEQ ID NO: 99, SEQ ID NO: 104, and SEQ ID NO: 115, respectively.
3. The method of claim 1 , wherein the heavy chain variable region comprises complementarity determining regions CDRH1, CDRH2 and CDRH3 having the amino acid sequences of SEQ ID NO: 117, SEQ ID NO: 123, and SEQ ID NO: 135, respectively.
4. The method of claim 1 , wherein the light chain variable region comprises complementarity determining regions CDRL1, CDRL2 and CDRL3 having the amino acid sequences of SEQ ID NO: 99, SEQ ID NO: 104, and SEQ ID NO: 115, respectively.
5. The method of claim 1 , wherein the anti-IL-13 antibody further comprises human framework regions.
6. The method of claim 2 , wherein the anti-IL-13 antibody comprises the amino acid sequence of SEQ ID NO: 142, and the amino acid sequence of SEQ ID NO: 143.
7. The method of claim 2 , wherein the anti-IL-13 antibody is an IgG antibody.
8. The method of claim 2 , wherein the anti-IL-13 antibody is an IgG1, an IgG2, an IgG3 or an IgG4 antibody.
9. The method of claim 1 , wherein the anti-IL-13 antibody is humanized.
10. The method of claim 2 , wherein the anti-IL-13 antibody is humanized.
11. The method of claim 1 , wherein the anti-IL-13 antibody is a monovalent antibody, a multispecific antibody, a chimeric antibody, a single chain antibody, a Fab fragment, or a F(ab′) fragment.
12. The method of claim 2 , wherein the anti-IL-13 antibody is a monovalent antibody, a multispecific antibody, a chimeric antibody, a single chain antibody, a Fab fragment, or a F(ab′) fragment.
13. The method of claim 1 , wherein the anti-IL-13 antibody is a bispecific antibody.
14. The method of claim 2 , wherein the anti-IL-13 antibody is a bispecific antibody.
15. The method of claim 6 , wherein the anti-IL-13 antibody is a bispecific antibody.
16. The method of claim 10 , wherein the anti-IL-13 antibody is a bispecific antibody.
17. The method of claim 1 , wherein the anti-IL-13 antibody is conjugated to a molecule.
18. The method of claim 2 , wherein the anti-IL-13 antibody is conjugated to a molecule.
19. The method of claim 6 , wherein the effective amount is between 0.1 mg/kg and 20 mg/kg.
20. A method for treating atopic dermatitis in a patient, comprising administering to a patient in need thereof an effective amount of a monoclonal anti-IL-13 antibody that specifically binds human IL-13, wherein the anti-IL-13 antibody comprises a heavy chain variable region comprising complementarity determining regions CDRH1, CDRH2 and CDRH3 and a light chain variable region comprising complementarity determining regions CDRL1, CDRL2 and CDRL3, wherein:
a. CDRH1 has the amino acid sequence of SEQ ID NO: 117, 118, 119, 120, 121 or 122;
b. CDRH2 has the amino acid sequence of SEQ ID NO: 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133 or 134;
c. CDRH3 has the amino acid sequence of SEQ ID NO: 135, 136, 137, 138, 139, 140 or 141;
d. CDRL1 has the amino acid sequence of SEQ ID NO: 99, 100, 101, 102, or 103;
e. CDRL2 has the amino acid sequence of SEQ ID NO: 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, or 114; and
f. CDRL3 has the amino acid sequence of SEQ ID NO: 115 or 116.
21. A method for treating atopic dermatitis in a patient, comprising administering to a patient in need thereof an effective amount of a monoclonal anti-IL-13 antibody that specifically binds human IL-13, wherein the anti-IL-13 antibody binds to the same epitope of human IL-13 as an antibody produced by the hybridoma designated with ATCC accession number PTA-5657.
22. The method of claim 21 , wherein said antibody competitively inhibits binding of an antibody produced by the hybridoma designated with ATCC accession number PTA-5657 to human IL-13 by at least 50%.
23. The method of claim 21 , wherein said antibody competitively inhibits binding of an antibody produced by the hybridoma designated with ATCC accession number PTA-5657 to human IL-13 by at least 60%.
24. The method of claim 21 , wherein said antibody competitively inhibits binding of an antibody produced by the hybridoma designated with ATCC accession number PTA-5657 to human IL-13 by at least 70%.