Method of modifying isoelectric point of antibody via amino acid substitution in CDR
US-9096651-B2 · Aug 4, 2015 · US
US12516115B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12516115-B2 |
| Application number | US-202318450863-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 16, 2023 |
| Priority date | Aug 5, 2016 |
| Publication date | Jan 6, 2026 |
| Grant date | Jan 6, 2026 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
For example, therapeutic methods and the like for novel IL-8-related diseases using an IL-8 signal inhibitor are provided. Alternatively, for example, therapeutic methods and the like for known or novel IL-8-related diseases using a novel anti-IL-8 antibody are provided.
Opening claim text (preview).
The invention claimed is: 1 . A method of inhibiting IL-8, which comprises administering an anti-IL-8 antibody that binds to human IL-8 to a subject in need thereof, wherein the subject suffers from an IL-8-related disease selected from the group consisting of chronic obstructive pulmonary disease (COPD), cystic fibrosis, psoriasis, hepatic fibrosis, renal fibrosis, and pulmonary fibrosis, and wherein the anti-IL-8 antibody comprises: (a) the amino acid sequence of SEQ ID NO: 23 as HVR-H1, (b) the amino acid sequence of SEQ ID NO: 29 as HVR-H2, (c) the amino acid sequence of SEQ ID NO: 30 as HVR-H3, (d) the amino acid sequence of SEQ ID NO: 26 as HVR-L1, (e) the amino acid sequence of SEQ ID NO: 31 as HVR-L2, and (f) the amino acid sequence of SEQ ID NO: 32 as HVR-L3. 2 . The method of claim 1 , wherein the anti-IL-8 antibody comprises a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 34 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 35. 3 . The method of claim 2 , wherein the anti-IL-8 antibody comprises a heavy chain comprising the amino acid sequence of SEQ ID NO: 36 and a light chain comprising the amino acid sequence of SEQ ID NO: 38. 4 . The method of claim 2 , wherein the anti-IL-8 antibody comprises a heavy chain comprising the amino acid sequence of SEQ ID NO: 37 and a light chain comprising the amino acid sequence of SEQ ID NO: 38. 5 . The method of claim 1 , wherein the disease is COPD. 6 . The method of claim 1 , wherein the disease is cystic fibrosis. 7 . The method of claim 1 , wherein the disease is psoriasis. 8 . The method of claim 1 , wherein the disease is hepatic fibrosis. 9 . The method of claim 1 , wherein the disease is renal fibrosis. 10 . The method of claim 1 , wherein the disease is pulmonary fibrosis. 11 . The method of claim 2 , wherein the disease is COPD. 12 . The method of claim 2 , wherein the disease is cystic fibrosis. 13 . The method of claim 2 , wherein the disease is psoriasis. 14 . The method of claim 2 , wherein the disease is hepatic fibrosis. 15 . The method of claim 2 , wherein the disease is renal fibrosis. 16 . The method of claim 2 , wherein the disease is pulmonary fibrosis.
Stability, e.g. half-life, pH, temperature or enzyme-resistance · CPC title
Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value · CPC title
Framework region [FR] · CPC title
Complementarity determining region [CDR] · CPC title
variable (Fv) region, i.e. VH and/or VL · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.