Anti-cd3 antibodies and methods of use
US-2015166661-A1 · Jun 18, 2015 · US
US11498965B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11498965-B2 |
| Application number | US-201816754431-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 22, 2018 |
| Priority date | Oct 20, 2017 |
| Publication date | Nov 15, 2022 |
| Grant date | Nov 15, 2022 |
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.
The present invention relates to an anti-CD3 antibody and a pharmaceutical composition for cancer treatment comprising same. The antibody according to the present invention has high affinity and specificity for CD3 and thus can be effectively used in cancer prevention or treatment.
Opening claim text (preview).
The invention claimed is: 1. An antibody or an antigen-binding fragment thereof, said antigen or antigen-binding fragment thereof comprising: (a-1) a light chain variable domain (VL domain) comprising the amino acid sequence of SEQ ID NO: 7 or 8; and (a-2) a heavy chain variable domain (VH domain) comprising the amino acid sequence of SEQ ID NO: 18, 19, 20, or 21, or (b-1) a light chain variable domain (VL domain) comprising the amino acid sequence of SEQ ID NO: 15 or 16; and (b-2) a heavy chain variable domain (VH domain) comprising the amino acid sequence of SEQ ID NO: 18, 19, 20, 21, 22, 23, 24, or 25, wherein the VL domain of (a-1) and (b-1) comprises complementarity determining region (CDR)1 comprising the amino acid sequence of SEQ ID NO: 29, CDR2 comprising the amino acid sequence of SEQ ID NO: 30, and CDR3 comprising the amino acid sequence of SEQ ID NO: 31; and wherein the VH domain of (a-2) and (b-2) comprises complementarity determining region (CDR)1 comprising the amino acid sequence of SEQ ID NO: 32, CDR2 comprising the amino acid sequence of SEQ ID NO: 33, and CDR3 comprising the amino acid sequence of SEQ ID NO: 34. 2. The antibody or the antigen-binding fragment thereof of claim 1 , wherein the antibody or the antigen-binding fragment thereof specifically binds to cluster of differentiation 3 (CD3). 3. The antibody or the antigen-binding fragment thereof of claim 2 , wherein the CD3 includes human-derived CD3 and monkey-derived CD3. 4. The antibody or the antigen-binding fragment thereof of claim 1 , wherein the antibody or the antigen-binding fragment thereof specifically binds to T cells. 5. The antibody or the antigen-binding fragment thereof of claim 4 , wherein the T cells include human-derived T cells and monkey-derived T cells. 6. The antibody or the antigen-binding fragment thereof of claim 1 , wherein the antibody is a humanized antibody. 7. A polynucleotide that encodes the light chain variable domain (VL domain) and the heavy chain variable domain (VH domain) of the antibody or the antigen-binding fragment thereof of claim 1 . 8. An expression vector comprising the polynucleotide of claim 7 . 9. A host cell transformed with the expression vector of claim 8 . 10. A method for producing an antibody that specifically binds to CD3, comprising culturing the host cell of claim 9 . 11. A pharmaceutical composition comprising the antibody or the antigen-biding fragment thereof of claim 1 . 12. A pharmaceutical composition comprising the antibody or the antigen-biding fragment thereof of claim 2 . 13. A pharmaceutical composition comprising the antibody or the antigen-biding fragment thereof of claim 3 . 14. A pharmaceutical composition comprising the antibody or the antigen-biding fragment thereof of claim 4 . 15. A pharmaceutical composition comprising the antibody or the antigen-biding fragment thereof of claim 5 . 16. A pharmaceutical composition comprising the antibody or the antigen-biding fragment thereof of claim 6 .
against the T-cell receptor (TcR)-CD3 complex · CPC title
Antineoplastic agents · CPC title
containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered · CPC title
variable (Fv) region, i.e. VH and/or VL · CPC title
Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.