Compositions and methods for increasing protein half-life in a serum
US-2019330370-A1 · Oct 31, 2019 · US
US9708409B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9708409-B2 |
| Application number | US-201414157061-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 16, 2014 |
| Priority date | Apr 12, 2000 |
| Publication date | Jul 18, 2017 |
| Grant date | Jul 18, 2017 |
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 invention concerns a method for obtaining and selecting monoclonal antibodies by an ADDC-type test, said antibodies capable of activating type III Fcy receptors and having a particular glycan structure. The inventive anti-D antibodies can be used for preventing Rhesus isoimmunisation in Rh negative persons, in particular for haemolytic disease in a new-born baby of for uses such as idiopathic thrombocytopenic pupura 9ITP).
Opening claim text (preview).
What is claimed is: 1. A cell culture producing monoclonal antibodies having on the Fcγ glycosylation site (Asn 297, EU numbering) bi-antennary glycan structures, wherein said glycan structures of the monoclonal antibodies have a fucose content less than 30%, and wherein said monoclonal antibodies are IgG antibodies directed against an antigen and activate effector cells expressing Fcγ type III receptors. 2. The cell culture of claim 1 , wherein the fucose content is less than 25%. 3. The cell culture of claim 2 , wherein the fucose content is less than 20%. 4. The cell culture of claim 1 , wherein the antigen is rhesus D. 5. The cell culture of claim 2 , wherein the antigen is rhesus D. 6. The cell culture of claim 1 , wherein the monoclonal antibodies are IgG1 antibodies. 7. The cell culture of claim 1 , wherein the monoclonal antibodies are IgG3 antibodies. 8. The cell culture of claim 1 , wherein said glycan structures of the monoclonal antibodies have a sialic acid content of less than 25%. 9. The cell culture of claim 1 , wherein the cell culture comprises a clone produced by transfection of a cell line with a gene coding for said monoclonal antibodies. 10. The cell culture of claim 9 , wherein the cell culture comprises a clone produced by transfection of a cell line deposited with the ATCC as accession number CRL-1662. 11. The cell culture of claim 1 , wherein the cell culture comprises a clone isolated from a cell line transfected with a gene coding for said monoclonal antibodies. 12. The cell culture of claim 11 , wherein the cell culture comprises a clone isolated from a cell line deposited with the ATCC as accession number CRL-1662 transfected with a gene coding for said monoclonal antibodies. 13. The cell culture of claim 1 , wherein the fucose content is between 20% and 30%. 14. The cell culture of claim 1 , wherein the fucose content is between 25% and 30%. 15. The cell culture of claim 1 , wherein the antigen is an infectious disease antigen. 16. The cell culture of claim 1 , wherein the antigen is a cancer antigen.
Immunosuppressants, e.g. drugs for graft rejection · CPC title
Drugs for disorders of the blood or the extracellular fluid · CPC title
Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents · CPC title
Immunostimulants · CPC title
Antibacterial agents · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.