http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2019290691-A1

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filingDate 2017-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3710fbc096e1923ccee86c58bb241fc0
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publicationDate 2019-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2019290691-A1
titleOfInvention Fusion protein for use in the treatment of hvg disease
abstract The invention provides a fusion protein for use in the treatment of HvG disease in a patient having received a transplant, for use in suppressing the host's immune response directed against the transplant. The fusion protein is adapted for use in suppressing the immune rejection of a transplant which contains or expresses HLA-A*02 or SLA-01*0401 in a recipient patient who is negative for HLA-A*02 or SLA-01*0401, i.e. the patient prior to transplantation does not express HLA-A*02 or SLA-01*0401. The fusion protein is a chimeric antigen receptor (CAR), which upon expression in regulatory T-cells (Treg) causes a specific suppressor activity of the regulatory T-cells in the presence of HLA-A*02 or SLA-01*0401.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2021230251-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2022165419-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2019248869-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11730764-B2
priorityDate 2016-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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