| CPC C07K 14/7051 (2013.01) [A61K 40/11 (2025.01); A61K 40/22 (2025.01); A61K 40/31 (2025.01); A61K 40/416 (2025.01); A61K 40/418 (2025.01); A61P 37/06 (2018.01); C07K 16/2833 (2013.01); C07K 19/00 (2013.01); C12N 15/85 (2013.01); A61K 2039/505 (2013.01); A61K 2239/38 (2023.05); C07K 2317/622 (2013.01); C07K 2319/00 (2013.01); C07K 2319/03 (2013.01); C07K 2319/33 (2013.01)] | 11 Claims |
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1. A method of treating HvG disease in a patient, comprising administering to said patient a fusion protein comprising a single-chain variable fragment antibody domain (scFv), a hinge, a transmembrane domain, an intracellular hCD28 signalling domain and an intracellular hCD3ζ (hCD3 zeta) signalling domain forming a chimeric antigen receptor having specificity for HLA-A*02 (CAR-A*02), wherein the fusion protein is expressed in a CD4+CD25+CD127low human regulatory T (Treg) cell, which Treg that express the CAR-A*02 is HLA-A*02 negative, wherein the patient is HLA-A*02 negative and contains or is intended to contain a solid tissue transplant which is HLA-A*02 positive.
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