| CPC A61K 39/39558 (2013.01) [A61K 39/12 (2013.01); A61K 39/245 (2013.01); A61K 39/285 (2013.01); A61K 40/11 (2025.01); A61K 40/31 (2025.01); A61K 40/4211 (2025.01); A61K 40/46 (2025.01); A61P 31/20 (2018.01); A61P 35/00 (2018.01); C07K 14/00 (2013.01); C07K 14/005 (2013.01); C07K 14/7051 (2013.01); C07K 14/70514 (2013.01); C07K 14/70517 (2013.01); C07K 14/70578 (2013.01); C07K 16/2803 (2013.01); C12N 5/0636 (2013.01); C12N 15/86 (2013.01); A61K 2039/5256 (2013.01); A61K 2039/585 (2013.01); C07K 2319/03 (2013.01); C07K 2319/33 (2013.01); C12N 2710/16122 (2013.01); C12N 2710/16134 (2013.01); C12N 2710/24134 (2013.01); C12N 2710/24143 (2013.01)] | 10 Claims |
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1. A method for treating a patient suffering from lymphoma expressing CD19 comprising:
(a) providing a composition comprising a population of T cells expressing both a chimeric antigen receptor (CAR) targeted to CD19 and a T cell receptor that binds a cytomegalovirus (CMV) antigen pp65;
(b) administering the composition of part (a) to the patient; and
(c) administering to the patient a viral vector encoding:
(i) CMV pp65 and
(ii) a fusion protein comprising exon 4 of CMV protein IE1 (e4) and exon 5 of CMV protein IE2 (e5).
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