AUTHOR=Omer Bilal , Castillo Paul A. , Tashiro Haruko , Shum Thomas , Huynh Mai T. A. , Cardenas Mara , Tanaka Miyuki , Lewis Andrew , Sauer Tim , Parihar Robin , Lapteva Natalia , Schmueck-Henneresse Michael , Mukherjee Malini , Gottschalk Stephen , Rooney Cliona M. TITLE=Chimeric Antigen Receptor Signaling Domains Differentially Regulate Proliferation and Native T Cell Receptor Function in Virus-Specific T Cells JOURNAL=Frontiers in Medicine VOLUME=5 YEAR=2018 URL=https://www.frontiersin.org/journals/medicine/articles/10.3389/fmed.2018.00343 DOI=10.3389/fmed.2018.00343 ISSN=2296-858X ABSTRACT=
The efficacy of T cells expressing chimeric antigen receptors (CARs) for solid tumors has been limited by insufficient CAR T cell expansion and persistence. The use of virus-specific T cells (VSTs) as carriers for CARs may overcome this limitation since CAR-VSTs can be boosted by viral vaccines or oncolytic viruses. However, there is limited understanding of the optimal combination of endodomains and their influence on the native T cell receptor (TCR) in VSTs. We therefore compared the function of GD2.CARs expressing the TCR zeta chain (ζ) alone or combined with endodomains from CD28 and 4-1BB in varicella zoster virus-specific (VZV) T cells. VZVSTs expressing GD2-CARs recognized VZV-derived peptides and killed GD2-expressing tumor cells. However, after repeated stimulation through their native TCR, the expansion of GD2-CAR.CD28ζ-VZVSTs was 3.3-fold greater (