| Literature DB >> 26525103 |
Philip D Greenberg1,2,3, Sunil R Hingorani1,4,3, Ingunn M Stromnes1,2, Thomas M Schmitt1, Ayaka Hulbert1, J Scott Brockenbrough1, Hieu Nguyen1, Carlos Cuevas5, Ashley M Dotson1, Xiaoxia Tan2, Jennifer L Hotes1.
Abstract
Pancreatic ductal adenocarcinomas (PDAs) erect physical barriers to chemotherapy and induce multiple mechanisms of immune suppression, creating a sanctuary for unimpeded growth. We tested the ability of T cells engineered to express an affinity-enhanced T cell receptor (TCR) against a native antigen to overcome these barriers in a genetically engineered model of autochthonous PDA. Engineered T cells preferentially accumulate in PDA and induce tumor cell death and stromal remodeling. However, tumor-infiltrating T cells become progressively dysfunctional, a limitation successfully overcome by serial T cell infusions that resulted in a near-doubling of survival without overt toxicities. Similarly engineered human T cells lyse PDA cells in vitro, further supporting clinical advancement of this TCR-based strategy for the treatment of PDA.Entities:
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Year: 2015 PMID: 26525103 PMCID: PMC4724422 DOI: 10.1016/j.ccell.2015.09.022
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743