| Literature DB >> 31715131 |
Rachel Grosser1, Leonid Cherkassky2, Navin Chintala1, Prasad S Adusumilli3.
Abstract
Checkpoint blockade (CPB) therapy can elicit durable clinical responses by reactivating an exhausted immune response. However, response rates remain limited, likely secondary to a lack of a tumor-reactive immune infiltrate. Chimeric antigen receptor (CAR) T cells may provide the necessary tumor-targeting immune infiltrate and a highly specific antitumor immune response. This can be further amplified by the addition of CPB agents, which serve to counteract the immune inhibitory environment undermining optimal CAR T cell efficacy. Herein, we review preclinical and clinical combination therapy with CAR T cells and CPB agents, with a focus on solid tumor malignancies.Entities:
Keywords: CAR T cell; PD-1; checkpoint blockade; chimeric antigen receptor; immunotherapy
Mesh:
Substances:
Year: 2019 PMID: 31715131 PMCID: PMC7171534 DOI: 10.1016/j.ccell.2019.09.006
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743