| Literature DB >> 26710685 |
Yun Ji1, James D Hocker2, Luca Gattinoni3.
Abstract
Adoptive T cell-based immunotherapies can mediate complete and durable regressions in patients with advanced cancer, but current response rates remain inadequate. Maneuvers to improve the fitness and antitumor efficacy of transferred T cells have been under extensive exploration in the field. Small non-coding microRNAs have emerged as critical modulators of immune system homeostasis and T cell immunity. Here, we summarize recent advances in our understanding of the role of microRNAs in regulating T cell activation, differentiation, and function. We also discuss how microRNA therapeutics could be employed to fine-tune T cell receptor signaling and enhance T cell persistence and effector functions, paving the way for the next generation of adoptive immunotherapies. Published by Elsevier Ltd.Entities:
Keywords: Adoptive cell transfer; CD8(+) T cells; Microrna (miRNA); T cell differentiation; Tumor immunotherapy
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Year: 2015 PMID: 26710685 PMCID: PMC4862908 DOI: 10.1016/j.smim.2015.11.006
Source DB: PubMed Journal: Semin Immunol ISSN: 1044-5323 Impact factor: 11.130