| Literature DB >> 29634943 |
Daniela S Thommen1, Ton N Schumacher2.
Abstract
Therapeutic reinvigoration of tumor-specific T cells has greatly improved clinical outcome in cancer. Nevertheless, many patients still do not achieve durable benefit. Recent evidence from studies in murine and human cancer suggest that intratumoral T cells display a broad spectrum of (dys-)functional states, shaped by the multifaceted suppressive signals that occur within the tumor microenvironment. Here we discuss the current understanding of T cell dysfunction in cancer, the value of novel technologies to dissect such dysfunction at the single cell level, and how our emerging understanding of T cell dysfunction may be utilized to develop personalized strategies to restore antitumor immunity.Entities:
Keywords: PD-1; T cell exhaustion; cancer; cancer immunotherapy; single cell technologies; tumor microenvironment
Mesh:
Year: 2018 PMID: 29634943 DOI: 10.1016/j.ccell.2018.03.012
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743