| Literature DB >> 21159627 |
Anita Q Gomes1, Duarte S Martins, Bruno Silva-Santos.
Abstract
Abundant interferon-γ secretion, potent cytotoxicity, and major histocompatibility complex-independent targeting of a large spectrum of tumors make γδ T cells attractive mediators of cancer immunotherapy. However, a better understanding of the molecular mechanisms involved in tumor cell recognition and γδ T-cell activation is required to improve the limited success of γδ T-cell-mediated treatments. Here, we review key advances in basic knowledge made over the past 3 years, and summarize the results of γδ T-cell-based clinical trials concluded to date. We also highlight new research directions on the basis of the modulation of receptors that control the function of γδ T cells. ©2010 AACR.Entities:
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Year: 2010 PMID: 21159627 DOI: 10.1158/0008-5472.CAN-10-3236
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701