4.7 Review

Antitumor T-cell Reconditioning: Improving Metabolic Fitness for Optimal Cancer Immunotherapy

Journal

CLINICAL CANCER RESEARCH
Volume 24, Issue 11, Pages 2473-2481

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-17-0894

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Funding

  1. Stand Up To Cancer Innovative Research Grant [SU2C-AACR-IRG 04-16]
  2. Sidney Kimmel Foundation for Cancer Research [SKF-015-036]
  3. NIH Director's New Innovator Award [DP2AI136598]
  4. UPCI Melanoma and Head and Neck Cancer SPOREs
  5. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [DP2AI136598] Funding Source: NIH RePORTER

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With the rapid rise of immunotherapy for cancer treatment, attention has focused on gaining a better understanding of T-cell biology in the tumor microenvironment. Elucidating the factors underlying changes in their function will allow for the development of new therapeutic strategies that could expand the patient population benefiting from immunotherapy, as well as circumvent therapy resistance. Cancers go beyond avoiding immune recognition and inducing T-cell dysfunction through coinhibitory molecules. Recent work has demonstrated that the tumor microenvironment elicits metabolic changes in T cells that dampen their ability to respond and that manipulating these metabolic changes can strengthen an antitumor immune response. Here we review the metabolic status of various types of T cells, the energetic state of the tumor microenvironment, and proposed modalities for improvement of immunotherapy through metabolic remodeling. (C) 2018 AACR.

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