4.5 Review

Modulation of GITR for cancer immunotherapy

Journal

CURRENT OPINION IN IMMUNOLOGY
Volume 24, Issue 2, Pages 217-224

Publisher

CURRENT BIOLOGY LTD
DOI: 10.1016/j.coi.2011.12.011

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Funding

  1. NIH [R01CA56821, P01CA59350, K12 CA120121-01, T32 CA09149-30]
  2. Swim Across America
  3. Cancer Research Institute
  4. Commonwealth Cancer Research Foundation/MSKCC Experimental Therapeutics Center
  5. John D. Proctor Foundation
  6. Margaret A. Cunningham Immune Mechanisms in Cancer Research Fellowship Award
  7. Melanoma Research Alliance

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Modulation of co-inhibitory and co-stimulatory receptors of the immune system has become a promising new approach for immunotherapy of cancer. With the recent FDA approval of CTLA-4 blockade serving as an important proof of principal, many new targets are now being translated into the clinic. Preclinical research has demonstrated that targeting glucocorticoid-induced tumor necrosis factor (TNF) receptor related gene (GITR), a member of TNF receptor superfamily, by agonist antibodies or natural ligand, can serve as an effective anti-tumor therapy. In this review, we will cover this research and the rationale that has led to initiation of two phase 1 clinical trials targeting GITR as a new immunotherapeutic approach for cancer.

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