Depletion of Tregs for adoptive T-cell therapy using CD44 and CD137 as selection markers

Author:

Till Brian G1,Press Oliver W23

Affiliation:

1. Clinical Research Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, Seattle, WA 98109, USA.

2. Clinical Research Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, Seattle, WA 98109, USA

3. Department of Medicine, University of Washington, Seattle, WA, USA

Abstract

Evaluation of: Goldstein MJ, Kohrt HE, Houot R et al. Adoptive cell therapy for lymphoma with CD4 T cells depleted of CD137-expressing regulatory T cells. Cancer Res. 72(5), 1239–1247 (2012). Several types of cancer have been shown to be susceptible to cellular immune responses, leading to investigations using various forms of T cell-based, tumor-directed immunotherapy. One potential obstacle for the successful application of these therapies is the suppressive function of Tregs. Goldstein and colleagues evaluate a strategy to identify and remove Tregs from an adoptive T-cell therapy product generated by in vivo vaccination. They demonstrate that the depletion of Tregs characterized by CD44 and CD137 expression enhances antitumor immunity in their mouse model.

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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