4.7 Article

Follicular lymphoma B cells induce the conversion of conventional CD4+ T cells to T-regulatory cells

Journal

INTERNATIONAL JOURNAL OF CANCER
Volume 124, Issue 1, Pages 239-244

Publisher

WILEY
DOI: 10.1002/ijc.23881

Keywords

tumor microenvironment; immune escape

Categories

Funding

  1. National Institute of Health
  2. Doris Duke Charitable Foundation
  3. Lymphoma Research Foundation
  4. American Society of Clinical Oncology Young Investigator
  5. Deutsche Krebshilfe, Germany

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There has been accumulating evidence that CD4(+)CD25(+) FoxP3 expressing regulatory T cells (Treg) are highly concentrated in tumors, thereby fostering an immune-privileged microenvironment. Some studies have shown that T-cell receptor (TCR) stimulation can convert conventional T cells into Treg. Follicular lymphoma (FL) It cells can enhance this Treg conversion. We investigated whether FL tumor B cells, as opposed to normal B cells, are unique in their ability to convert effector T cells into Treg. We found that tumor B cells alone, without artificial TCR stimulation, could induce conventional T cells to express FoxP3 and to acquire regulatory function. In contrast to their malignant counterpart, normal It cells did not induce Treg conversion. Treg conversion was independent of the T cell background, as T cells isolated from FL or normal peripheral blood were equally susceptible to being converted by tumor B cells. Our study provides evidence for a tumor-specific mechanism by which FL tumor cells promote immune escape through the induction of Treg. (C) 2008 Wiley-Liss, Inc.

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