T cells coexpressing CD3 and CD10 are a characteristic feature of angioimmunoblastic T-cell lymphoma (AITL) [1]. However, they are not unique to AITL, as these cells are also present in B cell lymphoma and reactive lymphoid hyperplasia [2]. To determine the significance of CD3+ CD10+ T cells, we use
Follicular lymphoma B cells induce the conversion of conventional CD4+ T cells to T-regulatory cells
β Scribed by Weiyun Z. Ai; Jing-Zhou Hou; Robert Zeiser; Debra Czerwinski; Robert S. Negrin; Ronald Levy
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- French
- Weight
- 288 KB
- Volume
- 124
- Category
- Article
- ISSN
- 0020-7136
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β¦ Synopsis
Abstract
There has been accumulating evidence that CD4^+^CD25^+^ FoxP3 expressing regulatory T cells (Treg) are highly concentrated in tumors, thereby fostering an immuneβprivileged microenvironment. Some studies have shown that Tβcell receptor (TCR) stimulation can convert conventional T cells into Treg. Follicular lymphoma (FL) B 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 B 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 tumorβspecific mechanism by which FL tumor cells promote immune escape through the induction of Treg. Β© 2008 WileyβLiss, Inc.
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