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Sci. Signal., 20 April 2010
Vol. 3, Issue 118, p. jc3
[DOI: 10.1126/scisignal.3118jc3]

JOURNAL CLUB

T Cells with Commitment Issues

Raphael Schneider*

Departments of Medicine and Microbiology and Immunology, Université de Montréal, CRCHUM-Notre-Dame Hospital, Pavilion JA DeSeve (room Y-3609), 1560 Sherbrooke E, Montreal, QC, Canada H2L 4M1.

Abstract: T cells are a central element of cell-mediated immunity. Host detection of infectious agents leads to antigen presentation and release of cytokines that cause naïve T cells to develop into effector T cells or regulatory T cells (Treg cells). Effector T cells act to control the invading agents and mediate tissue inflammation. Treg cells maintain immune homeostasis by suppressing effector T cell responses to prevent collateral damage. Until recently, T cell differentiation into distinct subsets with different functions had been considered irreversible. However, new evidence suggests that some differentiated T cell subsets are more phenotypically flexible than others. Studying the plasticity of T cells and the underlying signaling mechanisms may lead to important clues for understanding immunity and autoimmunity.

* E-mail, raphael.schneider{at}umontreal.ca

Citation: R. Schneider, T Cells with Commitment Issues. Sci. Signal. 3, jc3 (2010).

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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Journal Club: Intrathecal effects of daclizumab treatment of multiple sclerosis.
R. Schneider and N. Arbour (2012)
Neurology 78, e131-e133
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