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IL-2: A two-faced master regulator of autoimmunity

Journal

JOURNAL OF AUTOIMMUNITY
Volume 36, Issue 2, Pages 91-97

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jaut.2011.01.001

Keywords

IL-2; Regulatory T-cells; Th cytokines; Trafficking; Inflammation; Autoimmunity; Scurfy

Categories

Funding

  1. National Institutes of Health [DE-01759, AR-051203, AR-047988, AR-049449]

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CD4(+) T-cell (Th) cytokines provide important regulatory and effector functions of T-cells. Among them, IL-2 plays a unique role. IL-2 is required for the generation and maintenance of regulatory T-cells (Treg) to provide lifelong protection from autoimmune disease. Whether IL-2 is also required for autoimmune disease development is less clear as Il2(-/-) mice themselves spontaneously develop multi-organ inflammation (MOI). In this communication, we discuss evidence that support the thesis that IL-2 is required for the development of autoimmune response, although some aspects of autoimmune response are not regulated by IL-2. Potential IL-2-dependent mechanisms operating at specific stages of the inflammation process are presented. The interplays among Treg, IL-2, autoimmune response and adaptive immunity are discussed. Overall, available information indicates that IL-2 is a two-faced master regulator of autoimmunity: one to prevent autoimmunity while the other promotes autoimmune response. The latter is an unfortunate consequence of IL-2 function that is used to promote the adaptive immune response against foreign antigens and pathogens. (C) 2011 Elsevier Ltd. All rights reserved.

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