International Immunology Advance Access published online on March 30, 2006
International Immunology, doi:10.1093/intimm/dxh397
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1 Department of Pathology and Immunology, Washington University School of Medicine, 660 South Euclid Avenue, St Louis, MO 63110, USA
* To whom correspondence should be addressed. Incomplete T cell antigen receptor-mediated signaling induces an unresponsive state known as anergy. Previously, we had shown that anergy can be induced in antigen-primed but not naive T cells. In this report, we found that in vitro primed T cells from IL-2R
Received August 5, 2005
Accepted January 11, 2006
Article
Requirement of high-affinity IL-2-IL-2R interaction for T cell anergy induction
Robert J. Hayashi 1
and
Osami Kanagawa 2 *
2 Department of Pathology and Immunology, Washington University School of Medicine, 660 South Euclid Avenue, St Louis, MO 63110, USA; Riken Research Center for Allergy and Immunology, RIKEN Yokohama Institute, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa 230-0045, Japan
Osami Kanagawa, E-mail: kanagawa{at}rcai.riken.jp
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Abstract
-deficient mice were resistant to anergy induction in contrast to comparably treated wild-type T cells. This resistance persisted even after proliferation of IL-2R
chain-deficient CD4 T cells with high-dose IL-2-IL-2R
chains interaction. Thus, antigen activation, and/or progression through cell cycle are not sufficient to induce anergy susceptibility in T cells. The high-affinity IL-2-IL-2R interaction appears to play a critical role in this process.![]()
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