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The Initial Phase of an Immune Response Functions to Activate Regulatory T Cells
Author(s) -
William O’Gorman,
Hans Dooms,
Steve H. Thorne,
Wilson Kuswanto,
Erin F. Simonds,
Peter O. Krutzik,
Garry P. Nolan,
Abul K. Abbas
Publication year - 2009
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.0900691
Subject(s) - priming (agriculture) , stat5 , foxp3 , microbiology and biotechnology , cytokine , t cell , biology , immune system , endogeny , regulatory t cell , immunology , il 2 receptor , phosphorylation , endocrinology , botany , germination
An early reaction of CD4(+) T lymphocytes to Ag is the production of cytokines, notably IL-2. To detect cytokine-dependent responses, naive Ag-specific T cells were stimulated in vivo and the presence of phosphorylated STAT5 molecules was used to identify the cell populations responding to IL-2. Within hours of T cell priming, IL-2-dependent STAT5 phosphorylation occurred primarily in Foxp3(+) regulatory T cells. In contrast, the Ag-specific T cells received STAT5 signals only after repeated Ag exposure or memory differentiation. Regulatory T cells receiving IL-2 signals proliferated and developed enhanced suppressive activity. These results indicate that one of the earliest events in a T cell response is the activation of endogenous regulatory cells, potentially to prevent autoimmunity.

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