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Eur J Immunol. 2011 Nov;41(11):3351-60. doi: 10.1002/eji.201141629. Epub 2011 Oct 13.

IL-33 synergizes with TCR and IL-12 signaling to promote the effector function of CD8+ T cells.

Author information

1
Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.

Abstract

The effector functions of CD8(+) T cells are influenced by tissue inflammatory microenvironments. IL-33, a member of the IL-1 family, acts as a danger signal after its release during cell necrosis. The IL-33/ST2 axis has been implicated in various Th2 responses. Its role in CD8(+) T-cell-mediated immune response is, however, not known. Here we find that type 1 cytotoxic T (Tc1) cells cultured in vitro unexpectedly express high levels of the IL-33 receptor ST2. Interestingly, the expression of ST2 in Tc1 cells is dependent on T-bet, a master Th1/Tc1 transcription factor. In addition, IL-33 enhances TCR-triggered IFN-γ production. IL-33 together with IL-12 can stimulate IFN-γ production in Tc1 cells. Moreover, IL-33 synergizes with IL-12 to promote CD8(+) T-cell effector function. The synergistic effect of IL-33 and IL-12 is partly mediated by Gadd45b. Together, these in vitro data establish a novel role of IL-33 in promoting effector type 1 adaptive immune responses.

PMID:
21887788
PMCID:
PMC3332117
DOI:
10.1002/eji.201141629
[Indexed for MEDLINE]
Free PMC Article

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