| Literature DB >> 17513716 |
Takayuki Imanishi1, Hiromitsu Hara, Shinobu Suzuki, Nobutaka Suzuki, Shizuo Akira, Takashi Saito.
Abstract
Toll-like receptors recognize pathogen-associated molecular patterns, activate innate immunity, and consequently modulate adaptive immunity in response to infections. TLRs are also expressed on T cells, and it has been shown that T cell activation is modulated by TLR ligands. However, the functions of TLRs on Th1 and Th2 effector cells and the molecular mechanisms underlying TLR-mediated activation are not fully understood. We analyzed TLR functions and downstream signaling events in both effector T cells. In mouse Th1 cells the stimulation by TLR2 but not by other TLRs directly induced IFN-gamma production, cell proliferation, and cell survival without TCR stimulation, and these effects were greatly enhanced by IL-2 or IL-12 through the enhanced activation of MAPKs. In contrast, no TLR affected the function of effector Th2 cells. These results identify TLR2 as a new specific activator of Th1 cell function and imply the involvement in Th1-mediated responses.Entities:
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Year: 2007 PMID: 17513716 DOI: 10.4049/jimmunol.178.11.6715
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422