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Cutting Edge: The Mechanism of Invariant NKT Cell Responses to Viral Danger Signals
Author(s) -
Aaron J. Tyznik,
Emmanuel Tupin,
Niranjagarajan,
Min J. Her,
Chris A. Benedict,
Mitchell Kronenberg
Publication year - 2008
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.181.7.4452
Subject(s) - cd1d , tlr9 , secretion , biology , microbiology and biotechnology , immunology , cpg oligodeoxynucleotide , t cell receptor , natural killer t cell , mechanism (biology) , immune system , t cell , gene expression , gene , genetics , biochemistry , dna methylation , philosophy , epistemology
Invariant NK T (iNKT) cells influence the response to viral infections, although the mechanisms are poorly defined. In this study we show that these innate-like lymphocytes secrete IFN-gamma upon culture with CpG oligodeoxynucleotide-stimulated dendritic cells (DCs) from mouse bone marrow. This requires TLR9 signaling and IL-12 secretion by the activated DCs, but it does not require CD1d expression. iNKT cells also produce IFN-gamma in response to mouse CMV infection. Their mechanism of mouse CMV detection is quite similar to that of CpG, requiring both TLR9 signaling and IL-12 secretion, while the need for CD1d expression is relatively minor. Consequently, iNKT cells have the ability to respond to a variety of microbes, including viruses, in an Ag-independent manner, suggesting they may play a broad role in antipathogen defenses despite their limited TCR repertoire.

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