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IFN-γ-Producing γδ T Cells Help Control Murine West Nile Virus Infection
Author(s) -
Tian Wang,
Eileen P. Scully,
Zhinan Yin,
Jung Ho Kim,
Sha Wang,
Jun Yan,
Mark J. Mamula,
John F. Anderson,
Joe Craft,
Erol Fikrig
Publication year - 2003
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.171.5.2524
Subject(s) - biology , virology , adoptive cell transfer , virus , immunology , meningoencephalitis , t cell , immune system
West Nile (WN) virus causes fatal meningoencephalitis in laboratory mice, thereby partially mimicking human disease. Using this model, we have demonstrated that mice deficient in gammadelta T cells are more susceptible to WN virus infection. TCRdelta(-/-) mice have elevated viral loads and greater dissemination of the pathogen to the CNS. In wild-type mice, gammadelta T cells expanded significantly during WN virus infection, produced IFN-gamma in ex vivo assays, and enhanced perforin expression by splenic T cells. Adoptive transfer of gammadelta T cells to TCRdelta(-/-) mice reduced the susceptibility of these mice to WN virus, and this effect was primarily due to IFN-gamma-producing gammadelta T cells. These data demonstrate a distinct role for gammadelta T cells in the control of and prevention of mortality from murine WN virus infection.

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