Cutting Edge: The T Cell Chemoattractant IFN-Inducible Protein 10 Is Essential in Host Defense Against Viral-Induced Neurologic Disease

Michael T. Liu(University of California, Irvine), Benjamin P. Chen(University of California, Irvine), Patricia Oertel(University of California, Irvine), Michael J. Buchmeier(Scripps Research Institute), David A. Armstrong(University of California, Irvine), Thomas A. Hamilton(University of California, Irvine), Thomas E. Lane(University of California, Irvine)
The Journal of Immunology
September 1, 2000
Cited by 245Open Access
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Abstract

The contribution of the T cell chemoattractant chemokine IFN-inducible protein 10 (IP-10) in host defense following viral infection of the CNS was examined. IP-10 is expressed by astrocytes during acute encephalomyelitis in mouse hepatitis virus-infected mice, and the majority of T lymphocytes infiltrating into the CNS expressed the IP-10 receptor CXCR3. Treatment of mice with anti-IP-10 antisera led to increased mortality and delayed viral clearance from the CNS as compared with control mice. Further, administration of anti-IP-10 led to a >70% reduction (p </= 0.001) in CD4+ and CD8+ T lymphocyte infiltration into the CNS, which correlated with decreased (p </= 0.01) levels of IFN-gamma. These data indicate that IP-10 functions as a sentinel molecule in host defense and is essential in the development of a protective Th1 response against viral infection of the CNS.


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