Abstract |
Induction of a Th1 immune response against viral infection of the CNS is important in contributing to viral clearance. The present studies demonstrate a role for the T cell chemoattractant chemokine Mig (monokine induced by IFN-gamma) in contributing to a Th1 response against mouse hepatitis virus infection of the CNS. Analysis of the kinetics of Mig expression revealed mRNA transcripts present at days 7 and 12 postinfection (p.i.) but not early (day 2) or late (day 35) in the infection. To determine functional significance, mouse hepatitis virus-infected mice were treated with anti-Mig antisera, and the severity of disease was evaluated. Such treatment resulted in a marked increase in mortality that correlated with a >3 log increase in viral burden within the brains as compared with control mice treated with normal rabbit serum. Anti-Mig-treated mice displayed a significant decrease (p < 0.005) in CD4(+) and CD8(+) T cell recruitment into the CNS as compared with normal rabbit serum-treated mice. In addition, anti-Mig treatment resulted in a significant decrease (p < 0.05) in levels of IFN-gamma and IFN-beta that coincided with increased (p < 0.02) expression of the anti-inflammatory Th2 cytokine IL-10 within the CNS. Collectively, these data indicate that Mig is important in contributing to host defense by promoting a protective Th1 response against viral infection of the CNS.
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Authors | M T Liu, D Armstrong, T A Hamilton, T E Lane |
Journal | Journal of immunology (Baltimore, Md. : 1950)
(J Immunol)
Vol. 166
Issue 3
Pg. 1790-5
(Feb 01 2001)
ISSN: 0022-1767 [Print] United States |
PMID | 11160225
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- CXCL9 protein, human
- Chemokine CXCL9
- Chemokines, CXC
- Cytokines
- Immune Sera
- Intercellular Signaling Peptides and Proteins
- Interferon-gamma
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Topics |
- Amino Acid Sequence
- Animals
- Cell Movement
(immunology)
- Chemokine CXCL9
- Chemokines, CXC
(biosynthesis, immunology)
- Coronavirus Infections
(immunology, mortality, pathology, therapy)
- Cytokines
(metabolism)
- Encephalitis, Viral
(immunology, mortality, pathology)
- Immune Sera
(administration & dosage)
- Immunity, Innate
- Injections, Intraperitoneal
- Intercellular Signaling Peptides and Proteins
- Interferon-gamma
(physiology)
- Male
- Mice
- Mice, Inbred C57BL
- Molecular Sequence Data
- Murine hepatitis virus
(immunology)
- T-Lymphocytes
(immunology, metabolism, pathology)
- Tumor Cells, Cultured
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