Chemokines and the inflammatory response to viral infection in the centralnervous system with a focus on lymphocytic choriomeningitis virus

Citation
Vc. Asensio et al., Chemokines and the inflammatory response to viral infection in the centralnervous system with a focus on lymphocytic choriomeningitis virus, J NEUROVIRO, 5(1), 1999, pp. 65-75
Citations number
76
Categorie Soggetti
Neurosciences & Behavoir
Journal title
JOURNAL OF NEUROVIROLOGY
ISSN journal
13550284 → ACNP
Volume
5
Issue
1
Year of publication
1999
Pages
65 - 75
Database
ISI
SICI code
1355-0284(199902)5:1<65:CATIRT>2.0.ZU;2-L
Abstract
Leukocyte migration to the central nervous system (CNS) is a common process with often devastating consequences that follows infection of this tissue compartment with a variety of viruses. The mechanisms underlying this proce ss are poorly defined but, it is hypothesized that chemokines may be import ant regulatory signals for the cerebral recruitment and extravasation of le ukocytes. Here we discuss this hypothesis in the context of different viral infections of the CNS with emphasis on lymphocytic choriomeningitis virus (LCMV), In general, the pattern of chemokine gene expression in these CNS v iral infections is dynamic and complex with often overlapping expression of a number of different subclasses of chemokine genes. In the case of CNS in fection with LCMV, cerebral chemokine gene expression was observed in euthy mic and to a lesser extent athymic mice and preceded increases in cytokine gene expression and in euthymic mice, CNS leukocyte recruitment. These obse rvations together with the finding that CRG-2/IP-10, a prominently expresse d chemokine gene in many different CNS viral infections, was expressed by c ells intrinsic to the CNS e.g. astrocytes, suggest that activation of chemo kine gene expression may be a direct, early and localized host response to viral infection. These findings are consistent with the proposed involvemen t of chemokines as key signaling molecules for the migration of leukocytes to the CNS following virus infection.