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Increased Macrophage Chemoattractant Protein–1 in Cerebrospinal Fluid Precedes and Predicts Simian Immunodeficiency Virus Encephalitis
Author(s) -
M. Christine Zink,
Gary D. Coleman,
Joseph L. Mankowski,
Robert J. Adams,
Patrick M. Tarwater,
Kelly Fox,
Janice E. Clements
Publication year - 2001
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/323478
Subject(s) - cerebrospinal fluid , microglia , glial fibrillary acidic protein , encephalitis , simian immunodeficiency virus , biology , immunology , virus , pathology , virology , inflammation , medicine , immunohistochemistry
Macrophage chemoattractant protein-1 (MCP-1) may be a key trigger for the influx of macrophages into the brain in human immunodeficiency virus (HIV) encephalitis. In this study, simian immunodeficiency virus-infected macaques that developed moderate-to-severe encephalitis had significantly higher MCP-1 levels in cerebrospinal fluid (CSF) than in plasma as early as 28 days after inoculation, which was before the development of brain lesions. In contrast, CSF:plasma MCP-1 ratios remained constant at preinoculation levels in macaques that developed minimal or no encephalitis. Abundant MCP-1 protein and mRNA were detected in both macrophages and astrocytes in the brain. Macaques with increased MCP-1 in CSF had significantly greater expression of markers of macrophage and microglia activation and infiltration (CD68; P= .003) and astrocyte activation (glial fibrillary acidic protein; P= .019 and P= .031 in white and gray matter, respectively). The results suggest that the CSF:plasma MCP-1 ratio may be a valuable prognostic marker for the development of HIV-induced central nervous system disease.

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