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Angiocentric CD3 + T-Cell Infiltrates in Human Immunodeficiency Virus Type 1-Associated Central Nervous System Disease in Children
Journal article   Open access   Peer reviewed

Angiocentric CD3 + T-Cell Infiltrates in Human Immunodeficiency Virus Type 1-Associated Central Nervous System Disease in Children

Christos D. Katsetos, John E. Fincke, Agustin Legido, Harold W. Lischner, Jean-Pierre de Chadarevian, Edward M. Kaye, Chris D. Platsoucas and Emilia L. Oleszak
Clinical and diagnostic laboratory immunology, v 6(1)
Jan 1999
PMID: 9874673
url
https://doi.org/10.1128/cdli.6.1.105-114.1999View
Published, Version of Record (VoR) Open
url
https://doi.org/10.1128/CDLI.6.1.105-114.1999View
Published, Version of Record (VoR) Open

Abstract

ABSTRACT A significant proportion of brain tissue specimens from children with AIDS show evidence of vascular inflammation in the form of transmural and/or perivascular mononuclear-cell infiltrates at autopsy. Previous studies have shown that in contrast to inflammatory lesions observed in human immunodeficiency virus type 1 (HIV-1) encephalitis, in which monocytes/macrophages are the prevailing mononuclear cells, these infiltrates consist mostly of lymphocytes. Perivascular mononuclear-cell infiltrates were found in brain tissue specimens collected at autopsy from five of six children with AIDS and consisted of CD3 + T cells and equal or greater proportions of CD68 + monocytes/macrophages. Transmural (including endothelial) mononuclear-cell infiltrates were evident in one patient and comprised predominantly CD3 + T cells and small or, in certain vessels, approximately equal proportions of CD68 + monocytes/macrophages. There was a clear preponderance of CD3 + CD8 + T cells on the endothelial side of transmural infiltrates. In active lesions of transmural vasculitis, CD3 + T-cell infiltrates exhibited a distinctive zonal distribution. The majority of CD3 + cells were also CD8 + and CD45RO + . Scattered perivascular monocytes/macrophages in foci of florid vasculitis were immunoreactive for the p24 core protein. In contrast to the perivascular space, the intervening brain neuropil was dominated by monocytes/macrophages, microglia, and reactive astrocytes, containing only scant CD3 + CD8 + cells. Five of six patients showed evidence of calcific vasculopathy, but only two exhibited HIV-1 encephalitis. One patient had multiple subacute cerebral and brainstem infarcts associated with a widespread, fulminant mononuclear-cell vasculitis. A second patient had an old brain infarct associated with fibrointimal thickening of large leptomeningeal vessels. These infiltrating CD3 + T cells may be responsible for HIV-1-associated CNS vasculitis and vasculopathy and for endothelial-cell injury and the opening of the blood-brain barrier in children with AIDS.

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Collaboration types
Domestic collaboration
Web of Science research areas
Immunology
Infectious Diseases
Microbiology
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