T Cell Subsets and Cytomegalovirus Retinitis in Human Immunodeficiency Virus‐Infected Patients
Author(s) -
MeiLing TayKearney,
Cheryl Enger,
Richard D. Semba,
Walter Royal,
James P. Dunn,
Douglas A. Jabs
Publication year - 1997
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 - 10.1086/517303
Subject(s) - cytomegalovirus retinitis , retinitis , cd8 , human cytomegalovirus , flow cytometry , immunology , cytomegalovirus , cd28 , t cell , cd3 , lymphocyte , immunodeficiency , cluster of differentiation , medicine , biology , virology , antigen , virus , cell , herpesviridae , viral disease , immune system , genetics
A case-control study was done to investigate the relationship between T cell subsets and cytomegalovirus (CMV) retinitis in human immunodeficiency virus (HIV)-infected subjects with or without CMV retinitis and CD4+ cell counts of <0.050 x 10(9)/L. Cell surface markers on peripheral blood lymphocytes were evaluated using flow cytometry. Patients with CMV retinitis had significantly lower levels of CD8+ cells (median: 0.152 x 10(9)/L) compared with levels for controls (median: 0.296 x 10(9)/L, P < .001). Significant down-regulation of costimulatory molecule CD28+ and lymphocyte function-associated antigen-1 (LFA-1) expression was observed in patients versus controls (CD28+: 0.048 x 10(9)/L vs. 0.143 x 10(9)/L, P < .001; LFA-1: 0.238 x 10(9)/L vs. 0.400 x 10(9)/L, P < .001), but no significant differences were noted for NK cells. We propose that progressive loss of the CD3+ CD8+ cell subset and down-regulation of CD28 and LFA-1 accessory molecules are associated with an increased risk of CMV retinitis in HIV-infected patients.
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