Candida-Specific Systemic Cell-Mediated Immune Reactivities in Human Immunodeficiency Virus—Positive Persons with Mucosal Candidiasis

Oropharyngeal candidiasis (OPC), as opposed to vulvovaginal candidiasis (VVC), is a common opportunistic infection in human immunodeficiency virus (HIV)—positive persons that correlates with reduced CD4 T cell counts. Although cell-mediated immunity (CMI) by CD4 Th1-type cells is considered to be th...

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Bibliographic Details
Published in:The Journal of infectious diseases Vol. 183; no. 2; pp. 277 - 285
Main Authors: Leigh, Janet E., Barousse, Melissa, Swoboda, Rolf K., Myers, Tammy, Hager, Shannon, Wolf, Norbert A., Cutright, Jessica L., Thompson, James, Sobel, Jack D., Fidel, Paul L.
Format: Journal Article
Language:English
Published: Chicago, IL The University of Chicago Press 15-01-2001
University of Chicago Press
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Summary:Oropharyngeal candidiasis (OPC), as opposed to vulvovaginal candidiasis (VVC), is a common opportunistic infection in human immunodeficiency virus (HIV)—positive persons that correlates with reduced CD4 T cell counts. Although cell-mediated immunity (CMI) by CD4 Th1-type cells is considered to be the predominant host defense against mucosal candidiasis, the immune factors associated with susceptibility to OPC in HIV-positive persons are not well understood. This study investigated Candida-specific systemic CMI in HIV-positive persons with OPC and/or VVC. Reductions in delayed skin test reactivity to Candida antigen were observed in HIV-positive persons with CD4 cell counts <200 cells/µL, irrespective of the presence of mucosal infection. Likewise, despite the correlate of OPC with reduced CD4 cell counts in HIV-positive persons, differences in Candida-specific peripheral blood mononuclear cell proliferation and Th1/Th2 cytokine production between HIV-positive and HIV-negative persons were not consistent in a manner to suggest that deficiencies in Candida-specific systemic CMI account solely for the susceptibility to OPC.
Bibliography:ark:/67375/HXZ-XCWCV65Z-D
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ISSN:0022-1899
1537-6613
DOI:10.1086/317944