Human immunodeficiency virus gag and pol‐specific CD8 T cells in perinatal HIV infection

TW McCloskey, V Haridas, R Pahwa… - … : The Journal of the …, 2001 - Wiley Online Library
TW McCloskey, V Haridas, R Pahwa, S Pahwa
Cytometry: The Journal of the International Society for Analytical …, 2001Wiley Online Library
Background: Binding of fluorochrome‐conjugated MHC class I tetramers is a powerful
means to detect antigen‐specific CD8 T lymphocytes. In human immunodeficiency virus
(HIV) infection, cellular immune response is essential in curtailing HIV disease progression
but gaps persist in our understanding of HIV‐specific cells during the disease course. In this
study, we evaluated tetramer binding HIV‐specific CD8 T cells in HIV‐infected children.
Methods: Fluorescently labeled tetramers for HIV gag and pol were utilized to quantify …
Background
Binding of fluorochrome‐conjugated MHC class I tetramers is a powerful means to detect antigen‐specific CD8 T lymphocytes. In human immunodeficiency virus (HIV) infection, cellular immune response is essential in curtailing HIV disease progression but gaps persist in our understanding of HIV‐specific cells during the disease course. In this study, we evaluated tetramer binding HIV‐specific CD8 T cells in HIV‐infected children.
Methods
Fluorescently labeled tetramers for HIV gag and pol were utilized to quantify antigen‐specific cells by flow cytometry using a whole blood labeling method in a cohort of 19 HLA‐A2+ HIV‐ infected children (age range 1 month to 17 years).
Results
Fourteen children had detectable gag (median 0.4%) and pol (median 0.1%) binding CD8 T cells, three children had gag binding cells only, and two had neither. Numbers of gag and pol binding cells correlated with each other and each correlated independently with total CD8 T cells and total CD4 T cells.
Conclusions
HIV gag and pol‐specific CD8 T cells are maintained during the chronic phase of HIV infection in children and CD4 lymphocytes appear to be important for sustaining their levels. Cytometry (Comm. Clin. Cytometry) 46:265–270, 2001. © 2001 Wiley‐Liss, Inc.
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