Decline of CD3-positive T-cell counts by 6 months of age is associated with rapid disease progression in HIV-1–infected infants - 03/09/11
Abstract |
Because HIV-1 infected infants with rapid progression (RP) of disease might benefit from early and intense antiretroviral therapy, the identification of predictive factors of RP becomes extremely important. Currently, the best predictive factors of RP in HIV-1 infected children are HIV-1 RNA levels and CD4-positive T-cell counts. A decrease in CD3-positive T-cell count has been identified as a predictive factor of AIDS development in HIV-1 infected adults. Our objective was to evaluate decreased number of CD3-positive T-cells as a predictive factor of RP in infants. Peripheral blood lymphocytes from HIV-1 infected infants (up to 6 months of age) were analyzed for an association of lymphocyte subsets with RP, which was defined as the occurrence of AIDS or death before 18 months of age. In infants with RP (n = 32), CD3-positive T-cell counts were 3093 cells/μL at <1 month of age, 3092 cells/μL at 1 to 3 months, and 2062 cells/μL at 3 to 6 months. Non-RP infants (n = 49) maintained their CD3-positive T-cells counts at approximately 4000 cells/μL for at least 6 months of life. CD3-positive and CD4-positive T-cell counts were significantly associated with RP. Our results suggest that a decreased CD3-positive T-cell count may be used to predict RP in HIV-1 infected infants (RR = 2.16, P = .001). (J Allergy Clin Immunol 2001;108:265-8.)
Le texte complet de cet article est disponible en PDF.Keywords : HIV-1, AIDS, rapid disease progression, infants, CD3-positive T-cell counts
Abbreviations : RP:, RR:, CDC:, P2C2:, CD4-positive T-cells:, CD8-positive T-cells:
Plan
| Supported in part by National Heart, Lung and Blood Institute Grants N01-HR-96037, N01-HR-96038, N01-HR-96039, N01-HR-96040, N01-HR-96041, N01-HR, 96042 and N01-HR-96043; by National Institutes of Health General Clinical Research Center Grants RR-00071, RR-00188, RR-00533, RR-00643, RR-00645, RR-00865 and RR-02172; and by the Texas Children’s Hospital Immunology Research Fund. |
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| Reprint requests: Javier Chinen, MD, PhD, Texas Children’s Hospital, 6621 Fannin Street (MC: 1-3291), Houston, TX 77030. |
Vol 108 - N° 2
P. 265-268 - août 2001 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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