CHANGES IN LYMPHOCYTE-T SUBSETS IN INTRAVENOUS-DRUG-USERS WITH HIV-1 INFECTION
CHANGES IN LYMPHOCYTE-T SUBSETS IN INTRAVENOUS-DRUG-USERS WITH HIV-1 INFECTION
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DOI:
10.1001/jama.267.12.1631
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发表时间:
1992-03-25
影响因子:
120.7
通讯作者:
NELSON, KE
中科院分区:
文献类型:
--
作者:
MARGOLICK, JB;MUNOZ, A;NELSON, KE
Objective. - To evaluate changes in T-cell subsets in prevalent human immunodeficiency virus type 1 (HIV-1) seronegative and seropositive intravenous drug users (IVDUs) and in HIV-1 seropositive IVDUs with known time of seroconversion.Design. - Cohort study with a median 18-month follow-up.Setting. - Community-based clinic established to study the natural history of HIV infection in IVDUs.Subjects. - Eight hundred fifty-nine self-referred IVDUs aged 18 through 49 years who injected drugs within the last 10 years and who did not have an AIDS (acquired immunodeficiency syndrome)-defining illness; 152 were seronegative for HIV-1, 621 were seropositive, and 86 seroconverted during the study.Outcome Measures. - Proportions and absolute numbers of lymphocytes and CD3, CD4, and CD8 T cells as determined at 6-month intervals by flow cytometry and complete blood cell counts with automated differential.Results. - Median numbers of.CD4 lymphocytes at enrollment were 1061/mu-L (1.06 x 10(9)/L) for seronegative IVDUs, 508/mu-L for seropositive IVDUs, and 733/mu-L for those who seroconverted (enrolled a median of 4.5 months after seroconversion); the corresponding figures for CD8 lymphocytes were 628, 894, and 889/mu-L, respectively. Median rates of decline in absolute numbers and percentages of CD4 lymphocytes per 6 months were 7.6/mu-L (0.0%) for seropositive IVDUs and 55.1/mu-L (1.9%) for IVDUs who seroconverted (median follow-up after seroconversion was 12 months). Multivariate regression analysis that incorporated the within-individual correlation of the CD4 lymphocyte counts showed no significant change in these cells over time and no change due to use of drugs.Conclusion. - Our data suggest that progression of HIV-1 infection in IVDUs, as reflected in decline of CD4 cell counts, is no more rapid than that reported for other risk groups.