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CD4+细胞计数<200×10⁶/L但无艾滋病定义临床疾病的HIV感染同性恋男性疾病进展的预测因素。

Predictors of disease progression in HIV-infected homosexual men with CD4+ cells < 200 x 10(6)/l but free of AIDS-defining clinical disease.

作者信息

Keet I P, Krol A, Koot M, Roos M T, de Wolf F, Miedema F, Coutinho R A

机构信息

Municipal Health Service, Department of Public Health and Environment, Amsterdam, The Netherlands.

出版信息

AIDS. 1994 Nov;8(11):1577-83. doi: 10.1097/00002030-199411000-00009.

Abstract

OBJECTIVE

To study progression of HIV infection in individuals who are free of AIDS-defining clinical disease with CD4+ cell counts < 200 x 10(6)/l.

DESIGN

Prospective and nested case-control study.

SETTING

Amsterdam cohort study on HIV infection, The Netherlands.

PARTICIPANTS

Prospective study: 148 asymptomatic HIV-infected individuals with < 200 x 10(6)/l CD4+ cells. Nested case-control study: 58 men with AIDS-free follow-up more than 2 years after CD4 count < 200 x 10(6)/l, compared with 63 who progressed to AIDS within 2 years.

MAIN OUTCOME MEASURES

Progression to AIDS according to the 1987 Centers for Disease Control and Prevention case definition and death.

RESULTS

Median AIDS-free interval was 22 months, median interval to death 41 months. Presence of syncytium-inducing (SI) HIV variants, HIV p24 antigen, and a low T-cell response after stimulation with phytohaemagglutinin (PHA) were independent predictors of progression to AIDS. Probability of 1 year AIDS-free survival varied between 89 and 38% by the presence or absence of these additional markers. Effect of early treatment could only be detected in men with HIV p24 antigen and SI variants. Case-control analysis showed similar changes over time regarding prognostic markers in both groups although at a lower rate in the AIDS-free men. Eight men remained AIDS-free more than 4 years, SI variants were absent in seven, and all eight were p24-seronegative.

CONCLUSIONS

HIV-infected individuals can remain disease-free for more than 4 years with very low CD4+ cell counts, provided that they lack other progression markers: SI variants, p24 antigen and a low PHA-induced T-cell reactivity. A beneficiary effect of early treatment may be limited to men with SI variants and/or p24 antigen.

摘要

目的

研究CD4+细胞计数<200×10⁶/l且无艾滋病界定临床疾病的个体中HIV感染的进展情况。

设计

前瞻性巢式病例对照研究。

地点

荷兰阿姆斯特丹HIV感染队列研究。

参与者

前瞻性研究:148例无症状HIV感染个体,CD4+细胞<200×10⁶/l。巢式病例对照研究:58例CD4计数<200×10⁶/l后无艾滋病随访超过2年的男性,与63例在2年内进展为艾滋病的男性进行比较。

主要观察指标

根据1987年美国疾病控制与预防中心病例定义进展为艾滋病及死亡情况。

结果

无艾滋病的中位间隔时间为22个月,至死亡的中位间隔时间为41个月。合胞体诱导(SI)HIV变异体、HIV p24抗原的存在以及用植物血凝素(PHA)刺激后低T细胞反应是进展为艾滋病的独立预测因素。根据这些额外标志物的有无,1年无艾滋病生存概率在89%至38%之间变化。早期治疗的效果仅在有HIV p24抗原和SI变异体的男性中可检测到。病例对照分析显示两组预后标志物随时间的变化相似,尽管无艾滋病男性的变化率较低。8名男性无艾滋病超过4年,7名无SI变异体,且所有8名均为p24血清阴性。

结论

HIV感染个体CD4+细胞计数极低时,若缺乏其他进展标志物:SI变异体、p24抗原和低PHA诱导的T细胞反应性,可保持无病状态超过4年。早期治疗的有益效果可能仅限于有SI变异体和/或p24抗原的男性。

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