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血清转化时对HIV gag和env蛋白的体液免疫反应与HIV感染临床结局之间的关系。

Relation between humoral responses to HIV gag and env proteins at seroconversion and clinical outcome of HIV infection.

作者信息

Cheingsong-Popov R, Panagiotidi C, Bowcock S, Aronstam A, Wadsworth J, Weber J

机构信息

Department of Medicine, Royal Postgraduate Medical School, London.

出版信息

BMJ. 1991 Jan 5;302(6767):23-6. doi: 10.1136/bmj.302.6767.23.

Abstract

OBJECTIVE

To study the contribution of the humoral response to HIV-I at seroconversion to disease outcome after 84 months.

DESIGN

A retrospective longitudinal study.

SETTING

Two haemophilia centres in the United Kingdom.

PATIENTS

88 Haemophiliac patients infected with HIV-I for whom sera were available from before seroconversion and in whom clinical follow up data were available.

RESULTS

Kaplan-Meier survival analysis showed a significant difference between a high titre (greater than 1600) p24 antibody response at seroconversion and prolonged time before the development of HIV related disease (p = 0.0008). In contrast, higher titres of antibody to gp120 at seroconversion (greater than 25,600) correlated with more rapid clinical deterioration (p = 0.025).

CONCLUSIONS

The first humoral response to HIV proteins at seroconversion is associated with clinical outcome; patients with an initial low titre antibody response to the gagp24 protein have a significantly faster rate of progression to CDC stage IV disease. Patients with a high titre p24 antibody response progress to AIDS more slowly, and these data provide an explanation why p24 antigenaemia is not universally detected in patients with AIDS. It is unclear whether the association between a strong initial p24 antibody response and slower progression of HIV disease is causal and if so whether it is due to viral or host factors.

摘要

目的

研究血清转化时针对HIV-1的体液免疫反应对84个月后疾病转归的影响。

设计

一项回顾性纵向研究。

地点

英国的两个血友病中心。

患者

88例感染HIV-1的血友病患者,其血清转化前的血清样本及临床随访数据均可得。

结果

Kaplan-Meier生存分析显示,血清转化时p24抗体高滴度(大于1600)反应与HIV相关疾病发生前的较长时间存在显著差异(p = 0.0008)。相反,血清转化时gp120抗体较高滴度(大于25,600)与临床病情更快恶化相关(p = 0.025)。

结论

血清转化时对HIV蛋白的首次体液免疫反应与临床转归相关;对gagp24蛋白初始抗体滴度低的患者进展至疾病控制中心(CDC)IV期疾病的速度明显更快。p24抗体高滴度反应的患者进展至艾滋病的速度较慢,这些数据解释了为何艾滋病患者并非普遍检测到p24抗原血症。尚不清楚初始p24抗体强烈反应与HIV疾病进展较慢之间的关联是否具有因果关系,若有因果关系,是由于病毒因素还是宿主因素所致。

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