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病原体流行率可能决定 HIV 感染者体内抗原特异性 T 细胞应答的维持。

Pathogen prevalence may determine maintenance of antigen-specific T-cell responses in HIV-infected individuals.

机构信息

Department of Transplant and Infection Immunology, Saarland University, Homburg, Germany.

出版信息

AIDS. 2012 Mar 27;26(6):695-700. doi: 10.1097/QAD.0b013e3283519a89.

DOI:10.1097/QAD.0b013e3283519a89
PMID:22301414
Abstract

OBJECTIVE

To assess the effect of antigen-exposure on the T-cell repertoire in the chronic phase of HIV-infection.

DESIGN

This is a prospective cross-sectional study.

METHODS

HIV-seropositive patients and immunocompetent controls from tuberculosis low and high-endemic countries were recruited. Mycobacterium tuberculosis (purified protein derivative; PPD)-specific CD4 T-cell responses were quantified directly from whole blood using flow-cytometric analysis of intracellular cytokines after specific stimulation. T-cell reactivity toward cytomegalovirus (CMV) or Staphylococcus aureus Enterotoxin B (SEB) served as control.

RESULTS

In a low-endemic region, HIV-seropositive patients showed lower frequencies of PPD-specific T cells compared to immunocompetent individuals. This was not due to a general loss of immunity toward recall antigens, as T-cell immunity toward CMV or SEB was preserved. In line with continuous antigen exposure, HIV-seropositive patients from a high-endemic region showed preserved PPD-specific T-cell frequencies that were not different from those found in HIV-seronegative controls. Likewise, both groups did not differ in recall T-cell responses toward CMV or SEB.

CONCLUSION

A lower prevalence and frequency of PPD-specific immunity is a typical feature of HIV-related immunosuppression in low-endemic regions. In contrast, PPD-specific responses are maintained in HIV-seropositive individuals in regions with high tuberculosis prevalence. This suggests constant skewing and restriction of specific T-cell immunity toward environmental antigens in HIV-seropositive individuals.

摘要

目的

评估 HIV 感染慢性期抗原暴露对 T 细胞 repertoire 的影响。

设计

这是一项前瞻性的横断面研究。

方法

从低、高结核流行国家招募 HIV 血清阳性患者和免疫功能正常的对照者。使用流式细胞术分析细胞内细胞因子,直接从全血中定量检测结核分枝杆菌(纯化蛋白衍生物;PPD)特异性 CD4 T 细胞反应。巨细胞病毒(CMV)或金黄色葡萄球菌肠毒素 B(SEB)的 T 细胞反应作为对照。

结果

在低流行地区,与免疫功能正常者相比,HIV 血清阳性患者的 PPD 特异性 T 细胞频率较低。这不是由于对回忆抗原的一般免疫丧失,因为 CMV 或 SEB 的 T 细胞免疫仍然存在。与持续的抗原暴露一致,来自高流行地区的 HIV 血清阳性患者表现出保留的 PPD 特异性 T 细胞频率,与 HIV 血清阴性对照者无差异。同样,两组对 CMV 或 SEB 的回忆性 T 细胞反应也没有差异。

结论

在低流行地区,PPD 特异性免疫的低患病率和频率是 HIV 相关免疫抑制的典型特征。相比之下,在结核高流行地区,PPD 特异性反应在 HIV 血清阳性者中得以维持。这表明 HIV 血清阳性个体对环境抗原的特异性 T 细胞免疫持续偏倚和受限。

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