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HIV感染后CD4 + T细胞依赖性的丙型肝炎病毒特异性体液免疫反应降低

CD4+ T cell-dependent reduction in hepatitis C virus-specific humoral immune responses after HIV infection.

作者信息

Netski Dale M, Mosbruger Tim, Astemborski Jacquie, Mehta Shruti H, Thomas David L, Cox Andrea L

机构信息

Department of Medicine, Johns Hopkins Medical Institutions, Baltimore, MD, 21231, USA.

出版信息

J Infect Dis. 2007 Mar 15;195(6):857-63. doi: 10.1086/511826. Epub 2007 Feb 7.

Abstract

BACKGROUND

Human immunodeficiency virus (HIV) infection adversely affects all stages of hepatitis C virus (HCV) infection, leading to increased rates of viral persistence, higher levels of HCV viremia, and accelerated progression of HCV-related liver disease. These disease interactions may result in part from impairment of B cell function, which is CD4(+) T cell dependent.

METHODS

To determine the effect of HIV infection on B cell function, we compared HCV antibody levels and specificities in 29 HCV-infected persons before and after they acquired HIV and assessed the temporal correlation of these changes with overall CD4(+) T lymphocyte counts.

RESULTS

The pre-HIV infection HCV antibody titer was a predictor of the subsequent titer for all antigens, and decreasing CD4(+) T cell numbers was strongly associated with a decrease in anti-HCV titers for several antigens. CD4(+) T cells counts of <500 cells/mm(3) were significantly associated with lower HCV antibody end-point titers. Higher HCV end-point titers were associated with fewer years from HIV infection and, for Core antigen, current drug use.

CONCLUSIONS

HCV-specific antibody production is impaired by HIV infection, and loss of antibody production depends on CD4(+) T cell depletion. However, the decrease in titers is less significant in those who continue to actively inject drugs.

摘要

背景

人类免疫缺陷病毒(HIV)感染对丙型肝炎病毒(HCV)感染的各个阶段均产生不利影响,导致病毒持续存在率增加、HCV病毒血症水平升高以及HCV相关肝病进展加速。这些疾病相互作用可能部分源于B细胞功能受损,而B细胞功能依赖于CD4(+) T细胞。

方法

为确定HIV感染对B细胞功能的影响,我们比较了29例HCV感染者在感染HIV前后的HCV抗体水平和特异性,并评估了这些变化与总体CD4(+) T淋巴细胞计数的时间相关性。

结果

HIV感染前的HCV抗体滴度是所有抗原后续滴度的预测指标,CD4(+) T细胞数量减少与几种抗原的抗HCV滴度降低密切相关。CD4(+) T细胞计数<500个细胞/mm(3)与较低的HCV抗体终点滴度显著相关。较高的HCV终点滴度与感染HIV后的年限较短以及(针对核心抗原)当前吸毒有关。

结论

HIV感染会损害HCV特异性抗体的产生,抗体产生的丧失取决于CD4(+) T细胞耗竭。然而,在继续积极注射毒品的人群中,滴度下降的幅度较小。

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