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HIV阳性女性生殖道黏膜中细胞因子微环境的变化。

Changes to the cytokine microenvironment in the genital tract mucosa of HIV+ women.

作者信息

Olaitan A, Johnson M A, Reid W M, Poulter L W

机构信息

Department of Obstetrics and Gynaecology, The Royal Free Hospital and School of Medicine, London, UK.

出版信息

Clin Exp Immunol. 1998 Apr;112(1):100-4. doi: 10.1046/j.1365-2249.1998.00561.x.

Abstract

As previous studies have indicated that genital tract mucosal T cell function may be impaired in HIV infection, we investigated the T cell cytokine mRNA in the genital tract mucosa of HIV-infected women to determine if there are alterations in the cytokine profile which may explain the T cell impairment. The in situ hybridization technique was used to investigate the T helper-1 (Th1: IL-2, interferon-gamma (IFN-gamma)) and Th2 cytokine (IL-4, IL-5, IL-10) mRNA profile in cervical biopsies from 10 HIV+ and 10 HIV- subjects. Cervical intraepithelial neoplasia (CIN) and genital infection had previously been excluded and the distribution of immunocompetent cells within the cervical mucosa was known for each subject. Non-parametric tests were used to compare the optical density (OD) of cytokine mRNA in the HIV+ and HIV- groups. Comparisons were also made between peripheral CD4 lymphocyte counts, cervical CD4/CD8 T lymphocyte ratios and cytokine mRNA OD in HIV+ subjects. The HIV+ women had significantly higher mRNA OD for the Th2 cytokines IL-4, IL-5 and IL-10 than HIV women. There was also significantly lower IL-2 mRNA OD in the former group. HIV+ women had lower IFN-gamma mRNA than HIV- women, but the difference was not statistically significant. There was no correlation between cytokine mRNA OD and peripheral CD4 count or cervical CD4/CD8 ratio. The predominance of Th2 cytokines, which are immuno-inhibitory, in the cervical mucosa of HIV+ women may underlie the impaired cytotoxic potential observed in the CD8+ T lymphocytes and may contribute to the susceptibility of HIV-infected women to recurrent genital tract infections and cervical neoplasia.

摘要

正如先前的研究表明,HIV感染可能会损害生殖道黏膜T细胞功能,我们对HIV感染女性的生殖道黏膜中的T细胞细胞因子mRNA进行了研究,以确定细胞因子谱是否存在改变,这可能解释T细胞功能受损的原因。采用原位杂交技术研究了10名HIV阳性和10名HIV阴性受试者宫颈活检组织中辅助性T细胞1(Th1:白细胞介素-2、干扰素-γ(IFN-γ))和Th2细胞因子(白细胞介素-4、白细胞介素-5、白细胞介素-10)的mRNA谱。先前已排除宫颈上皮内瘤变(CIN)和生殖道感染,并且已知每个受试者宫颈黏膜内免疫活性细胞的分布情况。使用非参数检验比较HIV阳性组和HIV阴性组中细胞因子mRNA的光密度(OD)。还对HIV阳性受试者的外周血CD4淋巴细胞计数、宫颈CD4/CD8 T淋巴细胞比值和细胞因子mRNA OD进行了比较。HIV阳性女性的Th2细胞因子白细胞介素-4、白细胞介素-5和白细胞介素-10的mRNA OD显著高于HIV阴性女性。前一组的白细胞介素-2 mRNA OD也显著较低。HIV阳性女性的干扰素-γ mRNA低于HIV阴性女性,但差异无统计学意义。细胞因子mRNA OD与外周血CD4计数或宫颈CD4/CD8比值之间无相关性。免疫抑制性的Th2细胞因子在HIV阳性女性宫颈黏膜中的优势可能是CD8 + T淋巴细胞细胞毒性潜能受损的基础,并且可能导致HIV感染女性易患复发性生殖道感染和宫颈肿瘤。

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