Sabbaj Steffanie, Mestecky Jiri
Departments of Medicine, Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, AL.
Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL.
Curr Immunol Rev. 2019;15(1):41-48. doi: 10.2174/1573395514666180621152303.
The mucosal immune systems of the genital and intestinal tracts as the most frequent sites of HIV-1 entry, display remarkable immunological differences from the systemic immune compartment which must be considered in the evaluation of humoral and cellular immune responses to HIV-1. Marked differences in the fluids from the genital and intestinal tracts and in plasma with respect to the Ig isotypes, their levels, molecular forms and distinct effector functions must be taken into consideration in the evaluation and interpretation of humoral immune responses. Because of the low levels and highly pronounced variation in Ig content, HIV-1-specific antibody concentrations should be always related to the levels of total Ig of a given isotype. This practice will avoid inevitable differences due to the small volumes of collected fluids and sample dilution during the collection and processing of samples from external secretions. Furthermore, appropriate controls and immunochemical assays should be used to complement and confirm results generated by ELISA, which is prone to false positivity. In the evaluation of antibody-mediated virus neutralization in external secretions, precautions and rigorous controls must be used to exclude the effect of innate humoral factors. The evaluation of cell-mediated immune responses in mucosal tissues is difficult due to the low yields of cells obtained from tissue biopsies or cytobrush scrapings. Furthermore, tissue biopsies of, for example rectal mucosa, provide information pertinent exclusively to this local site, which due to the differences in distribution of cells of different phenotypes, do not provide information generalized to the entire intestinal tract. Importantly, studies concerning the kinetics of cellular responses are difficult to perform due to the limited availability of samples or to the inability of obtaining frequent repeated tissue biopsies. For sampling the female genital tract parallel collection of menstrual and peripheral blood yields high numbers of cells that permit their detailed phenotypic and functional analyses. In contrast to tissue biopsies, this non-traumatic collection procedure, results in high cell yields and repeated monthly sampling permits extensive and parallel functional studies of kinetics and unique characteristics of HIV-1-specific cellular responses in the female genital tract and peripheral blood.
作为HIV-1最常见的侵入部位,生殖道和肠道的黏膜免疫系统与全身免疫区室表现出显著的免疫学差异,在评估针对HIV-1的体液免疫和细胞免疫反应时必须予以考虑。在评估和解释体液免疫反应时,必须考虑生殖道和肠道分泌物以及血浆中Ig同种型、其水平、分子形式和独特效应功能的显著差异。由于Ig含量水平低且变化很大,HIV-1特异性抗体浓度应始终与给定同种型的总Ig水平相关。这种做法将避免因收集的分泌物体积小以及在收集和处理来自外分泌液的样本期间样本稀释而产生的不可避免的差异。此外,应使用适当的对照和免疫化学测定来补充和确认ELISA产生的结果,ELISA容易出现假阳性。在评估外分泌液中抗体介导的病毒中和作用时,必须采取预防措施并进行严格对照以排除先天性体液因子的影响。由于从组织活检或细胞刷刮取获得的细胞产量低,评估黏膜组织中的细胞介导免疫反应很困难。此外,例如直肠黏膜的组织活检仅提供与该局部部位相关的信息,由于不同表型细胞分布的差异,该信息不能推广到整个肠道。重要的是,由于样本可用性有限或无法频繁重复进行组织活检,关于细胞反应动力学的研究难以开展。对于女性生殖道采样,月经血和外周血的平行采集可获得大量细胞,从而允许对其进行详细的表型和功能分析。与组织活检不同,这种非侵入性采集程序可产生高细胞产量,并且每月重复采样允许对女性生殖道和外周血中HIV-1特异性细胞反应的动力学和独特特征进行广泛且平行的功能研究。