Shacklett Barbara L
Department of Medical Microbiology and Immunology, University of California, Davis, California, USA.
Curr Opin HIV AIDS. 2008 Sep;3(5):541-7. doi: 10.1097/COH.0b013e32830ab9ee.
This review summarizes recent literature in the field of mucosal immunology as it applies to HIV transmission and pathogenesis.
Pertinent recent findings include elucidation of the role of mucosal antigen-presenting cells and retinoic acid in imprinting a gut-homing phenotype on antigen-specific T and B cells, and the identification of Th17 and T regulatory cells as key modulators of the balance between tolerance and inflammation in mucosal tissues.
Mucosal surfaces of the body serve as the major portal of entry for HIV. These tissues also house a majority of the body's lymphocytes, including the CD4 T-cells that are the major cellular target for HIV infection. Elucidating mucosal immune responses is critical to our understanding of the host-pathogen relationship for two reasons: first, mucosal barriers are defended by a range of innate and adaptive defenses that might be exploited to develop effective vaccines or microbicides; second, adaptive immune responses in mucosal lymphoid tissues might serve to limit viral replication, decreasing the host's viral burden as well as reducing the likelihood of sexual transmission to a naïve host.
本综述总结了黏膜免疫学领域中与HIV传播和发病机制相关的近期文献。
近期的相关研究发现包括阐明黏膜抗原呈递细胞和视黄酸在赋予抗原特异性T细胞和B细胞肠道归巢表型方面的作用,以及确定Th17和调节性T细胞是黏膜组织中耐受性与炎症平衡的关键调节因子。
人体的黏膜表面是HIV进入的主要门户。这些组织还容纳了人体大部分淋巴细胞,包括作为HIV感染主要细胞靶点的CD4 T细胞。阐明黏膜免疫反应对于我们理解宿主与病原体的关系至关重要,原因有二:其一,黏膜屏障由一系列固有和适应性防御机制保护,这些机制可能被用于开发有效的疫苗或杀菌剂;其二,黏膜淋巴组织中的适应性免疫反应可能有助于限制病毒复制,降低宿主的病毒载量,并减少向未感染宿主性传播的可能性。