Fortis Claudio, Poli Guido
Immunology of Infectious Diseases Unit, DIBIT, San Raffaele Scientific Institute, Milan, Italy.
Immunol Res. 2005;33(1):1-21. doi: 10.1385/IR:33:1:001.
Dendritic cells (DC) and natural killer (NK) cells, the main cellular components of the innate immune system, participate in the most ancient first line of defense against infections. Both types of cells patrol peripheral tissues, whereas their rapid recruitment and activation at mucosal surfaces [the major entry point for the human immunodeficiency virus (HIV)] is a hallmark of acute inflammatory response. The ability of HIV to survive and replicate in the human host relies upon several molecular mechanisms eluding the immune surveillance of both adaptive immunity and of DC and NK cells beginning with the acute phase of primary HIV infection. DC and NK cells, unlike CD4+ T cells, are impaired more functionally rather than being depleted by HIV infection. In this article we will review some of the aspects of DC/NK cells interaction with HIV infection both in vitro and in vivo, and we will also speculate on the potential consequence for HIV pathogenesis and for the capacity of the virus to escape the surveillance of the innate immune system.
树突状细胞(DC)和自然杀伤(NK)细胞是固有免疫系统的主要细胞成分,参与对抗感染的最古老的第一道防线。这两种细胞在外周组织中巡逻,而它们在黏膜表面(人类免疫缺陷病毒(HIV)的主要侵入点)的快速募集和激活是急性炎症反应的一个标志。HIV在人类宿主中生存和复制的能力依赖于几种分子机制,这些机制从原发性HIV感染的急性期开始就避开了适应性免疫以及DC和NK细胞的免疫监视。与CD4+T细胞不同,DC和NK细胞在功能上受到的损害更大,而不是因HIV感染而耗竭。在本文中,我们将综述DC/NK细胞与HIV感染在体外和体内相互作用的一些方面,并且我们还将推测其对HIV发病机制以及病毒逃避固有免疫系统监视能力的潜在影响。