Kobelt D, Lechmann M, Steinkasserer A
Department of Dermatology, University of Erlangen, Hartmannstrasse 14, 91052 Erlangen, Germany.
Curr Top Microbiol Immunol. 2003;276:145-61. doi: 10.1007/978-3-662-06508-2_7.
Dendritic cells (DCs) are the most potent antigen-presenting cells, because they are also able to induce native T cells. Thus they are crucial in the induction of antiviral immune responses. Several viral immune escape mechanisms have been described; here we concentrate on the interaction between DCs and herpes simplex virus type 1 (HSV-1). DCs can be infected by HSV-1; however, only immature DCs generate infectious viral particles, whereas mature DCs do not support virus production and only immediate-early and early viral transcripts are generated. To induce potent immune responses DCs must mature. Interestingly, HSV-1 interferes with this maturation process, thus inhibiting antiviral T cell stimulation. Furthermore, HSV-1 strongly interferes with DC-mediated T cell proliferation. A striking finding was the complete degradation of CD83, the best-known marker for mature DC, after HSV-1 infection in lysosomal compartments. This CD83 degradation coincided with a clearly reduced T cell stimulation representing an additional new escape strategy. The functional role and the importance of CD83 are discussed in detail.
树突状细胞(DCs)是最有效的抗原呈递细胞,因为它们还能够激活天然T细胞。因此,它们在诱导抗病毒免疫反应中至关重要。已经描述了几种病毒免疫逃逸机制;在这里,我们专注于DCs与1型单纯疱疹病毒(HSV-1)之间的相互作用。HSV-1可以感染DCs;然而,只有未成熟的DCs能产生有传染性的病毒颗粒,而成熟的DCs不支持病毒产生,仅产生立即早期和早期病毒转录本。为了诱导有效的免疫反应,DCs必须成熟。有趣的是,HSV-1干扰了这个成熟过程,从而抑制了抗病毒T细胞的刺激。此外,HSV-1强烈干扰DC介导的T细胞增殖。一个显著的发现是,在溶酶体区室中HSV-1感染后,成熟DC最知名的标志物CD83完全降解。这种CD83降解与明显降低的T细胞刺激同时发生,代表了一种新的额外逃逸策略。文中详细讨论了CD83的功能作用及其重要性。