Department of Microbiology, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1124, New York, NY 10029, USA.
Immunol Res. 2012 Dec;54(1-3):140-51. doi: 10.1007/s12026-012-8304-8.
Members of the Herpesviridae family have the capacity to undergo both lytic and latent infection to establish a lifelong relationship with their host. Following primary infection, human cytomegalovirus (HCMV) can persist as a subclinical, recurrent infection for the lifetime of an individual. This quiescent portion of its life cycle is termed latency and is associated with periodic bouts of reactivation during times of immunosuppression, inflammation, or stress. In order to exist indefinitely and establish infection, HCMV encodes a multitude of immune modulatory mechanisms devoted to escaping the host antiviral response. HCMV has become a paradigm for studies of viral immune evasion of antigen presentation by both major histocompatibility complex (MHC) class I and II molecules. By restricting the presentation of viral antigens during both productive and latent infection, HCMV limits elimination by the human immune system. This review will focus on understanding how the virus manipulates the pathways of antigen presentation in order to modulate the host response to infection.
疱疹病毒家族的成员能够进行裂解和潜伏感染,从而与宿主建立终身关系。初次感染后,人类巨细胞病毒 (HCMV) 可以作为亚临床、复发性感染存在于个体的一生中。其生命周期的这个静止部分称为潜伏,并且与免疫抑制、炎症或应激期间周期性的再激活有关。为了无限期地存在并建立感染,HCMV 编码了多种免疫调节机制,致力于逃避宿主的抗病毒反应。HCMV 已成为研究病毒通过主要组织相容性复合体 (MHC) 类 I 和 II 分子逃避抗原呈递的范例。通过在产生活性和潜伏感染期间限制病毒抗原的呈递,HCMV 限制了人类免疫系统的清除。这篇综述将重点探讨病毒如何操纵抗原呈递途径,从而调节宿主对感染的反应。