Brenchley Jason M, Douek Daniel C
Viral Pathogenesis and Vaccine Section, Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
Curr Opin HIV AIDS. 2008 May;3(3):356-61. doi: 10.1097/COH.0b013e3282f9ae9c.
Significant gastrointestinal pathology occurs in progressive HIV and simian immunodeficiency virus (SIV) infections. This review will examine the relationship between the detrimental events to the gastrointestinal tract during the acute phase of infection and disease progression through the chronic phase and, ultimately, AIDS.
Gastrointestinal tract CD4 T cells are dramatically depleted in acutely HIV-infected humans and SIV-infected rhesus macaques, sooty mangabeys, and African green monkeys. In addition HIV infection of humans and SIV-infection of rhesus macaques are characterized by enteropathy and increased intestinal permeability. While SIV-infected rhesus macaques and HIV-infected humans manifest chronic and systemic immune activation and microbial translocation, and progress to chronic infection and AIDS, however, SIV-infected sooty mangabeys and African green monkeys do not.
Recent studies have increased our understanding of the mechanisms relating structural and immunological damage to the gastrointestinal tract during the acute phase of HIV/SIV infection to immune activation and disease progression in the chronic phase.
严重的胃肠道病变发生于进展性HIV和猴免疫缺陷病毒(SIV)感染中。本综述将探讨感染急性期胃肠道所发生的有害事件与疾病从慢性期最终发展至艾滋病之间的关系。
在急性HIV感染的人类以及感染SIV的恒河猴、乌黑白眉猴和非洲绿猴中,胃肠道CD4 T细胞显著耗竭。此外,人类的HIV感染和恒河猴的SIV感染均以肠道病变和肠道通透性增加为特征。虽然感染SIV的恒河猴和感染HIV的人类表现出慢性和全身性免疫激活以及微生物易位,并进展为慢性感染和艾滋病,然而,感染SIV的乌黑白眉猴和非洲绿猴却不会如此。
最近的研究增进了我们对HIV/SIV感染急性期胃肠道结构和免疫损伤与慢性期免疫激活及疾病进展之间关系机制的理解。