Derdeyn Cynthia A, Silvestri Guido
Division of Infectious Diseases, Department of Pathology, and Emory Vaccine Center, Emory University, 954 Gatewood Road NE, Atlanta, Georgia 30329, USA.
Curr Opin Immunol. 2005 Aug;17(4):366-73. doi: 10.1016/j.coi.2005.06.001.
Recent studies suggest that the pathogenesis of HIV infection and AIDS involves two distinct phases. During acute infection, massive depletion of CD4+CCR5+ memory T cells within the mucosal-associated lymphoid tissue leads to major and potentially irreversible damage to CD4+ T-cell-mediated immune functions. The emergence of potent, but ultimately ineffective, cell-mediated and humoral responses to HIV leads to the chronic phase of infection, which is characterized by partial control of viral replication, chronic immune activation, progressive decline of the naïve and memory T-cell pool, and systemic CD4+ T-cell depletion. The identification of these two pathogenic phases of HIV infection could have important implications in terms of HIV therapy and vaccine development.
近期研究表明,HIV感染及艾滋病的发病机制涉及两个不同阶段。在急性感染期间,黏膜相关淋巴组织内的CD4+CCR5+记忆T细胞大量耗竭,导致CD4+ T细胞介导的免疫功能遭受重大且可能不可逆转的损害。针对HIV的有效但最终无效的细胞介导和体液反应的出现,导致了感染的慢性阶段,其特征为病毒复制的部分控制、慢性免疫激活、初始和记忆T细胞库的逐渐减少以及全身性CD4+ T细胞耗竭。明确HIV感染的这两个致病阶段可能对HIV治疗和疫苗研发具有重要意义。