Barker E, Mackewicz C E, Reyes-Terán G, Sato A, Stranford S A, Fujimura S H, Christopherson C, Chang S Y, Levy J A
Department of Medicine, University of California, San Francisco, USA.
Blood. 1998 Nov 1;92(9):3105-14.
Infection with the human immunodeficiency virus (HIV) leads to a decrease in CD4(+) T cells and disease progression within a decade of seroconversion. However, a small group of infected people, despite being infected by HIV for 10 or more years, remain clinically asymptomatic and have stable CD4(+) cell counts without taking antiretroviral medication. To determine why these individuals, known as long-term survivors (LTS), remain healthy, the hematological profiles, viral load and properties, HIV coreceptor genotype, and anti-HIV immune responses of these people were compared with those of individuals who have progressed to disease (Progressors) over the same time period. Unlike Progressors, LTS have a low circulating viral load and a low number of HIV-infected cells. These differences in the levels of the viral load were not associated with a dominant biologic viral phenotype, varying growth kinetics of the virus, mutation in the cellular CCR5 gene, or the presence of neutralizing antibodies. Importantly, the difference in viral load could be explained by the enhanced ability of CD8(+) cells from LTS to suppress HIV replication.
感染人类免疫缺陷病毒(HIV)会导致CD4(+) T细胞数量减少,并在血清转化后的十年内出现疾病进展。然而,一小部分感染者尽管感染HIV达10年或更长时间,但在未服用抗逆转录病毒药物的情况下仍保持临床无症状,且CD4(+)细胞计数稳定。为了确定这些被称为长期存活者(LTS)的个体为何保持健康,将这些人的血液学特征、病毒载量及特性、HIV共受体基因型和抗HIV免疫反应与同期病情进展者(进展者)进行了比较。与进展者不同,LTS的循环病毒载量较低,HIV感染细胞数量也较少。病毒载量水平的这些差异与占主导的生物学病毒表型、病毒不同的生长动力学、细胞CCR5基因突变或中和抗体的存在无关。重要的是,病毒载量的差异可以用LTS的CD8(+)细胞抑制HIV复制能力增强来解释。