Saag M S
Department of Medicine, University of Alabama at Birmingham 35294.
AIDS Res Hum Retroviruses. 1994 Aug;10(8):887-92. doi: 10.1089/aid.1994.10.887.
Understanding of the immunopathogenesis of HIV infection is becoming more advanced as the activity of HIV infection in lymph nodes is appreciated and as improved virological measures permit more accurate quantitation of viral burden in patients at all stages of HIV disease. Although CD4+ cell counts remain important prognostic indicators, their role as a surrogate for direct antiviral activity has been questioned and increasing focus has been placed on more direct quantitative viral measures that are now available. After an initial explosive burst of viral replication during acute seroconversion that is downregulated by the immune system, these newer markers have revealed that viral replication is ongoing during the so-called "clinically latent" period of HIV infection. One of the most active sites of viral replication during this asymptomatic period is in lymphoid tissues. Over time, however, immunological control of HIV wanes, the site of replication shifts from the lymph nodes to other lymphoid organs, and disease progression ensues. The role of viral diversity in late-stage HIV disease is now well established, yet its role in pathogenesis and establishment of viruses resistant to antiviral agents is not fully established. Increased understanding of how HIV causes immune dysfunction may help us control direct and indirect (opportunistic) complications of HIV infection.
随着人们对淋巴结中HIV感染活动的认识不断加深,以及改进后的病毒学检测方法能够更准确地定量HIV疾病各个阶段患者的病毒载量,对HIV感染免疫发病机制的理解也日益深入。尽管CD4 +细胞计数仍然是重要的预后指标,但其作为直接抗病毒活性替代指标的作用受到了质疑,人们越来越关注目前可用的更直接的病毒定量检测方法。在急性血清转化期间病毒复制最初出现爆发性激增后,免疫系统会对其进行下调,这些更新的指标显示,在HIV感染所谓的“临床潜伏期”,病毒复制仍在持续。在此无症状期,病毒复制最活跃的部位之一是淋巴组织。然而,随着时间的推移,对HIV的免疫控制减弱,复制部位从淋巴结转移到其他淋巴器官,疾病随之进展。病毒多样性在晚期HIV疾病中的作用现已明确,但其在发病机制以及对抗病毒药物产生抗性的病毒形成过程中的作用尚未完全明确。对HIV如何导致免疫功能障碍的进一步了解,可能有助于我们控制HIV感染的直接和间接(机会性)并发症。