Suppr超能文献

来自对HIV感染者淋巴组织研究的致病机制见解。

Pathogenic insights from studies of lymphoid tissue from HIV-infected individuals.

作者信息

Cohen O J, Pantaleo G, Schwartzentruber D J, Graziosi C, Vaccarezza M, Fauci A S

机构信息

National Institute of Allergy and Infectious Diseases, Laboratory of Immunoregulation, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

J Acquir Immune Defic Syndr Hum Retrovirol. 1995;10 Suppl 1:S6-14.

PMID:8595512
Abstract

Studies of lymphoid tissue from HIV-infected individuals have provided critical insights into the pathogenesis of HIV disease. Systemic dissemination of virus via the lymphatic system occurs at a very early stage after infection. Explosive viral replication within lymphoid tissue ensues, before the development of cell-mediated and humoral immune responses. By the time potent immune responses downregulate viral expression, an immense viral reservoir within lymphoid tissue has already been established. During the stage of dichotomy in viral load between lymph node and peripheral blood, the viral reservoir is maintained by the ability of the follicular dendritic cells (FDC) network to efficiently trap extracellular virions, as well as by immunologic and microenvironmental factors favoring infection of susceptible cells and sequestration of cells already infected. Degeneration of the FDC network and wholesale disruption of lymphoid architecture herald late-stage disease. The dysfunctional lymphoid tissue contributes directly to immunodeficiency and to sharp increases in viral burden and replication as mechanical and immune controls are lost. Studies in HIV-infected long-term nonprogressors indicate that these individuals are able to maintain cell-mediated and humoral immune responses against HIV. These immune responses are responsible, at least in part, for the maintenance of intact lymphoid tissue architecture and the low levels of viral burden and replication detected in these individuals. Studies of the effect of antiretroviral therapy on HIV infection in lymphoid tissue show that decreases in plasma viremia are associated with and most likely are caused by decreases in viral replication within lymphoid tissue. Further understanding of the pathogenic mechanisms within lymphoid tissue will have important implications for early intervention aimed at inducing a long-term nonprogressor state (i.e., preventing disruption of lymphoid tissue integrity), and later intervention aimed at arresting or even reversing damage to the lymphoid system.

摘要

对HIV感染者淋巴组织的研究为深入了解HIV疾病的发病机制提供了关键见解。感染后很早阶段,病毒就通过淋巴系统发生全身播散。在细胞介导免疫和体液免疫反应形成之前,淋巴组织内就会发生病毒爆发性复制。当有效的免疫反应下调病毒表达时,淋巴组织内已形成了巨大的病毒储存库。在淋巴结和外周血病毒载量出现差异的阶段,滤泡树突状细胞(FDC)网络有效捕获细胞外病毒粒子的能力,以及有利于易感细胞感染和已感染细胞隔离的免疫和微环境因素,维持了病毒储存库。FDC网络退化和淋巴组织结构的全面破坏预示着疾病晚期。功能失调的淋巴组织直接导致免疫缺陷,并随着机械和免疫控制的丧失,使病毒载量和复制急剧增加。对HIV感染的长期不进展者的研究表明,这些个体能够维持针对HIV的细胞介导免疫和体液免疫反应。这些免疫反应至少部分负责维持完整的淋巴组织结构,以及这些个体中检测到的低水平病毒载量和复制。抗逆转录病毒疗法对淋巴组织中HIV感染影响的研究表明,血浆病毒血症的降低与淋巴组织内病毒复制的减少相关,并且很可能是由其引起的。进一步了解淋巴组织内的致病机制对于旨在诱导长期不进展状态(即防止淋巴组织完整性破坏)的早期干预,以及旨在阻止甚至逆转淋巴系统损伤的后期干预具有重要意义。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验