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食蟹猴中胸腺免疫病理学与猴免疫缺陷病毒(SIVsm)感染的进展

Thymic immunopathology and progression of SIVsm infection in cynomolgus monkeys.

作者信息

Li S L, Kaaya E E, Ordónez C, Ekman M, Feichtinger H, Putkonen P, Böttiger D, Biberfeld G, Biberfeld P

机构信息

Immunopathology Laboratory, Swedish Institute for Infectious Disease Control, Stockholm.

出版信息

J Acquir Immune Defic Syndr Hum Retrovirol. 1995 May 1;9(1):1-10.

PMID:7536107
Abstract

Thymuses from 22 cynomolgus monkeys infected with simian immunodeficiency virus (SIVsm) developed characteristic cortical and medullary changes including formation of B-cell follicles (8/21) and accumulation of virus immune complexes. Advanced thymic histopathology was correlated with more pronounced immunodeficiency. SIVsm provirus was detected by polymerase chain reaction (PCR) in most (16/18) thymuses and spliced viral env mRNA in 3 (3/7) thymuses with advanced histopathologic changes indicative of thymic SIVsm replication. By combined in situ hybridization (ISH) and immunohistochemistry, viral RNA was localized mainly to the follicular dendritic network, macrophages, multinucleated giant cells, and lymphocytes of the medullary regions. Latent infection by an Epstein-Barr-related herpesvirus (HVMF1) was also found by PCR and by ISH in medullary regions of three (3 of 8) thymuses with B-cell follicles, suggestive of an inductive role for B-cell proliferation in these thymuses. In a control group of HIV-2-infected nonimmunosuppressed monkeys, no comparable thymic changes were observed. Our results indicate that SIV, and probably by analogy HIV, can have direct and diverse pathogenic effects on the thymus that are important in the development of simian (human) AIDS.

摘要

对22只感染了猴免疫缺陷病毒(SIVsm)的食蟹猴的胸腺进行研究,发现其出现了特征性的皮质和髓质变化,包括B细胞滤泡形成(8/21)以及病毒免疫复合物的积累。严重的胸腺组织病理学变化与更明显的免疫缺陷相关。通过聚合酶链反应(PCR)在大多数(16/18)胸腺中检测到了SIVsm前病毒,在3只(3/7)有表明胸腺SIVsm复制的严重组织病理学变化的胸腺中检测到了剪接的病毒env mRNA。通过原位杂交(ISH)和免疫组织化学相结合的方法,发现病毒RNA主要定位于髓质区域的滤泡树突状网络、巨噬细胞、多核巨细胞和淋巴细胞中。在3只(8只中的3只)有B细胞滤泡的胸腺的髓质区域,通过PCR和ISH还发现了一种与爱泼斯坦-巴尔病毒相关的疱疹病毒(HVMF1)的潜伏感染,提示B细胞增殖在这些胸腺中具有诱导作用。在一组感染了HIV-2但未免疫抑制的猴的对照组中,未观察到类似的胸腺变化。我们的结果表明,SIV,可能类推到HIV,可对胸腺产生直接且多样的致病作用,这在猴(人类)艾滋病的发展中很重要。

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