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获得性免疫缺陷综合征中的胸腺。与其他类型免疫缺陷疾病的比较,以及1型人类免疫缺陷病毒成分的存在情况。

The thymus in acquired immune deficiency syndrome. Comparison with other types of immunodeficiency diseases, and presence of components of human immunodeficiency virus type 1.

作者信息

Schuurman H J, Krone W J, Broekhuizen R, van Baarlen J, van Veen P, Golstein A L, Huber J, Goudsmit J

机构信息

Department of Internal Medicine University Hospital, The Netherlands.

出版信息

Am J Pathol. 1989 Jun;134(6):1329-38.

PMID:2474255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1879947/
Abstract

The authors studied thymus specimens taken at autopsy from eight acquired immune deficiency syndrome (AIDS) patients and compared these with those taken from four patients with congenital immunodeficiency (unrelated to an intrinsic thymus defect) and seven patients after allogeneic bone marrow transplantation. In all cases, histology showed a severely involuted architecture, compatible with a debilitating disease before death. There were no major differences between thymus tissue in AIDS patients and in the other patients studied. This argues against the claim expressed in the literature that the epithelial microenvironment incurs particular HIV-1-induced injury in AIDS. This conclusion is substantiated by immunohistochemistry for HIV-1 gag and env proteins, and by hybridohistochemistry for gag/pol and env mRNA of HIV-1. Positive cells were observed only in low numbers, both inside the epithelial parenchyma and in the (expanded) perivascular areas. An interesting finding was the labeling of subcapsular/medullary epithelium in normal uninvoluted thymus by a number of antibodies to HIV-1 gag p17 and p24 proteins. Compatible with this labeling was the staining of epithelial stalks in hyperinvoluted thymuses irrespective of disease category. The previously reported cross-reactivity between HIV-1 core protein and thymosin alpha 1 cannot fully explain this observation, because the epithelium in the hyperinvoluted state is negative for thymosin alpha 1. This study confirms and extends previous reports on the endogenous presence of epitopes of retroviral antigens in thymic epithelium.

摘要

作者研究了8例获得性免疫缺陷综合征(艾滋病)患者尸检时获取的胸腺标本,并将其与4例先天性免疫缺陷患者(与胸腺固有缺陷无关)及7例异基因骨髓移植患者的胸腺标本进行比较。在所有病例中,组织学显示胸腺结构严重萎缩,这与患者生前患有消耗性疾病相符。艾滋病患者的胸腺组织与其他研究对象的胸腺组织之间无显著差异。这与文献中所声称的艾滋病中上皮微环境会遭受特定的HIV-1诱导损伤的观点相悖。这一结论通过针对HIV-1 gag和env蛋白的免疫组织化学以及针对HIV-1 gag/pol和env mRNA的杂交组织化学得以证实。仅在上皮实质内和(扩张的)血管周围区域观察到少量阳性细胞。一个有趣的发现是,在正常未萎缩的胸腺中,许多针对HIV-1 gag p17和p24蛋白的抗体标记了被膜下/髓质上皮。与此标记相符的是,无论疾病类别如何,高度萎缩胸腺中的上皮茎均有染色。先前报道的HIV-1核心蛋白与胸腺素α1之间的交叉反应无法完全解释这一观察结果,因为处于高度萎缩状态的上皮对胸腺素α1呈阴性。本研究证实并扩展了先前关于胸腺上皮中存在逆转录病毒抗原表位的报道。

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Monoclonal antibody against human T cell leukemia virus p19 defines a human thymic epithelial antigen acquired during ontogeny.抗人T细胞白血病病毒p19的单克隆抗体可识别一种在个体发育过程中获得的人胸腺上皮抗原。
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Rapid and irreversible CD4+ T-cell depletion induced by the highly pathogenic simian/human immunodeficiency virus SHIV(DH12R) is systemic and synchronous.高致病性猿猴/人类免疫缺陷病毒SHIV(DH12R)诱导的CD4 + T细胞快速且不可逆的耗竭是全身性和同步性的。
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Antiviral therapy reduces viral burden but does not prevent thymic involution in young cats infected with feline immunodeficiency virus.抗病毒疗法可降低病毒载量,但不能预防感染猫免疫缺陷病毒的幼猫的胸腺退化。
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