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在无胸腺裸鼠和免疫功能正常的大鼠中,不同亚群的T细胞与自然杀伤细胞、巨噬细胞和活化的小胶质细胞共同参与对刚地弓形虫的脑内免疫反应。

Different subsets of T cells in conjunction with natural killer cells, macrophages, and activated microglia participate in the intracerebral immune response to Toxoplasma gondii in athymic nude and immunocompetent rats.

作者信息

Schlüter D, Hein A, Dörries R, Deckert-Schlüter M

机构信息

Department of Medical Microbiology and Hygiene, Heidelberg University, Mannheim Clinic, Germany.

出版信息

Am J Pathol. 1995 Apr;146(4):999-1007.

Abstract

Oral infection of athymic nude and immunocompetent Lewis rats with Toxoplasma gondii induced a chronic nonlethal encephalitis. The histopathological pattern of Toxoplasma encephalitis was significantly different in both groups of animals and there were substantially larger numbers of Toxoplasma cysts in the brains of athymic rats. Combined immunohistochemical and flow cytometric analyses of intracerebral leukocytes identified alpha beta TCR+ CD4+ and CD8+ T cells; macrophages, and natural killer cells as inflammatory cell populations in immunocompetent rats, whereas in athymic rats natural killer cells, macrophages, and gamma delta TCR+ CD8+ CD3+ T cells contributed to the intracerebral inflammatory infiltrates. These findings not only point to a major participation of alpha beta TCR+ T cells to the intracerebral immune response, but also indicate that they are not essential to prevent the development of a lethal Toxoplasma encephalitis. In addition, microglia were strongly activated in both strains with simultaneous up-regulation of major histocompatibility complex class I and II antigens and CD4. Activation of microglia was most prominent in athymic rats, demonstrating that immunodeficiency does not preclude an up-regulation of these molecules including the human immunodeficiency virus receptor CD4 on microglial cells.

摘要

用刚地弓形虫经口感染无胸腺裸鼠和具有免疫活性的Lewis大鼠,可诱发慢性非致死性脑炎。两组动物的弓形虫脑炎组织病理学模式显著不同,无胸腺大鼠脑内的弓形虫囊肿数量明显更多。对脑内白细胞进行免疫组织化学和流式细胞术联合分析,在具有免疫活性的大鼠中确定αβTCR⁺CD4⁺和CD8⁺T细胞、巨噬细胞以及自然杀伤细胞为炎性细胞群体,而在无胸腺大鼠中,自然杀伤细胞、巨噬细胞以及γδTCR⁺CD8⁺CD3⁺T细胞构成脑内炎性浸润。这些发现不仅表明αβTCR⁺T细胞在脑内免疫反应中起主要作用,还表明它们对于预防致死性弓形虫脑炎的发生并非必不可少。此外,两种品系的小胶质细胞均被强烈激活,同时主要组织相容性复合体I类和II类抗原以及CD4上调。小胶质细胞的激活在无胸腺大鼠中最为显著,表明免疫缺陷并不妨碍这些分子上调,包括小胶质细胞上的人类免疫缺陷病毒受体CD4。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26e8/1869253/91ded89d038c/amjpathol00052-0224-a.jpg

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