首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >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.
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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.

机译:T细胞的不同子集与自然杀伤细胞巨噬细胞和活化的小胶质细胞一起参与无胸腺裸鼠和具有免疫能力的大鼠对弓形虫的脑内免疫反应。

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摘要

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.
机译:弓形虫口服感染无胸腺裸露和具有免疫能力的Lewis大鼠时,会引起慢性非致死性脑炎。两组动物中的弓形虫脑炎的组织病理学模式均存在显着差异,并且无胸腺大鼠大脑中的弓形虫囊肿数量明显较多。结合免疫组织化学和流式细胞术对脑白细胞进行了分析,鉴定出了αβTCR + CD4 +和CD8 + T细胞。巨噬细胞和天然杀伤细胞作为免疫活性大鼠中的炎症细胞种群,而在无胸腺大鼠中,天然杀伤细胞,巨噬细胞和γ-δTCR + CD8 + CD3 + T细胞有助于脑内炎性浸润。这些发现不仅表明αβTCR + T细胞主要参与了脑内免疫反应,而且还表明它们对于预防致命的弓形虫性脑炎的发展并非至关重要。此外,小胶质细胞在两种菌株中均被强烈激活,同时同时上调主要的组织相容性复合物I和II类抗原和CD4。小胶质细胞的激活在无胸腺大鼠中最为突出,表明免疫缺陷并不排除小胶质细胞上这些分子(包括人类免疫缺陷病毒受体CD4)的上调。

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