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幽门螺杆菌感染时,人胃黏膜中的淋巴细胞具有辅助性T细胞1表型。

Lymphocytes in the human gastric mucosa during Helicobacter pylori have a T helper cell 1 phenotype.

作者信息

Bamford K B, Fan X, Crowe S E, Leary J F, Gourley W K, Luthra G K, Brooks E G, Graham D Y, Reyes V E, Ernst P B

机构信息

Department of Microbiology and Immunology, The Queen's University of Belfast, Northern Ireland.

出版信息

Gastroenterology. 1998 Mar;114(3):482-92. doi: 10.1016/s0016-5085(98)70531-1.

Abstract

BACKGROUND & AIMS: Studies have shown that gastric T cells are increased during Helicobacter pylori infection. The purpose of this study was to characterize the human gastric T-cell responses in the presence or absence of H. pylori.

METHODS

T-cell surface antigens were examined by immunohistochemistry or after isolation for evaluation of surface antigens and cytoplasmic cytokines using flow cytometry.

RESULTS

CD4+ and CD8+ T cells were increased in situ during infection with H. pylori. Freshly isolated gastric T cells expressed cytoplasmic interferon gamma (IFN-gamma) and interleukin (IL)-2 after a brief stimulation. Simultaneous four-color flow cytometry demonstrated that both CD8+ and CD4+ T cells expressed IFN-gamma. Because stimulation through CD30 favors the induction of IL-5 and Th2 cells, gastric and colonic T cells were examined for CD30 expression. Consistent with the notion that Th2 cells are found in the intestine, CD30 was evident throughout the lamina propria of the colon but was virtually absent in the stomach. Furthermore, freshly isolated gastric T cells produced little IL-4 and virtually no IL-5 or tumor necrosis factor beta.

CONCLUSIONS

These observations show that gastric T cells resemble the Th1 type, which may explain their failure to induce immunity to H. pylori and their ability to contribute to the pathogenesis of gastric disease.

摘要

背景与目的

研究表明,幽门螺杆菌感染期间胃T细胞数量增加。本研究旨在描述幽门螺杆菌存在或不存在时人类胃T细胞的反应特征。

方法

通过免疫组织化学或分离后使用流式细胞术检测T细胞表面抗原,以评估表面抗原和细胞质细胞因子。

结果

幽门螺杆菌感染期间,原位CD4⁺和CD8⁺T细胞增加。新鲜分离的胃T细胞在短暂刺激后表达细胞质干扰素γ(IFN-γ)和白细胞介素(IL)-2。同时进行的四色流式细胞术显示,CD8⁺和CD4⁺T细胞均表达IFN-γ。由于通过CD30刺激有利于诱导IL-5和Th2细胞,因此检测了胃和结肠T细胞的CD30表达。与在肠道中发现Th2细胞的观点一致,CD30在结肠固有层中明显存在,但在胃中几乎不存在。此外,新鲜分离的胃T细胞产生的IL-4很少,几乎不产生IL-5或肿瘤坏死因子β。

结论

这些观察结果表明,胃T细胞类似于Th1型,这可能解释了它们无法诱导对幽门螺杆菌的免疫以及它们在胃部疾病发病机制中的作用。

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