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人肺泡巨噬细胞作为新型隐球菌感染中抗原呈递细胞的作用。

Role of human alveolar macrophages as antigen-presenting cells in Cryptococcus neoformans infection.

作者信息

Vecchiarelli A, Dottorini M, Pietrella D, Monari C, Retini C, Todisco T, Bistoni F

机构信息

Department of Experimental Medicine and Biochemical Sciences, University of Perugia, Italy.

出版信息

Am J Respir Cell Mol Biol. 1994 Aug;11(2):130-7. doi: 10.1165/ajrcmb.11.2.8049074.

Abstract

The contribution of human alveolar macrophages (AM) from normal subjects in Cryptococcus neoformans infection was investigated. AM were able to efficiently phagocytize the fungus after opsonization, but killing activity did not occur at an effector-to-target ratio of 10:1 in a 6-h incubation since there was an inhibition of phagosome-lysosome fusion. Moreover, the role of AM as antigen-presenting cells was investigated. Cryptococcus-laden AM were co-cultured with autologous T lymphocytes and lymphoproliferation was determined; a massive blastogenic response of alpha/beta TCR-bearing T lymphocytes was observed. The response started after 1 day of co-culture and was triggered and regulated by IL-1 produced by AM in response to C. neoformans. Finally, the antigen-presentation process was associated with HLA class II DR molecules. This finding suggests that AM play a key role in the lung as antigen-presenting cells and, through the secretion of IL-1, regulate proliferation and activation of T lymphocytes, which are important in mediating pulmonary clearance. We speculate that in immunodepressive conditions, the impairment of AM functions could contribute to the spread of C. neoformans infection from the lung.

摘要

研究了正常受试者的人肺泡巨噬细胞(AM)在新型隐球菌感染中的作用。调理后,AM能够有效地吞噬真菌,但在6小时孵育中,效应细胞与靶细胞比例为10:1时未出现杀伤活性,因为存在吞噬体-溶酶体融合的抑制。此外,还研究了AM作为抗原呈递细胞的作用。将载有隐球菌的AM与自体T淋巴细胞共培养,并测定淋巴细胞增殖;观察到携带α/βTCR的T淋巴细胞有大量的增殖反应。共培养1天后开始出现反应,由AM对新型隐球菌产生的IL-1触发和调节。最后,抗原呈递过程与HLA II类DR分子相关。这一发现表明,AM在肺中作为抗原呈递细胞起关键作用,并通过分泌IL-1调节T淋巴细胞的增殖和激活,这对介导肺部清除很重要。我们推测,在免疫抑制条件下,AM功能的损害可能导致新型隐球菌感染从肺部扩散。

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