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小鼠脾脏中单核细胞增生李斯特菌感染的早期发病机制。

Early pathogenesis of Listeria monocytogenes infection in the mouse spleen.

作者信息

Conlan J W

机构信息

Trudeau Institute Inc., Saranac Lake, NY 12983, USA.

出版信息

J Med Microbiol. 1996 Apr;44(4):295-302. doi: 10.1099/00222615-44-4-295.

Abstract

Histological observations suggested that in the spleen, blood-borne Listeria monocytogenes bacteria were preferentially ingested by two morphologically distinct mononuclear phagocyte populations present in the marginal zone of the white pulp. The morphologies of these phagocytes corresponded to those of marginal zone macrophages or marginal zone dendritic cells. Moreover, during the first day of infection, the same phagocytes containing listeria apparently translocated from the marginal zone into the white pulp where they established secondary infectious foci. This event was associated with a large influx of neutrophil polymorphonuclear leucocytes (PMNLs) into infected white pulp, and with the disappearance of lymphocytes from this compartment. White pulp lymphocytopenia also occurred in the spleens of listeria-infected mice selectively depleted of neutrophil PMNLs, indicating that these phagocytes were not responsible for displacing or destroying lymphocytes. The implications of these findings for explaining the virulence and immunogenicity of L. monocytogenes are discussed.

摘要

组织学观察表明,在脾脏中,血源单核细胞增生李斯特菌优先被白髓边缘区存在的两种形态不同的单核吞噬细胞群体摄取。这些吞噬细胞的形态与边缘区巨噬细胞或边缘区树突状细胞的形态相对应。此外,在感染的第一天,含有李斯特菌的相同吞噬细胞明显从边缘区转移到白髓,在那里它们形成了继发性感染灶。这一事件与大量中性粒细胞多形核白细胞(PMNLs)涌入受感染的白髓以及该区域淋巴细胞的消失有关。在选择性清除中性粒细胞PMNLs的李斯特菌感染小鼠的脾脏中也出现了白髓淋巴细胞减少,这表明这些吞噬细胞不是导致淋巴细胞移位或破坏的原因。本文讨论了这些发现对解释单核细胞增生李斯特菌的毒力和免疫原性的意义。

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