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肺泡巨噬细胞与星形诺卡菌的相互作用:吞噬作用、吞噬体-溶酶体融合及杀菌活性的免疫增强作用

Interaction of alveolar macrophages with Nocardia asteroides: immunological enhancement of phagocytosis, phagosome-lysosome fusion, and microbicidal activity.

作者信息

Davis-Scibienski C, Beaman B L

出版信息

Infect Immun. 1980 Nov;30(2):578-87. doi: 10.1128/iai.30.2.578-587.1980.

Abstract

Normal and specifically activated rabbit alveolar macrophages were infected in vitro with Nocardia asteroides GUH-2. In the presence of serum from normal rabbits, no significant differences were noted between normal and activated alveolar macrophages with respect to phagocytosis, incidence of phagosomelysosome fusion, or nocardicidal activity. However, all of these macrophage functions were enhanced by various immunological components. Serum from immunized rabbits enhanced phagocytosis of nocardial cells by activated macrophages, and there was an additional increase in phagocytosis observed when alveolar lining material was present. Complement had no effect on the ability of the macrophages to phagocytize nocardial cells. The greatest percentage of organisms phagocytized was observed when specifically primed lymph node cells, alveolar lining material, and serum from immunized rabbits were present in the incubation medium. N. asteroides GUH-2 inhibited phagosome-lysosome fusion in normal macrophages in the presence of serum from normal rabbits. However, addition of serum from immunized rabbits or the addition of specifically primed lymphocytes increased the amount of phagosome-lysosome fusion, whereas complement had no effect on this fusion process. Nocardial viability was not reduced when either normal or activated macrophages were infected with bacteria in the presence of normal serum, immune serum, or alveolar lining material. However, specifically activated macrophages incubated with primed lymph node cells obtained from immunized rabbits were able to both decrease the number of viable organisms recovered and to increase the incidence and extent of bacterial cell damage. The greatest number of organisms were killed by specifically activated macrophages when the bacterial cells were incubated with primed lymph node cells suspended in immune serum and alveolar lining material. These results indicate that activated macrophages alone are not sufficient to kill ingested N. asteroides GUH-2 and that specifically primed lymphocytes are important in host resistance to nocardial infections.

摘要

将正常及经特异性激活的兔肺泡巨噬细胞在体外感染星状诺卡菌GUH - 2。在正常兔血清存在的情况下,正常肺泡巨噬细胞与激活的肺泡巨噬细胞在吞噬作用、吞噬体 - 溶酶体融合发生率或杀诺卡菌活性方面未观察到显著差异。然而,所有这些巨噬细胞功能均被各种免疫成分增强。免疫兔血清增强了激活的巨噬细胞对诺卡菌细胞的吞噬作用,并且当存在肺泡衬里物质时观察到吞噬作用进一步增加。补体对巨噬细胞吞噬诺卡菌细胞的能力没有影响。当孵育培养基中存在经特异性致敏的淋巴结细胞、肺泡衬里物质和免疫兔血清时,观察到被吞噬的生物体百分比最高。在正常兔血清存在的情况下,星状诺卡菌GUH - 2抑制正常巨噬细胞中的吞噬体 - 溶酶体融合。然而,添加免疫兔血清或添加经特异性致敏的淋巴细胞会增加吞噬体 - 溶酶体融合的量,而补体对该融合过程没有影响。当正常或激活的巨噬细胞在正常血清、免疫血清或肺泡衬里物质存在的情况下感染细菌时,诺卡菌的活力并未降低。然而,与从免疫兔获得的经致敏的淋巴结细胞一起孵育的特异性激活的巨噬细胞能够减少回收的活生物体数量,并增加细菌细胞损伤的发生率和程度。当细菌细胞与悬浮在免疫血清和肺泡衬里物质中的经致敏的淋巴结细胞一起孵育时,特异性激活的巨噬细胞杀死的生物体数量最多。这些结果表明,仅激活的巨噬细胞不足以杀死摄入的星状诺卡菌GUH - 2,并且经特异性致敏的淋巴细胞在宿主抵抗诺卡菌感染中很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8bc/551350/437fadf456e3/iai00179-0263-a.jpg

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