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γ-干扰素激活的人肺泡巨噬细胞可抑制嗜肺军团菌的细胞内增殖。

IFN-gamma-activated human alveolar macrophages inhibit the intracellular multiplication of Legionella pneumophila.

作者信息

Nash T W, Libby D M, Horwitz M A

机构信息

Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York.

出版信息

J Immunol. 1988 Jun 1;140(11):3978-81.

PMID:3131422
Abstract

Human alveolar macrophages activated by human rIFN-gamma inhibit the intracellular multiplication of Legionella pneumophila, an intracellular bacterial pathogen and the agent of Legionnaires' disease. Activation of alveolar macrophages with IFN-gamma is dose dependent; significant inhibition of L. pneumophila multiplication (mean 1.60 +/- 0.20 logs) is achieved consistently with concentrations of IFN-gamma of greater than or equal to 2 x 10(-2) micrograms/ml (220 U/ml). Activation of alveolar macrophages is also time dependent. In macrophages treated continuously after explantation, macrophages infected at 48 to 96 h after explantation are more inhibitory than macrophages infected at 24 h after explantation. In macrophages not treated continuously after explantation but treated for various lengths of time before infection, the longer their exposure to IFN-gamma before infection, the greater the inhibition of L. pneumophila multiplication (96 greater than 72 greater than 48 greater than 24 h). IFN-gamma-activated alveolar macrophages exhibit morphologic signs of activation, including increased size, spreading, and aggregation. This paper demonstrates that a human resident macrophage can be activated with IFN-gamma such that it exhibits enhanced antimicrobial activity against a relevant pathogen.

摘要

人重组γ干扰素激活的人肺泡巨噬细胞可抑制嗜肺军团菌的细胞内增殖,嗜肺军团菌是一种细胞内细菌病原体,也是军团病的病原体。用γ干扰素激活肺泡巨噬细胞具有剂量依赖性;当γ干扰素浓度大于或等于2×10⁻²微克/毫升(220单位/毫升)时,可始终如一地显著抑制嗜肺军团菌的增殖(平均1.60±0.20对数)。肺泡巨噬细胞的激活也具有时间依赖性。在外植后持续处理的巨噬细胞中,外植后48至96小时感染的巨噬细胞比外植后24小时感染的巨噬细胞更具抑制性。在外植后不持续处理但在感染前处理不同时间长度的巨噬细胞中,感染前暴露于γ干扰素的时间越长,对嗜肺军团菌增殖的抑制作用越大(96小时大于72小时大于48小时大于24小时)。γ干扰素激活的肺泡巨噬细胞表现出激活的形态学特征,包括体积增大、铺展和聚集。本文证明,人常驻巨噬细胞可用γ干扰素激活,使其对相关病原体表现出增强的抗菌活性。

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