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两种连续的抗体介导控制嗜肺军团菌感染的方法。

Two sequential layers of antibody-mediated control of Legionella pneumophila infection.

机构信息

Institute of Microbiology, ETH Zürich, Vladimir-Prelog-Weg 1-5/10, Zürich, Switzerland.

Institute of Genetics, University of Erlangen-Nuernberg, Erwin-Rommelstr. 3, Erlangen, Germany.

出版信息

Eur J Immunol. 2019 Sep;49(9):1415-1420. doi: 10.1002/eji.201948106. Epub 2019 Jun 18.

Abstract

Protective immunity against intracellular pathogens, including bacteria, usually relies on cellular immunity. However, antibodies are also implicated in mediating protection against intracellular bacteria. In case of airway infection with Legionella pneumophila (Lpn), the causative agent of Legionnaires' disease, pre-existing Lpn-specific antibodies were shown to afford protection within two days of infection. Here we dissected the early kinetics of Ab-mediated protection against airway Lpn infection and observed two kinetically and mechanistically distinct phases of protection by passively administered antibodies. Within the first hour of infection, Lpn-opsonizing antibodies provided almost 10-fold protection in an antibody Fc-dependent, but FcR-independent manner. Later on, by two days post infection, Lpn-specific Ab-mediated protection strictly involved FcγR, Syk kinase activity in alveolar macrophages and induction of reactive oxygen species (ROS). The findings presented here contribute to the understanding of the mechanisms of Ab-mediated control of Lpn infection in actively or passively immunized individuals.

摘要

针对包括细菌在内的细胞内病原体的保护性免疫通常依赖于细胞免疫。然而,抗体也被认为在介导针对细胞内细菌的保护中发挥作用。在呼吸道感染嗜肺军团菌(Lpn),即军团病的病原体时,感染两天内预先存在的 Lpn 特异性抗体被证明提供了保护。在这里,我们剖析了抗体介导的针对气道 Lpn 感染的早期保护动力学,并观察到被动给予的抗体提供了两种具有不同动力学和机制的保护阶段。在感染后的第一个小时内,Lpn 调理抗体以抗体 Fc 依赖性但 FcR 非依赖性的方式提供了近 10 倍的保护。稍后,在感染后两天,Lpn 特异性 Ab 介导的保护严格涉及 FcγR、肺泡巨噬细胞中的 Syk 激酶活性和活性氧物质(ROS)的诱导。本研究结果有助于理解在主动或被动免疫个体中抗体介导的 Lpn 感染控制的机制。

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