Complement and Bacterial Infections: From Molecular Mechanisms to Therapeutic Applications

被引:129
作者
Heesterbeek, Dani A. C. [1 ]
Angelier, Mathieu L. [1 ]
Harrison, Richard A. [2 ]
Rooijakkers, Suzan H. M. [1 ]
机构
[1] Univ Utrecht, Med Ctr, Dept Med Microbiol, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[2] Cardiff Univ, Sch Med, Inst Infect & Immun, Cardiff, S Glam, Wales
关键词
Complement; Bacteria; Infections; Antibody therapy; Antibiotic resistance; Inflammatory diseases; Eculizumab; Neisseria; Membrane attack complex; PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA; MANNAN-BINDING LECTIN; STAPHYLOCOCCUS-AUREUS; PSEUDOMONAS-AERUGINOSA; NEISSERIA-MENINGITIDIS; ECULIZUMAB THERAPY; INHIBITORY PROTEIN; STRUCTURAL BASIS; PROPERDIN BINDS; NASAL CARRIAGE;
D O I
10.1159/000491439
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Complement is a complex protein network of plasma, and an integral part of the innate immune system. Complement activation results in the rapid clearance of bacteria by immune cells, and direct bacterial killing via large pore-forming complexes. Here we review important recent discoveries in the complement field, focusing on interactions relevant for the defense against bacteria. Understanding the molecular interplay between complement and bacteria is of great importance for future therapies for infectious and inflammatory diseases. Antibodies that support complement-dependent bacterial killing are of interest for the development of alternative therapies to treat infections with antibiotic-resistant bacteria. Furthermore, a variety of novel therapeutic complement inhibitors have been developed to prevent unwanted complement activation in autoimmune inflammatory diseases. A better understanding of how such inhibitors may increase the risk of bacterial infections is essential if such therapies are to be successful. (c) 2018 S. Karger AG, Basel
引用
收藏
页码:455 / 464
页数:10
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