Meningococcal disease and the complement system

被引:152
|
作者
Lewis, Lisa A. [1 ]
Ram, Sanjay [1 ]
机构
[1] Univ Massachusetts, Sch Med, Div Infect Dis & Immunol, Worcester, MA 01605 USA
关键词
Neisseria meningitidis; complement; meningococcus; sepsis; complement deficiency; MANNOSE-BINDING LECTIN; FACTOR-H BINDING; MEMBRANE COFACTOR PROTEIN; B NEISSERIA-MENINGITIDIS; MEDIATED LIPOPOLYSACCHARIDE RELEASE; ALTERNATIVE PATHWAY ACTIVATION; SERUM BACTERICIDAL ACTIVITY; ANTIGEN-ANTIBODY COMPLEXES; HUMAN C4B-BINDING PROTEIN; C3B/C4B RECEPTOR CR-1;
D O I
10.4161/viru.26515
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite considerable advances in the understanding of the pathogenesis of meningococcal disease, this infection remains a major cause of morbidity and mortality globally. The role of the complement system in innate immune defenses against invasive meningococcal disease is well established. Individuals deficient in components of the alternative and terminal complement pathways are highly predisposed to invasive, often recurrent meningococcal infections. Genome-wide analysis studies also point to a central role for complement in disease pathogenesis. Here we review the pathophysiologic events pertinent to the complement system that accompany meningococcal sepsis in humans. Meningococci use several often redundant mechanisms to evade killing by human complement. Capsular polysaccharide and lipooligosaccharide glycan composition play critical roles in complement evasion. Some of the newly described protein vaccine antigens interact with complement components and have sparked considerable research interest.
引用
收藏
页码:98 / 126
页数:29
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