Complement and its role in innate and adaptive immune responses

被引:1218
作者
Dunkelberger, Jason R. [2 ]
Song, Wen-Chao [1 ,2 ]
机构
[1] Univ Penn, Sch Med, Inst Translat Med & Therapeut, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Pharmacol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
complement; innate immunity; adaptive immunity; inflammation; host defense; DECAY-ACCELERATING FACTOR; ANAPHYLATOXIN-MEDIATED REGULATION; CHEMOTAXIS INHIBITORY PROTEIN; T-CELL IMMUNITY; CENTER B-CELLS; DENDRITIC CELLS; C5A RECEPTOR; C3A RECEPTOR; PATHWAY C3; FACTOR-H;
D O I
10.1038/cr.2009.139
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The complement system plays a crucial role in the innate defense against common pathogens. Activation of complement leads to robust and efficient proteolytic cascades, which terminate in opsonization and lysis of the pathogen as well as in the generation of the classical inflammatory response through the production of potent proinflammatory molecules. More recently, however, the role of complement in the immune response has been expanded due to observations that link complement activation to adaptive immune responses. It is now appreciated that complement is a functional bridge between innate and adaptive immune responses that allows an integrated host defense to pathogenic challenges. As such, a study of its functions allows insight into the molecular underpinnings of host-pathogen interactions as well as the organization and orchestration of the host immune response. This review attempts to summarize the roles that complement plays in both innate and adaptive immune responses and the consequences of these interactions on host defense.
引用
收藏
页码:34 / 50
页数:17
相关论文
共 162 条
[1]   Disruption of the Cr2 locus results in a reduction in B-1a cells and in an impaired B cell response to T-dependent antigen [J].
Ahearn, JM ;
Fischer, MB ;
Croix, D ;
Goerg, S ;
Ma, MH ;
Xia, JR ;
Zhou, XN ;
Howard, RG ;
Rothstein, TL ;
Carroll, MC .
IMMUNITY, 1996, 4 (03) :251-262
[2]  
Al-Sharif WZ, 1998, J IMMUNOL, V160, P2983
[3]  
AMATRUDA TT, 1993, J BIOL CHEM, V268, P10139
[4]   Genomic analysis of immunity in a Urochordate and the emergence of the vertebrate immune system: "waiting for Godot" [J].
Azumi, K ;
De Santis, R ;
De Tomaso, A ;
Rigoutsos, I ;
Yoshizaki, F ;
Pinto, MR ;
Marino, R ;
Shida, K ;
Ikeda, M ;
Ikeda, M ;
Arai, M ;
Inoue, Y ;
Shimizu, T ;
Satoh, N ;
Rokhsar, DS ;
Du Pasquier, L ;
Kasahara, M ;
Satake, M ;
Nonaka, M .
IMMUNOGENETICS, 2003, 55 (08) :570-581
[5]  
BACLE F, 1990, J IMMUNOL, V144, P147
[6]   Identification of the C1q-binding Sites of Human C1r and C1s A REFINED THREE-DIMENSIONAL MODEL OF THE C1 COMPLEX OF COMPLEMENT [J].
Bally, Isabelle ;
Rossi, Veronique ;
Lunardi, Thomas ;
Thielens, Nicole M. ;
Gaboriaud, Christine ;
Arlaud, Gerard J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (29) :19340-19348
[7]  
BAO L, 1992, Genomics, V13, P437, DOI 10.1016/0888-7543(92)90265-T
[8]   CD21/CD19 coreceptor signaling promotes B cell survival during primary immune responses [J].
Barrington, RA ;
Zhang, M ;
Zhong, XM ;
Jonsson, H ;
Holodick, N ;
Cherukuri, A ;
Pierce, SK ;
Rothstein, TL ;
Carroll, MC .
JOURNAL OF IMMUNOLOGY, 2005, 175 (05) :2859-2867
[9]   B lymphocyte memory:: Role of stromal cell complement and FcγRIIB receptors [J].
Barrington, RA ;
Pozdnyakova, O ;
Zafari, MR ;
Benjamin, CD ;
Carroll, MC .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (09) :1189-1199
[10]  
Blackmore TK, 1998, J IMMUNOL, V160, P3342