Regulation of B lymphocyte activation by complement C3 and the B cell coreceptor complex

被引:87
作者
Rickert, RC
机构
[1] Burnham Inst, Program Inflammatory Dis Res, Infect & Inflammatory Dis Ctr, La Jolla, CA 92037 USA
[2] Burnham Inst, Program Signal Transduct, Ctr Canc, La Jolla, CA 92037 USA
关键词
D O I
10.1016/j.coi.2005.03.001
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 an essential innate immune mechanism that recognizes and eradicates microbes and associated toxins. In addition, complement receptors (CD21 and CD35) on B cells cooperate with the B-cell antigen receptor (BCR) to efficiently recognize and respond to antigens bearing complement C3d(g). Fixation of C3d(g) to antigen confers adjuvant properties and therefore its deposition may need to be carefully regulated to avoid autoreactivity. CD21 and/or CD35 engagement is nonmitogenic, and B-cell activation via BCR-CD21 coligation is enhanced through the recruitment of CD19. Recent efforts have sought a better understanding of the topological and biochemical properties of BCR and coreceptor (CD19-CD21-CD81) signaling, as well as the context for complement activation in the response to foreign and self antigens.
引用
收藏
页码:237 / 243
页数:7
相关论文
共 57 条
[31]   Complement receptors CD21/35 link innate and protective immunity during Streptococcus pneumoniae infection by regulating IgG3 antibody responses [J].
Haas, KM ;
Hasegawa, M ;
Steeber, DA ;
Poe, JC ;
Zabel, MD ;
Bock, CB ;
Karp, DR ;
Briles, DE ;
Weis, JH ;
Tedder, TF .
IMMUNITY, 2002, 17 (06) :713-723
[32]   CD19 can regulate B lymphocyte signal transduction independent of complement activation [J].
Hasegawa, M ;
Fujimoto, M ;
Poe, JC ;
Steeber, DA ;
Tedder, TF .
JOURNAL OF IMMUNOLOGY, 2001, 167 (06) :3190-3200
[33]   Complement deficiency ameliorates collagen-induced arthritis in mice [J].
Hietala, MA ;
Jonsson, IM ;
Tarkowski, A ;
Kleinau, S ;
Pekna, M .
JOURNAL OF IMMUNOLOGY, 2002, 169 (01) :454-459
[34]   CD19-regulated signaling thresholds control peripheral tolerance and autoantibody production in B lymphocytes [J].
Inaoki, M ;
Sato, S ;
Weintraub, BC ;
Goodnow, CC ;
Tedder, TF .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (11) :1923-1931
[35]   Marginal zone and B1B cells unite in the early response against T-independent blood-borne particulate antigens [J].
Martin, F ;
Oliver, AM ;
Kearney, JF .
IMMUNITY, 2001, 14 (05) :617-629
[36]   Marginal-zone B cells [J].
Martin, F ;
Kearney, JF .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (05) :323-335
[37]   Positive selection from newly formed to marginal zone B cells depends on the rate of clonal production, CD19, and btk [J].
Martin, F ;
Kearney, JF .
IMMUNITY, 2000, 12 (01) :39-49
[38]   Markedly impaired humoral immune response in mice deficient in complement receptors 1 and 2 [J].
Molina, H ;
Holers, VM ;
Li, B ;
Fang, YF ;
Mariathasan, S ;
Goellner, J ;
StraussSchoenberger, J ;
Karr, RW ;
Chaplin, DD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) :3357-3361
[39]  
Morgan B.P., 1999, COMPLEMENT REGULATOR
[40]   Marginal zone B cells exhibit unique activation, proliferative and immunoglobulin secretory responses [J].
Oliver, AM ;
Martin, F ;
Gartland, GL ;
Carter, RH ;
Kearney, JF .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (09) :2366-2374