Regulation of Humoral Immunity by Complement

被引:340
作者
Carroll, Michael C. [1 ,2 ,3 ]
Isenman, David E. [4 ,5 ]
机构
[1] Harvard Univ, Childrens Hosp, Sch Med, Immune Dis Inst, Boston, MA 02115 USA
[2] Harvard Univ, Childrens Hosp, Sch Med, Program Mol & Cellular Med, Boston, MA 02115 USA
[3] Harvard Univ, Dept Pediat, Sch Med, Boston, MA 02115 USA
[4] Univ Toronto, Dept Biochem, Toronto, ON M5S 1A8, Canada
[5] Univ Toronto, Dept Immunol, Toronto, ON M5S 1A8, Canada
关键词
FOLLICULAR DENDRITIC CELLS; SUBCAPSULAR SINUS MACROPHAGES; EPSTEIN-BARR-VIRUS; RECEPTOR; B-CELLS; CRYSTAL-STRUCTURE; GERMINAL-CENTERS; BINDING PROTEIN; ANTIGEN; C3D;
D O I
10.1016/j.immuni.2012.08.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The complement system of innate immunity is important in regulating humoral immunity largely through the complement receptor CR2, which forms a coreceptor on B cells during antigen-induced activation. However, CR2 also retains antigens on follicular dendritic cells (FDCs). Display of antigen on FDCs is critical for clonal selection and affinity maturation of activated B cells. This review will discuss the role of complement in adaptive immunity in general with a focus on the interplay between CR2-associated antigen on B cells with CR2 expressed on FDCs. This latter interaction provides an opportunity for memory B cells to sample antigen over prolonged periods. The cocrystal structure of CR2 with its ligand C3d provides insight into how the complement system regulates access of antigen by B cells with implications for therapeutic manipulations to modulate aberrant B cell responses in the case of autoimmunity.
引用
收藏
页码:199 / 207
页数:9
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