Rickert Robert C
Program of Inflammatory Disease Research, Infectious and Inflammatory Disease Center, The Burnham Institute, La Jolla, California 92037, USA.
Curr Opin Immunol. 2005 Jun;17(3):237-43. doi: 10.1016/j.coi.2005.03.001.
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.
补体是一种重要的固有免疫机制,可识别并清除微生物及相关毒素。此外,B细胞上的补体受体(CD21和CD35)与B细胞抗原受体(BCR)协同作用,以有效识别并对抗携带补体C3d(g)的抗原作出反应。C3d(g)与抗原的结合赋予其佐剂特性,因此可能需要对其沉积进行严格调控以避免自身反应性。CD21和/或CD35的结合不具有促有丝分裂作用,并且通过募集CD19可增强经由BCR-CD21共结合的B细胞活化。最近的研究致力于更好地理解BCR和共受体(CD19-CD21-CD81)信号传导的拓扑学和生化特性,以及在对外源和自身抗原的应答中补体激活的背景情况。