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Regulation of B lymphocyte activation by complement C3 and the B cell co-receptor complex

Rickert R2005Current Opinion in ImmunologyReview
10.1016/j.coi.2005.03.001PubMed
Immune/Innate

Abstract

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.

Cited By (3)

  • Complement-mediated activation of the adaptive immune responses: role of C3d in linking the innate and adaptive immunityImmunologic Research · 2006
  • CD22: an inhibitory enigmaImmunology · 2008
  • CD21/35 Promotes Protective Immunity to Streptococcus pneumoniae through a Complement-Independent but CD19-Dependent Pathway That Regulates PD-1 ExpressionThe Journal of Immunology · 2009

References (2)

  • Mice deficient in complement receptors 1 and 2 lack a tissue injury-inducing subset of the natural antibody repertoireThe Journal of Immunology · 2002
  • The complement system in regulation of adaptive immunityNature Immunology · 2004

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