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CD21/CD35 in B cell activation

Carroll MC1998Seminars in ImmunologyReview
10.1006/smim.1998.0120PubMed
Immune/Innate

Abstract

The stimulus induced via the B cell receptor is a major factor in determination of the fate of naive B cells resulting in activation, elimination or anergy. The strength of B cell signal transduction is dependent not only on the affinity of antigen binding, but by positive signals via the co-receptor CD21/CD19/Tapa-1. Absence of CD21 expression by B cells results in an impaired humoral response to T-dependent antigens which is characterized by a reduction in B cell follicular retention and germinal center survival. The ligand for CD21 is complement C3d which becomes attached to antigen on activation of the complement system. Thus, the complement system of innate immunity is an important regulator of B lymphocytes.

Key Biomarkers

C3dCD19CD21CD35ComplementTapa-1

Cited By (1)

  • Regulation of humoral immune responses by CD21/CD35Immunological Reviews · 2000

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