BAFF selectively enhances the survival of plasmablasts generated from human memory B cells

J Clin Invest. 2003 Jul;112(2):286-97. doi: 10.1172/JCI18025.

Abstract

The generation of Ig-secreting cells (ISCs) from memory B cells requires interactions between antigen-specific (Ag-specific) B cells, T cells, and dendritic cells. This process must be strictly regulated to ensure sufficient humoral immunity while avoiding production of pathogenic autoantibodies. BAFF, a member of the TNF family, is a key regulator of B cell homeostasis. BAFF exerts its effect by binding to three receptors - transmembrane activator of and CAML interactor (TACI), B cell maturation antigen (BCMA), and BAFF receptor (BAFF-R). To elucidate the contribution of BAFF to the differentiation of B cells into ISCs, we tracked the fate of human memory B cells stimulated with BAFF or CD40L. BAFF and CD40L significantly increased the overall number of surviving B cells. This was achieved via distinct mechanisms. CD40L induced proliferation of nondifferentiated blasts, while BAFF prevented apoptosis of ISCs without enhancing proliferation. The altered responsiveness of activated memory B cells to CD40L and BAFF correlated with changes in surface phenotype such that expression of CD40 and BAFF-R were reduced on ISCs while BCMA was induced. These results suggest BAFF may enhance humoral immunity in vivo by promoting survival of ISCs via a BCMA-dependent mechanism. These findings have wide-ranging implications for the treatment of human immunodeficiencies as well as autoimmune diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADP-ribosyl Cyclase / biosynthesis
  • ADP-ribosyl Cyclase 1
  • Antigens, CD / biosynthesis
  • Apoptosis
  • B-Cell Activating Factor
  • B-Cell Activation Factor Receptor
  • B-Cell Maturation Antigen
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism
  • CD40 Ligand / metabolism
  • Cell Differentiation
  • Cell Division
  • Cell Line
  • Cell Separation
  • Cell Survival
  • Flow Cytometry
  • Humans
  • Immunologic Memory*
  • Interleukin-10 / biosynthesis
  • Interleukin-2 / biosynthesis
  • Membrane Glycoproteins
  • Membrane Proteins / metabolism
  • Membrane Proteins / physiology*
  • Microscopy, Fluorescence
  • Models, Biological
  • Neuropeptides / physiology
  • Nuclear Proteins / physiology
  • Protein Binding
  • Receptors, Tumor Necrosis Factor / metabolism
  • Spleen / cytology
  • Time Factors
  • Tumor Necrosis Factor-alpha / metabolism
  • Tumor Necrosis Factor-alpha / physiology*

Substances

  • ANP32B protein, human
  • Antigens, CD
  • B-Cell Activating Factor
  • B-Cell Activation Factor Receptor
  • B-Cell Maturation Antigen
  • Interleukin-2
  • Membrane Glycoproteins
  • Membrane Proteins
  • Neuropeptides
  • Nuclear Proteins
  • Receptors, Tumor Necrosis Factor
  • TNFRSF13C protein, human
  • TNFRSF17 protein, human
  • TNFSF13B protein, human
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • CD40 Ligand
  • ADP-ribosyl Cyclase
  • CD38 protein, human
  • ADP-ribosyl Cyclase 1