BAFF-driven autoimmunity requires CD19 expression

J Autoimmun. 2015 Aug:62:1-10. doi: 10.1016/j.jaut.2015.06.001. Epub 2015 Jun 20.

Abstract

B cell activating factor of the tumor necrosis factor family (BAFF or BLyS) is a critical factor for B cell survival and maturation. BAFF-transgenic (BAFF-Tg) mice develop autoimmunity that resembles systemic lupus erythematosus (SLE) in a T cell-independent but MyD88-dependent manner, implicating toll-like receptor (TLR) signaling. The specific B cell subtypes that make pro-inflammatory autoantibodies in BAFF-Tg mice are TLR-activated innate B cells known as marginal zone (MZ) and B1 B cells. These cells infiltrate the salivary glands and kidneys of diseased BAFF-Tg mice. However, loss of B1a or MZ B cells does not protect BAFF-Tg mice against disease, suggesting that B1b B cells might be the important pathogenic B cell subset. To test this hypothesis, we have generated BAFF-Tg mice that retained follicular B cells, but are deficient in B1a, B1b and MZ B cells, by crossing BAFF-Tg mice to CD19-deficient mice (BTg-CD19(-/-)). The BTg-CD19(-/-) mice did not produce autoantibodies and were protected from splenomegaly, kidney pathology and all signs of autoimmunity. This work suggests that B1b B cells, rather than MZ or B1a B cells, are sufficient and possibly required for the development of autoimmunity. Loss of the majority of innate-like B cells was able to protect BAFF-Tg mice from developing disease, so we can now conclude that autoimmunity induced by excessive BAFF production requires B1b B cells and CD19 signaling.

Keywords: Autoimmunity; B1b cells; BAFF; BAFF-transgenic; CD19; MZ B cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD19 / genetics*
  • Autoantibodies / immunology
  • Autoimmunity / genetics*
  • Autoimmunity / immunology*
  • B-Cell Activating Factor / metabolism*
  • B-Lymphocyte Subsets / immunology
  • B-Lymphocyte Subsets / metabolism
  • Complement C3 / immunology
  • Gene Expression Regulation*
  • Glomerulonephritis / genetics
  • Glomerulonephritis / immunology
  • Glomerulonephritis / metabolism
  • Glomerulonephritis / pathology
  • Immunoglobulin G / immunology
  • Immunoglobulin M / immunology
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Phenotype
  • Signal Transduction
  • Toll-Like Receptors / metabolism

Substances

  • Antigens, CD19
  • Autoantibodies
  • B-Cell Activating Factor
  • Complement C3
  • Immunoglobulin G
  • Immunoglobulin M
  • Toll-Like Receptors