Targeting B cells and antibody in transplantation

Am J Transplant. 2011 Jul;11(7):1359-67. doi: 10.1111/j.1600-6143.2011.03554.x. Epub 2011 Jun 10.

Abstract

There has been increasing interest in the role played by B cells, plasma cells and their associated antibody in the immune response to an allograft, driven by the need to undertake antibody-incompatible transplantation and evidence suggesting that B cells play a role in acute cellular rejection and in acute and chronic antibody-mediated rejection. A number of immunosuppressive agents have emerged which target B cells, plasma cells and/or antibody, for example, the B cell-depleting CD20 antibody rituximab. This review describes recent developments in the use of such agents, our understanding of the role of B cells in alloimmunity and the application of this knowledge toward novel therapies in transplantation. It also considers the evidence to date suggesting that B cells may act as regulators of an alloimmune response. Thus, future attempts to target B cells will need to address the problem of how to inhibit effector B cells, while enhancing those with regulatory capacity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antibodies, Monoclonal, Murine-Derived / pharmacology
  • Antigen-Presenting Cells / immunology
  • Antilymphocyte Serum / physiology
  • B-Lymphocytes / drug effects
  • B-Lymphocytes / immunology*
  • Graft Rejection / immunology
  • Humans
  • Lymphocyte Depletion
  • Rituximab
  • Transplantation Immunology

Substances

  • Antibodies, Monoclonal, Murine-Derived
  • Antilymphocyte Serum
  • Rituximab