Publication:
Regulatory B cells, A to Z

Research Projects

Organizational Units

Journal Issue

Abstract

B cells play a central role in the immune system through the production of antibodies. During the past two decades, it has become increasingly clear that B cells also have the capacity to regulate immune responses through mechanisms that extend beyond antibody production. Several types of human and murine regulatory B cells have been reported that suppress inflammatory responses in autoimmune disease, allergy, infection, transplantation, and cancer. Key suppressive molecules associated with regulatory B-cell function include the cytokines IL-10, IL-35, and TGF-beta as well as cell membrane-bound molecules such as programmed death-ligand 1, CD39, CD73, and aryl hydrocarbon receptor. Regulatory B cells can be induced by a range of different stimuli, including microbial products such as TLR4 or TLR9 ligands, inflammatory cytokines such as IL-6, IL-1 beta, and IFN-alpha, as well as CD40 ligation. This review provides an overview of our current knowledge on regulatory B cells. We discuss different types of regulatory B cells, the mechanisms through which they exert their regulatory functions, factors that lead to induction of regulatory B cells and their role in the alteration of inflammatory responses in different diseases.

Description

Keywords

Experimental autoimmune encephalomyelitis, Aryl-hydrocarbon receptor, B10 cells, T-cells, Rheumatoid-arthritis, Tnf-alpha, In-vitro, Il-10, Induction, Inflammation, Allergy, Autoimmunity, Breg cells, 10, Inflammation, Suppression, Tolerance, Allergy, Immunology

Citation

Collections


Metrikler

Search on Google Scholar


Total Views

1

Total Downloads

2