Mechanisms of Regulatory B cell Function in Autoimmune and Inflammatory Diseases beyond IL-10

被引:48
|
作者
Ray, Avijit [1 ,2 ]
Dittel, Bonnie N. [3 ]
机构
[1] Blood Ctr Wisconsin, Blood Res Inst, Milwaukee, WI 53226 USA
[2] AbbVie Inc, Oncol Discovery, N Chicago, IL 60064 USA
[3] Med Coll Wisconsin, Dept Microbiol & Mol Genet, Milwaukee, WI 53226 USA
来源
JOURNAL OF CLINICAL MEDICINE | 2017年 / 6卷 / 01期
基金
美国国家卫生研究院;
关键词
B cell; immune regulation; autoimmunity; inflammation; T-CELLS; TRANSPLANTATION TOLERANCE; MULTIPLE-SCLEROSIS; CHRONIC COLITIS; DEFICIENT MICE; ENCEPHALOMYELITIS; RITUXIMAB; DEPLETION; LYMPHOCYTE; INDUCTION;
D O I
10.3390/jcm6010012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the past two decades it has become clear that in addition to antigen presentation and antibody production B cells play prominent roles in immune regulation. While B cell-derived IL-10 has garnered much attention, B cells also effectively regulate inflammation by a variety of IL-10-independent mechanisms. B cell regulation has been studied in both autoimmune and inflammatory diseases. While collectively called regulatory B cells (Breg), no definitive phenotype has emerged for B cells with regulatory potential. This has made their study challenging and thus unique B cell regulatory mechanisms have emerged in a disease-dependent manner. Thus to harness the therapeutic potential of Breg, further studies are needed to understand how they emerge and are induced to evoke their regulatory activities.
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收藏
页数:7
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