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

期刊

JOURNAL OF CLINICAL MEDICINE
卷 6, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/jcm6010012

关键词

B cell; immune regulation; autoimmunity; inflammation

资金

  1. National Institutes of Health [R01 AI069358, 1R56AI122655]
  2. National Multiple Sclerosis Society [RG 1501-03034]
  3. Blood Center Research Foundation
  4. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R56AI122655, R56AI129348] Funding Source: NIH RePORTER

向作者/读者索取更多资源

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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