期刊文献+

Regulatory functions of innate-like B cells 被引量:12

Regulatory functions of innate-like B cells
原文传递
导出
摘要 Innate-like B cells (ILBs) are heterogeneous populations of unconventional B cells with innate sensing and responding properties. ILBs in mice are composed of B1 cells, marginal zone (MZ) B cells and other related B cells. ILBs maintain natural IgM levels at steady state, and after innate activation, they can rapidly acquire immune regulatory activities through the secretion of natural IgM and IL-IO. Thus, ILBs constitute an important source of IL-lO-producing regulatory B cells (Bregs), which have been shown to play critical roles in autoimmunity, inflammation and infection. The present review highlights the latest advances in the field of ILBs and focuses on their regulatory functions. Understanding the regulatory activities of ILBs and their underlying mechanisms could open new avenues in manipulating their functions in inflammatory, infectious and other relevant diseases. Innate-like B cells (ILBs) are heterogeneous populations of unconventional B cells with innate sensing and responding properties. ILBs in mice are composed of B1 cells, marginal zone (MZ) B cells and other related B cells. ILBs maintain natural IgM levels at steady state, and after innate activation, they can rapidly acquire immune regulatory activities through the secretion of natural IgM and IL-IO. Thus, ILBs constitute an important source of IL-lO-producing regulatory B cells (Bregs), which have been shown to play critical roles in autoimmunity, inflammation and infection. The present review highlights the latest advances in the field of ILBs and focuses on their regulatory functions. Understanding the regulatory activities of ILBs and their underlying mechanisms could open new avenues in manipulating their functions in inflammatory, infectious and other relevant diseases.
出处 《Cellular & Molecular Immunology》 SCIE CAS CSCD 2013年第2期113-121,共9页 中国免疫学杂志(英文版)
基金 This work was supported in part by grants from National Natural Science Foundation of China (31270961) and Shanghai Science and Technology Development Funds (12QA1403600). The author would like to thank Mr Yiyuan Fang for his help with figure preparation and Mr Brian Mozeleski for his critical reading.
关键词 immune regulation innate-like B cells interleukin 10 natural antibody regulatory B cells immune regulation innate-like B cells interleukin 10 natural antibody regulatory B cells
  • 相关文献

参考文献84

  • 1Bendelac A, Bonneville M, Kearney JF. Autoreactivity by design: innate B and T lymphocytes. IVatRev Immunol2001; 1: 177-186.
  • 2Kearney JF. Innate-like B cells. SprinEer Semin Immun 2005 26: 377-383.
  • 3Moore KW, de Waal Malefyt R, Coffman RL, O'Garra A. Interleukin-lO and the interleukin-lO receptor. Annu Rev Immunol2001; 19: 683- 765.
  • 4Kaveri SV, Silverman G J, Bayry J. Natural IgM in immune equilibrium and harnessing their therapeutic potential. J Immuno12012; 188: 939-945.
  • 5Baumgarth N, Herman OC, Jager GC, Brown L, Herzenberg LA. Innate and acquired humoral immunities to influenza virus are mediated by distinct arms of the immune system. Proc Natl Acad Sci USA 1999; 96: 2250-2255.
  • 6van Oudenaren A, Haaijman J J, Benner R. Frequencies of background cytoplasmic Ig-containing cells in various lymphoid organs of athymic and euthymic mice as a function of age and immune status. Immunology 1984; 51: 735-742.
  • 7Choi YS, Dieter JA, Rothaeusler K, Luo Z, Baumgarth N. B-1 cells in the bone marrow are a significant source of natural IgM. Eur J Immuno12012; 42: 120-129.
  • 8Martins G, Calame K. Regulation and functions of Blimp-1 in T and B lymphocytes. Annu Rev Irnmuno12008; 26: 133-169.
  • 9Tumang JR, Frances R, Yeo SG, Rothstein TL. Spontaneously Ig- secreting B-1 cells violate the accepted paradigm for expression of differentiation-associated transcription factors. J Immunol 2005; 174: 3173-3177.
  • 10Gunn KE, Brewer JW. Evidence that marginal zone B cells possess an enhanced secretory apparatus and exhibit superior secretory activity. .I Irnmuno12006; 177; 3791-3798.

同被引文献26

引证文献12

二级引证文献55

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部