Biragyn Arya, Aliseychik Maria, Rogaev Evgeny
Immunoregulation section, National Institute on Aging, 251 Bayview Blvd, Suite 100, Baltimore, MD, 21224, USA.
Brudnick Neuropsychiatric Research Institute, University of Massachusetts Medical School, Worcester, MA, USA.
Semin Immunopathol. 2017 Apr;39(3):283-294. doi: 10.1007/s00281-016-0615-8. Epub 2017 Jan 12.
Our understanding of B cells as merely antibody producers is slowly changing. Alone or in concert with antibody, they control outcomes of seemingly different diseases such as cancer, rheumatoid arthritis, diabetes, and multiple sclerosis. While their role in activation of effector immune cells is beneficial in cancer but bad in autoimmune diseases, their immunosuppressive and regulatory subsets (Bregs) inhibit autoimmune and anticancer responses. These pathogenic and suppressive functions are not static and appear to be regulated by the nature and strength of inflammation. Although aging increases inflammation and changes the composition and function of B cells, surprisingly, little is known whether the change affects aging-associated neurodegenerative disease, such as Alzheimer's disease (AD). Here, by analyzing B cells in cancer and autoimmune and neuroinflammatory diseases, we elucidate their potential importance in AD and other aging-associated neuroinflammatory diseases.
我们对B细胞仅仅作为抗体产生者的理解正在慢慢改变。它们单独或与抗体协同作用,控制着看似不同的疾病的结局,如癌症、类风湿性关节炎、糖尿病和多发性硬化症。虽然它们在激活效应免疫细胞方面的作用在癌症中是有益的,但在自身免疫性疾病中却是有害的,它们的免疫抑制和调节亚群(Bregs)会抑制自身免疫和抗癌反应。这些致病和抑制功能并非一成不变,似乎受炎症的性质和强度调节。尽管衰老会加剧炎症并改变B细胞的组成和功能,但令人惊讶的是,对于这种变化是否会影响与衰老相关的神经退行性疾病,如阿尔茨海默病(AD),我们知之甚少。在这里,通过分析癌症、自身免疫性疾病和神经炎症性疾病中的B细胞,我们阐明了它们在AD和其他与衰老相关的神经炎症性疾病中的潜在重要性。