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The immune potential and immunopathology of cytokine-producing B cell subsets: A comprehensive review

机译:产生细胞因子的B细胞子集的免疫潜力和免疫病理学:全面审查

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B lymphocytes are generally recognized for their potential to mediate humoral immunity by producing different antibody isotypes and being involved in opsonization and complement fixation. Nevertheless, the non-classical, antibody-independent immune potential of B cell subsets has attracted much attention especially in the past decade. These B cells can release a broad variety of cytokines (such as IL-2, IL-4, IL-6, IL-10, IL-17, IFN-a, IFN-y, TNF-a, TGF-|3, LT), and can be classified into distinct subsets depending on the particular cytokine profile, thus emerging the concept of cytokine-producing B cell subsets. Although there is still controversy surrounding the key cell surface markers, intracellular factors and cellular origins of cytokine-producing B cell subsets, accumulating evidence indicates that these B cells are endowed with great potential to regulate both innate and adaptive arms of immune system though releasing cytokines. On the one hand, they promote immune responses through mounting Thl/Th2/Thl7 and neutrophil response, inducing DC maturation and formation of lymphoid structures, increasing NK cell and macrophage activation, enhancing development of themselves and sustaining antibody production. On the other hand, they can negatively regulate immune responses by suppressing Th cell responses, inhibiting Trl cell and Foxp3+ Treg differentiation, impairing APC function and pro-inflammatory cytokine release by monocytes, and inducing CD8+ T cell anergy and CD4+ T cell apoptosis. Therefore, cytokine-producing B cell subsets have multifunctional functions in health and diseases, playing pathologic as well as protective roles in autoimmunity, infection, allergy, and even malignancy. In this review, we revisit the history of discovering cytokine-producing B cells, describe the identification of cytokine-producing B cell subsets, introduce the origins of cytokine-producing B cell subsets as well as molecular and cellular mechanisms for their differentiation, and summarize the recent progress made toward understanding the unexpectedly complex and potentially opposing roles of cytokine-producing B cells in immunological disorders.
机译:通常认识到淋巴细胞通过产生不同的抗体同种型并参与调理剂和补体固定来识别它们潜在的潜力。然而,B细胞子集的非古典抗体无关免疫潜力在过去十年中特别引起了很多关注。这些B细胞可以释放多种细胞因子(例如IL-2,IL-4,IL-6,IL-10,IL-17,IFN-A,IFN-Y,TNF-A,TGF- | 3, LT),并且可以根据特定的细胞因子谱分类为不同的亚群,从而产生了产生细胞因子的B细胞亚群的概念。虽然围绕关键细胞表面标志物,细胞因子产生的B细胞亚群的细胞内因子和细胞起源仍存在争议,但累积证据表明这些B细胞赋予诸多潜力,以调节免疫系统的先天和自适应武器,虽然释放细胞因子。一方面,它们通过安装THL / TH2 / THL7和中性粒细胞反应来促进免疫应答,诱导DC成熟和淋巴结形成,增加NK细胞和巨噬细胞活化,增强自身的发育和维持抗体产生。另一方面,它们可以通过抑制细胞应答,抑制TR1细胞和FoxP3 + Treg分化,损害APC函数和促炎细胞因子释放,并通过单核细胞抑制CD8 + T细胞毒性和CD4 + T细胞凋亡来对抗免疫反应。因此,产生细胞因子的B细胞子集具有健康和疾病的多功能功能,在自身免疫,感染,过敏甚至恶性肿瘤中发挥病理和保护作用。在本文中,我们重新发现发现细胞因子的B细胞的历史,描述了产生细胞因子的B细胞亚群的鉴定,介绍了产生细胞因子的B细胞亚群的起源以及分子和细胞机制的分化,并总结最近的进展,了解在免疫疾病中产生意外的复杂和潜在对立的细胞因子B细胞的作用。

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