Lowance Center for Human Immunology, Emory University, Atlanta, GA, United States.
Division of Rheumatology, Department of Medicine, Emory University, Atlanta, GA, United States.
Front Immunol. 2019 Oct 18;10:2458. doi: 10.3389/fimmu.2019.02458. eCollection 2019.
The increasingly recognized role of different types of B cells and plasma cells in protective and pathogenic immune responses combined with technological advances have generated a plethora of information regarding the heterogeneity of this human immune compartment. Unfortunately, the lack of a consistent classification of human B cells also creates significant imprecision on the adjudication of different phenotypes to well-defined populations. Additional confusion in the field stems from: the use of non-discriminatory, overlapping markers to define some populations, the extrapolation of mouse concepts to humans, and the assignation of functional significance to populations often defined by insufficient surface markers. In this review, we shall discuss the current understanding of human B cell heterogeneity and define major parental populations and associated subsets while discussing their functional significance. We shall also identify current challenges and opportunities. It stands to reason that a unified approach will not only permit comparison of separate studies but also improve our ability to define deviations from normative values and to create a clean framework for the identification, functional significance, and disease association with new populations.
不同类型的 B 细胞和浆细胞在保护性和致病性免疫反应中作用的日益被认可,加上技术的进步,产生了大量关于人类免疫区室异质性的信息。不幸的是,人类 B 细胞缺乏一致的分类,也导致对不同表型的判定存在显著的不准确性,无法明确界定为特定的群体。该领域的其他混淆源于:使用无差别、重叠的标志物来定义某些群体,将小鼠概念外推到人类,以及将功能意义赋予通常通过表面标志物不足来定义的群体。在这篇综述中,我们将讨论对人类 B 细胞异质性的现有理解,并定义主要的亲本群体及其相关亚群,同时讨论它们的功能意义。我们还将确定当前的挑战和机遇。不言而喻,统一的方法不仅可以允许对单独的研究进行比较,而且可以提高我们从正常值偏差中进行定义的能力,并为识别、功能意义和与新群体的疾病关联创建一个清晰的框架。