Baumgarth Nicole
Center for Comparative Medicine, Department of Pathology, Microbiology and Immunology, University of California Davis, Davis, CA 95616
J Immunol. 2017 Nov 15;199(10):3387-3394. doi: 10.4049/jimmunol.1700943.
A small population of B cells exists in lymphoid tissues and body cavities of mice that is distinct in development, phenotype, and function from the majority (B-2) B cell population. This population, originally termed "Ly-1" and now "B-1," has received renewed interest as an innate-like B cell population of fetal-derived hematopoiesis, responsible for natural Ab production and rapid immune responses. Molecular analyses have begun to define fetal and adult hematopoiesis, while cell-fate mapping studies have revealed complex developmental origins of B-1 cells. Together the studies provide a more detailed understanding of B-1 cell regulation and function. This review outlines studies that defined B-1 cells as natural Ab- and cytokine-producing B cells of fetal origin, with a focus on work conducted by R.R. Hardy, an early pioneer and codiscoverer of B-1 cells, whose seminal contributions enhanced our understanding of this enigmatic B cell population.
在小鼠的淋巴组织和体腔中存在一小部分B细胞,其在发育、表型和功能上与大多数(B-2)B细胞群体不同。这一群体最初被称为“Ly-1”,现在称为“B-1”,作为源自胎儿造血的类天然B细胞群体,因其负责天然抗体产生和快速免疫反应而重新受到关注。分子分析已开始明确胎儿和成人的造血过程,而细胞命运图谱研究揭示了B-1细胞复杂的发育起源。这些研究共同提供了对B-1细胞调节和功能更详细的理解。本综述概述了将B-1细胞定义为源自胎儿的天然抗体和细胞因子产生B细胞的研究,重点介绍了R.R. Hardy的工作,他是B-1细胞的早期先驱和共同发现者,其开创性贡献增进了我们对这一神秘B细胞群体的理解。