A Hard(y) Look at B-1 Cell Development and Function

被引:106
作者
Baumgarth, Nicole [1 ]
机构
[1] Univ Calif Davis, Ctr Comparat Med, Dept Pathol Microbiol & Immunol, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
HEMATOPOIETIC STEM-CELLS; LY-1; B-CELLS; CHRONIC LYMPHOCYTIC-LEUKEMIA; ANTIBODY-PRODUCING CELLS; FC-MU-R; BONE-MARROW; T-CELLS; MICE DEFICIENT; PHOSPHATIDYL CHOLINE; POSITIVE SELECTION;
D O I
10.4049/jimmunol.1700943
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:3387 / 3394
页数:8
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