Baum C M, Davie J M, McKearn J P
Crit Rev Immunol. 1985;5(4):349-70.
The review will examine B-cell differentiation with an emphasis on B-cell subpopulations. We will begin with an analysis of current evidence concerning B-cell ontogeny. The development of the B-cell repertoire will be traced from stem cell to effector cells. The CBA/N mouse, which expresses an X-linked immunodeficiency, will serve as a basis for discussing the delineation of B cells into subpopulations. The CBA/N mouse provides evidence for distinct populations of B cells which can be differentiated by cell surface antigens as well as function. We intend to focus on the functional diversity of B-cell subpopulations and how they develop. The CBA/N mouse is not the only evidence for distinct B cell subpopulations and we will attempt to organize these data into a coherent story of B-cell subsets.
本综述将着重于B细胞亚群来研究B细胞分化。我们将首先分析有关B细胞个体发生的现有证据。B细胞库的发育将从干细胞追溯到效应细胞。表达X连锁免疫缺陷的CBA/N小鼠将作为讨论将B细胞划分为亚群的基础。CBA/N小鼠为不同的B细胞群体提供了证据,这些群体可通过细胞表面抗原以及功能来区分。我们打算聚焦于B细胞亚群的功能多样性及其发育方式。CBA/N小鼠并非不同B细胞亚群的唯一证据,我们将尝试把这些数据整理成一个关于B细胞亚群的连贯故事。