DISTINCTIVE DEVELOPMENTAL ORIGINS AND SPECIFICITIES OF MURINE CD5(+)B CELLS

被引:130
作者
HARDY, RR
CARMACK, CE
LI, YS
HAYAKAWA, K
机构
[1] I. C. R., Fox Chase Cancer Center, Philadelphia, Pennsylvania, 19111
关键词
D O I
10.1111/j.1600-065X.1994.tb00660.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD5(+) B cells constitute a small fraction of cells in the spleen of adult mice that exhibit numerous features serving to distinguish them from the bulk of IgD(++)CD5(-) ''conventional'' B cells. In this review we focus on two major questions relating to this population: 1) the relationship of CD5(+) B cells to other B cells; and 2) the distinctive enrichment of particular autoreactive specificities in this subset. The nature of their origins is clarified by a thorough analysis of intermediate stages of early B-cell development in both fetal and adult tissues. The reactivity to bromelain-treated mouse red blood cells serves as a prototype system for the investigation of biased specificities in CD5(+) B cells. These lines of investigation lead us to propose that CD5(+) B cells in the adult are the remnant of a distinct fetal B-cell differentiation pathway wherein selection of cells from this fetal/neonatal population into the adult long-lived pool results in the overexpression of certain germline-encoded autoreactivities.
引用
收藏
页码:91 / 118
页数:28
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