Rosenberg Y J, Cunningham A J
Eur J Immunol. 1977 May;7(5):257-63. doi: 10.1002/eji.1830070503.
A role for antigen in the generation of fully mature splenic type B cells has been shown. In adoptive transfer experiments, cells from bone marrow or fetal liver required a longer period to give an anti-sheep red blood cell plaque-forming cell (PFC) response than those from spleen. This delay was not overcome by allowing the cells a 7-day sojourn in the irradiated host before antigen challenge. A two-stage protocol was designed in which the in vivo generation of fully mature cells could be measured by their ability to give PFC in lipopolysaccharide-stimulated cultures in vitro. These experiments showed that a critical factor which influences the final differentiation of bone marrow or fetal liver cells into mature, splenic type B cells is exposure to antigen.
抗原在完全成熟的脾型B细胞生成过程中的作用已得到证实。在过继转移实验中,来自骨髓或胎肝的细胞产生抗绵羊红细胞空斑形成细胞(PFC)反应所需的时间比来自脾脏的细胞更长。在抗原攻击前,让这些细胞在受辐照宿主体内停留7天,并不能消除这种延迟。设计了一个两阶段方案,通过在体外脂多糖刺激培养物中产生PFC的能力来衡量体内完全成熟细胞的生成情况。这些实验表明,影响骨髓或胎肝细胞最终分化为成熟脾型B细胞的关键因素是接触抗原。