Smith K G, Hewitson T D, Nossal G J, Tarlinton D M
The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia.
Eur J Immunol. 1996 Feb;26(2):444-8. doi: 10.1002/eji.1830260226.
The first product of the humoral response to antigen is low-affinity antibody, produced by extrafollicular foci of antibody-forming cells (AFC) in organs such as spleen and lymph node. These cells proliferate rapidly but then undergo an equally rapid decline, so that they are present in only small numbers 14 days after immunization. We have used 6-parameter flow cytometry to isolate and examine the characteristics of (4-hydroxy-5-nitrophenyl)acetyl-specific AFC, looking in particular for those markers that might differentiate them from cells of the intrafollicular (germinal center) arm of the T-dependent immune response. At day 7 of the primary response, most AFC were found to express surprisingly low levels of B220, high levels of syndecan, and retain significant levels of surface IgG1. We then used enzyme-linked immunospot assays to demonstrate that the rapid decline of these cells was not likely to be due to migration to organs such as the bone marrow. Their decline could, however, be explained by apoptosis in situ, which was demonstrated immunohistologically by nick-end labeling.
对抗原的体液免疫反应的首个产物是低亲和力抗体,由脾脏和淋巴结等器官中抗体形成细胞(AFC)的滤泡外灶产生。这些细胞迅速增殖,但随后同样迅速衰退,以至于在免疫后14天时仅少量存在。我们利用六参数流式细胞术分离并检测了(4-羟基-5-硝基苯基)乙酰特异性AFC的特征,尤其寻找那些可能将它们与T细胞依赖性免疫反应的滤泡内(生发中心)分支细胞区分开来的标志物。在初次反应的第7天,发现大多数AFC表达出人意料的低水平B220、高水平syndecan,并保留显著水平的表面IgG1。然后我们使用酶联免疫斑点分析来证明这些细胞的迅速衰退不太可能是由于迁移至骨髓等器官。然而,它们的衰退可以通过原位凋亡来解释,原位凋亡通过缺口末端标记进行免疫组织学证实。