Yazova A, Suslov A P, Brondz B D
Folia Biol (Praha). 1979;25(2):81-94.
Immunization of rats with mouse alpha-foetoprotein has been earlier shown to induce the antibody response to self AFP or rats. In this work a single injection of AFPm resulted in termination of natural tolerance of effector T-cells to AFPr, as shown by the macrophage migration inhibition test using peritoneal exudate cells from immunized animals. A significant reaction was elicited by both AFPm and AFPr in the course of primary, secondary and third immunization with AFPm. Pronounced MMI reaction to AFPm and AFPr has developed when AFPr was used as a booster antigen after primary injection with AFPm. Both the kinetics and magnitude of cell-mediated response to heterologous and self AFP injected either in CFA or without it were studied by the MMI test. T-cells of immune PEC were demonstrated by T-B separation to be responsible for MMI elicited by AFPm and AFPr.
早期研究表明,用小鼠甲胎蛋白免疫大鼠可诱导其产生针对自身甲胎蛋白或大鼠甲胎蛋白的抗体反应。在本研究中,单次注射小鼠甲胎蛋白(AFPm)可导致效应T细胞对大鼠甲胎蛋白(AFPr)的天然耐受性终止,这通过使用免疫动物的腹腔渗出细胞进行巨噬细胞移动抑制试验得以证实。在用AFPm进行初次、二次和三次免疫过程中,AFPm和AFPr均引发了显著反应。当在初次注射AFPm后使用AFPr作为加强抗原时,对AFPm和AFPr产生了明显的巨噬细胞移动抑制(MMI)反应。通过MMI试验研究了在弗氏完全佐剂(CFA)中或无CFA情况下注射异源和自身甲胎蛋白时细胞介导反应的动力学和强度。通过T细胞与B细胞分离证明,免疫的腹腔渗出细胞(PEC)中的T细胞是AFPm和AFPr引发MMI的原因。