Hausman P B, Goidl E A, Siskind G W, Weksler M E
J Immunol. 1985 Jun;134(6):3802-7.
Tolerance was induced in young and old mice by the i.v. injection of TNP-modified syngeneic spleen cells. The tolerant state was associated with the development of hapten-specific suppressor T cells. The specificity of suppressor T cells was studied by transferring T cells from tolerant donors to normal, nonirradiated, syngeneic recipients, which were then immunized with TNP-Ficoll or TNP-bovine gamma-globulin. Suppressor T cells induced in young mice depressed the plaque-forming cell response of young but not old mice to both antigens. Similarly, suppressor T cells induced in old mice depressed the response in old but not young mice. These findings suggest that aging is associated with changes in idiotype repertoire which influence the specificity of the suppressor T cells present in tolerant mice.
通过静脉注射经三硝基苯(TNP)修饰的同基因脾细胞,在年轻和年老小鼠中诱导出耐受性。耐受状态与半抗原特异性抑制性T细胞的产生有关。通过将来自耐受供体的T细胞转移到正常、未受照射的同基因受体中研究抑制性T细胞的特异性,然后用TNP-菲可(Ficoll)或TNP-牛γ球蛋白对这些受体进行免疫。在年轻小鼠中诱导产生的抑制性T细胞抑制了年轻而非年老小鼠对两种抗原的抗体形成细胞反应。同样,在年老小鼠中诱导产生的抑制性T细胞抑制了年老而非年轻小鼠的反应。这些发现表明,衰老与个体基因型库的变化有关,这些变化会影响耐受小鼠中存在的抑制性T细胞的特异性。