Ahmann G B, Sachs D H, Hodes R J
J Immunol. 1978 Nov;121(5):1981-9.
Pretreatment of murine lymphoid cells with anti-Ia and C abrogated the proliferative response of these cells to Con A, but not to PHA. Reconstitution experiments demonstrated that T cell-enriched populations failed to restore Con A responsiveness and that T cell-depleted populations were more effective in restoring responsiveness to Con A. In particular, a population of 1000 R resistant, glass-adherent, non-T spleen cells was capable of completely restoring responsiveness to Con A when added in numbers as low as 4% of cultured cells. These splenic adherent cells were found to express Ia determinants encoded by at least two genes: one in I-A and the other in I-B, I-J, and/or I-E/C, and it was demonstrated that determinants encoded in these two regions were expressed on the same cell. These results demonstrate that non-T accessory cells may be the Ia+ cells entirely responsible for the anti-Ia and C-induced abrogation of T cell proliferative responses to Con A.
用抗Ia和补体(C)预处理小鼠淋巴细胞可消除这些细胞对刀豆蛋白A(Con A)的增殖反应,但对植物血凝素(PHA)的反应不受影响。重建实验表明,富含T细胞的群体无法恢复对Con A的反应性,而去除T细胞的群体在恢复对Con A的反应性方面更有效。特别是,一群1000R抗性、玻璃黏附性、非T脾细胞,当以低至培养细胞4%的数量添加时,能够完全恢复对Con A的反应性。这些脾黏附细胞被发现表达由至少两个基因编码的Ia决定簇:一个在I-A区,另一个在I-B、I-J和/或I-E/C区,并且证明这两个区域编码的决定簇在同一细胞上表达。这些结果表明,非T辅助细胞可能是完全负责抗Ia和补体诱导的T细胞对Con A增殖反应消除的Ia+细胞。