Yeh N H, Dipre M, Reem G H
Thymus. 1984;6(4):255-61.
This study shows that anti-Tac antibody does not bind to human thymocytes unless they are activated. Human thymocytes could be induced to express Tac antigen (TCGF receptor) on their cell surface by Concanavalin A. B lymphoblastoid cells or 12-O-tetradecanoylphorbol 13-acetate alone did not induce TCGF receptors, but they did exert a very marked synergistic effect with Concanavalin A. This observation is consistent with our earlier finding that B lymphoblastoid cells secrete a factor which exerts a synergistic effect on the induction of lymphokine secretion by thymocytes and T-cells. The early expression of Tac antigen was independent of thymocyte proliferation. Anti-Tac antibody (10(-3)) inhibited the expression of TCGF receptors and late proliferation of thymocytes. TCGF did not reverse this inhibition nor did it prevent the binding of Tac antibody, but it enhanced the expression of Tac antigen.
本研究表明,抗 Tac 抗体不会与人类胸腺细胞结合,除非它们被激活。通过刀豆球蛋白 A 可诱导人类胸腺细胞在其细胞表面表达 Tac 抗原(TCGF 受体)。单独的 B 淋巴母细胞或 12 - O - 十四烷酰佛波醇 13 - 乙酸酯不会诱导 TCGF 受体,但它们与刀豆球蛋白 A 发挥非常显著的协同作用。这一观察结果与我们早期的发现一致,即 B 淋巴母细胞分泌一种对胸腺细胞和 T 细胞分泌淋巴因子的诱导具有协同作用的因子。Tac 抗原的早期表达与胸腺细胞增殖无关。抗 Tac 抗体(10⁻³)抑制 TCGF 受体的表达和胸腺细胞的晚期增殖。TCGF 不会逆转这种抑制作用,也不会阻止 Tac 抗体的结合,但它会增强 Tac 抗原的表达。