Heuer J, Kölsch E
J Immunol. 1985 Jun;134(6):4031-4.
The antigen-specific T suppressor (Ts) cell clone HF1 (Thy-1.2+, I-Ak+, I-Ek+) was isolated from a CBA/J mouse tolerized to low doses of bovine serum albumin (BSA), and a subclone was adapted to grow in the absence of antigen-presenting cells. The functional role of the I-Ak molecules endogenously expressed by HF1 Ts cells was analyzed by using anti-I-Ak monoclonal antibodies (mAb) in attempts to block the antigen-induced proliferation of these cells. Among a panel of anti-I-Ak mAb tested, only the H118-49 mAb directed against the private determinant Ia.m1 blocked BSA-induced proliferation. The data presented here suggest a selective regulatory role of membrane-bound I-Ak molecules in the antigen-induced signal transmission.
从对低剂量牛血清白蛋白(BSA)产生耐受的CBA/J小鼠中分离出抗原特异性T抑制(Ts)细胞克隆HF1(Thy-1.2 +,I-Ak +,I-Ek +),并使一个亚克隆适应于在无抗原呈递细胞的情况下生长。通过使用抗I-Ak单克隆抗体(mAb)来分析HF1 Ts细胞内源性表达的I-Ak分子的功能作用,试图阻断这些细胞的抗原诱导增殖。在测试的一组抗I-Ak mAb中,只有针对私有决定簇Ia.m1的H118-49 mAb阻断了BSA诱导的增殖。此处呈现的数据表明膜结合I-Ak分子在抗原诱导的信号传导中具有选择性调节作用。