Müllbacher A, Brenan M
Nature. 1980 May 1;285(5759):34-6. doi: 10.1038/285034a0.
Murine cytotoxic T-cell (Tc cell) responses to various antigens are controlled by immune response genes (Ir) mapping in the major histocompatibility complex (H-2). Both helper T cells, controlled by I region-coded genes, and Tc cells, controlled by K/D antigens, are necessary for a positive response. An H-2-restricted Tc-cell response to the male specific minor transplantation antigen (H-Y) can be elicited in B10 (H-2b) female mice primed with syngeneic male spleen cells intraperitoneally (i.p.) or intravenously (i.v.), or by skin grafting followed by restimulation in vitro in mixed lymphocyte culture (MLR) with male cells. CBA (H-2k) mice do not respond by these routes of in vivo priming, and this was thought to be due to a lack of permissible Ir genes for helper function. However, we now report that subcutaneous hind-footpad (fp) immunisation of 'non-responder' CBA mice with syngeneic male cells changes them to responders, a result which argues against a generalised Ir gene-controlled helper defect.
小鼠细胞毒性T细胞(Tc细胞)对各种抗原的反应受主要组织相容性复合体(H-2)中免疫反应基因(Ir)的控制。由I区编码基因控制的辅助性T细胞和由K/D抗原控制的Tc细胞对于阳性反应都是必需的。对雄性特异性次要移植抗原(H-Y)的H-2限制性Tc细胞反应可在经同基因雄性脾细胞腹腔内(i.p.)或静脉内(i.v.)致敏的B10(H-2b)雌性小鼠中引发,或通过皮肤移植,然后在体外与雄性细胞进行混合淋巴细胞培养(MLR)再刺激来引发。CBA(H-2k)小鼠通过这些体内致敏途径无反应,这被认为是由于缺乏辅助功能的许可性Ir基因。然而,我们现在报告,用同基因雄性细胞对“无反应者”CBA小鼠进行后足垫皮下(fp)免疫可使其转变为反应者,这一结果与普遍存在的Ir基因控制的辅助缺陷观点相悖。