Akagawa K S, Tokunaga T
Microbiol Immunol. 1979;23(5):403-14. doi: 10.1111/j.1348-0421.1979.tb00477.x.
Mice pretreated with an intravenous (i.v.) injection of BCG (BCG-sensitized mice) and then immunized intravenously with a high dose (10(8)--10(9)) of sheep red blood cells (SRBC) 2 weeks later developed strong delayed-type hypersensitivity (DTH) to SRBC, as in mice pretreated with cyclophosphamide (CY) (CY-treated mice) and then immunized with SRBC 2 days later; normal mice given the same dose of SRBC did not show such DTH. The mechanism of this strong DTH to SRBC which developed in BCG-sensitized mice was studied, by comparing it with that in CY-treated mice. The transfer of either whole spleen cells or thymus cells, but not serum, obtained from mice immunized with i.v. injections of 10(9) SRBC 4 days previously (hyperimmune mice) did not suppress either the induction or the expression of DTH to SRBC in BCG-sensitized mice, but suppressed those in CY-treated mice. The suppressor cells were SRBC-specific T cells. Adoptive transfer of DTH to SRBC by spleen cells from either BCG-sensitized mice of CY-treated mice to hyperimmune recipients failed. The adoptive transfer of DTH from BCG-sensitized mice to normal recipients also failed if the spleen cells from hyperimmune mice were cotransferred. Whole body irradiation (600 rad) of mice 2 hr before or after the time of immunization with SRBC reduced significantly DTH to SRBC in both BCG-sensitized and CY-treated mice. It was noticed that the total number of spleen cells in BCG-sensitized mice was 3--4 times larger than that in CY-treated mice. From these results, we conclude that the entity of effector T cells of DTH to SRBC induced in BCG-sensitized mice and in CY-treated mice was not different in terms of susceptibility to suppressor T cells and irradiation, but that the total numbers of effector T cells generated in these mice differed remarkably, resulting in the above-described different responsiveness to suppressor T cells transferred passively.
预先经静脉注射卡介苗处理的小鼠(卡介苗致敏小鼠),2周后再经静脉注射高剂量(10⁸ - 10⁹)的绵羊红细胞(SRBC)进行免疫,会对SRBC产生强烈的迟发型超敏反应(DTH),这与预先经环磷酰胺(CY)处理的小鼠(CY处理小鼠)、2天后再用SRBC免疫的情况相同;给予相同剂量SRBC的正常小鼠未表现出这种DTH。通过将卡介苗致敏小鼠中出现的这种对SRBC的强烈DTH与CY处理小鼠中的情况进行比较,研究了其机制。从4天前经静脉注射10⁹ SRBC免疫的小鼠(超免疫小鼠)获取的全脾细胞或胸腺细胞(而非血清)进行转移,不会抑制卡介苗致敏小鼠中对SRBC的DTH诱导或表达,但会抑制CY处理小鼠中的情况。抑制细胞是SRBC特异性T细胞。卡介苗致敏小鼠或CY处理小鼠的脾细胞将对SRBC的DTH过继转移给超免疫受体均失败。如果同时转移超免疫小鼠的脾细胞,卡介苗致敏小鼠向正常受体的DTH过继转移也失败。在用SRBC免疫前或免疫后2小时对小鼠进行全身照射(600拉德),会显著降低卡介苗致敏小鼠和CY处理小鼠中对SRBC的DTH。注意到卡介苗致敏小鼠的脾细胞总数比CY处理小鼠的大3 - 4倍。从这些结果我们得出结论,卡介苗致敏小鼠和CY处理小鼠中诱导产生的对SRBC的DTH效应T细胞实体,在对抑制性T细胞和照射的敏感性方面并无差异,但这些小鼠中产生的效应T细胞总数差异显著,导致对被动转移的抑制性T细胞产生上述不同的反应性。