Forman J
J Immunol. 1979 Dec;123(6):2451-5.
The specificity of H-2 unrestricted cytotoxic T cells was analyzed in secondary CML responses. A/J strain effector cells, sensitized against A.Tlab lymphoid cells, lysed target cells from strains with differing H-2 haplotypes but all sharing Qa-1b/Tlab alleles; whereas, target cells from strains with Qa-1a/Tlaa were not. When B6.Tlaa animals were in vivo-primed and challenged in vitro with B6 stimulator cells, no cytotoxic effector cell activity was generated. However, if B6.Tlaa animals were primed in vivo with A.BY cells and then rechallenged in vitro with either A.BY or B6 stimulator cells, cytotoxic effector cells were generated that lysed target cells from strains with Qa-1b/Tlab alleles. This suggests that factors in addition to Qa/Tla may play a role in the generation of anti-Qa/Tla effector cell activity. It was also noted that targets from strains with Qa-1a/Tlaa alleles were killed, although to a much lesser extent than the Qa-1b/Tlab targets. SWR anti-DBA/1 efffector cells strongly lysed target cells frrom strains with Qa-1b/Tlab, lysed Qa-1a/Tlaa targets to a lesser extent, and produced no cytotoxic effect on B6.Tlaa target cells. These data suggest that in addition to a CML target antigen associated with Qa-1b/Tlab, there may be an additional specificity recognized by cytotoxic T cells controlled by a gene outside of Qa-1b/Tlab.
在慢性粒细胞白血病(CML)的二次反应中分析了H-2非限制性细胞毒性T细胞的特异性。用A.Tlab淋巴细胞致敏的A/J品系效应细胞,可裂解来自具有不同H-2单倍型但均共享Qa-1b/Tlab等位基因的品系的靶细胞;而来自具有Qa-1a/Tlaa等位基因品系的靶细胞则不能被裂解。当B6.Tlaa动物在体内被致敏并在体外受到B6刺激细胞攻击时,未产生细胞毒性效应细胞活性。然而,如果B6.Tlaa动物在体内用A.BY细胞致敏,然后在体外再次受到A.BY或B6刺激细胞攻击,则会产生细胞毒性效应细胞,这些细胞可裂解来自具有Qa-1b/Tlab等位基因品系的靶细胞。这表明除了Qa/Tla之外的因素可能在抗Qa/Tla效应细胞活性的产生中起作用。还注意到,来自具有Qa-1a/Tlaa等位基因品系的靶细胞被杀死,尽管程度远低于Qa-1b/Tlab靶细胞。SWR抗DBA/1效应细胞强烈裂解来自具有Qa-1b/Tlab品系的靶细胞,对Qa-1a/Tlaa靶细胞的裂解程度较低,对B6.Tlaa靶细胞无细胞毒性作用。这些数据表明,除了与Qa-1b/Tlab相关的CML靶抗原外,可能还存在一种由Qa-1b/Tlab以外的基因控制的细胞毒性T细胞识别的额外特异性。