McDevitt H O, Tyan M L
J Exp Med. 1968 Jul 1;128(1):1-11.
The transfer of spleen cells from (C3H x C57Bl/6) F(1) mice, capable of responding to (T,G)-A--L, into irradiated C3H parental recipients, normally incapable of responding to (T,G)-A--L, transfers the ability to make either a primary or secondary immune response to this synthetic polypeptide antigen. This localizes the genetic control of the ability to respond to the spleen cell population and indicates that the genetic control is exerted upon a process directly related to antibody formation. Studies with congenic strains of mice and linkage studies in segregating backcross populations show that the ability to respond to (T,G)-A--L and (H,G)-A--L is linked to the H-2 locus and can thus be localized to the IXth mouse linkage group. Note Added in Proof: Of the three possible recombinant animals noted in Tables IV and V, two were infertile. The third animal was not a recombinant, since progeny testing and reimmunization showed that this animal was an H-2(2)/H-2(k) heterozygote capable of responding well to (T,G)-A--L.
将能够对(T,G)-A--L作出反应的(C3H×C57Bl/6)F(1)小鼠的脾细胞转移到经照射的C3H亲代受体中,这些亲代受体通常无法对(T,G)-A--L作出反应,这种转移赋予了对这种合成多肽抗原产生初次或二次免疫反应的能力。这将对该合成多肽抗原作出反应的能力的遗传控制定位到脾细胞群体上,并表明遗传控制作用于与抗体形成直接相关的过程。对同基因小鼠品系的研究以及在分离回交群体中的连锁研究表明,对(T,G)-A--L和(H,G)-A--L作出反应的能力与H-2基因座连锁,因此可以定位到小鼠第九连锁群。校样补注:表IV和表V中提到的三只可能的重组动物中,有两只不育。第三只动物不是重组体,因为子代测试和再次免疫表明这只动物是能够对(T,G)-A--L作出良好反应的H-2(2)/H-2(k)杂合子。