Green I, Paul W E, Benacerraf B
J Exp Med. 1967 Nov 1;126(5):959-67. doi: 10.1084/jem.126.5.959.
A study of the passive transfer of delayed hypersensitivity to DNP-poly-L-lysine and to DNP-GL was performed in Hartley guinea pigs. Delayed hypersensitivity to DNP-PLL and DNP-GL could be transferred successfully only by means of sensitized cells from genetic responder guinea pigs and in most cases, only into those guinea pigs genetically capable of responding to PLL. The inability to transfer delayed hypersensitivity to DNP-PLL or DNP-GL to genetic nonresponder guinea pigs is not the result of the early destruction of the transferred cells by an incompatible host, since it was shown that delayed hypersensitivity to ovalbumin could be successfully transferred from guinea pigs with the PLL gene into genetic nonresponder animals. The requirement of active participation of specific and genetically controlled host mechanisms in the successful passive transfer of delayed sensitivity to DNP-PLL and DNP-GL has been demonstrated.
在哈特利豚鼠身上进行了一项关于对二硝基苯 - 聚 -L-赖氨酸(DNP-poly-L-lysine)和二硝基苯 - 球蛋白(DNP-GL)迟发型超敏反应被动转移的研究。对DNP-PLL和DNP-GL的迟发型超敏反应仅能通过来自遗传性反应性豚鼠的致敏细胞成功转移,并且在大多数情况下,只能转移到那些在遗传上能够对PLL产生反应的豚鼠体内。无法将对DNP-PLL或DNP-GL的迟发型超敏反应转移到遗传性无反应性豚鼠身上,并非是由于不相容的宿主对转移细胞的早期破坏所致,因为已表明对卵清蛋白的迟发型超敏反应能够从具有PLL基因的豚鼠成功转移到遗传性无反应性动物体内。已经证明,在对DNP-PLL和DNP-GL迟发型超敏反应的成功被动转移中,特定的和受遗传控制的宿主机制需要积极参与。