Owens A H, Santos G W
J Exp Med. 1968 Aug 1;128(2):277-91. doi: 10.1084/jem.128.2.277.
In these studies adult mice treated with cyclophosphamide and foreign immunologically competent cells developed a graft versus host disease which outwardly resembled that encountered in other experimental systems. Progressively larger doses of cyclophosphamide produced an increasingly severe disease whereas comparable doses of mechlorethamine were ineffective. Increasingly larger cell inocula from parental, allogeneic, and xenogeneic donors resulted in a correspondingly more severe disease. Nucleated cells obtained from the peripheral blood were found to be the most potent inducers of this syndrome, while cells from the spleen, bone marrow, and thymus displayed lesser degrees of reactivity in that order. No such graft versus host disease occurred in mice given saline, lysed, or heat-killed cells in place of viable foreign cells. Neither did the disorder develop when comparable inocula of isogeneic cells were used.
在这些研究中,用环磷酰胺处理的成年小鼠与外来免疫活性细胞一起会发生移植物抗宿主病,其外在表现类似于在其他实验系统中所遇到的情况。逐渐增加环磷酰胺的剂量会导致病情越来越严重,而同等剂量的氮芥则无效。来自亲代、同种异体和异种供体的细胞接种量越来越大,导致相应更严重的疾病。发现从外周血获得的有核细胞是该综合征最有效的诱导剂,而来自脾脏、骨髓和胸腺的细胞按此顺序显示出较低程度的反应性。用盐水、裂解或热灭活的细胞代替活的外来细胞的小鼠未发生这种移植物抗宿主病。当使用同等接种量的同基因细胞时,该病症也不会发生。