Sjögren H O, Minowada J, Ankerst J
J Exp Med. 1967 Apr 1;125(4):689-701. doi: 10.1084/jem.125.4.689.
A specific isograft resistance against three different mouse adeno 12 sarcomas was demonstrated in mice treated with four to eight doses of viable or X-ray-killed adeno 12 mouse tumors. Whole-body X-ray irradiation with 350 R 24 hr previous to the test challenge did not abolish the resistance, indicating that it was due to a true anamnestic immune reaction. This was further proven by the finding that similar treatment with tumors of other origin did not induce any immunity, nor did the treatment with adeno 12 tumor material induce any immunity against two neoplasms of Schmidt-Ruppin-Rous viral origin. The previous report by Trentin et al. (17) that adeno 12 infection leads to a specific transplantation immunity was fully confirmed. When the specificity of this virus-induced immunity was studied it was discovered that besides adeno virus type 12, type 7 and probably type 18 also gave the same type of resistance while adenovirus type 5 did not. A contamination of the adeno 7-infected mice with adeno type 12 was excluded by testing pooled sera from these animals for anti-adeno 12 CF or HI antibodies.
在用四至八剂活的或经X射线灭活的腺病毒12型小鼠肿瘤处理的小鼠中,证实了对三种不同的小鼠腺病毒12型肉瘤存在特异性同基因抗性。在试验性攻击前24小时用350伦琴进行全身X射线照射并不能消除这种抗性,这表明它是由于真正的回忆性免疫反应所致。这一点通过以下发现得到进一步证实:用其他来源的肿瘤进行类似处理不会诱导任何免疫,用腺病毒12型肿瘤材料进行处理也不会诱导对两种施密特-鲁平-劳斯病毒起源的肿瘤的任何免疫。特伦丁等人(17)先前关于腺病毒12型感染导致特异性移植免疫的报告得到了充分证实。当研究这种病毒诱导的免疫的特异性时,发现除了腺病毒12型外,7型以及可能的18型也产生相同类型的抗性,而5型腺病毒则不会。通过检测这些动物的混合血清中抗腺病毒12型补体结合或血凝抑制抗体,排除了腺病毒7型感染小鼠被腺病毒12型污染的可能性。