Weiden P L, Storb R, Slichter S, Warren R P, Sale G E
J Immunol. 1976 Jul;117(1):143-50.
We have previously shown that blood transfusions can immunize a dog and lead to rejection of a subsequent marrow graft despite lethal total body irradiation (TBI). Sensitization to histocompatibility antigens induced by two prior transfusions of whole blood could be overcome by a regimen of procarbazine and anti-thymocyte serum (ATS) preceding TBI. The current study investigated a) whether this regimen could abrogate sensitization induced by six weekly transfusions given from days --50 to --15 preceding a marrow graft, and b) whether platelet survival studies and two in vitro tests of immunity could predict marrow graft rejection. All donor-recipient pairs were histoincompatible, unrelated, and of different breed. Twenty-two recipients received platelet concentrate transfusions and eight received whole blood transfusions. Recipients were given 1200 R TBI and a graft of marrow and peripheral blood leukocytes from the transfusion donor on day 0. Three of 15 recipients (20%) given procarbazine, 12.5 mg/kg i.v. on days --8, --6, and --4, and ATS, 0.6 ml/kg subcutaneously on days --7, --5 and --3, Rejected their grafts, whereas 11 of 15 dogs (73%) not given procarbazine and ATS rejected their grafts (p less than 0.01). Serum lymphocytotoxic antibodies, peripheral leukocyte migration inhibition, and in vivo donor platelet recovery and survival were studied in those recipients receiving six weekly transfusions and in 18 other recipients receiving a single donor transfusion 3 months before marrow grafting. No significant correlation was found among these in vitro and in vivo tests of sensitization. Sensitization to marrow grafts was not reliably detected by the presence of cytotoxic antibodies or leukocyte migration inhibition. Platelet survival, however, was positively correlated with the results of marrow grafting in 12 of 15 (80%) evaluable recipients (p approximately 0.15).
我们先前已表明,输血可使犬产生免疫反应,即使经过致死剂量的全身照射(TBI),也会导致随后的骨髓移植被排斥。在TBI之前,使用丙卡巴肼和抗胸腺细胞血清(ATS)的方案可克服因预先两次输注全血所诱导的对组织相容性抗原的致敏作用。当前研究调查了:a)该方案是否能消除在骨髓移植前从第-50天至-15天每周进行一次共六次输血所诱导的致敏作用;b)血小板存活研究以及两项体外免疫测试是否能够预测骨髓移植排斥反应。所有供体-受体对均为组织不相容、无亲缘关系且品种不同。22名受体接受了血小板浓缩物输血,8名接受了全血输血。受体在第0天接受1200拉德的TBI,并接受来自输血供体的骨髓和外周血白细胞移植。15名在第-8、-6和-4天静脉注射12.5毫克/千克丙卡巴肼,以及在第-7、-5和-3天皮下注射0.6毫升/千克ATS的受体中,有3名(20%)排斥了他们的移植,而15只未给予丙卡巴肼和ATS的犬中有11只(73%)排斥了他们的移植(p小于0.01)。在那些接受每周一次共六次输血的受体以及另外18名在骨髓移植前3个月接受单次供体输血的受体中,研究了血清淋巴细胞毒性抗体、外周白细胞迁移抑制以及体内供体血小板的恢复和存活情况。在这些体外和体内致敏测试之间未发现显著相关性。通过细胞毒性抗体的存在或白细胞迁移抑制并不能可靠地检测到对骨髓移植的致敏作用。然而,在15名可评估的受体中有12名(80%),血小板存活与骨髓移植结果呈正相关(p约为0.15)。