Gorin N C, Douay L, Laporte J P, Lopez M, Zittoun R, Rio B, Najman A, Jansen F K, Voisin G A, Stachowiak J
Presse Med. 1985 Nov 2;14(37):1909-13.
In order to consolidate a complete or partial remission, 4 patients with T-cell malignancy received cyclophosphamide 120 mg/kg plus total body irradiation, followed by reinfusion of cryopreserved autologous bone marrow purged in vitro by the immunotoxin T 101 (SR 41322) composed of the murine monoclonal T 101 antibody coupled with the A chain of ricin. The immunotoxin was applied in doses of 10(-9) and 10(-8) M for periods of 4 and 20 hours at 37 degrees C. The recovery of CFUc and BFUe progenitors was total following incubation with IT 101, but reduced after cryopreservation (1-15 to 80% for CFUc,-33 to 47% for BFUe), haematopoietic recovery occurred within normal delays, demonstrating that autologous bone marrow pretreated with the immunotoxin can be successfully transplanted. However, the slow increase in lymphocytes and the occurrence of lethal infection in 2 cases indicate that an in-depth study of immunological reconstitution after in vitro treatment of bone marrow with ITT 101 is necessary.
为巩固完全或部分缓解,4例T细胞恶性肿瘤患者接受了120mg/kg环磷酰胺加全身照射,随后回输经免疫毒素T 101(SR 41322)体外净化的冷冻保存自体骨髓,该免疫毒素由与蓖麻毒素A链偶联的鼠单克隆T 101抗体组成。免疫毒素以10(-9)和10(-8) M的剂量在37℃下应用4小时和20小时。与IT 101孵育后CFUc和BFUe祖细胞完全恢复,但冷冻保存后减少(CFUc为1 - 15%至80%,BFUe为 - 33%至47%),造血恢复在正常延迟时间内发生,表明经免疫毒素预处理的自体骨髓可成功移植。然而,淋巴细胞增加缓慢以及2例发生致命感染表明,有必要深入研究用ITT 101体外处理骨髓后的免疫重建情况。