Skórski T, Kawalec M
Department of Cytophysiology, Medical Centre of Postgraduate Education, Warsaw, Poland.
Exp Hematol. 1988 Oct;16(9):782-4.
Lymphatic leukemia L1210-bearing semisyngeneic Balb/c x DBA/2Wf F1 (CD2F1) mice were subjected to chemoradiotherapy (2 x 100 mg/kg of cyclophosphamide i.p. and 1000 cGy of total body irradiation) and reconstitution with 10(7) syngeneic bone marrow cells i.v. The bone marrow obtained from leukemic mice was previously ex vivo purged of the leukemia cells with mafosfamide (ASTA Z7654) and stored in liquid nitrogen. Eight weeks after cytoreductive therapy and bone marrow transplantation we tried to immunize the mice against the lethal dose of the leukemia by i.p. injections of L1210-Maf cells (L1210 cells treated in vitro with mafosfamide for inhibition of their growth). About 75% of such mice were able to reject the subsequent 10(3) L1210 leukemia cell challenge, as compared with 70% of normal immunized mice and 55% of mice reconstituted with bone marrow cells not treated with mafosfamide.
将携带L1210淋巴细胞白血病的半同基因Balb/c×DBA/2Wf F1(CD2F1)小鼠进行放化疗(腹腔注射2×100mg/kg环磷酰胺和全身照射1000cGy),并通过静脉注射10⁷个同基因骨髓细胞进行重建。从白血病小鼠获得的骨髓预先在体外用马磷酰胺(ASTA Z7654)清除白血病细胞,并储存在液氮中。在减瘤治疗和骨髓移植八周后,我们试图通过腹腔注射L1210-Maf细胞(体外经马磷酰胺处理以抑制其生长的L1210细胞)使小鼠对致死剂量的白血病产生免疫。与70%的正常免疫小鼠和55%用未用马磷酰胺处理的骨髓细胞重建的小鼠相比,约75%的此类小鼠能够排斥随后10³个L1210白血病细胞的攻击。