Körbling M, Fliedner T M, Calvo W, Ross W M, Nothdurft W, Steinbach I
Exp Hematol. 1979 Jul;7(6):277-88.
Long-term repopulation of the blood-forming organs of dogs, conditioned by wholebody X-irradiation (1200 R midplane dose), was achieved by transfusion of cryopreserved allogeneic blood mononuclear cells (MNC) without causing graft-versus-host-reaction (GVH-R). Donor and recipient dogs were DL-A identical, MLC-negative, no siblings, non-related. The blood stem cells (CFUc) were procured by a 3- to 4-hour continuous-flow leukapheresis. To increase the CFUc concentration in the peripheral blood, dextran sulfate (DS) was administered intravenously beforehand. About 1 x 10(10) MNC, among them about 1 x 10(7) CFUc, were collected and further segregated using a discontinuous albumin density gradient. Less dense cells were to be found in the upper part of the gradient (fraction 2). These cells included most of the CFUc, enriched by a factor of between 275 and 1730 compared to their concentration in the peripheral blood beforehand. After cryopreservation, these cells, when transfused into lethally irradiated dogs, completely repopulated the marrow and lymph nodes, caused no GVH-R and allowed long-term survival. These dogs received no immunosuppressive therapy, either before or after transfusion. More dense MNC were to be found in fraction 3; their transfusion caused a severe GVH-R, followed quickly by death. Fraction 4 was rich in lymphocytes and poor in CFUc. The transfusion of these cells produced a selective plasma-cell hyperplasia of the lymph nodes but failed to repopulate permanently the marrow. The reappearance of the different cell lineages in the marrow and in the peripheral blood after conditioning and transfusion of these cells produced a selective plasma-cell hyperplasia of the lymph nodes but failed to repopulate permanently the marrow. The reappearance of the different cell lineages in the marrow and in the peripheral blood after conditioning and transfusion of the segregated MNC is described in detail.
通过输注冷冻保存的同种异体血液单核细胞(MNC),在不引起移植物抗宿主反应(GVH-R)的情况下,实现了经全身X射线照射(中平面剂量1200拉德)处理的犬造血器官的长期再填充。供体犬和受体犬的DL-A相同,混合淋巴细胞培养阴性,无亲缘关系,非亲属。通过3至4小时的连续流式白细胞分离术采集血液干细胞(CFUc)。为了提高外周血中CFUc的浓度,预先静脉注射硫酸葡聚糖(DS)。收集约1×10¹⁰个MNC,其中约1×10⁷个CFUc,并使用不连续白蛋白密度梯度进一步分离。在梯度的上部(第2部分)发现密度较低的细胞。这些细胞包括大部分CFUc,与它们预先在外周血中的浓度相比,富集了275至1730倍。冷冻保存后,将这些细胞输注到接受致死性照射的犬体内时,它们完全重新填充了骨髓和淋巴结,未引起GVH-R,并使犬长期存活。这些犬在输血前后均未接受免疫抑制治疗。在第3部分中发现密度较高的MNC;输注它们会引起严重的GVH-R,随后很快死亡。第4部分富含淋巴细胞而CFUc较少。输注这些细胞会导致淋巴结选择性浆细胞增生,但未能永久性地重新填充骨髓。在对这些细胞进行预处理和输注后,骨髓和外周血中不同细胞系的重新出现导致了淋巴结选择性浆细胞增生,但未能永久性地重新填充骨髓。详细描述了分离的MNC在预处理和输注后骨髓和外周血中不同细胞系的重新出现情况。