Ildstad S T, Sachs D H
Nature. 1984;307(5947):168-70. doi: 10.1038/307168a0.
Clinical organ transplantation between genetically disparate individuals currently requires the use of chemotherapeutic agents to suppress the rejection reaction. The deleterious side effects of these reagents and their inability to prevent rejection completely has led to a continuing search for methods to induce specific transplantation tolerance in adult recipients. Numerous experimental animal models utilizing irradiation and bone marrow transplantation coincident with organ transplantation have been proposed. Bone marrow transplantation, however, has its own major complications, including graft-versus-host reactions and immunoincompetence, probably resulting from a failure of appropriate immune cell interactions in the reconstituted host. We have now attempted to overcome these difficulties by reconstituting the irradiated host with T-cell depleted bone marrow containing both host (syngeneic) and donor (allogeneic or xenogeneic) components. This technique leads to long-term survival of the reconstituted animals and specific prolongation of subsequent skin grafts of donor type. Animals reconstituted in this fashion are fully reactive to third-party allografts and xenografts and do not appear to manifest signs of graft-versus-host disease.
目前,在基因不同的个体之间进行临床器官移植需要使用化学治疗药物来抑制排斥反应。这些药物的有害副作用以及它们无法完全预防排斥反应,导致人们不断寻找在成年受者中诱导特异性移植耐受的方法。已经提出了许多利用照射和与器官移植同时进行的骨髓移植的实验动物模型。然而,骨髓移植有其自身的主要并发症,包括移植物抗宿主反应和免疫无能,这可能是由于重建宿主中适当的免疫细胞相互作用失败所致。我们现在试图通过用含有宿主(同基因)和供体(异基因或异种)成分的T细胞耗竭骨髓重建受照射宿主来克服这些困难。这种技术导致重建动物的长期存活以及供体类型后续皮肤移植的特异性延长。以这种方式重建的动物对第三方同种异体移植物和异种移植物具有完全反应性,并且似乎没有表现出移植物抗宿主病的迹象。