Vallera D A, Soderling C C, Carlson G J, Kersey J H
Transplantation. 1981 Mar;31(3):218-22. doi: 10.1097/00007890-198103000-00015.
The current studies were designed to evaluated optimal conditions for reduction of graft-versus-host disease (GVHD) by removal of donor T cells from bone marrow inoculum. A model was used in which the addition of spleen cells to donor marrow heavily favored the development of lethal GVHD. Treatment of donor bone marrow plus spleen cells with monoclonal anti-Thy-1.2 antibody plus complement protected lethally irradiated recipients from GVHD across major histocompatibility barriers better than donor cells treated with the same dilution of antibody alone. Engraftment was demonstrated by the presence of high percentages of donor cells in the peripheral blood of these animals and the long-term survival of donor skin grafts. These results may be important in light of the development of new antihuman T cell monoclonal antibodies which may be used in the treatment of donor marrow in clinical transplantation.
当前的研究旨在评估通过从骨髓接种物中去除供体T细胞来降低移植物抗宿主病(GVHD)的最佳条件。使用了一种模型,在该模型中,向供体骨髓中添加脾细胞极大地促进了致死性GVHD的发展。用单克隆抗Thy-1.2抗体加补体处理供体骨髓加脾细胞,比仅用相同稀释度抗体处理的供体细胞能更好地保护经致死性照射的受体免受主要组织相容性屏障的GVHD影响。这些动物外周血中高比例的供体细胞以及供体皮肤移植物的长期存活证明了植入的存在。鉴于可能用于临床移植中供体骨髓治疗的新型抗人T细胞单克隆抗体的开发,这些结果可能具有重要意义。