Storb R, Thomas E D, Buckner C D, Clift R A, Fefer A, Fernando L P, Giblett E R, Johnson F L, Neiman P E
Blood. 1976 Oct;48(4):485-90.
Eleven of twenty-four patients with severe aplastic anemia given marrow grafts from HLA-identical siblings between October 1970 and March 1973 are alive with normal marrow function and continued evidence of engraftment 3-5 yr later. Ten have been leading normal lives with no immunosuppressive or other drug therapy since day 100 postgrafting. One has had chronic graft-versus-host disease of the skin which is now slowly improving with no therapy. He returned to full-time employment in the summer of 1975. The long-term well-being of almost half of our initial patients emphasizes the importance of marrow transplantation for the treatment of severe aplastic anemia.
1970年10月至1973年3月期间,24例接受来自HLA相同同胞骨髓移植的严重再生障碍性贫血患者中,有11例存活,骨髓功能正常,3至5年后仍有植入证据。10例自移植后第100天起就过着正常生活,无需免疫抑制或其他药物治疗。1例患有慢性皮肤移植物抗宿主病,目前未经治疗正在缓慢改善。他于1975年夏天重返全职工作。我们最初近一半患者的长期健康状况凸显了骨髓移植治疗严重再生障碍性贫血的重要性。