Barrett A J, Brigden W D, Hobbs J R, Hugh-Jones K, Humble J G, James D C, Retsas S, Rogers T R, Selwyn S, Sneath P, Watson J G
Br Med J. 1977 Feb 12;1(6058):420-2. doi: 10.1136/bmj.1.6058.420.
A 15-year-old boy with Fanconi's anaemia, who required four units of blood each month, received a bone marrow graft from his 9-year-old brother, who has HLA identical and compatible on mixed lymphocyte reaction. Considerable immunosuppression was used and bacterial infection was prevented by vigorous decontamination in a Vickers-Trexler isolator. After the graft the patient's blood counts remained satisfactory for nine months, but it took six months before qualitative immune function was normal.
一名患有范科尼贫血的15岁男孩,每月需要4个单位的血液,接受了来自他9岁弟弟的骨髓移植,其弟弟的人类白细胞抗原(HLA)相同且在混合淋巴细胞反应中相匹配。使用了相当程度的免疫抑制措施,并在维克斯 - 特雷克斯勒隔离器中通过强力净化预防细菌感染。移植后,患者的血细胞计数在九个月内保持令人满意的水平,但定性免疫功能恢复正常则花了六个月时间。