Rieger C H, Lustig J V, Hirschhorn R, Rothberg R M
J Pediatr. 1977 May;90(5):707-12. doi: 10.1016/s0022-3476(77)81232-8.
In a 51/2-month-old male infant with adenosine deaminase-positive severe combined immunodeficiency disease, who had no suitable bone marrow donor, immunologic reconstitution was attempted with lymphoid cells obtained from the liver of a 4- to 5-week-old-male human embryo. A mild graft-versus-host reaction began three weeks later. T-cells, which were absent prior to infusion of hepatic lymphoid cells, rose to a maximum of 554/mm3 at 16 weeks post transplantation. A normal lymphocyte response to pokeweek mitogen was not present until 25 to 30 weeks and to allogeneic cells until 39 weeks. Postive in vitro lymphocyte responses to Candida albicans were found repeatedly after 52 weeks. Twenty months following transplantation the patient is free of clinical infection, although he requires regular injections of gamma globulin.
在一名5个半月大的腺苷脱氨酶阳性重症联合免疫缺陷病男婴中,由于没有合适的骨髓供体,尝试用从一名4至5周大的男性人类胚胎肝脏获取的淋巴细胞进行免疫重建。三周后开始出现轻度移植物抗宿主反应。在输注肝脏淋巴细胞之前不存在的T细胞,在移植后16周时升至最高554/mm³。直到25至30周才出现对商陆有丝分裂原的正常淋巴细胞反应,对同种异体细胞的正常反应直到39周才出现。52周后反复发现对白色念珠菌的体外淋巴细胞阳性反应。移植后20个月,患者没有临床感染,尽管他需要定期注射丙种球蛋白。