Keightley R G, Lawton A R, Cooper M D, Yunis E J
Lancet. 1975 Nov 1;2(7940):850-3. doi: 10.1016/s0140-6736(75)90238-x.
Following transplantation with allogeneic fetal liver, a boy with a severe combined immunodeficiency and adenosine-deaminase (A.D.A.) deficiency developed immunocompetent T and B cells in an orderly manner. Engraftment was indicated by appearance of A.D.A. activity and donor-lymphocyte and red-cell antigens. The child remained free of major infections until one year later when he developed an ultimately fatal nephrotic syndrome associated with immune-complex glomerulonephritis.
在接受同种异体胎儿肝脏移植后,一名患有严重联合免疫缺陷和腺苷脱氨酶(A.D.A.)缺乏症的男孩有序地产生了具有免疫活性的T细胞和B细胞。A.D.A.活性以及供体淋巴细胞和红细胞抗原的出现表明移植成功。该患儿在一年时间里未发生严重感染,直到后来患上了最终致命的肾病综合征,伴有免疫复合物性肾小球肾炎。