Donofrio J, Coleman M S, Hutton J J, Daoud A, Lampkin B, Dyminski J
J Clin Invest. 1978 Oct;62(4):884-7. doi: 10.1172/JCI109201.
The deoxynucleotide, dATP, is elevated 50- to 1,000-fold above normal in erythrocytes, lymphocytes, and bone marrow from a child with adenosine deaminase deficiency and severe combined immunodeficiency disease. The child, when 17 mo of age, was also excreting approximately 30 mg of deoxyadenosine per day in urine (normal is less than 0.1 mg/day). Urinary excretion of uric acid was decreased. Elevated dATP levels in lymphocytes and bone marrow, and increased urinary excretion of deoxyadenosine, persisted despite hypertransfusion of the child with irradiated erythrocytes from a donor with normal adenosine deaminase. Overproduction of deoxynucleotides by increased salvage of adenosine appears to be the primary metabolic abnormality in patients with adenosine de aminase deficiency.
在一名患有腺苷脱氨酶缺乏症和严重联合免疫缺陷病的儿童的红细胞、淋巴细胞和骨髓中,脱氧核苷酸dATP比正常水平升高了50至1000倍。该儿童17个月大时,每天尿中还排泄约30毫克脱氧腺苷(正常水平低于0.1毫克/天)。尿酸的尿排泄量减少。尽管用来自腺苷脱氨酶正常的供体的辐照红细胞对该儿童进行了大量输血,但淋巴细胞和骨髓中dATP水平升高以及脱氧腺苷尿排泄增加的情况仍然存在。腺苷补救途径增加导致脱氧核苷酸产生过多似乎是腺苷脱氨酶缺乏症患者的主要代谢异常。