Carson D A, Lakow E, Wasson D B, Kamatani N
Department of Clinical Research, Scripps Clinic and Research Foundation, La Jolla, CA 92037, U.S.A.
Immunol Today. 1981 Dec;2(12):234-8. doi: 10.1016/0167-5699(81)90010-4.
Two inborn errors of purine metabolism have been associated with autosomally inherited human immunodeficiency diseases. A lack of adenosine deaminase (ADA) produces severe lymphopenia and a combined immunodeficiency syndrome. A deficiency of purine nucleoside phosphorylase (PNP) is associated with a selective cellular immune depth. This article discusses the probable biochemical basis for lymphocyte-specific toxicity in these disorders.
两种嘌呤代谢的先天性缺陷与常染色体隐性遗传的人类免疫缺陷疾病相关。腺苷脱氨酶(ADA)缺乏会导致严重的淋巴细胞减少和联合免疫缺陷综合征。嘌呤核苷磷酸化酶(PNP)缺乏与选择性细胞免疫缺陷有关。本文讨论了这些疾病中淋巴细胞特异性毒性的可能生化基础。