Ariga T, Oda N, Yamaguchi K, Kawamura N, Kikuta H, Taniuchi S, Kobayashi Y, Terada K, Ikeda H, Hershfield M S, Kobayashi K, Sakiyama Y
Department of Human Gene Therapy and Department of Pediatrics, Hokkaido University School of Medicine, Sapporo, Japan.
Blood. 2001 May 1;97(9):2896-9. doi: 10.1182/blood.v97.9.2896.
Inherited deficiency of adenosine deaminase (ADA) results in one of the autosomal recessive forms of severe combined immunodeficiency. This report discusses 2 patients with ADA deficiency from different families, in whom a possible reverse mutation had occurred. The novel mutations were identified in the ADA gene from the patients, and both their parents were revealed to be carriers. Unexpectedly, established patient T-cell lines, not B-cell lines, showed half-normal levels of ADA enzyme activity. Reevaluation of the mutations in these T-cell lines indicated that one of the inherited ADA gene mutations was reverted in both patients. At least one of the patients seemed to possess the revertant cells in vivo; however, the mutant cells might have overcome the revertant after receiving ADA enzyme replacement therapy. These findings may have significant implications regarding the prospects for stem cell gene therapy for ADA deficiency.
腺苷脱氨酶(ADA)遗传性缺乏会导致严重联合免疫缺陷的常染色体隐性形式之一。本报告讨论了来自不同家庭的2例ADA缺乏患者,他们可能发生了反向突变。在患者的ADA基因中鉴定出了新的突变,并且发现他们的父母均为携带者。出乎意料的是,已建立的患者T细胞系而非B细胞系显示ADA酶活性水平为正常水平的一半。对这些T细胞系中的突变进行重新评估表明,两名患者中遗传性ADA基因突变之一均已回复突变。至少有一名患者体内似乎拥有回复突变细胞;然而,突变细胞在接受ADA酶替代疗法后可能已战胜了回复突变细胞。这些发现可能对ADA缺乏症的干细胞基因治疗前景具有重要意义。