Staal G E, Stoop J W, Zegers B J, Siegenbeek van Heukelom L H, van der Vlist M J, Wadman S K, Martin D W
J Clin Invest. 1980 Jan;65(1):103-8. doi: 10.1172/JCI109639.
Purine nucleoside phosphorylase deficiency is associated with a severely defective T-cell immunity. A patient with purine nucleoside phosphorylase deficiency was treated with transfusions of irradiated erythrocytes and plasma. This resulted in a remarkable correction of the metabolic disturbances in the patient. The urinary excretion of inosine, deoxyinosine, guanosine, and deoxyguanosine decreased, whereas uric acid excretion as well as serum uric acid concentration increased. It could be shown that the enzyme activity of the circulating erythrocytes correlated inversely with the urinary excretion of nucleosides and directly with the excretion of uric acid. As a consequence of the therapy, several glycolytic intermediates of the erythrocytes were increased, especially 2,3-diphosphoglycerate. The high 2,3-diphosphoglycerate level caused a shift to the right of the oxygen dissociation curve (P50 = 32.9 mm Hg). The immunological status of the patient showed definite improvement after the enzyme replacement therapy.
嘌呤核苷磷酸化酶缺乏与严重缺陷的T细胞免疫相关。一名嘌呤核苷磷酸化酶缺乏患者接受了辐照红细胞和血浆的输血治疗。这导致患者的代谢紊乱得到显著纠正。肌苷、脱氧肌苷、鸟苷和脱氧鸟苷的尿排泄减少,而尿酸排泄以及血清尿酸浓度增加。可以证明,循环红细胞的酶活性与核苷的尿排泄呈负相关,与尿酸排泄呈正相关。作为治疗的结果,红细胞的几种糖酵解中间产物增加,尤其是2,3-二磷酸甘油酸。高2,3-二磷酸甘油酸水平导致氧解离曲线右移(P50 = 32.9 mmHg)。酶替代治疗后患者的免疫状态有明显改善。