Schwartz A L, Polmar S H, Stern R C, Cowan D H
Br J Haematol. 1978 Jun;39(2):189-94. doi: 10.1111/j.1365-2141.1978.tb01088.x.
The platelets from a boy with adenosine deaminase deficiency-severe combined immunodeficiency disease (ADA-SCID) showed markedly subnormal aggregation in response to collagen and ADP. In contrast with normal platelets, ATP, AMP and adenosine had little effect in inhibiting ADP-induced aggregation of ADA-SCID platelets. These observations suggest that altered adenosine metabolism exists in ADA-SCID platelets.
一名患有腺苷脱氨酶缺乏症 - 严重联合免疫缺陷病(ADA - SCID)的男孩的血小板对胶原蛋白和二磷酸腺苷(ADP)的反应显示出明显低于正常水平的聚集。与正常血小板相比,三磷酸腺苷(ATP)、一磷酸腺苷(AMP)和腺苷对ADA - SCID血小板的ADP诱导聚集几乎没有抑制作用。这些观察结果表明ADA - SCID血小板中存在腺苷代谢改变。