San Raffaele Telethon Institute for Gene Therapy (SR-TIGET), IRCCS San Raffaele Scientific Institute, Milan, Italy.
Neurology Unit, Neurology Department, IRCCS San Raffaele Hospital, Milan, Italy.
Sci Rep. 2017 Jan 11;7:40136. doi: 10.1038/srep40136.
Adenosine Deaminase (ADA) deficiency is an autosomal recessive variant of severe combined immunodeficiency (SCID) caused by systemic accumulation of ADA substrates. Neurological and behavioral abnormalities observed in ADA-SCID patients surviving after stem cell transplantation or gene therapy represent an unresolved enigma in the field. We found significant neurological and cognitive alterations in untreated ADA-SCID patients as well as in two groups of patients after short- and long-term enzyme replacement therapy with PEG-ADA. These included motor dysfunction, EEG alterations, sensorineural hypoacusia, white matter and ventricular alterations in MRI as well as a low mental development index or IQ. Ada-deficient mice were significantly less active and showed anxiety-like behavior. Molecular and metabolic analyses showed that this phenotype coincides with metabolic alterations and aberrant adenosine receptor signaling. PEG-ADA treatment corrected metabolic adenosine-based alterations, but not cellular and signaling defects, indicating an intrinsic nature of the neurological and behavioral phenotype in ADA deficiency.
腺苷脱氨酶(ADA)缺乏症是一种常染色体隐性遗传的严重联合免疫缺陷(SCID),由 ADA 底物在体内积累引起。干细胞移植或基因治疗后存活的 ADA-SCID 患者出现的神经和行为异常是该领域尚未解决的难题。我们发现未经治疗的 ADA-SCID 患者以及接受 PEG-ADA 短期和长期酶替代治疗的两组患者均存在显著的神经和认知改变。这些改变包括运动功能障碍、脑电图改变、感觉神经性听力减退、MRI 中的白质和脑室改变以及智力发育指数或智商较低。Ada 缺陷小鼠的活动明显减少,表现出类似焦虑的行为。分子和代谢分析表明,这种表型与代谢改变和异常的腺苷受体信号传导一致。PEG-ADA 治疗可纠正代谢性基于腺苷的改变,但不能纠正细胞和信号缺陷,表明 ADA 缺乏症的神经和行为表型具有内在性质。