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慢病毒基因疗法治疗嘌呤核苷磷酸化酶缺乏症。

Lentivirus gene therapy for purine nucleoside phosphorylase deficiency.

作者信息

Liao Pu, Toro Ana, Min Weixian, Lee Shaun, Roifman Chaim M, Grunebaum Eyal

机构信息

Division of Allergy and Clinical Immunology, Research Institute, Hospital for Sick Children, Toronto, Canada.

出版信息

J Gene Med. 2008 Dec;10(12):1282-93. doi: 10.1002/jgm.1261.

Abstract

BACKGROUND

Purine nucleoside phosphorylase (PNP) deficiency causes the accumulation of toxic purine metabolites and lethal T cell immune defects, which might be corrected by expressing PNP by transplanting bone marrow (BM) cells transduced with lentiviral vectors containing the human PNP gene (lentiPNP).

METHODS

Lymphocytes from a single PNP-deficient patient as well as lymphocytes, fibroblasts and BM from PNP-deficient (PNP (-/-)) mice were transduced with lentiPNP. Female PNP (-/-) mice were transplanted with lentiPNP transduced BM cells from male PNP (-/-) mice or normal BM.

RESULTS

LentiPNP transduction significantly increased PNP expression in PNP-deficient human lymphocytes, murine lymphocytes, fibroblasts and BM cells. LentiPNP transduction also significantly improved the proliferation of PNP (-/-) murine lymphocyte and survival of irradiated PNP (-/-) fibroblasts. Polymerase chain reaction analysis demonstrated efficient transduction of lentiPNP into total and lineage-depleted BM cells grown ex vivo. LentiPNP transduced PNP (-/-) BM cells transplanted into PNP (-/-) mice expressed PNP in vivo, partially restored urinary uric acid secretion, improved thymocytes maturation, increased weight gain and extended survival of the mice. However, 12 weeks after transplant, the benefit of lentiPNP transduced cells and normal BM diminished and the percentage of engrafted donor cells decreased.

CONCLUSIONS

This short-term observational study provides the first in vivo proof that gene therapy may correct some of the abnormalities associated with PNP deficiency. Better gene transduction and expression, as well as improved cell engraftment, are required to further advance PNP gene therapy.

摘要

背景

嘌呤核苷磷酸化酶(PNP)缺乏会导致有毒嘌呤代谢产物的积累以及致命的T细胞免疫缺陷,通过移植用含有人类PNP基因的慢病毒载体转导的骨髓(BM)细胞来表达PNP,可能会纠正这些问题。

方法

用慢病毒载体转导单个PNP缺乏患者的淋巴细胞以及PNP缺乏(PNP(-/-))小鼠的淋巴细胞、成纤维细胞和骨髓。将雌性PNP(-/-)小鼠移植雄性PNP(-/-)小鼠或正常骨髓来源的慢病毒载体转导的BM细胞。

结果

慢病毒载体转导显著增加了PNP缺乏的人类淋巴细胞、小鼠淋巴细胞、成纤维细胞和BM细胞中PNP的表达。慢病毒载体转导还显著改善了PNP(-/-)小鼠淋巴细胞的增殖以及受辐射的PNP(-/-)成纤维细胞的存活。聚合酶链反应分析表明,慢病毒载体可有效转导至体外培养的全骨髓细胞和去除谱系细胞的骨髓细胞中。移植到PNP(-/-)小鼠体内的慢病毒载体转导的PNP(-/-)BM细胞在体内表达PNP,部分恢复了尿尿酸分泌,改善了胸腺细胞成熟,增加了体重增加并延长了小鼠的存活时间。然而,移植12周后,慢病毒载体转导的细胞和正常骨髓的益处减弱,移植的供体细胞百分比下降。

结论

这项短期观察性研究首次在体内证明基因治疗可能纠正与PNP缺乏相关的一些异常情况。需要更好的基因转导和表达以及改善细胞植入,以进一步推进PNP基因治疗。

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