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ADA 缺乏症患者和小鼠中 elapegademase 与 pegademase 的比较。

Comparison of elapegademase and pegademase in ADA-deficient patients and mice.

机构信息

Section of Hematology and Immunology, Department of Pediatrics, Alberta Children's Hospital and University of Calgary, Calgary, Canada.

Developmental and Stem Cell Biology Program, Research Institute, Hospital for Sick Children, Toronto, Canada.

出版信息

Clin Exp Immunol. 2020 May;200(2):176-184. doi: 10.1111/cei.13420. Epub 2020 Feb 9.

Abstract

The absence of adenosine deaminase (ADA) causes severe combined immune deficiency (SCID), which has been treated with PEGylated bovine-extracted ADA (ADAGEN). ADAGEN was recently replaced by a PEGylated recombinant bovine ADA, expressed in Escherichia coli (elapegademase, ELA-ADA). Limited information on ELA-ADA is available.  ADA enzymatic activity of ELA-ADA and ADAGEN was assessed in vitro at diverse dilutions. ADA activity and immune reconstitution in an ADA-SCID patient treated with ELA-ADA were compared with age-matched patients previously treated with ADAGEN. ADA activity and thymus reconstitution were evaluated in ADA-deficient mice following ELA-ADA or ADAGEN administered from 7 days postpartum. In vitro, ADA activity of ELA-ADA and ADAGEN were similar at all dilutions. In an ADA-SCID patient, ELA-ADA treatment led to a marked increase in trough plasma ADA activity, which was 20% higher than in a patient previously treated with ADAGEN. A marked increase in T cell numbers and generation of naive T cells was evident following 3 months of ELA-ADA treatment, while T cell numbers increased following 4 months in 3 patients previously treated with ADAGEN. T cell proliferations stimulation normalized and thymus shadow became evident following ELA-ADA treatment. ADA activity was significantly increased in the blood of ADA-deficient mice following ELA-ADA compared to ADAGEN, while both treatments improved the mice weights, the weight, number of cells in their thymus and thymocyte subpopulations. ELA-ADA has similar in- vitro and possibly better in-vivo activity than ADAGEN. Future studies will determine whether ELA-ADA results in improved long-term immune reconstitution.

摘要

腺苷脱氨酶(ADA)缺失会导致严重联合免疫缺陷(SCID),目前已采用聚乙二醇化牛源提取 ADA(ADAGEN)进行治疗。ADAGEN 最近已被在大肠杆菌中表达的聚乙二醇化重组牛 ADA(elapegademase,ELA-ADA)所取代。目前关于 ELA-ADA 的信息有限。本研究在体外不同稀释度下评估了 ELA-ADA 和 ADAGEN 的 ADA 酶活性。比较了 ELA-ADA 治疗的 ADA-SCID 患者与之前接受 ADAGEN 治疗的年龄匹配患者的 ADA 活性和免疫重建情况。在 ADA 缺陷型小鼠中,在产后 7 天给予 ELA-ADA 或 ADAGEN 后,评估 ADA 活性和胸腺重建情况。在体外,ELA-ADA 和 ADAGEN 的 ADA 活性在所有稀释度下均相似。在 ADA-SCID 患者中,ELA-ADA 治疗可显著增加谷值血浆 ADA 活性,比之前接受 ADAGEN 治疗的患者高 20%。接受 ELA-ADA 治疗 3 个月后,T 细胞数量和幼稚 T 细胞生成明显增加,而 3 名之前接受 ADAGEN 治疗的患者在接受治疗 4 个月后 T 细胞数量增加。ELA-ADA 治疗后 T 细胞增殖刺激恢复正常,胸腺阴影变得明显。与 ADAGEN 相比,ELA-ADA 可显著增加 ADA 缺陷型小鼠血液中的 ADA 活性,而两种治疗均改善了小鼠体重、胸腺重量、细胞数量及其胸腺细胞亚群。ELA-ADA 的体外活性与 ADAGEN 相似,体内活性可能更好。未来的研究将确定 ELA-ADA 是否会改善长期免疫重建。

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