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人脐带间充质干/基质细胞异体给药治疗支气管肺发育不良:4例越南婴儿的初步结果

Allogeneic administration of human umbilical cord-derived mesenchymal stem/stromal cells for bronchopulmonary dysplasia: preliminary outcomes in four Vietnamese infants.

作者信息

Nguyen Liem Thanh, Trieu Thai T H, Bui Hue T H, Hoang Van T, Nguyen Anh T T, Trinh Nhung T H, Nguyen Kien T, Hoang Duc M

机构信息

Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam.

Vinmec International Hospital-Times City, Vinmec Healthcare System, Hanoi, Vietnam.

出版信息

J Transl Med. 2020 Oct 20;18(1):398. doi: 10.1186/s12967-020-02568-6.


DOI:10.1186/s12967-020-02568-6
PMID:33081796
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7576694/
Abstract

BACKGROUND: Bronchopulmonary dysplasia (BPD) is a severe condition in premature infants that compromises lung function and necessitates oxygen support. Despite major improvements in perinatal care minimizing the devastating effects, BPD remains the most frequent complication of extreme preterm birth. Our study reports the safety of the allogeneic administration of umbilical cord-derived mesenchymal stem/stromal cells (allo-UC-MSCs) and the progression of lung development in four infants with established BPD. METHODS: UC tissue was collected from a healthy donor, followed by propagation at the Stem Cell Core Facility at Vinmec Research Institute of Stem Cell and Gene Technology. UC-MSC culture was conducted under xeno- and serum-free conditions. Four patients with established BPD were enrolled in this study between May 25, 2018, and December 31, 2018. All four patients received two intravenous doses of allo-UC-MSCs (1 million cells/kg patient body weight (PBW) per dose) with an intervening interval of 7 days. Safety and patient conditions were evaluated during hospitalization and at 7 days and 1, 6 and 12 months postdischarge. RESULTS: No intervention-associated severe adverse events or prespecified adverse events were observed in the four patients throughout the study period. At the time of this report, all patients had recovered from BPD and were weaned off of oxygen support. Chest X-rays and CT scans confirmed the progressive reductions in fibrosis. CONCLUSIONS: Allo-UC-MSC administration is safe in preterm infants with established BPD. Trial registration This preliminary study was approved by the Vinmec International Hospital Ethics Board (approval number: 88/2019/QĐ-VMEC; retrospectively registered March 12, 2019).

摘要

背景:支气管肺发育不良(BPD)是早产儿的一种严重病症,会损害肺功能并需要氧气支持。尽管围产期护理有了重大改善,将破坏性影响降至最低,但BPD仍是极早产最常见的并发症。我们的研究报告了4例已确诊BPD的婴儿接受异体脐带间充质干细胞(allo-UC-MSCs)输注的安全性以及肺发育进程。 方法:从一名健康供体采集脐带组织,随后在万美干细胞与基因技术研究所干细胞核心设施进行增殖培养。UC-MSC培养在无血清和无动物源成分条件下进行。2018年5月25日至2018年12月31日期间,4例已确诊BPD的患者纳入本研究。所有4例患者均接受两剂静脉注射allo-UC-MSCs(每剂100万个细胞/千克患者体重(PBW)),间隔7天。在住院期间以及出院后7天、1个月、6个月和12个月对安全性和患者状况进行评估。 结果:在整个研究期间,4例患者均未观察到与干预相关的严重不良事件或预设不良事件。在本报告发布时,所有患者均已从BPD中康复,且已停用氧气支持。胸部X光和CT扫描证实纤维化程度逐渐减轻。 结论:allo-UC-MSCs输注对于已确诊BPD的早产儿是安全的。试验注册 本初步研究已获得万美国际医院伦理委员会批准(批准号:88/2019/QĐ-VMEC;2019年3月12日追溯注册)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9630/7576694/53b4c67ade44/12967_2020_2568_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9630/7576694/1f795f1602ca/12967_2020_2568_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9630/7576694/16e7e322af58/12967_2020_2568_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9630/7576694/53b4c67ade44/12967_2020_2568_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9630/7576694/1f795f1602ca/12967_2020_2568_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9630/7576694/16e7e322af58/12967_2020_2568_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9630/7576694/53b4c67ade44/12967_2020_2568_Fig3_HTML.jpg

相似文献

[1]
Allogeneic administration of human umbilical cord-derived mesenchymal stem/stromal cells for bronchopulmonary dysplasia: preliminary outcomes in four Vietnamese infants.

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[2]
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[7]
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[2]
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[3]
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Int J Nanomedicine. 2025-2-27

[4]
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Respir Res. 2024-10-24

[5]
Progress in Research on Stem Cells in Neonatal Refractory Diseases.

J Pers Med. 2023-8-21

[6]
Innovations in cell therapy in pediatric diseases: a narrative review.

Transl Pediatr. 2023-6-30

[7]
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Stem Cells Transl Med. 2023-6-15

[8]
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[9]
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[10]
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本文引用的文献

[1]
Two-year outcomes of infants enrolled in the first-in-human study of amnion cells for bronchopulmonary dysplasia.

Stem Cells Transl Med. 2020-3

[2]
Update on Postnatal Corticosteroids to Prevent or Treat Bronchopulmonary Dysplasia.

Am J Perinatol. 2019-6-25

[3]
Bronchopulmonary Dysplasia: An Update of Current Pharmacologic Therapies and New Approaches.

Clin Med Insights Pediatr. 2018-12-11

[4]
Off-label mesenchymal stromal cell treatment in two infants with severe bronchopulmonary dysplasia: clinical course and biomarkers profile.

Cytotherapy. 2018-10-14

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First-In-Human Administration of Allogeneic Amnion Cells in Premature Infants With Bronchopulmonary Dysplasia: A Safety Study.

Stem Cells Transl Med. 2018-8-5

[6]
Paracetamol (acetaminophen) for patent ductus arteriosus in preterm or low birth weight infants.

Cochrane Database Syst Rev. 2018-4-6

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J Pediatr. 2018-6

[8]
Bronchopulmonary dysplasia: A review of pathogenesis and pathophysiology.

Respir Med. 2017-10-24

[9]
Mesenchymal Stromal Cell Therapy in Bronchopulmonary Dysplasia: Systematic Review and Meta-Analysis of Preclinical Studies.

Stem Cells Transl Med. 2017-10-17

[10]
Bone Marrow Mononuclear Cells Transplantation in Treatment of Established Bronchopulmonary Dysplasia: A Case Report.

Am J Case Rep. 2017-10-12

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