Advancing dentin-pulp regeneration: clinical perspectives and insights from stem/progenitor cell transplantation (part II).

IF 1.5 Q4 CELL BIOLOGY
American journal of stem cells Pub Date : 2024-06-15 eCollection Date: 2024-01-01 DOI:10.62347/BYPG4014
Sayna Shamszadeh, Mohammad Jafar Eghbal, Saeed Asgary
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Abstract

This systematic review evaluates clinical studies investigating regenerative endodontic procedures for mature/immature teeth utilizing stem cell transplantation. An electronic search of Scopus, PubMed, ISI Web Science, and Google Scholar was conducted up to January 2023. Outcome measures encompassed radiographic (periapical lesion, root length, apical foramen width, volume of the regenerated pulp) and clinical (post-operative pain, sensibility test) parameters. Among 3250 identified articles, five clinical studies were selected, comprising two randomized controlled trials (RCTs) for mature/immature teeth, and three case reports/series for mature teeth. Despite the promising potential, the included studies exhibited a notable risk of bias. The diversity in stem cells (e.g., dental pulp stem cells [DPSCs], umbilical cord mesenchymal stem cells [UC-MSCs]), scaffolds (Atecollagen, collagen membrane, platelet-poor plasma [PPP], leukocyte platelet-rich in fibrin [L-PRF]), and growth factors (granulocyte colony-stimulating factor [G-CSF]) emphasized the heterogeneity across interventions. In RCTs, DPSCs application increased root length and reduced apical foramen width in immature teeth, while UC-MSCs transplantation reduced apical lesions in mature teeth. Transplantation of DPSCs aggregates or UC-MSCs/PPP also elicited positive pulp responses and increased blood flow. In case reports/series, DPSCs application in teeth with irreversible pulpitis resulted in mineralization and increased the regenerated pulp' volume. Furthermore, transplantation of DPSCs with G-CSF/atelocollagen or L-PRF/collagen membrane led to positive pulp responses. While underscoring the potential of stem cell transplantation for regenerative endodontics in mature/immature teeth, the overall evidence quality and the limited number of available studies emphasize the need for cautious interpretation of results. Future well-designed clinical studies are essential to validate these findings further.

推进牙本质-牙髓再生:干细胞/祖细胞移植的临床视角和启示(第二部分)。
这篇系统性综述评估了利用干细胞移植对成熟/不成熟牙齿进行再生牙髓治疗的临床研究。对Scopus、PubMed、ISI Web Science和Google Scholar的电子检索截止到2023年1月。结果测量包括放射学参数(根尖周病变、牙根长度、根尖孔宽度、再生牙髓体积)和临床参数(术后疼痛、敏感性测试)。在已识别的 3250 篇文章中,选出了五项临床研究,包括两项针对成熟/不成熟牙齿的随机对照试验(RCT)和三项针对成熟牙齿的病例报告/系列研究。尽管这些研究很有潜力,但存在明显的偏差风险。干细胞(如牙髓干细胞[DPSCs]、脐带间充质干细胞[UC-MSCs])、支架(Atecollagen、胶原膜、贫血小板血浆[PPP]、富含纤维蛋白的白细胞血小板[L-PRF])和生长因子(粒细胞集落刺激因子[G-CSF])的多样性强调了不同干预措施的异质性。在临床试验中,应用 DPSCs 增加了未成熟牙的牙根长度并减少了根尖孔宽度,而 UC-MSCs 移植则减少了成熟牙的根尖病变。移植 DPSCs 聚合体或 UC-MSCs/PPP 还可引起积极的牙髓反应并增加血流量。在病例报告/系列报道中,在患有不可逆牙髓炎的牙齿中应用 DPSCs 可导致矿化,并增加再生牙髓的体积。此外,DPSCs与G-CSF/atelocollagen或L-PRF/collagen膜一起移植,可导致积极的牙髓反应。虽然强调了干细胞移植在成熟/未成熟牙齿牙髓再生中的潜力,但总体证据质量和可用研究数量有限,强调了谨慎解释结果的必要性。未来精心设计的临床研究对进一步验证这些发现至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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