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首页> 外文期刊>Tissue Engineering Part A >Injectable Tissue-Engineered Bone Using Autogenous Bone Marrow–Derived Stromal Cells for Maxillary Sinus Augmentation: Clinical Application Report from a 2–6-Year Follow-Up
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Injectable Tissue-Engineered Bone Using Autogenous Bone Marrow–Derived Stromal Cells for Maxillary Sinus Augmentation: Clinical Application Report from a 2–6-Year Follow-Up

机译:使用自体骨髓源性基质细胞进行上颌窦增强的可注射组织工程化骨:2至6年随访的临床应用报告

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摘要

This clinical study used injectable tissue-engineered bone, along with bone marrow–derived stromal cells (BMDSCs) and platelet-rich plasma (PRP), to conduct maxillary sinus floor augmentation by the simultaneous placement of bone graft and dental implants and to examine the state of regenerated bone after functional loading in 16 sinus augmentations in 12 patients whose alveolar crestal bone height was 2–10mm. We used PRP as an autologous scaffold—which provides signal molecules—with in vitro expanded BMDSCs to enhance osteogenesis. All 41 dental implants prepared with the materials were clinically stable after second-stage surgery. The height of mineralized tissue at 2 years showed the mean increases of 8.8±1.6mm compared to preoperative values, and no adverse effects and remarkable bone absorption were seen in the 2–6-year follow-up time. Although these results are preliminary, injectable tissue-engineered bone would stably predict the success of bone formation and dental implants, reduce patient burden, and provide minimally invasive cell therapy for patients.
机译:这项临床研究使用可注射的组织工程骨,以及骨髓源性基质细胞(BMDSC)和富血小板血浆(PRP),通过同时放置骨移植物和牙科植入物进行上颌窦底增强术,并检查12例牙槽骨高度为2–10mm的患者在16次窦增大后的功能负荷后的再生骨状态。我们将PRP用作自体支架(可提供信号分子)和体外扩增的BMDSC,以增强成骨作用。用该材料制备的所有41种牙科植入物在第二阶段手术后临床上均稳定。与手术前相比,2年时矿化组织的高度平均增加了8.8±1.6mm,并且在2至6年的随访时间内未观察到不良反应和明显的骨吸收。尽管这些结果是初步的,但可注射的组织工程化的骨将稳定地预测骨形成和牙科植入物的成功,减轻患者负担并为患者提供微创细胞治疗。

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  • 来源
    《Tissue Engineering Part A》 |2008年第10期|1699-1707|共9页
  • 作者单位

    Center for Genetic and Regenerative Medicine, Nagoya University School of Medicine, Nagoya, Japan.;

    Department of Oral and Maxillofacial Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.;

    Department of Oral and Maxillofacial Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.;

    Department of Oral and Maxillofacial Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.;

    Center for Genetic and Regenerative Medicine, Nagoya University School of Medicine, Nagoya, Japan.;

    Laboratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan.;

    Department of Oral and Maxillofacial Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.;

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