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血管内皮生长因子减弱的富血小板血浆可改善软骨修复的治疗效果。

VEGF-attenuated platelet-rich plasma improves therapeutic effect on cartilage repair.

机构信息

Department of Orthopedics and Rehabilitation, University of Wisconsin-Madison, Madison, WI, USA.

Linda & Mitch Hart Center for Regenerative and Personalized Medicine, Steadman Philippon Research Institute, Vail, CO, USA.

出版信息

Biomater Sci. 2022 May 4;10(9):2172-2181. doi: 10.1039/d1bm01873f.

Abstract

Autologous platelet-rich plasma (PRP) has gained popularity as a less invasive treatment for various musculoskeletal tissue injuries and conditions due to its favorable safety profile, minimal manipulation and cost-effectiveness. Although PRP treatment has been clinically used for the treatment of osteoarthritis (OA) and damaged cartilage, evidence on therapeutic efficacy has been inconsistent, which calls for a methodology to achieve consistent and improved treatment outcomes. Given that PRP contains numerous proteins, we hypothesized that attenuation of a growth factor known to be detrimental to the healing tissue would enhance efficacy of PRP treatment. Considering that VEGF-mediated angiogenesis inhibits the repair of articular cartilage, we developed VEGF-attenuated PRP by sequestering VEGF in PRP using VEGF-binding microspheres. We demonstrated that VEGF attenuation in PRP did not inhibit the effect of PRP on chondrogenic differentiation of stem cells . In addition, healing of rat OA cartilage was significantly improved after treatment with VEGF-attenuated PRP when compared to the PRP treatment group or PBS control group. We expect that attenuation of unwanted biological activity using growth factor-binding microspheres could provide a new PRP customization method broadly applicable to various tissue repair processes.

摘要

富血小板血浆 (PRP) 因其良好的安全性、最小的操作和成本效益而成为治疗各种肌肉骨骼组织损伤和疾病的一种微创治疗方法,越来越受到关注。虽然 PRP 治疗已在临床上用于治疗骨关节炎 (OA) 和受损软骨,但治疗效果的证据并不一致,这需要一种方法来实现一致和改善的治疗效果。鉴于 PRP 中含有许多蛋白质,我们假设抑制一种已知对愈合组织有害的生长因子会增强 PRP 治疗的效果。考虑到 VEGF 介导的血管生成会抑制关节软骨的修复,我们通过使用 VEGF 结合微球将 VEGF 隔离在 PRP 中来开发 VEGF 减弱的 PRP。我们证明,PRP 中 VEGF 的衰减不会抑制 PRP 对干细胞软骨分化的作用。此外,与 PRP 治疗组或 PBS 对照组相比,用 VEGF 减弱的 PRP 治疗大鼠 OA 软骨后,其愈合明显改善。我们期望使用生长因子结合微球减弱不需要的生物学活性可以为各种组织修复过程提供一种广泛适用的新的 PRP 定制方法。

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