自体肌腱细胞植入术(OrthoATI™)治疗髌腱和掌长肌腱时,年龄和供体部位不会影响细胞生长和生物活性。

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Droplet digital PCR (ddPCR) was utilized for gene expression analysis. Dichotomous results were compared between groups using x<sup>2</sup> or Fisher's exact tests with no adjustment for multiple comparisons. The nonparametric Mann–Whitney U and Kruskal–Wallis tests were utilized for the sex and age (&lt;35y, 35-44y, 45-54y, &gt;55y) analyses, respectively. All analyses were performed using IBM SPSS v27, and a two-tailed P-value of &lt;0.05 was considered statistically significant.</p></div><div><h3>Results</h3><p>149 patients were included in the analysis. The PT was biopsied in 63 patients, and PL in 86 patients. There were no observer effects for age and gender between the PT and PL groups. There was no statistical significance between the PT and PL tendons for cell morphology, average cell population doubling time (PDT) (PT 83.9 vs PL 82.7 ​h, p ​= ​0.482), cellular yield (PT 16.2 vs PL 15.2 ​× ​10<sup>6</sup>, p ​= ​0.099), and cell viability (PT 98.7 vs PL 99.0%, p ​= ​0.277). Additionally, ddPCR analyses showed no statistical significance found in tenogenic gene expression, including collagen type I (COL1, p ​= ​0.86), tenomodulin (TNMD, p ​= ​0.837) and scleraxis (SCX, p ​= ​0.331) between PT- and PL-derived tendon cells. An age stratification analysis found no effect on growth and gene expression. COL1 was found to be higher in males when compared to females (P ​&lt; ​0.001), but otherwise no difference was seen in growth and gene expression in the gender analysis. 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引用次数: 0

摘要

目的:自体肌腱细胞植入疗法(OrthoATI™)对治疗不同解剖部位的肌腱病患者具有显著疗效。本研究评估了患者年龄、性别和肌腱活检部位对用于治疗慢性肌腱病的自体肌腱细胞的形态、生长和基因表达的影响:2020年至2022年期间接受OrthoATI™治疗腱鞘炎的患者最初都是从髌腱(PT)或掌长肌腱(PL)上取活检组织进行治疗。自体腱细胞在良好生产规范(GMP)细胞实验室进行分离、培养和扩增,为期四至六周。细胞形态使用相衬显微镜进行评估。利用液滴数字 PCR (ddPCR) 进行基因表达分析。使用 x2 或费雪精确检验比较组间二分法结果,不进行多重比较调整。性别和年龄(55 岁)分析分别采用非参数 Mann-Whitney U 检验和 Kruskal-Wallis 检验。所有分析均使用 IBM SPSS v27 进行,结果采用双尾 P 值:149名患者被纳入分析。63名患者进行了PT活检,86名患者进行了PL活检。PT 组和 PL 组在年龄和性别方面没有观察者效应。在细胞形态、平均细胞群倍增时间 (PDT) (PT 83.9 小时 vs PL 82.7 小时,P=0.482)、细胞产量(PT 16.2 vs PL 15.2×106 ,P=0.099)和细胞存活率(PT 98.7 vs PL 99.0%,P=0.277)方面,PT 和 PL 肌腱之间没有统计学意义。此外,ddPCR 分析表明,PT 和 PL 衍生肌腱细胞之间的致韧带基因表达,包括 I 型胶原蛋白(COL1,p=0.86)、腱鞘蛋白(TNMD,p=0.837)和硬轴(SCX,p=0.331),均无统计学意义。年龄分层分析没有发现对生长和基因表达的影响。与女性相比,男性的 COL1 含量更高(PC结论:这项研究表明,用于 OrthoATI™ 的肌腱活检组织的肌腱细胞的生长和生物活性不受肌腱供体部位和年龄的影响:证据等级:IV。
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Impact of age and donor sites on bioactivities of tendon cells in autologous tenocyte implantation (OrthoATI™) for treatment of chronic tendinopathy

Objectives

Autologous tenocyte implantation (OrthoATI™) therapy has demonstrated efficacy in treating patients with tendinopathy at various anatomical sites. This study evaluates the effect of patient age, gender, and tendon biopsy site on morphology, growth, and gene expression of autologous tendon cells used to treat chronic tendinopathy.

Methods

Patients undergoing OrthoATI™ for tendinopathies between 2020 and 2022 were initially treated by biopsies taken from patella tendon (PT) or palmaris longus tendon (PL). The biopsies were sent to a Good Manufacturing Practice (GMP) cell laboratory where tendon cells were isolated, cultured, and expanded for four to six weeks. Cell morphology was assessed using phase contrast microscopy. Droplet digital PCR (ddPCR) was utilized for gene expression analysis. Dichotomous results were compared between groups using x2 or Fisher's exact tests with no adjustment for multiple comparisons. The nonparametric Mann–Whitney U and Kruskal–Wallis tests were utilized for the sex and age (<35y, 35-44y, 45-54y, >55y) analyses, respectively. All analyses were performed using IBM SPSS v27, and a two-tailed P-value of <0.05 was considered statistically significant.

Results

149 patients were included in the analysis. The PT was biopsied in 63 patients, and PL in 86 patients. There were no observer effects for age and gender between the PT and PL groups. There was no statistical significance between the PT and PL tendons for cell morphology, average cell population doubling time (PDT) (PT 83.9 vs PL 82.7 ​h, p ​= ​0.482), cellular yield (PT 16.2 vs PL 15.2 ​× ​106, p ​= ​0.099), and cell viability (PT 98.7 vs PL 99.0%, p ​= ​0.277). Additionally, ddPCR analyses showed no statistical significance found in tenogenic gene expression, including collagen type I (COL1, p ​= ​0.86), tenomodulin (TNMD, p ​= ​0.837) and scleraxis (SCX, p ​= ​0.331) between PT- and PL-derived tendon cells. An age stratification analysis found no effect on growth and gene expression. COL1 was found to be higher in males when compared to females (P ​< ​0.001), but otherwise no difference was seen in growth and gene expression in the gender analysis. No postbiopsy clinical complications were reported for either group.

Conclusion

This study has shown that the growth and bioactivities of tendon cells from tendon biopsies for OrthoATI™ are not affected by tendon donor site and age.

Level of evidence

IV.

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来源期刊
CiteScore
2.90
自引率
6.20%
发文量
61
审稿时长
108 days
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