用于异基因软骨治疗的软骨细胞的大规模生产。

IF 2.7 4区 医学 Q3 CELL & TISSUE ENGINEERING
Charlotte H Hulme, John K Garcia, Claire Mennan, Jade Perry, Sally Roberts, Kevin Norris, Duncan Baird, Larissa Rix, Robin Banerjee, Carl Meyer, Karina T Wright
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引用次数: 0

摘要

需要开发异基因软骨细胞疗法,以允许更多的人接受软骨修复细胞疗法的治疗,并降低目前两阶段自体手术的负担和成本。使用生物反应器大规模生产软骨细胞有助于提供现成的同种异体软骨细胞治疗,在一次生产过程中生产许多剂量。在本研究中,我们评估了一种用于成人软骨细胞制造的符合良好制造规范的中空纤维生物反应器(Quantum®)。软骨细胞是从膝关节置换术衍生的软骨中分离出来的(n = 5) 并在补充有10%胎牛血清(FBS)或5%人血小板裂解物(hPL)的培养基中在组织培养塑料(TCP)上扩增单代。补充hPL的培养物然后在Quantum生物反应器中扩增以进一步传代。在TCP上维持hPL或FBS中的匹配、平行培养物。对所有培养条件下的软骨细胞的生长动力学、形态、免疫特性、软骨形成潜力(软骨细胞颗粒测定)和单个端粒长度分析进行了表征。软骨细胞的量子膨胀导致86.4 ± 38.5 × 8.4中的106个细胞 ± 播种10.2后1.5天 ± 3.6 × 106个细胞。这与3.0有关 ± 量子生物反应器中的种群倍增为1.0,相比之下为2.1 ± 0.6和1.3 ± 在补充hPL和FBS的培养基中TCP上分别为1.0。Quantum和TCP扩增培养物保留了等效的软骨效力和间充质基质细胞标记物免疫图谱,只有整合素标记物CD49a在Quantum扩增后减少。量子膨胀软骨细胞与匹配的hPL-TCP群体表现出同等的软骨形成潜力(通过形成和维持软骨形成颗粒的能力来评估)。然而,与FBS培养物相比,hPL的制造导致软骨形成潜力降低,整合素CD49b、CD49c和CD51/61的细胞表面阳性率增加。与匹配的TCP培养物相比,软骨细胞的量子扩增并没有导致17p端粒长度缩短。这项研究表明,在Quantum中空纤维生物反应器中可以制造大量的成体软骨细胞。与匹配的TCP扩增相比,这种快速、高档扩增不会改变软骨细胞表型。因此,Quantum为临床应用提供了一种有吸引力的软骨细胞制造方法。然而,补充hPL用于软骨细胞扩增的培养基在保持软骨形成能力方面可能是不利的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Upscale Manufacture of Chondrocytes for Allogeneic Cartilage Therapies.

The Upscale Manufacture of Chondrocytes for Allogeneic Cartilage Therapies.

The Upscale Manufacture of Chondrocytes for Allogeneic Cartilage Therapies.

The Upscale Manufacture of Chondrocytes for Allogeneic Cartilage Therapies.

Allogeneic chondrocyte therapies need to be developed to allow more individuals to be treated with a cell therapy for cartilage repair and to reduce the burden and cost of the current two-stage autologous procedures. Upscale manufacture of chondrocytes using a bioreactor could help provide an off-the-shelf allogeneic chondrocyte therapy with many doses being produced in a single manufacturing run. In this study, we assess a good manufacturing practice-compliant hollow-fiber bioreactor (Quantum®) for adult chondrocyte manufacture. Chondrocytes were isolated from knee arthroplasty-derived cartilage (n = 5) and expanded in media supplemented with 10% fetal bovine serum (FBS) or 5% human platelet lysate (hPL) on tissue culture plastic (TCP) for a single passage. hPL-supplemented cultures were then expanded in the Quantum bioreactor for a further passage. Matched, parallel cultures in hPL or FBS were maintained on TCP. Chondrocytes from all culture conditions were characterized in terms of growth kinetics, morphology, immunoprofile, chondrogenic potential (chondrocyte pellet assays), and single telomere length analysis. Quantum expansion of chondrocytes resulted in 86.4 ± 38.5 × 106 cells in 8.4 ± 1.5 days, following seeding of 10.2 ± 3.6 × 106 cells. This related to 3.0 ± 1.0 population doublings in the Quantum bioreactor, compared with 2.1 ± 0.6 and 1.3 ± 1.0 on TCP in hPL- and FBS-supplemented media, respectively. Quantum- and TCP-expanded cultures retained equivalent chondropotency and mesenchymal stromal cell marker immunoprofiles, with only the integrin marker, CD49a, decreasing following Quantum expansion. Quantum-expanded chondrocytes demonstrated equivalent chondrogenic potential (as assessed by ability to form and maintain chondrogenic pellets) with matched hPL TCP populations. hPL manufacture, however, led to reduced chondrogenic potential and increased cell surface positivity of integrins CD49b, CD49c, and CD51/61 compared with FBS cultures. Quantum expansion of chondrocytes did not result in shortened 17p telomere length when compared with matched TCP cultures. This study demonstrates that large numbers of adult chondrocytes can be manufactured in the Quantum hollow-fiber bioreactor. This rapid, upscale expansion does not alter chondrocyte phenotype when compared with matched TCP expansion. Therefore, the Quantum provides an attractive method of manufacturing chondrocytes for clinical use. Media supplementation with hPL for chondrocyte expansion may, however, be unfavorable in terms of retaining chondrogenic capacity.

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来源期刊
Tissue engineering. Part C, Methods
Tissue engineering. Part C, Methods Medicine-Medicine (miscellaneous)
CiteScore
5.10
自引率
3.30%
发文量
136
期刊介绍: Tissue Engineering is the preeminent, biomedical journal advancing the field with cutting-edge research and applications that repair or regenerate portions or whole tissues. This multidisciplinary journal brings together the principles of engineering and life sciences in the creation of artificial tissues and regenerative medicine. Tissue Engineering is divided into three parts, providing a central forum for groundbreaking scientific research and developments of clinical applications from leading experts in the field that will enable the functional replacement of tissues. Tissue Engineering Methods (Part C) presents innovative tools and assays in scaffold development, stem cells and biologically active molecules to advance the field and to support clinical translation. Part C publishes monthly.
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