Wu Danielle, Lombaert Isabelle M A, DeLeon Maximilien, Pradhan-Bhatt Swati, Witt Robert L, Harrington Daniel Anton, Trombetta Mark G, Passineau Michael J, Farach-Carson Mary C
Department of Diagnostic and Biomedical Sciences, School of Dentistry, University of Texas Health Science Center at Houston, Houston, TX, United States.
Department of Bioengineering, Rice University, Houston, TX, United States.
Front Mol Biosci. 2021 Sep 30;8:711602. doi: 10.3389/fmolb.2021.711602. eCollection 2021.
An urgent need exists to develop large animal models for preclinical testing of new cell therapies designed to replace lost or damaged tissues. Patients receiving irradiation for treatment of head and neck cancers frequently develop xerostomia/dry mouth, a condition that could one day be treated by cell therapy to repopulate functional saliva-producing cells. Using immunosuppression protocols developed for patients receiving whole face transplants, we successfully used immunosuppressed miniswine as a suitable host animal to evaluate the long-term stability, biocompatibility, and fate of matrix-modified hyaluronate (HA) hydrogel/bioscaffold materials containing encapsulated salivary human stem/progenitor cells (hS/PCs). An initial biocompatibility test was conducted in parotids of untreated miniswine. Subsequent experiments using hS/PC-laden hydrogels were performed in animals, beginning an immunosuppression regimen on the day of surgery. Implant sites included the kidney capsule for viability testing and the parotid gland for biointegration time periods up to eight weeks. No transplant rejection was seen in any animal assessed by analysis of the tissues near the site of the implants. First-generation implants containing only cells in hydrogel proved difficult to handle in the surgical suite and were modified to adhere to a porcine small intestinal submucosa (SIS) membrane for improved handling and could be delivered through the da Vinci surgical system. Several different surgical techniques were assessed using the second-generation 3D-salivary tissue (3D-ST) for ease and stability both on the kidney capsule and in the capsule-less parotid gland. For the kidney, sliding the implant under the capsule membrane and quick stitching proved superior to other methods. For the parotid gland, creation of a tissue "pocket" for placement and immediate multilayer tissue closure were well tolerated with minimal tissue damage. Surgical clips were placed as fiduciary markers for tissue harvest. Some implant experiments were conducted with miniswine 90 days post-irradiation when salivation decreased significantly. Sufficient parotid tissue remained to allow implant placement, and animals tolerated immunosuppression. In all experiments, viability of implanted hS/PCs was high with clear signs of both vascular and nervous system integration in the parotid implants. We thus conclude that the immunosuppressed miniswine is a high-value emerging model for testing human implants prior to first-in-human trials.
迫切需要开发大型动物模型,用于对旨在替代受损组织的新型细胞疗法进行临床前测试。接受头颈癌放疗的患者经常会出现口干症,这种病症未来有一天可能通过细胞疗法来治疗,以重新填充产生功能性唾液的细胞。利用为接受全脸移植的患者开发的免疫抑制方案,我们成功地将免疫抑制小型猪作为合适的宿主动物,来评估含有包封唾液人类干细胞/祖细胞(hS/PCs)的基质修饰透明质酸(HA)水凝胶/生物支架材料的长期稳定性、生物相容性和转归。在未经处理的小型猪的腮腺中进行了初步生物相容性测试。随后,在动物身上使用载有hS/PCs的水凝胶进行实验,在手术当天开始免疫抑制方案。植入部位包括肾包膜用于活力测试,腮腺用于长达八周的生物整合时间段。通过对植入部位附近组织的分析,在任何评估的动物中均未观察到移植排斥反应。第一代仅在水凝胶中含有细胞的植入物在手术操作间难以处理,因此进行了改良,使其附着于猪小肠黏膜下层(SIS)膜以改善操作性,并且可以通过达芬奇手术系统进行递送。使用第二代3D唾液组织(3D-ST)评估了几种不同的手术技术,以提高在肾包膜和无包膜腮腺中的操作简便性和稳定性。对于肾脏,将植入物滑至包膜下并快速缝合被证明优于其他方法。对于腮腺,创建用于放置的组织“袋”并立即进行多层组织闭合,对组织损伤最小,耐受性良好。放置手术夹作为组织采集的基准标记。一些植入实验是在小型猪放疗90天后进行的,此时唾液分泌显著减少。仍有足够的腮腺组织允许植入物放置,并且动物耐受免疫抑制。在所有实验中,植入的hS/PCs活力很高,腮腺植入物中有明显的血管和神经系统整合迹象。因此,我们得出结论,免疫抑制小型猪是在首次人体试验之前测试人类植入物的一种高价值新兴模型。