Islam M Mirazul, Buznyk Oleksiy, Reddy Jagadesh C, Pasyechnikova Nataliya, Alarcon Emilio I, Hayes Sally, Lewis Philip, Fagerholm Per, He Chaoliang, Iakymenko Stanislav, Liu Wenguang, Meek Keith M, Sangwan Virender S, Griffith May
1Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
2Schepens Eye Research Institute and Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA USA.
NPJ Regen Med. 2018 Jan 31;3:2. doi: 10.1038/s41536-017-0038-8. eCollection 2018.
The severe worldwide shortage of donor organs, and severe pathologies placing patients at high risk for rejecting conventional cornea transplantation, have left many corneal blind patients untreated. Following successful pre-clinical evaluation in mini-pigs, we tested a biomaterials-enabled pro-regeneration strategy to restore corneal integrity in an open-label observational study of six patients. Cell-free corneal implants comprising recombinant human collagen and phosphorylcholine were grafted by anterior lamellar keratoplasty into corneas of unilaterally blind patients diagnosed at high-risk for rejecting donor allografts. They were followed-up for a mean of 24 months. Patients with acute disease (ulceration) were relieved of pain and discomfort within 1-2 weeks post-operation. Patients with scarred or ulcerated corneas from severe infection showed better vision improvement, followed by corneas with burns. Corneas with immune or degenerative conditions transplanted for symptom relief only showed no vision improvement overall. However, grafting promoted nerve regeneration as observed by improved touch sensitivity to near normal levels in all patients tested, even for those with little/no sensitivity before treatment. Overall, three out of six patients showed significant vision improvement. Others were sufficiently stabilized to allow follow-on surgery to restore vision. Grafting outcomes in mini-pig corneas were superior to those in human subjects, emphasizing that animal models are only predictive for patients with non-severely pathological corneas; however, for establishing parameters such as stable corneal tissue and nerve regeneration, our pig model is satisfactory. While further testing is merited, we have nevertheless shown that cell-free implants are potentially safe, efficacious options for treating high-risk patients.
全球范围内供体器官严重短缺,以及严重的病理状况使患者在接受传统角膜移植时面临高排斥风险,导致许多角膜盲患者得不到治疗。在小型猪身上进行成功的临床前评估后,我们在一项针对6名患者的开放标签观察性研究中测试了一种基于生物材料的促进再生策略,以恢复角膜完整性。由重组人胶原蛋白和磷酸胆碱组成的无细胞角膜植入物通过前板层角膜移植术移植到被诊断为高风险排斥供体同种异体移植物的单侧盲患者的角膜中。对他们进行了平均24个月的随访。患有急性疾病(溃疡)的患者在术后1-2周内疼痛和不适得到缓解。患有严重感染导致角膜瘢痕或溃疡的患者视力改善更好,其次是烧伤后的角膜。仅为缓解症状而移植的免疫或退行性角膜疾病患者总体上没有视力改善。然而,如在所有接受测试的患者中观察到的,移植促进了神经再生,即使是那些在治疗前几乎没有/没有感觉的患者,其触觉敏感性也提高到了接近正常水平。总体而言,6名患者中有3名视力有显著改善。其他患者病情充分稳定,可进行后续手术恢复视力。小型猪角膜的移植结果优于人类受试者,这强调动物模型仅对非严重病理角膜的患者具有预测性;然而,对于建立稳定角膜组织和神经再生等参数,我们的猪模型是令人满意的。虽然值得进一步测试,但我们已经表明,无细胞植入物对于治疗高风险患者可能是安全、有效的选择。