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首页> 外文期刊>Acta ophthalmologica >Clinical transplantation of ex vivo expanded autologous limbal epithelial cells using a culture medium with human serum as single supplement: A retrospective case series
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Clinical transplantation of ex vivo expanded autologous limbal epithelial cells using a culture medium with human serum as single supplement: A retrospective case series

机译:使用人血清作为单一补充剂的培养基离体扩增自体角膜缘上皮细胞的临床移植:回顾性病例系列

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Purpose: Presently, our clinic is the only centre in Scandinavia that offers patients with corneal surface pathology including limbal stem cell deficiency (LSCD) transplantation of ex vivo expanded limbal epithelial cells (LECs). We here present clinical data of the first nine patients with LSCD who were transplanted with autologous LECs expanded in medium completely free of any animal-derived products and non-human/recombinant growth factors (including Cholera Toxin), and with autologous human serum as the only growth supplement. Methods: We conducted a noncomparative retrospective study of patients with LSCD at our centre between 2009 and 2011. The diagnosis was based on history and clinical signs. A biopsy was taken from healthy limbus, and the epithelium was expanded on amniotic membrane (AM) in medium containing autologous serum and subsequently transplanted to the affected eye. Results: Successful outcome was defined as relief of pain and photophobia and/or improved best corrected visual acuity (BCVA) and/or reestablishment of a stable corneal epithelium and regression of corneal vascularization. Five of the nine transplanted patients (55.6%) had an improvement in either subjective symptoms or objective findings (11- to 28-month follow-up). Conclusions: Our clinical study shows that patients with LSCD can be treated successfully with transplantation of LECs expanded ex vivo in a medium with autologous serum as the only growth supplement. The use of this novel culture system, which is devoid of animal-derived products and non-human/recombinant growth factors (including Cholera Toxin), reduces the risks of inter-species disease transmission and host immune responses to xenogenic proteins, both obvious advantages for the patient.
机译:目的:目前,我们的诊所是斯堪的纳维亚半岛唯一为角膜表面病变患者提供服务的中心,其中包括角膜缘干细胞缺乏症(LSCD)移植离体扩大的角膜缘上皮细胞(LEC)。我们在此提供前9名LSCD患者的临床数据,这些患者移植了在完全不含任何动物源性产品和非人类/重组生长因子(包括霍乱毒素)的培养基中扩增的自体LEC,并以自体人类血清作为唯一的增长补充。方法:我们在2009年至2011年间对我们中心的LSCD患者进行了非比较性回顾性研究。诊断基于病史和临床体征。从健康角膜缘进行活检,然后在含有自体血清的培养基中在羊膜(AM)上扩增上皮,然后移植到患眼中。结果:成功的结果定义为疼痛和畏光缓解和/或改善的最佳矫正视力(BCVA)和/或稳定的角膜上皮重建和角膜血管形成消退。 9例移植患者中有5例(55.6%)的主观症状或客观发现均有改善(11-28个月的随访)。结论:我们的临床研究表明,在自体血清作为唯一生长补充剂的培养基中,通过离体扩增的LEC移植可以成功治疗LSCD患者。使用这种新颖的培养系统,该系统不含动物源性产品和非人类/重组生长因子(包括霍乱毒素),可降低种间疾病传播的风险和宿主对异种蛋白的免疫反应,这两个优点都很明显为病人。

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