Lath Yash V, Thool Archana R, Jadhav Indrayani
Medicine and Surgery, Jawaharlal Nehru Medical College, Datta Meghe Institute of Medical Sciences, Wardha, IND.
Ophthalmology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Medical Sciences, Wardha, IND.
Cureus. 2024 Feb 2;16(2):e53479. doi: 10.7759/cureus.53479. eCollection 2024 Feb.
Retinitis pigmentosa and age-related macular degeneration are the most frequent causes of irreversible visual impairment in the world. Existing therapeutic methods could be more effective, underscoring the necessity of new treatments. Reconstructing the retinal photoreceptors through the transplantation of human pluripotent stem cells, representing an attractive approach for restoring vision, has gained momentum. This paper gives an exhaustive account of what has been known in this field, the discoveries made, and the recent progress. This review paper outlines the retina's organisation, cell types, the pathophysiology of retinal injury/degeneration, and the reasoning behind using pluripotent stem cells in retinal regeneration. This article investigates differentiation strategies, molecular components that dictate cell type specification, and the recreation of retinal development in vitro, genetically engineering and manipulating epigenetic marks using various techniques for driving specific cell fates and improving therapy efficacy. Subretinal injection methods, cell encapsulation techniques, scaffold-based approaches, cell sheet transplantation, and their impact on integrating implanted cells into a functional retina are thoroughly reviewed. Using bioengineering approaches, biomaterials and growth factors form a favourable micro-ambience for grafted cells. Issues around safety and efficacy (tumorigenicity, immunological rejection, and long-term integration/functionality) are explored. Moreover, the paper emphasises the significance of rigorous characterisation, immunomodulatory strategies, and clinical and pre-clinical studies to ensure the safety and effectiveness of retinal regeneration therapy. Future perspectives and challenges are presented, looking at fine-tuning differentiation strategies, improving functional integration and regulatory aspects, and using co-therapy and supportive treatments.
视网膜色素变性和年龄相关性黄斑变性是全球不可逆视力损害的最常见原因。现有的治疗方法可能更有效,这凸显了新治疗方法的必要性。通过移植人类多能干细胞来重建视网膜光感受器,作为一种恢复视力的有吸引力的方法,已获得发展势头。本文详尽阐述了该领域已知的情况、已取得的发现以及最近的进展。这篇综述文章概述了视网膜的组织结构、细胞类型、视网膜损伤/变性的病理生理学,以及在视网膜再生中使用多能干细胞的依据。本文研究了分化策略、决定细胞类型特异性的分子成分,以及在体外重现视网膜发育、使用各种技术进行基因工程和操纵表观遗传标记以驱动特定细胞命运并提高治疗效果。对视网膜下注射方法、细胞封装技术、基于支架的方法、细胞片移植及其对将植入细胞整合到功能性视网膜中的影响进行了全面综述。利用生物工程方法,生物材料和生长因子为移植细胞形成有利的微环境。探讨了安全性和有效性方面的问题(致瘤性、免疫排斥以及长期整合/功能性)。此外,本文强调了严格表征、免疫调节策略以及临床和临床前研究对于确保视网膜再生治疗的安全性和有效性的重要性。还介绍了未来的前景和挑战,着眼于微调分化策略、改善功能整合和监管方面,以及使用联合治疗和支持性治疗。