Potential of mesenchymal stem cells as topical immunomodulatory cell therapies for ocular surface inflammatory disorders

被引:21
作者
Beeken, Lydia J. [1 ]
Ting, Darren S. J. [1 ]
Sidney, Laura E. [1 ]
机构
[1] Univ Nottingham, Div Clin Neurosci, Acad Ophthalmol, Queens Med Ctr Campus, Nottingham NG7 2UH, England
基金
英国工程与自然科学研究理事会;
关键词
cell therapy; cornea; inflammation mediators; mesenchymal stem cells; regenerative medicine; AMNIOTIC MEMBRANE TRANSPLANTATION; CORNEAL EPITHELIAL-CELLS; UMBILICAL-CORD BLOOD; DRY EYE DISEASE; STROMAL CELLS; BONE-MARROW; CONTACT-LENS; IMMUNOSUPPRESSIVE PROPERTIES; THERAPEUTIC-EFFICACY; ADIPOSE-TISSUE;
D O I
10.1002/sctm.20-0118
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Ocular surface inflammatory disorders (OSIDs) are a group of highly prevalent, heterogeneous diseases which display a variety of aetiologies and symptoms and are risk factors for serious complications including ocular and cornea impairment. Corneal inflammation is a common factor of all OSIDs, regardless of their cause or symptoms. Current medications include over-the-counter lubricating eye drops, corticosteroids, and ciclosporin, which either do not treat the corneal inflammation or have been associated with multiple side effects leading to alternative treatments being sought. Regenerative medicine cell therapies, particularly mesenchymal stem cells (MSCs), have shown great promise for immunosuppression and disease amelioration across multiple tissues, including the cornea. However, for successful development and clinical translation of MSC therapy for OSIDs, significant problems must be addressed. This review aims to highlight considerations, including whether the source of MSC isolation impacts the efficacy and safety of the therapy, in addition to assessing the feasibility of MSC topical application to the cornea and ocular surface through analysis of potential scaffolds and cell carriers for application to the eye. The literature contains limited data assessing MSCs incorporated into scaffolds for corneal administration, thus here we highlight the necessity of further investigations to truly exploit the potential of an MSC-based cell therapy for the treatment of OSIDs.
引用
收藏
页码:39 / 49
页数:11
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