Mesentier-Louro Louise A, Zaverucha-do-Valle Camila, Rosado-de-Castro Paulo H, Silva-Junior Almir J, Pimentel-Coelho Pedro M, Mendez-Otero Rosalia, Santiago Marcelo F
Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, 21941-902 Rio de Janeiro, RJ, Brazil.
Instituto Nacional de Infectologia Evandro Chagas (INI), Fundação Oswaldo Cruz, 21040-900 Rio de Janeiro, RJ, Brazil.
Stem Cells Int. 2016;2016:5078619. doi: 10.1155/2016/5078619. Epub 2015 Nov 16.
Following optic nerve injury associated with acute or progressive diseases, retinal ganglion cells (RGCs) of adult mammals degenerate and undergo apoptosis. These diseases have limited therapeutic options, due to the low inherent capacity of RGCs to regenerate and due to the inhibitory milieu of the central nervous system. Among the numerous treatment approaches investigated to stimulate neuronal survival and axonal extension, cell transplantation emerges as a promising option. This review focuses on cell therapies with bone marrow mononuclear cells and bone marrow-derived mesenchymal stem cells, which have shown positive therapeutic effects in animal models of optic neuropathies. Different aspects of available preclinical studies are analyzed, including cell distribution, potential doses, routes of administration, and mechanisms of action. Finally, published and ongoing clinical trials are summarized.
在与急性或进行性疾病相关的视神经损伤后,成年哺乳动物的视网膜神经节细胞(RGCs)会发生退化并凋亡。由于RGCs固有的再生能力较低以及中枢神经系统的抑制环境,这些疾病的治疗选择有限。在众多旨在刺激神经元存活和轴突延伸的治疗方法中,细胞移植成为一种有前景的选择。本综述聚焦于骨髓单个核细胞和骨髓源性间充质干细胞的细胞治疗,这些细胞在视神经病变动物模型中已显示出积极的治疗效果。分析了现有临床前研究的不同方面,包括细胞分布、潜在剂量、给药途径和作用机制。最后,总结了已发表和正在进行的临床试验。