Nucci Mariana Penteado, Filgueiras Igor Salerno, Ferreira João Matias, de Oliveira Fernando Anselmo, Nucci Leopoldo Penteado, Mamani Javier Bustamante, Rego Gabriel Nery Albuquerque, Gamarra Lionel Fernel
LIM44, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo 05529-060, Brazil.
Hospital Israelita Albert Einstein, São Paulo 05529-060, Brazil.
World J Stem Cells. 2020 May 26;12(5):381-405. doi: 10.4252/wjsc.v12.i5.381.
Stroke is the second leading cause of death worldwide. There is a real need to develop treatment strategies for reducing neurological deficits in stroke survivors, and stem cell (SC) therapeutics appear to be a promising alternative for stroke therapy that can be used in combination with approved thrombolytic or thrombectomy approaches. However, the efficacy of SC therapy depends on the SC homing ability and engraftment into the injury site over a long period of time. Nonetheless, tracking SCs from their niche to the target tissues is a complex process.
To evaluate SC migration homing, tracking and therapeutic efficacy in the treatment of stroke using nanoparticles.
A systematic literature search was performed to identify articles published prior to November 2019 that were indexed in PubMed and Scopus. The following inclusion criteria were used: (1) Studies that used models of stroke or ischemic brain lesions; (2) Studies of SCs labeled with some type of contrast agent for cell migration detection; and (3) Studies that involved cellular homing and tracking analysis.
A total of 82 articles were identified by indexing in Scopus and PubMed. After the inclusion criteria were applied, 35 studies were selected, and the articles were assessed for eligibility; ultimately, only 25 studies were included. Most of the selected studies used SCs from human and mouse bone marrow labeled with magnetic nanoparticles alone or combined with fluorophore dyes. These cells were administered in the stroke model (to treat middle cerebral artery occlusion in 74% of studies and for photothrombotic induction in 26% of studies). Fifty-three percent of studies used xenogeneic grafts for cell therapy, and the migration homing and tracking evaluation was performed by magnetic resonance imaging as well as other techniques, such as near-infrared fluorescence imaging (12%) or bioluminescence assays (12%).
Our systematic review provided an up-to-date evaluation of SC migration homing and the efficacy of cellular therapy for stroke treatment in terms of functional and structural improvements in the late stage.
中风是全球第二大死因。确实需要制定治疗策略以减少中风幸存者的神经功能缺损,干细胞(SC)疗法似乎是中风治疗的一种有前景的替代方法,可与已批准的溶栓或取栓方法联合使用。然而,SC疗法的疗效取决于SC的归巢能力以及长时间植入损伤部位的能力。尽管如此,追踪SC从其微环境到靶组织是一个复杂的过程。
使用纳米颗粒评估SC在中风治疗中的迁移归巢、追踪及治疗效果。
进行系统的文献检索,以识别2019年11月之前发表并被PubMed和Scopus索引的文章。使用以下纳入标准:(1)使用中风或缺血性脑损伤模型的研究;(2)对用某种造影剂标记的SC进行细胞迁移检测的研究;(3)涉及细胞归巢和追踪分析的研究。
通过在Scopus和PubMed中索引共识别出82篇文章。应用纳入标准后,选择了35项研究,并对文章进行了资格评估;最终,仅纳入25项研究。大多数所选研究使用单独用磁性纳米颗粒或与荧光染料联合标记的来自人和小鼠骨髓的SC。这些细胞被应用于中风模型(74%的研究用于治疗大脑中动脉闭塞,26%的研究用于光血栓形成诱导)。53%的研究使用异种移植物进行细胞治疗,迁移归巢和追踪评估通过磁共振成像以及其他技术进行,如近红外荧光成像(12%)或生物发光测定(12%)。
我们的系统评价对SC迁移归巢以及细胞疗法在中风治疗后期功能和结构改善方面的疗效提供了最新评估。