摘要
背景:眼睛具有独特的解剖特征,使其成为基因治疗应用的宝贵目标。 目的:本研究的目的是比较玻璃体内注射后四种病毒载体的转导效率,安全性和生物分布。 方法:将成纤维细胞腺病毒(AdV),腺相关病毒(AAV),杆状病毒(BV)和绿色荧光蛋白(GFP)慢病毒(LV)载体双侧玻璃体内注射入成年C57BL / 6OlaHsd小鼠。对照小鼠接受盐水。在3天至6个月的多个时间点对眼睛和其他器官进行了研究。用视网膜细胞标志物进行免疫组织化学染色以验证GFP阳性细胞。使用qPCR方法研究视网膜和各种非靶组织中的生物分布。从低温恒温器切片和血清样品研究炎症反应和毒性。 结果:从7天到6个月,AAV注射的眼睛显示GFP在内部和外部视网膜细胞中的表达。 LV眼睛显示持久的转基因表达主要在视网膜色素上皮中,而AdV主要瞬时转导前房中的细胞。在BV注射的眼中,GFP阳性非常低。 qPCR结果显示,AdV,AAV和LV扩散到视神经,但低于其他器官的检出限。通过玻璃体内注射AdV和BV诱发最强的免疫应答。在AdV治疗组中检测到最高浓度的抗GFP IgG,而AAV组显示最低浓度。血液化学筛选和细胞凋亡的细胞数量均未显示病毒载体和生理盐水注射组之间的任何差异。 结论:我们的研究结果显示,AAV,AdV和慢病毒载体玻璃体内基因传递是安全可行的。
关键词: 基因治疗,病毒载体,玻璃体内,生物分布,眼睛,转导。
Current Gene Therapy
Title:Comparative Study of Adeno-associated Virus, Adenovirus, Bacu lovirus and Lentivirus Vectors for Gene Therapy of the Eyes
Volume: 17 Issue: 3
关键词: 基因治疗,病毒载体,玻璃体内,生物分布,眼睛,转导。
摘要: Background: The eye possesses unique anatomical features that make it a valuable target for gene therapy applications.
Objective: The aim of the current study was to compare transduction efficiency, safety and biodistribution of four viral vectors following intravitreal injection.
Method: Adenovirus (AdV), Adeno-Associated Virus (AAV), Baculovirus (BV) and Lentivirus (LV) vectors encoding Green Fluorescent Protein (GFP) were injected bilaterally intravitreally into adult C57BL/6OlaHsd mice. Control mice received saline. Eyes and other organs were studied at multiple time points from 3 days to 6 months. Immunohistochemical stainings with retinal cell markers were performed to verify GFP-positive cells. Biodistribution in retina and various non-target tissues was studied using a qPCR method. Inflammatory responses and toxicity were investigated from cryostat eye sections and serum samples.
Results: AAV-injected eyes showed GFP expression both in inner and outer retinal cells from 7 days up to 6 months. LV eyes showed long lasting transgene expression mostly in retinal pigment epithelium whereas AdV transiently transduced mainly cells in the anterior chamber. In BV-injected eyes, GFP positivity was very low. qPCR results showed that AdV, AAV and LV spread into the optic nerve, but were below the detection limit in other organs. The strongest immune responses were evoked by intravitreal injections of AdV and BV. The highest concentration of anti-GFP IgG was detected in the AdV-treated group, whereas the AAV group showed the lowest concentration. Neither blood chemistry screen nor the number of apoptotic cells showed any differences between the viral vector and saline injected groups.
Conclusion: Our findings show that intravitreal gene delivery is safe and feasible with AAV, AdV and lentivirus vectors.
Export Options
About this article
Cite this article as:
Comparative Study of Adeno-associated Virus, Adenovirus, Bacu lovirus and Lentivirus Vectors for Gene Therapy of the Eyes, Current Gene Therapy 2017; 17 (3) . https://dx.doi.org/10.2174/1566523217666171003170348
DOI https://dx.doi.org/10.2174/1566523217666171003170348 |
Print ISSN 1566-5232 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5631 |
Call for Papers in Thematic Issues
Programmed Cell Death Genes in Oncology: Pioneering Therapeutic and Diagnostic Frontiers (BMS-CGT-2024-HT-45)
Programmed Cell Death (PCD) is recognized as a pivotal biological mechanism with far-reaching effects in the realm of cancer therapy. This complex process encompasses a variety of cell death modalities, including apoptosis, autophagic cell death, pyroptosis, and ferroptosis, each of which contributes to the intricate landscape of cancer development and ...read more
Related Journals
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers
- Announcements