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探索巨细胞病毒载体的潜力:综述。

Exploring the Potential of Cytomegalovirus-Based Vectors: A Review.

机构信息

Department of Microbiology and Molecular Genetics, New Jersey Medical School, Rutgers University, 225 Warren Street, Newark, NJ 070101, USA.

Department of Pain Medicine and Shenzhen Municipal Key Laboratory for Pain Medicine, Huazhong University of Science and Technology Union Shenzhen Hospital, Shenzhen 518060, China.

出版信息

Viruses. 2023 Oct 2;15(10):2043. doi: 10.3390/v15102043.

Abstract

Viral vectors have emerged as powerful tools for delivering and expressing foreign genes, playing a pivotal role in gene therapy. Among these vectors, cytomegalovirus (CMV) stands out as a promising viral vector due to its distinctive attributes including large packaging capacity, ability to achieve superinfection, broad host range, capacity to induce CD8+ T cell responses, lack of integration into the host genome, and other qualities that make it an appealing vector candidate. Engineered attenuated CMV strains such as Towne and AD169 that have a ~15 kb genomic DNA deletion caused by virus passage guarantee human safety. CMV's large genome enables the efficient incorporation of substantial foreign genes as demonstrated by CMV vector-based therapies for SIV, tuberculosis, cancer, malaria, aging, COVID-19, and more. CMV is capable of reinfecting hosts regardless of prior infection or immunity, making it highly suitable for multiple vector administrations. In addition to its broad cellular tropism and sustained high-level gene expression, CMV triggers robust, virus-specific CD8 T cell responses, offering a significant advantage as a vaccine vector. To date, successful development and testing of murine CMV (MCMV) and rhesus CMV (RhCMV) vectors in animal models have demonstrated the efficacy of CMV-based vectors. These investigations have explored the potential of CMV vectors for vaccines against HIV, cancer, tuberculosis, malaria, and other infectious pathogens, as well as for other gene therapy applications. Moreover, the generation of single-cycle replication CMV vectors, produced by deleting essential genes, ensures robust safety in an immunocompromised population. The results of these studies emphasize CMV's effectiveness as a gene delivery vehicle and shed light on the future applications of a CMV vector. While challenges such as production complexities and storage limitations need to be addressed, ongoing efforts to bridge the gap between animal models and human translation continue to fuel the optimism surrounding CMV-based vectors. This review will outline the properties of CMV vectors and discuss their future applications as well as possible limitations.

摘要

病毒载体已成为递呈和表达外源基因的有力工具,在基因治疗中发挥着关键作用。在这些载体中,巨细胞病毒(CMV)因其独特的属性脱颖而出,成为一种很有前途的病毒载体,其属性包括:大容量的包装能力、实现超感染的能力、广泛的宿主范围、诱导 CD8+T 细胞反应的能力、不整合到宿主基因组中、以及其他使其成为有吸引力的载体候选物的特性。经过工程改造的减毒 CMV 株,如 Towne 和 AD169,由于病毒传代导致约 15kb 基因组 DNA 缺失,从而保证了人类的安全性。CMV 的大基因组能够高效地整合大量的外源基因,这已被基于 CMV 载体的 SIV、结核病、癌症、疟疾、衰老、COVID-19 等的治疗方法所证明。CMV 能够重新感染宿主,无论宿主先前是否感染或具有免疫力,使其非常适合多次载体给药。除了广泛的细胞嗜性和持续的高水平基因表达外,CMV 还引发强烈的、针对病毒的 CD8+T 细胞反应,作为疫苗载体具有显著优势。迄今为止,鼠巨细胞病毒(MCMV)和恒河猴巨细胞病毒(RhCMV)载体在动物模型中的成功开发和测试证明了 CMV 载体的有效性。这些研究探讨了 CMV 载体在 HIV、癌症、结核病、疟疾和其他传染病病原体疫苗以及其他基因治疗应用中的潜力。此外,通过删除必需基因产生的单周期复制 CMV 载体,确保了在免疫功能低下人群中的强大安全性。这些研究的结果强调了 CMV 作为基因传递载体的有效性,并揭示了 CMV 载体的未来应用前景。尽管还需要解决生产复杂性和存储限制等挑战,但为弥合动物模型和人类转化之间的差距而进行的持续努力,继续为基于 CMV 的载体带来乐观情绪。本综述将概述 CMV 载体的特性,并讨论其未来的应用以及可能存在的限制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad77/10612100/3a732bf4320c/viruses-15-02043-g001.jpg

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