Suppr超能文献

反向工程保护:基于反向疫苗学的病毒病原体靶向疫苗的全面综述。

Reverse engineering protection: A comprehensive survey of reverse vaccinology-based vaccines targeting viral pathogens.

机构信息

Department of Medical Biotechnology, Aarupadai Veedu Medical College and Hospital, Vinayaka Mission's Research Foundation (Deemed to be University), Kirumampakkam, Puducherry 607402, India.

Division of Glycoscience, Department of Chemistry, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, AlbaNova University Center, Stockholm 106 91, Sweden.

出版信息

Vaccine. 2024 Apr 11;42(10):2503-2518. doi: 10.1016/j.vaccine.2024.02.087. Epub 2024 Mar 23.

Abstract

Vaccines have significantly reduced the impact of numerous deadly viral infections. However, there is an increasing need to expedite vaccine development in light of the recurrent pandemics and epidemics. Also, identifying vaccines against certain viruses is challenging due to various factors, notably the inability to culture certain viruses in cell cultures and the wide-ranging diversity of MHC profiles in humans. Fortunately, reverse vaccinology (RV) efficiently overcomes these limitations and has simplified the identification of epitopes from antigenic proteins across the entire proteome, streamlining the vaccine development process. Furthermore, it enables the creation of multiepitope vaccines that can effectively account for the variations in MHC profiles within the human population. The RV approach offers numerous advantages in developing precise and effective vaccines against viral pathogens, including extensive proteome coverage, accurate epitope identification, cross-protection capabilities, and MHC compatibility. With the introduction of RV, there is a growing emphasis among researchers on creating multiepitope-based vaccines aiming to stimulate the host's immune responses against multiple serotypes, as opposed to single-component monovalent alternatives. Regardless of how promising the RV-based vaccine candidates may appear, they must undergo experimental validation to probe their protection efficacy for real-world applications. The time, effort, and resources allocated to the laborious epitope identification process can now be redirected toward validating vaccine candidates identified through the RV approach. However, to overcome failures in the RV-based approach, efforts must be made to incorporate immunological principles and consider targeting the epitope regions involved in disease pathogenesis, immune responses, and neutralizing antibody maturation. Integrating multi-omics and incorporating artificial intelligence and machine learning-based tools and techniques in RV would increase the chances of developing an effective vaccine. This review thoroughly explains the RV approach, ideal RV-based vaccine construct components, RV-based vaccines designed to combat viral pathogens, its challenges, and future perspectives.

摘要

疫苗显著降低了许多致命病毒感染的影响。然而,鉴于反复出现的大流行和流行病,加快疫苗开发的需求日益增长。此外,由于多种因素,确定针对某些病毒的疫苗具有挑战性,特别是某些病毒无法在细胞培养物中培养,以及人类 MHC 谱的广泛多样性。幸运的是,反向疫苗学(RV)有效地克服了这些限制,并简化了整个蛋白质组中抗原蛋白表位的识别,简化了疫苗开发过程。此外,它还可以创建多表位疫苗,能够有效地考虑人类群体中 MHC 谱的变化。RV 方法在开发针对病毒病原体的精确有效的疫苗方面具有许多优势,包括广泛的蛋白质组覆盖、准确的表位识别、交叉保护能力和 MHC 兼容性。随着 RV 的引入,研究人员越来越重视创建基于多表位的疫苗,旨在刺激宿主针对多种血清型的免疫反应,而不是单一成分单价的替代品。无论 RV 为基础的候选疫苗看起来多么有希望,它们都必须经过实验验证,以探究其在实际应用中的保护效果。现在可以将用于费力的表位识别过程的时间、精力和资源重新用于验证通过 RV 方法识别的疫苗候选物。然而,要克服 RV 方法中的失败,必须努力将免疫原则纳入其中,并考虑针对疾病发病机制、免疫反应和中和抗体成熟中涉及的表位区域进行靶向。整合多组学并将基于人工智能和机器学习的工具和技术纳入 RV 中,将增加开发有效疫苗的机会。这篇综述详细解释了 RV 方法、理想的 RV 为基础的疫苗构建组件、针对病毒病原体设计的 RV 为基础的疫苗、它的挑战和未来展望。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验