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Recombinant vaccines and the development of new vaccine strategies

机译:重组疫苗和新疫苗策略的发展

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Vaccines were initially developed on an empirical basis, relying mostly on attenuation or inactivation of pathogens. Advances in immunology, molecular biology, biochemistry, genomics, and proteomics have added new perspectives to the vaccinology field. The use of recombinant proteins allows the targeting of immune responses focused against few protective antigens. There are a variety of expression systems with different advantages, allowing the production of large quantities of proteins depending on the required characteristics. Live recombinant bacteria or viral vectors effectively stimulate the immune system as in natural infections and have intrinsic adjuvant properties. DNA vaccines, which consist of non-replicating plasmids, can induce strong long-term cellular immune responses. Prime-boost strategies combine different antigen delivery systems to broaden the immune response. In general, all of these strategies have shown advantages and disadvantages, and their use will depend on the knowledge of the mechanisms of infection of the target pathogen and of the immune response required for protection. In this review, we discuss some of the major breakthroughs that have been achieved using recombinant vaccine technologies, as well as new approaches and strategies for vaccine development, including potential shortcomings and risks.
机译:疫苗最初是根据经验开发的,主要依靠病原体的减毒或灭活。免疫学,分子生物学,生物化学,基因组学和蛋白质组学的进步为疫苗学领域增添了新的视角。重组蛋白的使用允许靶向针对少量保护性抗原的免疫应答。有多种具有不同优势的表达系统,可根据所需特性生产大量蛋白质。活重组细菌或病毒载体可以像自然感染一样有效刺激免疫系统,并具有内在的佐剂特性。由非复制质粒组成的DNA疫苗可以诱导强烈的长期细胞免疫应答。初免-加强策略结合了不同的抗原递送系统以扩大免疫反应。总的来说,所有这些策略都显示了优缺点,其使用将取决于对靶病原体的感染机制和保护所需的免疫应答的了解。在这篇综述中,我们讨论了使用重组疫苗技术已经实现的一些重大突破,以及疫苗开发的新方法和策略,包括潜在的缺点和风险。

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