Biotechnological Interventions for the Production of Subunit Vaccines Against Group A Rotavirus

IF 2.8 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mukta Prajapati, Pooja Malik, Astha Sinha, Honey Yadav, Yachna K. Jaiwal, Yogesh K. Ahlawat, Darshna Chaudhary, Ranjana Jaiwal, Nisha Sharma, Pawan K. Jaiwal, Vijay K. Chattu
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Abstract

Group A rotavirus (RVA) is a major cause of severe gastroenteritis in infants and young children globally, despite the availability of live-attenuated vaccines. Challenges such as limited efficacy in low-income regions, safety concerns for immunocompromised individuals, and cold-chain dependency necessitate alternative vaccine strategies. Subunit vaccines, which use specific viral proteins to elicit immunity, provide a safer and more adaptable approach. This review highlights biotechnological advancements in producing subunit vaccines, focusing on recombinant expression systems like bacterial, yeast, insect, mammalian, and plant-based platforms for scalable and cost-effective production of viral proteins. Key innovations include molecular engineering, adjuvant development, and delivery system improvements to enhance vaccine immunogenicity and efficacy. Subunit vaccines and virus-like particles expressed in various systems have demonstrated promising preclinical and clinical results, with some candidates nearing commercial readiness. Reverse vaccinology, combined with Artificial Intelligence and Machine Learning, is driving the development of innovative multiepitope vaccines and antivirals. Strategies such as passive immunization, single-chain antibodies, immunobiotics, and novel antivirals are also explored as alternative management options. The review also underscores advanced genome editing and reverse genetics approaches to improve vaccine design and antiviral therapies. These biotechnological interventions offer hope for equitable and effective control of rotavirus diarrhea, particularly in resource-limited settings, and represent significant progress toward addressing current vaccine limitations.

Abstract Image

利用生物技术干预 A 组轮状病毒亚单位疫苗的生产
尽管有减毒活疫苗,但A组轮状病毒(RVA)是全球婴幼儿严重胃肠炎的主要病因。诸如在低收入地区效力有限、免疫功能低下个体的安全问题以及冷链依赖等挑战需要替代疫苗战略。亚单位疫苗使用特定的病毒蛋白引发免疫,提供了一种更安全、适应性更强的方法。这篇综述强调了生产亚单位疫苗的生物技术进展,重点是重组表达系统,如细菌、酵母、昆虫、哺乳动物和植物平台,用于可扩展和具有成本效益的病毒蛋白生产。关键的创新包括分子工程、佐剂开发和递送系统的改进,以增强疫苗的免疫原性和效力。亚单位疫苗和在各种系统中表达的病毒样颗粒已显示出有希望的临床前和临床结果,其中一些候选产品已接近商业化准备。反向疫苗学与人工智能和机器学习相结合,正在推动创新型多表位疫苗和抗病毒药物的开发。策略,如被动免疫,单链抗体,免疫生物制剂和新型抗病毒药物也被探索作为替代的管理选择。该综述还强调了先进的基因组编辑和反向遗传学方法,以改进疫苗设计和抗病毒疗法。这些生物技术干预措施为公平和有效地控制轮状病毒腹泻提供了希望,特别是在资源有限的情况下,并且在解决当前疫苗限制方面取得了重大进展。
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来源期刊
Cell Biochemistry and Function
Cell Biochemistry and Function 生物-生化与分子生物学
CiteScore
6.20
自引率
0.00%
发文量
93
审稿时长
6-12 weeks
期刊介绍: Cell Biochemistry and Function publishes original research articles and reviews on the mechanisms whereby molecular and biochemical processes control cellular activity with a particular emphasis on the integration of molecular and cell biology, biochemistry and physiology in the regulation of tissue function in health and disease. The primary remit of the journal is on mammalian biology both in vivo and in vitro but studies of cells in situ are especially encouraged. Observational and pathological studies will be considered providing they include a rational discussion of the possible molecular and biochemical mechanisms behind them and the immediate impact of these observations to our understanding of mammalian biology.
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