Suppr超能文献

登革热疫苗的研发:全球和印度的情况。

Dengue vaccine development: Global and Indian scenarios.

机构信息

Recombinant Gene Products Group, Molecular Medicine Division, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, India.

Recombinant Gene Products Group, Molecular Medicine Division, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, India; Translational Health Science and Technology Institute, NCR Biotech Science Cluster, Faridabad, India.

出版信息

Int J Infect Dis. 2019 Jul;84S:S80-S86. doi: 10.1016/j.ijid.2019.01.029. Epub 2019 Jan 23.

Abstract

India is home to nearly a third of the global population at risk of dengue, a viral disease caused by four antigenically and genetically distinct dengue viruses. Clinical illness following dengue virus infection can either be mild and self-limiting dengue fever or severe dengue hemorrhagic fever/dengue shock syndrome, with potentially fatal consequences. A live attenuated vaccine known as Dengvaxia, developed by Sanofi, was licensed in 2015. Following this, long-term follow-up of the Sanofi phase III efficacy trial participants has revealed potential safety concerns. This vaccine, which appears to predispose dengue-naïve recipients to an increased risk of hospitalization in the future, is recommended by the World Health Organization only for adults with a history of prior dengue virus infection. A safe and efficacious dengue vaccine continues to be sought globally. India has joined these efforts in recent years, and is poised to initiate the clinical development of two candidates in the near future, one licensed from abroad and the other developed indigenously. This article provides a glimpse of India's efforts to develop dengue vaccines in the context of the global dengue vaccine development and evaluation landscape and highlights key issues and questions confronting the dengue vaccine community.

摘要

印度拥有全球近三分之一的登革热风险人口,这是一种由四种具有不同抗原性和遗传特性的登革热病毒引起的病毒性疾病。登革热病毒感染后的临床疾病可能是轻微的、自限性的登革热,也可能是严重的登革出血热/登革休克综合征,可能导致致命后果。赛诺菲公司开发的一种名为 Dengvaxia 的减毒活疫苗于 2015 年获得许可。此后,对赛诺菲三期疗效试验参与者的长期随访揭示了潜在的安全问题。这种疫苗似乎使登革热初治者在未来有更高的住院风险,世界卫生组织仅建议有既往登革热病毒感染史的成年人使用。目前全球仍在寻求安全有效的登革热疫苗。近年来,印度也加入了这方面的努力,准备在不久的将来启动两种候选疫苗的临床开发,一种是从国外获得许可的,另一种是本土开发的。本文介绍了印度在全球登革热疫苗开发和评估背景下,为开发登革热疫苗所做的努力,并强调了登革热疫苗领域面临的关键问题和疑问。

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