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RTS,S malaria vaccine development: progress and considerations for postapproval introduction

机译:RTS,S疟疾疫苗开发:批准后引入的进展和注意事项

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Though the burden of malaria has decreased in the last decade in some sub-Saharan African countries, it is still high in others, and there is no malaria vaccine in use. The development of malaria vaccines in combination with current control programs could be effective in reducing the malaria burden. In this paper, we review and discuss the progress made in the RTS,S malaria vaccine development and considerations for its postapproval process. We conclude that the development of malaria vaccines has been a long process confronted with challenges of funding, difficulty in identifying malaria antigens that correlate with protection, and development of adjuvant systems among others. The scientific approval of the vaccine by the European Medicines Agency in July 2015 and subsequent recommendations for pilot implementation studies by the World Health Organization made history as the first human parasite vaccine. It is also a major public health achievement as the vaccine has the potential to prevent thousands of malaria cases. However, there are implementation challenges such as cold chain systems, community acceptance, and monitoring of adverse events post-licensure that need to be carefully addressed.
机译:尽管在过去的十年中,撒哈拉以南非洲一些国家的疟疾负担有所减轻,但在其他一些国家,疟疾负担仍然很高,并且没有使用疟疾疫苗。结合当前的控制计划开发疟疾疫苗可以有效减轻疟疾负担。在本文中,我们回顾并讨论了RTS,S疟疾疫苗开发的进展以及批准后过程的注意事项。我们得出结论,疟疾疫苗的开发是一个漫长的过程,面临着资金挑战,难以识别与保护相关的疟疾抗原以及佐剂系统的开发等问题。欧洲药品管理局于2015年7月对该疫苗进行了科学批准,随后世界卫生组织对试点实施研究提出了建议,这使它成为第一种人类寄生虫疫苗。这也是一项重大的公共卫生成就,因为该疫苗具有预防数千例疟疾的潜力。但是,存在实施挑战,例如冷链系统,社区接受度以及许可后不良事件的监测,需要认真解决。

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