疟疾
助推器(火箭)
疟疾疫苗
接种疫苗
免疫
增强剂量
医学
单发
免疫学
病毒学
计算机科学
抗原
恶性疟原虫
工程类
物理
光学
航空航天工程
作者
Romain Guyon,Sören Reinke,Adam Truby,Lee Sims,Adrian V. S. Hill,Luca Baù,Eleanor Stride,Anita Milicic
标识
DOI:10.1126/scitranslmed.adw2256
摘要
Inadequate booster uptake threatens the success of immunization campaigns as seen with the recently rolled-out R21 malaria vaccine. The ability to administer both prime and boost immunizations with a single injection would therefore save lives and alleviate health care burdens. We present a platform for delayed delivery of the booster dose that is scalable with existing technology, easily injectable, and protective against malaria in vivo. Using chip-based microfluidics, we encapsulated the R21 malaria vaccine in polymer microcapsules that release their content weeks to months postinjection. Coinjecting microcapsules with the priming dose of the R21 vaccine elicited strong antibody responses in a mouse model and provided 85% of the protection of a standard prime/boost schedule. If confirmed in humans, these results would pave the way for rapid deployment of single-shot prime/boost vaccination, an urgently needed global health intervention.
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