Walters Adam A, Krastev Christos, Hill Adrian V S, Milicic Anita
ORCRB, The Jenner Institute, University of Oxford, Oxford, UK.
J Pharm Pharmacol. 2015 Mar;67(3):400-8. doi: 10.1111/jphp.12367. Epub 2015 Feb 2.
Vaccination is considered the most successful health intervention; yet incomplete immunisation coverage continues to risk outbreaks of vaccine preventable diseases worldwide. Vaccination coverage improvement through a single-dose prime-boost technology would revolutionise modern vaccinology, impacting on disease prevalence, significantly benefiting health care and lowering economic burden of disease.
Over the past 30 years, there have been efforts to develop a single-dose delayed release vaccine technology that could replace the repeated prime-boost immunisations required for many current vaccines. Biocompatible polymers have been employed to encapsulate model vaccines for delayed delivery in vivo, using either continuous or pulsed release. Biomaterial considerations, safety aspects, particle characteristics and immunological aspects of this approach are discussed in detail.
Despite many studies showing the feasibility of vaccine encapsulation for single-dose prime-boost administration, none have been translated into convincing utility in animal models or human trials. Further development of the encapsulation technology, through optimising the particle composition, formulation, antigen loading efficacy and stability, could lead to the application of this important approach in vaccine deployment. If successful, this would provide a solution to better global vaccination coverage through a reduction in the number of immunisations needed to achieve protection against infectious diseases. This review provides an overview of single-dose vaccination in the context of today's vaccine needs and is derived from a body of literature that has not been reviewed for over a decade.
疫苗接种被认为是最成功的健康干预措施;然而,全球范围内免疫接种覆盖率不完整仍使疫苗可预防疾病爆发面临风险。通过单剂量初免-加强技术提高疫苗接种覆盖率将彻底改变现代疫苗学,影响疾病流行率,显著造福医疗保健并降低疾病经济负担。
在过去30年里,人们一直在努力开发一种单剂量缓释疫苗技术,该技术可取代许多现有疫苗所需的重复初免-加强免疫接种。生物相容性聚合物已被用于包裹模型疫苗,以便在体内实现持续或脉冲释放的延迟递送。详细讨论了这种方法的生物材料考量、安全性、颗粒特性和免疫学方面。
尽管许多研究表明疫苗包裹用于单剂量初免-加强给药具有可行性,但尚无研究在动物模型或人体试验中转化为令人信服的实用性。通过优化颗粒组成、配方、抗原负载效率和稳定性进一步开发包裹技术,可能会使这种重要方法应用于疫苗部署。如果成功,这将通过减少实现传染病防护所需的免疫接种次数,为提高全球疫苗接种覆盖率提供一种解决方案。本综述在当今疫苗需求的背景下概述了单剂量疫苗接种,其来源于十多年未被综述的一系列文献。