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减选佐剂疫苗制剂:一种用于协调评估的比较方法。

Down selecting adjuvanted vaccine formulations: a comparative method for harmonized evaluation.

机构信息

Biomedical Primate Research Centre, Department of Parasitology, Rijswijk, The Netherlands.

Vaccine Formulation Laboratory, University of Lausanne, Epalinges, Switzerland.

出版信息

BMC Immunol. 2018 Jan 31;19(1):6. doi: 10.1186/s12865-018-0245-0.

Abstract

BACKGROUND

The need for rapid and accurate comparison of panels of adjuvanted vaccine formulations and subsequent rational down selection, presents several challenges for modern vaccine development. Here we describe a method which may enable vaccine and adjuvant developers to compare antigen/adjuvant combinations in a harmonized fashion. Three reference antigens: Plasmodium falciparum apical membrane antigen 1 (AMA1), hepatitis B virus surface antigen (HBsAg), and Mycobacterium tuberculosis antigen 85A (Ag85A), were selected as model antigens and were each formulated with three adjuvants: aluminium oxyhydroxide, squalene-in-water emulsion, and a liposome formulation mixed with the purified saponin fraction QS21.

RESULTS

The nine antigen/adjuvant formulations were assessed for stability and immunogenicity in mice in order to provide benchmarks against which other formulations could be compared, in order to assist subsequent down selection of adjuvanted vaccines. Furthermore, mouse cellular immune responses were analyzed by measuring IFN-γ and IL-5 production in splenocytes by ELISPOT, and humoral responses were determined by antigen-specific ELISA, where levels of total IgG, IgG1, IgG2b and IgG2c in serum samples were determined.

CONCLUSIONS

The reference antigens and adjuvants described in this study, which span a spectrum of immune responses, are of potential use as tools to act as points of reference in vaccine development studies. The harmonized methodology described herein may be used as a tool for adjuvant/antigen comparison studies.

摘要

背景

快速准确地比较佐剂疫苗制剂的面板,然后进行合理的选择,这对现代疫苗开发提出了一些挑战。在这里,我们描述了一种方法,它可以使疫苗和佐剂开发人员以协调的方式比较抗原/佐剂组合。选择三种参考抗原:恶性疟原虫顶膜抗原 1(AMA1)、乙型肝炎病毒表面抗原(HBsAg)和结核分枝杆菌抗原 85A(Ag85A)作为模型抗原,并分别用三种佐剂进行配制:氢氧化铝、水包油佐剂和与纯化皂苷 QS21 混合的脂质体制剂。

结果

为了提供可与其他制剂进行比较的基准,以帮助随后选择佐剂疫苗,我们评估了这 9 种抗原/佐剂制剂在小鼠中的稳定性和免疫原性。此外,通过 ELISPOT 测定脾细胞中 IFN-γ和 IL-5 的产生来分析小鼠细胞免疫反应,并通过抗原特异性 ELISA 测定血清样品中总 IgG、IgG1、IgG2b 和 IgG2c 的水平来测定体液免疫反应。

结论

本研究中描述的参考抗原和佐剂涵盖了一系列免疫反应,它们具有作为疫苗开发研究中参考点的潜力。本文所述的协调方法可作为佐剂/抗原比较研究的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce87/5793412/7c07185e192c/12865_2018_245_Fig1_HTML.jpg

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