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明矾皮克林乳液作为提高疟疾疫苗效力的有效佐剂

Alum Pickering Emulsion as Effective Adjuvant to Improve Malaria Vaccine Efficacy.

作者信息

Chen Qiuting, Wu Nan, Gao Yuhui, Wang Xiaojun, Wu Jie, Ma Guanghui

机构信息

State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.

Department of Biochemistry, School of Environmental and Chemical Engineering, Xi'an Polytechnic University, Xi'an 710600, China.

出版信息

Vaccines (Basel). 2021 Oct 26;9(11):1244. doi: 10.3390/vaccines9111244.

Abstract

Malaria is a life-threatening global epidemic disease and has caused more than 400,000 deaths in 2019. To control and prevent malaria, the development of a vaccine is a potential method. An effective malaria vaccine should either combine antigens from all stages of the malaria parasite's life cycle, or epitopes of multiple key antigens due to the complexity of the Plasmodium parasite. Malaria's random constructed antigen-1 (M.RCAg-1) is one of the recombinant vaccines, which was selected from a DNA library containing thousands of diverse multi-epitope chimeric antigen genes. Moreover, besides selecting an antigen, using an adjuvant is another important procedure for most vaccine development procedures. Freund's adjuvant is considered an effective vaccine adjuvant for malaria vaccine, but it cannot be used in clinical settings because of its serious side effects. Traditional adjuvants, such as alum adjuvant, are limited by their unsatisfactory immune effects in malaria vaccines, hence there is an urgent need to develop a novel, safe and efficient adjuvant. In recent years, Pickering emulsions have attracted increasing attention as novel adjuvant. In contrast to classical emulsions, Pickering emulsions are stabilized by solid particles instead of surfactant, having pliability and lateral mobility. In this study, we selected aluminum hydroxide gel (termed as "alum") as a stabilizer to prepare alum-stabilized Pickering emulsions (ALPE) as a malaria vaccine adjuvant. In addition, monophosphoryl lipid A (MPLA) as an immunostimulant was incorporated into the Pickering emulsion (ALMPE) to further enhance the immune response. In vitro tests showed that, compared with alum, ALPE and ALMPE showed higher antigen load rates and could be effectively endocytosed by J774a.1 cells. In vivo studies indicated that ALMPE could induce as high antibody titers as Freund's adjuvant. The biocompatibility study also proved ALMPE with excellent biocompatibility. These results suggest that ALMPE is a potential adjuvant for a malaria vaccine.

摘要

疟疾是一种危及生命的全球性流行病,2019年已导致超过40万人死亡。为了控制和预防疟疾,开发疫苗是一种潜在的方法。由于疟原虫的复杂性,有效的疟疾疫苗应结合疟原虫生命周期所有阶段的抗原,或多种关键抗原的表位。疟疾随机构建抗原-1(M.RCAg-1)是重组疫苗之一,它是从包含数千种不同多表位嵌合抗原基因的DNA文库中筛选出来的。此外,除了选择抗原外,使用佐剂是大多数疫苗开发程序的另一个重要步骤。弗氏佐剂被认为是疟疾疫苗的有效疫苗佐剂,但由于其严重的副作用,不能用于临床。传统佐剂,如明矾佐剂,在疟疾疫苗中的免疫效果不尽人意,因此迫切需要开发一种新型、安全、高效的佐剂。近年来,Pickering乳液作为新型佐剂受到越来越多的关注。与传统乳液相比,Pickering乳液由固体颗粒而非表面活性剂稳定,具有柔韧性和横向流动性。在本研究中,我们选择氢氧化铝凝胶(称为“明矾”)作为稳定剂,制备明矾稳定的Pickering乳液(ALPE)作为疟疾疫苗佐剂。此外,将单磷酰脂质A(MPLA)作为免疫刺激剂掺入Pickering乳液(ALMPE)中,以进一步增强免疫反应。体外试验表明,与明矾相比,ALPE和ALMPE表现出更高的抗原负载率,并且可以被J774a.1细胞有效内吞。体内研究表明,ALMPE可以诱导与弗氏佐剂一样高的抗体滴度。生物相容性研究也证明ALMPE具有优异的生物相容性。这些结果表明,ALMPE是疟疾疫苗的潜在佐剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a53/8624716/7d28569ef81b/vaccines-09-01244-g001.jpg

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