Suppr超能文献

评估疟疾妊娠疫苗候选物的抗体功能活性和株特异性,使用体外吞噬作用测定法。

Evaluating antibody functional activity and strain-specificity of vaccine candidates for malaria in pregnancy using in vitro phagocytosis assays.

机构信息

Burnet Institute, Melbourne, VIC, Australia.

Department of Medicine, Peter Doherty Institute, University of Melbourne, Melbourne, VIC, Australia.

出版信息

Parasit Vectors. 2018 Jan 29;11(1):69. doi: 10.1186/s13071-018-2653-7.

Abstract

BACKGROUND

Malaria in pregnancy is a major cause of poor maternal and infant health, and is associated with the sequestration of P. falciparum-infected erythrocytes (IE) in the placenta. The leading vaccine candidate for pregnancy malaria, VAR2CSA, has been shown to induce antibodies that inhibit IE adhesion to the placental receptor chondroitin sulfate A (CSA), potentially preventing placental infection. However, the ability of vaccination-induced antibodies to promote opsonic phagocytosis is not well defined, but likely to be an important component of protective immunity.

METHODS

We investigated the use of an opsonic phagocytosis assay to evaluate antibodies induced by pregnancy malaria vaccine candidate antigens based on VAR2CSA. Opsonic phagocytosis was measured by flow cytometry and visualized by electron microscopy. We measured vaccine-induced antibody reactivity to placental type IEs from different geographical origins, and the functional ability of antibodies raised in immunized rabbits to induce phagocytosis by a human monocyte cell line.

RESULTS

Immunization-induced antibodies showed a mixture of strain-specific and cross-reactive antibody recognition of different placental-binding parasite lines. Antibodies generated against the DBL5 and DBL3 domains of VAR2CSA effectively promoted the opsonic phagocytosis of IEs by human monocytes; however, these functional antibodies were largely allele-specific and not cross-reactive. This has significant implications for the development of vaccines aiming to achieve a broad coverage against diverse parasite strains. Using competition ELISAs, we found that acquired human antibodies among pregnant women targeted both cross-reactive and allele-specific epitopes, consistent with what we observed with vaccine-induced antibodies.

CONCLUSIONS

Vaccines based on domains of VAR2CSA induced opsonic phagocytosis of IEs in a strain-specific manner. Assays measuring this phagocytic activity have the potential to aid the development and evaluation of vaccines against malaria in pregnancy.

摘要

背景

妊娠疟疾是母婴健康不良的主要原因,与恶性疟原虫感染红细胞(IE)在胎盘内的隔离有关。妊娠疟疾的主要候选疫苗 VAR2CSA 已被证明能诱导抑制 IE 与胎盘受体硫酸软骨素 A(CSA)结合的抗体,从而可能预防胎盘感染。然而,疫苗接种诱导的抗体促进调理吞噬的能力尚未得到很好的定义,但可能是保护性免疫的一个重要组成部分。

方法

我们研究了一种调理吞噬测定法,用于评估基于 VAR2CSA 的妊娠疟疾候选疫苗抗原诱导的抗体。通过流式细胞术测量调理吞噬作用,并通过电子显微镜进行可视化。我们测量了疫苗诱导的针对来自不同地理来源的胎盘 I 型 IE 的抗体反应性,以及在免疫兔中产生的抗体诱导人单核细胞系吞噬的功能能力。

结果

免疫诱导的抗体显示出针对不同胎盘结合寄生虫系的混合的菌株特异性和交叉反应性抗体识别。针对 VAR2CSA 的 DBL5 和 DBL3 结构域产生的抗体有效地促进了人类单核细胞对 IE 的调理吞噬作用;然而,这些功能性抗体主要是等位特异性的,不具有交叉反应性。这对旨在实现对多种寄生虫株广泛覆盖的疫苗开发具有重要意义。使用竞争 ELISA,我们发现孕妇获得的人抗体针对交叉反应性和等位特异性表位,与我们用疫苗诱导的抗体观察到的结果一致。

结论

基于 VAR2CSA 结构域的疫苗以菌株特异性方式诱导 IE 的调理吞噬作用。测量这种吞噬活性的测定法有可能有助于妊娠疟疾疫苗的开发和评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a79/5789608/f1c0475af00f/13071_2018_2653_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验