Xianghui Li , Zhiqiang Zhang , Zhenhuan Guo , Xia Ma , Xueting Ban , Xinghui Song , Yonglu Liu , Li Zhao , Qiqi Liu , Qigai He
{"title":"刺五加多糖负载碳酸钙纳米颗粒作为佐剂增强猪细小病毒疫苗免疫应答","authors":"Xianghui Li , Zhiqiang Zhang , Zhenhuan Guo , Xia Ma , Xueting Ban , Xinghui Song , Yonglu Liu , Li Zhao , Qiqi Liu , Qigai He","doi":"10.1016/j.medidd.2021.100094","DOIUrl":null,"url":null,"abstract":"<div><p>Recently, the strategy of using positively charged nanoparticles as new vaccine delivery systems has been widely investigated for enhancing the anti-infectious disease immune responses and has been found to efficiently improve the immune response through the targeting and activation of antigen-presenting cells. <em>Acanthopanax senticosus</em> polysaccharide (ASPS) is extracted from <em>Acanthopanax senticosus</em> and functions as an effective immunostimulatory drug. The present work encapsulated the ASPS immunopotentiator to the calcium carbonate (CaCO<sub>3</sub>) microspheres, and adopted polyethylenimine, a cationic polymer, for coating the microspheres, finally developing the novel nanoparticle (NP) delivery system with positive charge (CaCO<sub>3</sub>–ASPS–PEI). As a result, our constructed CaCO<sub>3</sub>–ASPS–PEI remarkably up-regulated CD86 and MHCII and activated macrophages, while increasing TNF-α and IL-1β production via macrophages. Moreover, the mice immunized with porcine parvovirus (PPV) antigen adsorbed onto CaCO<sub>3</sub>–ASPS–PEI nanoparticles had a significant enhancement in cytokine production, the PPV-specific IgG immune response, and the hybrid Th1/Th2 immune response (dominated by Th1), relative to the remaining groups. Based on the above results, our constructed CaCO<sub>3</sub>–ASPS–PEI NPs with positive charge may be used as the efficient adjuvant vaccine delivery system for inducing the long-time potent immune responses.</p></div>","PeriodicalId":33528,"journal":{"name":"Medicine in Drug Discovery","volume":"11 ","pages":"Article 100094"},"PeriodicalIF":0.0000,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.medidd.2021.100094","citationCount":"1","resultStr":"{\"title\":\"Acanthopanax senticosus polysaccharide-loaded calcium carbonate nanoparticle as an adjuvant to enhance porcine parvovirus vaccine immune responses\",\"authors\":\"Xianghui Li , Zhiqiang Zhang , Zhenhuan Guo , Xia Ma , Xueting Ban , Xinghui Song , Yonglu Liu , Li Zhao , Qiqi Liu , Qigai He\",\"doi\":\"10.1016/j.medidd.2021.100094\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Recently, the strategy of using positively charged nanoparticles as new vaccine delivery systems has been widely investigated for enhancing the anti-infectious disease immune responses and has been found to efficiently improve the immune response through the targeting and activation of antigen-presenting cells. <em>Acanthopanax senticosus</em> polysaccharide (ASPS) is extracted from <em>Acanthopanax senticosus</em> and functions as an effective immunostimulatory drug. 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引用次数: 1
摘要
近年来,利用带正电的纳米颗粒作为新型疫苗递送系统增强抗传染病免疫应答的研究越来越广泛,并发现其通过靶向和激活抗原呈递细胞有效地改善免疫应答。刺五加多糖(ASPS)是从刺五加中提取的一种有效的免疫刺激药物。本研究将免疫增强剂包裹在碳酸钙(CaCO3)微球中,并采用阳离子聚合物聚亚胺包覆微球,最终形成了一种新型的带正电荷(CaCO3 - ASPS - pei)的纳米粒子(NP)递送系统。结果,我们构建的caco3 - asp - pei显著上调CD86和MHCII,激活巨噬细胞,同时增加巨噬细胞产生TNF-α和IL-1β。此外,用CaCO3-ASPS-PEI纳米颗粒吸附猪细小病毒(PPV)抗原免疫小鼠的细胞因子产生、PPV特异性IgG免疫反应和Th1/Th2杂交免疫反应(以Th1为主)明显增强。基于以上结果,我们构建的带正电荷的caco3 - asp - pei NPs可以作为高效的佐剂疫苗递送系统,诱导长时间的强效免疫应答。
Acanthopanax senticosus polysaccharide-loaded calcium carbonate nanoparticle as an adjuvant to enhance porcine parvovirus vaccine immune responses
Recently, the strategy of using positively charged nanoparticles as new vaccine delivery systems has been widely investigated for enhancing the anti-infectious disease immune responses and has been found to efficiently improve the immune response through the targeting and activation of antigen-presenting cells. Acanthopanax senticosus polysaccharide (ASPS) is extracted from Acanthopanax senticosus and functions as an effective immunostimulatory drug. The present work encapsulated the ASPS immunopotentiator to the calcium carbonate (CaCO3) microspheres, and adopted polyethylenimine, a cationic polymer, for coating the microspheres, finally developing the novel nanoparticle (NP) delivery system with positive charge (CaCO3–ASPS–PEI). As a result, our constructed CaCO3–ASPS–PEI remarkably up-regulated CD86 and MHCII and activated macrophages, while increasing TNF-α and IL-1β production via macrophages. Moreover, the mice immunized with porcine parvovirus (PPV) antigen adsorbed onto CaCO3–ASPS–PEI nanoparticles had a significant enhancement in cytokine production, the PPV-specific IgG immune response, and the hybrid Th1/Th2 immune response (dominated by Th1), relative to the remaining groups. Based on the above results, our constructed CaCO3–ASPS–PEI NPs with positive charge may be used as the efficient adjuvant vaccine delivery system for inducing the long-time potent immune responses.