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异源初免-加强免疫接种 H3N2 流感病毒在无免疫个体中的效果:猪模型研究。

Efficacy of Heterologous Prime-Boost Vaccination with H3N2 Influenza Viruses in Pre-Immune Individuals: Studies in the Pig Model.

机构信息

Laboratory of Virology, Faculty of Veterinary Medicine, Department of Virology, Parasitology and Immunology, Ghent University, 9820 Merelbeke, Belgium.

Laboratory of Veterinary Pathology, Faculty of Veterinary Medicine, Ghent University, 9820 Merelbeke, Belgium.

出版信息

Viruses. 2020 Sep 1;12(9):968. doi: 10.3390/v12090968.

Abstract

In a previous study in influenza-naïve pigs, heterologous prime-boost vaccination with monovalent, adjuvanted whole inactivated vaccines (WIV) based on the European swine influenza A virus (SwIAV) strain, A/swine/Gent/172/2008 (G08), followed by the US SwIAV strain, A/swine/Pennsylvania/A01076777/2010 (PA10), was shown to induce broadly cross-reactive hemagglutination inhibition (HI) antibodies against 12 out of 15 antigenically distinct H3N2 influenza strains. Here, we used the pig model to examine the efficacy of that particular heterologous prime-boost vaccination regimen, in individuals with pre-existing infection-immunity. Pigs were first inoculated intranasally with the human H3N2 strain, A/Nanchang/933/1995. Seven weeks later, they were vaccinated intramuscularly with G08 followed by PA10 or vice versa. We examined serum antibody responses against the hemagglutinin and neuraminidase, and antibody-secreting cell (ASC) responses in peripheral blood, draining lymph nodes, and nasal mucosa (NMC), in ELISPOT assays. Vaccination induced up to 10-fold higher HI antibody titers than in naïve pigs, with broader cross-reactivity, and protection against challenge with an antigenically distant H3N2 strain. It also boosted ASC responses in lymph nodes and NMC. Our results show that intramuscular administration of WIV can lead to enhanced antibody responses and cross-reactivity in pre-immune subjects, and recall of ASC responses in lymph nodes and NMC.

摘要

在之前一项针对流感易感猪的研究中,使用基于欧洲猪流感病毒(SwIAV)株 A/swine/Gent/172/2008(G08)的单价、佐剂全灭活疫苗(WIV)进行异源初免-加强免疫,随后使用美国 SwIAV 株 A/swine/Pennsylvania/A01076777/2010(PA10)进行加强免疫,结果表明该方案诱导产生了针对 15 株具有不同抗原性的 H3N2 流感病毒株的广泛交叉反应性血凝抑制(HI)抗体。在此,我们使用猪模型研究了该特定异源初免-加强免疫方案在具有预先存在的感染-免疫个体中的效果。猪首先经鼻腔接种人源 H3N2 株 A/Nanchang/933/1995。7 周后,它们经肌肉注射接种 G08 随后接种 PA10 或反之。我们通过 ELISA 检测血清中针对血凝素和神经氨酸酶的抗体反应,通过 ELISPOT 检测外周血、引流淋巴结和鼻黏膜(NMC)中的抗体分泌细胞(ASC)反应。接种疫苗诱导的 HI 抗体滴度比未接种疫苗的猪高 10 倍,具有更广泛的交叉反应性,并能预防抗原性较远的 H3N2 株的攻击。它还增强了淋巴结和 NMC 中的 ASC 反应。我们的结果表明,WIV 经肌肉注射可在未免疫的个体中引起增强的抗体反应和交叉反应,并能在淋巴结和 NMC 中引发 ASC 反应的回忆。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fb6/7552030/5a3039ecd196/viruses-12-00968-g001.jpg

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