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探索使用不同甲型H1N1猪流感病毒株和疫苗平台的初免-加强疫苗接种方案。

Exploring Prime-Boost Vaccination Regimens with Different H1N1 Swine Influenza A Virus Strains and Vaccine Platforms.

作者信息

Parys Anna, Vandoorn Elien, Chiers Koen, Passvogel Katharina, Fuchs Walter, Mettenleiter Thomas C, Van Reeth Kristien

机构信息

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

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

出版信息

Vaccines (Basel). 2022 Oct 29;10(11):1826. doi: 10.3390/vaccines10111826.

Abstract

In a previous vaccination study in pigs, heterologous prime-boost vaccination with whole-inactivated H1N1 virus vaccines (WIV) induced superior antibody responses and protection compared to homologous prime-boost vaccination. However, no pan-H1 antibody response was induced. Therefore, to stimulate both local and systemic immune responses, we first vaccinated pigs intranasally with a pseudorabies vector vaccine expressing the pH1N1 hemagglutinin (prvCA09) followed by a homologous or heterologous WIV booster vaccine. Homologous and heterologous WIV-WIV vaccinated groups and mock-vaccinated or prvCA09 single-vaccinated pigs served as control groups. Five weeks after the second vaccination, pigs were challenged with a homologous pH1N1 or one of two heterologous H1N2 swine influenza A virus strains. A single prvCA09 vaccination resulted in complete protection against homologous challenge, and vector-WIV vaccinated groups were significantly better protected against heterologous challenge compared to the challenge control group or WIV-WIV vaccinated groups. Furthermore, vector-WIV vaccination resulted in broader hemagglutination inhibition antibody responses compared to WIV-WIV vaccination and higher numbers of antibody-secreting cells in peripheral blood, draining lymph nodes and nasal mucosa. However, even though vector-WIV vaccination induced stronger antibody responses and protection, we still failed to induce a pan-H1 antibody response.

摘要

在之前一项针对猪的疫苗接种研究中,与同源初免-加强免疫接种相比,用全灭活H1N1病毒疫苗(WIV)进行异源初免-加强免疫接种可诱导产生更强的抗体反应和保护作用。然而,并未诱导产生泛H1抗体反应。因此,为了刺激局部和全身免疫反应,我们首先给猪鼻内接种表达pH1N1血凝素的伪狂犬病载体疫苗(prvCA09),随后接种同源或异源WIV加强疫苗。同源和异源WIV-WIV接种组以及 mock 接种或prvCA09单接种猪作为对照组。第二次接种后五周,用同源pH1N1或两种异源H1N2甲型猪流感病毒株之一对猪进行攻毒。单次prvCA09接种可完全保护猪免受同源攻毒,与攻毒对照组或WIV-WIV接种组相比,载体-WIV接种组在抵御异源攻毒方面得到了显著更好的保护。此外,与WIV-WIV接种相比,载体-WIV接种可诱导产生更广泛的血凝抑制抗体反应,在外周血、引流淋巴结和鼻黏膜中产生更多的抗体分泌细胞。然而,尽管载体-WIV接种诱导产生了更强的抗体反应和保护作用,但我们仍然未能诱导产生泛H1抗体反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fd8/9699596/a27e8f3f2f39/vaccines-10-01826-g001.jpg

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