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掺入膜结合细胞因子佐剂的血凝素病毒样颗粒可保护老年小鼠免受同源和异源流感病毒攻击。

Hemagglutinin virus-like particles incorporated with membrane-bound cytokine adjuvants provide protection against homologous and heterologous influenza virus challenge in aged mice.

作者信息

Park Bo Ryoung, Bommireddy Ramireddy, Chung David Hyunjung, Kim Ki-Hye, Subbiah Jeeva, Jung Yu-Jin, Bhatnagar Noopur, Pack Christopher D, Ramachandiran Sampath, Reddy Shaker J C, Selvaraj Periasamy, Kang Sang-Moo

机构信息

Institute for Biomedical Sciences, Georgia State University, Atlanta, GA, 30303, USA.

Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, 30322, USA.

出版信息

Immun Ageing. 2023 May 11;20(1):20. doi: 10.1186/s12979-023-00344-w.

DOI:10.1186/s12979-023-00344-w
PMID:37170231
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10173218/
Abstract

BACKGROUND

Current influenza vaccines deliver satisfactory results in young people but are less effective in the elderly. Development of vaccines for an ever-increasing aging population has been an arduous challenge due to immunosenescence that impairs the immune response in the aged, both quantitatively and qualitatively.

RESULTS

To potentially enhance vaccine efficacy in the elderly, we investigated the immunogenicity and cross-protection of influenza hemagglutinin virus-like particles (HA-VLP) incorporated with glycosylphosphatidylinositol (GPI)-anchored cytokine-adjuvants (GPI-GM-CSF and GPI-IL-12) via protein transfer in aged mice. Lung viral replication against homologous and heterologous influenza viruses was significantly reduced in aged mice after vaccination with cytokine incorporated VLPs (HA-VLP-Cyt) in comparison to HA-VLP alone. Enhanced IFN-γCD4 and IFN-γCD8 T cell responses were also observed in aged mice immunized with HA-VLP-Cyt when compared to HA-VLP alone.

CONCLUSIONS

Cytokine-adjuvanted influenza HA-VLP vaccine induced enhanced protective response against homologous influenza A virus infection in aged mice. Influenza HA-VLP vaccine with GPI-cytokines also induced enhanced T cell responses correlating with better protection against heterologous infection in the absence of neutralizing antibodies. The results suggest that a vaccination strategy using cytokine-adjuvanted influenza HA-VLPs could be used to enhance protection against influenza A virus in the elderly.

摘要

背景

目前的流感疫苗在年轻人中效果良好,但在老年人中效果较差。由于免疫衰老会在数量和质量上损害老年人的免疫反应,因此为不断增加的老年人口开发疫苗一直是一项艰巨的挑战。

结果

为了潜在地提高老年人的疫苗效力,我们通过蛋白质转移研究了在老年小鼠中掺入糖基磷脂酰肌醇(GPI)锚定的细胞因子佐剂(GPI-GM-CSF和GPI-IL-12)的流感血凝素病毒样颗粒(HA-VLP)的免疫原性和交叉保护作用。与单独的HA-VLP相比,用掺入细胞因子的病毒样颗粒(HA-VLP-Cyt)对老年小鼠进行疫苗接种后,针对同源和异源流感病毒的肺部病毒复制显著减少。与单独的HA-VLP相比,在用HA-VLP-Cyt免疫的老年小鼠中也观察到增强的IFN-γCD4和IFN-γCD8 T细胞反应。

结论

细胞因子佐剂的流感HA-VLP疫苗在老年小鼠中诱导了针对同源甲型流感病毒感染的增强保护反应。含有GPI-细胞因子的流感HA-VLP疫苗还诱导了增强的T细胞反应,在没有中和抗体的情况下,这种反应与针对异源感染的更好保护相关。结果表明,使用细胞因子佐剂的流感HA-VLPs的疫苗接种策略可用于增强老年人对甲型流感病毒的保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/5a8dc2995415/12979_2023_344_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/576a5d5096b6/12979_2023_344_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/87babc0707e2/12979_2023_344_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/42fa7e074a56/12979_2023_344_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/461a0bce0289/12979_2023_344_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/b6be911771a2/12979_2023_344_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/3fd357d038e0/12979_2023_344_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/ac1d42c760a1/12979_2023_344_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/5a8dc2995415/12979_2023_344_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/576a5d5096b6/12979_2023_344_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/87babc0707e2/12979_2023_344_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/42fa7e074a56/12979_2023_344_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/461a0bce0289/12979_2023_344_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/b6be911771a2/12979_2023_344_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/3fd357d038e0/12979_2023_344_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/ac1d42c760a1/12979_2023_344_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5b/10173552/5a8dc2995415/12979_2023_344_Fig8_HTML.jpg

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