单次肌内注射植物制造的病毒样颗粒疫苗可引起平衡的体液和细胞反应,并保护年轻和老年小鼠免受甲型H1N1流感病毒的攻击,尽管存在适度或不存在体液反应。

Q2 Biochemistry, Genetics and Molecular Biology
Clinical and Vaccine Immunology Pub Date : 2017-12-05 Print Date: 2017-12-01 DOI:10.1128/CVI.00273-17
Breanna Hodgins, Karen K Yam, Kaitlin Winter, Stephane Pillet, Nathalie Landry, Brian J Ward
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引用次数: 22

摘要

病毒样颗粒(VLP)流感疫苗可以肌肉注射(i.m)或鼻内注射(i.n),对于老年人可能比分裂病毒粒子制剂更有优势。我们测试了一种携带病毒血凝素(HA)的植物制造的VLP候选疫苗,该疫苗可以在年轻和年老小鼠中通过i.m.或i.n.传递。年轻成年(5- 8周龄)和成年(16- 20月龄)雌性BALB/c小鼠接受单次3 μg剂量(基于HA (a/ California/07/2009 H1N1)含量的植物制造的H1-VLP (i.m.或i.m.)分裂病毒粒子疫苗(i.m.)或不接种。接种疫苗后,评估体液和脾细胞反应,并对一些小鼠进行攻击。注射VLP和分离疫苗都能100%保护幼鼠,但VLP组体重减轻最少,并且有更强的体液和细胞反应。与分离疫苗接种者相比,接种了VLP的老龄动物更有可能存活(80%对60%)。注射VLP后肺病毒载量最低。接种VLP的小鼠几乎没有可检测到的免疫反应,但存活率显著提高。在这两个年龄组中,注射H1-VLP疫苗引起了更平衡的体液和细胞反应,并提供了比分裂病毒粒子疫苗更好的同源攻击保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Single Intramuscular Dose of a Plant-Made Virus-Like Particle Vaccine Elicits a Balanced Humoral and Cellular Response and Protects Young and Aged Mice from Influenza H1N1 Virus Challenge despite a Modest/Absent Humoral Response.

A Single Intramuscular Dose of a Plant-Made Virus-Like Particle Vaccine Elicits a Balanced Humoral and Cellular Response and Protects Young and Aged Mice from Influenza H1N1 Virus Challenge despite a Modest/Absent Humoral Response.

A Single Intramuscular Dose of a Plant-Made Virus-Like Particle Vaccine Elicits a Balanced Humoral and Cellular Response and Protects Young and Aged Mice from Influenza H1N1 Virus Challenge despite a Modest/Absent Humoral Response.

Virus-like-particle (VLP) influenza vaccines can be given intramuscularly (i.m.) or intranasally (i.n.) and may have advantages over split-virion formulations in the elderly. We tested a plant-made VLP vaccine candidate bearing the viral hemagglutinin (HA) delivered either i.m. or i.n. in young and aged mice. Young adult (5- to 8-week-old) and aged (16- to 20-month-old) female BALB/c mice received a single 3-μg dose based on the HA (A/California/07/2009 H1N1) content of a plant-made H1-VLP (i.m. or i.n.) split-virion vaccine (i.m.) or were left naive. After vaccination, humoral and splenocyte responses were assessed, and some mice were challenged. Both VLP and split vaccines given i.m. protected 100% of the young animals, but the VLP group lost the least weight and had stronger humoral and cellular responses. Compared to split-vaccine recipients, aged animals vaccinated i.m. with VLP were more likely to survive challenge (80% versus 60%). The lung viral load postchallenge was lowest in the VLP i.m. groups. Mice vaccinated with VLP i.n. had little detectable immune response, but survival was significantly increased. In both age groups, i.m. administration of the H1-VLP vaccine elicited more balanced humoral and cellular responses and provided better protection from homologous challenge than the split-virion vaccine.

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来源期刊
Clinical and Vaccine Immunology
Clinical and Vaccine Immunology 医学-传染病学
CiteScore
2.88
自引率
0.00%
发文量
0
审稿时长
1.5 months
期刊介绍: Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.
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