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M2 缺陷型单复制流感疫苗诱导的免疫应答与对高度漂移 H3N2 流感株人体挑战的保护作用相关。

M2-Deficient Single-Replication Influenza Vaccine-Induced Immune Responses Associated With Protection Against Human Challenge With Highly Drifted H3N2 Influenza Strain.

机构信息

Celyn Consulting, Lewes, Delaware, USA.

SGS Life Sciences, Antwerp, Belgium.

出版信息

J Infect Dis. 2022 Aug 12;226(1):83-90. doi: 10.1093/infdis/jiab374.

DOI:10.1093/infdis/jiab374
PMID:34323977
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9373152/
Abstract

BACKGROUND

Current influenza vaccines are strain specific and demonstrate low vaccine efficacy against H3N2 influenza disease, especially when vaccine is mismatched to circulating virus. The novel influenza vaccine candidate, M2-deficient single replication (M2SR), induces a broad, multi-effector immune response.

METHODS

A phase 2 challenge study was conducted to assess the efficacy of an M2SR vaccine expressing hemagglutinin and neuraminidase from A/Brisbane/10/2007 (Bris2007 M2SR H3N2; clade 1). Four weeks after vaccination, recipients were challenged with antigenically distinct H3N2 virus (A/Belgium/4217/2015, clade 3C.3b) and assessed for infection and clinical symptoms.

RESULTS

Adverse events after vaccination were mild and similar in frequency for placebo and M2SR recipients. A single dose of Bris2007 M2SR induced neutralizing antibody to the vaccine (48% of recipients) and challenge strain (27% of recipients). Overall, 54% of M2SR recipients were infected after challenge, compared with 71% of placebo recipients. The subset of M2SR recipients with a vaccine-induced microneutralization response against the challenge virus had reduced rates of infection after challenge (38% vs 71% of placebo recipients; P = .050) and reduced illness.

CONCLUSIONS

Study participants with vaccine-induced neutralizing antibodies were protected against infection and illness after challenge with an antigenically distinct virus. This is the first demonstration of vaccine-induced protection against a highly drifted H3N2 challenge virus.

摘要

背景

目前的流感疫苗是针对特定毒株的,对 H3N2 流感疾病的疫苗效果较低,尤其是当疫苗与流行病毒不匹配时。新型流感疫苗候选物 M2 缺失的单复制(M2SR)可诱导广泛的多效免疫反应。

方法

进行了一项 2 期挑战研究,以评估表达 A/Brisbane/10/2007(Bris2007 M2SR H3N2;谱系 1)血凝素和神经氨酸酶的 M2SR 疫苗的疗效。接种疫苗 4 周后,受种者用抗原性不同的 H3N2 病毒(A/Belgium/4217/2015,谱系 3C.3b)进行挑战,并评估感染和临床症状。

结果

接种后的不良事件轻微,且在安慰剂和 M2SR 受种者中的发生频率相似。单次剂量的 Bris2007 M2SR 诱导出针对疫苗(48%的受种者)和挑战株(27%的受种者)的中和抗体。总体而言,54%的 M2SR 受种者在挑战后感染,而安慰剂受种者为 71%。在 M2SR 受种者中,具有针对挑战病毒的疫苗诱导的微量中和反应的亚组,在挑战后感染率降低(38%比安慰剂受种者的 71%;P=0.050),疾病也减轻。

结论

具有疫苗诱导的中和抗体的研究参与者在接受抗原性不同的病毒挑战后,可免受感染和疾病的影响。这是首次证明疫苗可预防高度漂移的 H3N2 挑战病毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a41/9373152/11d5ef325dd8/jiab374_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a41/9373152/2bebc9847097/jiab374_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a41/9373152/72976c63b2be/jiab374_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a41/9373152/67fb852b4887/jiab374_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a41/9373152/11d5ef325dd8/jiab374_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a41/9373152/2bebc9847097/jiab374_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a41/9373152/72976c63b2be/jiab374_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a41/9373152/67fb852b4887/jiab374_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a41/9373152/11d5ef325dd8/jiab374_fig4.jpg

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