未接种天花疫苗者接种JYNNEOS后对猴痘病毒的短期中和抗体反应

IF 7.2 2区 医学 Q1 IMMUNOLOGY
Kara Phipps, Jennifer Yates, Jessica Pettit, Sean Bialosuknia, Danielle Hunt, Alan P. DuPuis, Anne Payne, William Lee, Kathleen A. McDonough
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引用次数: 0

摘要

第三代天花疫苗JYNNEOS是猴痘病毒(MPXV)控制工作不可或缺的一部分,但这种改良的安卡拉-巴伐利亚-北欧牛痘(MVA-BN)疫苗的有效性能否持久尚不明确。我们优化并使用了一种含有真枝IIa MPXV和牛痘病毒的斑块减少中和试验(PRNT)来评估8名接种了2剂JYNNEOS的供者在12个月内的抗体反应。一名捐助者以前接受过ACAM2000疫苗;7名捐赠者未接种天花疫苗。供者对牛痘病毒(L1, B5和A33)或MPXV (E8, H3, A35)抗原的IgG反应和对两种病毒的PRNT滴度在接种疫苗后8周达到峰值,此后在幼稚供者中迅速下降。MPXV PRNT滴度特别低;没有早期供体显示斑块减少90%。鉴于最近的临床数据支持MVA-BN疫苗对MPXV的有效性,尽管抗体反应较低,但这些数据表明需要改进MPXV免疫的相关因素,以便进行MVA-BN耐久性研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Short-Lived Neutralizing Antibody Responses to Monkeypox Virus in Smallpox Vaccine–Naive Persons after JYNNEOS Vaccination

JYNNEOS, a third-generation smallpox vaccine, is integral to monkeypox virus (MPXV) control efforts, but the durability of this modified vaccinia Ankara–Bavarian Nordic (MVA-BN) vaccine’s effectiveness is undefined. We optimized and used a plaque reduction neutralization test (PRNT) with authentic clade IIa MPXV and vaccinia virus to assess antibody responses over 12 months in 8 donors vaccinated with 2 doses of JYNNEOS. One donor previously received the ACAM2000 vaccine; 7 donors were smallpox vaccine–naive. IgG responses of the donors to vaccinia virus (L1, B5, and A33) or MPXV (E8, H3, A35) antigens and PRNT titers to both viruses peaked at 8 weeks postvaccination and waned rapidly thereafter in naive donors. MPXV PRNT titers were especially low; no naive donors demonstrated 90% plaque reduction. These data indicate a need for improved correlates of MPXV immunity to enable MVA-BN durability studies, given that recent clinical data support MVA-BN vaccine efficacy against MPXV despite low antibody responses.

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来源期刊
Emerging Infectious Diseases
Emerging Infectious Diseases 医学-传染病学
CiteScore
17.30
自引率
1.70%
发文量
505
审稿时长
1 months
期刊介绍: Emerging Infectious Diseases is a monthly open access journal published by the Centers for Disease Control and Prevention. The primary goal of this peer-reviewed journal is to advance the global recognition of both new and reemerging infectious diseases, while also enhancing our understanding of the underlying factors that contribute to disease emergence, prevention, and elimination. Targeted towards professionals in the field of infectious diseases and related sciences, the journal encourages diverse contributions from experts in academic research, industry, clinical practice, public health, as well as specialists in economics, social sciences, and other relevant disciplines. By fostering a collaborative approach, Emerging Infectious Diseases aims to facilitate interdisciplinary dialogue and address the multifaceted challenges posed by infectious diseases.
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