Intestinal mucosal immune responses induced by novel oral poliovirus vaccine type 2 and Sabin monovalent oral poliovirus vaccine type 2: an analysis of data from four clinical trials.

IF 20.9 1区 生物学 Q1 INFECTIOUS DISEASES
Audrey Godin, Elizabeth B Brickley, Ruth I Connor, Wendy F Wieland-Alter, Margaret E Ackerman, Joshua A Weiner, John Modlin, Minetaro Arita, Ananda S Bandyopadhyay, Chris Gast, Xavier Sáez-Llorens, Ricardo W Rüttimann, Pierre Van Damme, Ilse De Coster, Peter F Wright
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引用次数: 0

Abstract

Background: A novel oral polio vaccine type 2 (nOPV2), which is more genetically stable (ie, lower risks of reverting to neurovirulence) than the Sabin monovalent OPV2 (mOPV2), has been deployed to interrupt circulating vaccine-derived poliovirus type 2 (PV2) outbreaks. This study compares intestinal mucosal immune responses induced by nOPV2 and mOPV2.

Methods: In this analysis, we evaluated intestinal mucosal immune responses in healthy participants of different ages (ie, infants aged 18-22 weeks, children aged 1-4 years, and adults aged 18-50 years) and vaccine backgrounds (ie, OPV2-experienced vs OPV2-naive). Participants were selected from two phase 2 trials of nOPV2, conducted in 2018-19 (infants and children, NCT03554798 [Panama]; adults, EudraCT 2018-001684-22-NCT04544787 [Belgium]), and two phase 4 historical control trials of mOPV2, conducted in 2015-16 (infants and children, NCT02521974 [Panama]; adults, EudraCT 2015-003325-33 [Belgium]). We measured PV2-specific neutralising activity and IgA concentrations in stools collected before and 14 days after vaccination.

Findings: We compared data from 160 participants (ie, 47 infants, 47 children, and 66 adults) in the nOPV2 trials to 188 participants (ie, 42 infants, 46 children, and 100 adults) in the mOPV2 trials. Within each age group, one dose of nOPV2 or mOPV2 induced similar intestinal PV2-specific neutralisation and IgA responses on day 14. Responses diminished with age: among the OPV2-naive participants who received nOPV2, 27 (82%) of 33 infants, 17 (61%) of 28 children, and four (25%) of 16 adults had detectable PV2-specific neutralisation on day 14. Despite having similar median log10 IgA responses (1·4 [IQR 1·0-2·2] vs 1·4 [1·1-1·7], p=0·34) and median log2 neutralisation titres (1 [IQR 1-1] vs 1 [1-1·5], p=0·89) on day 14, a smaller percentage of OPV2-experienced adults shed vaccine virus than OPV2-naive adults upon nOPV2 challenge (20% vs 82%, p<0·0001).

Interpretation: We found no evidence of differences in the intestinal mucosal immune responses induced by nOPV2 or Sabin mOPV2 and observed the strongest responses in infants.

Funding: The Bill & Melinda Gates Foundation, Japan Agency for Medical Research and Development.

新型口服脊髓灰质炎病毒疫苗2型和Sabin单价口服脊髓灰质炎病毒疫苗2型诱导的肠黏膜免疫应答:四项临床试验数据分析
背景:与Sabin单价脊髓灰质炎疫苗(mOPV2)相比,新型口服脊髓灰质炎疫苗2型(nOPV2)在遗传上更稳定(即恢复神经毒力的风险更低),已被用于阻断循环疫苗衍生的2型脊髓灰质炎病毒(PV2)暴发。本研究比较了nOPV2和mOPV2诱导的肠黏膜免疫应答。方法:在本分析中,我们评估了不同年龄(即18-22周的婴儿、1-4岁的儿童和18-50岁的成年人)和疫苗背景(即经历过opv2与未接种opv2)的健康参与者的肠黏膜免疫反应。参与者从2018- 2019年进行的两项nOPV2二期试验中选择(婴儿和儿童,NCT03554798[巴拿马];成人,EudraCT 2018-001684-22-NCT04544787[比利时]),以及2015- 2016年进行的两项mOPV2 4期历史对照试验(婴儿和儿童,NCT02521974[巴拿马]);成人,EudraCT 2015-003325-33[比利时])。我们测量了接种前和接种后14天收集的粪便中pv2特异性中和活性和IgA浓度。研究结果:我们比较了nOPV2试验中160名参与者(即47名婴儿、47名儿童和66名成人)和mOPV2试验中188名参与者(即42名婴儿、46名儿童和100名成人)的数据。在每个年龄组中,一剂nOPV2或mOPV2在第14天诱导类似的肠道pv2特异性中和和IgA反应。反应随着年龄的增长而减弱:在接受nOPV2的opv2新手参与者中,33名婴儿中有27名(82%),28名儿童中有17名(61%),16名成年人中有4名(25%)在第14天检测到pv2特异性中和。尽管在第14天具有相似的中位log10 IgA应答(1.4 [IQR 1 . 0-2 . 2] vs 1.4 [1 . 1-1 . 7], p= 0.34)和中位log2中和滴度(1 [IQR 1-1] vs 1 [1-1 . 5], p= 0.89),但经历过opv2的成年人在遭遇nOPV2攻击时,排出疫苗病毒的比例低于未经历过opv2的成年人(20% vs 82%)。解释:我们没有发现nOPV2或Sabin mOPV2诱导的肠黏膜免疫应答存在差异的证据,并观察到婴儿的反应最强。资助:比尔及梅琳达·盖茨基金会、日本医学研究与开发机构。
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来源期刊
Lancet Microbe
Lancet Microbe Multiple-
CiteScore
27.20
自引率
0.80%
发文量
278
审稿时长
6 weeks
期刊介绍: The Lancet Microbe is a gold open access journal committed to publishing content relevant to clinical microbiologists worldwide, with a focus on studies that advance clinical understanding, challenge the status quo, and advocate change in health policy.
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