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人体挑战研究与志贺氏菌生物缀合疫苗:临床疗效和保护相关因素分析。

Human challenge study with a Shigella bioconjugate vaccine: Analyses of clinical efficacy and correlate of protection.

机构信息

Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.

LimmaTech Biologics AG, Schlieren, Switzerland.

出版信息

EBioMedicine. 2021 Apr;66:103310. doi: 10.1016/j.ebiom.2021.103310. Epub 2021 Apr 13.

DOI:10.1016/j.ebiom.2021.103310
PMID:33862589
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8054157/
Abstract

BACKGROUND

Shigellosis is a major cause of moderate to severe diarrhoea and dysentery in children under 5 years of age in low and middle-income countries. The Flexyn2a vaccine conjugates the O-polysaccharide of Shigella flexneri 2a to Pseudomonas aeruginosa exotoxin A. We describe a Phase 2b proof-of-concept challenge study that evaluated safety, immunogenicity, and efficacy of the Flexyn2a vaccine to protect against shigellosis.

METHODS

In this randomized, double blind, placebo-controlled trial, healthy adults were randomized 1:1 to receive Flexyn2a (10 µg) or placebo intramuscularly, twice, 4 weeks apart, followed by challenge 4 weeks later with 1500 colony forming units (CFUs) of S. flexneri 2a strain 2457T. The primary outcome was vaccine-induced protection. S. flexneri 2a lipopolysaccharide (LPS)-specific immune responses were assessed.

FINDINGS

Sixty-seven subjects were enrolled, 34 received vaccine and 33 placebo. The vaccine was well tolerated; the majority of adverse events were mild in nature. Thirty vaccinees and 29 placebo recipients received the S. flexneri 2a challenge. Vaccination resulted in a 30.2% reduction in shigellosis compared with placebo (13/30 vs. 18/29; p = 0.11; 95% CI -15 to 62.6). Vaccine efficacy was more robust against severe disease, reaching 51.7% (p = 0.015, 95% CI 5.3 to 77.9) against moderate/severe diarrhoea or dysentery concurrent with fever or severe enteric symptoms and 72.4% (p = 0.07) against more severe diarrhoea (≥10 lose stools or ≥1000 g loose stools/24 h). Vaccinated subjects were less likely to need early antibiotic intervention following challenge (protective efficacy 51.7%, p = 0.01; 95% CI 9 to 76.8). In those who developed shigellosis, vaccinated subjects had a lower disease severity score (p = 0.002) than placebo-recipients. Additionally, LPS-specific serum IgG responses in Flexyn2a recipients were associated with protection against disease (p = 0.0016) and with a decreased shigellosis disease score (p = 0.002).

INTERPRETATION

The Flexyn2a bioconjugate vaccine was immunogenic, well tolerated and protected against severe illness after Shigella challenge and is a promising Shigella vaccine construct. We identified a strong association between anti-S. flexneri 2a serum IgG and a reduction in disease outcomes. (Clinicaltrials.gov, NCT02646371.) FUNDING: Funding for this study was through a grant from the Wellcome Trust.

摘要

背景

志贺菌病是中低收入国家 5 岁以下儿童中度至重度腹泻和痢疾的主要病因。Flexyn2a 疫苗将福氏志贺菌 2a 的 O-多糖与铜绿假单胞菌外毒素 A 结合在一起。我们描述了一项 2b 期概念验证挑战研究,评估了 Flexyn2a 疫苗预防志贺菌病的安全性、免疫原性和疗效。

方法

在这项随机、双盲、安慰剂对照试验中,健康成年人按 1:1 比例随机接受 Flexyn2a(10μg)或安慰剂肌内注射,间隔 4 周,随后在 4 周后用 1500 个福氏志贺菌 2a 株 2457T 的菌落形成单位(CFU)进行挑战。主要终点是疫苗诱导的保护。评估了福氏志贺菌 2a 脂多糖(LPS)特异性免疫反应。

结果

共纳入 67 名受试者,34 名接受疫苗,33 名接受安慰剂。疫苗耐受性良好;大多数不良事件性质轻微。30 名疫苗接种者和 29 名安慰剂接受者接受了福氏志贺菌 2a 挑战。与安慰剂相比,疫苗接种使痢疾发病率降低 30.2%(13/30 与 18/29;p=0.11;95%CI-15 至 62.6)。疫苗对严重疾病的疗效更显著,达到 51.7%(p=0.015,95%CI5.3 至 77.9),针对发热或严重肠道症状伴中度/重度腹泻或痢疾,以及 72.4%(p=0.07),针对更严重的腹泻(≥10 次稀便或≥1000g 稀便/24h)。接种疫苗的受试者在接受挑战后更不可能需要早期抗生素干预(保护效力 51.7%,p=0.01;95%CI9 至 76.8)。在发生痢疾的患者中,接种疫苗的患者的疾病严重程度评分较低(p=0.002)。此外,Flexyn2a 接受者的 LPS 特异性血清 IgG 反应与疾病预防(p=0.0016)和痢疾疾病评分降低(p=0.002)相关。

结论

Flexyn2a 生物缀合物疫苗具有免疫原性,耐受性良好,可预防志贺菌感染后的严重疾病,是一种很有前途的志贺菌疫苗构建体。我们发现,抗福氏志贺菌 2a 血清 IgG 与疾病结局的降低之间存在很强的关联。(临床试验.gov,NCT02646371。)资金来源:本研究的资金来自惠康信托基金。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08e8/8054157/4bc568119e9a/gr7.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08e8/8054157/4bc568119e9a/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08e8/8054157/0f52799860b5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08e8/8054157/616bda930bac/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08e8/8054157/e8afb60486b9/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08e8/8054157/97da25ba9db5/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08e8/8054157/01d38473f41c/gr5.jpg
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