Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
LimmaTech Biologics AG, Schlieren, Switzerland.
EBioMedicine. 2021 Apr;66:103310. doi: 10.1016/j.ebiom.2021.103310. Epub 2021 Apr 13.
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.
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.
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).
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.
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。
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。
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。
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。