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两种佐剂剂型与季节性流感 A/H7N9 疫苗联用的剂量节约效应:一项随机、双盲、安慰剂对照、1 期临床试验。

Dose-sparing effect of two adjuvant formulations with a pandemic influenza A/H7N9 vaccine: A randomized, double-blind, placebo-controlled, phase 1 clinical trial.

机构信息

Instituto Butantan, São Paulo, Brazil.

World Health Organization, Geneva, Switzerland.

出版信息

PLoS One. 2022 Oct 18;17(10):e0274943. doi: 10.1371/journal.pone.0274943. eCollection 2022.

Abstract

The emergence of potentially pandemic viruses has resulted in preparedness efforts to develop candidate vaccines and adjuvant formulations. We evaluated the dose-sparing effect and safety of two distinct squalene-based oil-in-water adjuvant emulsion formulations (IB160 and SE) with influenza A/H7N9 antigen. This phase I, randomized, double-blind, placebo-controlled, dose-finding trial (NCT03330899), enrolled 432 healthy volunteers aged 18 to 59. Participants were randomly allocated to 8 groups: 1A) IB160 + 15μg H7N9, 1B) IB160 + 7.5μg H7N9, 1C) IB160 + 3.75μg H7N9, 2A) SE + 15μg H7N9, 2B) SE + 7.5μg H7N9, 2C) SE + 3.75μg H7N9, 3) unadjuvanted vaccine 15μg H7N9 and 4) placebo. Immunogenicity was evaluated through haemagglutination inhibition (HI) and microneutralization (MN) tests. Safety was evaluated by monitoring local and systemic, solicited and unsolicited adverse events (AE) and reactions (AR) 7 and 28 days after each study injection, respectively, whereas serious adverse events (SAE) were monitored up to 194 days post-second dose. A greater increase in antibody geometric mean titers (GMT) was observed in groups receiving adjuvanted vaccines. Vaccinees receiving IB160-adjuvanted formulations showed the greatest response in group 1B, which induced an HI GMT increase of 4.7 times, HI titers ≥40 in 45.2% of participants (MN titers ≥40 in 80.8%). Vaccinees receiving SE-adjuvanted vaccines showed the greatest response in group 2A, with an HI GMT increase of 2.5 times, HI titers ≥40 in 22.9% of participants (MN titers ≥40 in 65.7%). Frequencies of AE and AR were similar among groups. Pain at the administration site and headache were the most frequent local and systemic solicited ARs. The vaccine candidates were safe and the adjuvanted formulations have a potential dose-sparing effect on immunogenicity against influenza A/H7N9. The magnitude of this effect could be further explored.

摘要

潜在大流行病毒的出现促使人们努力开发候选疫苗和佐剂配方。我们评估了两种不同的角鲨烯水包油佐剂乳剂配方(IB160 和 SE)与甲型流感病毒 A/H7N9 抗原联合使用的剂量节约效应和安全性。这项 I 期、随机、双盲、安慰剂对照、剂量发现试验(NCT03330899)纳入了 432 名年龄在 18 至 59 岁的健康志愿者。参与者被随机分配到 8 组:1A)IB160 + 15μg H7N9,1B)IB160 + 7.5μg H7N9,1C)IB160 + 3.75μg H7N9,2A)SE + 15μg H7N9,2B)SE + 7.5μg H7N9,2C)SE + 3.75μg H7N9,3)未佐剂疫苗 15μg H7N9 和 4)安慰剂。通过血凝抑制(HI)和微量中和(MN)试验评估免疫原性。通过监测局部和全身、应征和未应征的不良事件(AE)和反应(AR),分别在每次研究注射后 7 天和 28 天评估安全性,而严重不良事件(SAE)在第二次注射后 194 天内进行监测。接受佐剂疫苗的人群抗体几何平均滴度(GMT)增加更多。接受 IB160 佐剂制剂的接种者在 1B 组中表现出最大的反应,该组 HI GMT 增加了 4.7 倍,45.2%的参与者 HI 滴度≥40(MN 滴度≥40,80.8%)。接受 SE 佐剂疫苗的接种者在 2A 组中表现出最大的反应,HI GMT 增加了 2.5 倍,22.9%的参与者 HI 滴度≥40(MN 滴度≥40,65.7%)。各组 AE 和 AR 的频率相似。接种部位疼痛和头痛是最常见的局部和全身应征 AR。候选疫苗是安全的,佐剂配方对甲型流感病毒 A/H7N9 具有潜在的免疫原性节约效应。这种效应的程度可以进一步探讨。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4aa8/9578608/9831c7716b8c/pone.0274943.g001.jpg

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