Suppr超能文献

健康成年人中 2 种病毒样颗粒诺如病毒候选疫苗制剂抗体的持久性:记忆探针疫苗接种 1 年随访。

Persistence of Antibodies to 2 Virus-Like Particle Norovirus Vaccine Candidate Formulations in Healthy Adults: 1-Year Follow-up With Memory Probe Vaccination.

机构信息

Department of Medicine, Baylor College of Medicine, Houston, Texas.

Takeda Pharmaceuticals International, Zurich, Switzerland.

出版信息

J Infect Dis. 2019 Jul 19;220(4):603-614. doi: 10.1093/infdis/jiz170.

Abstract

BACKGROUND

We previously reported the tolerability and immunogenicity 1 month after intramuscular administration of 2 bivalent virus-like particle (VLP)-based candidate norovirus vaccine formulations in adults. We now describe the persistence of immunity and responses to a memory probe vaccination 1 year later.

METHODS

A total of 454 healthy men and women aged 18-49 years in 3 equal groups received placebo (saline) or 15/50 or 50/50 vaccine formulations (ie, 15 or 50 µg of GI.1 genotype VLPs, respectively, and 50 µg of GII.4c VLPs) with MPL and Al(OH)3. Immunogenicity and safety were assessed up to day 365, when 351 participants received a memory probe vaccination of 15 µg each of GI.1 and GII.4c VLPs with Al(OH)3.

RESULTS

No safety signals were detected up to 1 year after the first vaccination. Pan-immunoglobulin, immunoglobulin A, and histo-blood group antigen-blocking (HBGA) antibody levels among vaccinees waned but remained higher than levels before vaccination and levels in placebo recipients on days 180 and 365. Memory probe vaccination increased all antibody titers. Levels of HBGA antibodies to GI.1 but not GII.4c were higher after the first vaccination in candidate vaccine groups, compared with those in the placebo group.

CONCLUSION

Levels of antibodies to both candidate norovirus VLP formulations persisted above baseline levels for at least 1 year after primary vaccination. HBGA-blocking responses to the memory probe for GI.1 but not GII.4c displayed characteristics of immune memory.

CLINICAL TRIALS REGISTRATION

NCT02142504.

摘要

背景

我们之前报告了肌肉内给予两种单价病毒样颗粒(VLP)候选诺如病毒疫苗制剂后 1 个月的成人耐受性和免疫原性。我们现在描述了 1 年后免疫持久性和对记忆探针疫苗接种的反应。

方法

总共 454 名年龄在 18-49 岁的健康男性和女性分为 3 组,分别接受安慰剂(生理盐水)或 15/50 或 50/50 疫苗制剂(即分别为 15 或 50μg GI.1 基因型 VLP 和 50μg GII.4c VLP)与 MPL 和 Al(OH)3。免疫原性和安全性评估至第 365 天,此时 351 名参与者接受了 15μg GI.1 和 GII.4c VLP 与 Al(OH)3 的记忆探针疫苗接种。

结果

首次接种后 1 年内未发现安全信号。疫苗接种者的全免疫球蛋白、免疫球蛋白 A 和组织血型抗原阻断(HBGA)抗体水平下降,但仍高于接种前和安慰剂组在第 180 天和第 365 天的水平。记忆探针疫苗接种增加了所有抗体滴度。与安慰剂组相比,候选疫苗组在初次接种后 GI.1 的 HBGA 抗体水平更高,但 GII.4c 则不然。

结论

两种候选诺如病毒 VLP 制剂的抗体水平在初次接种后至少 1 年内持续高于基线水平。对 GI.1 但不是 GII.4c 的记忆探针的 HBGA 阻断反应显示出免疫记忆的特征。

临床试验注册

NCT02142504。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验