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3岁以下儿童季节性流感疫苗的免疫原性和安全性。

Immunogenicity and safety of seasonal influenza vaccines in children under 3 years of age.

作者信息

Aoun Tia, Borrow Ray, Arkwright Peter D

机构信息

Lydia Becker Institute of Immunology and Inflammation, University of Manchester, Manchester, UK.

Vaccine Evaluation Unit, UK Health Security Agency, Manchester Royal Infirmary, Manchester, UK.

出版信息

Expert Rev Vaccines. 2023 Jan-Dec;22(1):226-242. doi: 10.1080/14760584.2023.2181797.

Abstract

INTRODUCTION

Despite children aged 6-35 months developing more severe influenza infections, not all countries include influenza vaccines in their national immunization programs.

AREAS COVERED

This literature review examines the efficacy, immunogenicity, and safety of seasonal trivalent influenza vaccines (TIVs) and quadrivalent influenzae vaccines (QIVs) in children 6-35 months old to determine if greater valency promotes greater protection while maintaining a similar safety profile.

EXPERT OPINION

TIVs and QIVs are safe for children under 3 years old. TIVs and QIVs provided good seroprotection, and immunogenicity (GMT, SCR, and SPR) meeting recommended levels set by CHMP (European) and CBER (USA). However, as QIVs carry two influenza B strains and TIVs only one, QIVs has an overall higher seroprotection against particularly influenza B. Vaccines containing adjuncts had better immunogenicity, particularly after the first dose. Seroprotection of all vaccines lasted 12 months. Increasing the dosage from 0.25 mL to 0.5 mL did not cause more systemic or local side-effects. Further comparisons of efficacy, and wider promotion of influenza vaccines in general are required in preschool children.

摘要

引言

尽管6至35个月大的儿童更容易感染严重的流感,但并非所有国家都将流感疫苗纳入其国家免疫规划。

涵盖领域

本文献综述研究了季节性三价流感疫苗(TIV)和四价流感疫苗(QIV)在6至35个月大儿童中的疗效、免疫原性和安全性,以确定更高的价数是否能在保持相似安全性的同时提供更好的保护。

专家意见

TIV和QIV对3岁以下儿童是安全的。TIV和QIV提供了良好的血清保护,其免疫原性(几何平均滴度、血清转化率和血清保护率)达到了欧洲药品管理局(CHMP)和美国生物制品评估和研究中心(CBER)设定的推荐水平。然而,由于QIV含有两种乙型流感病毒株,而TIV仅含一种,QIV对乙型流感的总体血清保护率更高。含有佐剂的疫苗具有更好的免疫原性,尤其是在首剂接种后。所有疫苗的血清保护作用持续12个月。将剂量从0.25毫升增加到0.5毫升不会导致更多的全身或局部副作用。需要对学龄前儿童流感疫苗的疗效进行进一步比较,并更广泛地推广流感疫苗。

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