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活疫苗和灭活流感疫苗可诱导相似的体液免疫应答,但只有活疫苗可诱导幼儿产生多样化的 T 细胞应答。

Live and inactivated influenza vaccines induce similar humoral responses, but only live vaccines induce diverse T-cell responses in young children.

机构信息

Department of Internal Medicine, Saint Louis University Vaccine and Treatment Evaluation Unit, Missouri, USA.

出版信息

J Infect Dis. 2011 Sep 15;204(6):845-53. doi: 10.1093/infdis/jir436. Epub 2011 Aug 15.

Abstract

BACKGROUND

Two doses of either trivalent live attenuated or inactivated influenza vaccines (LAIV and TIV, respectively) are approved for young children (≥ 24 months old for LAIV and ≥ 6 months old for TIV) and induce protective antibody responses. However, whether combinations of LAIV and TIV are safe and equally immunogenic is unknown. Furthermore, LAIV is more protective than TIV in children for unclear reasons.

METHODS

Children 6-35 months old were administered, 1 month apart, 2 doses of either TIV or LAIV, or combinations of LAIV and TIV in both prime/boost sequences. Influenza-specific antibodies were measured by hemagglutination inhibition (HAI), and T cells were studied in flow cytometric and functional assays. Highly conserved M1, M2, and NP peptides predicted to be presented by common HLA class I and II were used to stimulate interferon-γ enzyme-linked immunospot responses.

RESULTS

All LAIV and/or TIV combinations were well tolerated and induced similar HAI responses. In contrast, only regimens containing LAIV induced influenza-specific CD4(+), CD8(+), and γδ T cells, including T cells specific for highly conserved influenza peptides.

CONCLUSIONS

Prime/boost combinations of LAIV and TIV in young children were safe and induced similar protective antibodies. Only LAIV induced CD4(+), CD8(+), and γδ T cells relevant for broadly protective heterosubtypic immunity.

CLINICAL TRIALS REGISTRATION

NCT00231907.

摘要

背景

两种剂量的三价减毒活流感疫苗(LAIV)或灭活流感疫苗(TIV)(LAIV 适用于≥24 个月龄儿童,TIV 适用于≥6 个月龄儿童)均被批准用于儿童,并能诱导保护性抗体反应。然而,LAIV 和 TIV 的联合应用是否安全且具有同等的免疫原性尚不清楚。此外,LAIV 在儿童中的保护作用优于 TIV,但原因尚不清楚。

方法

6-35 月龄儿童间隔 1 个月分别接种 2 剂 TIV 或 LAIV,或 LAIV 和 TIV 的序贯联合接种。通过血凝抑制(HAI)测定流感特异性抗体,流式细胞术和功能测定研究 T 细胞。使用高度保守的 M1、M2 和 NP 肽预测由常见 HLA I 类和 II 类呈递,以刺激干扰素-γ酶联免疫斑点反应。

结果

所有 LAIV 和/或 TIV 联合方案均具有良好的耐受性,并诱导相似的 HAI 反应。相比之下,只有含有 LAIV 的方案能诱导流感特异性 CD4+、CD8+和γδ T 细胞,包括针对高度保守的流感肽的特异性 T 细胞。

结论

LAIV 和 TIV 在儿童中的序贯联合应用安全,能诱导相似的保护性抗体。只有 LAIV 能诱导与广泛保护异源免疫相关的 CD4+、CD8+和γδ T 细胞。

临床试验注册

NCT00231907。

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