Assessment of the humoral immune response in children after immunization with different types of inactivated influenza vaccines in the 2019-2020 season

Q4 Medicine
Z. Buzitskaya, A. Popov, E. Romanovskaya-Romanko, M. Sergeeva, E. Varyushina, M. K. Erofeeva, M. Stukova, D. Lioznov
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引用次数: 0

Abstract

Causing millions of cases worldwide every year, influenza is one of the most common respiratory infections. The effectiveness of influenza vaccination and the nature of the resulting immune response may vary depending on the vaccine composition and age group. Since children are at the highest risk of disease and act as the main carriers of influenza, the assessment of the immunological efficacy of vaccines in this group is crucial for controlling the epidemic. Therefore, this study aimed to evaluate the characteristics of the humoral immune response in children after immunization with various types of inactivated influenza vaccines. An observational study was conducted in the 2019-2020 season and involved 230 children (< 18 years old) and a comparison group of 87 adults aged 18 to 60 years. The subjects, who provided informed consent to participate, were vaccinated with one of three vaccines (Grippol Plus, Sovigripp, or Ultrix) in an open-label fashion. The humoral immune response was assessed by measuring the hemagglutination inhibition (HI) titer in the paired sera taken before and three weeks after vaccination. The immunogenicity of the vaccines in the age group under 18, met the CPMP criteria for the assessment of inactivated influenza vaccines in terms of the fold increase in antibody titers and the proportion of individuals with seroconversion to all three components (A/H1N1pdm09, A/H3N2, and B/Victoria). Although 6 to 18-year-old participants showed a more robust immune response to the B/Victoria component compared to the adult participants (aged 18 to 60), it was insufficient to ensure that 70% of the participants have a protective antibody titer. A comparative analysis of the vaccines’ immunogenicity was carried out for a subgroup of children aged 6-18 who had initially low antibody levels at the time of vaccination. The analysis showed that the split vaccine Ultrix outperformed the adjuvanted vaccine Grippol Plus in generating an antibody response to the component B/Victoria; however, the antibody responses to the A/H1N1pdm09 and A/H3N2 components did not differ between the two vaccines. The children under 6 years of age demonstrated a less pronounced humoral immune response to vaccination compared with the other age groups, which may be due to the age-related characteristics of the immune system in children of preschool age.
2019-2020季节接种不同类型流感灭活疫苗后儿童体液免疫应答的评价
流感是最常见的呼吸道感染之一,每年在全球造成数百万例病例。流感疫苗接种的有效性和由此产生的免疫反应的性质可能因疫苗成分和年龄组而异。由于儿童患病风险最高,并且是流感的主要携带者,因此评估疫苗在这一群体中的免疫功效对于控制流感流行至关重要。因此,本研究旨在评价儿童接种不同类型流感灭活疫苗后体液免疫反应的特点。在2019-2020赛季进行了一项观察性研究,涉及230名儿童(18岁以下)和87名18至60岁的成年人。提供知情同意参与的受试者以开放标签方式接种三种疫苗(Grippol Plus、Sovigripp或Ultrix)中的一种。体液免疫反应是通过测量疫苗接种前和接种后三周的配对血清中的血凝抑制(HI)滴度来评估的。在18岁以下年龄组中,疫苗的免疫原性符合CPMP对灭活流感疫苗的评估标准,抗体滴度增加了两倍,血清转化为所有三种成分(A/H1N1pdm09、A/H3N2和B/Victoria)的个体比例也达到了这一标准。虽然6至18岁的参与者对B/Victoria组分的免疫反应比成年参与者(18至60岁)更强,但这不足以确保70%的参与者具有保护性抗体滴度。对接种疫苗时抗体水平较低的6-18岁儿童亚组进行了疫苗免疫原性的比较分析。分析表明,分离疫苗Ultrix在产生对B/Victoria组分的抗体应答方面优于佐剂疫苗Grippol Plus;然而,对A/H1N1pdm09和A/H3N2组分的抗体反应在两种疫苗之间没有差异。与其他年龄组相比,6岁以下儿童对疫苗接种表现出较不明显的体液免疫反应,这可能是由于学龄前儿童免疫系统的年龄相关特征。
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来源期刊
Medical Immunology (Russia)
Medical Immunology (Russia) Medicine-Immunology and Allergy
CiteScore
0.70
自引率
0.00%
发文量
88
审稿时长
12 weeks
期刊介绍: The journal mission is to promote scientific achievements in fundamental and applied immunology to various medical fields, the publication of reviews, lectures, essays by leading domestic and foreign experts in the field of fundamental and experimental immunology, clinical immunology, allergology, immunodiagnostics and immunotherapy of infectious, allergy, autoimmune diseases and cancer.
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