Potential determinants of antibody responses after vaccination against SARS-CoV-2 in older persons: the Doetinchem Cohort Study.

IF 5.2 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Yunus Kuijpers, H Susan J Picavet, Lia de Rond, Mary-Lène de Zeeuw-Brouwer, Ryanne Rutkens, Esther Gijsbers, Irene Slits, Peter Engelfriet, Anne-Marie Buisman, W M Monique Verschuren
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引用次数: 0

Abstract

Background: Immune responses to vaccination vary widely between individuals. The aim of this study was to identify health-related variables potentially underlying the antibody responses to SARS-CoV-2 vaccination in older persons. We recruited participants in the long-running Doetinchem Cohort Study (DCS) who underwent vaccination as part of the national COVID-19 program, and measured antibody concentrations to SARS-CoV-2 Spike protein (S1) and Nucleoprotein (N) at baseline (T0), and a month after both the first vaccination (T1), and the second vaccination (T2). Associations between the antibody concentrations and demographic variables, including age, sex, socio-economic status (SES), comorbidities (cardiovascular diseases and immune mediated diseases), various health parameters (cardiometabolic markers, inflammation markers, kidney- and lung function) and a composite measure of frailty ('frailty index', ranging from 0 to 1) were tested using multivariate models.

Results: We included 1457 persons aged 50 to 92 years old. Of these persons 1257 were infection naïve after their primary vaccination series. The majority (N = 954) of these individuals were vaccinated with two doses of BNT162b2 (Pfizer) and their data were used for further analysis. A higher frailty index was associated with lower anti-S1 antibody responses at T1 and T2 for both men (RT1 = -0.095, PT1 = 0.05; RT2 = -0.11, PT2 = 0.02) and women (RT1 = -0.24, PT1 < 0.01; RT2 = -0.15, PT2 < 0.01). After correcting for age and sex the frailty index was also associated with the relative increase in anti-S1 IgG concentrations between the two vaccinations (β = 1.6, P < 0.01). Within the construct of frailty, history of a cardiac catheterization, diabetes, gastrointestinal disease, a cognitive speed in the lowest decile of the population distribution, and impaired lung function were associated with lower antibody responses after both vaccinations.

Conclusions: Components of frailty play a key role in the primary vaccination response to the BNT162b2 vaccine within an ageing population. Older persons with various comorbidities have a lowered immune response after their first vaccination, and while frail and sick older persons see a stronger increase after their second vaccination compared to healthy people, they still have a lower antibody response after their second vaccination.

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老年人接种严重急性呼吸系统综合征冠状病毒2型疫苗后抗体反应的潜在决定因素:Doetinchem队列研究。
背景:不同个体对疫苗接种的免疫反应差异很大。这项研究的目的是确定可能导致老年人对严重急性呼吸系统综合征冠状病毒2型疫苗的抗体反应的健康相关变量。我们招募了长期Doetinchem队列研究(DCS)的参与者,他们作为国家新冠肺炎计划的一部分接受了疫苗接种,并在基线(T0)和第一次疫苗接种(T1)和第二次疫苗接种后一个月(T2)测量了SARS-CoV-2刺突蛋白(S1)和核蛋白(N)的抗体浓度。抗体浓度与人口统计学变量之间的相关性,包括年龄、性别、社会经济地位(SES)、合并症(心血管疾病和免疫介导的疾病),使用多变量模型测试了各种健康参数(心脏代谢标志物、炎症标志物、肾和肺功能)和虚弱的综合指标(“虚弱指数”,范围从0到1)。结果:我们纳入了1457名年龄在50至92岁之间的患者。在这些人中,1257人在初次接种疫苗后感染了幼稚型。多数(N = 954)接种两剂BNT162b2(辉瑞),并将其数据用于进一步分析。较高的虚弱指数与两名男性在T1和T2时较低的抗S1抗体反应有关(RT1 = -0.095,PT1 = 0.05;RT2 = -0.11,PT2 = 0.02)和妇女(RT1 = -0.24,PT1 T2 = -0.15,PT2 结论:在老龄化人群中,虚弱的成分在BNT162b2疫苗的初级疫苗接种反应中起着关键作用。患有各种合并症的老年人在第一次接种疫苗后免疫反应较低,尽管与健康人相比,体弱多病的老年人第二次接种后免疫反应增强,但他们第二次疫苗接种后抗体反应仍然较低。
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来源期刊
Immunity & Ageing
Immunity & Ageing GERIATRICS & GERONTOLOGY-IMMUNOLOGY
CiteScore
10.20
自引率
3.80%
发文量
55
期刊介绍: Immunity & Ageing is a specialist open access journal that was first published in 2004. The journal focuses on the impact of ageing on immune systems, the influence of aged immune systems on organismal well-being and longevity, age-associated diseases with immune etiology, and potential immune interventions to increase health span. All articles published in Immunity & Ageing are indexed in the following databases: Biological Abstracts, BIOSIS, CAS, Citebase, DOAJ, Embase, Google Scholar, Journal Citation Reports/Science Edition, OAIster, PubMed, PubMed Central, Science Citation Index Expanded, SCImago, Scopus, SOCOLAR, and Zetoc.
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