Maccabi Institute for Research & Innovation, Maccabi Healthcare Services, Tel Aviv, Israel.
CSL Vifor, Glattbrugg, Switzerland.
PLoS One. 2023 May 22;18(5):e0285606. doi: 10.1371/journal.pone.0285606. eCollection 2023.
Iron plays a key role in human immune responses; however, the influence of iron deficiency on the coronavirus disease 2019 (COVID-19) vaccine effectiveness is unclear.
To assess the effectiveness of the BNT162b2 messenger RNA COVID-19 vaccine in preventing severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and COVID-19-related hospitalization and death in individuals with or without iron deficiency.
This large retrospective, longitudinal cohort study analyzed real-world data from the Maccabi Healthcare Services database (covering 25% of Israeli residents). Eligible adults (aged ≥16 years) received a first BNT162b2 vaccine dose between December 19, 2020, and February 28, 2021, followed by a second dose as per approved vaccine label. Individuals were excluded if they had SARS-CoV-2 infection before vaccination, had hemoglobinopathy, received a cancer diagnosis since January 2020, had been treated with immunosuppressants, or were pregnant at the time of vaccination. Vaccine effectiveness was assessed in terms of incidence rates of SARS-CoV-2 infection confirmed by real-time polymerase chain reaction assay, relative risks of COVID-19-related hospitalization, and mortality in individuals with iron deficiency (ferritin <30 ng/mL or transferrin saturation <20%). The two-dose protection period was Days 7 to 28 after the second vaccination.
Data from 184,171 individuals with (mean [standard deviation; SD] age 46.2 [19.6] years; 81.2% female) versus 1,072,019 without (mean [SD] age 46.9 [18.0] years; 46.2% female) known iron deficiency were analyzed. Vaccine effectiveness in the two-dose protection period was 91.9% (95% confidence interval [CI] 83.7-96.0%) and 92.1% (95% CI 84.2-96.1%) for those with versus without iron deficiency (P = 0.96). Of patients with versus without iron deficiency, hospitalizations occurred in 28 and 19 per 100,000 during the reference period (Days 1-7 after the first dose), and in 19 and 7 per 100,000 during the two-dose protection period, respectively. Mortality rates were comparable between study groups: 2.2 per 100,000 (4/181,012) in the population with iron deficiency and 1.8 per 100,000 (19/1,055,298) in those without known iron deficiency.
Results suggest that the BNT162b2 COVID-19 vaccine is >90% effective in preventing SARS-CoV-2 infection in the 3 weeks after the second vaccination, irrespective of iron-deficiency status. These findings support the use of the vaccine in populations with iron deficiency.
铁在人体免疫反应中起着关键作用;然而,铁缺乏症对 2019 年冠状病毒病(COVID-19)疫苗效果的影响尚不清楚。
评估 BNT162b2 信使 RNA COVID-19 疫苗在预防严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)感染和 COVID-19 相关住院和死亡方面的有效性,包括有或没有铁缺乏症的个体。
这是一项大型回顾性、纵向队列研究,分析了 Maccabi 医疗保健服务数据库(覆盖以色列居民的 25%)的真实世界数据。符合条件的成年人(年龄≥16 岁)在 2020 年 12 月 19 日至 2021 年 2 月 28 日之间接受了第一剂 BNT162b2 疫苗,随后按照批准的疫苗标签接种了第二剂。如果个体在接种疫苗前有 SARS-CoV-2 感染、血红蛋白病、自 2020 年 1 月以来被诊断患有癌症、接受过免疫抑制剂治疗或在接种疫苗时怀孕,则将其排除在外。通过实时聚合酶链反应检测确诊的 SARS-CoV-2 感染发生率、COVID-19 相关住院的相对风险和铁缺乏症(血清铁蛋白<30ng/mL 或转铁蛋白饱和度<20%)个体的死亡率来评估疫苗的有效性。两剂保护期是第二次接种后 7 至 28 天。
分析了 184171 名有(平均[标准差;SD]年龄 46.2[19.6]岁;81.2%女性)与 1072019 名无(平均[SD]年龄 46.9[18.0]岁;46.2%女性)已知铁缺乏症的个体的数据。在两剂保护期内,有与无铁缺乏症的个体的疫苗有效性分别为 91.9%(95%置信区间[CI]83.7-96.0%)和 92.1%(95% CI 84.2-96.1%)(P=0.96)。在参考期(第一次接种后 1-7 天),有和无铁缺乏症的个体中,每 100000 人中有 28 和 19 人住院,在两剂保护期内,每 100000 人中有 19 和 7 人住院。研究组的死亡率相当:铁缺乏症人群为 2.2/100000(4/181012),无铁缺乏症人群为 1.8/100000(19/1055298)。
结果表明,BNT162b2 COVID-19 疫苗在第二次接种后 3 周内预防 SARS-CoV-2 感染的有效性超过 90%,无论铁缺乏症状态如何。这些发现支持在铁缺乏症人群中使用该疫苗。