Annual Variant-Targeted Vaccination to Prevent Severe COVID-19 in Cohorts With Vaccine-Derived and Hybrid Immunity.

IF 7.3 1区 医学 Q1 IMMUNOLOGY Clinical Infectious Diseases Pub Date : 2025-09-16 DOI:10.1093/cid/ciaf124
J Daniel Kelly, Katherine J Hoggatt, Nathan C Lo, Samuel Leonard, W John Boscardin, Hye Sun Kim, Emily N Lum, Charles C Austin, Amy L Byers, Phyllis C Tien, Peter C Austin, Dawn M Bravata, Salomeh Keyhani
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Abstract

Background: Current coronavirus disease 2019 (COVID-19) vaccine recommendations in the United States (US) provide guidance for adults to receive at least annual variant-targeted vaccination. We sought to estimate the strength and durability of protection from annual variant-targeted vaccination against severe COVID-19 illness in individuals with vaccine-derived and hybrid immunity.

Methods: We emulated a target trial using an electronic health record-based, propensity score-matched (1:1) cohort of US Veterans. Booster-vaccinated adults were eligible for a variant-targeted messenger RNA (mRNA) booster starting 1 September 2022. Matched sets of those who did and did not receive the variant-targeted booster dose were identified on a weekly basis, and the cohort was followed until 31 August 2023. Outcomes were hospitalization due to COVID-19 pneumonia and in-hospital severe illness. We fit Cox models, overall and stratified by last documented severe acute respiratory syndrome coronavirus 2 infection (pre-Omicron, Omicron), to estimate relative vaccine effectiveness (rVE).

Results: The propensity score-matched cohort consisted of 1 576 626 COVID-19 booster-vaccinated adults. Estimates of rVE from variant-targeted mRNA booster against hospitalization due to COVID-19 pneumonia were significant and similar in the cohort with vaccine-derived immunity (rVE, 29% [95% confidence interval {CI}, 25%-34%]) and cohort with hybrid immunity (rVE, 38% [95% CI, 27%-47%]). These protective gains were significant from 0 to 6 months but not 6 to 12 months after vaccination and during pre-XBB and XBB variant eras. Findings were similar for in-hospital severe illness.

Conclusions: In cohorts with vaccine-derived and hybrid immunity, modest but significant gains in protection against hospitalization and severe COVID-19 illness were conferred by the annual variant-targeted booster dose but not sustained beyond 6 months.

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在疫苗衍生免疫和混合免疫队列中,每年接种靶向变异疫苗以预防COVID-19严重疾病。
背景:目前美国的COVID-19疫苗建议为成年人至少每年接受变异靶向疫苗接种提供了指导。我们试图估计疫苗衍生和混合免疫个体每年接种针对COVID-19严重疾病的变异靶向疫苗的保护强度和持久性。方法:我们模拟了一项目标试验,使用基于电子健康记录,倾向评分匹配(1:1)的美国退伍军人队列。从2022年9月1日开始,接种强化疫苗的成年人有资格接种变异靶向mRNA强化疫苗。每周确定接受和未接受变异靶向加强剂量的匹配组,并对该队列进行随访,直到2023年8月31日。结果为COVID-19肺炎住院和住院重症。我们拟合Cox模型,根据最后记录的SARS-CoV-2感染(pre-Omicron, Omicron)进行总体和分层,以估计相对疫苗有效性(VE)。结果:倾向评分匹配的队列包括1,576,626名接种了COVID-19加强疫苗的成年人。变异靶向mRNA增强剂对COVID-19肺炎住院治疗的相对疫苗有效性(rVE)估计在疫苗来源免疫队列中显著且相似(rVE: 29%;95%CI: 25%, 34%)和混合免疫队列(rVE: 38%;95%ci: 27%, 47%)。在接种疫苗后的0-6个月,以及XBB和XBB变异前,这些保护性增益显著,但在6-12个月则不显著。住院重症患者的调查结果相似。结论:在疫苗衍生免疫和混合免疫队列中,每年变体靶向加强剂量在预防住院和COVID-19严重疾病方面获得了适度但显著的收益,但持续时间不超过6个月。
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来源期刊
Clinical Infectious Diseases
Clinical Infectious Diseases 医学-传染病学
CiteScore
25.00
自引率
2.50%
发文量
900
审稿时长
3 months
期刊介绍: Clinical Infectious Diseases (CID) is dedicated to publishing original research, reviews, guidelines, and perspectives with the potential to reshape clinical practice, providing clinicians with valuable insights for patient care. CID comprehensively addresses the clinical presentation, diagnosis, treatment, and prevention of a wide spectrum of infectious diseases. The journal places a high priority on the assessment of current and innovative treatments, microbiology, immunology, and policies, ensuring relevance to patient care in its commitment to advancing the field of infectious diseases.
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