Mak Josephine, Khan Sana, Britton Amadea, Rose Spencer, Gwynn Lisa, Ellingson Katherine D, Meece Jennifer, Feldstein Leora R, Tyner Harmony, Edwards Laura J, Thiese Matthew S, Naleway Allison, Gaglani Manjusha, Solle Natasha, Burgess Jefferey L, Lamberte Julie Mayo, Shea Meghan, Hunt-Smith Taryn, Caban-Martinez Alberto, Porter Cynthia, Wiegand Ryan, Rai Ramona, Hegmann Kurt T, Hollister James, Fowlkes Ashley, Wesley Meredith, Philips Andrew L, Rivers Patrick, Bloodworth Robin, Newes-Adeyi Gabriella, Olsho Lauren E W, Yoon Sarang K, Saydah Sharon, Lutrick Karen
National Center for Immunization and Respiratory Disease, Centers for Disease Control and Prevention, Atlanta, Georgia.
Department of Epidemiology and Biostatistics, Mel and Enid Zuckerman College of Public Health, University of Arizona, Tucson, Arizona.
J Infect Dis. 2025 Mar 17;231(3):665-676. doi: 10.1093/infdis/jiae556.
Data are limited on whether vaccination reduces post COVID conditions (PCCs) risk after less severe nonhospitalized coronavirus disease 2019 (COVID-19). This study assessed whether COVID-19 vaccination protected against PCCs in persons with mild initial infections during Delta and Omicron variant predominance.
This study utilized a case-control design, nested within the HEROES-RECOVER cohort. Participants aged ≥18 years with test-confirmed severe acute respiratory syndrome coronavirus disease 2 (SARS-CoV-2) between 28 June 2021 and 14 September 2022 were surveyed for PCCs, defined by symptoms lasting >4 weeks after initial infection. Cases self-reported PCCs and controls self-reported no PCCs. The exposure was messenger RNA (mRNA) COVID-19 vaccination (2 or 3 monovalent doses). Odds of PCCs among vaccinated and unvaccinated persons were compared with logistic regression.
Of 936 participants, 23.6% reported PCCs and 83.2% were vaccinated. Participants who received 3 vaccine doses had lower odds of PCC-related gastrointestinal, neurological, and other symptoms compared to unvaccinated participants (adjusted odds ratio [95% confidence interval]: 0.37 [.16-.85], 0.56 [.32-.97], and 0.48 [.25-.91], respectively).
COVID-19 vaccination protected against development of PCCs among persons with mild infection during both Delta and Omicron variant predominance, supporting vaccination as an important PCCs prevention tool.
关于在症状较轻的非住院2019冠状病毒病(COVID-19)后接种疫苗是否能降低新冠后遗症(PCCs)风险的数据有限。本研究评估了在德尔塔和奥密克戎变异株占主导期间,COVID-19疫苗接种对初始感染较轻的人群预防PCCs的作用。
本研究采用病例对照设计,嵌套于HEROES-RECOVER队列中。对2021年6月28日至2022年9月14日期间年龄≥18岁且经检测确诊为严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的参与者进行PCCs调查,PCCs定义为初始感染后症状持续超过4周。病例自我报告有PCCs,对照自我报告无PCCs。暴露因素为信使核糖核酸(mRNA)COVID-19疫苗接种(2剂或3剂单价疫苗)。采用逻辑回归比较接种和未接种人群中发生PCCs的几率。
在936名参与者中,23.6%报告有PCCs,83.2%接种了疫苗。与未接种疫苗的参与者相比,接种3剂疫苗的参与者出现与PCCs相关的胃肠道、神经和其他症状的几率较低(调整后的优势比[95%置信区间]分别为:0.37[.16-.85]、0.56[.32-.97]和0.48[.25-.91])。
在德尔塔和奥密克戎变异株占主导期间,COVID-19疫苗接种可预防轻度感染人群发生PCCs,支持将疫苗接种作为预防PCCs的重要工具。