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Association of mRNA COVID-19 vaccination and reductions in Post-COVID Conditions following SARS-CoV-2 infection in a US prospective cohort of essential workers
The Journal of Infectious Diseases ( IF 5.0 ) Pub Date : 2024-11-12 , DOI: 10.1093/infdis/jiae556
Josephine Mak, Sana Khan, Amadea Britton, Spencer Rose, Lisa Gwynn, Katherine D Ellingson, Jennifer Meece, Leora Feldstein, Harmony Tyner, Laura Edwards, Matthew S Thiese, Allison Naleway, Manjusha Gaglani, Natasha Solle, Jefferey L Burgess, Julie Mayo Lamberte, Meghan Shea, Taryn Hunt-Smith, Alberto Caban-Martinez, Cynthia Porter, Ryan Wiegand, Ramona Rai, Kurt T Hegmann, James Hollister, Ashley Fowlkes, Meredith Wesley, Andrew L Philips, Patrick Rivers, Robin Bloodworth, Gabriella Newes-Adeyi, Lauren E W Olsho, Sarang K Yoon, Sharon Saydah, Karen Lutrick

Background While there is evidence that COVID-19 vaccination protects against development of post-COVID conditions (PCC) after severe infection data are limited on whether vaccination reduces the risk after cases of less-severe non-hospitalized COVID-19 disease with more recent SARS-CoV-2 variant viruses. This study assessed whether COVID-19 vaccination was protective against subsequent development of PCC in persons with predominantly mild initial infections during both Delta and Omicron variant predominance. Methods This study utilized a case-control design, nested within the HEROES-RECOVER cohort. Participants aged ≥18 years with PCR-confirmed SARS-CoV-2 infection between 6/28/2021 and 9/14/2022 were surveyed for PCC, defined by symptoms lasting >1 month after initial infection Cases were participants self-reporting PCC and controls were participants that did not self-report PCC. The exposure was mRNA COVID-19 vaccination (2 or 3 monovalent doses) versus no COVID-19 vaccination. Logistic regression was used to compare the odds of PCC among vaccinated and unvaccinated persons; additional analyses evaluating PCC subtypes were also performed. Results A total of 936 participants with documented SARS-CoV-2 infection were included; of these 23.6% (221) reported PCC and 83.3% (779) were vaccinated. Participants who received a 3rd COVID-19 monovalent mRNA dose prior to infection had lower odds of PCC-related gastrointestinal, neurological, and other symptoms compared to unvaccinated participants (aOR: 0.37; 95% CI: 0.16-0.85; aOR: 0.56; 95% CI: 0.32-0.97; aOR:0.48; 95% CI: 0.25-0.91). Conclusions COVID-19 vaccination protected against development of PCC among persons with mild infection during both Delta and Omicron variant predominance, supporting vaccination as an important tool for PCC prevention.

中文翻译:


在美国前瞻性基本工作者队列中,mRNA COVID-19 疫苗接种与 SARS-CoV-2 感染后 COVID 后病情减少的关联



背景 虽然有证据表明 COVID-19 疫苗接种可以防止严重感染后 COVID 后疾病 (PCC) 的发展,但关于疫苗接种是否能降低较轻的非住院 COVID-19 疾病与最近的 SARS-CoV-2 变体病毒病例发生的风险的数据有限。本研究评估了在 Delta 和 Omicron 变体占主导地位期间,COVID-19 疫苗接种是否能防止主要为轻度初始感染的人随后发生 PCC。方法 本研究采用病例对照设计,嵌套在 HEROES-RECOVER 队列中。在 2021 年 6 月 28 日至 2022 年 9 月 14 日期间,年龄≥ 18 岁且经 PCR 确认感染 SARS-CoV-2 的参与者接受了 PCC 调查,其定义为症状在初始感染后持续 >1 个月病例是参与者自我报告 PCC,对照组是未自我报告 PCC 的参与者。暴露是 mRNA COVID-19 疫苗接种(2 或 3 剂单价剂量)与不接种 COVID-19 疫苗。采用 Logistic 回归比较接种疫苗和未接种疫苗者 PCC 的几率;还进行了评估 PCC 亚型的额外分析。结果 共纳入 936 名有 SARS-CoV-2 感染记录的参与者;其中 23.6% (221) 报告了 PCC,83.3% (779) 接种了疫苗。与未接种疫苗的参与者相比,在感染前接受第 3 剂 COVID-19 单价 mRNA 的参与者出现 PCC 相关胃肠道、神经和其他症状的几率较低(aOR:0.37;95% CI:0.16-0.85;aOR:0.56;95% CI:0.32-0.97;aOR:0.48;95% CI:0.25-0.91)。 结论 在 Delta 和 Omicron 变体占主导地位期间,COVID-19 疫苗接种可防止轻度感染者发生 PCC,支持疫苗接种作为预防 PCC 的重要工具。
更新日期:2024-11-12
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