Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill.
North Carolina Department of Health and Human Services, Raleigh.
JAMA. 2022 Oct 11;328(14):1415-1426. doi: 10.1001/jama.2022.17876.
Data about the association of COVID-19 vaccination and prior SARS-CoV-2 infection with risk of SARS-CoV-2 infection and severe COVID-19 outcomes may guide prevention strategies.
To estimate the time-varying association of primary and booster COVID-19 vaccination and prior SARS-CoV-2 infection with subsequent SARS-CoV-2 infection, hospitalization, and death.
DESIGN, SETTING, AND PARTICIPANTS: Cohort study of 10.6 million residents in North Carolina from March 2, 2020, through June 3, 2022.
COVID-19 primary vaccine series and boosters and prior SARS-CoV-2 infection.
Rate ratio (RR) of SARS-CoV-2 infection and hazard ratio (HR) of COVID-19-related hospitalization and death.
The median age among the 10.6 million participants was 39 years; 51.3% were female, 71.5% were White, and 9.9% were Hispanic. As of June 3, 2022, 67% of participants had been vaccinated. There were 2 771 364 SARS-CoV-2 infections, with a hospitalization rate of 6.3% and mortality rate of 1.4%. The adjusted RR of the primary vaccine series compared with being unvaccinated against infection became 0.53 (95% CI, 0.52-0.53) for BNT162b2, 0.52 (95% CI, 0.51-0.53) for mRNA-1273, and 0.51 (95% CI, 0.50-0.53) for Ad26.COV2.S 10 months after the first dose, but the adjusted HR for hospitalization remained at 0.29 (95% CI, 0.24-0.35) for BNT162b2, 0.27 (95% CI, 0.23-0.32) for mRNA-1273, and 0.35 (95% CI, 0.29-0.42) for Ad26.COV2.S and the adjusted HR of death remained at 0.23 (95% CI, 0.17-0.29) for BNT162b2, 0.15 (95% CI, 0.11-0.20) for mRNA-1273, and 0.24 (95% CI, 0.19-0.31) for Ad26.COV2.S. For the BNT162b2 primary series, boosting in December 2021 with BNT162b2 had the adjusted RR relative to primary series of 0.39 (95% CI, 0.38-0.40) and boosting with mRNA-1273 had the adjusted RR of 0.32 (95% CI, 0.30-0.34) against infection after 1 month and boosting with BNT162b2 had the adjusted RR of 0.84 (95% CI, 0.82-0.86) and boosting with mRNA-1273 had the adjusted RR of 0.60 (95% CI, 0.57-0.62) after 3 months. Among all participants, the adjusted RR of Omicron infection compared with no prior infection was estimated at 0.23 (95% CI, 0.22-0.24) against infection, and the adjusted HRs were 0.10 (95% CI, 0.07-0.14) against hospitalization and 0.11 (95% CI, 0.08-0.15) against death after 4 months.
Receipt of primary COVID-19 vaccine series compared with being unvaccinated, receipt of boosters compared with primary vaccination, and prior infection compared with no prior infection were all significantly associated with lower risk of SARS-CoV-2 infection (including Omicron) and resulting hospitalization and death. The associated protection waned over time, especially against infection.
关于 COVID-19 疫苗接种和先前 SARS-CoV-2 感染与 SARS-CoV-2 感染和严重 COVID-19 结局风险的关联的数据可能指导预防策略。
评估初级和加强 COVID-19 疫苗接种以及先前 SARS-CoV-2 感染与随后 SARS-CoV-2 感染、住院和死亡的时间变化关联。
设计、设置和参与者:2020 年 3 月 2 日至 2022 年 6 月 3 日期间北卡罗来纳州 1060 万居民的队列研究。
COVID-19 初级疫苗系列和加强针以及先前的 SARS-CoV-2 感染。
SARS-CoV-2 感染的比率比(RR)和 COVID-19 相关住院和死亡的危险比(HR)。
在 1060 万参与者中,中位年龄为 39 岁;51.3%为女性,71.5%为白人,9.9%为西班牙裔。截至 2022 年 6 月 3 日,67%的参与者已接种疫苗。有 2771364 例 SARS-CoV-2 感染,住院率为 6.3%,死亡率为 1.4%。与未接种疫苗相比,初级疫苗系列对感染的调整后的 RR 为 BNT162b2 的 0.53(95%CI,0.52-0.53),mRNA-1273 的 0.52(95%CI,0.51-0.53),Ad26.COV2.S 的 0.51(95%CI,0.50-0.53)接种第一剂后 10 个月,但住院的调整 HR 仍为 BNT162b2 的 0.29(95%CI,0.24-0.35),mRNA-1273 的 0.27(95%CI,0.23-0.32),Ad26.COV2.S 的 0.35(95%CI,0.29-0.42),死亡的调整 HR 仍为 BNT162b2 的 0.23(95%CI,0.17-0.29),mRNA-1273 的 0.15(95%CI,0.11-0.20),Ad26.COV2.S 的 0.24(95%CI,0.19-0.31)。对于 BNT162b2 初级系列,2021 年 12 月用 BNT162b2 加强针接种与初级系列相比,感染的调整 RR 为 0.39(95%CI,0.38-0.40),用 mRNA-1273 加强针接种的调整 RR 为 0.32(95%CI,0.30-0.34),接种后 1 个月,用 BNT162b2 加强针接种的调整 RR 为 0.84(95%CI,0.82-0.86),用 mRNA-1273 加强针接种的调整 RR 为 0.60(95%CI,0.57-0.62),接种后 3 个月。在所有参与者中,与无既往感染相比,估计 Omicron 感染的调整 RR 为 0.23(95%CI,0.22-0.24),感染后 4 个月的调整 HR 分别为 0.10(95%CI,0.07-0.14)、0.11(95%CI,0.08-0.15)。
与未接种疫苗相比,接受初级 COVID-19 疫苗接种系列、接种加强针以及先前的感染与 SARS-CoV-2 感染(包括 Omicron)以及随后的住院和死亡风险降低显著相关。这种关联的保护作用随着时间的推移而减弱,尤其是对感染的保护作用。