Protection conferred by SARS-CoV-2 infection across a spectrum of reinfection symptoms and severities
Author | Sukik, Layan |
Author | Chemaitelly, Hiam |
Author | Ayoub, Houssein H |
Author | Coyle, Peter |
Author | Tang, Patrick |
Author | Hasan, Mohammad R |
Author | Yassine, Hadi M |
Author | Al Thani, Asmaa A |
Author | Al-Kanaani, Zaina |
Author | Al-Kuwari, Einas |
Author | Jeremijenko, Andrew |
Author | Kaleeckal, Anvar Hassan |
Author | Latif, Ali Nizar |
Author | Shaik, Riyazuddin Mohammad |
Author | Abdul-Rahim, Hanan F |
Author | Nasrallah, Gheyath K |
Author | Al-Kuwari, Mohamed Ghaith |
Author | Butt, Adeel |
Author | Al-Romaihi, Hamad Eid |
Author | Al-Thani, Mohamed H |
Author | Al-Khal, Abdullatif |
Author | Bertollini, Roberto |
Author | Abu-Raddad, Laith J |
Available date | 2025-05-27T05:41:22Z |
Publication Date | 2025 |
Publication Name | BMJ Open Respiratory Research |
Resource | Scopus |
Identifier | http://dx.doi.org/10.1136/bmjresp-2024-002718 |
ISSN | 20524439 |
Abstract | Background SARS-CoV-2 infection is associated with protection against reinfection. This study analysed this protection across different reinfection symptoms and severities, comparing the preomicron and omicron eras. Methods A nationwide, matched, test-negative, case-control study was conducted in Qatar from 5 February 2020 to 12 March 2024. The preomicron analysis used a sample of 509 949 positive and 8 494 782 negative tests, while the omicron analysis included 682 257 positive and 6 904 044 negative tests. Data were sourced from Qatar's national databases for COVID-19 laboratory testing, vaccination, hospitalisation and death. Results Effectiveness of preomicron infection against preomicron reinfection was estimated at 80.9% (95% CI: 79.1% to 82.6%) for asymptomatic reinfection, 87.5% (95% CI: 86.1% to 88.9%) for symptomatic reinfection, 97.8% (95% CI: 95.7% to 98.9%) for severe COVID-19 reinfection, 100.0% (95% CI: 97.5% to 100.0%) for critical COVID-19 reinfection and 88.1% (95% CI: 50.3% to 97.2%) for fatal COVID-19 reinfection. For omicron infection against omicron reinfection, the estimates were 46.4% (95% CI: 36.9% to 54.4%) for asymptomatic reinfection, 52.8% (95% CI: 44.4% to 60.0%) for symptomatic reinfection, 100.0% (95% CI: 55.4% to 100.0%) for severe COVID-19 reinfection, 100.0% (95% CI: 15.1% to 100.0%) for critical COVID-19 reinfection, and 75.2% (95% CI: -58.8% to 97.5%) for fatal COVID-19 reinfection. Effectiveness over time since previous infection showed no discernible decline in protection against all forms of reinfection in the preomicron era, but a rapid decline against asymptomatic and symptomatic reinfections in the omicron era. Conclusions A gradient of protection against reinfection is evident, with the highest protection observed against severe forms of COVID-19. Over time, this gradient becomes more pronounced, as protection against asymptomatic and symptomatic reinfections decreases, while protection against severe outcomes remains strong. |
Sponsor | Funding text 1: The authors acknowledge the many dedicated individuals at Hamad Medical Corporation, the Ministry of Public Health, the Primary Health Care Corporation, Qatar Biobank, Sidra Medicine, and Weill Cornell Medicine-Qatar for their diligent efforts and contributions to make this study possible. The authors are also grateful for institutional salary support from the Biomedical Research Program and the Biostatistics, Epidemiology and Biomathematics Research Core, both at Weill Cornell Medicine-Qatar, as well as for institutional salary support provided by the Ministry of Public Health, Hamad Medical Corporation and Sidra Medicine. The authors are also grateful for the Qatar Genome Programme and Qatar University Biomedical Research Center for institutional support for the reagents needed for the viral genome sequencing. ; Funding text 2: This work was supported by the Biomedical Research Program and the Biostatistics, Epidemiology and the Biomathematics Research Core, both at Weill Cornell Medicine-Qatar, as well as the Ministry of Public Health, Hamad Medical Corporation, Sidra Medicine, Qatar Genome Programme and Qatar University Biomedical Research Center. No award or grant number was associated with this funding. ; Funding text 3: The authors acknowledge the many dedicated individuals at Hamad Medical Corporation, the Ministry of Public Health, the Primary Health Care Corporation, Qatar Biobank, Sidra Medicine, and Weill Cornell Medicine-Qatar for their diligent efforts and contributions to make this study possible. The authors are also grateful for institutional salary support from the Biomedical Research Program and the Biostatistics, Epidemiology and Biomathematics Research Core, both at Weill Cornell Medicine-Qatar, as well as for institutional salary support provided by the Ministry of Public Health, Hamad Medical Corporation and Sidra Medicine. The authors are also grateful for the Qatar Genome Programme and Qatar University Biomedical Research Center for institutional support for the reagents needed for the viral genome sequencing. This work was supported by the Biomedical Research Program and the Biostatistics, Epidemiology and the Biomathematics Research Core, both at Weill Cornell Medicine-Qatar, as well as the Ministry of Public Health, Hamad Medical Corporation, Sidra Medicine, Qatar Genome Programme and Qatar University Biomedical Research Center. No award or grant number was associated with this funding. |
Language | en |
Publisher | BMJ Publishing Group |
Subject | COVID-19 Innate Immunity Respiratory Infection Viral infection |
Type | Article |
Issue Number | 1 |
Volume Number | 12 |
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