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Protective effectiveness of prior SARS-CoV-2 infection and hybrid immunity against Omicron infection and severe disease: a systematic review and meta-regression
Niklas Bobrovitz; Harriet Ware; Xiaomeng Ma; Zihan Li; Reza Hosseini; Christian Cao; Anabel Selemon; Mairead Whelan; Zahra Premji; Hanane Issa; Brianna Cheng; Laith J Abu-Raddad; David L Buckeridge; Maria Van Kerkhove; Vanessa Piechotta; Melissa M Higdon; Annelies Wilder-Smith; Isabel Bergeri; Daniel Feikin; Rahul Krishan Arora; Minal K Patel; Lorenzo Subissi.
Affiliation
  • Niklas Bobrovitz; Temerty Faculty of Medicine, University of Toronto, Canada. Department of Critical Care Medicine, University of Calgary, Canada. Centre for Health Informatics,
  • Harriet Ware; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Canada.
  • Xiaomeng Ma; Institute of Health Policy Management & Evaluation, University of Toronto, Canada.
  • Zihan Li; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Canada. Department of Bioengineering, University of California, Berkeley, USA.
  • Reza Hosseini; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Canada. School of Population and Public Health, University of British Columbia
  • Christian Cao; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Canada. Temerty Faculty of Medicine, University of Toronto, Canada.
  • Anabel Selemon; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Canada.
  • Mairead Whelan; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Canada.
  • Zahra Premji; Libraries, University of Victoria, Canada.
  • Hanane Issa; Institute of Health Informatics, University College London, United Kingdom.
  • Brianna Cheng; Temerty Faculty of Medicine, University of Toronto, Canada.
  • Laith J Abu-Raddad; Infectious Disease Epidemiology Group, Weill Cornell Medicine Qatar, Cornell University, Doha, Qatar.
  • David L Buckeridge; Department of Epidemiology and Biostatistics, School of Population and Global Health, McGill University, Montreal, Canada.
  • Maria Van Kerkhove; Health Emergency Program, World Health Organization, Geneva, Switzerland.
  • Vanessa Piechotta; Department of Infectious Disease Epidemiology, Robert Koch Institute, Berlin, Germany.
  • Melissa M Higdon; International Vaccine Access Center, Department of International Health, John Hopkins Bloomberg School of Public Health, Baltimore, MA, USA.
  • Annelies Wilder-Smith; Department of Immunizations, Vaccines and Biologicals, World Health Organization, Geneva, Switzerland.
  • Isabel Bergeri; Health Emergency Program, World Health Organization, Geneva, Switzerland.
  • Daniel Feikin; Department of Immunizations, Vaccines and Biologicals, World Health Organization, Geneva, Switzerland.
  • Rahul Krishan Arora; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Canada. Institute of Biomedical Engineering, University of Oxford, United King
  • Minal K Patel; Department of Immunizations, Vaccines and Biologicals, World Health Organization, Geneva, Switzerland.
  • Lorenzo Subissi; Health Emergency Program, World Health Organization, Geneva, Switzerland
Preprint in English | medRxiv | ID: ppmedrxiv-22280610
ABSTRACT
BackgroundWe aimed to systematically review the magnitude and duration of the protective effectiveness of prior infection (PE) and hybrid immunity (HE) against Omicron infection and severe disease. MethodsWe searched pre-print and peer-reviewed electronic databases for controlled studies from January 1, 2020, to June 1, 2022. Risk of bias (RoB) was assessed using the Risk of Bias In Non-Randomized Studies of Interventions (ROBINS-I)-Tool. We used random-effects meta-regression to estimate the magnitude of protection at 1-month intervals and the average change in protection since the last vaccine dose or infection from 3 months to 6 or 12 months. We compared our estimates of PE and HE to previously published estimates of the magnitude and durability of vaccine effectiveness (VE) against Omicron. FindingsEleven studies of prior infection and 15 studies of hybrid immunity were included. For prior infection, there were 97 estimates (27 at moderate RoB and 70 at serious RoB), with the longest follow up at 15 months. PE against hospitalization or severe disease was 82{middle dot}5% [71{middle dot}8-89{middle dot}7%] at 3 months, and 74{middle dot}6% [63{middle dot}1-83{middle dot}5%] at 12 months. PE against reinfection was 65{middle dot}2% [52{middle dot}9-75{middle dot}9%] at 3 months, and 24{middle dot}7% [16{middle dot}4-35{middle dot}5%] at 12 months. For HE, there were 153 estimates (78 at moderate RoB and 75 at serious RoB), with the longest follow up at 11 months for primary series vaccination and 4 months for first booster vaccination. Against hospitalization or severe disease, HE involving either primary series vaccination or first booster vaccination was consistently >95% for the available follow up. Against reinfection, HE involving primary series vaccination was 69{middle dot}0% [58{middle dot}9-77{middle dot}5%] at 3 months after the most recent infection or vaccination, and 41{middle dot}8% [31{middle dot}5-52{middle dot}8%] at 12 months, while HE involving first booster vaccination was 68{middle dot}6% [58{middle dot}8-76{middle dot}9%] at 3 months, and 46{middle dot}5% [36{middle dot}0-57{middle dot}3%] at 6 months. Against hospitalization or severe disease at 6 months, hybrid immunity with first booster vaccination (effectiveness 95{middle dot}3% [81{middle dot}9-98{middle dot}9%]) or with primary series alone (96{middle dot}5% [90{middle dot}2-98{middle dot}8%]) provided significantly greater protection than prior infection alone (80{middle dot}1% [70{middle dot}3-87{middle dot}2%]), first booster vaccination alone (76{middle dot}7% [72{middle dot}5-80{middle dot}4%]), or primary series alone (64{middle dot}6% [54{middle dot}5-73{middle dot}6%]). Results for protection against reinfection were similar. InterpretationPrior infection and hybrid immunity both provided greater and more sustained protection against Omicron than vaccination alone. All protection estimates waned quickly against infection but remained high for hospitalisation or severe disease. Individuals with hybrid immunity had the highest magnitude and durability of protection against all outcomes, reinforcing the global imperative for vaccination. FundingWHO COVID-19 Solidarity Response Fund and the Coalition for Epidemic Preparedness Innovations. Research in contextO_ST_ABSEvidence before this studyC_ST_ABSThe global emergence and rapid spread of Omicron (B.1.1.529) variant of concern, characterized by their ability to escape immunity, has required scientists and policymakers to reassess the population protection against Omicron infection and severe disease. So far, few systematic reviews have incorporated data on Omicron, and none have examined the protection against Omicron conferred by hybrid immunity (i.e. the immunity gained from the combination of vaccination and prior infection) which is now widespread globally. While one preprint has recently reported protection from prior infection over time, no systematic review has systematically compared the magnitude and duration of vaccination, prior infection, and hybrid immunity. A large single-country study has reported that protection from either infection or hybrid immunity against Omicron infection wanes to low levels at 15 months, but is relatively stable against severe disease. Added value of this studyPrior infection and hybrid immunity both provided greater and more sustained protection against Omicron than vaccination alone. Individuals with hybrid immunity had the highest magnitude and durability of protection against all outcomes; protection against severe disease remained above 95% until the end of available follow-up at 11 months after hybrid immunity with primary series and 4 months after hybrid immunity with booster vaccination, and was sustained at these high levels of protection in projections to 12 months and 6 months, respectively. Implications of all the available evidenceThese results may serve to tailor guidance on the optimal number and timing of vaccinations. At the public health level, these findings can be combined with data on local infection prevalence, vaccination rates, and their timing. In settings with high seroprevalence, limited resources, and competing health priorities, it may be reasonable to focus on achieving high coverage rates with primary series among individuals who are at higher risk of poor outcome, as this will provide a high level of protection against severe disease for at least one year among those with prior infection. Furthermore, given the waning protection for both infection-and vaccine induced immunity against infection or reinfection, mass vaccination could be timed for roll-out prior to periods of expected increased incidence, such as the winter season. At the individual level, these results can be combined with knowledge of a persons infection and vaccination history. A six-month delay in booster may be justified after the last infection or vaccination for individuals with a known prior infection and full primary series vaccination. Further follow-up of the protective effectiveness of hybrid immunity against hospitalization or severe disease for all vaccines is needed to clarify how much waning of protection might occur with longer duration since the last infection or vaccination. Producing estimates of protection for new variant-containing vaccines will be crucial for COVID-19 vaccine policy and decision-making bodies. Policy makers considering the use and timing of vaccinations should include the local extent of past infection, the protection conferred by prior infection or hybrid immunity, and the duration of this protection as key considerations to inform their decision-making.
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Experimental_studies / Observational study / Prognostic study / Rct / Review / Systematic review Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Experimental_studies / Observational study / Prognostic study / Rct / Review / Systematic review Language: English Year: 2022 Document type: Preprint
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