Avishay Spitzer1,2,3, Yoel Angel2,4,5, Or Marudi2, David Zeltser2,6, Esther Saiag2,7, Hanoch Goldshmidt2,8, Ilana Goldiner2,8, Moshe Stark2,8, Ora Halutz2,8, Ronni Gamzu2,9, Marina Slobodkin2,10, Nadav Amrami2,10, Eugene Feigin2,10, Meital Elbaz2,11, Moran Furman2,12, Yotam Bronstein2,10, Amanda Chikly2,11, Anna Eshkol2,12, Victoria Furer2,13, Talia Mayer2,12, Suzy Meijer2,11, Ariel Melloul2,10, Michal Mizrahi2,10, Michal Yakubovsky2,11, Dana Rosenberg2,13, Ari Safir2,12, Liron Spitzer2,12, Eyal Taleb2,12, Ori Elkayam2,13, Adi Silberman2,13, Tali Eviatar2,13, Ofir Elalouf2,13, Tal Levinson2,11, Katia Pozyuchenko14, Ayelet Itzhaki-Alfia2,14, Eli Sprecher2,12,15, Ronen Ben-Ami2,11, Oryan Henig2,11. 1. Department of Oncology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. 2. Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. 3. Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel. 4. Department of Anesthesia, Pain Management and Intensive Care, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. 5. Department of Physician Affairs, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. 6. Department of Emergency Medicine, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. 7. Department of Information Systems and Operations, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. 8. Department of Clinical Laboratories, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. 9. Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. 10. Department of Internal Medicine "D," Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. 11. Department of Infectious Diseases and Infection Control, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. 12. Department of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. 13. Department of Rheumatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. 14. Department of Pathology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. 15. Department of Research and Development, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Abstract
Importance: Administration of a BNT162b2 booster dose (Pfizer-BioNTech) to fully vaccinated individuals aged 60 years and older was significantly associated with lower risk of SARS-CoV-2 infection and severe illness. Data are lacking on the effectiveness of booster doses for younger individuals and health care workers. Objective: To estimate the association of a BNT162b2 booster dose with SARS-CoV-2 infections among health care workers who were previously vaccinated with a 2-dose series of BNT162b2. Design, Setting, and Participants: This was a prospective cohort study conducted at a tertiary medical center in Tel Aviv, Israel. The study cohort included 1928 immunocompetent health care workers who were previously vaccinated with a 2-dose series of BNT162b2, and had enrolled between August 8 and 19, 2021, with final follow-up reported through September 20, 2021. Screening for SARS-CoV-2 infection was performed every 14 days. Anti-spike protein receptor binding domain IgG titers were determined at baseline and 1 month after enrollment. Cox regression with time-dependent analysis was used to estimate hazard ratios of SARS-CoV-2 infection between booster-immunized status and 2-dose vaccinated (booster-nonimmunized) status. Exposures: Vaccination with a booster dose of BNT162b2 vaccine. Main Outcomes and Measures: The primary outcome was SARS-CoV-2 infection, as confirmed by reverse transcriptase-polymerase chain reaction. Results: Among 1928 participants, the median age was 44 years (IQR, 36-52 years) and 1381 were women (71.6%). Participants completed the 2-dose vaccination series a median of 210 days (IQR, 205-213 days) before study enrollment. A total of 1650 participants (85.6%) received the booster dose. During a median follow-up of 39 days (IQR, 35-41 days), SARS-CoV-2 infection occurred in 44 participants (incidence rate, 60.2 per 100 000 person-days); 31 (70.5%) were symptomatic. Five SARS-CoV-2 infections occurred in booster-immunized participants and 39 in booster-nonimmunized participants (incidence rate, 12.8 vs 116 per 100 000 person-days, respectively). In a time-dependent Cox regression analysis, the adjusted hazard ratio of SARS-CoV-2 infection for booster-immunized vs booster-nonimmunized participants was 0.07 (95% CI, 0.02-0.20). Conclusions and Relevance: Among health care workers at a single center in Israel who were previously vaccinated with a 2-dose series of BNT162b2, administration of a booster dose compared with not receiving one was associated with a significantly lower rate of SARS-CoV-2 infection over a median of 39 days of follow-up. Ongoing surveillance is required to assess durability of the findings.
Importance: Administration of a BNT162b2 booster dose (Pfizer-BioNTech) to fully vaccinated individuals aged 60 years and older was significantly associated with lower risk of SARS-CoV-2 infection and severe illness. Data are lacking on the effectiveness of booster doses for younger individuals and health care workers. Objective: To estimate the association of a BNT162b2 booster dose with SARS-CoV-2 infections among health care workers who were previously vaccinated with a 2-dose series of BNT162b2. Design, Setting, and Participants: This was a prospective cohort study conducted at a tertiary medical center in Tel Aviv, Israel. The study cohort included 1928 immunocompetent health care workers who were previously vaccinated with a 2-dose series of BNT162b2, and had enrolled between August 8 and 19, 2021, with final follow-up reported through September 20, 2021. Screening for SARS-CoV-2 infection was performed every 14 days. Anti-spike protein receptor binding domain IgG titers were determined at baseline and 1 month after enrollment. Cox regression with time-dependent analysis was used to estimate hazard ratios of SARS-CoV-2 infection between booster-immunized status and 2-dose vaccinated (booster-nonimmunized) status. Exposures: Vaccination with a booster dose of BNT162b2 vaccine. Main Outcomes and Measures: The primary outcome was SARS-CoV-2 infection, as confirmed by reverse transcriptase-polymerase chain reaction. Results: Among 1928 participants, the median age was 44 years (IQR, 36-52 years) and 1381 were women (71.6%). Participants completed the 2-dose vaccination series a median of 210 days (IQR, 205-213 days) before study enrollment. A total of 1650 participants (85.6%) received the booster dose. During a median follow-up of 39 days (IQR, 35-41 days), SARS-CoV-2 infection occurred in 44 participants (incidence rate, 60.2 per 100 000 person-days); 31 (70.5%) were symptomatic. Five SARS-CoV-2 infections occurred in booster-immunized participants and 39 in booster-nonimmunized participants (incidence rate, 12.8 vs 116 per 100 000 person-days, respectively). In a time-dependent Cox regression analysis, the adjusted hazard ratio of SARS-CoV-2 infection for booster-immunized vs booster-nonimmunized participants was 0.07 (95% CI, 0.02-0.20). Conclusions and Relevance: Among health care workers at a single center in Israel who were previously vaccinated with a 2-dose series of BNT162b2, administration of a booster dose compared with not receiving one was associated with a significantly lower rate of SARS-CoV-2 infection over a median of 39 days of follow-up. Ongoing surveillance is required to assess durability of the findings.
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