Association of a Third Dose of BNT162b2 Vaccine With Incidence of SARS-CoV-2 Infection Among Health Care Workers in Israel.
Adult
Aged
Antibodies, Viral
/ blood
BNT162 Vaccine
/ administration & dosage
COVID-19
/ diagnosis
COVID-19 Nucleic Acid Testing
COVID-19 Vaccines
/ immunology
Female
Health Personnel
/ statistics & numerical data
Humans
Immunization, Secondary
Immunoglobulin G
/ blood
Incidence
Israel
/ epidemiology
Male
Middle Aged
Proportional Hazards Models
Prospective Studies
SARS-CoV-2
/ immunology
Spike Glycoprotein, Coronavirus
/ immunology
Vaccine Efficacy
Journal
JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160
Informations de publication
Date de publication:
25 01 2022
25 01 2022
Historique:
pubmed:
11
1
2022
medline:
2
2
2022
entrez:
10
1
2022
Statut:
ppublish
Résumé
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. 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. 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. Vaccination with a booster dose of BNT162b2 vaccine. The primary outcome was SARS-CoV-2 infection, as confirmed by reverse transcriptase-polymerase chain reaction. 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). 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.
Identifiants
pubmed: 35006256
pii: 2788104
doi: 10.1001/jama.2021.23641
pmc: PMC8749710
doi:
Substances chimiques
Antibodies, Viral
0
COVID-19 Vaccines
0
Immunoglobulin G
0
Spike Glycoprotein, Coronavirus
0
BNT162 Vaccine
N38TVC63NU
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
341-349Commentaires et corrections
Type : CommentIn
Références
N Engl J Med. 2021 Dec 9;385(24):e85
pubmed: 34706170
JAMA. 2021 Jun 22;325(24):2457-2465
pubmed: 33956048
JAMA. 2021 Dec 7;326(21):2203-2204
pubmed: 34739043
Lancet. 2021 Dec 4;398(10316):2093-2100
pubmed: 34756184
N Engl J Med. 2021 Apr 15;384(15):1412-1423
pubmed: 33626250
JAMA. 2013 Nov 27;310(20):2191-4
pubmed: 24141714
N Engl J Med. 2021 Oct 7;385(15):1393-1400
pubmed: 34525275
MMWR Morb Mortal Wkly Rep. 2021 Aug 27;70(34):1167-1169
pubmed: 34437521
N Engl J Med. 2021 Oct 14;385(16):1474-1484
pubmed: 34320281
Lancet. 2021 May 15;397(10287):1819-1829
pubmed: 33964222
Front Microbiol. 2020 Oct 19;11:584251
pubmed: 33193227
Lancet. 2021 Jun 19;397(10292):2331-2333
pubmed: 34090624
N Engl J Med. 2021 Sep 23;385(13):1244-1246
pubmed: 34379917
JAMA. 2021 Jul 23;:
pubmed: 34297036
Clin Chem Lab Med. 2021 Apr 09;59(8):1453-1462
pubmed: 33837679
Isr J Health Policy Res. 2021 Jan 26;10(1):6
pubmed: 33499905
Nat Med. 2021 Jul;27(7):1205-1211
pubmed: 34002089
MMWR Morb Mortal Wkly Rep. 2021 Sep 24;70(38):1337-1343
pubmed: 34555004
N Engl J Med. 2020 Dec 31;383(27):2603-2615
pubmed: 33301246
Lancet Respir Med. 2021 Sep;9(9):999-1009
pubmed: 34224675