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Durability of Protection Post-Primary COVID-19 Vaccination in the United States.
Zheutlin, Amanda; Ott, Miles; Sun, Ran; Zemlianskaia, Natalia; Meyer, Craig S; Rubel, Meagan; Hayden, Jennifer; Neri, Breno; Kamath, Tripthi; Khan, Najat; Schneeweiss, Sebastian; Sarsour, Khaled.
  • Zheutlin A; Data Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
  • Ott M; Data Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
  • Sun R; Data Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
  • Zemlianskaia N; Data Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
  • Meyer CS; Data Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
  • Rubel M; Data Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
  • Hayden J; Data Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
  • Neri B; Data Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
  • Kamath T; Data Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
  • Khan N; Data Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
  • Schneeweiss S; Division of Pharmacoepidemiology, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02120, USA.
  • Sarsour K; Data Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
Vaccines (Basel) ; 10(9)2022 Sep 03.
Article in English | MEDLINE | ID: covidwho-2071884
ABSTRACT
The durability of immune responses after COVID-19 vaccination will drive long-term vaccine effectiveness across settings and may differ by vaccine type. To determine durability of protection of COVID-19 vaccines (BNT162b2, mRNA-1273, and Ad26.COV2.S) following primary vaccination in the United States, a matched case-control study was conducted in three cohorts between 1 January and 7 September 2021 using de-identified data from a database covering 168 million lives. Odds ratios (ORs) for developing outcomes of interest (breakthrough SARS-CoV-2 infection, hospitalization, or intensive care unit admission) were determined for each vaccine (no direct comparisons). In total, 17,017,435 individuals were identified. Relative to the baseline, stable protection was observed for Ad26.COV2.S against infections (OR [95% confidence interval (CI)], 1.31 [1.18-1.47]) and hospitalizations (OR [95% CI], 1.25 [0.86-1.80]). Relative to the baseline, protection waned over time against infections for BNT162b2 (OR [95% CI], 2.20 [2.01-2.40]) and mRNA-1273 (OR [95% CI], 2.07 [1.87-2.29]) and against hospitalizations for BNT162b2 (OR [95% CI], 2.38 [1.79-3.17]). Baseline protection remained stable for intensive care unit admissions for all three vaccines. Calculated baseline VE was consistent with published literature. This study suggests that the three vaccines in three separate populations may have different durability profiles.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Language: English Year: 2022 Document Type: Article Affiliation country: Vaccines10091458

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Language: English Year: 2022 Document Type: Article Affiliation country: Vaccines10091458