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Prior SARS-CoV-2 infection and COVID-19 vaccine effectiveness against outpatient illness during widespread circulation of SARS-CoV-2 Omicron variant, US Flu VE network.
Tartof, Sara Y; Xie, Fagen; Yadav, Ruchi; Wernli, Karen J; Martin, Emily T; Belongia, Edward A; Gaglani, Manjusha; Zimmerman, Richard K; Talbot, H Keipp; Thornburg, Natalie; Flannery, Brendan.
  • Tartof SY; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California, USA.
  • Xie F; Department of Health Systems Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, California, USA.
  • Yadav R; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California, USA.
  • Wernli KJ; Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • Martin ET; Kaiser Permanente Washington Health Research Institute, Seattle, Washington, USA.
  • Belongia EA; University of Michigan School of Public Health, Ann Arbor, Michigan, USA.
  • Gaglani M; Marshfield Clinic Research Institute, Marshfield, Wisconsin, USA.
  • Zimmerman RK; Baylor Scott & White Health, Temple, Texas, USA.
  • Talbot HK; Texas A&M University College of Medicine, Temple, Texas, USA.
  • Thornburg N; University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Flannery B; Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Influenza Other Respir Viruses ; 17(5): e13143, 2023 05.
Artículo en Inglés | MEDLINE | ID: covidwho-20231202
ABSTRACT

BACKGROUND:

We estimated combined protection conferred by prior SARS-CoV-2 infection and COVID-19 vaccination against COVID-19-associated acute respiratory illness (ARI).

METHODS:

During SARS-CoV-2 Delta (B.1.617.2) and Omicron (B.1.1.529) variant circulation between October 2021 and April 2022, prospectively enrolled adult patients with outpatient ARI had respiratory and filter paper blood specimens collected for SARS-CoV-2 molecular testing and serology. Dried blood spots were tested for immunoglobulin-G antibodies against SARS-CoV-2 nucleocapsid (NP) and spike protein receptor binding domain antigen using a validated multiplex bead assay. Evidence of prior SARS-CoV-2 infection also included documented or self-reported laboratory-confirmed COVID-19. We used documented COVID-19 vaccination status to estimate vaccine effectiveness (VE) by multivariable logistic regression by prior infection status.

RESULTS:

Four hundred fifty-five (29%) of 1577 participants tested positive for SARS-CoV-2 infection at enrollment; 209 (46%) case-patients and 637 (57%) test-negative patients were NP seropositive, had documented previous laboratory-confirmed COVID-19, or self-reported prior infection. Among previously uninfected patients, three-dose VE was 97% (95% confidence interval [CI], 60%-99%) against Delta, but not statistically significant against Omicron. Among previously infected patients, three-dose VE was 57% (CI, 20%-76%) against Omicron; VE against Delta could not be estimated.

CONCLUSIONS:

Three mRNA COVID-19 vaccine doses provided additional protection against SARS-CoV-2 Omicron variant-associated illness among previously infected participants.
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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Asunto principal: Vacunas contra la Influenza / COVID-19 Tipo de estudio: Estudios diagnósticos / Estudio experimental / Estudio observacional / Estudio pronóstico Tópicos: Vacunas / Variantes Límite: Adulto / Humanos Idioma: Inglés Revista: Influenza Other Respir Viruses Asunto de la revista: Virología Año: 2023 Tipo del documento: Artículo País de afiliación: Irv.13143

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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Asunto principal: Vacunas contra la Influenza / COVID-19 Tipo de estudio: Estudios diagnósticos / Estudio experimental / Estudio observacional / Estudio pronóstico Tópicos: Vacunas / Variantes Límite: Adulto / Humanos Idioma: Inglés Revista: Influenza Other Respir Viruses Asunto de la revista: Virología Año: 2023 Tipo del documento: Artículo País de afiliación: Irv.13143