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The Effect of Third Dose of Pfizer/BioNTech and Moderna COVID-19 mRNA Vaccines on IgG Antibody Titers.
Khuc, Thao A; Pequeno, Gregery; Betancourt-Garcia, Monica; Casciato, Adrienne M; Gomez-Martinez, Marissa; Arroyo, Carlos D; Pope, Bill D; Narmala, Shravan; Rao, Sohail.
Afiliação
  • Khuc TA; Medicine, Doctor's Hospital Renaissance (DHR) Health Institute for Research and Development, Edinburg, USA.
  • Pequeno G; Medicine, Doctor's Hospital Renaissance (DHR) Health Institute for Research and Development, Edinburg, USA.
  • Betancourt-Garcia M; Center of Excellence for Trauma Research in the Border Region, Doctor's Hospital Renaissance (DHR) Health Institute for Research and Development, Edinburg, USA.
  • Casciato AM; Medicine, Doctor's Hospital Renaissance (DHR) Health Institute for Research and Development, Edinburg, USA.
  • Gomez-Martinez M; Family Medicine, Doctor's Hospital Renaissance (DHR) Health Institute for Research and Development, Edinburg, USA.
  • Arroyo CD; Medicine, Doctor's Hospital Renaissance (DHR) Health Institute for Research and Development, Edinburg, USA.
  • Pope BD; Medicine, University of Texas Rio Grande Valley School of Medicine, Edinburg, USA.
  • Narmala S; Hematology and Oncology, Doctor's Hospital Renaissance (DHR) Health, Edinburg, USA.
  • Rao S; Medicine, Doctor's Hospital Renaissance (DHR) Health Institute for Research and Development, Edinburg, USA.
Cureus ; 15(7): e41696, 2023 Jul.
Article em En | MEDLINE | ID: mdl-37575726
ABSTRACT
With the emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants, the Centers for Disease Control and Prevention (CDC) authorized the third dose of the Pfizer-BioNTech (BNT162b2) vaccine with the rationale for prolonged elevation of anti-SARS-CoV-2 antibody titers and protection against the SARS-CoV-2 virus. To better understand how administration of the third dose of the Pfizer/BioNTech coronavirus disease 2019 (COVID-19) vaccine affects the incidence and severity of SARS-CoV-2 infections, we administered the third dose of the Pfizer-BioNTech (BNT162b2) to 189 participants. Blood samples were collected from participants during each of their scheduled visits (baseline, week two, week 12, and week 24) and tested for semi-quantitative anti-SARS-CoV-2 immunoglobulin G (IgG) titers. Our results showed that administration of the third dose of the Pfizer-BioNTech (BNT162b2) vaccine elicited elevated anti-SARS-CoV-2 IgG antibodies for the 24-week duration of the study. IgG antibody titers were greatest in week two, and progressively decreased by week 12 and week 24, with statistically significant differences between the IgG antibody titers for each collection date.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article