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Dynamics of SARS-CoV-2 VOC Neutralization and Novel mAb Reveal Protection against Omicron.
Hao, Linhui; Hsiang, Tien-Ying; Dalmat, Ronit R; Ireton, Renee; Morton, Jennifer F; Stokes, Caleb; Netland, Jason; Hale, Malika; Thouvenel, Chris; Wald, Anna; Franko, Nicholas M; Huden, Kristen; Chu, Helen Y; Sigal, Alex; Greninger, Alex L; Tilles, Sasha; Barrett, Lynn K; Van Voorhis, Wesley C; Munt, Jennifer; Scobey, Trevor; Baric, Ralph S; Rawlings, David J; Pepper, Marion; Drain, Paul K; Gale, Michael.
Afiliação
  • Hao L; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA 98109, USA.
  • Hsiang TY; Center for Emerging & Re-Emerging Infectious Diseases, University of Washington, Seattle, WA 98109, USA.
  • Dalmat RR; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA 98109, USA.
  • Ireton R; Center for Emerging & Re-Emerging Infectious Diseases, University of Washington, Seattle, WA 98109, USA.
  • Morton JF; International Clinical Research Center, Department of Global Health, Schools of Medicine and Public Health, University of Washington, Seattle, WA 98104, USA.
  • Stokes C; Department of Epidemiology, School of Public Health, University of Washington, Seattle, WA 98195, USA.
  • Netland J; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA 98109, USA.
  • Hale M; Center for Emerging & Re-Emerging Infectious Diseases, University of Washington, Seattle, WA 98109, USA.
  • Thouvenel C; International Clinical Research Center, Department of Global Health, Schools of Medicine and Public Health, University of Washington, Seattle, WA 98104, USA.
  • Wald A; Department of Epidemiology, School of Public Health, University of Washington, Seattle, WA 98195, USA.
  • Franko NM; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA 98109, USA.
  • Huden K; Center for Emerging & Re-Emerging Infectious Diseases, University of Washington, Seattle, WA 98109, USA.
  • Chu HY; Department of Pediatrics, School of Medicine, University of Washington, Seattle, WA 98195, USA.
  • Sigal A; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA 98109, USA.
  • Greninger AL; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA 98109, USA.
  • Tilles S; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA 98109, USA.
  • Barrett LK; Department of Epidemiology, School of Public Health, University of Washington, Seattle, WA 98195, USA.
  • Van Voorhis WC; Division of Allergy and Infectious Diseases, Department of Medicine, School of Medicine, University of Washington, Seattle, WA 98195, USA.
  • Munt J; Allergy and Infectious Diseases Division, Laboratory Medicine & Pathology, & Epidemiology, University of Washington, Seattle, WA 98195, USA.
  • Scobey T; Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
  • Baric RS; Division of Allergy and Infectious Diseases, Department of Medicine, School of Medicine, University of Washington, Seattle, WA 98195, USA.
  • Rawlings DJ; Division of Allergy and Infectious Diseases, Department of Medicine, School of Medicine, University of Washington, Seattle, WA 98195, USA.
  • Pepper M; Division of Allergy and Infectious Diseases, Department of Medicine, School of Medicine, University of Washington, Seattle, WA 98195, USA.
  • Drain PK; Africa Health Research Institute, Durban 4001, South Africa.
  • Gale M; School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Mayville 4058, South Africa.
Viruses ; 15(2)2023 02 14.
Article em En | MEDLINE | ID: mdl-36851745
New variants of SARS-CoV-2 continue to emerge and evade immunity. We isolated SARS-CoV-2 temporally across the pandemic starting with the first emergence of the virus in the western hemisphere and evaluated the immune escape among variants. A clinic-to-lab viral isolation and characterization pipeline was established to rapidly isolate, sequence, and characterize SARS-CoV-2 variants. A virus neutralization assay was applied to quantitate humoral immunity from infection and/or vaccination. A panel of novel monoclonal antibodies was evaluated for antiviral efficacy. We directly compared all variants, showing that convalescence greater than 5 months post-symptom onset from ancestral virus provides little protection against SARS-CoV-2 variants. Vaccination enhances immunity against viral variants, except for Omicron BA.1, while a three-dose vaccine regimen provides over 50-fold enhanced protection against Omicron BA.1 compared to a two-dose. A novel Mab neutralizes Omicron BA.1 and BA.2 variants better than the clinically approved Mabs, although neither can neutralize Omicron BA.4 or BA.5. Thus, the need remains for continued vaccination-booster efforts, with innovation for vaccine and Mab improvement for broadly neutralizing activity. The usefulness of specific Mab applications links with the window of clinical opportunity when a cognate viral variant is present in the infected population.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: COVID-19 Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: COVID-19 Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article