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SARS-CoV-2 Omicron: Viral Evolution, Immune Evasion, and Alternative Durable Therapeutic Strategies.
Guo, Hailong; Ha, Sha; Botten, Jason W; Xu, Kai; Zhang, Ningyan; An, Zhiqiang; Strohl, William R; Shiver, John W; Fu, Tong-Ming.
Afiliación
  • Guo H; IGM Biosciences, Mountain View, CA 94043, USA.
  • Ha S; IGM Biosciences, Mountain View, CA 94043, USA.
  • Botten JW; Department of Medicine, Division of Pulmonary Disease and Critical Care Medicine, Robert Larner, M.D. College of Medicine, University of Vermont, Burlington, VT 05405, USA.
  • Xu K; Department of Microbiology and Molecular Genetics, Robert Larner, M.D. College of Medicine, University of Vermont, Burlington, VT 05405, USA.
  • Zhang N; Texas Therapeutics Institute, Brown Foundation Institute of Molecular Medicine, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
  • An Z; Texas Therapeutics Institute, Brown Foundation Institute of Molecular Medicine, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
  • Strohl WR; Texas Therapeutics Institute, Brown Foundation Institute of Molecular Medicine, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
  • Shiver JW; IGM Biosciences, Mountain View, CA 94043, USA.
  • Fu TM; IGM Biosciences, Mountain View, CA 94043, USA.
Viruses ; 16(5)2024 04 28.
Article en En | MEDLINE | ID: mdl-38793580
ABSTRACT
Since the SARS-CoV-2 Omicron virus has gained dominance worldwide, its continual evolution with unpredictable mutations and patterns has revoked all authorized immunotherapeutics. Rapid viral evolution has also necessitated several rounds of vaccine updates in order to provide adequate immune protection. It remains imperative to understand how Omicron evolves into different subvariants and causes immune escape as this could help reevaluate the current intervention strategies mostly implemented in the clinics as emergency measures to counter the pandemic and, importantly, develop new solutions. Here, we provide a review focusing on the major events of Omicron viral evolution, including the features of spike mutation that lead to immune evasion against monoclonal antibody (mAb) therapy and vaccination, and suggest alternative durable options such as the ACE2-based experimental therapies superior to mAbs to address this unprecedented evolution of Omicron virus. In addition, this type of unique ACE2-based virus-trapping molecules can counter all zoonotic SARS coronaviruses, either from unknown animal hosts or from established wild-life reservoirs of SARS-CoV-2, and even seasonal alpha coronavirus NL63 that depends on human ACE2 for infection.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Evasión Inmune / Glicoproteína de la Espiga del Coronavirus / SARS-CoV-2 / COVID-19 Límite: Animals / Humans Idioma: En Revista: Viruses Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Evasión Inmune / Glicoproteína de la Espiga del Coronavirus / SARS-CoV-2 / COVID-19 Límite: Animals / Humans Idioma: En Revista: Viruses Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza