1. Academic Validation
  2. Adjunct Immunotherapies for the Management of Severely Ill COVID-19 Patients

Adjunct Immunotherapies for the Management of Severely Ill COVID-19 Patients

  • Cell Rep Med. 2020 May 19;1(2):100016. doi: 10.1016/j.xcrm.2020.100016.
Srinivasa Reddy Bonam 1 Srini V Kaveri 1 Anavaj Sakuntabhai 2 Laurent Gilardin 3 Jagadeesh Bayry 1
Affiliations

Affiliations

  • 1 Institut National de la Santé et de la Recherche Médicale, Centre de Recherche des Cordeliers, Equipe - Immunopathologie et Immunointervention Thérapeutique, Sorbonne Université, Université de Paris, Paris 75006, France.
  • 2 Unité de Génétique Fonctionnelle des Maladies Infectieuses, Institut Pasteur, CNRS UMR2000 Génomique Évolutive, Modélisation et Santé, Institut Pasteur, Paris 75015, France.
  • 3 Hôpital Bégin, Saint Mandé 94160, France.
Abstract

Coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It has infected millions, with more than 275,000 fatal cases as of May 8, 2020. Currently, there are no specific COVID-19 therapies. Most patients depend on mechanical ventilation. Current COVID-19 data clearly highlight that cytokine storm and activated immune cell migration to the lungs characterize the early immune response to COVID-19 that causes severe lung damage and development of acute respiratory distress syndrome. In view of uncertainty associated with immunosuppressive treatments, such as corticosteroids and their possible secondary effects, including risks of secondary infections, we suggest immunotherapies as an adjunct therapy in severe COVID-19 cases. Such immunotherapies based on inflammatory cytokine neutralization, immunomodulation, and passive viral neutralization not only reduce inflammation, inflammation-associated lung damage, or viral load but could also prevent intensive care unit hospitalization and dependency on mechanical ventilation, both of which are limited resources.

Keywords

COVID-19; IVIG; SARS-CoV-2; convalescent plasma; cytokine storm syndrome; cytokines; hyperimmune globulin; immunotherapy; inflammation; monoclonal antibody; passive immunotherapy.

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