Risk of Severe COVID-19 in Four Immunocompromised Populations: A French Expert Perspective.

Paul Loubet, Ilies Benotmane, Slim Fourati, Florent Malard, Fanny Vuotto, Elodie Blanchard, François Raffi, Stéphanie Nguyen, Nicolas de Prost, Jérôme Avouac
Author Information
  1. Paul Loubet: VBIC, INSERM U1047, Université de Montpellier, Service des Maladies Infectieuses et Tropicales, Centre Hospitalier Universitaire (CHU) de Nîmes, Place du Pr Robert Debré, 30029, Nîmes Cedex 9, France. paul.loubet@chu-nimes.fr. ORCID
  2. Ilies Benotmane: Service de Nephrologie-Dialyse-Transplantation, CHU de Strasbourg, Strasbourg, France. ORCID
  3. Slim Fourati: Université Paris-Est-Créteil (UPEC), Créteil, France.
  4. Florent Malard: Sorbonne Université, Centre de Recherche Saint-Antoine, INSERM UMRs938, Service d'Hématologie Clinique et de Thérapie Cellulaire, AP-HP Hôpital Saint-Antoine, Paris, France. ORCID
  5. Fanny Vuotto: Service de Maladies Infectieuses, CHU de Lille, Lille, France.
  6. Elodie Blanchard: Service de Pneumologie, Hôpital Haut Lévêque, CHU de Bordeaux, Pessac, France. ORCID
  7. François Raffi: Department of Infectious Diseases, INSERM CIC 1413, Nantes Université, CHU de Nantes, Nantes, France.
  8. Stéphanie Nguyen: Sorbonne Université, INSERM U1135, CNRS EMR 8255, Centre d'Immunologie et des Maladies Infectieuses (CIMI), Service d'Hématologie et de Thérapies Cellulaires, AP-HP Hôpital de la Pitié-Salpêtrière, Paris, France.
  9. Nicolas de Prost: Université Paris-Est-Créteil (UPEC), Créteil, France. ORCID
  10. Jérôme Avouac: Service de Rhumatologie, Hôpital Cochin, AP-HP Centre Université Paris Cité, INSERM U1016/UMR 8104, Paris, France.

Abstract

Immunocompromised patients are disproportionately impacted by severe disease, hospitalization, and mortality associated with coronavirus disease 2019 (COVID-19). To optimize the management of these patients in clinical practice, we convened an expert panel to review current evidence on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine responses and severe COVID-19 in immunocompromised populations. We identified four main immunocompromised groups-solid organ transplant recipients, patients receiving allogeneic hematopoietic stem cell transplantation or chimeric antigen receptor (CAR) T cell therapy, patients treated for hematologic malignancies, and patients treated for inflammatory diseases-who mount suboptimal humoral responses to SARS-CoV-2 vaccination and are at increased risk of severe COVID-19-related outcomes. A wide range of risk factors were associated with reduced vaccine responses and/or poor outcomes, most commonly older age, comorbidities, and the type and number of immunosuppressive therapies. We believe that early identification and close monitoring of these at-risk patients, plus regular booster vaccinations, prophylactic monoclonal antibody therapy, non-pharmacologic prevention measures, prompt antiviral treatment, and other risk mitigation strategies, are critical to protect against SARS-CoV-2 infection and severe COVID-19.

Keywords

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