Antiviral therapies for the management of persistent coronavirus disease 2019 in immunocompromised hosts: A narrative review

Author:

Kinsella Paul M.12ORCID,Moso Michael A.23ORCID,Morrissey Catherine Orla4,Dendle Claire56,Guy Stephen78ORCID,Bond Katherine91011,Sasadeusz Joseph23,Slavin Monica A.1312ORCID

Affiliation:

1. Department of Infectious Diseases Peter MacCallum Cancer Centre Melbourne Australia

2. Department of Infectious Diseases University of Melbourne at the Doherty Institute of Infection and Immunity Melbourne Australia

3. Victorian Infectious Diseases Service Royal Melbourne Hospital at the Doherty Institute of Infection and Immunity Melbourne Australia

4. Department of Infectious Diseases Alfred Health and Monash University Melbourne Australia

5. Monash Infectious Diseases Monash Health Melbourne Australia

6. School of Clinical Sciences Monash University Melbourne Australia

7. Department of Infectious Diseases Eastern Health Melbourne Australia

8. Eastern Health Clinical School Monash University Melbourne Australia

9. Department of Microbiology Royal Melbourne Hospital Melbourne Australia

10. Victorian Infectious Diseases Reference Laboratory (VIDRL) at the Peter Doherty Institute for Infection and Immunity Melbourne Australia

11. Department of Microbiology and Immunology University of Melbourne at the Doherty Institute of Infection and Immunity Melbourne Australia

12. Sir Peter MacCallum Department of Oncology Peter MacCallum Cancer Centre Melbourne Australia

Abstract

AbstractAntiviral agents with activity against severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) have played a critical role in disease management; however, little is known regarding the efficacy of these medications in the treatment of SARS‐CoV‐2 infection in immunocompromised patients, particularly in the management of persistent SARS‐CoV‐2 positivity.This narrative review discusses the management of persistent coronavirus disease 2019 in immunocompromised hosts, with a focus on antiviral therapies. We identified 84 cases from the literature describing a variety of approaches, including prolonged antiviral therapy (n = 11), combination antivirals (n = 13), and mixed therapy with antiviral and antibody treatments (n = 60). A high proportion had an underlying haematologic malignancy (n = 67, 80%), and were in receipt of anti‐CD20 agents (n = 51, 60%). Success was reported in 70 cases (83%) which varied according to the therapy type. Combination therapies with antivirals may be an effective approach for individuals with persistent SARS‐CoV‐2 positivity, particularly those that incorporate treatments aimed at increasing neutralizing antibody levels. Any novel approaches taken to this difficult management dilemma should be mindful of the emergence of antiviral resistance.

Publisher

Wiley

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