SARS-CoV-2 viral load dynamics in immunocompromised critically ill patients on remdesivir treatment.

Lahmer, Tobias; Erber, Johanna; Schmid, Roland M; Schneider, Jochen; Spinner, Christoph D; Luppa, Peter; Sörgel, Fritz; Kinzig, Martina; Rasch, Sebastian

doi:10.4081/mrm.2022.825

2022

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Title:: SARS-CoV-2 viral load dynamics in immunocompromised critically ill patients on remdesivir treatment.
Document type:: Article; Journal Article
Author(s):: Lahmer, Tobias; Erber, Johanna; Schmid, Roland M; Schneider, Jochen; Spinner, Christoph D; Luppa, Peter; Sörgel, Fritz; Kinzig, Martina; Rasch, Sebastian
Abstract:: The relationship between SARS-CoV-2 quantitative viral load and risk of disease progression, morbidity such as long- COVID or mortality in immunosuppressed, remains largely undefined in COVID-19 patients. Critically ill immunosuppressed patients potentially benefit from remdesivir treatment because of the prolonged course of their infection. Four critically ill immunocompromised patients and the impact of remdesivir on viral dynamics in lower respiratory samples were studied. Bronchoalveolar lavage (BAL) samples were assessed to measure SARS-CoV-2 quantitative viral load using real-time PCR. Corresponding plasma levels of remdesivir and its metabolite GS-441524 were determined. Mean virus load of 39.74 x 107 geq/ml (±33.25 x 107 geq/ml) on day 1 dropped significantly (p<0.008) to 3.54 x 106 geq/ml (±6.93 x 106 geq/ml) on day 3 and to 1.4 x 105 geq/ml (±2.35 x 105 geq/ml) on day 5 of remdesivir treatment. Mean virus load dropped below <1% between day 1 and 5 of remdesivir treatment. Parent prodrug remdesivir and also GS441524 metabolite levels of antiviral activity in our patients were far in excess of EC 50. Our data present that remdesivir treatment potentially reduces the SARS-CoV-2 viral load in immunosuppressed critically ill patients. However, the implication of viral load reduction on morbidity and mortality needs further investigation.
Journal title abbreviation:: Multidiscip Respir Med
Year:: 2022
Journal volume:: 17
Fulltext / DOI:: doi:10.4081/mrm.2022.825
Pubmed ID:: http://view.ncbi.nlm.nih.gov/pubmed/35646346
Print-ISSN:: 1828-695X
TUM Institution:: Institut für Klinische Chemie und Pathobiochemie; Klinik und Poliklinik für Innere Medizin II, Gastroenterologie
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