Severe Acute Respiratory Syndrome Coronavirus 2 Monoclonal Antibody Combination Therapy in Patients With Coronavirus Disease 2019 and Primary Antibody Deficiency

Abstract Background Previous reports highlighted the efficacy of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-specific monoclonal antibodies (mAbs) against coronavirus disease 2019. Methods We conducted a prospective study on the clinical outcome and antiviral effects of mAbs added t...

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Published inThe Journal of infectious diseases Vol. 225; no. 5; pp. 820 - 824
Main Authors Pulvirenti, Federica, Milito, Cinzia, Cinetto, Francesco, Fernandez Salinas, Ane, Terreri, Sara, Piano Mortari, Eva, Auria, Stefania, Soccodato, Valentina, Miriam, Lichtner, Nicastri, Emanuele, Vincenzi, Laura, Carsetti, Rita, D’Offizi, Gianpiero, Quinti, Isabella
Format Journal Article
LanguageEnglish
Published US Oxford University Press 02.03.2022
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Summary:Abstract Background Previous reports highlighted the efficacy of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-specific monoclonal antibodies (mAbs) against coronavirus disease 2019. Methods We conducted a prospective study on the clinical outcome and antiviral effects of mAbs added to standard of care therapy in SARS-CoV-2-infected patients with primary antibody defects. Results Median time of SARS-CoV-2 quantitative polymerase chain reaction (qPCR) positivity was shorter in 8 patients treated with mAbs (22 days) than in 10 patients treated with standard of care therapy only (37 days, P=.026). Median time of SARS-CoV-2 qPCR positivity from mAb administration was 10 days. Conclusions The SARS-CoV-2 mAbs treatment was effective and well tolerated in patients with primary antibody defects. Anti-SARS-CoV-2 monoclonal antibodies are emerging as a potential therapeutic option for high-risk patients. Here we showed that early administration of monoclonal antibodies in patients with primary antibody defects and COVID-19 reduced the time of viral replication and avoid disease evolution.
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F. P. and C. M. are co-first authors.
ISSN:0022-1899
1537-6613
DOI:10.1093/infdis/jiab554