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Combination therapy with nirmatrelvir and molnupiravir improves the survival of SARS-CoV-2 infected mice

As the SARS-CoV-2 pandemic remains uncontrolled owing to the continuous emergence of variants of concern, there is an immediate need to implement the most effective antiviral treatment strategies, especially for risk groups. Here, we evaluated the therapeutic potency of nirmatrelvir, remdesivir and...

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Autores principales: Jeong, Ju Hwan, Chokkakula, Santosh, Min, Seong Cheol, Kim, Beom Kyu, Choi, Won-Suk, Oh, Sol, Yun, Yu Soo, Kang, Da Hyeon, Lee, Ok-Jun, Kim, Eung-Gook, Choi, Jang-Hoon, Lee, Joo-Yeon, Choi, Young Ki, Baek, Yun Hee, Song, Min-Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier B.V. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535923/
https://www.ncbi.nlm.nih.gov/pubmed/36209984
http://dx.doi.org/10.1016/j.antiviral.2022.105430
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author Jeong, Ju Hwan
Chokkakula, Santosh
Min, Seong Cheol
Kim, Beom Kyu
Choi, Won-Suk
Oh, Sol
Yun, Yu Soo
Kang, Da Hyeon
Lee, Ok-Jun
Kim, Eung-Gook
Choi, Jang-Hoon
Lee, Joo-Yeon
Choi, Young Ki
Baek, Yun Hee
Song, Min-Suk
author_facet Jeong, Ju Hwan
Chokkakula, Santosh
Min, Seong Cheol
Kim, Beom Kyu
Choi, Won-Suk
Oh, Sol
Yun, Yu Soo
Kang, Da Hyeon
Lee, Ok-Jun
Kim, Eung-Gook
Choi, Jang-Hoon
Lee, Joo-Yeon
Choi, Young Ki
Baek, Yun Hee
Song, Min-Suk
author_sort Jeong, Ju Hwan
collection PubMed
description As the SARS-CoV-2 pandemic remains uncontrolled owing to the continuous emergence of variants of concern, there is an immediate need to implement the most effective antiviral treatment strategies, especially for risk groups. Here, we evaluated the therapeutic potency of nirmatrelvir, remdesivir and molnupiravir, and their combinations in SARS-CoV-2 infected K18-hACE2 transgenic mice. Systemic treatment of mice with each drug (20 mg/kg) resulted in slightly enhanced antiviral efficacy and yielded an increased life expectancy of only about 20–40% survival. However, combination therapy with nirmatrelvir (20 mg/kg) and molnupiravir (20 mg/kg) in lethally infected mice showed profound inhibition of SARS-CoV-2 replication in both the lung and brain and synergistically improved survival rates up to 80% compared to those with nirmatrelvir (36%, P < 0.001) and molnupiravir (43%, P < 0.001) administered alone. This combination therapy effectively reduced clinical severity score, virus-induced tissue damage, and viral distribution compared to those in animals treated with these monotherapies. Furthermore, all these assessments associated with this combination were also significantly higher than that of mice receiving remdesivir monotherapy (P < 0.001) and the nirmatrelvir (20 mg/kg) and remdesivir (20 mg/kg) combination (P < 0.001), underscored the clinical significance of this combination. By contrast, the nirmatrelvir and remdesivir combination showed less antiviral efficacy, with lower survival compared to nirmatrelvir monotherapy due to the insufficient plasma exposure of the remdesivir, demonstrating the inefficient therapeutic effect of this combination in the mouse model. The combination therapy with nirmatrelvir and molnupiravir contributes to alleviated morbidity and mortality, which can serve as a basis for the design of clinical studies of this combination in the treatment of COVID-19 patients.
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spelling pubmed-95359232022-10-06 Combination therapy with nirmatrelvir and molnupiravir improves the survival of SARS-CoV-2 infected mice Jeong, Ju Hwan Chokkakula, Santosh Min, Seong Cheol Kim, Beom Kyu Choi, Won-Suk Oh, Sol Yun, Yu Soo Kang, Da Hyeon Lee, Ok-Jun Kim, Eung-Gook Choi, Jang-Hoon Lee, Joo-Yeon Choi, Young Ki Baek, Yun Hee Song, Min-Suk Antiviral Res Article As the SARS-CoV-2 pandemic remains uncontrolled owing to the continuous emergence of variants of concern, there is an immediate need to implement the most effective antiviral treatment strategies, especially for risk groups. Here, we evaluated the therapeutic potency of nirmatrelvir, remdesivir and molnupiravir, and their combinations in SARS-CoV-2 infected K18-hACE2 transgenic mice. Systemic treatment of mice with each drug (20 mg/kg) resulted in slightly enhanced antiviral efficacy and yielded an increased life expectancy of only about 20–40% survival. However, combination therapy with nirmatrelvir (20 mg/kg) and molnupiravir (20 mg/kg) in lethally infected mice showed profound inhibition of SARS-CoV-2 replication in both the lung and brain and synergistically improved survival rates up to 80% compared to those with nirmatrelvir (36%, P < 0.001) and molnupiravir (43%, P < 0.001) administered alone. This combination therapy effectively reduced clinical severity score, virus-induced tissue damage, and viral distribution compared to those in animals treated with these monotherapies. Furthermore, all these assessments associated with this combination were also significantly higher than that of mice receiving remdesivir monotherapy (P < 0.001) and the nirmatrelvir (20 mg/kg) and remdesivir (20 mg/kg) combination (P < 0.001), underscored the clinical significance of this combination. By contrast, the nirmatrelvir and remdesivir combination showed less antiviral efficacy, with lower survival compared to nirmatrelvir monotherapy due to the insufficient plasma exposure of the remdesivir, demonstrating the inefficient therapeutic effect of this combination in the mouse model. The combination therapy with nirmatrelvir and molnupiravir contributes to alleviated morbidity and mortality, which can serve as a basis for the design of clinical studies of this combination in the treatment of COVID-19 patients. The Authors. Published by Elsevier B.V. 2022-12 2022-10-06 /pmc/articles/PMC9535923/ /pubmed/36209984 http://dx.doi.org/10.1016/j.antiviral.2022.105430 Text en © 2022 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Jeong, Ju Hwan
Chokkakula, Santosh
Min, Seong Cheol
Kim, Beom Kyu
Choi, Won-Suk
Oh, Sol
Yun, Yu Soo
Kang, Da Hyeon
Lee, Ok-Jun
Kim, Eung-Gook
Choi, Jang-Hoon
Lee, Joo-Yeon
Choi, Young Ki
Baek, Yun Hee
Song, Min-Suk
Combination therapy with nirmatrelvir and molnupiravir improves the survival of SARS-CoV-2 infected mice
title Combination therapy with nirmatrelvir and molnupiravir improves the survival of SARS-CoV-2 infected mice
title_full Combination therapy with nirmatrelvir and molnupiravir improves the survival of SARS-CoV-2 infected mice
title_fullStr Combination therapy with nirmatrelvir and molnupiravir improves the survival of SARS-CoV-2 infected mice
title_full_unstemmed Combination therapy with nirmatrelvir and molnupiravir improves the survival of SARS-CoV-2 infected mice
title_short Combination therapy with nirmatrelvir and molnupiravir improves the survival of SARS-CoV-2 infected mice
title_sort combination therapy with nirmatrelvir and molnupiravir improves the survival of sars-cov-2 infected mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535923/
https://www.ncbi.nlm.nih.gov/pubmed/36209984
http://dx.doi.org/10.1016/j.antiviral.2022.105430
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