Cargando…
Ribavirin for treating Lassa fever: A systematic review of pre-clinical studies and implications for human dosing
Ribavirin is currently the standard of care for treating Lassa fever. However, the human clinical trial data supporting its use suffer from several serious flaws that render the results and conclusions unreliable. We performed a systematic review of available pre-clinical data and human pharmacokine...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000057/ https://www.ncbi.nlm.nih.gov/pubmed/35353804 http://dx.doi.org/10.1371/journal.pntd.0010289 |
_version_ | 1784685340191096832 |
---|---|
author | Salam, Alex P. Duvignaud, Alexandre Jaspard, Marie Malvy, Denis Carroll, Miles Tarning, Joel Olliaro, Piero L. Horby, Peter W. |
author_facet | Salam, Alex P. Duvignaud, Alexandre Jaspard, Marie Malvy, Denis Carroll, Miles Tarning, Joel Olliaro, Piero L. Horby, Peter W. |
author_sort | Salam, Alex P. |
collection | PubMed |
description | Ribavirin is currently the standard of care for treating Lassa fever. However, the human clinical trial data supporting its use suffer from several serious flaws that render the results and conclusions unreliable. We performed a systematic review of available pre-clinical data and human pharmacokinetic data on ribavirin in Lassa. In in-vitro studies, the EC50 of ribavirin ranged from 0.6 μg/ml to 21.72 μg/ml and the EC90 ranged from 1.5 μg/ml to 29 μg/ml. The mean EC50 was 7 μg/ml and the mean EC90 was 15 μg/ml. Human PK data in patients with Lassa fever was sparse and did not allow for estimation of concentration profiles or pharmacokinetic parameters. Pharmacokinetic modelling based on healthy human data suggests that the concentration profiles of current ribavirin regimes only exceed the mean EC50 for less than 20% of the time and the mean EC90 for less than 10% of the time, raising the possibility that the current ribavirin regimens in clinical use are unlikely to reliably achieve serum concentrations required to inhibit Lassa virus replication. The results of this review highlight serious issues with the evidence, which, by today standards, would be unlikely to support the transition of ribavirin from pre-clinical studies to human clinical trials. Additional pre-clinical studies are needed before embarking on expensive and challenging clinical trials of ribavirin in Lassa fever. |
format | Online Article Text |
id | pubmed-9000057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-90000572022-04-12 Ribavirin for treating Lassa fever: A systematic review of pre-clinical studies and implications for human dosing Salam, Alex P. Duvignaud, Alexandre Jaspard, Marie Malvy, Denis Carroll, Miles Tarning, Joel Olliaro, Piero L. Horby, Peter W. PLoS Negl Trop Dis Research Article Ribavirin is currently the standard of care for treating Lassa fever. However, the human clinical trial data supporting its use suffer from several serious flaws that render the results and conclusions unreliable. We performed a systematic review of available pre-clinical data and human pharmacokinetic data on ribavirin in Lassa. In in-vitro studies, the EC50 of ribavirin ranged from 0.6 μg/ml to 21.72 μg/ml and the EC90 ranged from 1.5 μg/ml to 29 μg/ml. The mean EC50 was 7 μg/ml and the mean EC90 was 15 μg/ml. Human PK data in patients with Lassa fever was sparse and did not allow for estimation of concentration profiles or pharmacokinetic parameters. Pharmacokinetic modelling based on healthy human data suggests that the concentration profiles of current ribavirin regimes only exceed the mean EC50 for less than 20% of the time and the mean EC90 for less than 10% of the time, raising the possibility that the current ribavirin regimens in clinical use are unlikely to reliably achieve serum concentrations required to inhibit Lassa virus replication. The results of this review highlight serious issues with the evidence, which, by today standards, would be unlikely to support the transition of ribavirin from pre-clinical studies to human clinical trials. Additional pre-clinical studies are needed before embarking on expensive and challenging clinical trials of ribavirin in Lassa fever. Public Library of Science 2022-03-30 /pmc/articles/PMC9000057/ /pubmed/35353804 http://dx.doi.org/10.1371/journal.pntd.0010289 Text en © 2022 Salam et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Salam, Alex P. Duvignaud, Alexandre Jaspard, Marie Malvy, Denis Carroll, Miles Tarning, Joel Olliaro, Piero L. Horby, Peter W. Ribavirin for treating Lassa fever: A systematic review of pre-clinical studies and implications for human dosing |
title | Ribavirin for treating Lassa fever: A systematic review of pre-clinical studies and implications for human dosing |
title_full | Ribavirin for treating Lassa fever: A systematic review of pre-clinical studies and implications for human dosing |
title_fullStr | Ribavirin for treating Lassa fever: A systematic review of pre-clinical studies and implications for human dosing |
title_full_unstemmed | Ribavirin for treating Lassa fever: A systematic review of pre-clinical studies and implications for human dosing |
title_short | Ribavirin for treating Lassa fever: A systematic review of pre-clinical studies and implications for human dosing |
title_sort | ribavirin for treating lassa fever: a systematic review of pre-clinical studies and implications for human dosing |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000057/ https://www.ncbi.nlm.nih.gov/pubmed/35353804 http://dx.doi.org/10.1371/journal.pntd.0010289 |
work_keys_str_mv | AT salamalexp ribavirinfortreatinglassafeverasystematicreviewofpreclinicalstudiesandimplicationsforhumandosing AT duvignaudalexandre ribavirinfortreatinglassafeverasystematicreviewofpreclinicalstudiesandimplicationsforhumandosing AT jaspardmarie ribavirinfortreatinglassafeverasystematicreviewofpreclinicalstudiesandimplicationsforhumandosing AT malvydenis ribavirinfortreatinglassafeverasystematicreviewofpreclinicalstudiesandimplicationsforhumandosing AT carrollmiles ribavirinfortreatinglassafeverasystematicreviewofpreclinicalstudiesandimplicationsforhumandosing AT tarningjoel ribavirinfortreatinglassafeverasystematicreviewofpreclinicalstudiesandimplicationsforhumandosing AT olliaropierol ribavirinfortreatinglassafeverasystematicreviewofpreclinicalstudiesandimplicationsforhumandosing AT horbypeterw ribavirinfortreatinglassafeverasystematicreviewofpreclinicalstudiesandimplicationsforhumandosing |