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An Engineered Human-Antibody Fragment with Fentanyl Pan-Specificity that Reverses Carfentanil-Induced Respiratory Depression

The opioid overdose crisis primarily driven by potent synthetic opioids resulted in more than 500,000 deaths in the US over the last 20 years. Though naloxone, a short acting medication, remains the primary treatment option for temporarily reversing opioid overdose effects, alternative countermeasur...

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Autores principales: Eubanks, Lisa M., Pholcharee, Tossapol, Oyen, David, Natori, Yoshihiro, Zhou, Bin, Wilson, Ian A., Janda, Kim D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349930/
https://www.ncbi.nlm.nih.gov/pubmed/37461607
http://dx.doi.org/10.1101/2023.07.04.547721
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author Eubanks, Lisa M.
Pholcharee, Tossapol
Oyen, David
Natori, Yoshihiro
Zhou, Bin
Wilson, Ian A.
Janda, Kim D.
author_facet Eubanks, Lisa M.
Pholcharee, Tossapol
Oyen, David
Natori, Yoshihiro
Zhou, Bin
Wilson, Ian A.
Janda, Kim D.
author_sort Eubanks, Lisa M.
collection PubMed
description The opioid overdose crisis primarily driven by potent synthetic opioids resulted in more than 500,000 deaths in the US over the last 20 years. Though naloxone, a short acting medication, remains the primary treatment option for temporarily reversing opioid overdose effects, alternative countermeasures are needed. Monoclonal antibodies present a versatile therapeutic opportunity that can be tailored for synthetic opioids and that can help prevent post-treatment renarcotization. The ultrapotent analog carfentanil, is especially concerning due to its unique pharmacological properties. With this in mind, we generated a fully human antibody through a drug-specific B cell sorting strategy with a combination of carfentanil and fentanyl probes. The resulting pan-specific antibody was further optimized through scFv phage display. This antibody, C10-S66K, displays high affinity to carfentanil, fentanyl, and other analogs, and reversed carfentanil-induced respiratory depression. Additionally, x-ray crystal structures with carfentanil and fentanyl bound provided structural insight into key drug:antibody interactions.
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spelling pubmed-103499302023-07-17 An Engineered Human-Antibody Fragment with Fentanyl Pan-Specificity that Reverses Carfentanil-Induced Respiratory Depression Eubanks, Lisa M. Pholcharee, Tossapol Oyen, David Natori, Yoshihiro Zhou, Bin Wilson, Ian A. Janda, Kim D. bioRxiv Article The opioid overdose crisis primarily driven by potent synthetic opioids resulted in more than 500,000 deaths in the US over the last 20 years. Though naloxone, a short acting medication, remains the primary treatment option for temporarily reversing opioid overdose effects, alternative countermeasures are needed. Monoclonal antibodies present a versatile therapeutic opportunity that can be tailored for synthetic opioids and that can help prevent post-treatment renarcotization. The ultrapotent analog carfentanil, is especially concerning due to its unique pharmacological properties. With this in mind, we generated a fully human antibody through a drug-specific B cell sorting strategy with a combination of carfentanil and fentanyl probes. The resulting pan-specific antibody was further optimized through scFv phage display. This antibody, C10-S66K, displays high affinity to carfentanil, fentanyl, and other analogs, and reversed carfentanil-induced respiratory depression. Additionally, x-ray crystal structures with carfentanil and fentanyl bound provided structural insight into key drug:antibody interactions. Cold Spring Harbor Laboratory 2023-07-04 /pmc/articles/PMC10349930/ /pubmed/37461607 http://dx.doi.org/10.1101/2023.07.04.547721 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Eubanks, Lisa M.
Pholcharee, Tossapol
Oyen, David
Natori, Yoshihiro
Zhou, Bin
Wilson, Ian A.
Janda, Kim D.
An Engineered Human-Antibody Fragment with Fentanyl Pan-Specificity that Reverses Carfentanil-Induced Respiratory Depression
title An Engineered Human-Antibody Fragment with Fentanyl Pan-Specificity that Reverses Carfentanil-Induced Respiratory Depression
title_full An Engineered Human-Antibody Fragment with Fentanyl Pan-Specificity that Reverses Carfentanil-Induced Respiratory Depression
title_fullStr An Engineered Human-Antibody Fragment with Fentanyl Pan-Specificity that Reverses Carfentanil-Induced Respiratory Depression
title_full_unstemmed An Engineered Human-Antibody Fragment with Fentanyl Pan-Specificity that Reverses Carfentanil-Induced Respiratory Depression
title_short An Engineered Human-Antibody Fragment with Fentanyl Pan-Specificity that Reverses Carfentanil-Induced Respiratory Depression
title_sort engineered human-antibody fragment with fentanyl pan-specificity that reverses carfentanil-induced respiratory depression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349930/
https://www.ncbi.nlm.nih.gov/pubmed/37461607
http://dx.doi.org/10.1101/2023.07.04.547721
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