Literature DB >> 35153198

Pharmacological Profiling of Antifentanyl Monoclonal Antibodies in Combination with Naloxone in Pre- and Postexposure Models of Fentanyl Toxicity.

Carly A Baehr1, Mariah M Wu2, Sujata G Pandit2, Jose Arias-Umana2, David AuCoin2, Marco Pravetoni2.   

Abstract

The incidence of fatal drug overdoses in the United States is an alarming public health threat that has been exacerbated by the COVID-19 pandemic, resulting in over 100,000 deaths between April 2020 and April 2021. A significant portion of this is attributable to widespread access to fentanyl and other synthetic opioids, alone or in combination with heroin or psychostimulants, such as cocaine or methamphetamine. Monoclonal antibodies (mAb) offer prophylactic and therapeutic interventions against opioid overdose by binding opioids in serum, reducing distribution of drug to the brain and other organs. Here, we investigated the efficacy of a leading antifentanyl mAb, clone HY6-F9, in reversal and prevention of fentanyl-induced toxicity compared with the opioid receptor antagonist naloxone (NLX) in rats. In postexposure models, rats were challenged with fentanyl, followed by HY6-F9, NLX, or both. HY6-F9 reversed fentanyl-induced antinociception, respiratory depression, and bradycardia, and rats retained protection against additional challenges for at least 1 week. Although intravenous NLX reversed fentanyl-induced respiratory depression more rapidly than mAb alone, kinetics of reversal by intravenous mAb were similar to subcutaneous NLX. Coadministration of mAb and NLX provided greater protection than individual treatments against high doses of fentanyl. Prophylactic administration of mAb reduced the ED50 of NLX approximately twofold against 2.25 mg/kg of fentanyl. Finally, mAb sequestered fentanyl and its metabolite norfentanyl in serum and reduced brain concentrations of fentanyl. These results support the translation of mAb as medical interventions alone or in combination with NLX to prevent and reverse fentanyl-related overdose. SIGNIFICANCE STATEMENT: Fentanyl-related overdoses have increased dramatically in the US and worldwide. Currently, approved pharmacotherapies for treatment of opioid use disorder and reversal of overdose are not sufficient to curb the incidence of opioid-related deaths. Additionally, fentanyl and its potent analogs present a potential risk from use in deliberate poisoning or chemical attacks. This study demonstrates the use of monoclonal antibodies as a countermeasure to fentanyl-induced toxicity in pre- and postexposure scenarios, supporting their use in combination with the opioid antagonist naloxone.
Copyright © 2022 by The American Society for Pharmacology and Experimental Therapeutics.

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Year:  2022        PMID: 35153198      PMCID: PMC9048265          DOI: 10.1124/jpet.121.001048

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.402


  21 in total

Review 1.  Naloxone dosage for opioid reversal: current evidence and clinical implications.

Authors:  Rachael Rzasa Lynn; J L Galinkin
Journal:  Ther Adv Drug Saf       Date:  2017-12-13

2.  The effects of a repeated dose of a recombinant humanized anti-cocaine monoclonal antibody on cocaine self-administration in rats.

Authors:  Hanna N Wetzel; Vladimir L Tsibulsky; Andrew B Norman
Journal:  Drug Alcohol Depend       Date:  2016-10-06       Impact factor: 4.492

3.  Monoclonal nicotine-specific antibodies reduce nicotine distribution to brain in rats: dose- and affinity-response relationships.

Authors:  D E Keyler; S A Roiko; E Benlhabib; M G LeSage; J V St Peter; S Stewart; S Fuller; C T Le; P R Pentel
Journal:  Drug Metab Dispos       Date:  2005-04-20       Impact factor: 3.922

4.  Fentanyl causes naloxone-resistant vocal cord closure: A platform for testing opioid overdose treatments.

Authors:  Nicholas B Miner; William E Schutzer; Yalda Zarnegarnia; Aaron Janowsky; Randy Torralva
Journal:  Drug Alcohol Depend       Date:  2021-08-28       Impact factor: 4.492

Review 5.  Noradrenergic Mechanisms in Fentanyl-Mediated Rapid Death Explain Failure of Naloxone in the Opioid Crisis.

Authors:  Randy Torralva; Aaron Janowsky
Journal:  J Pharmacol Exp Ther       Date:  2019-09-06       Impact factor: 4.030

6.  A Monoclonal Antibody against 6-Acetylmorphine Protects Female Mice Offspring from Adverse Behavioral Effects Induced by Prenatal Heroin Exposure.

Authors:  Anne Marte Sjursen Kvello; Jannike Mørch Andersen; Elisabeth Leere Øiestad; Synne Steinsland; Audun Aase; Jørg Mørland; Inger Lise Bogen
Journal:  J Pharmacol Exp Ther       Date:  2018-10-25       Impact factor: 4.030

7.  Fentanyl depression of respiration: Comparison with heroin and morphine.

Authors:  Rob Hill; Rakulan Santhakumar; William Dewey; Eamonn Kelly; Graeme Henderson
Journal:  Br J Pharmacol       Date:  2019-12-23       Impact factor: 8.739

8.  First human study of a chimeric anti-methamphetamine monoclonal antibody in healthy volunteers.

Authors:  Misty W Stevens; Ralph L Henry; S Michael Owens; Ralph Schutz; W Brooks Gentry
Journal:  MAbs       Date:  2014       Impact factor: 5.857

9.  Higher naloxone dosing in a quantitative systems pharmacology model that predicts naloxone-fentanyl competition at the opioid mu receptor level.

Authors:  Ronald B Moss; Meghan McCabe Pryor; Rebecca Baillie; Katherine Kudrycki; Christina Friedrich; Mike Reed; Dennis J Carlo
Journal:  PLoS One       Date:  2020-06-16       Impact factor: 3.240

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