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Nucleic Acid Polymers with Accelerated Plasma and Tissue Clearance for Chronic Hepatitis B Therapy

REP 2139 is a nucleic acid polymer (NAP) currently under clinical development for chronic hepatitis B (HBV) therapy. This preclinical study investigated different REP 2139 analogs that would display reduced accumulation in the serum and tissues, while retaining an antiviral effect against HBV infect...

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Autores principales: Roehl, Ingo, Seiffert, Stephan, Brikh, Celia, Quinet, Jonathan, Jamard, Catherine, Dorfler, Nadine, Lockridge, Jennifer A., Cova, Lucyna, Vaillant, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466589/
https://www.ncbi.nlm.nih.gov/pubmed/28918011
http://dx.doi.org/10.1016/j.omtn.2017.04.019
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author Roehl, Ingo
Seiffert, Stephan
Brikh, Celia
Quinet, Jonathan
Jamard, Catherine
Dorfler, Nadine
Lockridge, Jennifer A.
Cova, Lucyna
Vaillant, Andrew
author_facet Roehl, Ingo
Seiffert, Stephan
Brikh, Celia
Quinet, Jonathan
Jamard, Catherine
Dorfler, Nadine
Lockridge, Jennifer A.
Cova, Lucyna
Vaillant, Andrew
author_sort Roehl, Ingo
collection PubMed
description REP 2139 is a nucleic acid polymer (NAP) currently under clinical development for chronic hepatitis B (HBV) therapy. This preclinical study investigated different REP 2139 analogs that would display reduced accumulation in the serum and tissues, while retaining an antiviral effect against HBV infection. REP 2139 analogs were evaluated in human plasma, CD-1 mice, cynomolgus monkeys, and Pekin ducks. Discrete ribose transformation to 2′OH in selected riboadenosines resulted in a slow degradation in acidified human plasma that plateaued after 48 hr. REP 2165, a REP 2139 analog containing three unmodified riboadenosines equally spaced throughout the polymer, showed similar plasma clearance and tissue distribution as REP 2139 in mice and cynomolgus monkeys after a single dose. Interestingly, after repeated administration, accumulation of REP 2165 in plasma and organs was reduced, indicating a dramatically faster rate of clearance from organs after therapy was ended in both species. Both REP 2139 and REP 2165 were well tolerated at clinically relevant doses, with no alterations in liver, kidney, or hematological function. In chronic duck HBV (DHBV) infection, REP 2165 displayed significantly reduced liver accumulation after repeated dosing but retained antiviral activity similar to REP 2139. These results indicate the therapeutic potential of REP 2165 against chronic HBV infection in patients is similar to REP 2139, but with significantly reduced drug accumulation and improved tissue clearance.
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spelling pubmed-54665892017-06-16 Nucleic Acid Polymers with Accelerated Plasma and Tissue Clearance for Chronic Hepatitis B Therapy Roehl, Ingo Seiffert, Stephan Brikh, Celia Quinet, Jonathan Jamard, Catherine Dorfler, Nadine Lockridge, Jennifer A. Cova, Lucyna Vaillant, Andrew Mol Ther Nucleic Acids Original Article REP 2139 is a nucleic acid polymer (NAP) currently under clinical development for chronic hepatitis B (HBV) therapy. This preclinical study investigated different REP 2139 analogs that would display reduced accumulation in the serum and tissues, while retaining an antiviral effect against HBV infection. REP 2139 analogs were evaluated in human plasma, CD-1 mice, cynomolgus monkeys, and Pekin ducks. Discrete ribose transformation to 2′OH in selected riboadenosines resulted in a slow degradation in acidified human plasma that plateaued after 48 hr. REP 2165, a REP 2139 analog containing three unmodified riboadenosines equally spaced throughout the polymer, showed similar plasma clearance and tissue distribution as REP 2139 in mice and cynomolgus monkeys after a single dose. Interestingly, after repeated administration, accumulation of REP 2165 in plasma and organs was reduced, indicating a dramatically faster rate of clearance from organs after therapy was ended in both species. Both REP 2139 and REP 2165 were well tolerated at clinically relevant doses, with no alterations in liver, kidney, or hematological function. In chronic duck HBV (DHBV) infection, REP 2165 displayed significantly reduced liver accumulation after repeated dosing but retained antiviral activity similar to REP 2139. These results indicate the therapeutic potential of REP 2165 against chronic HBV infection in patients is similar to REP 2139, but with significantly reduced drug accumulation and improved tissue clearance. American Society of Gene & Cell Therapy 2017-05-04 /pmc/articles/PMC5466589/ /pubmed/28918011 http://dx.doi.org/10.1016/j.omtn.2017.04.019 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Roehl, Ingo
Seiffert, Stephan
Brikh, Celia
Quinet, Jonathan
Jamard, Catherine
Dorfler, Nadine
Lockridge, Jennifer A.
Cova, Lucyna
Vaillant, Andrew
Nucleic Acid Polymers with Accelerated Plasma and Tissue Clearance for Chronic Hepatitis B Therapy
title Nucleic Acid Polymers with Accelerated Plasma and Tissue Clearance for Chronic Hepatitis B Therapy
title_full Nucleic Acid Polymers with Accelerated Plasma and Tissue Clearance for Chronic Hepatitis B Therapy
title_fullStr Nucleic Acid Polymers with Accelerated Plasma and Tissue Clearance for Chronic Hepatitis B Therapy
title_full_unstemmed Nucleic Acid Polymers with Accelerated Plasma and Tissue Clearance for Chronic Hepatitis B Therapy
title_short Nucleic Acid Polymers with Accelerated Plasma and Tissue Clearance for Chronic Hepatitis B Therapy
title_sort nucleic acid polymers with accelerated plasma and tissue clearance for chronic hepatitis b therapy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5466589/
https://www.ncbi.nlm.nih.gov/pubmed/28918011
http://dx.doi.org/10.1016/j.omtn.2017.04.019
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