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Toxicological and Safety Pharmacological Profiling of the Anti-Infective and Anti-Inflammatory Peptide Pep19-2.5
Aspidasept (Pep19-2.5) and its derivative Pep19-4LF (“Aspidasept II”) are anti-infective and anti-inflammatory synthetic polypeptides currently in development for application against a variety of moderate to severe bacterial infections that could lead to systemic inflammation, as in the case of seve...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782211/ https://www.ncbi.nlm.nih.gov/pubmed/36557665 http://dx.doi.org/10.3390/microorganisms10122412 |
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author | Möller, Clemens Heinbockel, Lena Garidel, Patrick Gutsmann, Thomas Mauss, Karl Weindl, Günther Fukuoka, Satoshi Loser, Dominik Danker, Timm Brandenburg, Klaus |
author_facet | Möller, Clemens Heinbockel, Lena Garidel, Patrick Gutsmann, Thomas Mauss, Karl Weindl, Günther Fukuoka, Satoshi Loser, Dominik Danker, Timm Brandenburg, Klaus |
author_sort | Möller, Clemens |
collection | PubMed |
description | Aspidasept (Pep19-2.5) and its derivative Pep19-4LF (“Aspidasept II”) are anti-infective and anti-inflammatory synthetic polypeptides currently in development for application against a variety of moderate to severe bacterial infections that could lead to systemic inflammation, as in the case of severe sepsis and septic shock, as well as application to non-systemic diseases in the case of skin and soft tissue infections (SSTI). In the present study, Aspidasept and Aspidasept II and their part structures were analysed with respect to their toxic behavior in different established models against a variety of relevant cells, and in electrophysiological experiments targeting the hERG channel according to ICH S7B. Furthermore, the effects in mouse models of neurobiological behavior and the local lymph node according to OECD test guideline 429 were investigated, as well as a rat model of repeated dose toxicology according to ICH M3. The data provide conclusive information about potential toxic effects, thus specifying a therapeutic window for the application of the peptides. Therefore, these data allow us to define Aspidasept concentrations for their use in clinical studies as parenteral application. |
format | Online Article Text |
id | pubmed-9782211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97822112022-12-24 Toxicological and Safety Pharmacological Profiling of the Anti-Infective and Anti-Inflammatory Peptide Pep19-2.5 Möller, Clemens Heinbockel, Lena Garidel, Patrick Gutsmann, Thomas Mauss, Karl Weindl, Günther Fukuoka, Satoshi Loser, Dominik Danker, Timm Brandenburg, Klaus Microorganisms Article Aspidasept (Pep19-2.5) and its derivative Pep19-4LF (“Aspidasept II”) are anti-infective and anti-inflammatory synthetic polypeptides currently in development for application against a variety of moderate to severe bacterial infections that could lead to systemic inflammation, as in the case of severe sepsis and septic shock, as well as application to non-systemic diseases in the case of skin and soft tissue infections (SSTI). In the present study, Aspidasept and Aspidasept II and their part structures were analysed with respect to their toxic behavior in different established models against a variety of relevant cells, and in electrophysiological experiments targeting the hERG channel according to ICH S7B. Furthermore, the effects in mouse models of neurobiological behavior and the local lymph node according to OECD test guideline 429 were investigated, as well as a rat model of repeated dose toxicology according to ICH M3. The data provide conclusive information about potential toxic effects, thus specifying a therapeutic window for the application of the peptides. Therefore, these data allow us to define Aspidasept concentrations for their use in clinical studies as parenteral application. MDPI 2022-12-06 /pmc/articles/PMC9782211/ /pubmed/36557665 http://dx.doi.org/10.3390/microorganisms10122412 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Möller, Clemens Heinbockel, Lena Garidel, Patrick Gutsmann, Thomas Mauss, Karl Weindl, Günther Fukuoka, Satoshi Loser, Dominik Danker, Timm Brandenburg, Klaus Toxicological and Safety Pharmacological Profiling of the Anti-Infective and Anti-Inflammatory Peptide Pep19-2.5 |
title | Toxicological and Safety Pharmacological Profiling of the Anti-Infective and Anti-Inflammatory Peptide Pep19-2.5 |
title_full | Toxicological and Safety Pharmacological Profiling of the Anti-Infective and Anti-Inflammatory Peptide Pep19-2.5 |
title_fullStr | Toxicological and Safety Pharmacological Profiling of the Anti-Infective and Anti-Inflammatory Peptide Pep19-2.5 |
title_full_unstemmed | Toxicological and Safety Pharmacological Profiling of the Anti-Infective and Anti-Inflammatory Peptide Pep19-2.5 |
title_short | Toxicological and Safety Pharmacological Profiling of the Anti-Infective and Anti-Inflammatory Peptide Pep19-2.5 |
title_sort | toxicological and safety pharmacological profiling of the anti-infective and anti-inflammatory peptide pep19-2.5 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782211/ https://www.ncbi.nlm.nih.gov/pubmed/36557665 http://dx.doi.org/10.3390/microorganisms10122412 |
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