Evidence map›Paper›PMID 36557665›Full record

ArticleMicroorganisms2022

Toxicological and Safety Pharmacological Profiling of the Anti-Infective and Anti-Inflammatory Peptide Pep19-2.5.

Clemens Möller, Lena Heinbockel, Patrick Garidel, Thomas Gutsmann, Karl Mauss, Günther Weindl, Satoshi Fukuoka, Dominik Loser, Timm Danker, Klaus Brandenburg

Open access · goldAbstract read
In one paragraph

Article in Microorganisms, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 1 country.

Clemens MöllerLife Sciences Faculty, Albstadt-Sigmaringen University, 72488 Sigmaringen, Germany.
Lena HeinbockelBrandenburg Antiinfektiva GmbH, c/o Forschungszentrum Borstel, 23845 Borstel, Germany.
Patrick GaridelBiophysikalische Chemie, Martin-Luther-Universität Halle-Wittenberg, 06120 Halle (Saale), Germany.
Thomas GutsmannFG Biophysik, Leibniz Lungenzentrum, Forschungszentrum Borstel, 23845 Borstel, Germany.
Karl MaussBrandenburg Antiinfektiva GmbH, c/o Forschungszentrum Borstel, 23845 Borstel, Germany.
Günther WeindlAbteilung Pharmakologie und Toxikologie, Pharmazeutisches Institut, Universität Bonn, 53121 Bonn, Germany.ORCID 0000-0002-4493-7597
Satoshi FukuokaBrandenburg Antiinfektiva GmbH, c/o Forschungszentrum Borstel, 23845 Borstel, Germany.
Dominik LoserLife Sciences Faculty, Albstadt-Sigmaringen University, 72488 Sigmaringen, Germany.
Timm DankerNMI-TT GmbH, 72770 Reutlingen, Germany.
Klaus BrandenburgBrandenburg Antiinfektiva GmbH, c/o Forschungszentrum Borstel, 23845 Borstel, Germany.
Research Center Borstel - Leibniz Lung Center · DENatural and Medical Sciences Institute · DEAlbstadt-Sigmaringen University · DEMartin Luther University Halle-Wittenberg · DEUniversity of Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

antiinfectiveantiinflammatoryantimicrobial peptidesepsis

Identifiers

PMID36557665
PMCPMC9782211
OpenAlexW4311633591

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.