Evidence map›Paper›PMID 37483220›Full record

ArticleACS omega2023

Design of Glycoengineered IL-4 Antagonists Employing Chemical and Biosynthetic Glycosylation.

Sarah Thomas, Juliane E Fiebig, Eva-Maria Kuhn, Dominik S Mayer, Sebastian Filbeck, Werner Schmitz, Markus Krischke, Roswitha Gropp, Thomas D Mueller

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2023. 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
1.4field-weighted citation impact, top 19% 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, 6 citations in OpenAlex.

  1. The importance of B cells for osteogenic homeostasis.Cell communication and signaling : CCS · 2026
    Article
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

9 authors at 3 institutions in 1 country.

Sarah ThomasDepartment of Molecular Plant Physiology and Biophysics, Julius-von-Sachs Institute of the University Wuerzburg, Julius-von-Sachs Platz 2, D-97082 Wuerzburg, Germany.
Juliane E FiebigDepartment of Molecular Plant Physiology and Biophysics, Julius-von-Sachs Institute of the University Wuerzburg, Julius-von-Sachs Platz 2, D-97082 Wuerzburg, Germany.
Eva-Maria KuhnDepartment of Molecular Plant Physiology and Biophysics, Julius-von-Sachs Institute of the University Wuerzburg, Julius-von-Sachs Platz 2, D-97082 Wuerzburg, Germany.
Dominik S MayerDepartment of Molecular Plant Physiology and Biophysics, Julius-von-Sachs Institute of the University Wuerzburg, Julius-von-Sachs Platz 2, D-97082 Wuerzburg, Germany.
Sebastian FilbeckDepartment of Molecular Plant Physiology and Biophysics, Julius-von-Sachs Institute of the University Wuerzburg, Julius-von-Sachs Platz 2, D-97082 Wuerzburg, Germany.
Werner SchmitzDepartment of Biochemistry and Molecular Biology, Biocenter of the University Wuerzburg, Am Hubland, D-97074 Wuerzburg, Germany.
Markus KrischkeDepartment of Pharmaceutical Biology, Julius-von-Sachs Institute of the University Wuerzburg, Julius-von-Sachs Platz 2, D-97082 Wuerzburg, Germany.
Roswitha GroppDepartment of General- Visceral-, Vascular- and Transplantation Surgery, Hospital of the LMU, Nussbaumstr. 20, 80336 Munich, Germany.
Thomas D MuellerDepartment of Molecular Plant Physiology and Biophysics, Julius-von-Sachs Institute of the University Wuerzburg, Julius-von-Sachs Platz 2, D-97082 Wuerzburg, Germany.ORCID https://orcid.org/0000-0003-1862-7357
Leibniz Association · DELMU Klinikum · DEUniversity of Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin-4 (IL-4) plays a key role in atopic diseases. It coordinates T-helper cell differentiation to subtype 2, thereby directing defense toward humoral immunity. Together with Interleukin-13, IL-4 further induces immunoglobulin class switch to IgE. Antibodies of this type activate mast cells and basophilic and eosinophilic granulocytes, which release pro-inflammatory mediators accounting for the typical symptoms of atopic diseases. IL-4 and IL-13 are thus major targets for pharmaceutical intervention strategies to treat atopic diseases. Besides neutralizing antibodies against IL-4, IL-13, or its receptors, IL-4 antagonists can present valuable alternatives. Pitrakinra, an

Identifiers

PMID37483220
PMCPMC10357448
OpenAlexW4383198391

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.