Evidence map›Paper›PMID 36897792›Full record

ArticleMolecular pharmaceutics2023

Discovery of a Non-competitive TNFR1 Antagonist Affibody with Picomolar Monovalent Potency That Does Not Affect TNFR2 Function.

Nagamani Vunnam, MaryJane Been, Evan Huber, Carolyn Paulson, Sophia Szymonski, Benjamin J Hackel, Jonathan N Sachs

Open access · greenAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Peptide-based allosteric inhibitor targets TNFR1 conformationally active region and disables receptor-ligand signaling complex.Proceedings of the National Academy of Sciences of the United States of America · 2024
    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

7 authors at 1 institution in 1 country.

Nagamani VunnamDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota 55455, United States.ORCID 0000-0003-3915-1159
MaryJane BeenDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota 55455, United States.ORCID 0000-0001-7315-616X
Evan HuberDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Carolyn PaulsonDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota 55455, United States.ORCID 0000-0001-8564-7345
Sophia SzymonskiDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Benjamin J HackelDepartment of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States.ORCID 0000-0003-3561-9463
Jonathan N SachsDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota 55455, United States.ORCID 0000-0003-1403-5960
University of Minnesota · US

Funding

Understanding the structural dynamics of TNF receptorsR35GM131814 · NIGMS · UNIVERSITY OF MINNESOTA · PI SACHS, JONATHAN N · 2019 to 2023
$2.0M
Engineering synthetic ligands with potent allosteric inhibition of tumornecrosis factor receptorsR01EB028274 · NIBIB · UNIVERSITY OF MINNESOTA · PI HACKEL, BENJAMIN, SACHS, JONATHAN N · 2019 to 2022
$1.5M
Engineering Gp2 as a small ligand scaffoldR01EB023339 · NIBIB · UNIVERSITY OF MINNESOTA · PI HACKEL, BENJAMIN · 2017 to 2020
$1.3M
NIBIB NIH HHS R01 EB023339NIBIB NIH HHS R01 EB028274NIGMS NIH HHS R35 GM131814
6 · The paper itself

Abstract

Tumor necrosis factor (TNF) is a key regulator of immune responses and plays a significant role in the initiation and maintenance of inflammation. Upregulation of TNF expression leads to several inflammatory diseases, such as Crohn's, ulcerative colitis, and rheumatoid arthritis. Despite the clinical success of anti-TNF treatments, the use of these therapies is limited because they can induce adverse side effects through inhibition of TNF biological activity, including blockade of TNF-induced immunosuppressive function of TNFR2. Using yeast display, we identified a synthetic affibody ligand (ABY

Indexed as

Receptors, Tumor Necrosis Factor, Type IReceptors, Tumor Necrosis Factor, Type IILigandsTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsLigandsReceptors, Tumor Necrosis Factor, Type IReceptors, Tumor Necrosis Factor, Type IITumor Necrosis Factor-alphaTumor Necrosis Factor Inhibitorsaffibodyinflammatory diseasesNF-κB activationTNFTNFR1yeast surface display

Identifiers

PMID36897792
PMCPMC10849843
OpenAlexW4323807086

What OpenQuestion holds

Textmetadata
LicenceTDM
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.