Evidence map›Paper›PMID 41142466›Full record

Articlenpj biomedical innovations2025

Indoleamine 2,3-dioxygenase-galectin-3 fusion protein remodels inflammatory and fibrotic programs, ameliorating imiquimod-induced psoriasis.

Jennifer A Simonovich, Sabrina L Macias, Mingqi Zhou, Marija Portelli, Isha Verma, Arun Wanchoo, Alexander J Kwiatkowski, Eric Y Helm, Tran B Ngo, Shamima Islam and 7 more

Abstract read
In one paragraph

Article in npj biomedical innovations, 2025. 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
–field-weighted citation impact
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.

  1. 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

17 authors.

Jennifer A Simonovich *J. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL USA.
Sabrina L Macias *J. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL USA.
Mingqi Zhou *J. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL USA.
Marija PortelliJ. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL USA.
Isha VermaJ. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL USA.
Arun WanchooJ. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL USA.
Alexander J KwiatkowskiJ. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL USA.
Eric Y HelmDepartment of Anatomy and Cell Biology, College of Medicine, University of Florida, Gainesville, FL USA.
Tran B NgoJ. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL USA.
Shamima IslamDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL USA.
Carlos Moran SeguraAdv Analytic Digital Lab, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL USA.
Jonathan V NguyenAdv Analytic Digital Lab, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL USA.
Robert MaileDepartment of Surgery, College of Medicine, University of Florida, Gainesville, FL USA.
Shannon M WalletDepartment of Oral Biology, College of Dentistry, University of Florida, Gainesville, FL USA.
Gregory A HudallaJ. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL USA.
Dorina AvramDepartment of Anatomy and Cell Biology, College of Medicine, University of Florida, Gainesville, FL USA.
Benjamin G KeselowskyJ. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL USA.

Funding

Tissue-Anchored vs. Circulating Engineered Enzyme Constructs for Immunometabolic Resolution of PsoriasisR01AI171045 · NIAID · UNIVERSITY OF FLORIDA · PI Dorina Avram, Benjamin George Keselowsky · 2023 to 2026
$3.1M
Diversity Supplement: Directing Tryptophan Immunometabolism to Ameliorate Liver Ischemic-Reperfusion InjuryR01DK129690 · NIDDK · UNIVERSITY OF FLORIDA · PI KESELOWSKY, BENJAMIN GEORGE, ZARRINPAR, ALI · 2022 to 2025
$2.7M
Tissue-Targeted Enzyme for Localized Tryptophan Catabolism to Direct Subcutaneous and Oral Mucosal Inflammatory ResponsesR01DE027301 · NIDCR · UNIVERSITY OF FLORIDA · PI KESELOWSKY, BENJAMIN GEORGE · 2017 to 2020
$2.0M
NIAID NIH HHS R01 AI171045NIDCR NIH HHS R01 DE027301NIDDK NIH HHS R01 DK129690
6 · The paper itself

Abstract

Localized anti-inflammatory treatment options for psoriasis are limited. Addressing this, a fusion protein was created consisting of the regulatory enzyme indoleamine 2,3-dioxygenase (IDO) fused to carbohydrate-binding protein galectin-3 (Gal3), termed IDO-Gal3, and therapeutic potential was investigated in a murine model of imiquimod-induced psoriasis. Prior work established that Gal3 fusion provides prolonged localized tissue retention of injected fusion protein, which colocalizes therapeutic to the site of inflammation, limits systemic distribution, and reduces potential for off-target side-effects. A single subcutaneous administration at disease onset remarkably decreased the disease metrics of skin redness, scaling and thickening, as measured by the psoriasis area and severity index (PASI) composite score. Infiltrating immune cells, particularly neutrophils and gamma delta T cells, and inflammatory responses were significantly reduced. Transcriptomic analyses indicated inflammation and fibrosis-associated programs were also substantially reduced following IDO-Gal3 treatment. These data demonstrate IDO-Gal3 treatment ameliorated psoriasis with concomitant remodeling of inflammatory and fibrotic programs.

Indexed as

BiotechnologyDrug discoveryImmunologyMolecular medicine

Identifiers

PMID41142466
PMCPMC12545190

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.