Evidence map›Paper›PMID 41053100›Full record

ArticleCell death & disease2025

Transferrin is a drug candidate for the treatment of dry age-related macular degeneration (AMD).

Jenny Youale, Karine Bigot, Thara Jaworski, Cécile Lebon, Anaïs Françon, Kimberley Delaunay, Romain Bénard, Thaïs De Bastard, Alejandra Daruich, Naël Kaddour and 3 more

Abstract read
In one paragraph

Article in Cell death & disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

13 authors.

Jenny YoualeCentre de Recherche des Cordeliers, Inserm, Physiopathology of Ocular Diseases to Clinical Development, Université Paris Cité, Sorbonne Université, Paris, France.
Karine BigotPulseSight Therapeutics (formerly Eyevensys), Paris, France.
Thara JaworskiCentre de Recherche des Cordeliers, Inserm, Physiopathology of Ocular Diseases to Clinical Development, Université Paris Cité, Sorbonne Université, Paris, France.
Cécile LebonCentre de Recherche des Cordeliers, Inserm, Physiopathology of Ocular Diseases to Clinical Development, Université Paris Cité, Sorbonne Université, Paris, France.
Anaïs FrançonCentre de Recherche des Cordeliers, Inserm, Physiopathology of Ocular Diseases to Clinical Development, Université Paris Cité, Sorbonne Université, Paris, France.
Kimberley DelaunayCentre de Recherche des Cordeliers, Inserm, Physiopathology of Ocular Diseases to Clinical Development, Université Paris Cité, Sorbonne Université, Paris, France.
Romain BénardPulseSight Therapeutics (formerly Eyevensys), Paris, France.
Thaïs De BastardCentre de Recherche des Cordeliers, Inserm, Physiopathology of Ocular Diseases to Clinical Development, Université Paris Cité, Sorbonne Université, Paris, France.
Alejandra DaruichOphthalmology Department, Necker-Enfants Malades University Hospital, AP-HP, Paris Cité University, Paris, France.
Naël KaddourCentre de Recherche des Cordeliers, Inserm, Physiopathology of Ocular Diseases to Clinical Development, Université Paris Cité, Sorbonne Université, Paris, France.
Thierry BordetPulseSight Therapeutics (formerly Eyevensys), Paris, France.ORCID http://orcid.org/0000-0002-3648-2270
Francine Behar-CohenCentre de Recherche des Cordeliers, Inserm, Physiopathology of Ocular Diseases to Clinical Development, Université Paris Cité, Sorbonne Université, Paris, France.ORCID http://orcid.org/0000-0001-8571-9513
Emilie PicardCentre de Recherche des Cordeliers, Inserm, Physiopathology of Ocular Diseases to Clinical Development, Université Paris Cité, Sorbonne Université, Paris, France. picardemilie@gmail.com.ORCID http://orcid.org/0000-0002-2689-0510

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-20-CE18-0023
6 · The paper itself

Abstract

Dysregulation of iron homeostasis plays a crucial role in retinal diseases, contributing to oxidative stress, inflammation, and ferroptosis, key processes that drive the degeneration of the retinal pigment epithelium (RPE) and photoreceptors in age-related macular degeneration (AMD). Previous studies, though limited in patient numbers, have reported elevated iron levels in the aqueous humor, RPE, and Bruch's membrane of AMD patients. In this study, we aimed to confirm iron imbalance in a larger cohort of AMD patients and assess its correlation with disease stage. Elevated iron levels and a reduction in transferrin (TF) iron-binding capacity were observed in patients with early geographic atrophy (GA). RPE cells derived from human stem cells exhibited AMD-like features when exposed to iron overload or oxidized lipids. Treatment with TF appeared to restore aspects of iron homeostasis and reduce oxidative stress, mitochondrial damage, inflammation, complement activation, and ferroptosis in this model. These findings suggest that TF supplementation may represent a potential therapeutic strategy to help prevent or slow AMD progression.

Indexed as

Geographic AtrophyMacular DegenerationTransferrinAgedAged, 80 and overFemaleFerroptosisHomeostasisHumansIronMaleOxidative StressRetinal Pigment EpitheliumIronTransferrin

Identifiers

PMID41053100
PMCPMC12501284

What OpenQuestion holds

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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.