Evidence map›Paper›PMID 41750387›Full record

ArticleBiomolecules2026

Immunomodulatory Effects of Nintedanib on Human Blood Monocytes/Macrophages from Patients with Idiopathic Pulmonary Fibrosis.

Maria Talmon, Arianna Mares, Hari Baskar Balasubramanian, Chiara Mocchetti, Lara Camillo, Piero Balbo, Luigia Grazia Fresu, Filippo Patrucco

Abstract read
In one paragraph

Article in Biomolecules, 2026. 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. 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

8 authors.

Maria TalmonDepartment of Pharmaceutical Sciences, University of Piemonte Orientale, Via Bovio 6, 28100 Novara, Italy.
Arianna MaresDepartment of Health Sciences, School of Medicine, University of Piemonte Orientale, Via Solaroli, 17, 28100 Novara, Italy.
Hari Baskar BalasubramanianDepartment of Health Sciences, School of Medicine, University of Piemonte Orientale, Via Solaroli, 17, 28100 Novara, Italy.ORCID 0000-0001-7713-3133
Chiara MocchettiDepartment of Health Sciences, School of Medicine, University of Piemonte Orientale, Via Solaroli, 17, 28100 Novara, Italy.ORCID 0009-0003-6638-975X
Lara CamilloDepartment of Health Sciences, School of Medicine, University of Piemonte Orientale, Via Solaroli, 17, 28100 Novara, Italy.ORCID 0000-0003-2148-3454
Piero BalboDivision of Respiratory Diseases, Maggiore della Carità University Hospital, C.so Mazzini 18, 28100 Novara, Italy.
Luigia Grazia FresuDepartment of Health Sciences, School of Medicine, University of Piemonte Orientale, Via Solaroli, 17, 28100 Novara, Italy.ORCID 0000-0002-8605-9040
Filippo PatruccoDivision of Respiratory Diseases, Maggiore della Carità University Hospital, C.so Mazzini 18, 28100 Novara, Italy.

Funding

Boehringer Ingelheim (Italy) MaMoIPF 16/07/2020
6 · The paper itself

Abstract

backgroundNintedanib (NTD) is an inhibitor of several tyrosine kinases whose role in the pathogenesis of idiopathic pulmonary fibrosis (IPF) is well recognized. Therefore, NTD was approved for the management of IPF about ten years ago. NTD has been demonstrated to have immunomodulatory effects in vitro. We now evaluated the effects of NTD on monocyte/macrophage phenotype isolated from IPF patients treated with NTD.

methodsMonocytes were isolated from IPF patients naïve for treatments and used as such or differentiated into M1- and M2-like macrophages. The cellular phenotype (characterized by the expression pro- and anti-fibrotic surface markers) and responsiveness (characterized by oxidative stress and cytokine expression/release) were evaluated, at T0 (before treatment starts) and after 6 months of treatment with a 150 mg capsule of NTD twice a day (T1).

resultsFollowing differentiation, both M1 and M2 macrophage populations, derived from monocytes isolated from patients treated with NTD, present a higher percentage of cells positive for anti-fibrotic CD80/CD86 and expressing less profibrotic CD206/CD163. Importantly, gene expression and release of the pro-fibrotic factor TGF-β were significantly decreased at T1.

conclusionsThese results show that although it does not have a direct effect on monocyte phenotype/responsiveness, NTD in vivo appears to prime monocytes to differentiate preferentially towards an anti-fibrotic macrophage phenotype, suggesting that it has an immunomodulatory effect on macrophage polarization. This data leads us to hypothesize that NTD could also induce this change in vivo, thus contributing to the improvement of the patient's fibrotic state.

Indexed as

Idiopathic Pulmonary FibrosisImmunologic FactorsIndolesMacrophagesMonocytesAgedCell DifferentiationFemaleHumansMaleMiddle AgedOxidative StressTransforming Growth Factor betaImmunologic FactorsIndolesnintedanibTransforming Growth Factor betaidiopathic pulmonary fibrosisIPFmacrophagemonocytenintedaniboxidative stress

Identifiers

PMID41750387
PMCPMC12938255

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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.