Evidence map›Paper›PMID 41356371›Full record

ArticleResearch square2025

Airway Delivery of Encapsulated Cytokine-Secreting Cells for Local Immunomodulation in Inflammatory Lung Diseases.

Omid Veiseh, Samira Aghlara-Fotovat, Kailyn Nunez, Miguel Mendez-Sosa, Michael Guinn, Saad Malik, Saliha Pathan, Jacob Cabler, Maheshwari Ramineni, Suridh Chakravarty and 3 more

Abstract readPreprint
In one paragraph

Article in Research square, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Samira Aghlara-FotovatRice University.
Kailyn NunezRice University.
Miguel Mendez-SosaBaylor College of Medicine.
Michael GuinnRice University.
Saad MalikBaylor College of Medicine.
Saliha PathanBaylor College of Baylor.
Jacob CablerRice University.
Maheshwari RamineniHouston Methodist Research Institute.
Suridh ChakravartyBaylor College of Medicine.
Julia GoldmanBaylor College Of Medicine.
Michael DiehlRice University.
Ravi GhantaBaylor College of Medicine.

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Suzanne AW Fuqua · 2007 to 2026
$73.9M
Consortium for Broad Based Disease Phenotyping of Knockout MiceU54HG006348 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI BEAUDET, ARTHUR L., PAYLOR, RICHARD E · 2011 to 2015
$17.0M
Research Training Program in Cardiovascular SurgeryT32HL139430 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI Todd K Rosengart · 2018 to 2026
$2.9M
Cell Based Immunomodulation to Promote Post-Infarct Myocardial RepairR01HL163258 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI RAVI K GHANTA · 2023 to 2026
$2.8M
Cell Based Immunomodulation to Suppress Lung Inflammation and Promote RepairR01HL174616 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI RAVI K GHANTA, Omid Veiseh · 2024 to 2026
$2.1M
BD Biosciences Special Order LSRIIS10RR024574 · NCRR · BAYLOR COLLEGE OF MEDICINE · PI LUMPKIN, ELLEN A · 2009 to 2009
$430k
Single Cell Spatial Transcriptomics Shared Instrument at the BCM Core FacilityS10OD032189 · OD · BAYLOR COLLEGE OF MEDICINE · PI CHEN, RUI · 2022 to 2022
$304k
NCI NIH HHS P30 CA125123NCRR NIH HHS S10 RR024574NHGRI NIH HHS U54 HG006348NHLBI NIH HHS R01 HL163258NHLBI NIH HHS R01 HL174616NHLBI NIH HHS T32 HL139430NIH HHS S10 OD032189
6 · The paper itself

Abstract

Dysregulated lung immunity drives excessive inflammation, leading to diseases like acute respiratory distress syndrome (ARDS) and pulmonary fibrosis that have high morbidity and mortality. Immunomodulation can attenuate inflammation and improve outcomes, however off-target effects from systemic delivery lead to adverse events that limit clinical translation. Herein, we develop a modular cell-based microcapsule platform that can be administered via the airway for localized, durable, and tunable delivery of various immunomodulatory proteins to the lungs. With this system, we demonstrate therapeutic efficacy of localized delivery of two proteins, interleukin-10 (IL-10) and interleukin-1 receptor antagonist (IL-1Ra), in a lipopolysaccharide-induced rodent model of ARDS. Single-cell RNA sequencing revealed that IL-10-secreting capsules reprogram the lung immune landscape in ARDS by altering myeloid cell composition, suppressing pro-inflammatory gene expression, and promoting the resolution of inflammation. In a bleomycin pulmonary fibrosis model, the platform enables durable and sustained delivery of IL-10 to alleviate hypoxemia and rescue lung architecture. Safety and biocompatibility were further confirmed in a large animal model, highlighting the clinical potential of the platform for the treatment of inflammatory lung diseases.

Identifiers

PMID41356371
PMCPMC12676441

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Registered trials

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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.