Evidence map›Paper›PMID 42465746›Full record

ArticleFrontiers in immunology2026

Stem cell factor 248 shapes ILC2 transcriptional programs and promotes mucosal inflammation in allergic asthma.

Nobuhiro Asai, Grace K Lombardo, Ramon Ocadiz-Ruiz, Yao Gu, Andrew J Rasky, Dana S Garcia, Angela J Montoya, Sarita Montaño, Kazuma Yagi, Wendy Fonseca

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. 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
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0citing papers in PubMed
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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

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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

10 authors.

Nobuhiro Asai *Department of Pathology. University of Michigan, Ann Arbor, MI, United States.
Grace K Lombardo *Department of Pathology. University of Michigan, Ann Arbor, MI, United States.
Ramon Ocadiz-RuizDepartment of Pathology. University of Michigan, Ann Arbor, MI, United States.
Yao GuDepartment of Pathology. University of Michigan, Ann Arbor, MI, United States.
Andrew J RaskyDepartment of Pathology. University of Michigan, Ann Arbor, MI, United States.
Dana S GarciaDepartment of Pathology. University of Michigan, Ann Arbor, MI, United States.
Angela J MontoyaDepartment of Pathology. University of Michigan, Ann Arbor, MI, United States.
Sarita MontañoDepartment of Pathology. University of Michigan, Ann Arbor, MI, United States.
Kazuma YagiDepartment of Pathology. University of Michigan, Ann Arbor, MI, United States.
Wendy FonsecaDepartment of Pathology. University of Michigan, Ann Arbor, MI, United States.

Funding

Long-term Phenotypic Alteration in the Lung Epithelium Following Early-life RSV InfectionR01HL174633 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Wendy Fonseca Aguilar · 2025 to 2026
$1.4M
Long-term alteration of the airway epithelium after early life RSV infectionR56HL167750 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FONSECA AGUILAR, WENDY · 2024 to 2024
$566k
NHLBI NIH HHS R01 HL174633NHLBI NIH HHS R56 HL167750
6 · The paper itself

Abstract

Stem cell factor (SCF), also known as Kit ligand, is a pleiotropic cytokine that signals through the c-Kit receptor to regulate cellular development, survival, and proliferation. Although SCF is classically recognized for its essential role in hematopoiesis and mast cell biology, c-Kit is also expressed by innate lymphoid cell progenitors (ILCp) and subsets of mature innate lymphoid cells (ILCs), suggesting broader immunoregulatory functions. Group 2 innate lymphoid cells (ILC2s) are critical mediators of type 2 airway inflammation and serve as an important source of type 2 cytokines during allergic responses. We previously demonstrated increased expression of the pro-inflammatory SCF248 isoform in the lungs of mice with chronic allergic inflammation, while elevated soluble SCF levels have also been reported in patients with asthma. In the present study, we further observed that SCF248 is upregulated in the bone marrow during allergic inflammation, suggesting that SCF248 may contribute to both local and systemic regulation of allergic immune responses. To define the role of SCF/c-Kit signaling in ILC2 biology, we first performed transcriptional profiling of SCF-deficient ILC2s, which revealed reduced expression of genes associated with cytokine signaling, activation, and effector function, including

Indexed as

AsthmaImmunity, InnateLymphocytesStem Cell FactorAnimalsCytokinesDisease Models, AnimalInflammationMiceMice, KnockoutProto-Oncogene Proteins c-kitSignal TransductionCytokinesProto-Oncogene Proteins c-kitStem Cell Factorallergyasthmac-kitILC2ILCPSCF

Identifiers

PMID42465746
PMCPMC13372909

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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.