Evidence map›Paper›PMID 42686065›Full record

ArticleCellular and molecular gastroenterology and hepatology2026

Control of Intestinal Type 3 Immunity by the Unfolded Protein Response Sensor Inositol-Requiring Enzyme 1α in Antigen-Presenting Cells.

Dominique Fernández, Antonia Geisse, Pamela González-Maldonado, Ailiñ Tapia, Francisca Gutiérrez-Ballesteros, Valentina Ugalde, Felipe Tapia, Felipe Flores-Santibañez, Takao Iwawaki, Karina Pino-Lagos and 5 more

Abstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 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
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

15 authors.

Dominique FernándezLaboratorio de Inmunología y Estrés Celular, Núcleo Interdisciplinario de Farmacología e Inmunología, Instituto de Ciencias Biomédicas (ICBM), Facultad de Medicina, Universidad de Chile, Santiago, Chile; Laboratorio de Inmunología, Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Antonia GeisseLaboratorio de Inmunología y Estrés Celular, Núcleo Interdisciplinario de Farmacología e Inmunología, Instituto de Ciencias Biomédicas (ICBM), Facultad de Medicina, Universidad de Chile, Santiago, Chile; Laboratorio de Inmunología, Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Pamela González-MaldonadoLaboratorio de Inmunología y Estrés Celular, Núcleo Interdisciplinario de Farmacología e Inmunología, Instituto de Ciencias Biomédicas (ICBM), Facultad de Medicina, Universidad de Chile, Santiago, Chile; Laboratorio de Inmunología, Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Ailiñ TapiaLaboratorio de Inmunología y Estrés Celular, Núcleo Interdisciplinario de Farmacología e Inmunología, Instituto de Ciencias Biomédicas (ICBM), Facultad de Medicina, Universidad de Chile, Santiago, Chile; Laboratorio de Inmunología, Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Francisca Gutiérrez-BallesterosLaboratorio de Inmunología y Estrés Celular, Núcleo Interdisciplinario de Farmacología e Inmunología, Instituto de Ciencias Biomédicas (ICBM), Facultad de Medicina, Universidad de Chile, Santiago, Chile; Laboratorio de Inmunología, Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Valentina UgaldeLaboratorio de Neuroinmunología, Centro Científico y Tecnológico de Excelencia Ciencia and Vida, Fundación Ciencia and Vida, Santiago, Chile.
Felipe TapiaLaboratorio de Inmunología y Estrés Celular, Núcleo Interdisciplinario de Farmacología e Inmunología, Instituto de Ciencias Biomédicas (ICBM), Facultad de Medicina, Universidad de Chile, Santiago, Chile; Laboratorio de Inmunología, Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Felipe Flores-SantibañezLaboratorio de Inmunología y Estrés Celular, Núcleo Interdisciplinario de Farmacología e Inmunología, Instituto de Ciencias Biomédicas (ICBM), Facultad de Medicina, Universidad de Chile, Santiago, Chile; Laboratorio de Inmunología, Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Takao IwawakiDivision of Cell Medicine, Department of Life Science, Medical Research Institute, Kanazawa Medical University, Uchinada, Ishikawa, Japan.
Karina Pino-LagosFacultad de Medicina, Centro de Investigación e Innovación Biomédica, Universidad de los Andes, Santiago, Chile.
Louis BoonJJP Biologics, Warsaw, Poland.
María Rosa BonoLaboratorio de Inmunología, Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Carolina PradoLaboratorio de Neuroinmunología, Centro Científico y Tecnológico de Excelencia Ciencia and Vida, Fundación Ciencia and Vida, Santiago, Chile; Facultad de Medicina y Ciencia, Universidad San Sebastián, Santiago, Chile.
Rodrigo PachecoLaboratorio de Neuroinmunología, Centro Científico y Tecnológico de Excelencia Ciencia and Vida, Fundación Ciencia and Vida, Santiago, Chile; Facultad de Medicina y Ciencia, Universidad San Sebastián, Santiago, Chile.
Fabiola OsorioLaboratorio de Inmunología y Estrés Celular, Núcleo Interdisciplinario de Farmacología e Inmunología, Instituto de Ciencias Biomédicas (ICBM), Facultad de Medicina, Universidad de Chile, Santiago, Chile; Laboratorio de Inmunología, Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile. Electronic address: fabiola.osorio@uchile.cl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsThe unfolded protein response is an essential cellular program maintaining intestinal homeostasis by acting on several cell types. However, whether the unfolded protein response sensor inositol-requiring enzyme 1α acts on dendritic cells and other antigen-presenting cells for shaping intestinal immunity remains poorly defined.

methodsHere, we dissect the role of the endoribonuclease domain of the unfolded protein response sensor inositol-requiring enzyme 1α in intestinal CD11c

resultsWe identify robust inositol-requiring enzyme 1α endoribonuclease activity in intestinal conventional dendritic cell subsets, dendritic cells associated with crypto patches and isolated lymphoid follicles, and macrophages, independently of microbial signals. Targeted ablation of inositol-requiring enzyme 1α endoribonuclease in the intestinal CD11c

conclusionsCollectively, our findings uncover inositol-requiring enzyme 1α endoribonuclease in intestinal CD11c

Indexed as

APCsIntestineIRE1Type 3 Immunity

Identifiers

PMID42686065
PMCPMC13677055

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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.