Evidence map›Paper›PMID 41292922›Full record

ArticlebioRxiv : the preprint server for biology2025

Immunomodulatory Functions of Intercalated Cells in Kidney Autoimmunity.

Maria C Avenatti, Maia L Elizagaray, Micah C Purba, Ferran Barrachina, Angela Chen, Isinsu Bastepe, Katherine Radovanovic, Maria A Battistone

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

8 authors.

Maria C AvenattiProgram in Membrane Biology, Nephrology Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, 02129, MA, United States.ORCID 0009-0004-3658-0390
Maia L ElizagarayProgram in Membrane Biology, Nephrology Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, 02129, MA, United States.ORCID 0000-0002-4570-172X
Micah C PurbaProgram in Membrane Biology, Nephrology Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, 02129, MA, United States.ORCID 0009-0004-5898-787X
Ferran BarrachinaProgram in Membrane Biology, Nephrology Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, 02129, MA, United States.ORCID 0000-0003-3138-4142
Angela ChenProgram in Membrane Biology, Nephrology Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, 02129, MA, United States.ORCID 0009-0009-3025-0864
Isinsu BastepeProgram in Membrane Biology, Nephrology Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, 02129, MA, United States.ORCID 0009-0000-4985-2448
Katherine RadovanovicProgram in Membrane Biology, Nephrology Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, 02129, MA, United States.ORCID 0009-0005-6623-076X
Maria A BattistoneProgram in Membrane Biology, Nephrology Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, 02129, MA, United States.ORCID 0000-0003-0490-9548

Funding

P&F programP30DK135043 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Dennis Brown · 2023 to 2026
$5.4M
Proton-secreting epithelial cells as key modulators of epididymal mucosal immunity - Administrative SupplementR01HD104672 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI Maria Agustina Battistone · 2021 to 2026
$2.5M
NICHD NIH HHS R01 HD104672NIDDK NIH HHS P30 DK135043
6 · The paper itself

Abstract

Various autoimmune diseases frequently cause both acute and chronic kidney injuries through complex mechanisms involving autoantibodies and cellular immune responses that result in tissue damage. Intercalated cells (ICs), specialized renal tubular epithelial cells responsible for proton secretion, are strategically positioned at the epithelial-immune interface, making them ideal sensors of stress signals and potential triggers of immune responses. This study investigates the molecular mechanisms by which ICs interact with immune cells to maintain renal immune homeostasis and contribute to the development of autoimmune kidney disease. We depleted Foxp3

Indexed as

epithelial cellsinflammationRegulatory T cellrenal injury

Identifiers

PMID41292922
PMCPMC12642325

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.