Evidence map›Paper›PMID 42025270›Full record

ReviewCurrent opinion in immunology2026

CRAC channels as targets for immunotherapy.

Kenneth Stauderman, Sudarshan Hebbar, Stefan Feske

Abstract readReview
In one paragraph

Review in Current opinion in immunology, 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

3 authors.

Kenneth StaudermanCalciMedica Inc., La Jolla, CA 92037, USA.
Sudarshan HebbarCalciMedica Inc., La Jolla, CA 92037, USA.
Stefan FeskeDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA. Electronic address: stefan.feske@nyulangone.org.

Funding

Regulation of encephalitogenic T cells by CRAC channelsR01AI137004 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FESKE, STEFAN · 2018 to 2022
$2.4M
ATP1B3: novel regulator of T cell-mediated immunityR01AI180128 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI STEFAN FESKE · 2024 to 2026
$1.9M
NIAID NIH HHS R01 AI137004NIAID NIH HHS R01 AI180128
6 · The paper itself

Abstract

Ca²⁺ release-activated Ca²⁺ (CRAC) channels facilitate store-operated Ca²⁺ entry in both immune and nonimmune cells. They are crucial for the function of many immune cell types and strongly associated with the pathophysiology of immune-related disorders. Inherited null mutations in the genes encoding the CRAC channel, ORAI1, and its activator STIM1, are linked to inborn errors of immunity in patients, highlighting the essential role of these channels in immunity. Preclinical studies using knockout mice and CRAC channel inhibitors (CRACi) have further demonstrated their pivotal function in the pathophysiology of immune-related conditions, including immunity to infection, autoimmunity, allergy, and other inflammatory diseases. Clinical trials in patients with inflammatory disorders underscore the potential utility of CRACi for immunotherapy. Here, we provide an overview of CRAC channels in immune cell function, review their roles in preclinical models of immune diseases, and discuss the outcomes of clinical trials involving CRACi.

Indexed as

Calcium Channel BlockersCalcium Release Activated Calcium ChannelsImmune System DiseasesImmunotherapyAnimalsHumansMolecular Targeted TherapyORAI1 ProteinStromal Interaction Molecule 1Calcium Channel BlockersCalcium Release Activated Calcium ChannelsORAI1 ProteinStromal Interaction Molecule 1

Identifiers

PMID42025270
PMCPMC13273768

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.