Evidence map›Paper›PMID 41906618›Full record

ArticleEuropean journal of immunology2026

Irgm1 Restrains CD8

Caitlyn T Molloy, Yazan Alwarawrah, Jonathan A Cohen, Brian E Fee, Jason K Whitmire, Gregory A Taylor, Nancie J MacIver

Abstract read
In one paragraph

Article in European journal of 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
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

7 authors.

Caitlyn T MolloyDepartment of Microbiology and Immunology, University of North Carolina, Chapel Hill, North Carolina, USA.
Yazan AlwarawrahDepartment of Pediatrics, Division of Pediatric Endocrinology, University of North Carolina, Chapel Hill, North Carolina, USA.
Jonathan A CohenDepartment of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA.
Brian E FeeDepartment of Medicine, Division of Geriatrics, and Center for the Study of Aging and Human Development, Duke University Medical Center, Durham, North Carolina, USA.
Jason K WhitmireDepartment of Microbiology and Immunology, University of North Carolina, Chapel Hill, North Carolina, USA.
Gregory A TaylorDepartment of Medicine, Division of Geriatrics, and Center for the Study of Aging and Human Development, Duke University Medical Center, Durham, North Carolina, USA.
Nancie J MacIverDepartment of Microbiology and Immunology, University of North Carolina, Chapel Hill, North Carolina, USA.ORCID 0000-0003-3676-9391

Funding

UNIV OF NORTH CAROLINA CLINICAL NUTRITION RESEARCH UNITP30DK056350 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SUSAN M. SMITH · 1999 to 2026
$31.6M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
Vanderbilt Clinical Oncology Research Career Development ProgramK12CA090625 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Debra L. Friedman, Paula Jill Hurley · 2001 to 2026
$16.9M
IRGM proteins as regulators of inflammationR01AI148243 · NIAID · DUKE UNIVERSITY · PI COERS, JOERN, TAYLOR, GREGORY A · 2020 to 2024
$2.4M
Role of IRGM proteins in immunity to enteric bacteriaR01AI145929 · NIAID · DUKE UNIVERSITY · PI TAYLOR, GREGORY A · 2019 to 2023
$1.6M
Leptin as a Regulator of T Cell Metabolism and FunctionK08DK087944 · NIDDK · DUKE UNIVERSITY · PI MACIVER, NANCIE · 2010 to 2014
$678k
Regulation of T cell metabolism and function by IRGM proteinsR21AI135398 · NIAID · DUKE UNIVERSITY · PI MACIVER, NANCIE, TAYLOR, GREGORY A · 2019 to 2020
$442k
Metabolic reprogramming to improve EGFRvIII CAR T cell persistenceR21CA253163 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MACIVER, NANCIE, SAMPSON, JOHN H. · 2021 to 2022
$402k
National Institute of Allergy and Infectious Diseases R21AI135398NCI NIH HHS K12 CA090625NCI NIH HHS R21 CA253163NIAID NIH HHS R01 AI145929NIAID NIH HHS R01 AI148243NIAID NIH HHS R21 AI135398NIDDK NIH HHS K08 DK087944NIDDK NIH HHS P30 DK056350NIGMS NIH HHS T32 GM007171
6 · The paper itself

Abstract

Immunity-related GTPases (IRGs) are a family of proteins that maintain cellular homeostasis by promoting autophagy and mitophagy. Mutations in human IRGM and genetic deletion of mouse Irgm1 have been linked to increased severity of inflammatory bowel disease, cancer, sepsis, and various infections. While IRGM/Irgm1 are known cell-intrinsic regulators of inflammation, their roles in T cell function remain poorly understood. We previously demonstrated that Irgm1 deficiency leads to increased production of proinflammatory mediators, including Granzyme B and interferon-γ, and increased apoptosis in CD8

Indexed as

ApoptosisCD8-Positive T-LymphocytesCytokinesGTP-Binding ProteinsInterferon Type ILymphocytic ChoriomeningitisAnimalsLymphocytic choriomeningitis virusMiceMice, Inbred C57BLMice, KnockoutSignal TransductionCytokinesGTP-Binding ProteinsIfi1 protein, mouseInterferon Type IapoptosisCD8+ T cellsimmunity‐related GTPase M1 (Irgm1)inflammationtype I interferon

Identifiers

PMID41906618
PMCPMC13078172

What OpenQuestion holds

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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.