Evidence map›Paper›PMID 40217124›Full record

ArticleNature cardiovascular research2025

The immune checkpoint regulator CD40 potentiates myocardial inflammation.

Jesus Jimenez, Junedh Amrute, Pan Ma, Xiaoran Wang, Shibali Das, Raymond Dai, Yohei Komaru, Andreas Herrlich, Matthias Mack, Kory J Lavine

Abstract read
In one paragraph

Article in Nature cardiovascular research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. The Immune Microenvironment: New Therapeutic Implications in Organ Fibrosis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    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

10 authors.

Jesus JimenezCenter for Cardiovascular Research, Department of Medicine, Cardiovascular Division, Washington University School of Medicine, St. Louis, MO, USA.ORCID http://orcid.org/0000-0001-5399-8538
Junedh AmruteCenter for Cardiovascular Research, Department of Medicine, Cardiovascular Division, Washington University School of Medicine, St. Louis, MO, USA.ORCID http://orcid.org/0000-0002-6851-0168
Pan MaCenter for Cardiovascular Research, Department of Medicine, Cardiovascular Division, Washington University School of Medicine, St. Louis, MO, USA.
Xiaoran WangCenter for Cardiovascular Research, Department of Medicine, Cardiovascular Division, Washington University School of Medicine, St. Louis, MO, USA.
Shibali DasCenter for Cardiovascular Research, Department of Medicine, Cardiovascular Division, Washington University School of Medicine, St. Louis, MO, USA.
Raymond DaiWashington University, St. Louis, MO, USA.
Yohei KomaruDivision of Nephrology, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.ORCID http://orcid.org/0000-0002-7970-5518
Andreas HerrlichDivision of Nephrology, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Matthias MackDivision of Nephrology, Department of Medicine, University Hospital Regensburg, Regensburg, Germany.
Kory J LavineCenter for Cardiovascular Research, Department of Medicine, Cardiovascular Division, Washington University School of Medicine, St. Louis, MO, USA. klavine@wustl.edu.ORCID http://orcid.org/0000-0003-1948-9945

Funding

Washington University Rheumatic DiseasesResearch Resource-based CenterP30AR073752 · NIAMS · WASHINGTON UNIVERSITY · PI Alfred Hyoungju Kim · 2018 to 2026
$7.6M
Program to Increase Diversity in Cardiovascular Health-Related Research(PRIDE-CVD)R25HL105446 · NHLBI · SUNY DOWNSTATE MEDICAL CENTER · PI Mohamed Boutjdir · 2010 to 2026
$5.9M
PRIDE SUMMER INSTITUTE IN CARDIOVASCULAR GENETIC EPIDEMIOLOGYR25HL105400 · NHLBI · WASHINGTON UNIVERSITY · PI DAVILA-ROMAN, VICTOR G., DE LAS FUENTES, LISA · 2010 to 2025
$5.2M
Specification and Function of Tissue Resident and Recruited Macrophages in Cardiac Remodeling and Heart FailureR35HL161185 · NHLBI · WASHINGTON UNIVERSITY · PI Kory J. Lavine · 2022 to 2026
$4.3M
The Role of Donor Innate Immune Responses in Regulating Alloimmunity after Heart TransplantationR01HL151078 · NHLBI · WASHINGTON UNIVERSITY · PI KREISEL, DANIEL, LAVINE, KORY J. · 2020 to 2023
$2.6M
Role of Amphiregulin in kidney fibrosisR01DK121200 · NIDDK · WASHINGTON UNIVERSITY · PI HERRLICH, ANDREAS · 2019 to 2023
$2.1M
MACROPHAGE HETEROGENEITY IN HEART FAILURE PROGRESSION AND CARDIAC RECOVERYR01HL138466 · NHLBI · WASHINGTON UNIVERSITY · PI LAVINE, KORY J. · 2017 to 2021
$1.9M
MACROPHAGE ONTOGENY SHIFTS IN ISCHEMIC HEART DISEASER01HL139714 · NHLBI · WASHINGTON UNIVERSITY · PI LAVINE, KORY J. · 2018 to 2021
$1.5M
CD40 Immunotherapy Effect on the Cardiac Immune Landscape and Response to Myocardial DiseaseK08HL163518 · NHLBI · WASHINGTON UNIVERSITY · PI Jesus Jimenez · 2024 to 2026
$489k
Emerging Immune Checkpoint Therapies Reshape the Cardiac Immune Landscape and Promote Myocardial VulnerabilityK99HL171935 · NHLBI · WASHINGTON UNIVERSITY · PI MA, PAN · 2024 to 2025
$205k
BLRD VA I01 BX005322Burroughs Wellcome Fund (BWF) 1014782Fondation Leducq 20CVD02MEXT | Japan Society for the Promotion of Science (JSPS) 202360162NHLBI NIH HHS K08 HL163518NHLBI NIH HHS K99 HL171935NHLBI NIH HHS R01 HL138466NHLBI NIH HHS R01 HL139714NHLBI NIH HHS R01 HL151078NHLBI NIH HHS R25 HL105400NHLBI NIH HHS R25 HL105446NHLBI NIH HHS R35 HL161185NIAMS NIH HHS P30 AR073752NIDDK NIH HHS R01 DK121200U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) 1K08HL163518-01A1U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01 HL161185U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases) R01DK121200
6 · The paper itself

Abstract

Immune checkpoint therapeutics including CD40 agonists have tremendous promise to elicit antitumor responses in patients resistant to current therapies. Conventional immune checkpoint inhibitors (PD-1, PD-L1 and CTLA-4 antagonists) are associated with serious adverse cardiac events including life-threatening myocarditis. However, little is known regarding the potential for CD40 agonists to trigger myocardial inflammation or myocarditis. Here we leverage genetic mouse models, single-cell sequencing and cell depletion studies to show that an anti-CD40 agonist antibody reshapes the cardiac immune landscape through activation of CCR2

Indexed as

CD40 AntigensHeart FailureMacrophagesMyocarditisMyocardiumAnimalsCD8-Positive T-LymphocytesDisease Models, AnimalImmunologic MemoryMaleMiceMice, Inbred C57BLMice, KnockoutReceptors, CCR2Signal TransductionVentricular RemodelingCcr2 protein, mouseCD40 AntigensReceptors, CCR2

Identifiers

PMID40217124
PMCPMC12641230

What OpenQuestion 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 OpenQuestion graph.