Evidence map›Paper›PMID 42460471›Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2026

Innate Immune Memory Responses in Organ Transplantation.

Lisanne C de Jong, Nils Rother, Raphaël Duivenvoorden

Abstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 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

3 authors.

Lisanne C de JongDepartment of Nephrology, Radboud University Medical Center, Nijmegen, the Netherlands (L.C.d.J., N.R., R.D.).ORCID 0000-0002-7188-3184
Nils RotherDepartment of Nephrology, Radboud University Medical Center, Nijmegen, the Netherlands (L.C.d.J., N.R., R.D.).
Raphaël DuivenvoordenDepartment of Nephrology, Radboud University Medical Center, Nijmegen, the Netherlands (L.C.d.J., N.R., R.D.).ORCID 0000-0003-1446-8336

Funding

Using trained immunity-inhibiting nanobiologics to achieve tolerance of heart allografts in non-human primatesP01AI168258 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Zahi A. Fayad, Joren C Madsen · 2023 to 2026
$14.7M
NIAID NIH HHS P01 AI168258
6 · The paper itself

Abstract

Innate immunity is a critical contributor to graft rejection and cardiovascular complications after organ transplantation, with increasing evidence indicating that innate immune memory significantly influences graft outcomes. The most extensively studied form, trained immunity, involves epigenetic and metabolic reprogramming of innate immune cells, altering their inflammatory responsiveness. Numerous transplantation-related factors, including metabolic disturbances such as hypercholesterolemia and hyperglycemia, can induce trained immunity, and both experimental and clinical studies have linked it to graft survival. Although trained immunity reflects responses to nonspecific stimuli, innate allogeneic memory shows that innate immune cells can recognize nonself and mount donor-specific memory responses. This review covers the current knowledge on both forms of innate immune memory in the context of solid organ transplantation.

Indexed as

Graft RejectionGraft SurvivalImmunity, InnateImmunologic MemoryOrgan TransplantationAnimalsEpigenesis, GeneticHumansSignal TransductionTrained Immunityepigenomicsgraft rejectiongraft survivalorgan transplantationtrained immunity

Identifiers

PMID42460471
PMCPMC13392995

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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.