Evidence map›Paper›PMID 40603793›Full record

ReviewAdvances in experimental medicine and biology2025

Iron, Hepcidin, and Immunity.

Daisy Crisell, Nick Talbot, Hal Drakesmith

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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.

Daisy CrisellClinical Medical School, University of Oxford, Oxford, UK.
Nick TalbotDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.
Hal DrakesmithMRC Translational Immune Discovery Unit, MRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, John Radcliffe Hospital, University of Oxford, Oxford, UK. alexander.drakesmith@imm.ox.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infection involves the utilization of host nutritional resources by the pathogen. Genetic, experimental, and clinical evidence supports the critical role of iron as a focus for both pathogen attack and host defense. The molecular basis of how mammals regulate iron transport to maintain homeostasis, and in response to infection, has been well characterized since the discovery of the hormone hepcidin. The multiple activities of iron in host innate and adaptive immune cell function have also been studied in increasing depth. Recently these research strands have been converging, showing how host regulation of iron affects not only classical "nutritional immunity" as a defense against pathogens but also influences the development and magnitude of immune responses. These findings are discussed in the context of different types of infectious micro-organisms, against a background of host disease states (including respiratory disorders), and in relation to iron supplementation, vaccination, and pathological immune responses.

Indexed as

HepcidinsIronAdaptive ImmunityAnimalsHomeostasisHumansImmunity, InnateHepcidinsIronHepcidinHypoferremiaImmune responsesInfectionVaccination

Identifiers

PMID40603793

What OpenQuestion holds

Textmetadata
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.