Evidence map›Paper›PMID 39107476›Full record

ReviewCellular & molecular immunology2024

The immunology of sickness metabolism.

Felix M Wensveen, Marko Šestan, Bojan Polić

Abstract readReview
In one paragraph

Review in Cellular & molecular immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Temperature control in acute brain injury.Intensive care medicine · 2026
    Review
  7. Review
  8. Article
  9. The cycle of infectious fever - how it affects bacterial infections.Frontiers in cellular and infection microbiology · 2026
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Tissue-specific antiviral immunity.Cellular & molecular immunology · 2024
    Article
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.

Felix M Wensveen *University of Rijeka Faculty of Medicine, Rijeka, Croatia. Felix.Wensveen@uniri.hr.
Marko Šestan *University of Rijeka Faculty of Medicine, Rijeka, Croatia.ORCID 0000-0002-1473-6647
Bojan PolićUniversity of Rijeka Faculty of Medicine, Rijeka, Croatia.

Funding

EC | European Regional Development Fund (Europski Fond za Regionalni Razvoj) KK.01.1.1.01.0006Hrvatska Zaklada za Znanost (Croatian Science Foundation) IP-2020-02-7928Hrvatska Zaklada za Znanost (Croatian Science Foundation) IP-2022-10-3414Hrvatska Zaklada za Znanost (Croatian Science Foundation) IPCH-2020-10-8440
6 · The paper itself

Abstract

Everyone knows that an infection can make you feel sick. Although we perceive infection-induced changes in metabolism as a pathology, they are a part of a carefully regulated process that depends on tissue-specific interactions between the immune system and organs involved in the regulation of systemic homeostasis. Immune-mediated changes in homeostatic parameters lead to altered production and uptake of nutrients in circulation, which modifies the metabolic rate of key organs. This is what we experience as being sick. The purpose of sickness metabolism is to generate a metabolic environment in which the body is optimally able to fight infection while denying vital nutrients for the replication of pathogens. Sickness metabolism depends on tissue-specific immune cells, which mediate responses tailored to the nature and magnitude of the threat. As an infection increases in severity, so do the number and type of immune cells involved and the level to which organs are affected, which dictates the degree to which we feel sick. Interestingly, many alterations associated with metabolic disease appear to overlap with immune-mediated changes observed following infection. Targeting processes involving tissue-specific interactions between activated immune cells and metabolic organs therefore holds great potential for treating both people with severe infection and those with metabolic disease. In this review, we will discuss how the immune system communicates in situ with organs involved in the regulation of homeostasis and how this communication is impacted by infection.

Indexed as

HomeostasisAnimalsHumansImmune SystemInfectionsMetabolic Diseasesimmune systemImmunometabolisminfectioninflammasomemetabolic disease

Identifiers

PMID39107476
PMCPMC11364700

What Socratic holds

Textmetadata
LicenceCC BY
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.