Evidence map›Paper›PMID 38947335›Full record

ReviewFrontiers in immunology2024

SOCS1 is a critical checkpoint in immune homeostasis, inflammation and tumor immunity.

Grace M Bidgood, Narelle Keating, Karen Doggett, Sandra E Nicholson

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Article
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  6. Manipulation therapy alleviates neuropathic painThe Korean journal of pain · 2026
    Article
  7. Article
  8. T-bet Fate Mapping Reveals Gestational Stage-Specific Transcriptional Adaptation of Decidual NK Cells.American journal of reproductive immunology (New York, N.Y. : 1989) · 2026
    Article
  9. Review
  10. Review
  11. Lypd6b depletion promotes CD8Nature communications · 2025
    Article
  12. Article
  13. Immunoregulatory Microenvironment in the Elderly Skin.JID innovations : skin science from molecules to population health · 2025
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

4 authors.

Grace M BidgoodInflammation Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Narelle KeatingInflammation Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Karen DoggettInflammation Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.
Sandra E NicholsonInflammation Division, Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Suppressor of Cytokine Signaling (SOCS) family proteins are important negative regulators of cytokine signaling. SOCS1 is the prototypical member of the SOCS family and functions in a classic negative-feedback loop to inhibit signaling in response to interferon, interleukin-12 and interleukin-2 family cytokines. These cytokines have a critical role in orchestrating our immune defence against viral pathogens and cancer. The ability of SOCS1 to limit cytokine signaling positions it as an important immune checkpoint, as evidenced by the detection of detrimental

Indexed as

HomeostasisInflammationNeoplasmsSuppressor of Cytokine Signaling 1 ProteinAnimalsAutoimmunityCytokinesHumansSignal TransductionCytokinesSOCS1 protein, humanSuppressor of Cytokine Signaling 1 ProteinautoimmunitycancercytokineimmunotherapyJAK-STATSOCS1

Identifiers

PMID38947335
PMCPMC11211259

What OpenQuestion holds

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LicenceCC BY
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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.