Evidence map›Paper›PMID 40719862›Full record

ReviewCellular and molecular life sciences : CMLS2025

ISG-15, beyond its functions in the cell: a mini review.

Mudassir S Ali, Yun Sang Tang, Horace Hok Yeung Lee, Susan C Baker, Chris Ka Pun Mok

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. cGAMP suppresses FTO expression to promote mCellular and molecular life sciences : CMLS · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. 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

5 authors.

Mudassir S Ali *Department of Microbiology and Immunology, Stritch School of Medicine, Loyola University, Chicago, Maywood, IL, 60153, USA.ORCID http://orcid.org/0000-0003-2600-2277
Yun Sang Tang *The Jockey Club School of Public Health and Primary Care, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, P.R. China.
Horace Hok Yeung LeeCentre for Regenerative Medicine and Health, Hong Kong Institute of Science & Innovation, Chinese Academy of Sciences, Beijing, China.
Susan C BakerDepartment of Microbiology and Immunology, Stritch School of Medicine, Loyola University, Chicago, Maywood, IL, 60153, USA.
Chris Ka Pun MokThe Jockey Club School of Public Health and Primary Care, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, P.R. China. kapunmok@cuhk.edu.hk.

Funding

Investigating Interferon Antagonists in Delaying Innate Immune Responses to SARS-CoV-2R01AI159945 · NIAID · LOYOLA UNIVERSITY CHICAGO · PI BAKER, SUSAN C. · 2021 to 2025
$4.0M
Regulation of Host Innate Immunity Against Viral InfectionR37AI087846 · NIAID · CLEVELAND CLINIC LERNER COM-CWRU · PI Michaela Ulrike Gack · 2021 to 2026
$2.8M
NIAID NIH HHS R01 AI159945NIAID NIH HHS R37 AI087846RGC theme-based research schemes T11-705/21-NRGC theme-based research schemes T11-712/19-Nthe Emergency Key Program of Guangzhou Laboratory EKPG22-30-6the National Institutes of Health, USA R01 AI159945 and R37 AI087846
6 · The paper itself

Abstract

Interferon-stimulated gene 15 (ISG15) is an interferon-stimulated gene and a ubiquitin-like protein, traditionally known for its role in ISGylation. In addition to its intracellular functions, recent studies have revealed a novel role for extracellular ISG15, particularly in the context of viral infections. Beyond type I interferons, various stimuli, including viral and bacterial infections, have been found to trigger its secretion. Notably, the integrin receptor LFA-1 has been identified as a receptor for extracellular ISG15. Despite these advancements, the precise mechanisms by which extracellular ISG15 functions-such as the pathways regulating its secretion and receptor interactions-remain unclear. Viral proteins and de-ISGylating enzymes are known to influence ISG15 secretion levels, thereby impacting its immunomodulatory potential. This mini-review summarizes the existing studies aimed at understanding the mechanisms behind the secretion and functions of extracellular ISG15, with a particular focus on its immunomodulatory effects during infection. We also explore the contrasting roles of extracellular ISG15 in mice and humans, highlighting the need for more species-specific research. Further investigation into the role of extracellular ISG15 may uncover novel therapeutic strategies for infectious diseases, cancer, and inflammatory conditions.

Indexed as

CytokinesUbiquitinsAnimalsHumansMiceVirus DiseasesCytokinesISG15 protein, humanUbiquitinsExtracellularInnate immunityInterferonISG-15LFA-1

Identifiers

PMID40719862
PMCPMC12304407

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.