Evidence map›Paper›PMID 39474427›Full record

ArticleFrontiers in immunology2024

PD-1 and CTLA-4 serve as major gatekeepers for effector and cytotoxic T-cell potentiation by limiting a CXCL9/10-CXCR3-IFNγ positive feedback loop.

Noor Abdala-Saleh, Jennie Lugassy, Akshatha Shivakumar-Kalvhati, Abeer Turky, Sari Abu Ras, Hila Razon, Nir Berger, Dana Bar-On, Yotam Bar-On, Tetsuya Taura and 2 more

Abstract read
In one paragraph

Article 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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Engineered chemokines, resistant to cancer-mediated post-transcriptional modifications, as drugs to improve cancer immunotherapy.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Development of DPP-4-resistant CXCL9-Fc and CXCL10-Fc chemokines for effective cancer immunotherapy.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  13. 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

12 authors.

Noor Abdala-Saleh *Department of Immunology, Faculty of Medicine, Technion, Haifa, Israel.
Jennie Lugassy *Department of Immunology, Faculty of Medicine, Technion, Haifa, Israel.
Akshatha Shivakumar-KalvhatiDepartment of Immunology, Faculty of Medicine, Technion, Haifa, Israel.
Abeer TurkyDepartment of Immunology, Faculty of Medicine, Technion, Haifa, Israel.
Sari Abu RasDepartment of Immunology, Faculty of Medicine, Technion, Haifa, Israel.
Hila RazonDepartment of Immunology, Faculty of Medicine, Technion, Haifa, Israel.
Nir BergerResearch and Development, Teva Pharmaceutical Industries, Ltd., Netanya, Israel.
Dana Bar-OnResearch and Development, Teva Pharmaceutical Industries, Ltd., Netanya, Israel.
Yotam Bar-OnDepartment of Immunology, Faculty of Medicine, Technion, Haifa, Israel.
Tetsuya TauraBiologics Discovery, Teva Pharmaceutical Industries Ltd, Redwood City, CA, United States.
David WilsonBiologics Discovery, Teva Pharmaceutical Industries Ltd, Redwood City, CA, United States.
Nathan KarinDepartment of Immunology, Faculty of Medicine, Technion, Haifa, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CXCR3 is a chemokine receptor with three ligands: CXCL9, CXCL10 and CXCL11. We report that in addition to attracting CXCR3+ T cells to tumor sites a key role of CXCL9 and CXCL10 is in inducing a self-feeding feedback loop that accelerates effector/cytotoxic activities of both CD4+ and CD8+ T cells while downregulating immunoregulatory protein TIM3. CXCR3KO mice displayed a markedly reduced response to anti-PD-1 and anti-CTLA-4 therapy. Results from a panel of

Indexed as

Chemokine CXCL10Chemokine CXCL9CTLA-4 AntigenInterferon-gammaMice, KnockoutProgrammed Cell Death 1 ReceptorReceptors, CXCR3AnimalsCD8-Positive T-LymphocytesCell Line, TumorFeedback, PhysiologicalHumansImmune Checkpoint InhibitorsMiceMice, Inbred C57BLChemokine CXCL10Chemokine CXCL9CTLA-4 AntigenCtla4 protein, mouseCxcl10 protein, mouseCxcl9 protein, mouseCxcr3 protein, mouseImmune Checkpoint InhibitorsInterferon-gammaPdcd1 protein, mouseProgrammed Cell Death 1 ReceptorReceptors, CXCR3CXCL10CXCL9CXCR3ICIPD-1

Identifiers

PMID39474427
PMCPMC11519525

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.