Evidence map›Paper›PMID 36325490›Full record

ArticleClinical & translational immunology2022

Diabetes induced by checkpoint inhibition in nonobese diabetic mice can be prevented or reversed by a JAK1/JAK2 inhibitor.

Tingting Ge, Amber-Lee Phung, Gaurang Jhala, Prerak Trivedi, Nicola Principe, David J De George, Evan G Pappas, Sara Litwak, Laura Sanz-Villanueva, Tara Catterall and 6 more

Abstract read
In one paragraph

Article in Clinical & translational immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. The Immune Checkpoint Inhibitors Journey: From Early Promise to Lasting Impact.Journal of immunotherapy and precision oncology · 2026
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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

16 authors.

Tingting GeImmunology and Diabetes Unit St Vincent's Institute Fitzroy VIC Australia.
Amber-Lee PhungNational Centre for Asbestos Related Diseases, Institute for Respiratory Health The University of Western Australia Crawley WA Australia.
Gaurang JhalaImmunology and Diabetes Unit St Vincent's Institute Fitzroy VIC Australia.
Prerak TrivediImmunology and Diabetes Unit St Vincent's Institute Fitzroy VIC Australia.
Nicola PrincipeNational Centre for Asbestos Related Diseases, Institute for Respiratory Health The University of Western Australia Crawley WA Australia.
David J De GeorgeImmunology and Diabetes Unit St Vincent's Institute Fitzroy VIC Australia.
Evan G PappasImmunology and Diabetes Unit St Vincent's Institute Fitzroy VIC Australia.
Sara LitwakImmunology and Diabetes Unit St Vincent's Institute Fitzroy VIC Australia.
Laura Sanz-VillanuevaImmunology and Diabetes Unit St Vincent's Institute Fitzroy VIC Australia.ORCID https://orcid.org/0000-0003-3318-4224
Tara CatterallImmunology and Diabetes Unit St Vincent's Institute Fitzroy VIC Australia.
Stacey FynchImmunology and Diabetes Unit St Vincent's Institute Fitzroy VIC Australia.
Louis BoonJJP Biologics Warsaw Poland.
Thomas W KayImmunology and Diabetes Unit St Vincent's Institute Fitzroy VIC Australia.ORCID https://orcid.org/0000-0002-7273-2556
Jonathan CheeNational Centre for Asbestos Related Diseases, Institute for Respiratory Health The University of Western Australia Crawley WA Australia.ORCID https://orcid.org/0000-0002-7986-2708
Balasubramanian KrishnamurthyImmunology and Diabetes Unit St Vincent's Institute Fitzroy VIC Australia.
Helen E ThomasImmunology and Diabetes Unit St Vincent's Institute Fitzroy VIC Australia.ORCID https://orcid.org/0000-0001-6604-6640

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Immune checkpoint inhibitors have achieved clinical success in cancer treatment, but this treatment causes immune-related adverse events, including type 1 diabetes (T1D). Our aim was to test whether a JAK1/JAK2 inhibitor, effective at treating spontaneous autoimmune diabetes in nonobese diabetic (NOD) mice, can prevent diabetes secondary to PD-L1 blockade. Methods: Anti-PD-L1 antibody was injected into NOD mice to induce diabetes, and JAK1/JAK2 inhibitor LN3103801 was administered by oral gavage to prevent diabetes. Flow cytometry was used to study T cells and beta cells. Mesothelioma cells were inoculated into BALB/c mice to induce a transplantable tumour model. Results: Anti-PD-L1-induced diabetes was associated with increased immune cell infiltration in the islets and upregulated MHC class I on islet cells. Anti-PD-L1 administration significantly increased islet T cell proliferation and islet-specific CD8 Conclusion: A JAK1/JAK2 inhibitor can prevent and reverse anti-PD-L1-induced diabetes by blocking IFNγ and γc cytokine activities. Our study provides preclinical validation of JAK1/JAK2 inhibitor use in checkpoint inhibitor-induced diabetes.

Indexed as

CD8+ T cellscytokinesimmune checkpoint inhibitor‐induced diabetesJAK inhibitorNOD mice

Identifiers

PMID36325490
PMCPMC9618467

What OpenQuestion holds

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Registered trials

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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.