Evidence map›Paper›PMID 40416970›Full record

ArticleFrontiers in immunology2025

Wip1 inhibitor CCT007093 alleviates immune exhaustion of lymphocytes via p65 NF-κB and YY1 in chronic hepatitis B virus infection in mice.

Yu-Syuan You, Wan-Ting Chang, Chia-Lang Hsu, Hui-Ying Wang, Yan-Fong Lu, InKyeom Kim, Shiang-Jong Tzeng

Abstract read
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Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Yu-Syuan YouGraduate Institute of Pharmacology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Wan-Ting ChangGraduate Institute of Pharmacology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Chia-Lang HsuDepartment of Medical Research, National Taiwan University Hospital, Taipei, Taiwan.
Hui-Ying WangGraduate Institute of Pharmacology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Yan-Fong LuGraduate Institute of Pharmacology, College of Medicine, National Taiwan University, Taipei, Taiwan.
InKyeom KimDepartment of Pharmacology, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Shiang-Jong TzengGraduate Institute of Pharmacology, College of Medicine, National Taiwan University, Taipei, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Prolonged viral infections often lead to lymphocyte exhaustion, marked by heightened inhibitory receptor expression like PD-1, compromising host defense mechanisms. The unexplored potential of chemical checkpoint inhibitors in rejuvenating immune responses prompted our investigation. Methods: We focused on CCT007093, a Wip1 inhibitor, screened for its distinctive capacity to simultaneously decrease PD-1 and FcγRIIB expression in B cells. Results: In this study, we harnessed a murine model of immune exhaustion induced by chronic hepatitis B virus (HBV) infection using hydrodynamic injection. Treatment with CCT007093 resulted in decreased levels of PD-1 expression, resulting in reduced percentages of PD-1 Discussion: Our study highlights the prowess of chemical checkpoint inhibitors, exemplified by CCT007093, in alleviating immune exhaustion in HBV-infected mice, particularly by enhancing adaptive immunity.

Indexed as

Hepatitis B, ChronicHepatitis B virusTranscription Factor RelAAnimalsB-LymphocytesDisease Models, AnimalImmune System ExhaustionMiceMice, Inbred C57BLProgrammed Cell Death 1 ReceptorReceptors, IgGProgrammed Cell Death 1 ReceptorReceptors, IgGRela protein, mouseTranscription Factor RelACCT007093FcγRIIBhepatitis B virus (HBV)immune exhaustionp65 NF-kBPD-1wild-type p53-induced phosphatase (Wip1)Ying Yang 1 (YY1)

Identifiers

PMID40416970
PMCPMC12098592

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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.