Evidence map›Paper›PMID 39340067›Full record

ArticleVaccines2024

GSK-3β in Dendritic Cells Exerts Opposite Functions in Regulating Cross-Priming and Memory CD8 T Cell Responses Independent of β-Catenin.

Chunmei Fu, Jie Wang, Tianle Ma, Congcong Yin, Li Zhou, Björn E Clausen, Qing-Sheng Mi, Aimin Jiang

Abstract read
In one paragraph

Article in Vaccines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Tim-3-targeted vaccines overcome tumor immunosuppression and reduce cDC1 dependence to elicit potent anti-tumor immunity.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  2. Review
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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

8 authors.

Chunmei FuCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health, Detroit, MI 48202, USA.
Jie WangCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health, Detroit, MI 48202, USA.ORCID 0000-0001-9732-1975
Tianle MaDepartment of Computer Science and Engineering, School of Engineering and Computer Science, Oakland University, Rochester, MI 48309, USA.ORCID 0000-0003-2309-1489
Congcong YinCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health, Detroit, MI 48202, USA.ORCID 0000-0003-0865-2823
Li ZhouCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health, Detroit, MI 48202, USA.ORCID 0000-0002-7028-3865
Björn E ClausenInstitute for Molecular Medicine, Paul Klein Center for Immune Intervention, University Medical Center of the Johannes Gutenberg-University Mainz, Langenbeckstrasse 1, 55131 Mainz, Germany.ORCID 0000-0002-2484-7842
Qing-Sheng MiCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health, Detroit, MI 48202, USA.ORCID 0000-0002-1411-6827
Aimin JiangCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health, Detroit, MI 48202, USA.ORCID 0000-0001-9161-5729

Funding

VPS72 controls Treg cell stability and adaptation to tumor microenvironmentR01CA284740 · NCI · HENRY FORD HEALTH + MICHIGAN STATE UNIVERSITY HEALTH SCIENCES · PI FANG, DEYU, MI, QING-SHENG · 2023 to 2025
$3.1M
b-catenin in vaccine-induced anti-tumor CD8 T cell immunityR01CA198105 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI JIANG, AIMIN · 2015 to 2019
$2.0M
Decoding TGF-beta signaling pathways in skin langerhans cellsR56AI165991 · NIAID · HENRY FORD HEALTH SYSTEM · PI MI, QING-SHENG, ZHOU, LI · 2022 to 2022
$376k
DFG, German Science Foundation CL419/2-2 (project #315501751)DFG, German Science Foundation CRC1292/2-TP20 (Project # 318346496)DFG, German Science Foundation TRR355/1-A09 (Project # 490846870)NCI NIH HHS R01 CA198105NCI NIH HHS R01 CA284740NIAID NIH HHS R56 AI165991NIH HHS 1R01CA198105NIH HHS 1R01CA284740NIH HHS 1R56AI165991
6 · The paper itself

Abstract

GSK-3β plays a critical role in regulating the Wnt/β-catenin signaling pathway, and manipulating GSK-3β in dendritic cells (DCs) has been shown to improve the antitumor efficacy of DC vaccines. Since the inhibition of GSK-3β leads to the activation of β-catenin, we hypothesize that blocking GSK-3β in DCs negatively regulates DC-mediated CD8 T cell immunity and antitumor immunity. Using CD11c-GSK-3β

Indexed as

CD8 T cell immunitydendritic cellsGSK-3βmemory responsesβ-catenin

Identifiers

PMID39340067
PMCPMC11436163

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.