Evidence map›Paper›PMID 38460167›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Metabolism/Immunity Dual-Regulation Thermogels Potentiating Immunotherapy of Glioblastoma Through Lactate-Excretion Inhibition and PD-1/PD-L1 Blockade.

Tianliang Li, Dan Xu, Zhao Ruan, Jie Zhou, Wenbo Sun, Bo Rao, Haibo Xu

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
10.1field-weighted citation impact, top 1% of its field
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

54 citing papers in PubMed, 42 citations in OpenAlex.

  1. HAdvanced materials (Deerfield Beach, Fla.) · 2026
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  6. Targeting Lactate and Lactylation in Cancer Metabolism and Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
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  14. SLC2A1Nature cell biology · 2026
    Article
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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

7 authors at 1 institution in 1 country.

Tianliang LiDepartment of Radiology, Zhongnan Hospital of Wuhan University, 169 Donghu Road, Wuhan, 430071, China.
Dan XuDepartment of Nuclear Medicine, Zhongnan Hospital of Wuhan University, 169 Donghu Road, Wuhan, 430071, China.
Zhao RuanDepartment of Radiology, Zhongnan Hospital of Wuhan University, 169 Donghu Road, Wuhan, 430071, China.
Jie ZhouDepartment of Radiology, Zhongnan Hospital of Wuhan University, 169 Donghu Road, Wuhan, 430071, China.
Wenbo SunDepartment of Radiology, Zhongnan Hospital of Wuhan University, 169 Donghu Road, Wuhan, 430071, China.
Bo RaoDepartment of Radiology, Zhongnan Hospital of Wuhan University, 169 Donghu Road, Wuhan, 430071, China.
Haibo XuDepartment of Radiology, Zhongnan Hospital of Wuhan University, 169 Donghu Road, Wuhan, 430071, China.ORCID 0000-0002-8451-8979
Wuhan University · CN

Funding

China Postdoctoral Science Foundation 2022M712472General Program of National Natural Science Foundation of China 8227071086Science and Technology Innovation Cultivation Fund of Zhongnan Hospital CXPY2022030Young Scientists Fund of the National Natural Science Foundation of China 82203005
6 · The paper itself

Abstract

Intrinsic immunosuppressive tumor microenvironment (ITM) and insufficient tumor infiltration of T cells severely impede the progress of glioblastoma (GBM) immunotherapy. In this study, it is identify that inhibiting the expression of glucose transporter 1 (GLUT1) can facilitate the prevention of lactate excretion from tumor glycolysis, which significantly alleviates the lactate-driven ITM by reducing immunosuppressive tumor-associated macrophages (TAMs) and regulatory T cells (Tregs). Simultaneously, the findings show that the generated inflammatory cytokine IFN-γ during immune activation aggravates the immune escape by upregulating immune checkpoint programmed death-ligand 1 (PD-L1) in tumor cells and TAMs. Therefore, an injectable thermogel loaded with a GLUT1 inhibitor BAY-876 and a PD-1/PD-L1 blocker BMS-1 (Gel@B-B) for dual-regulation of metabolism and immunity of GBM is developed. Consequently, in situ injection of Gel@B-B significantly delays tumor growth and prolongs the survival of the orthotopic GBM mouse model. By actively exposing tumor antigens to antigen-presenting cells, the GBM vaccine combined with Gel@B-B is found to significantly increase the fraction of effector T cells (Th1/CTLs) in the tumor microenvironment, thereby remarkably mitigating tumor recurrence long-term. This study may provide a promising strategy for GBM immunotherapy.

Indexed as

B7-H1 AntigenGlioblastomaImmunotherapyLactic AcidAnimalsBrain NeoplasmsCell Line, TumorDisease Models, AnimalGelsHumansImmune Checkpoint InhibitorsMiceProgrammed Cell Death 1 ReceptorTumor-Associated MacrophagesTumor MicroenvironmentB7-H1 AntigenGelsImmune Checkpoint InhibitorsLactic AcidProgrammed Cell Death 1 Receptordrug‐loading thermogelsglioblastomaimmune checkpointlactatevaccines

Identifiers

PMID38460167
PMCPMC11095231
OpenAlexW4392620936

What OpenQuestion 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 OpenQuestion graph.