Evidence map›Paper›PMID 37399358›Full record

ArticleJournal for immunotherapy of cancer2023

Inhibition of lactate transport by MCT-1 blockade improves chimeric antigen receptor T-cell therapy against B-cell malignancies.

Ernesto Lopez, Rajesh Karattil, Francesco Nannini, Gordon Weng-Kit Cheung, Lilian Denzler, Felipe Galvez-Cancino, Sergio Quezada, Martin A Pule

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 2 pooled it
11.7field-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

47 citing papers in PubMed, 2 syntheses or guidelines pooled it, 51 citations in OpenAlex.

  1. Pooled it
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  5. Targeting Lactate and Lactylation in Cancer Metabolism and Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  16. Lactate, a Spearhead of Cancer Aggressiveness: Metabolic Reprogramming, Immune Suppression, and Metastatic Progression.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2026
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  18. [Progress in metabolomics of multiple myeloma].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2025
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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 at 2 institutions in 2 countries.

Ernesto LopezHaematology Department, Cancer Institute, University College London, London, UK.ORCID 0000-0003-1012-2899
Rajesh KarattilHaematology Department, Cancer Institute, University College London, London, UK.
Francesco NanniniCancer Immunology Unit, Cancer Institute, University College London, London, UK.ORCID 0000-0001-9589-5107
Gordon Weng-Kit CheungHaematology Department, Cancer Institute, University College London, London, UK.ORCID 0000-0002-7016-1059
Lilian DenzlerDivision of Biosciences, Institute of Structural and Molecular Biology, University College London, London, UK.
Felipe Galvez-CancinoCancer Immunology Unit, Cancer Institute, University College London, London, UK.
Sergio QuezadaCancer Immunology Unit, Cancer Institute, University College London, London, UK.ORCID 0000-0002-9763-1700
Martin A PuleHaematology Department, Cancer Institute, University College London, London, UK martin.pule@ucl.ac.uk.ORCID 0000-0002-8347-9867
Cancer Institute (WIA) · INInstitute of Structural and Molecular Biology · GB

Funding

Cancer Research UK C33499/A20265Cancer Research UK C36463/A20764Cancer Research UK C36463/A22246Cancer Research UK C416/A18088Cancer Research UK C7893/A26233
6 · The paper itself

Abstract

backgroundChimeric antigen receptor (CAR) T cells have shown remarkable results against B-cell malignancies, but only a minority of patients have long-term remission. The metabolic requirements of both tumor cells and activated T cells result in production of lactate. The export of lactate is facilitated by expression of monocarboxylate transporter (MCTs). CAR T cells express high levels of MCT-1 and MCT-4 on activation, while certain tumors predominantly express MCT-1.

methodsHere, we studied the combination of CD19-specific CAR T-cell therapy with pharmacological blockade of MCT-1 against B-cell lymphoma.

resultsMCT-1 inhibition with small molecules AZD3965 or AR-C155858 induced CAR T-cell metabolic rewiring but their effector function and phenotype remained unchanged, suggesting CAR T cells are insensitive to MCT-1 inhibition. Moreover, improved cytotoxicity in vitro and antitumoral control on mouse models was found with the combination of CAR T cells and MCT-1 blockade.

conclusionThis work highlights the potential of selective targeting of lactate metabolism via MCT-1 in combination with CAR T cells therapies against B-cell malignancies.

Indexed as

Lymphoma, B-CellReceptors, Chimeric AntigenAnimalsCell- and Tissue-Based TherapyImmunotherapy, AdoptiveLactatesMiceLactatesReceptors, Chimeric AntigenImmunotherapyMetabolic Networks and PathwaysReceptors, Chimeric AntigenT-Lymphocytes

Identifiers

PMID37399358
PMCPMC10314680
OpenAlexW4382935546

What OpenQuestion holds

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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.