Evidence map›Paper›PMID 32876369›Full record

ArticleCancer science2020

Synergistic effect of ibrutinib and CD19 CAR-T cells on Raji cells in vivo and in vitro.

Meijing Liu, Xuelin Wang, Zheng Li, Rui Zhang, Juan Mu, Yanyu Jiang, Qi Deng, Lei Sun

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 28 citations in OpenAlex.

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  8. [Analysis of infection in B-cell lymphoma patients treated with BTK inhibitors].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2023
    Article
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  19. Pharmacologic Control of CAR T Cells.International journal of molecular sciences · 2021
    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 at 3 institutions in 1 country.

Meijing LiuThe First Central Clinical College of Tianjin Medical University, Tianjin, China.
Xuelin WangInstitute of Developmental Biology and Molecular Medicine, Fudan University, Shanghai, China.
Zheng LiThe First Central Clinical College of Tianjin Medical University, Tianjin, China.
Rui ZhangDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Juan MuDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.ORCID https://orcid.org/0000-0003-2339-0892
Yanyu JiangDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Qi DengDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.ORCID https://orcid.org/0000-0002-3646-4953
Lei SunInstitute of Developmental Biology and Molecular Medicine, Fudan University, Shanghai, China.
Tianjin First Center Hospital · CNFudan University · CNTianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ibrutinib might improve the efficacy of anti-CD19 chimeric antigen receptor (CD19 CAR) T-cell therapy in chronic lymphocytic leukemia (CLL). We studied the possibility and mechanism of the synergistic effect of ibrutinib and CAR-T cells in other types of lymphoma. In this study, we selected the CD19 CAR-T cells of a patient with lymphoma who failed in his CD19 CAR-T-cell therapy and a dose of 8 mg/kg/d ibrutinib. Subcutaneous and tail vein tumorigenic mice were established with Raji cells. The differences in the synergistic effect between these 2 models were compared by bioluminescence imaging (BLI) monitoring and flow cytometry (FCM). The expression of the STAT-3 signaling pathway was assessed by western blot analysis. There was no synergistic effect of ibrutinib and CD19 CAR-T cells in vitro. Programmed cell death-ligand 1 (PD-L1) was expressed in 0.23 ± 0.06% of Raji cells. In the subcutaneous tumorigenic model, the luciferase signal was reduced significantly in the group receiving ibrutinib combined with CD19 CAR-T cells. Moreover, the proportion of CD19 CAR-T cells was higher in the polytherapy group than in the CAR-T-cell monotherapy group. However, we did not get an analogous synergistic effect in the tail vein tumorigenic model. STAT-3 signaling pathway expression in the residual tumor cells did not differ between those with and those without ibrutinib, suggesting that the IL-10/STAT-3/PD-L1 pathway was not involved in the synergistic effect. Therefore, some other mechanism might be a target for ibrutinib. Our results provide evidence for the use of ibrutinib in polytherapy for other types of B-cell lymphoma.

Indexed as

Immunotherapy, AdoptiveAdenineAdultAgedAnimalsAntigens, CD19Biomarkers, TumorCell Line, TumorCombined Modality TherapyDisease Models, AnimalFemaleHumansImmunophenotypingLymphoma, Large B-Cell, DiffuseMaleMiceAdenineAntigens, CD19Biomarkers, TumoribrutinibPiperidinesProtein Kinase InhibitorsReceptors, Antigen, T-CellSTAT3 protein, humanSTAT3 Transcription FactorBruton tyrosine kinase inhibitorchimeric antigen receptorprogrammed cell death-ligand 1Raji cell linetumor microenvironment

Identifiers

PMID32876369
PMCPMC7648031
OpenAlexW3082625327

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.