Evidence map›Paper›PMID 36944898›Full record

ArticleMedical oncology (Northwood, London, England)2023

CD27 agonism coordinates with CD28 and 4-1BB signal to augment the efficacy of CAR-T cells in colorectal tumor.

Chengcheng Zhang, Jiankun Jia, Gang Heng, Yunyan Li, Meilin Wang, Jun Chen, Linling Wang, Di Jiang, Zhi Yang, Cheng Qian

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Chengcheng Zhang *Department of hepatobiliary surgery, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, 400038, China.
Jiankun Jia *Department of general surgery, General Hospital of central theater command, Wuhan, 430000, China.
Gang Heng *Department of general surgery, General Hospital of central theater command, Wuhan, 430000, China.
Yunyan LiCenter for Precision Medicine of Cancer, Chongqing Key Laboratory of Translational Research for Cancer Metastasis and Individualized Treatment, Chongqing University Cancer Hospital, Chongqing, 400030, China.
Meilin WangCenter for Precision Medicine of Cancer, Chongqing Key Laboratory of Translational Research for Cancer Metastasis and Individualized Treatment, Chongqing University Cancer Hospital, Chongqing, 400030, China.
Jun ChenCenter for Precision Medicine of Cancer, Chongqing Key Laboratory of Translational Research for Cancer Metastasis and Individualized Treatment, Chongqing University Cancer Hospital, Chongqing, 400030, China.
Linling WangCenter for Precision Medicine of Cancer, Chongqing Key Laboratory of Translational Research for Cancer Metastasis and Individualized Treatment, Chongqing University Cancer Hospital, Chongqing, 400030, China.
Di JiangDepartment of hepatobiliary surgery, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, 400038, China.
Zhi YangCenter for Precision Medicine of Cancer, Chongqing Key Laboratory of Translational Research for Cancer Metastasis and Individualized Treatment, Chongqing University Cancer Hospital, Chongqing, 400030, China.
Cheng QianCenter for Precision Medicine of Cancer, Chongqing Key Laboratory of Translational Research for Cancer Metastasis and Individualized Treatment, Chongqing University Cancer Hospital, Chongqing, 400030, China. cqian8634@gmail.com.ORCID http://orcid.org/0000-0003-1500-9991
Chongqing University · CNArmy Medical University · CNWuhan General Hospital of Guangzhou · CN

Funding

National Natural Science Foundation of China 81520108025National Natural Science Foundation of China 81903157
6 · The paper itself

Abstract

Chimeric antigen receptor T cell (CAR-T) is regarded as a promising therapy for malignancies. In our previous clinical trial targeted colorectal tumors, we found that CAR-T cells experienced poor proliferation and persistence in tumor sites. To improve the efficacy of CAR-T cells, we introduced CD27 co-stimulation signal into the established system and found that the CEA28BB27Z CAR-T cells exhibited enhanced proliferation and anti-tumor activity. Next, we demonstrated that the CEA28BB27Z CAR-T cells expressed less immune checkpoint receptors and generated more CD4

Indexed as

Colorectal NeoplasmsReceptors, Chimeric AntigenTumor Necrosis Factor Receptor Superfamily, Member 7CD28 AntigensHumansImmunotherapy, AdoptiveT-LymphocytesTumor Necrosis Factor Receptor Superfamily, Member 9Xenograft Model Antitumor AssaysCD28 AntigensReceptors, Chimeric AntigenTNFRSF9 protein, humanTumor Necrosis Factor Receptor Superfamily, Member 7Tumor Necrosis Factor Receptor Superfamily, Member 9CAR-T cellsCD27Colorectal tumorMemory stem T cellsMitochondrial dynamics

Identifiers

PMID36944898
OpenAlexW4353017195

What OpenQuestion holds

Textmetadata
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.