Evidence map›Paper›PMID 35925286›Full record

ArticleCancer immunology, immunotherapy : CII2023

Anti-mesothelin CAR-T immunotherapy in patients with ovarian cancer.

Jiannan Chen, Jianhua Hu, Lili Gu, Feng Ji, Fan Zhang, Miaomiao Zhang, Jun Li, Zhengliang Chen, Longwei Jiang, Yan Zhang and 9 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 51 citations in OpenAlex.

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  9. Targeting orthotopic and metastatic pancreatic cancer with allogeneic stem cell-engineered mesothelin-redirected CAR-NKT cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 5 institutions in 2 countries.

Jiannan Chen *Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
Jianhua Hu *Department of Biotherapy, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
Lili Gu *Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
Feng JiJiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
Fan ZhangJiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
Miaomiao ZhangJiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
Jun LiNanjing Blue Shield Biotechnology Co., Ltd., Nanjing, 210023, China.
Zhengliang ChenNanjing Blue Shield Biotechnology Co., Ltd., Nanjing, 210023, China.
Longwei JiangDepartment of Biotherapy, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
Yan ZhangDepartment of Biotherapy, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
Ruifang ShiDepartment of Biotherapy, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
Lihua MaDepartment of Biotherapy, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
Shaochang JiaDepartment of Biotherapy, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
Ying ZhangDepartment of Pathology, Jinling Hospital of Nanjing University School of Medicine, Nanjing, 210002, China.
Qi ZhangCenter of Interventional Radiology and Vascular Surgery, Department of Radiology, Zhongda Hospital, Medical School, Southeast University, Nanjing, 210009, China.
Junqing LiangInner Mongolia Autonomous Region Cancer Hospital, Hohhot, 010010, China.
Shunyu YaoBaylor University, 1311 S 5th St, Waco, USA.
Zhigang HuJiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China. huzg_2000@126.com.ORCID http://orcid.org/0000-0002-5265-3535
Zhigang GuoJiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China. guo@njnu.edu.cn.
Nanjing General Hospital of Nanjing Military Command · CNNanjing Normal University · CNBaylor University · USInner Mongolia Autonomous Region Hospital of Traditional Chinese Medicine · CNZhongda Hospital Southeast University · CN

Funding

Innovative Research Group Project of the National Natural Science Foundation of China 81872284
6 · The paper itself

Abstract

Recently, chimeric antigen receptor T cell (CAR-T) therapy has received increasing attention as an adoptive cellular immunotherapy that targets tumors. However, numerous challenges remain for the effective use of CAR-T to treat solid tumors, including ovarian cancer, which is an aggressive and metastatic cancer with a poor therapeutic response. We screened for an effective anti-MSLN single-chain Fv antibody with comparable binding activity and non-off-target properties using human phage display library. A second-generation of anti-MSLN CAR was designed and generated. We demonstrated the efficacy of our anti-MSLN CAR-T cells for ovarian cancer treatment in an in vitro experiment to kill ovarian tumor cell lines. The anti-MSLN CAR-T cells impeded MSLN-positive tumor growth concomitant with a significant increase in cytokine levels compared with the control. Then, we demonstrated the efficacy of anti-MSLN CAR-T cells in an in vivo experiment against ovarian cancer cell-derived xenografts. Furthermore, we herein report three cases with ovarian cancer who were treated with autologous anti-MSLN CAR-T cells and evaluate the safety and effectiveness of adoptive cell therapy. In this investigator-initiated clinical trials, no patients experienced cytokine release syndrome or neurological symptoms over 2 grads. Disease stabilized in two patients, with progression-free survival times of 5.8 and 4.6 months. Transient CAR expression was detected in patient blood after infusion each time. The tumor partially subsided, and the patient's condition was relieved. In conclusion, this work proves the efficacy of the anti-MSLN CAR-T treatment strategy in ovarian cancer and provides preliminary data for the development of further clinical trials.

Indexed as

Immunotherapy, AdoptiveOvarian NeoplasmsReceptors, Chimeric AntigenAnimalsCell Line, TumorFemaleGPI-Linked ProteinsHumansImmunotherapyGPI-Linked ProteinsReceptors, Chimeric AntigenCAR-TImmunotherapyInvestigator-initiated clinical trialMesothelinOvarian cancer

Identifiers

PMID35925286
PMCPMC10991348
OpenAlexW4289780861

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.