Evidence map›Paper›PMID 35338087›Full record

ArticleJournal for immunotherapy of cancer2022

Development of a TCR-like antibody and chimeric antigen receptor against NY-ESO-1/HLA-A2 for cancer immunotherapy.

Xin Liu, Yixiang Xu, Wei Xiong, Bingnan Yin, Yuqian Huang, Junjun Chu, Changsheng Xing, Chen Qian, Yang Du, Tianhao Duan and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.4field-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

39 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  4. Article
  5. KRASScience advances · 2026
    Article
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  8. Article
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  18. Article
  19. NY-ESO-1 antigen: A promising frontier in cancer immunotherapy.Clinical and translational medicine · 2024
    Review
  20. Review
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

15 authors at 4 institutions in 2 countries.

Xin LiuKeck School of Medicine, University of Southern California, Los Angeles, California, USA.
Yixiang XuTexas Therapeutics Institute, Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center at Houston, Houston, Texas, USA.
Wei XiongTexas Therapeutics Institute, Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center at Houston, Houston, Texas, USA.ORCID 0000-0002-8087-5047
Bingnan YinKeck School of Medicine, University of Southern California, Los Angeles, California, USA.
Yuqian HuangCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, Texas, USA.
Junjun ChuKeck School of Medicine, University of Southern California, Los Angeles, California, USA.
Changsheng XingKeck School of Medicine, University of Southern California, Los Angeles, California, USA.
Chen QianKeck School of Medicine, University of Southern California, Los Angeles, California, USA.
Yang DuKeck School of Medicine, University of Southern California, Los Angeles, California, USA.
Tianhao DuanKeck School of Medicine, University of Southern California, Los Angeles, California, USA.
Helen Y WangKeck School of Medicine, University of Southern California, Los Angeles, California, USA.
Ningyan ZhangTexas Therapeutics Institute, Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center at Houston, Houston, Texas, USA.
John S YuNeurosurgical Oncology in the Department of Neurosurgery, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Zhiqiang AnTexas Therapeutics Institute, Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center at Houston, Houston, Texas, USA Zhiqiang.An@uth.tmc.edu rongfuwa@usc.edu.
Rongfu WangKeck School of Medicine, University of Southern California, Los Angeles, California, USA Zhiqiang.An@uth.tmc.edu rongfuwa@usc.edu.ORCID 0000-0002-8834-2763
University of Southern California · USBrown Foundation · USCedars-Sinai Medical Center · USHouston Methodist · US

Funding

Transport Oncophysics CoreU54CA210181 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI SHEN, HAIFA · 2016 to 2020
$9.3M
Novel Strategies for Intervention of Inflammatory Diseases and Cancer - Research Supplement to R01-CA101795R01CA101795 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI WANG, RONGFU · 2004 to 2022
$4.6M
CD4+ T cells and neoantigens in melanoma immunotherapy.R01CA246547 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI WANG, RONGFU · 2021 to 2025
$3.1M
NCI NIH HHS R01 CA101795NCI NIH HHS R01 CA246547NCI NIH HHS U54 CA210181
6 · The paper itself

Abstract

backgroundThe current therapeutic antibodies and chimeric antigen receptor (CAR) T cells are capable of recognizing surface antigens, but not of intracellular proteins, thus limiting the target coverage for drug development. To mimic the feature of T-cell receptor (TCR) that recognizes the complex of major histocompatibility class I and peptide on the cell surface derived from the processed intracellular antigen, we used NY-ESO-1, a cancer-testis antigen, to develop a TCR-like fully human IgG1 antibody and its derivative, CAR-T cells, for cancer immunotherapy.

methodsHuman single-chain variable antibody fragment (scFv) phage library (~10

resultsMonoclonal antibody 2D2 identified from phage-displayed library specifically bound to NY-ESO-1

conclusionsThis study showed the specificity of the antibody identified from human scFv phage library and demonstrated the potential antitumor activity by TCR-like CAR-T cells both in vitro and in vivo, warranting further preclinical and clinical evaluation of the TCR-like antibody in patients. The generation of TCR-like antibody and its CAR-T cells provides the state-of-the-art platform and proof-of-concept validation to broaden the scope of target antigen recognition and sheds light on the development of novel therapeutics for cancer immunotherapy.

Indexed as

MelanomaReceptors, Chimeric AntigenTriple Negative Breast NeoplasmsAnimalsAntibodiesAntigens, NeoplasmCell Line, TumorHLA-A2 AntigenHumansImmunotherapyMaleMicePeptidesReceptors, Antigen, T-CellAntibodiesAntigens, NeoplasmHLA-A2 AntigenPeptidesReceptors, Antigen, T-CellReceptors, Chimeric Antigenantibody affinityantibody specificityimmunotherapyreceptors, chimeric antigen

Identifiers

PMID35338087
PMCPMC8961179
OpenAlexW4220670463

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.