Evidence map›Paper›PMID 41012104›Full record

ArticleVaccines2025

TCR-T Cell Recognition of an NY-ESO-1 Epitope Presented by HLA-A2 Supertype: Implications for Cancer Immunotherapy.

Qingqing Lin, Fenglan Liu, Yipeng Ma, Yanwei Li, Tong Lin, Xiaochun Chen, Jinling Zhang, Heng Sun, Zhi Wang, Xiaojun Xia and 3 more

Abstract read
In one paragraph

Article in Vaccines, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Article
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

13 authors.

Qingqing LinShenzhen Innovation Immunotechnology Co., Ltd., Shenzhen International Biological Valley-Life Science Industrial Park, Dapeng New District, Shenzhen 518119, China.
Fenglan LiuShenzhen Innovation Immunotechnology Co., Ltd., Shenzhen International Biological Valley-Life Science Industrial Park, Dapeng New District, Shenzhen 518119, China.
Yipeng MaShenzhen Innovation Immunotechnology Co., Ltd., Shenzhen International Biological Valley-Life Science Industrial Park, Dapeng New District, Shenzhen 518119, China.
Yanwei LiShenzhen Innovation Immunotechnology Co., Ltd., Shenzhen International Biological Valley-Life Science Industrial Park, Dapeng New District, Shenzhen 518119, China.
Tong LinShenzhen Innovation Immunotechnology Co., Ltd., Shenzhen International Biological Valley-Life Science Industrial Park, Dapeng New District, Shenzhen 518119, China.
Xiaochun ChenShenzhen Innovation Immunotechnology Co., Ltd., Shenzhen International Biological Valley-Life Science Industrial Park, Dapeng New District, Shenzhen 518119, China.
Jinling ZhangShenzhen Innovation Immunotechnology Co., Ltd., Shenzhen International Biological Valley-Life Science Industrial Park, Dapeng New District, Shenzhen 518119, China.
Heng SunNational Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen 518116, China.
Zhi WangShenzhen Innovation Immunotechnology Co., Ltd., Shenzhen International Biological Valley-Life Science Industrial Park, Dapeng New District, Shenzhen 518119, China.
Xiaojun XiaState Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou 510060, China.ORCID 0000-0003-4444-7472
Geng TianDepartment of Oncology, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University, Shenzhen 518035, China.
Shi JinNational Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen 518116, China.
Mingjun WangShenzhen Innovation Immunotechnology Co., Ltd., Shenzhen International Biological Valley-Life Science Industrial Park, Dapeng New District, Shenzhen 518119, China.

Funding

Guangdong Basic and Applied Basic Research Foundation 2020B1515120018Shenzhen Basic Research Program JCYJ20180507182902330 and JCYJ20190809115811354Shenzhen Major Science and Technology Special Project KJZD20240903102713018Shenzhen Peacock Plan KQTD20130416114522736Shenzhen Science and Technology Program RCJC20200714114436049Shenzhen Science and Technology Research and Development Fund CJGJZD20200617102403009Special Funds for Dapeng New District Industry Development KJYF202001-13, KJYF202001-12, KY20180214, PT201901-12the Cancer Hospital, Chinese Academy of Medical Sciences, Shenzhen Center/ Shenzhen Cancer Hospital Research Project SZ2020ZD006
6 · The paper itself

Abstract

backgroundT-cell receptor (TCR)-engineered T-cell therapy (TCR-T) has become a promising anticancer therapy. Recognition of tumor cells by TCR-T cells requires matched human leukocyte antigen (HLA) alleles and tumor antigens, which seriously limits their population coverage. One strategy to expand the population coverage of a specific TCR-T cell therapy is to enable TCR-T cells to recognize target peptides presented by more HLA alleles.

methodsIn this study, HLA alleles were selected based on the Chinese population frequency and HLA supertype classification. Then, COS-7 and two tumor cell lines (586 mel and 5637) were transduced with selected HLA alleles for functional evaluation of TCR-T cells. HLA-A2 alleles capable of both exogenously and endogenously presenting the NY-ESO-1-derived epitope and thereby being recognized by TCR-T cells were tested.

resultsWe demonstrated that a given TCR-T cell product can recognize the NY-ESO-1 peptide exogenously and endogenously presented not only by HLA-A*02:01 but also by HLA-A*02:03, HLA-A*02:06, and HLA-A*02:10, almost doubling the population coverage in the Chinese population from 12.01% to 21.05%.

conclusionsOur study suggests that cancer patients expressing members of the HLA-A2 supertype may benefit from the TCR-T cell product, and other TCR-T cell products could similarly expand their population coverage even within the non-Chinese population through an analogous approach.

Indexed as

cancer immunotherapyHLA-A2 allelesHLA-A2 supertypeNY-ESO-1TCR-T

Identifiers

PMID41012104
PMCPMC12474311

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.