Evidence map›Paper›PMID 40011760›Full record

ArticleCell research2025

TCR catch bonds nonlinearly control CD8 cooperation to shape T cell specificity.

Rui Qin, Yong Zhang, Jiawei Shi, Peng Wu, Chenyi An, Zhenhai Li, Nuo Liu, Ziyan Wan, Ting Hua, Xiaolong Li and 3 more

Abstract read
In one paragraph

Article in Cell research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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  12. Adoptive T-cell therapy for virus-associated diseases.Clinical microbiology reviews · 2025
    Review
  13. Article
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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

13 authors.

Rui Qin *Department of Cardiology of the Second Affiliated Hospital and Department of Cell Biology, Zhejiang University School of Medicine, Liangzhu Laboratory, Zhejiang University, Hangzhou, Zhejiang, China.
Yong Zhang *State Key Laboratory of Epigenetic Regulation and Intervention, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.ORCID 0000-0001-6664-435X
Jiawei Shi *Key Laboratory for Biomedical Engineering of the Ministry of Education, and Zhejiang Provincial Key Laboratory of Cardio-Cerebral Vascular Detection Technology and Medicinal Effectiveness Appraisal, and College of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou, Zhejiang, China.
Peng Wu *Tianjian Laboratory of Advanced Biomedical Sciences, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Chenyi AnSchool of Biology and Engineering, Guizhou Medical University, Guiyang, Guizhou, China.
Zhenhai LiShanghai Key Laboratory of Mechanics in Energy Engineering, Shanghai Institute of Applied Mathematics and Mechanics, School of Mechanics and Engineering Science, Shanghai University, Shanghai, China.ORCID 0000-0002-0720-2807
Nuo LiuDepartment of Hematology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Ziyan WanDepartment of Hematology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Ting HuaDepartment of Hematology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Xiaolong LiDepartment of Hematology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Jizhong LouState Key Laboratory of Epigenetic Regulation and Intervention, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China. jlou@ibp.ac.cn.ORCID 0000-0003-4031-6125
Weiwei YinKey Laboratory for Biomedical Engineering of the Ministry of Education, and Zhejiang Provincial Key Laboratory of Cardio-Cerebral Vascular Detection Technology and Medicinal Effectiveness Appraisal, and College of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou, Zhejiang, China. wwyin@zju.edu.cn.
Wei ChenDepartment of Cardiology of the Second Affiliated Hospital and Department of Cell Biology, Zhejiang University School of Medicine, Liangzhu Laboratory, Zhejiang University, Hangzhou, Zhejiang, China. jackweichen@zju.edu.cn.ORCID 0000-0001-5366-7253

Funding

Chinese Academy of Sciences (CAS) KJ2070000094National Natural Science Foundation of China (National Science Foundation of China) 12102389National Natural Science Foundation of China (National Science Foundation of China) 12172371National Natural Science Foundation of China (National Science Foundation of China) 12272216National Natural Science Foundation of China (National Science Foundation of China) 12272348National Natural Science Foundation of China (National Science Foundation of China) 31600751National Natural Science Foundation of China (National Science Foundation of China) 31971237National Natural Science Foundation of China (National Science Foundation of China) 32090044National Natural Science Foundation of China (National Science Foundation of China) 32101052National Natural Science Foundation of China (National Science Foundation of China) T2394511National Natural Science Foundation of China (National Science Foundation of China) T2394512University of Science and Technology of China (USTC) KY9100000092
6 · The paper itself

Abstract

Naturally evolved T-cell receptors (TCRs) exhibit remarkably high specificity in discriminating non-self antigens from self-antigens under dynamic biomechanical modulation. In contrast, engineered high-affinity TCRs often lose this specificity, leading to cross-reactivity with self-antigens and off-target toxicity. The underlying mechanism for this difference remains unclear. Our study reveals that natural TCRs exploit mechanical force to form optimal catch bonds with their cognate antigens. This process relies on a mechanically flexible TCR-pMHC binding interface, which enables force-enhanced CD8 coreceptor binding to MHC-α

Indexed as

CD8 AntigensLymphocyte ActivationReceptors, Antigen, T-CellT-LymphocytesHumansLigandsMolecular Docking SimulationMolecular Dynamics SimulationProtein BindingProtein EngineeringProtein Structure, QuaternaryCD8 AntigensLigandsReceptors, Antigen, T-Cell

Identifiers

PMID40011760
PMCPMC11958657

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.