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T cell receptor β-chain-targeting chimeric antigen receptor T cells against T cell malignancies

Author

Listed:
  • Fanlin Li

    (Shanghai Jiao Tong University)

  • Huihui Zhang

    (Shanghai Jiao Tong University
    Shanghai Jiao Tong University)

  • Wanting Wang

    (Shanghai Jiao Tong University
    Shanghai Jiao Tong University)

  • Puyuan Yang

    (Shanghai Jiao Tong University)

  • Yue Huang

    (Shanghai Jiao Tong University)

  • Junshi Zhang

    (Shanghai Jiao Tong University)

  • Yaping Yan

    (Shanghai Jiao Tong University)

  • Yuan Wang

    (Shanghai Jiao Tong University)

  • Xizhong Ding

    (Shanghai Jiao Tong University)

  • Jie Liang

    (Shanghai Jiao Tong University)

  • Xinyue Qi

    (Shanghai Jiao Tong University)

  • Min Li

    (Shanghai Jiao Tong University)

  • Ping Han

    (Shanghai Jiao Tong University)

  • Xiaoqing Zhang

    (Shanghai Jiao Tong University)

  • Xin Wang

    (Shanghai Longyao Biotechnology Limited)

  • Jiang Cao

    (Affiliated Hospital of Xuzhou Medical University)

  • Yang-Xin Fu

    (University of Texas Southwestern Medical Center)

  • Xuanming Yang

    (Shanghai Jiao Tong University
    Shanghai Jiao Tong University)

Abstract

The success of chimeric antigen receptor (CAR) T cells in treating B cell malignancies comes at the price of eradicating normal B cells. Even though T cell malignancies are aggressive and treatment options are limited, similar strategies for T cell malignancies are constrained by the severe immune suppression arising from bystander T cell aplasia. Here, we show the selective killing of malignant T cells without affecting normal T cell-mediated immune responses in vitro and in a mouse model of disseminated leukemia. Further, we develop a CAR construct that carries the single chain variable fragment of a subtype-specific antibody against the variable TCR β-chain region. We demonstrate that these anti-Vβ8 CAR-T cells are able to recognize and kill all Vβ8+ malignant T cells that arise from clonal expansion while sparing malignant or healthy Vβ8− T cells, allowing sufficient T cell-mediated cellular immunity. In summary, we present a proof of concept for a selective CAR-T cell therapy to eradicate T cell malignancies while maintaining functional adaptive immunity, which opens the possibility for clinical development.

Suggested Citation

  • Fanlin Li & Huihui Zhang & Wanting Wang & Puyuan Yang & Yue Huang & Junshi Zhang & Yaping Yan & Yuan Wang & Xizhong Ding & Jie Liang & Xinyue Qi & Min Li & Ping Han & Xiaoqing Zhang & Xin Wang & Jiang, 2022. "T cell receptor β-chain-targeting chimeric antigen receptor T cells against T cell malignancies," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-32092-8
    DOI: 10.1038/s41467-022-32092-8
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    Cited by:

    1. Jingjing Ren & Xiaofeng Liao & Julia M. Lewis & Jungsoo Chang & Rihao Qu & Kacie R. Carlson & Francine Foss & Michael Girardi, 2024. "Generation and optimization of off-the-shelf immunotherapeutics targeting TCR-Vβ2+ T cell malignancy," Nature Communications, Nature, vol. 15(1), pages 1-16, December.

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