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

Fanlin LiHuihui ZhangWanting WangPuyuan YangYue HuangJunshi ZhangYaping YanYuan WangXizhong DingJie LiangXinyue QiMin LiPing HanXiaoqing ZhangXin WangJiang CaoYang-Xin FuXuanming Yang
Published in: Nature communications (2022)
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.
Keyphrases
  • cell therapy
  • immune response
  • mouse model
  • stem cells
  • acute myeloid leukemia
  • regulatory t cells
  • inflammatory response
  • robot assisted
  • cancer therapy
  • minimally invasive
  • endoplasmic reticulum stress