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Defining a TCF1-expressing progenitor allogeneic CD8+ T cell subset in acute graft-versus-host disease

Author

Listed:
  • Solhwi Lee

    (Sungkyunkwan University School of Medicine)

  • Kunhee Lee

    (Sungkyunkwan University School of Medicine)

  • Hyeonjin Bae

    (Sungkyunkwan University School of Medicine)

  • Kyungmin Lee

    (Sungkyunkwan University School of Medicine)

  • Junghwa Lee

    (Sungkyunkwan University School of Medicine)

  • Junhui Ma

    (Sungkyunkwan University School of Medicine)

  • Ye Ji Lee

    (GENINUS Inc.)

  • Bo Ryeong Lee

    (GENINUS Inc.)

  • Woong-Yang Park

    (GENINUS Inc.
    Samsung Medical Center)

  • Se Jin Im

    (Sungkyunkwan University School of Medicine)

Abstract

Graft-versus-host disease (GvHD) is a severe complication of hematopoietic stem cell transplantation driven by activated allogeneic T cells. Here, we identify a distinct subset of T cell factor-1 (TCF1)+ CD8+ T cells in mouse allogeneic and xenogeneic transplant models of acute GvHD. These TCF1+ cells exhibit distinct characteristics compared to TCF1- cells, including lower expression of inhibitory receptors and higher expression of costimulatory molecules. Notably, the TCF1+ subset displays exclusive proliferative potential and could differentiate into TCF1- effector cells upon antigenic stimulation. Pathway analyses support the role of TCF1+ and TCF1- subsets as resource cells and effector cells, respectively. Furthermore, the TCF1+ CD8+ T cell subset is primarily present in the spleen and exhibits a resident phenotype. These findings provide insight into the differentiation of allogeneic and xenogeneic CD8+ T cells and have implications for the development of immunotherapeutic strategies targeting acute GvHD.

Suggested Citation

  • Solhwi Lee & Kunhee Lee & Hyeonjin Bae & Kyungmin Lee & Junghwa Lee & Junhui Ma & Ye Ji Lee & Bo Ryeong Lee & Woong-Yang Park & Se Jin Im, 2023. "Defining a TCF1-expressing progenitor allogeneic CD8+ T cell subset in acute graft-versus-host disease," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-41357-9
    DOI: 10.1038/s41467-023-41357-9
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