TOX regulates T lymphocytes differentiation and its function in tumor

Front Immunol. 2023 Mar 9:14:990419. doi: 10.3389/fimmu.2023.990419. eCollection 2023.

Abstract

Thymocyte selection-associated high mobility group box protein (TOX) is expressed differently at all T lymphocytes development stages. Owing to more advanced scientific and technological means, including single-cell sequencing technology, heterogeneity of T lymphocytes and TOX has gradually been revealed. Further exploration of such heterogeneity will help us comprehend the developmental stage and functional characteristics of T lymphocytes in greater detail. Emerging evidence supports its regulation not only in exhausting, but also in activating T lymphocytes, thereby verifying TOX heterogeneity. TOX can be used not only as a latent intervention target for tumor diseases and chronic infections, and a therapeutic strategy for autoimmune diseases, but also as a critical factor predicting the drug response and overall survival of patients with malignant tumors.

Keywords: CD4; CD8; T-cell exhaustion; TOX; tumor.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cell Differentiation
  • High Mobility Group Proteins* / metabolism
  • Humans
  • Neoplasms*
  • T-Lymphocytes* / metabolism

Substances

  • High Mobility Group Proteins
  • TOX protein, human

Grants and funding

This project is partly supported by Key Technology Research and Development Program of Tianjin (18ZXDBSY00140 to HW), Scientific research projects (tjsyljkxh016 to HW) was supported by Tianjin Association of Medical and Health.