The effects of T-DXd on the expression of HLA class I and chemokines CXCL9/10/11 in HER2-overexpressing gastric cancer cells

Sci Rep. 2021 Aug 19;11(1):16891. doi: 10.1038/s41598-021-96521-2.

Abstract

Trastuzumab deruxtecan (T-DXd), a HER2-targeting antibody-drug conjugate with a topoisomerase I inhibitor deruxtecan (DXd), exhibits an excellent anti-tumor effect in previously treated HER2-positive tumors. A recent study demonstrated that T-DXd not only suppressed tumor growth but also enhanced anti-tumor immunity through increasing the number of tumor-infiltrating CD8+ T cells and enhancement of major-histocompatibility-complex class I expression on tumor cells in a mouse model. However, the effect of T-DXd on anti-tumor immune responses in human cancers is largely unknown. We investigated the effect of T-DXd on the expression of HLA class I and CXCL9/10/11, T-cell chemoattractants, in HER2-positive human gastric cancer (GC) cells. We found that T-DXd significantly inhibited GC cell proliferation in a HER2-dependent manner, while it slightly increased the expression of HLA class I in HER2-positive GC cells. Moreover, we revealed that T-DXd significantly induced mRNA expression of CXCL9/10/11 in HER2-positive GC cells. T-DXd-triggered up-regulation of these chemokines was mediated through the activation of DNA damage signaling pathways. These results suggest that T-DXd triggers anti-tumor immune responses at least in part through induction of the expression of HLA class I and CXCL9/10/11 on HER2-positive GC cells, resulting in the enhancement of anti-tumor immunity in human GC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Camptothecin / analogs & derivatives*
  • Camptothecin / pharmacology
  • Camptothecin / therapeutic use
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Chemokine CXCL10 / genetics*
  • Chemokine CXCL10 / metabolism
  • Chemokine CXCL11 / genetics*
  • Chemokine CXCL11 / metabolism
  • Chemokine CXCL9 / genetics*
  • Chemokine CXCL9 / metabolism
  • Chemotactic Factors / pharmacology
  • DNA Damage
  • Gene Expression Regulation, Neoplastic / drug effects
  • Histocompatibility Antigens Class I / metabolism*
  • Humans
  • Immunoconjugates / pharmacology
  • Immunoconjugates / therapeutic use*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptor, ErbB-2 / metabolism*
  • Stomach Neoplasms / drug therapy*
  • Stomach Neoplasms / genetics
  • Stomach Neoplasms / immunology*
  • Trastuzumab / pharmacology
  • Trastuzumab / therapeutic use*
  • Up-Regulation / drug effects

Substances

  • Chemokine CXCL10
  • Chemokine CXCL11
  • Chemokine CXCL9
  • Chemotactic Factors
  • Histocompatibility Antigens Class I
  • Immunoconjugates
  • RNA, Messenger
  • trastuzumab deruxtecan
  • Receptor, ErbB-2
  • Trastuzumab
  • Camptothecin