CD40×HER2 bispecific antibody overcomes the CCL2-induced trastuzumab resistance in HER2-positive gastric cancer

J Immunother Cancer. 2022 Jul;10(7):e005063. doi: 10.1136/jitc-2022-005063.

Abstract

Background: There was much hard work to study the trastuzumab resistance in HER2-positive gastric cancer (GC), but the information which would reveal this abstruse mechanism is little. In this study, we aimed to investigate the roles of tumor cell-derived CCL2 on trastuzumab resistance and overcome the resistance by treatment with the anti-CD40-scFv-linked anti-HER2 (CD40 ×HER2) bispecific antibody (bsAb).

Methods: We measured the levels of CCL2 expression in HER2-positive GC tissues, and revealed biological functions of tumor cell-derived CCL2 on tumor-associated macrophages (TAMs) and the trastuzumab resistance. Then, we developed CD40 ×HER2 bsAb, and examined the targeting roles on HER2 and CD40, to overcome the trastuzumab resistance without systemic toxicity.

Results: We found the level of CCL2 expression in HER2-postive GC was correlated with infiltration of TAMs, polarization status of infiltrated TAMs, trastuzumab resistance and survival outcomes of GC patients. On exposure to CCL2, TAMs decreased the M1-like phenotype, thereby eliciting the trastuzumab resistance. CCL2 activated the transcription of ZC3H12A, which increased K63-linked deubiquitination and K48-linked auto-ubiquitination of TRAF6/3 to inactivate NF-κB signaling in TAMs. CD40 ×HER2 bsAb, which targeted the CD40 to restore the ubiquitination level of TRAF6/3, increased the M1-like phenotypic transformation of TAMs, and overcame trastuzumab resistance without immune-related adversary effects (irAEs).

Conclusions: We revealed a novel mechanism of trastuzumab resistance in HER2-positive GC via the CCL2-ZC3H12A-TRAF6/3 signaling axis, and presented a CD40 ×HER2 bsAb which showed great antitumor efficacy with few irAEs.

Keywords: gastrointestinal neoplasms; immunotherapy; macrophages; tumor microenvironment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD40 Antigens / metabolism
  • Chemokine CCL2 / metabolism
  • Chemokine CCL2 / pharmacology
  • Humans
  • Receptor, ErbB-2 / metabolism
  • Signal Transduction
  • Stomach Neoplasms* / pathology
  • TNF Receptor-Associated Factor 6 / metabolism
  • TNF Receptor-Associated Factor 6 / pharmacology
  • Trastuzumab / pharmacology
  • Trastuzumab / therapeutic use

Substances

  • CCL2 protein, human
  • CD40 Antigens
  • Chemokine CCL2
  • TNF Receptor-Associated Factor 6
  • Receptor, ErbB-2
  • Trastuzumab