Impact of mouse model tumor implantation site on acquired resistance to anti-PD-1 immune checkpoint therapy

Front Immunol. 2023 Jan 10:13:1011943. doi: 10.3389/fimmu.2022.1011943. eCollection 2022.

Abstract

Introduction: The use of tumor subcutaneous (SC) implantations rather than orthotopic sites is likely to induce a significant bias, in particular, in the field of immunotherapy.

Methods: In this study, we developed and characterized MC38 models, implanted subcutaneously and orthotopically, which were either sensitive or rendered resistant to anti-PD1 therapy. We characterized the tumor immune infiltrate by flow cytometry at baseline and after treatment.

Results and discussion: Our results demonstrate several differences between SC and orthotopic models at basal state, which tend to become similar after therapy. These results emphasize the need to take into account tumor implantation sites when performing preclinical studies with immunotherapeutic agents.

Keywords: orthotopic; MC38; anti-PD-1; preclinical model; subcutaneous.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Disease Models, Animal
  • Drug Resistance, Neoplasm*
  • Immune Checkpoint Inhibitors* / pharmacology
  • Immunotherapy / methods
  • Mice
  • Neoplasms* / therapy

Substances

  • Immune Checkpoint Inhibitors

Grants and funding

This work was supported in part by the Lyric Grant INCa-DGOS-4664. The National Association Research and Technology (ANRT) supported MD for their PhD thesis (CIFRE funding) during a 3-year contract with Antineo.