Dual blockage of both PD-L1 and CD47 enhances the therapeutic effect of oxaliplatin and FOLFOX in CT-26 mice tumor model

Sci Rep. 2023 Feb 11;13(1):2472. doi: 10.1038/s41598-023-29363-9.

Abstract

Colorectal cancer is a poorly immunogenic. Such property can be reverted by using ICD. However, ICD inducers can also induce the expression of inhibitory checkpoint receptors CD47 and PD-L1 on tumor cells, making CRC tumors resistant to mainly CD8 T cell killing and macrophage-mediated phagocytosis. In this study, we examined the therapeutic effect of Oxaliplatin and FOLFOX regimen in combination with blocking antibodies against CD47 and PD-L1. FOLFOX and Oxaliplatin treatment lead to an increase in CD47 and PD-L1 expression on CT-26 cells invitro and invivo. Combining blocking antibodies against CD47 and PD-L1 with FOLFOX leads to a significant increase in survival and a decrease in tumor size. This triple combining regimen also leads to a significant decrease in Treg and MDSC and a significant increase in CD8 + INF-γ + lymphocytes and M1/M2 macrophage ratio in the tumor microenvironment. Our study showed triple combining therapy with FOLFOX, CD47 and PD-L1 is an effective treatment regimen in CT-26 mice tumor model and may consider as a potential to translate to the clinic.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Blocking
  • Antineoplastic Combined Chemotherapy Protocols* / pharmacology
  • B7-H1 Antigen* / metabolism
  • CD47 Antigen* / metabolism
  • Colorectal Neoplasms* / drug therapy
  • Fluorouracil
  • Leucovorin
  • Mice
  • Organoplatinum Compounds
  • Oxaliplatin* / pharmacology
  • Tomography, X-Ray Computed
  • Tumor Microenvironment*

Substances

  • Antibodies, Blocking
  • B7-H1 Antigen
  • CD47 Antigen
  • Oxaliplatin

Supplementary concepts

  • Folfox protocol