The Tumor-Immune Response Is Not Compromised by Mesenchymal Stromal Cells in Humanized Mice

J Immunol. 2019 Nov 15;203(10):2735-2745. doi: 10.4049/jimmunol.1900807. Epub 2019 Oct 2.

Abstract

Therapeutic uses of mesenchymal stromal cells (MSCs) have emerged over the past decade. Yet, their effect on tumor growth remains highly debated, particularly in an immune competent environment. In this study, we wanted to investigate the impact of human umbilical cord-derived MSCs (hUC-MSCs) on tumor growth in humanized mice generated by the human adoptive transfer of PBMCs or the cotransplantation of hematopoietic stem cells and human thymic tissue (human BLT [Hu-BLT]). Our results showed that the growth and immune rejection of engineered human fibroblastic tumors was not altered by the injection of hUC-MSCs in immune-deficient or humanized mice, respectively. This was observed whether tumor cells were injected s.c. or i.v. and independently of the injection route of the hUC-MSCs. Moreover, only in Hu-BLT mice did hUC-MSCs have some effects on the tumor-immune infiltrate, yet without altering tumor growth. These results demonstrate that hUC-MSCs do not promote fibroblastic tumor growth and neither do they prevent tumor infiltration and rejection by immune cells in humanized mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adoptive Transfer
  • Animals
  • Cell Line, Transformed / transplantation
  • Fibroblasts / transplantation
  • Genetic Vectors
  • Graft Rejection / immunology
  • Heterografts
  • Humans
  • Injections, Intravenous
  • Injections, Subcutaneous
  • Lymphocytes, Tumor-Infiltrating / immunology*
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / immunology*
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Neoplasm Transplantation
  • Neoplasms, Experimental / immunology
  • Radiation Chimera
  • Specific Pathogen-Free Organisms
  • Telomerase / genetics
  • Telomerase / physiology
  • Thymus Gland / transplantation
  • Wharton Jelly / cytology

Substances

  • TERT protein, human
  • Telomerase

Grants and funding