Cannabinoids Reduce Inflammation but Inhibit Lymphocyte Recovery in Murine Models of Bone Marrow Transplantation

Int J Mol Sci. 2019 Feb 4;20(3):668. doi: 10.3390/ijms20030668.

Abstract

Cannabinoids, the biologically active constituents of Cannabis, have potent neuronal and immunological effects. However, the basic and medical research dedicated to medical cannabis and cannabinoids is limited. The influence of these treatments on hematologic reconstitution and on the development of graft versus host disease (GVHD) after bone marrow transplantation (BMT) is largely unknown. In this research, we compared the influence of D9 tetrahydrocannabinol (THC) and cannabidiol (CBD) on lymphocyte activation in vitro and in murine BMT models. Our in vitro results demonstrate that these treatments decrease activated lymphocyte proliferation and affect cytokine secretion. We also discovered that CBD and THC utilize different receptors to mediate these effects. In vivo, in a syngeneic transplantation model, we demonstrate that all treatments inhibit lymphocyte reconstitution and show the inhibitory role of the cannabinoid receptor type 2 (CB2) on lymphocyte recovery. Although pure cannabinoids exhibited a superior effect in vitro, in an allogeneic (C57BL/6 to BALB/c) BMT mouse model, THC-high and CBD-high cannabis extracts treatment reduced the severity of GVHD and improved survival significantly better than the pure cannabinoids. Our results highlights the complexity of using cannabinoids-based treatments and the need for additional comparative scientific results.

Keywords: D9 tetrahydrocannabinol; bone marrow transplantation; cannabidiol; cannabinoid receptor 2; cannabis; graft versus host disease; hematopoiesis; immune; lymphocyte; phytocannabinoids.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Bone Marrow Transplantation / adverse effects*
  • Cannabidiol / pharmacology*
  • Cannabidiol / therapeutic use
  • Disease Models, Animal
  • Dronabinol / pharmacology*
  • Dronabinol / therapeutic use
  • Female
  • Graft vs Host Disease / drug therapy*
  • Graft vs Host Disease / etiology
  • Graft vs Host Disease / pathology
  • Inflammation / drug therapy*
  • Inflammation / etiology
  • Lymphocyte Activation / drug effects*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Treatment Outcome

Substances

  • Cannabidiol
  • Dronabinol