ImmunoTargets and Therapy (Aug 2020)

Cannabidiol as a Novel Therapeutic for Immune Modulation

  • Peyravian N,
  • Deo S,
  • Daunert S,
  • Jimenez JJ

Journal volume & issue
Vol. Volume 9
pp. 131 – 140

Abstract

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Nadia Peyravian,1,2 Sapna Deo,1,2 Sylvia Daunert,1– 3 Joaquin J Jimenez1,2,4 1Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, FL, USA; 2Dr. JT Macdonald Foundation Biomedical Nanotechnology Institute of the University of Miami, Miami, FL, USA; 3University of Miami Clinical and Translational Science Institute, Miami, FL, USA; 4Department of Dermatology & Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, FL, USACorrespondence: Joaquin J Jimenez; Sylvia DaunertDepartment of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, 1011 NW 15th Street, Miami, FL 33136, USATel +1 305 243 6586Email [email protected]; [email protected]: The immune-suppressive effects of cannabidiol (CBD) are attributed to the modulation of essential immunological signaling pathways and receptors. Mechanistic understanding of the pharmacological effects of CBD emphasizes the therapeutic potential of CBD as a novel immune modulator. Studies have observed that the antagonists of CB1 and CB2 receptors and transient receptor potential vanilloid 1 reverse the immunomodulatory effects of CBD. CBD also inhibits critical activators of the Janus kinase/signal transducer and activator of transcription signaling pathway, as well as the nucleotide-binding oligomerization domain-like receptor signaling pathway, in turn decreasing pro-inflammatory cytokine production. Furthermore, CBD protects against cellular damage incurred during immune responses by modulating adenosine signaling. Ultimately, the data overwhelmingly support the immunosuppressive effects of CBD and this timely review draws attention to the prospective development of CBD as an effective immune modulatory therapeutic.Keywords: cannabidiol, CBD, immune modulation, CB1 and CB2 receptors, TRPV1, JAK/STAT, inflammasome

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