Abstract The legalization of cannabinoids for medical use has reinforced their emerging role as a treatment of chronic pain in patients with cancer or rheumatic diseases.1,2 In addition to their role as pain relievers, evidence obtained from animal models suggests that cannabinoids have immunosuppressive properties.3 However, a definite immunosuppressive function of cannabinoids has not yet been confirmed in clinical trials.4 We therefore analyzed the influence of the cannabis derivative cannabidiol (CBD) and the endogenous cannabinoid anandamide (AEA) on T helper type 17 (Th17) cells from patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and psoriatic arthritis (PsA). Interestingly, in vitro culture in the...