Aswad Miran, Pechkovsky Antonina, Ghanayiem Narmeen, Hamza Haya, Louria-Hayon Igal
The Shanti Center For Medical Cannabis Research, Rambam Health Care Campus, Haifa, Israel.
Clinical Research Institute at Rambam (CRIR), Rambam Health Care Campus, Haifa, Israel.
Front Immunol. 2025 Jul 10;16:1599109. doi: 10.3389/fimmu.2025.1599109. eCollection 2025.
Rheumatoid arthritis (RA) is a debilitating autoimmune disease affecting approximately 1% of the global population and is associated with significant morbidity and mortality. Given the known anti-inflammatory effects of cannabinoids, we investigated the therapeutic potential of a high-CBD extract, termed CBD-X, by assessing its effects on immune cells and disease progression. This study investigates the therapeutic potential of a high-CBD extract (CBD-X) in RA.
We evaluated the effects of CBD-X on cells involved in RA pathogenesis using macrophages and primary human neutrophils as ex vivo models. In addition, two murine models of RA were applied: collagen-induced arthritis (CIA) and collagen antibody-induced arthritis (CAIA).
Ex vivo experiments demonstrated that CBD-X inhibited the secretion of pro-inflammatory cytokines, including IL-1β from macrophages and IL-8, IL-6, and TNF-α from human neutrophils, suggesting its potential to modulate inflammatory responses. Moreover, CBD-X attenuated NF-κB p65 and Akt phosphorylation downstream LPS-activation signal in neutrophils. To further evaluate its therapeutic effects, we employed two murine models of RA: collagen-induced arthritis (CIA) and collagen antibody-induced arthritis (CAIA). In both models, CBD-X treatment resulted in a significant reduction of leukocyte levels in the blood, primarily through the suppression of neutrophil and monocyte populations, which play a central role in RA pathogenesis. Additionally, CBD-X reduced neutrophil migration to the joints in the CAIA model, highlighting its potential to alleviate joint inflammation. Furthermore, it modulated the neutrophil-to-macrophage ratio (NMR), an important marker of RA progression, an effect that was not observed with dexamethasone treatment, suggesting a distinct mechanism of immune regulation. Notably, CBD-X promoted the pro-resolving macrophages to the rheumatic joints. Importantly, CBD-X exerted its anti-inflammatory effect by downregulating TNF-α and MCP-1 while upregulating IL-10, a key anti-inflammatory cytokine involved in immune homeostasis.
These findings indicate that CBD-X has a significant potential as a therapeutic agent for RA, offering a promising approach to modulate immune responses and reduce inflammation in RA patients.
类风湿性关节炎(RA)是一种使人衰弱的自身免疫性疾病,影响着全球约1%的人口,且与显著的发病率和死亡率相关。鉴于大麻素已知的抗炎作用,我们通过评估一种名为CBD-X的高CBD提取物对免疫细胞和疾病进展的影响,来研究其治疗潜力。本研究调查了高CBD提取物(CBD-X)在类风湿性关节炎中的治疗潜力。
我们使用巨噬细胞和原代人中性粒细胞作为体外模型,评估了CBD-X对参与类风湿性关节炎发病机制的细胞的影响。此外,应用了两种类风湿性关节炎小鼠模型:胶原诱导的关节炎(CIA)和胶原抗体诱导的关节炎(CAIA)。
体外实验表明,CBD-X抑制促炎细胞因子的分泌,包括巨噬细胞分泌的IL-1β以及人中性粒细胞分泌的IL-8、IL-6和TNF-α,表明其具有调节炎症反应的潜力。此外,CBD-X减弱了中性粒细胞中LPS激活信号下游的NF-κB p65和Akt磷酸化。为了进一步评估其治疗效果,我们采用了两种类风湿性关节炎小鼠模型:胶原诱导的关节炎(CIA)和胶原抗体诱导的关节炎(CAIA)。在这两种模型中,CBD-X治疗均导致血液中白细胞水平显著降低,主要是通过抑制在类风湿性关节炎发病机制中起核心作用的中性粒细胞和单核细胞群体。此外,在CAIA模型中,CBD-X减少了中性粒细胞向关节的迁移,突出了其减轻关节炎症的潜力。此外,它调节了中性粒细胞与巨噬细胞的比例(NMR)——类风湿性关节炎进展的一个重要标志物,而地塞米松治疗未观察到这种效果,这表明其免疫调节机制独特。值得注意的是,CBD-X促使促消退巨噬细胞向风湿性关节迁移。重要的是,CBD-X通过下调TNF-α和MCP-1,同时上调IL-10发挥其抗炎作用,IL-10是参与免疫稳态的关键抗炎细胞因子。
这些发现表明,CBD-X作为类风湿性关节炎的治疗药物具有巨大潜力,为调节类风湿性关节炎患者的免疫反应和减轻炎症提供了一种有前景的方法。