Lu Chuanjian, Liu Huazhen, Jin Xiaowei, Chen Yuchao, Liang Chun-Ling, Qiu Feifei, Dai Zhenhua
Section of Immunology and Joint Immunology Program, Guangdong Provincial Hospital of Chinese Medicine, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.
Department of Integrative Chinese-Western Medicine, The Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Front Pharmacol. 2018 Feb 12;9:88. doi: 10.3389/fphar.2018.00088. eCollection 2018.
A recipient usually rejects a transplanted organ and thus needs immunosuppressive treatments to prevent rejection. Achieving long-term allograft survival without continuous global immunosuppression is highly desirable in transplantation as long-term immunosuppression causes various side effects. Therefore, it is necessary to search for medicine with potentially less side effects. Traditional Chinese medicine PSORI-CM01 (Yin Xie Ling), a formula with seven natural herbs, has been used to treat patients with psoriasis. Here, we investigated a "sharpened" formula, PSORI-CM02 consisting of only five herbs from PSORI-CM01: Curcumae rhizoma, Radix paeoniae rubra, Rhizoma smilacis glabrae, Mume fructus, and Sarcandrae herba. We examined whether or not PSORI-CM02 would suppress alloimmunity and found that PSORI-CM02 significantly inhibited murine skin allograft rejection and reduced graft-infiltration of CD3+ T cells. Interestingly, omitting any single herbal component rendered the whole formula ineffective in suppression, indicating that these herbal components exert their effects cooperatively as a whole. Moreover, PSORI-CM02 increased CD8+CD122+PD-1+ Treg frequency with CD4+FoxP3+ Tregs remaining unchanged in recipient mice, whereas CsA reduced CD4+FoxP3+ Treg frequency. PSORI-CM02 also hindered CD11c+ DC maturation posttransplantation. Importantly, PSORI-CM02-induced CD8+CD122+PD-1+ Tregs were more potent in suppression of allograft rejection in Rag-/- mice than control Tregs. On the other hand, PSORI-CM02 suppressed T cell proliferation and reduced their phosphorylation of P70S6K and P50/P65, suggesting that it inhibits both mTOR and NFκB signaling pathways. It also increased IL-10 production while reducing IFNγ level in the supernatant of activated T cells co-cultured with CD8+CD122+PD-1+ Tregs. Furthermore, HPLC fingerprinting ruled out that PSORI-CM02 contained CsA or rapamycin. PSORI-CM02 also did not cause any illness and toxic injury in recipient mice. Thus, we demonstrate that PSORI-CM02 formula suppresses allograft rejection without toxicity.
接受者通常会排斥移植器官,因此需要进行免疫抑制治疗以防止排斥反应。在移植过程中,在不进行持续全面免疫抑制的情况下实现长期同种异体移植存活是非常理想的,因为长期免疫抑制会导致各种副作用。因此,有必要寻找副作用可能较小的药物。传统中药PSORI-CM01(银屑灵)是一种由七种天然草药组成的配方,已用于治疗银屑病患者。在此,我们研究了一种“精简”配方PSORI-CM02,它仅由PSORI-CM01中的五种草药组成:莪术、赤芍、土茯苓、乌梅和肿节风。我们检测了PSORI-CM02是否会抑制同种免疫,发现PSORI-CM02显著抑制小鼠皮肤同种异体移植排斥反应,并减少移植组织中CD3+T细胞的浸润。有趣的是,省略任何一种草药成分都会使整个配方失去抑制作用,这表明这些草药成分作为一个整体协同发挥作用。此外,PSORI-CM02可增加受体小鼠中CD8+CD122+PD-1+调节性T细胞(Treg)的频率,而CD4+FoxP3+Treg保持不变,而环孢素(CsA)会降低CD4+FoxP3+Treg的频率。PSORI-CM02还会阻碍移植后CD11c+树突状细胞(DC)的成熟。重要的是,PSORI-CM02诱导的CD8+CD122+PD-1+Treg在Rag-/-小鼠中对同种异体移植排斥反应的抑制作用比对照Treg更强。另一方面,PSORI-CM02抑制T细胞增殖,并降低其P70S6K和P50/P65的磷酸化水平,这表明它同时抑制雷帕霉素靶蛋白(mTOR)和核因子κB(NFκB)信号通路。在与CD8+CD122+PD-1+Treg共培养的活化T细胞上清液中,它还增加白细胞介素-10(IL-10)的产生,同时降低干扰素γ(IFNγ)水平。此外,高效液相色谱指纹图谱排除了PSORI-CM02含有CsA或雷帕霉素的可能性。PSORI-CM02在受体小鼠中也未引起任何疾病和毒性损伤情况。因此,我们证明PSORI-CM02配方可抑制同种异体移植排斥反应且无毒性。