Toldi Gergely, Munoz Luis, Herrmann Martin, Schett Georg, Balog Attila
First Department of Pediatrics, Semmelweis University, Bókay u. 53, Budapest, 1083, Hungary.
MTA-SE, Pediatrics and Nephrology Research Group, Budapest, Hungary.
Immunol Res. 2016 Apr;64(2):627-31. doi: 10.1007/s12026-015-8683-8.
Kv1.3 and IKCa1 lymphocyte potassium channels have been implicated as important targets of selective immunomodulation. We compared the alterations in cytokine production upon selective inhibition of Kv1.3 or IKCa1 channels (by MGTX and TRAM, respectively) in healthy donors (HD), RA and AS patients. We also determined calcium influx kinetics and its sensitivity to Kv1.3 and IKCa1 channel inhibition following PHA activation in CD4, Th1, Th2 and CD8 cells as well as monocytes. The application of TRAM resulted in a lower production of TNF-a and IL1-RA in all three study groups. Inhibition by TRAM had contrary effects on the production of IL-1b and IL-5: While their production was increased by PBMCs of RA patients, this effect was not observed in HD and AS PBMCs. While treatment with MGTX resulted in a similar decrease in calcium influx in the CD4 and Th2 subsets across all study groups, TRAM treatment had opposite effects on RA and HD samples: It decreased calcium influx in the Th2 and CD8 subsets in RA, while only Th1 cells were affected in HDs. The effects of IKCa1 channel inhibition are controversial in samples of RA and AS patients, since it shifts the inflammatory balance into the pro-inflammatory direction.
Kv1.3和IKCa1淋巴细胞钾通道被认为是选择性免疫调节的重要靶点。我们比较了在健康供体(HD)、类风湿关节炎(RA)和强直性脊柱炎(AS)患者中,分别通过MGTX和TRAM选择性抑制Kv1.3或IKCa1通道后细胞因子产生的变化。我们还测定了在CD4、Th1、Th2和CD8细胞以及单核细胞中,经PHA激活后钙内流动力学及其对Kv1.3和IKCa1通道抑制的敏感性。TRAM的应用导致所有三个研究组中TNF-α和IL-1RA的产生减少。TRAM的抑制作用对IL-1β和IL-5的产生有相反的影响:虽然RA患者的PBMC增加了它们的产生,但在HD和AS的PBMC中未观察到这种效应。虽然MGTX处理导致所有研究组中CD4和Th2亚群的钙内流有类似的减少,但TRAM处理对RA和HD样本有相反的影响:它降低了RA中Th2和CD8亚群的钙内流,而在HD中仅Th1细胞受到影响。在RA和AS患者的样本中,IKCa1通道抑制的作用存在争议,因为它将炎症平衡转向促炎方向。