Zhevago Natalya A, Samoilova Kira A
Photobiology Unit, Institute of Cytology of the Russian Academy of Sciences, St. Petersburg.
Photomed Laser Surg. 2006 Apr;24(2):129-39. doi: 10.1089/pho.2006.24.129.
The aim of this randomized, placebo-controlled, double-blind trial was to investigate changes in the content of 10 cytokines in the human peripheral blood after transcutaneous and in vitro irradiation with polychromatic visible and infrared (IR) polarized light at therapeutic dose.
The role of cytokines in development of anti-inflammatory, immunomodulatory, and wound-healing effects of visible and IR light remains poorly studied.
The sacral area of volunteers was exposed (480-3400 nm, 95% polarization, 12 J/cm(2)); in parallel, the blood samples of the same subjects were irradiated in vitro (2.4 J/cm(2)). Determination of cytokine content was performed using enzyme-linked immunosorbent assay (ELISA).
A dramatic decrease in the level of pro-inflammatory cytokines TNF-alpha, IL-6, and IFN-gamma was revealed: at 0.5 h after exposure of volunteers (with the initial parameters exceeding the norm), the cytokine contents fell, on average, 34, 12, and 1.5 times. The reduced concentrations of TNF-alpha and IL-6 were preserved after four daily exposures, whereas levels of IFN-gamma and IL-12 decreased five and 15 times. At 0.5 h and at later times, the amount of anti-inflammatory cytokines was found to rise: that of IL-10 rose 2.7-3.5 times (in subjects with normal initial parameters) and of TGF-beta1 1.4-1.5 times (in the cases of its decreased level). A peculiarity of the light effect was a fast rise of IFN-gamma at 3.3-4.0 times in subjects with normal initial values. The content of IL-1beta, IL-2, IFN-alpha, and IL-4 did not change. Similar regularities of the light effects were recorded after in vitro irradiation of blood, as well as on mixing the irradiated and non-irradiated autologous blood at a volume ratio 1:10 (i.e., at modeling the events in a vascular bed of the exposed person when a small amount of the transcutaneously photomodified blood contacts its main circulating volume).
Exposure of a small area of the human body to light leads to a fast decrease in the elevated pro-inflammatory cytokine plasma content and to an increase in the the anti-inflammatory factor concentration, which may be an important mechanism of the anti-inflammatory effect of phototherapy. These changes result from transcutaneous photomodification of a small volume of blood and a fast transfer of the light-induced changes to the entire pool of circulating blood.
本随机、安慰剂对照、双盲试验旨在研究以治疗剂量的多色可见光和红外(IR)偏振光经皮和体外照射后,人外周血中10种细胞因子含量的变化。
细胞因子在可见光和红外光的抗炎、免疫调节及伤口愈合作用中的作用仍研究不足。
对志愿者的骶部区域进行照射(480 - 3400nm,95%偏振,12J/cm²);同时,对同一受试者的血样进行体外照射(2.4J/cm²)。使用酶联免疫吸附测定(ELISA)法测定细胞因子含量。
发现促炎细胞因子TNF-α、IL-6和IFN-γ水平显著降低:在志愿者照射后0.5小时(初始参数超过正常范围),细胞因子含量平均下降34倍、12倍和1.5倍。每日照射4次后,TNF-α和IL-6浓度仍维持在较低水平,而IFN-γ和IL-12水平分别下降5倍和15倍。在0.5小时及之后,发现抗炎细胞因子数量增加:IL-10增加2.7 - 3.5倍(初始参数正常的受试者),TGF-β1增加1.4 - 1.5倍(其水平降低的情况)。光效应的一个特点是初始值正常的受试者中IFN-γ迅速升高3.3 - 倍。IL-1β、IL-2、IFN-α和IL-4的含量未发生变化。在血液体外照射后,以及将照射和未照射的自体血液按体积比1:10混合时(即在模拟暴露个体血管床中的情况,当少量经皮光修饰的血液接触其主要循环血量时),也记录到了类似的光效应规律。
人体小面积受光照射会导致血浆中升高的促炎细胞因子含量迅速降低,抗炎因子浓度增加,这可能是光疗抗炎作用的重要机制。这些变化是由少量血液的经皮光修饰以及光诱导变化向整个循环血液池的快速传递引起的。