Fujii Hidetaka, Shimada Yuka, Hasegawa Minoru, Takehara Kazuhiko, Sato Shinichi
Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
J Dermatol Sci. 2004 Jun;35(1):43-51. doi: 10.1016/j.jdermsci.2004.03.001.
Although abnormalities of various chemokines are detected in systemic sclerosis (SSc), there are few findings concerning Th1 or Th2 chemoattractants.
To determine whether serum levels of chemokines preferentially chemotactic for Th1 cells (IP-10 and MIG) and predominantly chemotactic for Th2 cells (TARC and MDC) are elevated and whether they correlate with clinical features in patients with SSc.
Serum samples from patients with diffuse cutaneous SSc (dSSc; n = 34), limited cutaneous SSc (lSSc; n = 30), dermatomyositis (DM; n = 15), systemic lupus erythematosus (SLE; n = 22), and normal controls (n = 30) were examined by sandwich ELISA.
Serum TARC levels were significantly elevated in dSSc patients (P < 0.0002) and lSSc patients (P < 0.0001) compared with normal controls. Similarly, serum MDC levels were significantly increased in patients with dSSc (P < 0.02) or lSSc (P < 0.05) relative to normal controls. In addition, serum IP-10 was detected significantly more frequently in patients with dSSc (44%), lSSc (30%), or DM (53%) than normal controls (0%) and patients with SLE (0%). Furthermore, elevated TARC levels correlated with the presence of pitting scars and anti-topoisomerase I antibody, increased titers of anti-topoisomerase I and antinuclear antibody, and decreased glomerular filtration rate. Increased MDC levels were associated with pitting scars and younger ages at onset.
These results suggest that both Th2 chemoattractants, TARC and MDC, and a Th1 chemoattractant IP-10 play a role in the development of SSc.
尽管在系统性硬化症(SSc)中检测到多种趋化因子异常,但关于Th1或Th2趋化因子的研究结果较少。
确定对Th1细胞具有优先趋化作用的趋化因子(IP - 10和MIG)以及对Th2细胞具有主要趋化作用的趋化因子(TARC和MDC)的血清水平是否升高,以及它们是否与SSc患者的临床特征相关。
采用夹心ELISA法检测弥漫性皮肤型SSc(dSSc;n = 34)、局限性皮肤型SSc(lSSc;n = 30)、皮肌炎(DM;n = 15)、系统性红斑狼疮(SLE;n = 22)患者及正常对照者(n = 30)的血清样本。
与正常对照相比,dSSc患者(P < 0.0002)和lSSc患者(P < 0.0001)的血清TARC水平显著升高。同样,相对于正常对照,dSSc(P < 0.02)或lSSc(P < 0.05)患者的血清MDC水平显著升高。此外,dSSc患者(44%)、lSSc患者(30%)或DM患者(53%)血清IP - 10的检出频率显著高于正常对照者(0%)和SLE患者(0%)。此外,TARC水平升高与凹陷性瘢痕、抗拓扑异构酶I抗体的存在、抗拓扑异构酶I和抗核抗体滴度升高以及肾小球滤过率降低相关。MDC水平升高与凹陷性瘢痕和发病年龄较小有关。
这些结果表明,Th2趋化因子TARC和MDC以及Th1趋化因子IP - 10在SSc的发病机制中均起作用。