临床皮肤科杂志
臨床皮膚科雜誌
림상피부과잡지
JOURNAL OF CLINICAL DERMATOLOGY
2014年
7期
389-392
,共4页
贾近博%张乔安%陈明华
賈近博%張喬安%陳明華
가근박%장교안%진명화
蕈样肉芽肿%趋化因子受体4%T淋巴细胞,调节性%Foxp3
蕈樣肉芽腫%趨化因子受體4%T淋巴細胞,調節性%Foxp3
심양육아종%추화인자수체4%T림파세포,조절성%Foxp3
mycosis fungoides%CCR4%regulatory T cells%Foxp3
目的:探讨趋化因子受体(CCR)4与叉头框转录因子Foxp3+调节性T细胞在不同临床分期蕈样肉芽肿(MF)患者皮损中的表达,并初步探讨其意义。方法:收集22例MF患者的皮损组织,采用免疫组化方法,分别检测CCR4与Foxp3的表达水平。结果:Foxp3在MF斑块期表达明显增多,红斑期次之,而在肿瘤期几乎不表达;尽管CCR4在各期MF中均有表达,但其表达程度以红斑期最强,斑块期次之,肿瘤期最弱,差异有统计学意义(P<0.001),且CCR4与Foxp3在皮损中的阳性表达存在正相关关系(相关系数为0.489)。结论:CCR4与Foxp3在不同分期MF皮损中的表达对了解MF免疫功能的变化和新的治疗提供帮助。
目的:探討趨化因子受體(CCR)4與扠頭框轉錄因子Foxp3+調節性T細胞在不同臨床分期蕈樣肉芽腫(MF)患者皮損中的錶達,併初步探討其意義。方法:收集22例MF患者的皮損組織,採用免疫組化方法,分彆檢測CCR4與Foxp3的錶達水平。結果:Foxp3在MF斑塊期錶達明顯增多,紅斑期次之,而在腫瘤期幾乎不錶達;儘管CCR4在各期MF中均有錶達,但其錶達程度以紅斑期最彊,斑塊期次之,腫瘤期最弱,差異有統計學意義(P<0.001),且CCR4與Foxp3在皮損中的暘性錶達存在正相關關繫(相關繫數為0.489)。結論:CCR4與Foxp3在不同分期MF皮損中的錶達對瞭解MF免疫功能的變化和新的治療提供幫助。
목적:탐토추화인자수체(CCR)4여차두광전록인자Foxp3+조절성T세포재불동림상분기심양육아종(MF)환자피손중적표체,병초보탐토기의의。방법:수집22례MF환자적피손조직,채용면역조화방법,분별검측CCR4여Foxp3적표체수평。결과:Foxp3재MF반괴기표체명현증다,홍반기차지,이재종류기궤호불표체;진관CCR4재각기MF중균유표체,단기표체정도이홍반기최강,반괴기차지,종류기최약,차이유통계학의의(P<0.001),차CCR4여Foxp3재피손중적양성표체존재정상관관계(상관계수위0.489)。결론:CCR4여Foxp3재불동분기MF피손중적표체대료해MF면역공능적변화화신적치료제공방조。
To investigate the expression of CC chemokine receptor (CCR) 4 and Foxp3+ regulatory T cells (Tregs)in different stages of mycosis fungoides (MF)and subsequently explore their significance for the development of MF. Methods:Tissue specimens were obtained from the lesions of 22 patients with MF. Immunohistochemistry was performed to de-tect the expression of CCR4 and Foxp3 in the tissue specimens. Results: Immunohistochemical staining showed that the ex-pression of Foxp3 in the plaque stage was significantly increased compared to the erythematous stage and hardly any expression observed in the tumor stage. Although CCR4 were expressed in all groups, the positive rate showed obvious difference, higher in erythematous lesions, median in plaque and lower in tumor lesions(P<0.001). Furthermore, expression of CCR4 had a posi-tively correlated with expression of Foxp3+ Tregs in MF lesions(correlation factor=0.489). Conclusions:The results indicate that the expressions of CCR4 and Foxp3 in the different stages of MF may help us better understanding the immunologic changes, and providing new ideas for treatment of MF.