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首页> 外文期刊>Archives of dermatological research. >Combination therapy with oral PUVA and corticosteroid for recalcitrant alopecia areata.
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Combination therapy with oral PUVA and corticosteroid for recalcitrant alopecia areata.

机译:口服PUVA和皮质类固醇联合治疗顽固性秃发斑。

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摘要

Alopecia areata (AA) is regarded as a tissue-specific autoimmune disease for which several therapies have been suggested to modify the immune reaction against HFs, such as contact immunotherapy, psoralen plus ultraviolet A (PUVA), corticosteroids, cyclosporine, minoxidil, and dithranol. However, severe type AA, such as alopecia totalis (AT) and alopecia universalis (AU), often show resistance against these therapies. We applied a combination therapy with oral corticosteroid and oral PUVA for intractable cases of AT and AU. These patients took 20 mg/day corticosteroid and were irradiated with UVA on the whole body 2 h after taking methoxsalen for 1 month. In all patients, the terminal hair on the whole scalp regrew after 2 months. Two patients had a relapse of hair loss 3 months after the termination of the treatment. FACS analysis revealed that the CD4+CD25(high) and CD4+CD25+FOXP3+ Treg population in PBMC was increased after the combination therapy. Furthermore, the number of infiltrating cells decreased and FOXP3+ cells were often found in lesion skin after the combination therapy. Mitogen-induced proliferation tests showed low responses against PHA and Con A after the combination therapy. Taken together, the combination therapy may modify the systemic immune system and increase the number of Treg cells, resulting in improvement of recalcitrant AA.
机译:斑秃(AA)被认为是一种组织特异性自身免疫性疾病,已提出了多种疗法来改善针对HF的免疫反应,例如接触免疫疗法,补骨脂素加紫外线A(PUVA),皮质类固醇,环孢菌素,米诺地尔和二乙醇。但是,严重的AA型,例如总脱发(AT)和通用脱发(AU),通常显示出对这些疗法的抵抗力。我们对顽固性AT和AU病例应用了口服糖皮质激素和口服PUVA联合治疗。这些患者每天服用20 mg皮质类固醇,并在服用甲氧沙林1个月后2小时用UVA照射全身。在所有患者中,两个月后,整个头皮上的末梢毛发会重新生长。两名患者在治疗终止后3个月复发了脱发。 FACS分析显示,联合治疗后PBMC中CD4 + CD25(高)和CD4 + CD25 + FOXP3 + Treg群体增加。此外,联合治疗后病变皮肤中浸润细胞数量减少,并且经常发现FOXP3 +细胞。丝裂原诱导的增殖试验显示,联合治疗后,对PHA和Con A的反应低。两者合计,联合疗法可能会改变全身免疫系统并增加Treg细胞的数量,从而导致顽固性AA的改善。

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