Kalimo K, Lammintausta K, Viander M, Jansén C T
Department of Dermatology, University of Turku, Finland.
Photodermatol. 1989 Feb;6(1):16-9.
Five females with nickel contact allergy and longstanding hand dermatitis were treated with oral methoxsalen and a series of whole-body UVA irradiations with a cumulative UVA dose of 30 to 58 J/cm2. Lymphocyte stimulation to nickel sulphate was determined prior to PUVA therapy, and monitored during the treatment and at 1 year after treatment. In 4 patients the cutaneous threshold to nickel sulphate patch testing was determined immediately post-PUVA and at 1 year. In all cases, the dermatosis cleared during the PUVA treatment. In 2 patients the immediate post-PUVA skin nickel reactivity was low compared with the 1-year follow-up value, while in 2 patients a progressive diminution of the skin reactivity was noticed. One patient was in clinical remission and had negative skin test at 1-year follow-up. In spite of diminished cutaneous sensitivity and/or clinical remission, the sensitivity of blood lymphocytes to nickel was approximately the same or increased, as determined by the lymphocyte transformation test. Thus no evidence was found to indicate that systemic, nickel-specific suppressive immune regulative mechanisms would have been activated by the treatment.
五名患有镍接触性过敏和长期手部皮炎的女性接受了口服甲氧沙林治疗,并进行了一系列全身UVA照射,累积UVA剂量为30至58 J/cm²。在PUVA治疗前测定对硫酸镍的淋巴细胞刺激,并在治疗期间和治疗后1年进行监测。在4名患者中,在PUVA治疗后立即和1年后测定对硫酸镍斑贴试验的皮肤阈值。在所有病例中,皮肤病在PUVA治疗期间均消退。2名患者在PUVA治疗后立即的皮肤镍反应性低于1年随访值,而2名患者则注意到皮肤反应性逐渐降低。1名患者临床缓解,在1年随访时皮肤试验为阴性。尽管皮肤敏感性降低和/或临床缓解,但通过淋巴细胞转化试验确定,血液淋巴细胞对镍的敏感性大致相同或增加。因此,没有发现证据表明该治疗激活了全身性、镍特异性抑制性免疫调节机制。