Utsinger P D, Young W J
Am J Med. 1976 Aug;61(2):287-94. doi: 10.1016/0002-9343(76)90179-0.
A patient with allopurinol hypersensitivity, manifested by fever, lymphadenopathy and a severe erythematous, morbilliform, maculopapular rash was studied. On immunofluorescent staining of the patient's skin, heavy granular deposits of immunoglobulin M (IgM) were found at the dermal-epidermal junction. Transformation of the patient's lymphocytes could not be effected by a variety of combinations of allopurinol, allopurinol metabolites and serum. These data suggested that the hypersensitivity reaction caused by allopurinol had immune complex deposition as the central feature in pathogenesis. The predominance of IgM may provide a distinctive feature from the deposits generally seen in systemic and discoid lupus erythematosus.
对一名出现发热、淋巴结病以及严重的红斑、麻疹样、斑丘疹皮疹等表现的别嘌醇超敏反应患者进行了研究。对该患者的皮肤进行免疫荧光染色时,在真皮-表皮交界处发现了大量免疫球蛋白M(IgM)颗粒状沉积物。该患者的淋巴细胞不能被别嘌醇、别嘌醇代谢产物和血清的多种组合所转化。这些数据表明,别嘌醇引起的超敏反应在发病机制中以免疫复合物沉积为核心特征。IgM的优势可能使其与系统性红斑狼疮和盘状红斑狼疮中常见的沉积物有所区别。