Beatriz Rodríguez-Bayona, Sandrine Ruchaud, Carmen Rodríguez, Mario Linares, Antonio Astola, Manuela Ortiz, William C Earnshaw, Manuel M Valdivia
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引用次数: 25
摘要
背景:Graham Little - Piccardi - Lassueur (GLPL)综合征是一种罕见的皮肤病,其特征是瘢痕性脱发,阴毛和腋毛脱落,以及不同位置的毛囊丘疹的进行性发展。我们报告第一例自身免疫反应的患者患有GLPL综合征。方法:对人、猴、仓鼠、小鼠和牛等多种细胞培养物进行免疫荧光和免疫印迹分析,分析GLPL患者体内自身抗体的存在。结果:自身免疫血清显示着丝粒和纺锤体微管染色模式,类似于染色体客运蛋白复合体。通过使用杆状病毒中表达的蛋白复合物,免疫印迹分析表明,在该GLPL综合征患者中,INCENP蛋白是主要的自身抗原。结论:GLPL综合征的自身免疫反应是针对着丝粒蛋白的。GLPL患者中偶尔出现的自身免疫可以作为一种检测这种疾病的持续努力和基于自身抗原反应的更直接治疗的测试。
Autoantibodies against the chromosomal passenger protein INCENP found in a patient with Graham Little-Piccardi-Lassueur syndrome.
Background: Graham Little - Piccardi - Lassueur (GLPL) syndrome is a rare dermatosis characterized by scarring alopecia, loss of pubic and axillary hair, and progressive development of variously located follicular papules. We report a first case ever of an autoimmune response in a patient suffering from GLPL syndrome.
Methods: Immunofluorescence and immunoblot analysis were used in a variety of cell cultures including human, monkey, hamster, mouse and bovine cells to analyze the presence of autoantibodies in a GLPL patient.
Results: The autoimmune serum showed a pattern of centromere and spindle microtubule staining resembling that of the chromosomal passenger protein complex. By using a complex of proteins expressed in baculovirus, immunoblot analysis demonstrated that the INCENP protein is a major autoantigen in this patient with GLPL syndrome.
Conclusion: An autoimmune response in GLPL syndrome is reported against the INCENP centromere protein. The occasional development of autoimmunity in GLPL patients could serve as a test in continuing efforts to detect this disease and for a more directed therapy based on the autoantigen response.