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蕈样肉芽肿患者白癜风的发病机制。

Pathogenetic mechanisms of vitiligo in a patient with Sézary syndrome.

作者信息

Knol A C, Quéreux G, Marques-Briand S, Pandolfino M C, Khammari A, Guilloux Y, Dreno B

机构信息

INSERM U601, CHU Hôtel-Dieu, 9 quai Moncousu, 44093 Nantes cedex 01, France.

出版信息

Br J Dermatol. 2005 Dec;153(6):1207-12. doi: 10.1111/j.1365-2133.2005.06877.x.

DOI:10.1111/j.1365-2133.2005.06877.x
PMID:16307660
Abstract

Patients exhibiting association between vitiligo and cutaneous T-cell lymphoma (CTCL) remain rare and it is not known whether some T-cell subpopulations of CTCL in the skin are able to recognize specific melanocytic epitopes and thus induce vitiligo. The aim of our study was to determine whether T cells specific to melanocyte differentiation antigens were detectable among tumour-infiltrating lymphocytes (TIL) in the hypopigmented skin of a patient with Sézary syndrome (SS). A 71-year-old patient presented with SS and developed vitiligo during the course of her disease. Immunohistochemical studies showed staining with HMB45 and MelanA antibodies in the pigmented skin biopsy, whereas no staining was observed in the hypopigmented skin biopsy. To analyse responses to melanocyte differentiation antigens, we used a transient COS transfection assay that permits an estimation of CD8 T-cell responses against a large number of HLA/antigen combinations. This technique allowed the detection of melanocyte differentiation antigen-specific T lymphocytes, directed mainly against Melan-A/MART1 antigen in the HLA-A*23 context. Our study supports the concept that vitiligo that has developed during the evolution of a CTCL is related to the presence of a T-lymphocyte subpopulation reactive against melanocyte differentiation antigens (mainly Melan-A/MART1) present in skin lesions. The role of interferon in the induction of this T-lymphocyte subpopulation is discussed.

摘要

白癜风与皮肤T细胞淋巴瘤(CTCL)相关的患者仍然罕见,目前尚不清楚皮肤中CTCL的某些T细胞亚群是否能够识别特定的黑素细胞表位,从而诱发白癜风。我们研究的目的是确定在一名 Sézary 综合征(SS)患者色素减退皮肤的肿瘤浸润淋巴细胞(TIL)中,是否能检测到黑素细胞分化抗原特异性T细胞。一名71岁的患者患有SS,在疾病过程中出现了白癜风。免疫组化研究显示,在色素沉着皮肤活检中HMB45和MelanA抗体呈阳性染色,而在色素减退皮肤活检中未观察到染色。为了分析对黑素细胞分化抗原的反应,我们使用了瞬时COS转染试验,该试验可以评估CD8 T细胞对大量HLA/抗原组合的反应。这项技术能够检测到黑素细胞分化抗原特异性T淋巴细胞,主要针对HLA-A*23背景下的Melan-A/MART1抗原。我们的研究支持这样一种观点,即在CTCL演变过程中出现的白癜风与皮肤病变中存在对黑素细胞分化抗原(主要是Melan-A/MART1)有反应的T淋巴细胞亚群有关。文中还讨论了干扰素在诱导这种T淋巴细胞亚群中的作用。

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