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福尔马林固定石蜡包埋的原发性和转移性黑色素瘤中Melan A/MART-1免疫反应性:频率与分布

Melan A/MART-1 immunoreactivity in formalin-fixed paraffin-embedded primary and metastatic melanoma: frequency and distribution.

作者信息

Hofbauer G F, Kamarashev J, Geertsen R, Böni R, Dummer R

机构信息

Department of Dermatology, University Hospital, Zürich, Switzerland.

出版信息

Melanoma Res. 1998 Aug;8(4):337-43. doi: 10.1097/00008390-199808000-00007.

Abstract

Monoclonal antibody (MAb) A103 specifically detects Melan A/MART-1 protein expression. Melan A/MART-1-derived peptides are recognized by CD8+ T-cells and are used in immunotherapy. We examined formalin-fixed paraffin-embedded tissue from 57 melanomas (34 primary, 23 metastatic) and 39 control cases (junctional, dermal, compound, Spitz, Reed and balloon-cell naevi) using the alkaline phosphatase and anti-alkaline phosphatase immunochemical method after antigen retrieval. Immunoreactivity was rated as low, medium or high, and staining pattern as homogeneous or heterogeneous. Staining with MAb A103 showed a sensitivity of 88% for melanoma, with a very high specificity for melanocytic cells. Immunopositivity decreased along with clinical stage, with stage I showing 100%, stage II 88%, stage III 90% and stage IV 75% immunoreactivity. Staining changed from an exclusively homogeneous pattern in the early clinical stages to a more heterogeneous pattern in the later stages. Melanocytic control tissues consisting of naevi of different subtypes all showed weak to moderate homogeneous immunoreactivity, with polarity towards the epidermis. Analysis of short-term melanoma cell cultures using reverse transcription-polymerase chain reaction (RT-PCR) enzyme-linked immunosorbent assay (ELISA) demonstrated mRNA expression in only one third of the originally immunopositive tumours, suggesting rapid mRNA expression loss in culture. MAb A103 allows the detection of melanoma-associated Melan A/MART-1 protein expression in routine archival tissue and thus enables the profiling of melanomas suited for immunotherapy approaches involving Melan A/MART-1 derived epitopes.

摘要

单克隆抗体(MAb)A103可特异性检测黑色素A/MART-1蛋白的表达。黑色素A/MART-1衍生肽可被CD8+T细胞识别,并用于免疫治疗。我们采用碱性磷酸酶和抗碱性磷酸酶免疫化学方法,在抗原修复后,检测了57例黑色素瘤(34例原发性,23例转移性)和39例对照病例(交界痣、皮内痣、复合痣、Spitz痣、Reed痣和气球细胞痣)的福尔马林固定石蜡包埋组织。免疫反应性分为低、中、高三个等级,染色模式分为均匀或不均匀。MAb A103染色显示黑色素瘤的敏感性为88%,对黑素细胞具有很高的特异性。免疫阳性率随临床分期而降低,I期显示100%的免疫反应性,II期为88%,III期为90%,IV期为75%。染色从临床早期的完全均匀模式转变为后期的更不均匀模式。由不同亚型痣组成的黑素细胞对照组织均显示出弱至中度的均匀免疫反应性,且朝向表皮呈极性。使用逆转录聚合酶链反应(RT-PCR)和酶联免疫吸附测定(ELISA)对短期黑色素瘤细胞培养物进行分析,结果表明,在最初免疫阳性的肿瘤中,只有三分之一表达mRNA,这表明培养物中mRNA表达迅速丧失。MAb A1A103可在常规存档组织中检测与黑色素瘤相关的黑色素A/MART-1蛋白表达,从而能够对适合涉及黑色素A/MART-1衍生表位的免疫治疗方法的黑色素瘤进行分析。

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