Savino W, Berrih S, Dardenne M
Lab Invest. 1984 Sep;51(3):292-6.
The protein defined by the anti-p19 monoclonal antibody (raised against a 19-kilodalton protein from human T leukemia virus) and normally acquired during the ontogenesis of the human thymic epithelium was studied by indirect immunofluorescence in thymomas and thymic hyperplasias. Hyperplastic (and involuted) thymuses from patients with myasthenia gravis exhibited a clear-cut expression of this differentiation antigen exclusively in epithelial cells, thus qualitatively similar to what was observed in the normal thymus. In thymoma epithelial cells, however, this expression was strongly altered: in the 12 malignant thymomas studied, no anti-p19 reactivity was found. In the four benign cases, a variable number of epithelial cells expressed this antigen. These results suggest that the differentiation antigen of the human thymic epithelium defined by the anti-p19 monoclonal antibody is lost during the malignant transformation occurring in thymomas. Furthermore, this monoclonal antibody provides an additional tool for the study of the degree of dedifferentiation of thymomas.
利用间接免疫荧光法,对胸腺瘤和胸腺增生组织中由抗p19单克隆抗体(针对人T淋巴细胞白血病病毒的一种19千道尔顿蛋白制备)所定义的、通常在人胸腺上皮发育过程中获得的蛋白质进行了研究。重症肌无力患者的增生性(及萎缩性)胸腺仅在上皮细胞中呈现出这种分化抗原的清晰表达,在性质上与正常胸腺中观察到的情况相似。然而,在胸腺瘤上皮细胞中,这种表达发生了强烈改变:在所研究的12例恶性胸腺瘤中,未发现抗p19反应性。在4例良性病例中,有数量不等的上皮细胞表达了这种抗原。这些结果表明,由抗p19单克隆抗体所定义的人胸腺上皮分化抗原在胸腺瘤发生的恶性转化过程中丧失。此外,这种单克隆抗体为研究胸腺瘤的去分化程度提供了一种额外的工具。