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原发性肿瘤与黑色素瘤转移灶个体匹配对的抗原谱。

Antigenic profiles of individual-matched pairs of primary and melanoma metastases.

作者信息

Meije Clifton B, Swart Guido W M, Lepoole Caroline, Das Pranab K, Van den Oord Joost J

机构信息

Department of Pathology, Academical Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Hum Pathol. 2009 Oct;40(10):1399-407. doi: 10.1016/j.humpath.2008.11.018. Epub 2009 Apr 22.

DOI:10.1016/j.humpath.2008.11.018
PMID:19386352
Abstract

A unique collection of individual-matched pairs of primary and melanoma metastases were studied immunohistochemically with a panel of 6 monoclonal antibodies directed to gp-100, pigmentation-associated antigen, tyrosinase-related protein, human leukocyte antigen DR, MAA-1, and MAA-2 (high molecular weight melanoma-associated antigens). The antigenic profile of immunoreactive pigment cells was compared with the stage of tumor progression. Our data show consistent antigenic profiles of primary melanomas and their metastases within the same patient. Expression of tyrosinase-related protein and pigmentation-associated antigen was observed in the radial growth phase of primary melanomas but showed diminished or complete loss of expression in the vertical growth phase and in metastatic melanomas. HLA-DR was negative in the most primary lesions, but melanoma cells and a larger proportion of immunoreactive cells were observed at the metastatic site. The melanoma-associated antigens MAA-1 and MAA-2 were expressed throughout tumor progression. Although no clear distinction could be made between primary and secondary melanoma lesions for both melanoma-associated antigens, there was a profound variability in the topographical antigen distribution when compared with HLA-DR. The loss of expression of pigmentation-associated antigen and tyrosinase-related protein in the vertical growth phase of the primary lesions and metastatic melanomas did not reach statistical significance but still may be related to tumor progression. This indicates that primary melanomas can be distinguished from their metastases by evaluation of the antigenic profile and in this respect facilitate the recognition of tumor progression stages.

摘要

我们使用一组针对gp-100、色素沉着相关抗原、酪氨酸酶相关蛋白、人类白细胞抗原DR、MAA-1和MAA-2(高分子量黑色素瘤相关抗原)的6种单克隆抗体,对一组独特的原发性和黑色素瘤转移灶个体匹配对进行了免疫组织化学研究。将免疫反应性色素细胞的抗原谱与肿瘤进展阶段进行了比较。我们的数据显示,同一患者体内原发性黑色素瘤及其转移灶具有一致的抗原谱。在原发性黑色素瘤的放射状生长阶段观察到酪氨酸酶相关蛋白和色素沉着相关抗原的表达,但在垂直生长阶段和转移性黑色素瘤中表达减弱或完全丧失。HLA-DR在大多数原发性病变中呈阴性,但在转移部位观察到黑色素瘤细胞和更大比例的免疫反应性细胞。黑色素瘤相关抗原MAA-1和MAA-2在肿瘤进展过程中均有表达。虽然对于这两种黑色素瘤相关抗原,原发性和继发性黑色素瘤病变之间没有明显区别,但与HLA-DR相比,抗原的地形分布存在很大差异。原发性病变和转移性黑色素瘤垂直生长阶段色素沉着相关抗原和酪氨酸酶相关蛋白表达的丧失未达到统计学意义,但仍可能与肿瘤进展有关。这表明,通过评估抗原谱可以区分原发性黑色素瘤及其转移灶,在这方面有助于识别肿瘤进展阶段。

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Antigenic profiles of individual-matched pairs of primary and melanoma metastases.原发性肿瘤与黑色素瘤转移灶个体匹配对的抗原谱。
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