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原发性葡萄膜黑色素瘤、其细胞系及其四处转移灶中的人类白细胞抗原(HLA)表达情况。

HLA expression in a primary uveal melanoma, its cell line, and four of its metastases.

作者信息

Blom D J, Schurmans L R, De Waard-Siebinga I, De Wolff-Rouendaal D, Keunen J E, Jager M J

机构信息

Department of Ophthalmology, Leiden University Hospital, Netherlands.

出版信息

Br J Ophthalmol. 1997 Nov;81(11):989-93. doi: 10.1136/bjo.81.11.989.

Abstract

BACKGROUND

The level of HLA expression on a tumour may influence the immunological response against this tumour, and vice versa. HLA expression was determined in a primary uveal melanoma, its metastases, and on a cell line derived from this melanoma, and the presence and type of infiltrate in tissue sections were also studied.

METHODS

Immunohistochemistry with monoclonal antibodies (MAbs) against HLA class I and II, T cells, NK cells, and macrophages.

RESULTS

Primary and metastatic lesions, as well as the cell line showed high levels of expression of the monomorphic determinants of HLA class I. Expression of the polymorphic HLA-A2 and HLA-A3 antigens was decreased on metastases to the skin and liver. HLA-Bw4 expression was low on all lesions, as well as expression of HLA class II. Tumour infiltrating cells consisted mainly of CD3, CD4, and CD8 positive cells. Expression on the cell line corresponded to expression on the primary tumour.

CONCLUSION

The primary uveal melanoma as well as the cell line showed a high expression of monomorphic and polymorphic HLA-A antigens, while metastases showed a high expression of monomorphic and a lower expression of polymorphic antigens. This variation in expression may support tumour cell escape from NK cells as well as CTL mediated lysis.

摘要

背景

肿瘤上HLA表达水平可能影响针对该肿瘤的免疫反应,反之亦然。测定了原发性葡萄膜黑色素瘤、其转移灶以及源自该黑色素瘤的细胞系中的HLA表达,并研究了组织切片中浸润物的存在情况和类型。

方法

使用针对HLA I类和II类、T细胞、NK细胞及巨噬细胞的单克隆抗体进行免疫组织化学检测。

结果

原发性和转移性病变以及细胞系均显示出HLA I类单态决定簇的高表达。皮肤和肝脏转移灶上多态性HLA - A2和HLA - A3抗原的表达降低。所有病变上HLA - Bw4表达均较低,HLA II类表达也较低。肿瘤浸润细胞主要由CD3、CD4和CD8阳性细胞组成。细胞系上的表达与原发性肿瘤上的表达一致。

结论

原发性葡萄膜黑色素瘤以及细胞系显示出单态和多态性HLA - A抗原的高表达,而转移灶显示出单态的高表达和多态性抗原的低表达。这种表达差异可能支持肿瘤细胞逃避NK细胞以及CTL介导的裂解。

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