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MHC I类抗原表达缺陷在高度恶性的B细胞淋巴瘤中很常见。

Defective expression of MHC class I antigens is frequent in B-cell lymphomas of high-grade malignancy.

作者信息

Möller P, Herrmann B, Moldenhauer G, Momburg F

出版信息

Int J Cancer. 1987 Jul 15;40(1):32-9. doi: 10.1002/ijc.2910400107.

DOI:10.1002/ijc.2910400107
PMID:3298077
Abstract

An unselected series of 66 immunohistologically proven B-cell lymphomas was examined for the expression of MHC class I antigens with monoclonal antibodies directed against non-polymorphic determinants of HLA-A,B,C heavy chain and beta 2-microglobulin. The tumors were classified according to the Kiel classification. No significant differences were observed in the reaction for HLA-A,B,C and beta 2m which may be indicative of a coordinate expression in our lymphoma series. In 37 cases (56%), all tumor cells exhibited strong staining for class I antigens as observed in normal B cells. The remaining 29 cases (44%) showed abnormally low or undetectable class I expression in varying tumor cell subsets; 13 cases were completely devoid of HLA-A,B,C. Twenty-two out of 30 lymphomas of high-grade malignancy but only 7/36 lymphomas of low-grade malignancy presented defective class I expression. This difference in proportion is highly significant (p less than 0.00002). Eleven of the 13 class I-negative lymphomas belonged to the group of high-grade malignancy. Centrocytic lymphoma, which has the poorest prognosis among the B-cell lymphomas of low-grade malignancy, was defective in 40% of the cases examined. The lymphoblastic type represented an exception within the lymphomas of high-grade malignancy as no defective expression was observed. In addition to the correlation between the high-grade malignancy and defective class I expression, defects occurred more frequently in lymphomas with an extra-nodal primary manifestation (p less than 0.05). The grade of malignancy, however, was not correlated with the primary site of the lymphoma.

摘要

对一组未经选择的66例经免疫组织学证实的B细胞淋巴瘤进行检测,使用针对HLA-A、B、C重链和β2-微球蛋白非多态性决定簇的单克隆抗体检测MHC I类抗原的表达。根据 Kiel 分类法对肿瘤进行分类。在HLA-A、B、C和β2m的反应中未观察到显著差异,这可能表明在我们的淋巴瘤系列中存在协同表达。在37例(56%)中,所有肿瘤细胞均表现出与正常B细胞中观察到的相同的I类抗原强染色。其余29例(44%)在不同的肿瘤细胞亚群中表现出异常低或无法检测到的I类表达;13例完全缺乏HLA-A、B、C。30例高度恶性淋巴瘤中有22例,但低度恶性淋巴瘤中只有7/36例出现I类表达缺陷。这种比例差异具有高度统计学意义(p<0.00002)。13例I类阴性淋巴瘤中有11例属于高度恶性组。在低度恶性的B细胞淋巴瘤中预后最差的中心细胞淋巴瘤,在40%的检测病例中存在缺陷。淋巴母细胞型在高度恶性淋巴瘤中是个例外,未观察到表达缺陷。除了高度恶性与I类表达缺陷之间的相关性外,结外原发性淋巴瘤中缺陷出现的频率更高(p<0.05)。然而,恶性程度与淋巴瘤的原发部位无关。

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