Weiss L M, Trela M J, Cleary M L, Turner R R, Warnke R A, Sklar J
Am J Pathol. 1985 Dec;121(3):369-73.
The authors have analyzed the DNA of immunoglobulin and T-cell receptor genes in a series of 6 malignancies which were judged to be of histiocytic derivation on the basis of morphologic criteria. They found that 4 of these cases showed rearrangements of the beta T-cell receptor genes in spite of the lack of any specific immunohistochemical markers for B or T cells. One case showed rearrangements of both heavy and light chain immunoglobulin genes and probably represents either a sinusoidal large cell lymphoma or a B-cell lymphoma with activation of histiocytes simulating malignant histiocytosis. A single case lacked both immunoglobulin and T-cell receptor rearrangements consistent with immunologic analyses that suggested its origin from an interdigitating reticulum cell. The result of this study in conjunction with the authors' previous immunologic observations suggests that many presumed histiocytic malignancies actually represent T-cell lymphomas. Alternatively, beta T-cell receptor rearrangement may be a common feature of tumors that show monocyte/histiocytic differentiation.
作者分析了一系列6种恶性肿瘤的免疫球蛋白和T细胞受体基因的DNA,这些肿瘤根据形态学标准被判定为组织细胞来源。他们发现,尽管缺乏B细胞或T细胞的任何特异性免疫组化标志物,但其中4例显示β T细胞受体基因重排。1例显示重链和轻链免疫球蛋白基因均重排,可能代表窦状大细胞淋巴瘤或伴有组织细胞活化模拟恶性组织细胞增多症的B细胞淋巴瘤。1例既缺乏免疫球蛋白重排也缺乏T细胞受体重排,这与免疫分析结果一致,提示其起源于交错突网状细胞。这项研究的结果与作者之前的免疫学观察结果表明,许多推测的组织细胞恶性肿瘤实际上代表T细胞淋巴瘤。或者,β T细胞受体重排可能是显示单核细胞/组织细胞分化的肿瘤的一个共同特征。