Yumoto N, Furukawa M, Kurosu K, Mikata A
First Department of Pathology, School of Medicine, Chiba University, Japan.
Lab Invest. 1998 Mar;78(3):261-8.
To clarify the origin of tumor cells and the possible role of antigen in the pathogenesis of mucosa-associated lymphoid tissue (MALT) lymphoma, we analyzed the third complementarity determining region of IgH gene in nine primary gastric B-cell lymphomas by PCR. The presence of vacA gene of Helicobacter pylori was also determined. These cases were diagnosed histopathologically as three low (extranodal marginal zone B-cell lymphoma)- and three high-grade MALT lymphomas and three diffuse large-cell lymphomas without evidence of MALT lymphoma. All cases showed a monoclonally rearranged JH band. A single dominant clone was detected by sequencing the IgH CDR3 regions in eight cases. In the remaining cases. In the remaining case, two major sequences were identified. Complementarity-determining region 3 (CDR3) sequences in lymphoma cell clones of seven cases showed 61% to 81% homology with autoantibody-associated lymphocyte clones including rheumatoid factor. The N-D-N region in the low-grade MALT lymphoma group was significantly longer than in the high-grade lymphoma groups. Although vacA gene of H. pylori was detected in five of nine cases, all lymphoma cell clones showed no association with foreign antigen. These results indicate that autoantigen may be responsible for the clonal selection of lymphoma cells, and thus autoimmunity may play a role in the pathogenesis of primary gastric B-cell lymphomas.
为阐明肿瘤细胞的起源以及抗原在黏膜相关淋巴组织(MALT)淋巴瘤发病机制中的可能作用,我们通过聚合酶链反应(PCR)分析了9例原发性胃B细胞淋巴瘤中免疫球蛋白重链(IgH)基因的第三个互补决定区。同时还检测了幽门螺杆菌的空泡毒素A(vacA)基因。这些病例经组织病理学诊断为3例低级别(结外边缘区B细胞淋巴瘤)和3例高级别MALT淋巴瘤,以及3例无MALT淋巴瘤证据的弥漫性大细胞淋巴瘤。所有病例均显示单克隆重排的JH条带。通过对8例病例的IgH互补决定区3(CDR3)区域进行测序,检测到一个单一的优势克隆。在其余病例中,鉴定出两个主要序列。7例淋巴瘤细胞克隆中的互补决定区3(CDR3)序列与包括类风湿因子在内的自身抗体相关淋巴细胞克隆显示出61%至81%的同源性。低级别MALT淋巴瘤组中的N-D-N区域明显长于高级别淋巴瘤组。虽然9例中有5例检测到幽门螺杆菌的vacA基因,但所有淋巴瘤细胞克隆均显示与外来抗原无关联。这些结果表明自身抗原可能是淋巴瘤细胞克隆选择的原因,因此自身免疫可能在原发性胃B细胞淋巴瘤的发病机制中起作用。