Zelenetz A D, Chen T T, Levy R
Department of Medicine, Stanford Medical School, California 94305.
J Exp Med. 1991 Jan 1;173(1):197-207. doi: 10.1084/jem.173.1.197.
To investigate the clonal relationship between follicular lymphoma (FL) and transformed diffuse lymphoma (tDL), we examined the expression of tumor idiotype, immunoglobulin (Ig) gene rearrangements and sequence of Ig variable genes in paired tissue specimens. All 16 cases analyzed expressed surface immunoglobulin (sIg) on both the FL and the tDL, though the immunophenotype of one case of FL could not be definitively determined. In 14 of 15 cases, the surface immunophenotype was preserved; the exception was likely secondary to a class switch from IgM to IgG. In 12 of 13 cases, antiidiotypic monoclonal antibodies prepared against the FL reacted with the paired tDL. Analysis of Ig gene rearrangements in four cases by Southern blot hybridization showed evidence of clonal relationships in all cases though concordance was not seen with all probes tested (C kappa, C lambda, JH, PFL1, and PFL2). In the one case that had a discordant L chain rearrangement, sequence analysis of the L chain demonstrated a common mature B cell origin for both the FL and tDL. To determine whether tDL arose from one or more FL cells, the sequences of the H chain variable genes were analyzed. Individual clones of the V region gene of the FL showed a random distribution of changes throughout the sequence. In contrast, individual clones of the V region gene from tDL shared numerous nonrandom sequence alterations, implying a common single cell origin. In conclusion, tDL is a mature B cell and arises by transformation of a single FL cell.
为了研究滤泡性淋巴瘤(FL)与转化型弥漫性淋巴瘤(tDL)之间的克隆关系,我们检测了配对组织标本中肿瘤独特型的表达、免疫球蛋白(Ig)基因重排以及Ig可变基因序列。分析的所有16例病例中,FL和tDL均表达表面免疫球蛋白(sIg),不过1例FL的免疫表型无法明确确定。15例中的14例,表面免疫表型得以保留;例外情况可能是由于从IgM到IgG的类别转换所致。13例中的12例,针对FL制备的抗独特型单克隆抗体与配对的tDL发生反应。通过Southern印迹杂交对4例病例的Ig基因重排进行分析,结果显示所有病例均有克隆关系的证据,不过并非与所有检测探针(Cκ、Cλ、JH、PFL1和PFL2)都一致。在1例轻链重排不一致的病例中,轻链序列分析表明FL和tDL均起源于共同的成熟B细胞。为了确定tDL是否源自一个或多个FL细胞,我们分析了重链可变基因序列。FL的V区基因单个克隆在整个序列中呈现出随机分布的变化。相比之下,tDL的V区基因单个克隆存在众多非随机序列改变,这意味着其起源于共同的单个细胞。总之,tDL是一种成熟B细胞,由单个FL细胞转化而来。