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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >The IGHV1-69/IGHJ3 recombinations of unmutated CLL are distinct from those of normal B cells
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The IGHV1-69/IGHJ3 recombinations of unmutated CLL are distinct from those of normal B cells

机译:未突变的CLL的IGHV1-69 / IGHJ3重组与正常B细胞​​不同

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IGHV1-69/51p1 is expressed by ~ 30% of unmutated chronic lymphocytic leukemia (U-CLL) and combines with selected IGHD and IGHJ genes generating stereotypes if HCDR3 amino acid homology is > 60%. We had previously revealed stereotypic IGHV1-69/IGHJ6 rearrangements in normal naive B cells, thereby identifying potential counterparts of U-CLL. A different stereotypic IGHV1-69/IGHD3-16(RF2)/IGHJ3 rearrangement carrying the CAR(GGx)YD motif in the N1-region, recurrent in 6% IGHV1-69+ve CLL, is exceptionally sequence restricted, strongly suggestive of shared antigen recognition. We have now analyzed IGHV1-69/IGHJ3 rearrangements in circulating B cells of healthy individuals using several PCR-based approaches with IGHV1-69/IGHJ3 CLL sequences for reference. Stereotypes were found, but all were distinct from CLL. Remarkably, even a highly sensitive semi-nested PCR, specific for the CLL-expressed IGHV1-69/IGHD3-16(RF2)/ IGHJ3 stereotype, failed to identify the CAR(GGx)YD sequence, although similar motifs were found. These highly specific B cells are not apparent in the accessible normal repertoire and may expand in response to rarely expressed antigens important in the pathogenesis of CLL.
机译:IGHV1-69 / 51p1由约30%的未突变慢性淋巴细胞性白血病(U-CLL)表达,并且如果HCDR3氨基酸同源性> 60%,则与选定的IGHD和IGHJ基因结合产生定型。先前我们已经揭示了正常幼稚B细​​胞中的定型IGHV1-69 / IGHJ6重排,从而确定了U-CLL的潜在对应物。在N1区中携带CAR(GGx)YD基序的另一种刻板印象IGHV1-69 / IGHD3-16(RF2)/ IGHJ3重排在6%IGHV1-69 + ve CLL中复发,异常受序列限制,强烈提示共享抗原识别。现在,我们使用几种基于PCR的方法分析了健康个体循环B细胞中的IGHV1-69 / IGHJ3重排,并以IGHV1-69 / IGHJ3 CLL序列作为参考。发现了刻板印象,但都不同于CLL。值得注意的是,即使发现了相似的基序,即使是对CLL表达的IGHV1-69 / IGHD3-16(RF2)/ IGHJ3刻板印象特异的高灵敏度半巢式PCR也无法鉴定CAR(GGx)YD序列。这些高度特异性的B细胞在可访问的正常库中并不明显,并且可能会响应于CLL发病机理中重要的罕见表达抗原而扩增。

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