Swaminathan Srividya, Klemm Lars, Park Eugene, Papaemmanuil Elli, Ford Anthony, Kweon Soo-Mi, Trageser Daniel, Hasselfeld Brian, Henke Nadine, Mooster Jana, Geng Huimin, Schwarz Klaus, Kogan Scott C, Casellas Rafael, Schatz David G, Lieber Michael R, Greaves Mel F, Müschen Markus
Department of Laboratory Medicine, University of California San Francisco, CA, 94143.
University of Freiburg, Faculty of Biology, 79104 Freiburg, Germany.
Nat Immunol. 2015 Jul;16(7):766-774. doi: 10.1038/ni.3160. Epub 2015 May 18.
Childhood acute lymphoblastic leukemia (ALL) can often be traced to a pre-leukemic clone carrying a prenatal genetic lesion. Postnatally acquired mutations then drive clonal evolution toward overt leukemia. The enzymes RAG1-RAG2 and AID, which diversify immunoglobulin-encoding genes, are strictly segregated in developing cells during B lymphopoiesis and peripheral mature B cells, respectively. Here we identified small pre-BII cells as a natural subset with increased genetic vulnerability owing to concurrent activation of these enzymes. Consistent with epidemiological findings on childhood ALL etiology, susceptibility to genetic lesions during B lymphopoiesis at the transition from the large pre-BII cell stage to the small pre-BII cell stage was exacerbated by abnormal cytokine signaling and repetitive inflammatory stimuli. We demonstrated that AID and RAG1-RAG2 drove leukemic clonal evolution with repeated exposure to inflammatory stimuli, paralleling chronic infections in childhood.
儿童急性淋巴细胞白血病(ALL)通常可追溯到携带产前遗传损伤的白血病前期克隆。出生后获得的突变随后推动克隆进化为明显的白血病。在B淋巴细胞生成过程中,使免疫球蛋白编码基因多样化的酶RAG1-RAG2和AID分别在发育中的细胞和外周成熟B细胞中严格分离。在这里,我们确定小前BII细胞是一个天然亚群,由于这些酶的同时激活,其遗传易感性增加。与儿童ALL病因的流行病学研究结果一致,从大前BII细胞阶段向小前BII细胞阶段转变过程中,B淋巴细胞生成期间对遗传损伤的易感性因异常细胞因子信号传导和反复炎症刺激而加剧。我们证明,AID和RAG1-RAG2在反复接触炎症刺激后推动白血病克隆进化,这与儿童期慢性感染情况相似。