IGHV@
CD5型
淋巴细胞增多症
生物
先证者
免疫学
单克隆
慢性淋巴细胞白血病
遗传学
流式细胞术
抗体
基因
白血病
单克隆抗体
突变
作者
Fatima Abbasi,Nancy S. Longo,Peter E. Lipsky,Elizabeth Raveché,Thérèse Aurran Schleinitz,Maryalice Stetler‐Stevenson,Neil E. Caporaso,Gerald E. Marti
标识
DOI:10.1111/j.1365-2141.2007.06857.x
摘要
Monoclonal B cell lymphocytosis (MBL) was detected in four unaffected first-degree relatives (FDR) in a familial chronic lymphocytic leukaemia (CLL) kindred. The proband remains untreated and two male siblings have died. The four unaffected siblings have been followed for a five-year period. All four FDR developed a kappa(+)CD5(+) MBL detected by flow cytometry. Poymerase chain reaction (PCR) for IGHV rearrangement showed evidence of oligoclonality in three of these individuals. Single cell PCR of flow cytometric sorted kappa(+) cells combined with Ig kappa light chain gene sequencing revealed further evidence of monoclonality in two of these individuals. Three of these individuals all showed evidence of hyper-somatic mutations. The B-cell repertoire in unaffected FDR in familial CLL offers a new area to investigate the interface between the immune system and lymphoid neoplasm.
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