生发中心
B细胞
生物
细胞
淋巴瘤
幼稚B细胞
起源细胞
弥漫性大B细胞淋巴瘤
抗原
细胞生物学
B细胞淋巴瘤
分子生物学
T细胞
免疫学
抗体
遗传学
抗原提呈细胞
免疫系统
作者
Antony B. Holmes,Clarissa Corinaldesi,Qiong Shen,Rahul Kumar,Nicolò Compagno,Zhong Wang,Mor Nitzan,Eli Grunstein,Laura Pasqualucci,Riccardo Dalla‐Favera,Katia Basso
摘要
In response to T cell–dependent antigens, mature B cells are stimulated to form germinal centers (GCs), the sites of B cell affinity maturation and the cell of origin (COO) of most B cell lymphomas. To explore the dynamics of GC B cell development beyond the known dark zone and light zone compartments, we performed single-cell (sc) transcriptomic analysis on human GC B cells and identified multiple functionally linked subpopulations, including the distinct precursors of memory B cells and plasma cells. The gene expression signatures associated with these GC subpopulations were effective in providing a sc-COO for ∼80% of diffuse large B cell lymphomas (DLBCLs) and identified novel prognostic subgroups of DLBCL.
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