体细胞突变
生发中心
表观遗传学
生物
B细胞
记忆B细胞
免疫球蛋白类转换
V(D)J复合
亲和力成熟
获得性免疫系统
体细胞
遗传学
基因组
抗原
克隆选择
Cre-Lox重组
计算生物学
免疫学
抗体
基因
重组
转基因
转基因小鼠
摘要
The adaptive immune system has evolved to allow effective responses against a virtually unlimited number of invading pathogens. This process requires the transient formation of germinal centers (GC), a dynamic environment that ensures the generation and selection of B cells capable to produce antibodies with high antigen affinity, or to maintain the memory of that antigen for life. However, this comes at a cost, as the unique events accompanying the GC reaction pose a significant risk to the genome of B cells, which must endure elevated levels of replication stress, while proliferating at high rates and undergoing DNA breaks introduced by somatic hypermutation and class switch recombination. Indeed, the genetic/epigenetic disruption of programs implicated in normal GC biology has emerged as a hallmark of most B cell lymphomas. This improved understanding provides a conceptual framework for the identification of cellular pathways that could be exploited for precision medicine approaches.
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