Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Mol Med. 2013 Aug 28;19(1):230-6. doi: 10.2119/molmed.2013.00042.
Chronic lymphocytic leukemia (CLL) patients assigned to stereotyped subset 4 possess distinctive patterns of intraclonal diversification (ID) within their immunoglobulin (IG) genes. Although highly indicative of an ongoing response to antigen(s), the critical question concerning the precise timing of antigen involvement is unresolved. Hence, we conducted a large-scale longitudinal study of eight subset 4 cases totaling 511 and 398 subcloned IG heavy and kappa sequences. Importantly, we could establish a hierarchical pattern of subclonal evolution, thus revealing which somatic hypermutations were negatively or positively selected. In addition, distinct clusters of subcloned sequences with cluster-specific mutational profiles were observed initially; however, at later time points, the minor cluster had often disappeared and hence not been selected. Despite the high intensity of ID, it was remarkable that certain residues remained essentially unaltered. These novel findings strongly support a role for persistent antigen stimulation in the clonal evolution of CLL subset 4.
慢性淋巴细胞白血病(CLL)患者被分配到定型亚组 4 后,其免疫球蛋白(IG)基因内存在独特的克隆内多样化(ID)模式。尽管这高度提示了对抗原的持续反应,但关于抗原参与的确切时间的关键问题仍未解决。因此,我们对 8 个亚组 4 病例进行了大规模的纵向研究,共对 511 和 398 个克隆 IG 重链和κ序列进行了克隆。重要的是,我们能够建立一个克隆进化的层次模式,从而揭示哪些体细胞突变是被负选择还是正选择。此外,最初观察到具有簇特异性突变特征的克隆序列的不同簇;然而,在稍后的时间点,小簇通常已经消失,因此没有被选择。尽管 ID 强度很高,但令人惊讶的是,某些残基基本保持不变。这些新发现强烈支持持续性抗原刺激在 CLL 亚组 4 的克隆进化中的作用。