B-cell receptor immunoglobulin stereotypy in chronic lymphocytic leukemia: Key to understanding disease biology and stratifying patients

被引:5
作者
Agathangelidis, Andreas [1 ]
Chatzikonstantinou, Thomas [2 ]
Stamatopoulos, Kostas [2 ,3 ]
机构
[1] Natl & Kapodistrian Univ Athens, Dept Biol, Div Genet & Biotechnol, Athens, Greece
[2] Ctr Res & Technol Hellas, Inst Appl Biosci, 6th km Charilaou Thermi Rd, Thermi 57001, Thessaloniki, Greece
[3] Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden
关键词
Chronic lymphocytic leukemia; Immunogenetics; B-cell receptor; Stereotypy; IGHV genes; Somatic hypermutation; N-GLYCOSYLATION SITES; ANTIGEN RECEPTORS; PATHOGENETIC IMPLICATIONS; NOTCH1; MUTATIONS; VARIABLE REGION; GENE-MUTATIONS; RISK-FACTOR; SUBSETS; CLL; PATTERNS;
D O I
10.1053/j.seminhematol.2023.12.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sequence convergence, otherwise stereotypy, of B-cell receptor immunoglobulin (BcR IG) from unrelated patients is a distinctive feature of the IG gene repertoire in chronic lymphocytic leukemia (CLL) whereby patients expressing a particular BcR IG archetype are classified into groups termed stereotyped subsets. From a biological perspective, the fact that a considerable fraction ( similar to 41%) of patients with CLL express (quasi)identical or stereotyped BcR IG underscores the key role of antigen selection in the natural history of CLL. From a clinical perspective, at odds with the pronounced heterogeneity of CLL at large, patients belonging to the same stereotyped subset display consistent clinical presentation and outcome, including response to treatment, likely as a reflection of consistent biological background. Many major stereotyped subsets were recently shown to have satellites, that is, smaller subsets that are immunogenetically similar. Preliminary evidence supports that this similarity extends to shared biological and even clinical features, with important implications for patient stratification. Consequently, BcR IG stereotypy emerges as a powerful tool for dissecting the heterogeneity of CLL toward refined risk stratification and, eventually, more precise therapeutic interventions. (c) 2024 Elsevier Inc. All rights reserved.
引用
收藏
页码:91 / 99
页数:9
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