TY - JOUR
T1 - Higher-order connections between stereotyped subsets
T2 - implications for improved patient classification in CLL
AU - ERIC, the European Research Initiative on CLL
AU - Agathangelidis, Andreas
AU - Chatzidimitriou, Anastasia
AU - Gemenetzi, Katerina
AU - Giudicelli, Veronique
AU - Karypidou, Maria
AU - Plevova, Karla
AU - Davis, Zadie
AU - Yan, Xiao Jie
AU - Jeromin, Sabine
AU - Schneider, Christof
AU - Pedersen, Lone Bredo
AU - Tschumper, Renee C.
AU - Sutton, Lesley Ann
AU - Baliakas, Panagiotis
AU - Scarfò, Lydia
AU - van Gastel, Ellen J.
AU - Armand, Marine
AU - Tausch, Eugen
AU - Biderman, Bella
AU - Baer, Constance
AU - Bagnara, Davide
AU - Navarro, Alba
AU - Langlois de Septenville, Anne
AU - Guido, Valentina
AU - Mitterbauer-Hohendanner, Gerlinde
AU - Dimovski, Aleksandar
AU - Brieghel, Christian
AU - Lawless, Sarah
AU - Meggendorfer, Manja
AU - Brazdilova, Kamila
AU - Ritgen, Matthias
AU - Facco, Monica
AU - Tresoldi, Cristina
AU - Visentin, Andrea
AU - Patriarca, Andrea
AU - Catherwood, Mark
AU - Bonello, Lisa
AU - Sudarikov, Andrey
AU - Vanura, Katrina
AU - Roumelioti, Maria
AU - Skuhrova Francova, Hana
AU - Moysiadis, Theodoros
AU - Veronese, Silvio
AU - Giannopoulos, Krzysztof
AU - Mansouri, Larry
AU - Karan-Djurasevic, Teodora
AU - Sandaltzopoulos, Raphael
AU - Bödör, Csaba
AU - Fais, Franco
AU - Gaidano, Gianluca
N1 - Publisher Copyright:
© 2021 American Society of Hematology
PY - 2021/3/11
Y1 - 2021/3/11
N2 - Chronic lymphocytic leukemia (CLL) is characterized by the existence of subsets of patients with (quasi)identical, stereotyped B-cell receptor (BcR) immunoglobulins. Patients in certain major stereotyped subsets often display remarkably consistent clinicobiological profiles, suggesting that the study of BcR immunoglobulin stereotypy in CLL has important implications for understanding disease pathophysiology and refining clinical decision-making. Nevertheless, several issues remain open, especially pertaining to the actual frequency of BcR immunoglobulin stereotypy and major subsets, as well as the existence of higher-order connections between individual subsets. To address these issues, we investigated clonotypic IGHV-IGHD-IGHJ gene rearrangements in a series of 29 856 patients with CLL, by far the largest series worldwide. We report that the stereotyped fraction of CLL peaks at 41% of the entire cohort and that all 19 previously identified major subsets retained their relative size and ranking, while 10 new ones emerged; overall, major stereotyped subsets had a cumulative frequency of 13.5%. Higher-level relationships were evident between subsets, particularly for major stereotyped subsets with unmutated IGHV genes (U-CLL), for which close relations with other subsets, termed “satellites,” were identified. Satellite subsets accounted for 3% of the entire cohort. These results confirm our previous notion that major subsets can be robustly identified and are consistent in relative size, hence representing distinct disease variants amenable to compartmentalized research with the potential of overcoming the pronounced heterogeneity of CLL. Furthermore, the existence of satellite subsets reveals a novel aspect of repertoire restriction with implications for refined molecular classification of CLL. Key Points: • In a series of 29 856 CLL patients, the incidence of BcR stereotypy peaked at 41%. • Higher-order relations exist between stereotyped subsets, particularly for those from U-CLL, for which satellite subsets were identified.
AB - Chronic lymphocytic leukemia (CLL) is characterized by the existence of subsets of patients with (quasi)identical, stereotyped B-cell receptor (BcR) immunoglobulins. Patients in certain major stereotyped subsets often display remarkably consistent clinicobiological profiles, suggesting that the study of BcR immunoglobulin stereotypy in CLL has important implications for understanding disease pathophysiology and refining clinical decision-making. Nevertheless, several issues remain open, especially pertaining to the actual frequency of BcR immunoglobulin stereotypy and major subsets, as well as the existence of higher-order connections between individual subsets. To address these issues, we investigated clonotypic IGHV-IGHD-IGHJ gene rearrangements in a series of 29 856 patients with CLL, by far the largest series worldwide. We report that the stereotyped fraction of CLL peaks at 41% of the entire cohort and that all 19 previously identified major subsets retained their relative size and ranking, while 10 new ones emerged; overall, major stereotyped subsets had a cumulative frequency of 13.5%. Higher-level relationships were evident between subsets, particularly for major stereotyped subsets with unmutated IGHV genes (U-CLL), for which close relations with other subsets, termed “satellites,” were identified. Satellite subsets accounted for 3% of the entire cohort. These results confirm our previous notion that major subsets can be robustly identified and are consistent in relative size, hence representing distinct disease variants amenable to compartmentalized research with the potential of overcoming the pronounced heterogeneity of CLL. Furthermore, the existence of satellite subsets reveals a novel aspect of repertoire restriction with implications for refined molecular classification of CLL. Key Points: • In a series of 29 856 CLL patients, the incidence of BcR stereotypy peaked at 41%. • Higher-order relations exist between stereotyped subsets, particularly for those from U-CLL, for which satellite subsets were identified.
UR - http://www.scopus.com/inward/record.url?scp=85102607193&partnerID=8YFLogxK
U2 - 10.1182/blood.2020007039
DO - 10.1182/blood.2020007039
M3 - Article
SN - 0006-4971
VL - 137
SP - 1365
EP - 1376
JO - Blood
JF - Blood
IS - 10
ER -