TY - JOUR
T1 - Common-variable immunodeficiency-related lymphomas associate with mutations and rearrangements of BCL-6
T2 - Pathogenetic and histogenetic implications
AU - Ariatti, Cristiano
AU - Vivenza, Daniela
AU - Capello, Daniela
AU - Migliazza, Anna
AU - Parvis, Guido
AU - Fassone, Lucia
AU - Buonaiuto, Daniela
AU - Savinelli, Francesco
AU - Rossi, Davide
AU - Saglio, Giuseppe
AU - Gaidano, Gianluca
N1 - Funding Information:
Supported by the Istituto Superiore di Sanità, II Programma Nazionale di Ricerca sull’AIDS 1998, Progetto Patologia, Clinica e Terapia dell’AIDS, Rome, Italy; Fondazione ‘‘Piera Pietro e Giovanni Ferrero,’’ Alba, Italy; and ‘‘Fondazione CRT,’’ Torino, Italy. D.C. is being supported by a fellowship from Fondazione Italiana Ricera Contro Il Cancro (FIRC), Milan, Italy.
PY - 2000
Y1 - 2000
N2 - Common-variable immunodeficiency (CVI) patients develop non-Hodgkin's lymphomas (NHL), mainly B-lineage diffuse large-cell lymphomas (DLCL), with a high relative risk. The molecular pathogenesis of CVI-related NHL (CVI-NHL) is unknown. Here we aimed at providing a detailed molecular characterization of CVI-NHL. Rearrangements of BCL-6 were detected in two thirds of CVI-NHL cases examined. All 3 CVI-NHL also harbored point mutations of the BCL-6 5' noncoding regions, which constitute a marker of B-cell transit through the germinal center (GC). The number and molecular pattern of BCL-6 mutations in CVI-NHL were similar to that detected in DLCL of immunocompetent hosts and in DLCL arising in other immunodeficiency settings. Microsatellite instability occured in one CVI-NHL devoid of a BCL.6 rearrangement. All CVI-NHL scored negative for genetic lesions of BCL-2, p53, c-MYC, REL as well as for viral infection by EBV and HHV-8. Overall, these data indicate that: similarly to other immunodeficiency-related NHL, involvement of BCL-6 occurs frequently also in CVI-NHL; and because BCL.6 mutations are acquired by B cells during GC transit, their occurrence in CVI-NHL suggest that these lymphomas are histogenetically related to GC B cells. (C) 2000 by W.B. Saunders Company.
AB - Common-variable immunodeficiency (CVI) patients develop non-Hodgkin's lymphomas (NHL), mainly B-lineage diffuse large-cell lymphomas (DLCL), with a high relative risk. The molecular pathogenesis of CVI-related NHL (CVI-NHL) is unknown. Here we aimed at providing a detailed molecular characterization of CVI-NHL. Rearrangements of BCL-6 were detected in two thirds of CVI-NHL cases examined. All 3 CVI-NHL also harbored point mutations of the BCL-6 5' noncoding regions, which constitute a marker of B-cell transit through the germinal center (GC). The number and molecular pattern of BCL-6 mutations in CVI-NHL were similar to that detected in DLCL of immunocompetent hosts and in DLCL arising in other immunodeficiency settings. Microsatellite instability occured in one CVI-NHL devoid of a BCL.6 rearrangement. All CVI-NHL scored negative for genetic lesions of BCL-2, p53, c-MYC, REL as well as for viral infection by EBV and HHV-8. Overall, these data indicate that: similarly to other immunodeficiency-related NHL, involvement of BCL-6 occurs frequently also in CVI-NHL; and because BCL.6 mutations are acquired by B cells during GC transit, their occurrence in CVI-NHL suggest that these lymphomas are histogenetically related to GC B cells. (C) 2000 by W.B. Saunders Company.
KW - BCL-6
KW - Common variable immunodeficiency
KW - Lymphoma
KW - Pathogenesis
UR - http://www.scopus.com/inward/record.url?scp=0033942516&partnerID=8YFLogxK
U2 - 10.1053/hupa.2000.7626
DO - 10.1053/hupa.2000.7626
M3 - Article
SN - 0046-8177
VL - 31
SP - 871
EP - 873
JO - Human Pathology
JF - Human Pathology
IS - 7
ER -