TY - JOUR
T1 - Primary effusion lymphoma cell lines harbouring human herpesvirus type-8
AU - Carbone, Antonino
AU - Cilia, Anna M.
AU - Gloghini, Annunziata
AU - Capello, Daniela
AU - Perin, Tiziana
AU - Bontempo, Daniela
AU - Canzonieri, Vincenzo
AU - Tirelli, Umberto
AU - Volpe, Rachele
AU - Gaidano, Gianluca
N1 - Funding Information:
This work has been supported by ISS, I1 Programma nazionale di ricerca sull’AIDS 1998 - Progetto Pato-logia clinica e terapia dell’ AIDS, Rome, Italy.
PY - 2000
Y1 - 2000
N2 - Primary effusion lymphoma (PEL) is a novel lymphoma entity consistently infected by HHV-8 that occurs predominantly in immunodeficient patients and is characterized by liquid growth in the serous body cavities. In order to facilitate the understanding of PEL pathogenesis and histogenesis, we have established three PEL cell lines termed CRO-AP/2, CRO-AP/3 and CRO-AP/5. All cell lines have been derived from HIV positive homosexual men affected by PEL with (in the case of CRO-AP/2 and CRO-AP/5) or without (in the case of CRO-AP/3) a previous history of Kaposi's sarcoma. The cell lines are representative of both virologic variants of PEL, i.e. HHV-8+ EBV+ PEL (CRO-AP/2 and CRO-AP/5) and HHV-8+ EBV PEL (CRO-AP/3). Morphologic and phenotypic features of CRO-AP/2 CRO-AP/3 and CRO-AP/5 are typical of PEL, and include morphology bridging immunoblastic and anaplastic features as well as an indeterminate (non B- non T-cell) phenotype. The B-cell nature of the cell lines is documented by the presence of rearranged immunoglobulin genes. The detailed analysis of the molecular and phenotypic features of CRO-AP/2, CRO-AP/3 and CRO-AP/5 has allowed the identification of recurrent chromosomal abnormalities of PEL and has contributed to the definition of PEL as a lymphoma of post-germinal center, pre-terminally differentiated B-cells.
AB - Primary effusion lymphoma (PEL) is a novel lymphoma entity consistently infected by HHV-8 that occurs predominantly in immunodeficient patients and is characterized by liquid growth in the serous body cavities. In order to facilitate the understanding of PEL pathogenesis and histogenesis, we have established three PEL cell lines termed CRO-AP/2, CRO-AP/3 and CRO-AP/5. All cell lines have been derived from HIV positive homosexual men affected by PEL with (in the case of CRO-AP/2 and CRO-AP/5) or without (in the case of CRO-AP/3) a previous history of Kaposi's sarcoma. The cell lines are representative of both virologic variants of PEL, i.e. HHV-8+ EBV+ PEL (CRO-AP/2 and CRO-AP/5) and HHV-8+ EBV PEL (CRO-AP/3). Morphologic and phenotypic features of CRO-AP/2 CRO-AP/3 and CRO-AP/5 are typical of PEL, and include morphology bridging immunoblastic and anaplastic features as well as an indeterminate (non B- non T-cell) phenotype. The B-cell nature of the cell lines is documented by the presence of rearranged immunoglobulin genes. The detailed analysis of the molecular and phenotypic features of CRO-AP/2, CRO-AP/3 and CRO-AP/5 has allowed the identification of recurrent chromosomal abnormalities of PEL and has contributed to the definition of PEL as a lymphoma of post-germinal center, pre-terminally differentiated B-cells.
KW - Cell lines
KW - EBV
KW - Human herpesvirus type 8
KW - PEL
KW - Primary effusion lymphoma
UR - http://www.scopus.com/inward/record.url?scp=18744424715&partnerID=8YFLogxK
U2 - 10.3109/10428190009148391
DO - 10.3109/10428190009148391
M3 - Review article
SN - 1042-8194
VL - 36
SP - 447
EP - 456
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
IS - 5-6
ER -