EPSTEIN-BARR-VIRUS INFECTION IN THE NEOPLASTIC AND NONNEOPLASTIC CELLS OF LYMPHOID MALIGNANCIES

Citation
N. Teramoto et al., EPSTEIN-BARR-VIRUS INFECTION IN THE NEOPLASTIC AND NONNEOPLASTIC CELLS OF LYMPHOID MALIGNANCIES, Cancer, 77(11), 1996, pp. 2339-2347
Citations number
30
Categorie Soggetti
Oncology
Journal title
CancerACNP
ISSN journal
0008543X
Volume
77
Issue
11
Year of publication
1996
Pages
2339 - 2347
Database
ISI
SICI code
0008-543X(1996)77:11<2339:EIITNA>2.0.ZU;2-8
Abstract
BACKGROUND. The Epstein-Barr virus (EBV) has been frequently detected in lymphoid malignancies. However, EBV infection in the nonneoplastic cells of lymphoid malignancies has not been extensively studied. METHO DS. Four hundred nine cases of lymphoid malignancies including 377 non -Hodgkin's lymphoma (NHL) and 32 Hodgkin's disease (HD) were examined for EBV infection by EBER-1 in situ hybridization (EBER-ISH), immunost aining against LMP-1, Epstein-Barr nuclear antigen 2 (EBNA2) and ZEBRA , and Southern hybridization using a BamHIW fragment as a probe. Doubl e staining with EBER-ISH and immunostaining against CD20, CD45RO, and LMP-1 was performed in selected cases. RESULTS. Although EBER-1-positi ve cells (EPCs) were detected in 49 of 276 B-cell lymphomas, 31 of 100 T-cell lymphomas, 1 of 1 natural killer-cell lymphoma, and 17 of 32 H Ds, almost all of the tumor cells were exclusively EBER-1-positive in the 10 NHL cases. Some EPCs were of different cell lineages than the t umor cells in 15 of the 26 NHLs examined by double staining. LMP-1, EB NA2, and ZEBRA were detected in 22, 4, and 3 cases, respectively. In 4 LMP-1-positive HDs, double staining revealed that some EBER-1-positiv e Reed-Sternberg cells were negative for LMP-1. EBV genomic DNA was de tected in 8 of the 39 examined cases. CONCLUSIONS. T-cell lymphomas co ntained EPCs more frequently than B-cell lymphomas. Nonneoplastic lymp hocytes were infected with EBV more frequently than lymphoma cells. Ro we's latency II may be unstable in lymphoid malignancies. Some NHLs, e specially T-cell lymphoma, may provide favorable conditions for EBV in fection of nonneoplastic lymphocytes. (C) 1996 American Cancer Society .