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PRESENCE OF EPSTEIN‐BARR VIRUS DNA IN NASAL LYMPHOMAS OF B AND ‘T’ CELL TYPE
Author(s) -
Ho F. C. S.,
Srivastava G.,
Loke S. L.,
Fu K. H.,
Leung B. P. Y.,
Liang R.,
Choy D.
Publication year - 1990
Publication title -
hematological oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 44
eISSN - 1099-1069
pISSN - 0278-0232
DOI - 10.1002/hon.2900080505
Subject(s) - biology , gene rearrangement , southern blot , lymphoma , epstein–barr virus , virus , immunophenotyping , immunoglobulin gene , t cell receptor , virology , gene , lineage (genetic) , antibody , dna , ecori , microbiology and biotechnology , t cell , genetics , immunology , antigen , restriction enzyme , immune system
We studied 12 tumours from 11 Chinese patients with primary nasal lymphoma for presence of Epstein‐Barr Virus (EBV) DNA, using Southern‐blot analysis. These results were correlated with immunophenotype and T‐cell receptor (TcR) or immunoglobulin gene rearrangement patterns. EBV DNA was detected in all nine tumours with a ‘T’ phenotype, in both primary and secondary sites. When the structure of the viral genomic termini was studied using the EcoRI‐Dhet probe, a single clonal episomal band was demonstrated in five tumour samples, with one other case showing a biclonal pattern. However, none of these cases showed clonal rearrangement of TcR β chain gene, and TcR γ rearrangement was found only in one. The lineage of these phenotypic ‘T’ lymphomas therefore require further studies for confirmation. Two out of three B‐lymphomas were also EBV DNA+; clonal EBV DNA was found in one. Their B‐lineage was confirmed by detection of clonal immunoglobulin gene rearrangements. The association of EBV with an increasing number of lymphomas of different types highlights the need for continued study into its role in oncogenesis.