Gene Expression Profiling of Epstein-Barr Virus-positive and -negative Monomorphic B-cell Posttransplant Lymphoproliferative Disorders

Although most posttransplant lymphoproliferative disorders (PTLD) are related to Epstein-Barr virus (EBV) infection, approximately 20% lack detectable EBV (EBV−). It is uncertain whether the latter cases are truly distinct from EBV+ PTLD or possibly relate to another infectious agent. This study use...

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Veröffentlicht in:Diagnostic molecular pathology 2007-09, Vol.16 (3), p.158-168
Hauptverfasser: Craig, Fiona E, Johnson, Lawrence R, Harvey, Stephen A. K, Nalesnik, Michael A, Luo, Jianhua H, Bhattacharya, Soumyaroop D, Swerdlow, Steven H
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Sprache:eng
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Zusammenfassung:Although most posttransplant lymphoproliferative disorders (PTLD) are related to Epstein-Barr virus (EBV) infection, approximately 20% lack detectable EBV (EBV−). It is uncertain whether the latter cases are truly distinct from EBV+ PTLD or possibly relate to another infectious agent. This study used gene expression profiling to further investigate the relationship between EBV+ and EBV− monomorphic B-cell PTLD, and to search for clues to their pathogenesis. Affymetrix HU133A GeneChips were used to compare 4 EBV+ and 4 EBV− cases of monomorphic B-cell PTLD. Hierarchical clustering successfully distinguished the EBV+ and EBV− groups. Relative to EBV− PTLD, 54 transcripts were over-expressed in EBV+ PTLD. The transcripts identified included IRF7 (a known regulator of EBV LMP1 expression), EBI2 (EBV-induced gene 2), and 3 that are interferon induced (MX1, IFITM1, and IFITM3). In addition, the EBV+ group contained 232 transcripts decreased relative to the EBV− group, including changes concordant with those previously reported after EBV infection of cultured B-cell lines. In summary, in a small group of monomorphic B-cell PTLD, EBV+ cases demonstrated a subset of gene expression changes associated with EBV infection of B cells. By contrast, EBV− PTLD lacked viral-associated changes suggesting that they are biologically distinct.
ISSN:1052-9551
1533-4066
DOI:10.1097/PDM.0b013e31804f54a9