The tumor virus landscape of AIDS-related lymphomas.

Blood
Authors
Keywords
Abstract

Immunodeficiency dramatically increases susceptibility to cancer as a result of reduced immune surveillance and enhanced opportunities for virus-mediated oncogenesis. Although AIDS-related lymphomas (ARLs) are frequently associated with known oncogenic viruses, many cases contain no known transforming virus. To discover novel transforming viruses, we profiled a set of ARL samples using whole transcriptome sequencing. We determined that Epstein-Barr virus (EBV) was the only virus detected in the tumor samples of this cohort, suggesting that if unidentified pathogens exist in this disease, they are present in 10% of cases or undetectable by our methods. To evaluate the role of EBV in ARL pathogenesis, we analyzed viral gene expression and found highly heterogeneous patterns of viral transcription across samples. We also found significant heterogeneity of viral antigen expression across a large cohort, with many patient samples presenting with restricted type I viral latency, indicating that EBV latency proteins are under increased immunosurveillance in the post-combined antiretroviral therapies era. Furthermore, EBV infection of lymphoma cells in HIV-positive individuals was associated with a distinct host gene expression program. These findings provide insight into the joint host-virus regulatory network of primary ARL tumor samples and expand our understanding of virus-associated oncogenesis. Our findings may also have therapeutic implications, as treatment may be personalized to target specific viral and virus-associated host processes that are only present in a subset of patients.

Year of Publication
2015
Journal
Blood
Volume
125
Issue
20
Pages
e14-22
Date Published
2015 May 14
ISSN
1528-0020
URL
DOI
10.1182/blood-2014-11-599951
PubMed ID
25827832
PubMed Central ID
PMC4432014
Links
Grant list
1RC2CA148317 / CA / NCI NIH HHS / United States
RC2 CA148317 / CA / NCI NIH HHS / United States
U01CA121947 / CA / NCI NIH HHS / United States
UM1 CA181255 / CA / NCI NIH HHS / United States
1UM1CA181255 / CA / NCI NIH HHS / United States
UM1 CA121947 / CA / NCI NIH HHS / United States
U01 CA121947 / CA / NCI NIH HHS / United States