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Analysis of Simian Immunodeficiency Virus-specific CD8+ T-cells in Rhesus Macaques by Peptide-MHC-I Tetramer Staining
Published on: December 23, 2016
Macaque homologs of EBV and KSHV show uniquely different associations with simian AIDS-related lymphomas
A Gregory Bruce1, Helle Bielefeldt-Ohmann, Serge Barcy
1Seattle Children's Research Institute, Seattle, Washington, United States of America.
Abstract:
Two gammaherpesviruses, Epstein-Barr virus (EBV) (Lymphocryptovirus genus) and Kaposi's sarcoma-associated herpesvirus (KSHV) (Rhadinovirus genus) have been implicated in the etiology of AIDS-associated lymphomas. Homologs of these viruses have been identified in macaques and other non-human primates. In order to assess the association of these viruses with non-human primate disease, archived lymphoma samples were screened for the presence of macaque lymphocryptovirus (LCV) homologs of EBV, and macaque rhadinoviruses belonging to the RV1 lineage of KSHV homologs or the more distant RV2 lineage of Old World primate rhadinoviruses. Viral loads were determined by QPCR and infected cells were identified by immunolabeling for different viral proteins. The lymphomas segregated into three groups. The first group (n = 6) was associated with SIV/SHIV infections, contained high levels of LCV (1-25 genomes/cell) and expressed the B-cell antigens CD20 or BLA.36. A strong EBNA-2 signal was detected in the nuclei of the neoplastic cells in one of the LCV-high lymphomas, indicative of a type III latency stage. None of the lymphomas in this group stained for the LCV viral capsid antigen (VCA) lytic marker. The second group (n = 5) was associated with D-type simian retrovirus-2 (SRV-2) infections, contained high levels of RV2 rhadinovirus (9-790 genomes/cell) and expressed the CD3 T-cell marker. The third group (n = 3) was associated with SIV/SHIV infections, contained high levels of RV2 rhadinovirus (2-260 genomes/cell) and was negative for both CD20 and CD3. In both the CD3-positive and CD3/CD20-negative lymphomas, the neoplastic cells stained strongly for markers of RV2 lytic replication. None of the lymphomas had detectable levels of retroperitoneal fibromatosis herpesvirus (RFHV), the macaque RV1 homolog of KSHV. Our data suggest etiological roles for both lymphocryptoviruses and RV2 rhadinoviruses in the development of simian AIDS-associated lymphomas and indicate that the virus-infected neoplastic lymphoid cells are derived from different lymphocyte lineages and differentiation stages.
Insights
Macaque lymphomas are linked to lymphocryptoviruses and RV2 rhadinoviruses, similar to human AIDS-associated lymphomas. These viruses infect different cell types, suggesting varied roles in simian lymphoma development.
Area of Science:
- Virology
- Oncology
- Immunology
Background:
- Epstein-Barr virus (EBV) and Kaposi's sarcoma-associated herpesvirus (KSHV) are linked to AIDS-associated lymphomas in humans.
- Viral homologs of EBV and KSHV exist in non-human primates, including macaques.
- Understanding these viral associations in non-human primates can provide insights into human disease pathogenesis.
Purpose of the Study:
- To investigate the association of macaque lymphocryptovirus (LCV) and macaque rhadinoviruses (RV1 and RV2 lineages) with simian lymphomas.
- To determine viral loads and identify infected cell types in archived lymphoma samples.
- To explore the etiological roles of these viruses in the development of simian AIDS-associated lymphomas.
Main Methods:
- Screening of archived macaque lymphoma samples for macaque lymphocryptovirus (LCV) and macaque rhadinoviruses (RV1/RV2).
- Quantification of viral loads using quantitative PCR (QPCR).
- Identification of infected cells via immunolabeling for viral proteins and lymphocyte markers (CD20, CD3).
Main Results:
- Lymphomas segregated into three groups based on viral association and cell markers: LCV with B-cell markers (CD20), RV2 with T-cell markers (CD3), and RV2 with neither B nor T-cell markers.
- High viral loads of LCV and RV2 were detected in specific lymphoma groups.
- Evidence of viral latency (EBNA-2) in LCV-associated lymphomas and lytic replication markers in RV2-associated lymphomas were observed. No RFHV (RV1 homolog) was detected.
Conclusions:
- Both lymphocryptoviruses and RV2 rhadinoviruses play significant etiological roles in simian AIDS-associated lymphomas.
- The infected neoplastic lymphoid cells in these lymphomas originate from diverse lymphocyte lineages and differentiation stages.
- These findings highlight the importance of studying non-human primate models for understanding herpesvirus-driven oncogenesis.
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