GB virus C (GBV-C) is a common human infection that, until recently, was not thought to be associated with any disease. Due to the perceived lack of pathogenicity, blood products are not screened for GBV-C, even though ~2% of U.S. blood donors are viremic at the time of donation. A recent large, Canadian, population-based case- control study found an association between GBV-C and non-Hodgkin lymphoma (NHL; odds ratio of 2.72 [95% CI 1.22-6.69]). Unfortunately, due to an imbalance in sample availability, the cases were not well matched with the controls. Nevertheless, previous studies, and several lines of evidence support biological plausibility for a relationship between GBV-C and NHL, the 6th most common cancer in the US. Specifically, GBV-C infection causes persistent infection of humans, replicates in B and T lymphocytes, prolongs survival of lymphocytes and is associated with delayed apoptosis in vivo and in vitro. Specifically, two viral proteins (nonstructural protein 5A and envelope glycoprotein E2) inhibit Fas-mediated apoptosis in lymphocyte cell lines. In addition, hepatitis C virus is an accepted risk for NHL, and GBV-C is closely related to HCV, sharing considerable amino acid homology (up to 80%) in several conserved nonstructural, replication-related proteins.
In Specific Aim 1, we will determine whether GBV-C viremia is associated with the risk of developing NHL by using an existing clinic-based case-control study of 2500 cases and 2500 controls from the upper Midwestern US.
In Aim 2 we will assess the relationship of past GBV-C infection (antibody positivity) on risk of NHL and prognosis, and in Aim 3 we will determine if GBV-C is associated with event-free and overall survival in NHL. As a secondary analysis, the association of GBV-C with NHL subtypes (diffuse large B cell lymphoma, other B-cell lymphomas, follicular lymphoma, or T cell lymphomas) will be examined, although power to assess subtype-specific associations was limited. This study fills a critical need to determine in an independent, rigorously-designed, and well-powered case-control study from North America whether GBV-C virus is associated with NHL risk and prognosis. Screening blood donors for GBV-C would be costly and require deferral of approximately 2% of donors. However, if GBV-C is associated with NHL, reconsideration of current blood donor screening testing would be necessary to protect the blood supply. By using an established case-control study cohort, for which the samples will be available at the start of this grant, and by working with leaders in GBV-C and lymphoma epidemiology and clinical research, the study has a high probability of success. The laboratory that will perform the GBV-C diagnostic testing developed the state-of-the-art approaches to be utilized, and has extensive published experience related to GBV-C research. The evaluation of a role for this virus in NHL prognosis is novel and innovative. Regardless of the results obtained, this study has the potential to have a great impact on public health regarding transfusion medicine, and potentially in the clinical management of NHL patients.

Public Health Relevance

GB virus C, a common viral infection of humans, is present in ~ 2% of healthy blood donors, and each day in the U.S. there are an estimated 300,000 units of GBV-C contaminated blood products transfused. A recent study suggests that GBV-C may be a risk of developing non-Hodgkins lymphoma. In this Clinical Science Merit Review application we propose a large, case-control study to determine if GBV-C is related to NHL, and if so, this will be important for transfusion medicine.

Agency
National Institute of Health (NIH)
Institute
Veterans Affairs (VA)
Type
Non-HHS Research Projects (I01)
Project #
5I01CX000821-04
Application #
8958794
Study Section
Epidemiology (EPID)
Project Start
2012-10-01
Project End
2016-09-30
Budget Start
2015-10-01
Budget End
2016-09-30
Support Year
4
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Iowa City VA Medical Center
Department
Type
DUNS #
028084333
City
Iowa City
State
IA
Country
United States
Zip Code
52246
Fama, Angelo; Xiang, Jinhua; Link, Brian K et al. (2018) Human Pegivirus infection and lymphoma risk and prognosis: a North American study. Br J Haematol 182:644-653
Simmonds, Peter; Becher, Paul; Bukh, Jens et al. (2017) ICTV Virus Taxonomy Profile: Flaviviridae. J Gen Virol 98:2-3
Bhattarai, Nirjal; McLinden, James H; Xiang, Jinhua et al. (2017) Hepatitis C virus infection inhibits a Src-kinase regulatory phosphatase and reduces T cell activation in vivo. PLoS Pathog 13:e1006232
McLinden, James H; Bhattarai, Nirjal; Stapleton, Jack T et al. (2017) Yellow Fever Virus, but Not Zika Virus or Dengue Virus, Inhibits T-Cell Receptor-Mediated T-Cell Function by an RNA-Based Mechanism. J Infect Dis 216:1164-1175
Dogan, Meeshanthini V; Xiang, Jinhua; Beach, Steven R H et al. (2015) Ethnicity and Smoking-Associated DNA Methylation Changes at HIV Co-Receptor GPR15. Front Psychiatry 6:132
Chivero, Ernest T; Bhattarai, Nirjal; McLinden, James H et al. (2015) Human Pegivirus (HPgV; formerly known as GBV-C) inhibits IL-12 dependent natural killer cell function. Virology 485:116-27
Chivero, Ernest T; Stapleton, Jack T (2015) Tropism of human pegivirus (formerly known as GB virus C/hepatitis G virus) and host immunomodulation: insights into a highly successful viral infection. J Gen Virol 96:1521-32
Lanteri, Marion C; Vahidnia, Farnaz; Tan, Sylvia et al. (2015) Downregulation of Cytokines and Chemokines by GB Virus C After Transmission Via Blood Transfusion in HIV-Positive Blood Recipients. J Infect Dis 211:1585-96
Stapleton, Jack T; Xiang, Jinhua; McLinden, James H et al. (2014) A novel T cell evasion mechanism in persistent RNA virus infection. Trans Am Clin Climatol Assoc 125:14-24; discussion 24-6
Chang, Cindy M; Stapleton, Jack T; Klinzman, Donna et al. (2014) GBV-C infection and risk of NHL among U.S. adults. Cancer Res 74:5553-60

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