GBV-C Infection and Risk of NHL among U.S. Adults

Author:

Chang Cindy M.1,Stapleton Jack T.2,Klinzman Donna2,McLinden James H.2,Purdue Mark P.1,Katki Hormuzd A.1,Engels Eric A.1

Affiliation:

1. 1Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.

2. 2Department of Internal Medicine, Iowa City Veterans Affairs Medical Center, University of Iowa, Iowa City, Iowa.

Abstract

AbstractSome retrospective studies suggest an association between infection with GB virus-C (GBV-C) and non-Hodgkin lymphoma (NHL). We evaluated this association prospectively in a nested case–control study within the U.S. Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial. Cases (N = 658) and controls (N = 1,316) were individually matched by age, sex, race/ethnicity, timing of study entry, and sample selection. Prediagnostic PLCO serum samples were tested for GBV-C RNA (as a measure of active infection) and E2 antibody (active or resolved infection). Logistic regression was used to estimate odds ratios (OR) for the association between GBV-C and NHL overall and NHL subtypes. Twelve cases (1.8%) and seven controls (0.5%) were GBV-C RNA-positive. GBV-C RNA positivity was associated with NHL overall [OR, 3.43; 95% confidence interval (CI), 1.35–8.71] and, based on small numbers, diffuse large B-cell lymphoma (OR, 5.31; 95% CI, 1.54–18.36). The association with NHL persisted when the interval between testing and selection was greater than 4 years (OR, 6.00; 95% CI, 1.21–29.73). In contrast, E2 antibody positivity was not associated with NHL risk (OR, 1.08; 95% CI, 0.74–1.58). Our study demonstrates that GBV-C infection precedes development of NHL. GBV-C infection may play an etiologic role in a small proportion of NHL cases, perhaps by causing chronic immune stimulation or impaired immunosurveillance. Cancer Res; 74(19); 5553–60. ©2014 AACR.

Publisher

American Association for Cancer Research (AACR)

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