Abstract

Epstein-Barr virus (EBV) is transmitted by saliva and is a major cause of cancer, particularly in people living with HIV/AIDS. Here, we describe the frequency and quantity of EBV detection in the saliva of Ugandan adults with and without HIV-1 infection and use these data to develop a novel mathematical model of EBV infection in the tonsils. Eligible cohort participants were not taking antiviral medications, and those with HIV-1 infection had a CD4 count >200 cells/mm3. Over a 4-week period, participants provided daily oral swabs that we analysed for the presence and quantity of EBV. Compared with HIV-1 uninfected participants, HIV-1 coinfected participants had an increased risk of EBV detection in their saliva (IRR = 1.27, 95% CI = 1.10-1.47) and higher viral loads in positive samples. We used these data to develop a stochastic, mechanistic mathematical model that describes the dynamics of EBV, infected cells, and immune response within the tonsillar epithelium to analyse potential factors that may cause EBV infection to be more severe in HIV-1 coinfected participants. The model, fit using Approximate Bayesian Computation, showed high fidelity to daily oral shedding data and matched key summary statistics. When evaluating how model parameters differed among participants with and without HIV-1 coinfection, results suggest HIV-1 coinfected individuals have higher rates of B cell reactivation, which can seed new infection in the tonsils and lower rates of an EBV-specific immune response. Subsequently, both these traits may explain higher and more frequent EBV detection in the saliva of HIV-1 coinfected individuals.

Highlights

  • Epstein-Barr virus (EBV) infection is associated with the development of approximately 200,000 malignancies per year worldwide, including B cell lymphomas and nasopharyngeal carcinoma [1]

  • Epstein-Barr virus (EBV) is a ubiquitous infection worldwide associated with the development of several kinds of cancer, including B cell lymphoma and nasopharyngeal carcinoma

  • HIV-1 infection is associated with increased B cell activation as well as immunodeficiency resulting from loss of T cells; whether these factors contribute to higher rates of EBV replication during coinfection, and by how much, has remained unknown

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Summary

Introduction

Epstein-Barr virus (EBV) infection is associated with the development of approximately 200,000 malignancies per year worldwide, including B cell lymphomas and nasopharyngeal carcinoma [1]. EBV is thought first to infect oral epithelial cells overlying the lymphoid tissue known as Waldeyer’s ring [9]. B cells latently infected with EBV can return to Waldeyer’s ring, encounter cognate antigen, and become activated to mature into plasma cells, triggering lytic reactivation and production of infectious virions [13,14,15]. This process initiates a new round of epithelial infection in the tonsils and viral shedding in the saliva

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