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Published on: July 9, 2014
Primary gamma-herpesviral infection in Zambian children
Veenu Minhas1, Brad P Brayfield, Kay L Crabtree
1Nebraska Center for Virology and School of Biological Sciences, University of Nebraska-Lincoln, Lincoln, NE 68583 USA.
Insights
HHV-8 and Epstein-Barr virus (EBV) infections in Zambian children are largely asymptomatic and not correlated. HIV infection is a significant risk factor for both HHV-8 and EBV acquisition in early childhood.
Area of Science:
- Pediatric Infectious Diseases
- Viral Immunology
- Epidemiology
Background:
- Human herpesvirus 8 (HHV-8) and Epstein-Barr virus (EBV) are common childhood infections, but their early clinical presentations and co-infection patterns remain unclear.
- Zambia is an area endemic for HHV-8, making it a key location to study these viral infections in young children.
Purpose of the Study:
- To compare the natural history, clinical manifestations, and risk factors of HHV-8 and EBV infections in 12-month-old Zambian children.
- To investigate potential correlations between HHV-8 and EBV infections in early childhood.
Main Methods:
- A cohort of 677 Zambian infants aged 12 months were assessed for HHV-8 and EBV serostatus.
- Logistic regression analysis was used to identify associations between socio-economic status, clinical manifestations, and viral serostatus.
Main Results:
- EBV seroprevalence (58.9%) was significantly higher than HHV-8 (13.4%).
- HIV-1 infected children had a higher risk of HHV-8 infection (OR 3.69). Maternal HIV-1 infection increased EBV acquisition risk (OR 1.86) but not HHV-8.
- Rash was marginally associated with primary HHV-8 and EBV infection.
Conclusions:
- HHV-8 and EBV infections are not correlated in early childhood; infection with one does not increase susceptibility to the other.
- Primary HHV-8 and EBV infections in this population are often asymptomatic, presenting potentially as rash.
- Maternal and child HIV infection are significant risk factors for acquiring HHV-8 and EBV.
Background:
HHV-8 is closely related to Epstein-Barr virus (EBV), but the clinical presentations of these two infections in early childhood are not well understood. Also, it is not known whether infection by one virus correlates with another. Here, we compare the natural history of infection by these two viruses along with the clinical manifestations and risk factors that are associated with early childhood infection in Zambia, which is an endemic area for HHV-8.
Methods:
This study was conducted in a cohort of 12 month old Zambian children (N = 677). Data on socio-economic status and a wide range of clinical manifestations were collected. Logistic regression was used to test for significant associations between the collected variables and HHV-8 or EBV serostatus at 12 months of age.
Results:
We observed a significantly higher seroprevalence for EBV (58.9%) as compared to HHV-8 (13.4%). HIV-1 infected children had at a significantly higher risk of being infected with HHV-8 (Odds ratio [OR] 3.69, 95% confidence interval [CI] 1.64 - 8.32). HIV-1 infection of the mothers was a significant risk factor for increased acquisition of EBV but not HHV-8 by children (OR 1.86, 05% CI 1.20 - 2.87). Self reported rash was marginally associated with primary infection for HHV-8 and EBV.
Conclusions:
These results suggest that there is no correlation between EBV and HHV-8 infections. Infection by one does not increase the susceptibility for the second virus. Primary HHV-8 and EBV infection in early childhood may clinically present as rash but remains largely asymptomatic and may remain undetected in this population. HIV infection in the mother or child are important risk factors that contribute to EBV or HHV-8 infection.
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