AI Article Synopsis

  • The study examined the presence of Epstein-Barr virus (EBV) DNA in the cerebrospinal fluid (CSF) of 470 adults living with HIV in Zambia who showed neurological symptoms, finding that 28.9% tested positive for EBV DNA.
  • Key associations with EBV positivity included younger age, shorter HIV duration, and specific CSF findings like low glucose and high protein and white blood cell levels.
  • Despite the high EBV detection rate, the study concluded that EBV DNA load in CSF and blood had limited clinical significance and was not linked to patient mortality.

Article Abstract

The significance of Epstein-Barr virus (EBV) detection in the cerebrospinal spinal fluid (CSF) in people living with HIV (PLWH) is not entirely understood. The detection of EBV DNA may represent active central nervous system (CNS) infection, reactivation in the setting of another CNS pathogen or due to impaired immunity, or detection of quiescent virus. We screened 470 adult PLWH in Zambia with neurological symptoms for the presence of EBV DNA in the CSF. We performed quantitative EBV PCR on the CSF and blood. We then performed quantitative EBV DNA PCR on the blood of controls with documented HIV viral suppression without CNS symptoms. The prevalence of EBV DNA in the CSF of patients with CNS symptoms was 28.9% (136/470). EBV DNA positivity was associated with younger age, shorter duration of HIV diagnosis, lower CSF glucose levels, higher CSF protein and white blood cell levels, and a positive CSF Mycobacterium tuberculosis result. The median EBV DNA load was 8000 cps/mL in both the CSF and blood with a range of 2000-2,753,000 cps/mL in the CSF and 1000 to 1,871,000 cps/mL in the blood. Molecular screening of CSF for other possible causes of infection identified Mycobacterium tuberculosis in 30.1% and cytomegalovirus (CMV) in 10.5% of samples. EBV DNA load in the blood and CSF was not associated with mortality. Our results suggest that even though EBV DNA was commonly detected in the CSF of our population, it appears to have limited clinical significance regardless of EBV DNA load.

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Source
http://dx.doi.org/10.1007/s13365-023-01178-4DOI Listing

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