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Epstein-Barr virus and human immunodeficiency virus serological responses and viral burdens in HIV-infected patients treated with HAART

✍ Scribed by Cathal E. O'Sullivan; RongSheng Peng; Kelly Stefano Cole; Ronald C. Montelaro; Timothy Sturgeon; Hal B. Jenson; Paul D. Ling


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
122 KB
Volume
67
Category
Article
ISSN
0146-6615

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✦ Synopsis


Abstract

Epstein‐Barr virus (EBV) associated non‐Hodgkin lymphoma is recognized as a complication of human immunodeficiency virus (HIV) infection. Little is known regarding the influence of highly active antiretroviral therapy (HAART) on the biology of EBV in this population. To characterize the EBV‐ and HIV‐specific serological responses together with EBV DNA levels in a cohort of HIV‐infected adults treated with HAART, a study was conducted to compare EBV and HIV serologies and EBV DNA copy number (DNAemia) over a 12‐month period after the commencement of HAART. All patients were seropositive for EBV at baseline. Approximately 50% of patients had detectable EBV DNA at baseline, and 27/30 had detectable EBV DNA at some point over the follow‐up period of 1 year. Changes in EBV DNA copy number over time for any individual were unpredictable. Significant increases in the levels of Epstein‐Barr nuclear antigen (EBNA) and Epstein‐Barr early antigen (EA) antibodies were demonstrated in the 17 patients who had a good response to HAART. Of 29 patients with paired samples tested, four‐fold or greater increases in titers were detected for EA in 12/29 (41%), for EBNA in 7/29 (24%), for VCA‐IgG in 4/29 (14%); four‐fold decreases in titers were detected in 2/29 (7%) for EA and 12/29 (41%) for EBNA. A significant decline in the titer of anti‐HIV antibodies was also demonstrated. It was concluded that patients with advanced HIV infection who respond to HAART have an increase in their EBV specific antibodies and a decrease in their HIV‐specific antibodies. For the cohort overall, there was a transient increase in EBV DNA levels that had declined by 12 months. J. Med Virol. 67:320–326, 2002. © 2002 Wiley‐Liss, Inc.


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