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Reconstitution of Herpes Simplex Virus–Specific T Cell Immunity in HIV‐Infected Patients Receiving Highly Active Antiretroviral Therapy

2007; Oxford University Press; Volume: 195; Issue: 3 Linguagem: Inglês

10.1086/510623

1537-6613

Meghna Ramaswamy, Anele Waters, Colette Smith, Emma Hainsworth, Gareth Hardy, Margaret Johnson, Jonathan Ainsworth, Andrew Phillips, Anna María Geretti,

HIV Research and Treatment

Production of herpes simplex virus (HSV)-specific interferon-γ by peripheral-blood mononuclear cells (PBMCs) of HSV-seropositive healthy donors and human immunodeficiency virus-infected persons was determined by use of ELISPOT. The mean ± SD number of spot-forming cells/106 PBMCs was 314 ± 74 in 11 healthy donors, 360 ± 69 in 3 long-term nonprogressors (LTNPs), 186 ± 52 in 9 newly diagnosed patients, and 181 ± 59 in 33 patients who were receiving highly active antiretroviral therapy (HAART) for a median period of 30 months (range, 1–109 months). In 9 patients monitored prospectively while receiving virologi-cally and immunologically successful first-line HAART, the number of spot-forming cells increased by 5.6/month (95% confidence interval, 1.2–9.9 [P=.01]) and 21.3/100 CD4 cells/mm3 gained (95% confidence interval, 13.8–28.7 [P<.0001]). Responses were correlated with LTNP status and CD4 cell count.