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Please use this identifier to cite or link to this item: http://hdl.handle.net/10390/888

Authors: Florence, E.
Lundgren, J.
Dreezen, C.
Fisher, M.
Kirk, O.
Blaxhult, A.
Panos, G.
Katlama, C.
Vella, S.
Phillips, A.
Corporate Authors: EuroSIDA Study Group
Title: Factors associated with a reduced CD4 lymphocyte count response to HAART despite full viral suppression in the EuroSIDA study
Journal Name: HIV Medicine
Issue Date: 2003
Volume: 4
Issue: 3
Pages: 255-262
Publisher ©: Blackwell Publishing
Place: Oxford
DOI: http://dx.doi.org/10.1111/j.1468-1293.2003.00156.x
Pubmed ID: http://www.ncbi.nlm.nih.gov/pubmed/12859325
Language: English
Type: ARTICLE
Keywords: Viral diseases
HIV
Viral load
CD4 lymphocyte count
Antiretrovirals
HAART
Immune reconstitution
Abstract: OBJECTIVES: To describe the prevalence and risk factors of poor CD4 count rise despite a good virological response on highly active antiretroviral treatment (HAART). METHODS: The patients from the EuroSIDA study who started HAART with a baseline CD4 count of <350 cells/microL and where all viral load (pVL) measures remained below 500 HIV-1 RNA copies/mL between 6 and 12 months after the start of HAART were included. The risk factors for poor CD4 count rise were analyzed by multiple regression. RESULTS: Seven hundred and eighty patients were included. A low CD4 count response was observed in 225 patients (29%). The risk factors for this condition were older age, lower CD4 count at baseline, higher increase from the nadir to baseline CD4 count and lower pVL at baseline. Patients taking > or =one drug from each of the three antiviral classes were more likely to have a good CD4 response but a minority of the study participants was taking this treatment regimen (3.1%) and the confidence interval was large. CONCLUSIONS: A poor immune reconstitution despite a good virological control is frequent after initiation of HAART among patients with a baseline CD4 count of <350 cells/microL. The underlying mechanisms leading to this condition seems mainly driven by the age and the baseline immunological and virological status of the patients.
Appears in Collections:Dept. Clinical Sciences - Articles

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