BACKGROUND: We aimed to compare rates of virologic response and CD4 changes after combination antiretroviral (cART) initiation in individuals infected with B and specific non-B HIV subtypes. METHODS: Using CASCADE data we analyzed HIV-RNA and CD4 counts for persons infected ≥1996, ≥15 years of age. We used survival and longitudinal modeling to estimate probabilities of virologic response (confirmed HIV-RNA <500 c/ml), and failure (HIV-RNA>500 c/ml at 6 months or ≥1000 c/ml following response) and CD4 increase after cART initiation. RESULTS: 2003 (1706 B, 142 CRF02_AG, 55 A, 53 C, 47 CRF01_AE) seroconverters were included in analysis. There was no evidence of subtype effect overall for response or failure (p = 0.075 and 0.317, respectively) although there was a suggestion that those infected with subtypes CRF01_AE and A responded sooner than those with subtype B infection [HR (95% CI):1.37 (1.01-1.86) and 1.29 (0.96-1.72), respectively]. Rates of CD4 increase were similar in all subtypes except subtype A, which tended to have lower initial, but faster long-term, increases. CONCLUSIONS: Virologic and immunologic response to cART was similar across all studied subtypes but statistical power was limited by the rarity of some non-B subtypes. Current antiretroviral agents seem to have similar efficacy in subtype B and most widely encountered non-B infections in high-income countries.

Virologic and Immunologic Response to cART by HIV-1 Subtype in the CASCADE Collaboration / G. Touloumi, N. Pantazis, M.L. Chaix, H.C. Bucher, R. Zangerle, A.M. Kran, R. Thiebaut, B. Masquelier, C. Kucherer, A. D’Arminio Monforte, L. Meyer, K. Porter, for CASCADE Collaboration in EuroCoord. - In: PLOS ONE. - ISSN 1932-6203. - 8:7(2013 Jul 30), pp. e71174.1-e71174.8. [10.1371/journal.pone.0071174]

Virologic and Immunologic Response to cART by HIV-1 Subtype in the CASCADE Collaboration

A. D’Arminio Monforte;
2013

Abstract

BACKGROUND: We aimed to compare rates of virologic response and CD4 changes after combination antiretroviral (cART) initiation in individuals infected with B and specific non-B HIV subtypes. METHODS: Using CASCADE data we analyzed HIV-RNA and CD4 counts for persons infected ≥1996, ≥15 years of age. We used survival and longitudinal modeling to estimate probabilities of virologic response (confirmed HIV-RNA <500 c/ml), and failure (HIV-RNA>500 c/ml at 6 months or ≥1000 c/ml following response) and CD4 increase after cART initiation. RESULTS: 2003 (1706 B, 142 CRF02_AG, 55 A, 53 C, 47 CRF01_AE) seroconverters were included in analysis. There was no evidence of subtype effect overall for response or failure (p = 0.075 and 0.317, respectively) although there was a suggestion that those infected with subtypes CRF01_AE and A responded sooner than those with subtype B infection [HR (95% CI):1.37 (1.01-1.86) and 1.29 (0.96-1.72), respectively]. Rates of CD4 increase were similar in all subtypes except subtype A, which tended to have lower initial, but faster long-term, increases. CONCLUSIONS: Virologic and immunologic response to cART was similar across all studied subtypes but statistical power was limited by the rarity of some non-B subtypes. Current antiretroviral agents seem to have similar efficacy in subtype B and most widely encountered non-B infections in high-income countries.
African ; article ; Caucasian ; CD4 lymphocyte count ; controlled study ; drug efficacy ; drug response ; drug treatment failure ; ethnic group ; female ; human ; Human immunodeficiency virus 1 infection ; immune response ; major clinical study ; male ; population research; seroconversion ; treatment duration ; viremia
Settore MED/17 - Malattie Infettive
30-lug-2013
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/224780
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