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

被引:12
作者
Touloumi, Giota [1 ]
Pantazis, Nikos [1 ]
Chaix, Marie-Laure [2 ]
Bucher, Heiner C. [3 ]
Zangerle, Robert [4 ]
Kran, Anne-Marte Bakken [5 ]
Thiebaut, Rodolphe [6 ]
Masquelier, Bernard [7 ]
Kucherer, Claudia [8 ]
Monforte, Antonella d'Arminio [9 ]
Meyer, Laurence [10 ]
Porter, Kholoud [11 ]
机构
[1] Univ Athens, Sch Med, GR-11527 Athens, Greece
[2] Univ Paris 05, CHU Necker Enfants Malad, AP HP, Lab Virol,EA 3620, Paris, France
[3] Basel Inst Clin Epidemiol & Biostat, Basel, Switzerland
[4] Univ Innsbruck Hosp, A-6020 Innsbruck, Austria
[5] Oslo Univ Hosp Ulleval, Dept Microbiol, Oslo, Norway
[6] Univ Bordeaux, INSERM, ISPED, Ctr INSERM Epidemiol Biostat U897, Bordeaux, France
[7] Hosp Pellegrin, Bordeaux, France
[8] Robert Koch Inst, Berlin, Germany
[9] Univ Milan, Inst Infect Dis, San Paolo Hosp, Milan, Italy
[10] Univ Paris 11, INSERM, AP HP, U1018, Paris, France
[11] MRC Clin Trials Unit, London, England
关键词
NON-B SUBTYPES; ACTIVE ANTIRETROVIRAL THERAPY; DISEASE PROGRESSION; DRUG-RESISTANCE; TYPE-1; SUBTYPE; IMPACT; INDIVIDUALS; DIVERSITY; EPIDEMIOLOGY; INFECTION;
D O I
10.1371/journal.pone.0071174
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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