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Tipranavir resistance associated mutations in protease inhibitor-naive patients with HIV-1 subtype A/E infection
被引:6
|作者:
Sungkanuparph, Somnuek
[1
]
Sukasem, Chonlaphat
[2
]
Manosuthi, Weerawat
[1
,3
]
Wiboonchutikul, Surasak
[1
]
Piyavong, Bucha
[1
]
Chantratita, Wasun
[2
]
机构:
[1] Mahidol Univ, Fac Med, Ramathibodi Hosp, Dept Med, Bangkok 10400, Thailand
[2] Mahidol Univ, Fac Med, Ramathibodi Hosp, Dept Pathol, Bangkok 10400, Thailand
[3] Minist Publ Hlth, Bamrasnaradura Infect Dis Inst, Nonthaburi 11000, Thailand
关键词:
HIV;
Tipranavir;
Resistance;
Mutations;
Subtype A/E;
CRF01;
AE;
D O I:
10.1016/j.jcv.2008.07.002
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Background: Tipranavir-resistance associated mutations (TPV-RAMs) are often observed among patients with HIV-1 Subtype A/E infection. Data regarding TPV resistance in subtype A/E is still limited. Objectives: To determine the prevalence of TPV-RAMs among protease inhibitor-naive, HIV-1 subtype A/E infected patients. Study design: Genotypic resistance testing was conducted among HIV-1-infected patients who were Pl-naive. Results: We studied 112 patients (mean age, 40.7 years; 58% male). Median CD4 cell count and HIV-1 RNA were 192 cells/mm(3) and 4.2 log copies/mL, respectively. Ninety-three patients (83%) infected with subtype A/E; the others had subtype B.The most common TPV-RAMs were M361(88%), H69K (61%), and 113V(48%). Median number of TPV-RAMs was 3 mutations. Patients with subtype A/E had higher prevalence of 113V (54% vs. 21%, P=0.011), M361(96% vs. 53%, P<0.001), H69K (68% vs. 26%, P=0.001), and >2 TPV-RAMs (62% vs. 21%, P=0.002). In multivariate analysis, only subtype A/E was associated with the occurrence of >2 TPV-RAMs (OR 9.83: 95%Cl, 1.95-39.57: P=0.006). Conclusions: TPV-RAMs previously described by IAS-USA are commonly observed in Pl-naive patients with HIV-1 subtype A/E infection. Further studies to define virologic response of subtype A/E to TPV and clinical validation of TPV-RAMs in HIV-1 subtype A/E are essentially needed. (C) 2008 Elsevier B.V. All rights reserved.
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页码:284 / 286
页数:3
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