Objectives: To evaluate the frequency and progression over time of the WHO-defined transmitted HIV-1 drug resistance mutations (DRMs) among antiretroviral treatment (ART)-naive HIV-1-infected patients in Cameroon. Design: We analyzed HIV-1 DRM data generated from 369 ART-naive individuals consecutively recruited between 1996 and 2007 in urban and rural areas in Cameroon. Methods: HIV-1 drug resistance genotyping was performed in the pol gene using plasma samples and surveillance DRMs were identified using the 2009 WHO-DRM list. Results: We observed in Yaounde, the capital city, an increasing prevalence of DRMs over time: 0.0% (none of 61 participants) in 1996-1999; 1.9% (one of 53 participants) in 2001; 4.1% (two of 49 participants) in 2002; and 12.3% (10 of 81 participants) in 2007. In the rural areas with more recently implemented ART programs, we found DRMs in six of 125 (4.8%) ART-naive individuals recruited in 2006-2007. DRMs identified in both areas included resistance mutations to protease inhibitors, nucleoside reverse transcriptase inhibitors (NRTIs) and non-NRTIs (NNRTIs) that might impair the efficacy of available first-line and second-line treatments. Conclusion: This report showed an increase in transmitted DRMs in areas where antiretroviral drugs were introduced earlier, although other factors such as natural viral polymorphisms and acquired DRMs through exposure to antiretroviral cannot be totally excluded. Further surveillances are needed to confirm this evolution and inform public health policies on adequate actions to help limit the selection and transmission of drug-resistant HIV, while scaling up access to ART in developing countries. (C) 2011 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins
机构:
Fred Hutchinson Canc Res Ctr, Div Med Oncol Vaccine & Infect Dis Div, Div Global Oncol, Dept Med, 1124 Columbia St, Seattle, WA 98104 USANCI, Mol Pharmacol Sect, NIH, Bethesda, MD 20892 USA
Uldrick, Thomas S.
Yarchoan, Robert
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NCI, HIV AIDS Malignancy Branch, NIH, Bethesda, MD 20892 USANCI, Mol Pharmacol Sect, NIH, Bethesda, MD 20892 USA
机构:
Univ British Columbia, Sch Populat & Publ Hlth, Fac Med, British Columbia Ctr Excellence HIV AIDS, Vancouver, BC V5Z 1M9, CanadaUniv British Columbia, Sch Populat & Publ Hlth, Fac Med, British Columbia Ctr Excellence HIV AIDS, Vancouver, BC V5Z 1M9, Canada
Shannon, Kate
Kaida, Angela
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Univ British Columbia, Sch Populat & Publ Hlth, Fac Med, British Columbia Ctr Excellence HIV AIDS, Vancouver, BC V5Z 1M9, CanadaUniv British Columbia, Sch Populat & Publ Hlth, Fac Med, British Columbia Ctr Excellence HIV AIDS, Vancouver, BC V5Z 1M9, Canada
Kaida, Angela
Rachlis, Beth
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Univ British Columbia, Sch Populat & Publ Hlth, Fac Med, British Columbia Ctr Excellence HIV AIDS, Vancouver, BC V5Z 1M9, CanadaUniv British Columbia, Sch Populat & Publ Hlth, Fac Med, British Columbia Ctr Excellence HIV AIDS, Vancouver, BC V5Z 1M9, Canada
Rachlis, Beth
Lloyd-Smith, Elisa
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Univ British Columbia, Sch Populat & Publ Hlth, Fac Med, British Columbia Ctr Excellence HIV AIDS, Vancouver, BC V5Z 1M9, CanadaUniv British Columbia, Sch Populat & Publ Hlth, Fac Med, British Columbia Ctr Excellence HIV AIDS, Vancouver, BC V5Z 1M9, Canada
Lloyd-Smith, Elisa
Gray, Glenda
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Univ Witwatersrand, Perinatal HIV Res Unit, Soweto, South AfricaUniv British Columbia, Sch Populat & Publ Hlth, Fac Med, British Columbia Ctr Excellence HIV AIDS, Vancouver, BC V5Z 1M9, Canada
Gray, Glenda
Strathdee, Steffanie A.
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Univ Calif San Diego, Div Int Hlth & Cross Cultural Med, Sch Med, La Jolla, CA 92093 USAUniv British Columbia, Sch Populat & Publ Hlth, Fac Med, British Columbia Ctr Excellence HIV AIDS, Vancouver, BC V5Z 1M9, Canada