Assessing subtype and drug-resistance-associated mutations among antiretroviral-treated HIV-infected patients

被引:20
|
作者
Hamkar, Rasool [1 ]
Mohraz, Minoo [2 ]
Lorestani, Shima [3 ]
Aghakhani, Arezoo [4 ]
Truong, Hong-Ha M. [5 ]
McFarland, Willi [5 ]
Banifazl, Mohammad [6 ]
Eslamifar, Ali [4 ]
Foroughi, Maryam [2 ]
Pakfetrat, Atessa [7 ]
Ramezani, Amitis [4 ]
机构
[1] Univ Tehran Med Sci, Tehran, Iran
[2] Iranian Res Ctr HIV AIDS, Tehran, Iran
[3] Islamic AZAD Univ, Sch Sci, Qom, Iran
[4] Pasteur Inst Iran, Dept Clin Res, Tehran 13164, Iran
[5] Univ Calif San Francisco, San Francisco, CA 94143 USA
[6] Iranian Soc Support Patients Infect Dis, Tehran, Iran
[7] Mashhad Univ Med Sci, Sch Med, Mashhad, Iran
关键词
antiretroviral therapy; drug resistance; HIV; IMMUNODEFICIENCY-VIRUS TYPE-1; RIO-DE-JANEIRO; GENOTYPIC RESISTANCE; GENETIC DIVERSITY; PREVALENCE; THERAPY; IMPACT;
D O I
10.1097/01.aids.0000386738.32919.67
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Several studies have reported an increasing number of therapeutic failures with antiretroviral drugs in HIV-infected patients. The emergence of viral-resistant strains is a major problem for the medical management of infected individuals. The aim of this study is to determine viral subtypes and drug-resistance mutations among antiretroviral-treated HIV-infected patients. Methods: A total of 42 antiretroviral-treated but still viremic HIV-infected patients were enrolled. The HIV pol regions were amplified and sequenced to determine subtypes and antiretroviral-resistant mutations. Results: The subtype distribution was 48% A/D recombinants, 43% subtype B, 5% subtype A and 5% CRF01-AE recombinants. Drug-resistant mutations were most common in subtype B (53%) and A/D recombinant strains (44%). Virus samples from 19% of participants had no drug-resistant mutations; 2, 2 and 76% of samples carried one, two and at least three drug-resistant mutations, respectively. The prevalence of nucleoside transcriptase inhibitor mutations was 76%, with M184V and L74V present in 60 and 38% of samples, respectively. The prevalence of nonnucleoside transcriptase inhibitor mutations was 74%, with P225H present in 55% of study specimens. The prevalence of protease inhibitor mutations was 45%, with major mutation L90M seen in 33% and minor mutation A71V in 36% of samples. Of note, the P225H and A71V are 'minor' drug-resistance mutations conferring only minimal drug-resistance phenotypes in the absence of major mutations. Conclusion: Our study found a high prevalence of drug-resistant mutations in Iranian HIV-infected patients. Our data support the need for continued surveillance of resistance patterns to help guide therapeutic approaches and limit transmission of these variants. (C) 2010 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins
引用
收藏
页码:S85 / S91
页数:7
相关论文
共 50 条
  • [21] Low emergence of secondary antiretroviral drug resistance mutations among HIV-1 subtype C-infected Ethiopian patients
    Mulu, A.
    Maier, M.
    Liebert, U.
    JOURNAL OF THE INTERNATIONAL AIDS SOCIETY, 2012, 15 : 139 - 139
  • [22] Role of In Vitro Stimulation with Lipopolysaccharide on T-Cell Activation in HIV-Infected Antiretroviral-Treated Patients
    Tincati, Camilla
    Bellistri, Giusi M.
    Ancona, Giuseppe
    Merlini, Esther
    Monforte, Antonella d'Arminio
    Marchetti, Giulia
    CLINICAL & DEVELOPMENTAL IMMUNOLOGY, 2012,
  • [23] Subtype distribution and drug resistance mutations in naive HIV-infected people, Istanbul, Turkey
    Kuskucu, M. A.
    Tok, Y. Tuyji
    Erdem, H.
    Yucebag, E.
    Mete, B.
    Yildiz, D.
    Oncul, A.
    Zerdali, E.
    Karaosmanoglu, H. Kumbasar
    Aydin, O. Altuntas
    Gunduz, A.
    Koc, M. Meric
    Tabak, F.
    Midilli, K.
    HIV MEDICINE, 2021, 22 : 59 - 61
  • [24] Impact of Vaccination on Distribution of T Cell Subsets in Antiretroviral-Treated HIV-Infected Children
    Thitilertdecha, Premrutai
    Khowawisetsut, Ladawan
    Ammaranond, Palanee
    Poungpairoj, Poonsin
    Tantithavorn, Varangkana
    Onlamoon, Nattawat
    DISEASE MARKERS, 2017, 2017
  • [25] Longitudinal changes of bone mineral density and metabolism in antiretroviral-treated HIV-infected children
    Vigano, A
    Zamproni, I
    Beccio, S
    Bianchi, R
    Giacomet, V
    Mora, S
    ANTIVIRAL THERAPY, 2003, 8 (04) : L96 - L96
  • [26] Long-term body composition changes in antiretroviral-treated HIV-infected individuals
    Grant, Philip M.
    Kitch, Douglas
    McComsey, Grace A.
    Collier, Ann C.
    Bartali, Benedetta
    Koletar, Susan L.
    Erlandson, Kristine M.
    Lake, Jordan E.
    Yin, Michael T.
    Melbourne, Kathy
    Ha, Belinda
    Brown, Todd T.
    AIDS, 2016, 30 (18) : 2805 - 2813
  • [27] Long-term body composition changes in antiretroviral-treated HIV-infected individuals
    Grant, P. M.
    Kitch, D.
    McComsey, G.
    Collier, A.
    Bartali, B.
    Koletar, S. L.
    Erlandson, K.
    Lake, J. E.
    Yin, M.
    Melbourne, K.
    Ha, B.
    Brown, T. T.
    ANTIVIRAL THERAPY, 2015, 20 : A18 - A18
  • [28] HIV drug resistance among nave HIV-infected patients in Iran
    Farrokhi, Molood
    Gholami, Mohammad
    Mohraz, Minoo
    McFarland, Willi
    Baesi, Kazem
    Abbasian, Ladan
    JOURNAL OF RESEARCH IN MEDICAL SCIENCES, 2019, 24
  • [29] HIV Drug Resistance and Its Impact on Antiretroviral Therapy in Chinese HIV-Infected Patients
    Xing, Hui
    Ruan, Yuhua
    Li, Jingyun
    Shang, Hong
    Zhong, Ping
    Wang, Xia
    Liao, Lingjie
    Li, Hanping
    Zhang, Min
    Xue, Yile
    Wang, Zhe
    Su, Bin
    Liu, Wei
    Dong, Yonghui
    Ma, Yanling
    Li, Huiqin
    Qin, Guangming
    Chen, Lin
    Pan, Xiaohong
    Chen, Xi
    Peng, Guoping
    Fu, Jihua
    Chen, Ray Y.
    Kang, Laiyi
    Shao, Yiming
    PLOS ONE, 2013, 8 (02):
  • [30] Comparison of antiretroviral drug resistance among treatment-naive and treated HIV-infected individuals in Shiraz, Iran
    Mohammad Ali Davarpanah
    Nasrin Motazedian
    Hassan Joulaei
    Mohammad Reza Aghasadeghi
    Hossein Faramarzi
    Ehsan Aghah
    Archives of Virology, 2018, 163 : 99 - 104