A humanized mouse model for HIV-2 infection and efficacy testing of a single-pill triple-drug combination anti-retroviral therapy

被引:13
作者
Hu, Shuang [1 ]
Neff, Charles Preston [1 ,2 ]
Kumar, Dipu Mohan [1 ]
Habu, Yuichiro [1 ]
Akkina, Sarah R. [1 ,3 ]
Seki, Takahiro [1 ,4 ]
Akkina, Ramesh [1 ]
机构
[1] Colorado State Univ, Dept Microbiol Immunol & Pathol, Ft Collins, CO 80523 USA
[2] Univ Colorado Anschutz Med Campus, Dept Med, Aurora, CO 80045 USA
[3] Univ Washington, Dept Otolaryngol Head & Neck Surg, Seattle, WA 98195 USA
[4] Shionogi & Co Ltd, Drug Discovery & Dis Res Lab, Osaka 5610825, Japan
关键词
Animal model for HIV-2 infection and therapy; HIV-2 therapeutic testing in humanized mice; Single-pill triple-drug therapy fot HIV-2; Triple-drug Triumeq therapy for HIV; Combinatorial ART for HIV; Humanized mice for HIV research; IMMUNODEFICIENCY-VIRUS TYPE-2; REVERSE-TRANSCRIPTASE; HU MOUSE; RESISTANCE; INHIBITORS; MICE;
D O I
10.1016/j.virol.2016.11.013
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
While HIV-2 is a causative agent for AIDS in addition to the better studied HIV-1, there is currently no suitable animal model for experimental studies for HIV-2 infection and evaluating promising drugs in vivo. Here we evaluated humanized mice for their susceptibility to HIV-2 infection and tested a single-pill three drug formulation of anti-retrovirals (NRTIs abacavir and lamivudine, integrase inhibitor dolutegravir) (trade name, Triumeq(R)). Our results showed that hu-mice are susceptible to HIV-2 infection showing persistent viremia and CD4 T cell loss, key hallmarks of AIDS pathogenesis. Oral drug treatment led to full viral suppression and protection from CD4 T cell depletion. Cessation of therapy resulted in viral rebound and CD4 T cell loss. These proof-of-concept studies establish the utility of hu-mice for evaluating HIV-2 pathogenesis in more detail in the future, testing novel therapies and providing pre-clinical efficacy data of a three drug combination to treat HIV-2 infections.
引用
收藏
页码:115 / 118
页数:4
相关论文
共 27 条
  • [1] New generation humanized mice for virus research: Comparative aspects and future prospects
    Akkina, Ramesh
    [J]. VIROLOGY, 2013, 435 (01) : 14 - 28
  • [2] AKKINA RK, 1994, BLOOD, V84, P1393
  • [3] HIV-1 Antiretroviral Drug Therapy
    Arts, Eric J.
    Hazuda, Daria J.
    [J]. COLD SPRING HARBOR PERSPECTIVES IN MEDICINE, 2012, 2 (04):
  • [4] Mucosal transmission of R5 and X4 tropic HIV-1 via vaginal and rectal routes in humanized Rag-/- γc-/- (RAG-hu) mice
    Berges, Bradford K.
    Akkina, Sarah R.
    Folkvord, Joy M.
    Connick, Elizabeth
    Akkina, Ramesh
    [J]. VIROLOGY, 2008, 373 (02) : 342 - 351
  • [5] HIV-1 infection and CD4 T cell depletion in the humanized Rag2-/-γc-/- (RAG-hu) mouse model
    Berges, Bradford K.
    Wheat, William H.
    Palmer, Brent E.
    Connick, Elizabeth
    Akkina, Ramesh
    [J]. RETROVIROLOGY, 2006, 3 (1)
  • [6] Humanized Rag2-/-γc-/- (RAG-hu) mice can sustain long-term chronic HIV-1 infection lasting more than a year
    Berges, Bradford K.
    Akkina, Sarah R.
    Remling, Leila
    Akkina, Ramesh
    [J]. VIROLOGY, 2010, 397 (01) : 100 - 103
  • [7] HIV-1 and HIV-2 Reverse Transcriptases: Different Mechanisms of Resistance to Nucleoside Reverse Transcriptase Inhibitors
    Boyer, Paul L.
    Clark, Patrick K.
    Hughes, Stephen H.
    [J]. JOURNAL OF VIROLOGY, 2012, 86 (10) : 5885 - 5894
  • [8] Buggert M., 2016, AIDS
  • [9] Update on Human Immunodeficiency Virus (HIV)-2 Infection
    Campbell-Yesufu, Omobolaji T.
    Gandhi, Rajesh T.
    [J]. CLINICAL INFECTIOUS DISEASES, 2011, 52 (06) : 780 - 787
  • [10] HIV-2 Integrase Polymorphisms and Longitudinal Genotypic Analysis of HIV-2 Infected Patients Failing a Raltegravir-Containing Regimen
    Cavaco-Silva, Joana
    Abecasis, Ana
    Miranda, Ana Claudia
    Pocas, Jose
    Narciso, Jorge
    Aguas, Maria Joao
    Maltez, Fernando
    Almeida, Isabel
    Germano, Isabel
    Diniz, Antonio
    de Fatima Goncalves, Maria
    Gomes, Perpetua
    Cunha, Celso
    Camacho, Ricardo Jorge
    [J]. PLOS ONE, 2014, 9 (03):