Intensification of Antiretroviral Therapy with a CCR5 Antagonist in Patients with Chronic HIV-1 Infection: Effect on T Cells Latently Infected

被引:78
作者
Gutierrez, Carolina [1 ,2 ]
Diaz, Laura [3 ]
Vallejo, Alejandro [1 ,2 ]
Hernandez-Novoa, Beatriz [1 ,2 ]
Abad, Maria [1 ,2 ]
Madrid, Nadia [1 ,2 ]
Dahl, Viktor [4 ]
Rubio, Rafael [5 ]
Moreno, Ana M. [1 ,2 ]
Dronda, Fernando [1 ,2 ]
Luis Casado, Jose [1 ,2 ]
Navas, Enrique [1 ,2 ]
Jesus Perez-Elias, Maria [1 ,2 ]
Zamora, Javier [2 ,6 ]
Palmer, Sarah [4 ]
Munoz, Eduardo [7 ]
Angeles Munoz-Fernandez, Maria [3 ]
Moreno, Santiago [1 ,2 ]
机构
[1] Hosp Univ Ramon Y Cajal, Dept Infect Dis, Madrid, Spain
[2] IRYCIS, Madrid, Spain
[3] Hosp Gen Univ Gregorio Maranon, Inmunobiol Lab, Madrid, Spain
[4] Karolinska Inst, Stockholm, Sweden
[5] Hosp Gen Univ Doce Octubre, Infect Dis Unit, Madrid, Spain
[6] Hosp Univ Ramon Y Cajal, Dept Biostat, Madrid, Spain
[7] Univ Cordoba, Dept Immunol, Cordoba, Spain
来源
PLOS ONE | 2011年 / 6卷 / 12期
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; LOW-LEVEL VIREMIA; PLASMA VIREMIA; RALTEGRAVIR INTENSIFICATION; IMMUNE ACTIVATION; EXTENDED PERIODS; IN-VIVO; RESERVOIR; REPLICATION; COMBINATION;
D O I
10.1371/journal.pone.0027864
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
Objective: The primary objective was to assess the effect of MVC intensification on latently infected CD4(+) T cells in chronically HIV-1-infected patients receiving antiretroviral therapy. Methods: We performed an open-label pilot phase II clinical trial involving chronically HIV-1-infected patients receiving stable antiretroviral therapy whose regimen was intensified with 48 weeks of maraviroc therapy. We analyzed the latent reservoir, the residual viremia and episomal 2LTR DNA to examine the relationship between these measures and the HIV-1 latent reservoir, immune activation, lymphocyte subsets (including effector and central memory T cells), and markers associated with bacterial translocation. Results: Overall a non significant reduction in the size of the latent reservoir was found (p = 0.068). A mean reduction of 1.82 IUPM was observed in 4 patients with detectable latent reservoir at baseline after 48 weeks of intensification. No effect on plasma residual viremia was observed. Unexpectedly, all the patients had detectable 2LTR DNA circles at week 24, while none of them showed those circles at the end of the study. No changes were detected in CD4(+) or CD8(+) counts, although a significant decrease was found in the proportion of HLA-DR(+)/CD38(+) CD4(+) and CD8(+) T-cells. LPS and sCD14 levels increased. Conclusions: Intensification with MVC was associated with a trend to a decrease in the size of the latent HIV-1 reservoir in memory T cells. No impact on residual viremia was detected. Additional studies with larger samples are needed to confirm the results.
引用
收藏
页数:9
相关论文
共 51 条
[11]   Relationship Between Residual Plasma Viremia and the Size of HIV Proviral DNA Reservoirs in Infected Individuals Receiving Effective Antiretroviral Therapy [J].
Chun, Tae-Wook ;
Murray, Danielle ;
Justement, J. Shawn ;
Hallahan, Claire W. ;
Moir, Susan ;
Kovacs, Colin ;
Fauci, Anthony S. .
JOURNAL OF INFECTIOUS DISEASES, 2011, 204 (01) :135-138
[12]   Rebound of plasma viremia following cessation of antiretroviral therapy despite profoundly low levels of HIV reservoir: implications for eradication [J].
Chun, Tae-Wook ;
Justement, J. Shawn ;
Murray, Danielle ;
Hallahan, Claire W. ;
Maenza, Janine ;
Collier, Ann C. ;
Sheth, Prameet M. ;
Kaul, Rupert ;
Ostrowski, Mario ;
Moir, Susan ;
Kovacs, Colin ;
Fauci, Anthony S. .
AIDS, 2010, 24 (18) :2803-2808
[13]   HIV-infected individuals receiving effective antiviral therapy for extended periods of time continually replenish their viral reservoir [J].
Chun, TW ;
Nickle, DC ;
Justement, JS ;
Large, D ;
Semerjian, A ;
Curlin, ME ;
O'Shea, MA ;
Hallahan, CW ;
Daucher, M ;
Ward, DJ ;
Moir, S ;
Mullins, JI ;
Kovacs, C ;
Fauci, AS .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (11) :3250-3255
[14]   Presence of an inducible HIV-1 latent reservoir during highly active antiretroviral therapy [J].
Chun, TW ;
Stuyver, L ;
Mizell, SB ;
Ehler, LA ;
Mican, JAM ;
Baseler, M ;
Lloyd, AL ;
Nowak, MA ;
Fauci, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (24) :13193-13197
[15]   The integrin α4β7 forms a complex with cell-surface CD4 and defines a T-cell subset that is highly susceptible to infection by HIV-1 [J].
Cicala, Claudia ;
Martinelli, Elena ;
McNally, Jonathan P. ;
Goode, Diana J. ;
Gopaul, Ravindra ;
Hiatt, Joseph ;
Jelicic, Katija ;
Kottilil, Shyamasundaran ;
Macleod, Katilyn ;
O'Shea, Angeline ;
Patel, Nikita ;
Van Ryk, Donald ;
Wei, Danlan ;
Pascuccio, Massimiliano ;
Yi, Ling ;
McKinnon, Lyle ;
Izulla, Preson ;
Kimani, Joshua ;
Kaul, Rupert ;
Fauci, Anthony S. ;
Arthos, James .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (49) :20877-20882
[16]   Maraviroc versus Efavirenz, Both in Combination with Zidovudine-Lamivudine, for the Treatment of Antiretroviral-Naive Subjects with CCR5-Tropic HIV-1 Infection [J].
Cooper, David A. ;
Heera, Jayvant ;
Goodrich, James ;
Tawadrous, Margaret ;
Saag, Michael ;
DeJesus, Edwin ;
Clumeck, Nathan ;
Walmsley, Sharon ;
Ting, Naitee ;
Coakley, Eoin ;
Reeves, Jacqueline D. ;
Reyes-Teran, Gustavo ;
Westby, Mike ;
Van Der Ryst, Elna ;
Ive, Prudence ;
Mohapi, Lerato ;
Mingrone, Horacio ;
Horban, Andrzej ;
Hackman, Frances ;
Sullivan, John ;
Mayer, Howard .
JOURNAL OF INFECTIOUS DISEASES, 2010, 201 (06) :803-813
[17]   Treatment intensification does not reduce residual HIV-1 viremia in patients on highly active antiretroviral therapy [J].
Dinoso, J. B. ;
Kim, S. Y. ;
Wiegand, A. M. ;
Palmer, S. E. ;
Gange, S. J. ;
Cranmer, L. ;
O'Shea, A. ;
Callender, M. ;
Spivak, A. ;
Brennan, T. ;
Kearney, M. F. ;
Proschan, M. A. ;
Mican, J. M. ;
Rehm, C. A. ;
Coffin, J. M. ;
Mellors, J. W. ;
Siliciano, R. F. ;
Maldarelli, F. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (23) :9403-9408
[18]   Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity [J].
Dorr, P ;
Westby, M ;
Dobbs, S ;
Griffin, P ;
Irvine, B ;
Macartney, M ;
Mori, J ;
Rickett, G ;
Smith-Burchnell, C ;
Napier, C ;
Webster, R ;
Armour, D ;
Price, D ;
Stammen, B ;
Wood, A ;
Perros, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (11) :4721-4732
[19]   Effects of Maraviroc and Efavirenz on Markers of Immune Activation and Inflammation and Associations with CD4+ Cell Rises in HIV-Infected Patients [J].
Funderburg, Nicholas ;
Kalinowska, Magdalena ;
Eason, James ;
Goodrich, James ;
Heera, Jayvant ;
Mayer, Howard ;
Rajicic, Natasa ;
Valdez, Hernan ;
Lederman, Michael M. .
PLOS ONE, 2010, 5 (10)
[20]   No Evidence for Decay of the Latent Reservoir in HIV-1-Infected Patients Receiving Intensive Enfuvirtide-Containing Antiretroviral Therapy [J].
Gandhi, Rajesh T. ;
Bosch, Ronald J. ;
Aga, Evgenia ;
Albrecht, Mary ;
Demeter, Lisa M. ;
Dykes, Carrie ;
Bastow, Barbara ;
Para, Michael ;
Lai, Jun ;
Siliciano, Robert F. ;
Siliciano, Janet D. ;
Eron, Joseph J. .
JOURNAL OF INFECTIOUS DISEASES, 2010, 201 (02) :293-296