Peptide-loaded dendritic-cell vaccination followed by treatment interruption for chronic HIV-1 infection: A phase 1 trial

Immune response enhanced by therapeutic HIV‐1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adj...

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Published inJournal of Medical Virology Vol. 78; no. 6; pp. 711 - 718
Main Authors Ide, Fuyuaki, Nakamura, Tetsuya, Tomizawa, Mariko, Kawana-Tachikawa, Ai, Odawara, Takashi, Hosoya, Noriaki, Iwamoto, Aikichi
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Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.06.2006
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Abstract Immune response enhanced by therapeutic HIV‐1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV‐1‐infected individuals. The safety and efficacy of DC‐based vaccine loaded with HIV‐1‐derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA‐A*2402 restriction were immunized to four HIV‐1‐infected individuals under HAART. In terms of safety, peptide‐loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN‐γ production in CD8+ lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non‐responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV‐1 infection. J. Med. Virol. 78:711–718, 2006. © 2006 Wiley‐Liss, Inc.
AbstractList Immune response enhanced by therapeutic HIV-1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV-1-infected individuals. The safety and efficacy of DC-based vaccine loaded with HIV-1-derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA-A*2402 restriction were immunized to four HIV-1-infected individuals under HAART. In terms of safety, peptide-loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN-gamma production in CD8(+) lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non-responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV-1 infection.Immune response enhanced by therapeutic HIV-1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV-1-infected individuals. The safety and efficacy of DC-based vaccine loaded with HIV-1-derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA-A*2402 restriction were immunized to four HIV-1-infected individuals under HAART. In terms of safety, peptide-loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN-gamma production in CD8(+) lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non-responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV-1 infection.
Immune response enhanced by therapeutic HIV-1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV-1-infected individuals. The safety and efficacy of DC-based vaccine loaded with HIV-1-derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA-A*2402 restriction were immunized to four HIV-1-infected individuals under HAART. In terms of safety, peptide-loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN-gamma production in CD8(+) lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non-responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV-1 infection.
Immune response enhanced by therapeutic HIV-1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV-1-infected individuals. The safety and efficacy of DC-based vaccine loaded with HIV-1-derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA-A*2402 restriction were immunized to four HIV-1-infected individuals under HAART. In terms of safety, peptide-loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN- production in CD8+ lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non-responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV-1 infection. J. Med. Virol. 78:711-718, 2006.
Immune response enhanced by therapeutic HIV‐1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV‐1‐infected individuals. The safety and efficacy of DC‐based vaccine loaded with HIV‐1‐derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA‐A*2402 restriction were immunized to four HIV‐1‐infected individuals under HAART. In terms of safety, peptide‐loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN‐γ production in CD8+ lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non‐responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV‐1 infection. J. Med. Virol. 78:711–718, 2006. © 2006 Wiley‐Liss, Inc.
Immune response enhanced by therapeutic HIV‐1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV‐1‐infected individuals. The safety and efficacy of DC‐based vaccine loaded with HIV‐1‐derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA‐A*2402 restriction were immunized to four HIV‐1‐infected individuals under HAART. In terms of safety, peptide‐loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN‐γ production in CD8 + lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non‐responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV‐1 infection. J. Med. Virol. 78:711–718, 2006. © 2006 Wiley‐Liss, Inc.
Author Tomizawa, Mariko
Iwamoto, Aikichi
Kawana-Tachikawa, Ai
Hosoya, Noriaki
Nakamura, Tetsuya
Odawara, Takashi
Ide, Fuyuaki
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  fullname: Iwamoto, Aikichi
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Issue 6
Keywords HIV-1
Immunopathology
Dendritic cell
Peptides
HIV-1 virus
Vaccination
Retroviridae
AIDS
Vaccine
Immune deficiency
Lentivirus
Infection
Virus
treatment interruption
Chronic
Treatment
Viral disease
Antiviral
Human immunodeficiency virus
HAART
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Kinloch-de Loes S, Hoen B, Smith DE, Autran B, Lampe FC, Phillips AN, Goh LE, Andersson J, Tsoukas C, Sonnerborg A, Tambussi G, Girard PM, Bloch M, Battegay M, Carter N, El Habib R, Theofan G, Cooper DA, Perrin L, QUEST Study Group. 2005. Impact of therapeutic immunization on HIV-1 viremia after discontinuation of antiretroviral therapy initiated during acute infection. J Infect Dis 192: 607-617.
Kuzushima K, Hayashi N, Kimura H, Tsurumi T. 2001. Efficient identification of HLA-A*2402-restricted cytomegalovirus-specific CD8+ T-cell epitopes by a computer algorithm and an enzyme-linked immunospot assay. Blood 98: 1872-1881.
Borrow P, Lewicki H, Hahn BH, Shaw GM, Oldstone MB. 1994. Virus-specific CD8 cytotoxic T-lymphocyte activity associated with control of viremia in primary human immunodeficiency virus type 1 infection. J Virol 68: 6103-6110.
Koup RA, Safrit JT, Cao Y, Andrews CA, McLeod G, Borkowsky W, Farthing C, Ho DD. 1994. Temporal association of cellular immune responses with the initial control of viremia in primary human immunodeficiency virus type 1 syndrome. J Virol 68: 4650-4655.
Lu W, Arraes LC, Ferreira WT, Andrieu JM. 2004. Therapeutic dendritic-cell vaccine for chronic HIV-1 infection. Nat Med 10: 1359-1365.
Bostrom AC, Hejdeman B, Matsuda R, Fredriksson M, Fredriksson EL, Bratt G, Sandstrom E, Wahren B. 2004. Long-term persistence of vaccination and HAART to human immunodeficiency virus (HIV). Vaccine 22: 1683-1691.
Metzner KJ, Bonhoeffer S, Fischer M, Karanicolas R, Allers K, Joos B, Weber R, Hirschel B, Kostrikis LG, Gunthard HF, The Swiss HIV Cohort Study. 2003. Emergence of minor populations of human immunodeficiency virus type 1 carrying the M184V and L90M mutations in subjects undergoing structured treatment interruptions. J Infect Dis 188: 1433-1443.
Ramratnam B, Mittler JE, Zhang L, Boden D, Hurley A, Fang F, Macken CA, Perelson AS, Markowitz M, Ho DD. 2000. The decay of the latent reservoir of replication-competent HIV-1 is inversely correlated with the extent of residual viral replication during prolonged anti-retroviral therapy. Nat Med 6: 82-85.
Dorrell L, Dong T, Ogg GS, Lister S, McAdam S, Rostron T, Conlon C, McMichael AJ, Rowland-Jones SL. 1999. Distinct recognition of non-clade B human immunodeficiency virus type 1 epitopes by cytotoxic T lymphocytes generated from donors infected in Africa. J Virol 73: 1708-1714.
Furutsuki T, Hosoya N, Kawana-Tachikawa A, Tomizawa M, Odawara T, Goto M, Kitamura Y, Nakamura T, Kelleher AD, Cooper DA, Iwamoto A. 2004. Frequent transmission of cytotoxic-T-lymphocyte escape mutants of human immunodeficiency virus type 1 in the highly HLA-A24-positive Japanese population. J Virol 78: 8437-8445.
Lisziewicz J, Trocio J, Xu J, Whitman L, Ryder A, Bakare N, Lewis MG, Wagner W, Pistorio A, Arya S, Lori F. 2005. Control of viral rebound through therapeutic immunization with DermaVir. AIDS 19: 35-43.
Oxenius A, Price DA, Gunthard HF, Dawson SJ, Fagard C, Perrin L, Fischer M, Weber R, Plana M, Garcia F, Hirschel B, McLean A, Phillips RE. 2002. Stimulation of HIV-specific cellular immunity by structured treatment interruption fails to enhance viral control in chronic HIV infection. Proc Natl Acad Sci USA 99: 13747-13752.
Ikeda-Moore Y, Tomiyama H, Miwa K, Oka S, Iwamoto A, Kaneko Y, Takiguchi M. 1997. Identification and characterization of multiple HLA-A24-restricted HIV-1 CTL epitopes: Strong epitopes are derived from V regions of HIV-1. J Immunol 159: 6242-6252.
Tanaka H, Akaza T, Juji T. 1996. Report of the Japanese Central Bone Marrow Data Center. Clin Transpl 139-144.
Kaufmann DE, Lichterfeld M, Altfeld M, Addo MM, Johnston MN, Lee PK, Wagner BS, Kalife ET, Strick D, Rosenberg ES, Walker BD. 2004. Limited durability of viral control following treated acute HIV infection. PLoS Med 1: e36.
Watanabe N, Tomizawa M, Tachikawa-Kawana A, Goto M, Ajisawa A, Nakamura T, Iwamoto A. 2001. Quantitative and qualitative abnormalities in HIV-1-specific T cells. AIDS 15: 711-715.
Kawamura T, Gatanaga H, Borris DL, Connors M, Mitsuya H, Blauvelt A. 2003. Decreased stimulation of CD4+ T cell proliferation and IL-2 production by highly enriched populations of HIV-infected dendritic cells. J Immunol 170: 4260-4266.
Tremblay CL, Hicks JL, Sutton L, Giguel F, Flynn T, Johnston M, Sax PE, Walker BD, Hirsch MS, Rosenberg ES, D'Aquila RT. 2003. Antiretroviral resistance associated with supervised treatment interruptions in treated acute HIV infection. AIDS 17: 1086-1089.
Garcia F, Lejeune M, Climent N, Gil C, Alcami J, Morente V, Alos L, Ruiz A, Setoain J, Fumero E, Castro P, Lopez A, Cruceta A, Piera C, Florence E, Pereira A, Libois A, Gonzalez N, Guila M, Caballero M, Lomena F, Joseph J, Miro JM, Pumarola T, Plana M, Gatell JM, Gallart T. 2005. Therapeutic immunization with dendritic cells loaded with heat-inactivated autologous HIV-1 in patients with chronic HIV-1 infection. J Infect Dis 191: 1680-1685.
Banchereau J, Palucka AK. 2005. Dendritic cells as therapeutic vaccines against cancer. Nat Rev Immunol 5: 296-306.
Schweighardt B, Ortiz GM, Grant RM, Wellons M, Miralles GD, Kostrikis LG, Bartlett JA, Nixon DF. 2002. Emergence of drug-resistant HIV-1 variants in patients undergoing structured treatment interruptions. AIDS 16: 2342-2344.
McMichael AJ, Rowland-Jones SL. 2001. Cellular immune responses to HIV. Nature 410: 980-987.
Fagard C, Oxenius A, Gunthard H, Garcia F, Le Braz M, Mestre G, Battegay M, Furrer H, Vernazza P, Bernasconi E, Telenti A, Weber R, Leduc D, Yerly S, Price D, Dawson SJ, Klimkait T, Perneger TV, McLean A, Clotet B, Gatell JM, Perrin L, Plana M, Phillips R, Hirschel B, Swiss HIV Cohort Study. 2003. A prospective trial of structured treatment interruptions in human immunodeficiency virus infection. Arch Intern Med 163: 1220-1226.
Siliciano JD, Kajdas J, Finzi D, Quinn TC, Chadwick K, Margolick JB, Kovacs C, Gange SJ, Siliciano RF. 2003. Long-term follow-up studies confirm the stability of the latent reservoir for HIV-1 in resting CD4+ T cells. Nat Med 9: 727-728.
Tubiana R, Carcelain G, Vray M, Gourlain K, Dalban C, Chermak A, Rabian C, Vittecoq D, Simon A, Bouvet E, El Habib R, Costagliola D, Calvez V, Autran B, Katlama C, the Vacciter Study group. 2005. Therapeutic immunization with a human immunodeficiency virus (HIV) type 1-recombinant canarypox vaccine in chronically HIV-infected patients: The Vacciter Study (ANRS 094). Vaccine 23: 4292-4301.
Wu L, Kong WP, Nabel GJ. 2005. Enhanced breadth of CD4 T-cell immunity by DNA prime and adenovirus boost immunization to human immunodeficiency virus Env and Gag immunogens. J Virol 79: 8024-8031.
Yu JS, Liu G, Ying H, Yong WH, Black KL, Wheeler CJ. 2004. Vaccination with tumor lysate-pulsed dendritic cells elicits antigen-specific, cytotoxic T-cells in patients with malignant glioma. Cancer Res 64: 4973-4979.
Harrer E, Bauerle M, Ferstl B, Chaplin P, Petzold B, Mateo L, Handley A, Tzatzaris M, Vollmar J, Bergmann S, Rittmaier M, Eismann K, Muller S, Kalden JR, Spriewald B, Willbold D, Harrer T. 2005. Therapeutic vaccination of HIV-1-infected patients on HAART with a recombinant HIV-1 nef-expressing MVA: Safety, immunogenicity and influence on viral load during treatment interruption. Antivir Ther 10: 285-300.
Ikeda-Moore Y, Tomiyama H, Ibe M, Oka S, Miwa K, Kaneko Y, Takiguchi M. 1998. Identification of a novel HLA-A24-restricted cytotoxic T-lymphocyte epitope derived from HIV-1 Gag protein. AIDS 12: 2073-2074.
Lange CG, Lederman MM, Medvik K, Asaad R, Wild M, Kalayjian R, Valdez H. 2003. Nadir CD4+ T-cell count and numbers of CD28+ CD4+ T-cells predict functional responses to immunizations in chronic HIV-1 infection. AIDS 17: 2015-2023.
Foung SK, Taidi B, Ness D, Grumet FC. 1986. A monoclonal antibody against HLA-A11 and A24. Hum Immunol 15: 316-319.
Hejdeman B, Leandersson AC, Fredriksson EL, Sandstrom E, Wahren B, Bratt G. 2003. Better preserved immune responses after immunization with rgp 160 in HIV-1 infected patients treated with highly active antiretroviral therapy than in untreated patients with similar CD4 levels during at 2 years' follow-up. HIV Med 4: 101-110.
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References_xml – reference: Yu JS, Liu G, Ying H, Yong WH, Black KL, Wheeler CJ. 2004. Vaccination with tumor lysate-pulsed dendritic cells elicits antigen-specific, cytotoxic T-cells in patients with malignant glioma. Cancer Res 64: 4973-4979.
– reference: Kinloch-de Loes S, Hoen B, Smith DE, Autran B, Lampe FC, Phillips AN, Goh LE, Andersson J, Tsoukas C, Sonnerborg A, Tambussi G, Girard PM, Bloch M, Battegay M, Carter N, El Habib R, Theofan G, Cooper DA, Perrin L, QUEST Study Group. 2005. Impact of therapeutic immunization on HIV-1 viremia after discontinuation of antiretroviral therapy initiated during acute infection. J Infect Dis 192: 607-617.
– reference: Wu L, Kong WP, Nabel GJ. 2005. Enhanced breadth of CD4 T-cell immunity by DNA prime and adenovirus boost immunization to human immunodeficiency virus Env and Gag immunogens. J Virol 79: 8024-8031.
– reference: Tanaka H, Akaza T, Juji T. 1996. Report of the Japanese Central Bone Marrow Data Center. Clin Transpl 139-144.
– reference: Hejdeman B, Leandersson AC, Fredriksson EL, Sandstrom E, Wahren B, Bratt G. 2003. Better preserved immune responses after immunization with rgp 160 in HIV-1 infected patients treated with highly active antiretroviral therapy than in untreated patients with similar CD4 levels during at 2 years' follow-up. HIV Med 4: 101-110.
– reference: Kawamura T, Gatanaga H, Borris DL, Connors M, Mitsuya H, Blauvelt A. 2003. Decreased stimulation of CD4+ T cell proliferation and IL-2 production by highly enriched populations of HIV-infected dendritic cells. J Immunol 170: 4260-4266.
– reference: Ikeda-Moore Y, Tomiyama H, Ibe M, Oka S, Miwa K, Kaneko Y, Takiguchi M. 1998. Identification of a novel HLA-A24-restricted cytotoxic T-lymphocyte epitope derived from HIV-1 Gag protein. AIDS 12: 2073-2074.
– reference: McMichael AJ, Rowland-Jones SL. 2001. Cellular immune responses to HIV. Nature 410: 980-987.
– reference: Oxenius A, Price DA, Gunthard HF, Dawson SJ, Fagard C, Perrin L, Fischer M, Weber R, Plana M, Garcia F, Hirschel B, McLean A, Phillips RE. 2002. Stimulation of HIV-specific cellular immunity by structured treatment interruption fails to enhance viral control in chronic HIV infection. Proc Natl Acad Sci USA 99: 13747-13752.
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– reference: Foung SK, Taidi B, Ness D, Grumet FC. 1986. A monoclonal antibody against HLA-A11 and A24. Hum Immunol 15: 316-319.
– reference: Tremblay CL, Hicks JL, Sutton L, Giguel F, Flynn T, Johnston M, Sax PE, Walker BD, Hirsch MS, Rosenberg ES, D'Aquila RT. 2003. Antiretroviral resistance associated with supervised treatment interruptions in treated acute HIV infection. AIDS 17: 1086-1089.
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Snippet Immune response enhanced by therapeutic HIV‐1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART)....
Immune response enhanced by therapeutic HIV-1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART)....
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SubjectTerms Adult
Antiretroviral Therapy, Highly Active
Biological and medical sciences
CD4 Lymphocyte Count
Chronic Disease
Chronic Disease - therapy
Dendritic Cells
Dendritic Cells - immunology
Dendritic Cells - metabolism
Dendritic Cells - transplantation
Drug Resistance, Viral
Drug Resistance, Viral - genetics
Epitopes, T-Lymphocyte
Epitopes, T-Lymphocyte - immunology
Fundamental and applied biological sciences. Psychology
HAART
HIV Antigens
HIV Antigens - administration & dosage
HIV Antigens - immunology
HIV Infections
HIV Infections - drug therapy
HIV Infections - immunology
HIV Infections - therapy
HIV-1
HIV-1 - drug effects
HIV-1 - genetics
HIV-1 - immunology
Human immunodeficiency virus 1
Human viral diseases
Humans
Immunotherapy
Immunotherapy - methods
Infectious diseases
Male
Medical sciences
Microbiology
Middle Aged
Miscellaneous
Mutation
T-Lymphocytes, Cytotoxic
T-Lymphocytes, Cytotoxic - immunology
treatment interruption
vaccine
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies
Viral diseases
Viral diseases of the lymphoid tissue and the blood. Aids
Viral Load
Virology
Title Peptide-loaded dendritic-cell vaccination followed by treatment interruption for chronic HIV-1 infection: A phase 1 trial
URI https://api.istex.fr/ark:/67375/WNG-G48GLR61-N/fulltext.pdf
https://cir.nii.ac.jp/crid/1871709542524873728
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjmv.20612
https://www.ncbi.nlm.nih.gov/pubmed/16628588
https://www.proquest.com/docview/20550923
https://www.proquest.com/docview/67901505
Volume 78
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