4.5 Article

The PEDVAC trial: Preliminary data from the first therapeutic DNA vaccination in HIV-infected children

Journal

VACCINE
Volume 29, Issue 39, Pages 6810-6816

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2010.12.058

Keywords

HIV; Children; Therapeutic vaccine; Multigene HIV DNA vaccine

Funding

  1. European Union
  2. Ministry of Health, Rome [FIRB RBNEOI-RB9B.003, FIRB RBIP064CRT-006]
  3. Italian Health Institute, Rome [AIDS 40G.33, 45G.17, 50G.25]
  4. CIPE (Rome)
  5. Regione Liguria, Genoa
  6. EU [LSHP-CT-2005-018680]
  7. EVA Centre for AIDS Reagents, NIBSC, UK [ARP631 Rec HIV-1 RT, ARP694 HIV p17/24 B Clade, ARP695 HIV-1 p17/24 C Clade, ARP698 HIV-1 UG37 gp140, ARP699 CN54 gp140]
  8. EC
  9. Bill and Melinda Gates GHRC
  10. GLAXO, Wellcome [ARP631]
  11. FIT BIOTECH Oyj Plc Eesti Filiaal, TARTU, ESTONIA [ARP694, ARP695]
  12. Polymun, Vienna, Austria [ARP698, ARP699]
  13. Immunogenetics Inc. [EVA620]

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The PEDVAC study is the first trial designed to analyze safety and immunogenicity of a therapeutic vaccination with a multiclade multigene HIV DNA vaccine (HIVIS) in infected children. Twenty HIV-1 vertically infected children (6-16 years of age), on stable antiretroviral treatment for at least 6 months with HIV-1 RNA < 50 copies/ml and stable CD4 counts (>400 cells/mm(3) or 25%) over 12 months of follow-up, were recruited into the study. Enrolled patients have been randomized into two arms: a control group of 10 children who continued previous antiretroviral treatment (HAART) (arm A) and a group of 10 children immunized intramuscularly with the HIVIS DNA vaccine in addition to previous HAART (arm B). Immunizations took place at week 0, 4, 12 and the boosting dose is planned at week 36. The 10 children in the vaccine group have received the first 3 priming doses of the HIVIS vaccine. Safety data showed good tolerance to the vaccination schedule. Mild cutaneous self-limeted reactions consisted of local irritation, usually itching or erythema +/- swelling at the injection site, were reported. No severe systemic adverse events have been observed. No vaccinated children had a decrease of CD4 T-cell counts from baseline. None experienced virological failure. Analysis of cellular immune responses was scheduled at week 0, 4, 12, 16, 20, 40, 60, 72 and 96 by standard lymphoproliferation assay, intracellular cytokine staining and cell-ELISA, a miniaturized assay to measure antigen-induced IFN gamma secretion. Evaluation of these results is in progress and will provide key information on the status and changes of antigen specific immunity during HIV DNA immunization. (C) 2010 Elsevier Ltd. All rights reserved.

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