TY - JOUR
T1 - A therapeutic dendritic cell-based vaccine for HIV-1 infection
AU - García, Felipe
AU - Climent, Núria
AU - Assoumou, Lambert
AU - Gil, Cristina
AU - González, Nuria
AU - Alcamí, José
AU - León, Agathe
AU - Romeu, Joan
AU - Dalmau, Judith
AU - Martínez-Picado, Javier
AU - Lifson, Jeff
AU - Autran, Brigitte
AU - Costagliola, Dominique
AU - Clotet, Bonaventura
AU - Gatell, Josep M.
AU - Plana, Montserrat
AU - Gallart, Teresa
N1 - Funding Information:
This study was partially supported by grants: FIS PS09/01297, FIPSE 36750/08, SAF2008-04395, SAF 05/05566, FIPSE 36536/05, FIS 040503, FIS 070291, contract FIS 03/0072, Mutua Madrileña del Automóvil, STREP (UE) Life sciences, genomics and biotechnology for health LSH2005_2.3.0.10, PROFIT (FIT 090100-2005-9), MARATÓTV3, RIS**, ORVACS***.
Funding Information:
Dr Felipe García was recipient of a Research Grant from IDIBAPS****, Barcelona, Spain.
PY - 2011/2/15
Y1 - 2011/2/15
N2 - A double-blinded, controlled study of vaccination of untreated patients with chronic human immunodeficiency virus type 1 (HIV-1) infection with 3 doses of autologous monocyte-derived dendritic cells (MD-DCs) pulsed with heat inactivated autologous HIV-1 was performed. Therapeutic vaccinations were feasible, safe, and well tolerated. At week 24 after first vaccination (primary end point), a modest significant decrease in plasma viral load was observed in vaccine recipients, compared with control subjects (P = .03). In addition, the change in plasma viral load after vaccination tended to be inversely associated with the increase in HIV-specific T cell responses in vaccinated patients but tended to be directly correlated with HIV-specific T cell responses in control subjects. Clinical trial.gov NCT00402142.
AB - A double-blinded, controlled study of vaccination of untreated patients with chronic human immunodeficiency virus type 1 (HIV-1) infection with 3 doses of autologous monocyte-derived dendritic cells (MD-DCs) pulsed with heat inactivated autologous HIV-1 was performed. Therapeutic vaccinations were feasible, safe, and well tolerated. At week 24 after first vaccination (primary end point), a modest significant decrease in plasma viral load was observed in vaccine recipients, compared with control subjects (P = .03). In addition, the change in plasma viral load after vaccination tended to be inversely associated with the increase in HIV-specific T cell responses in vaccinated patients but tended to be directly correlated with HIV-specific T cell responses in control subjects. Clinical trial.gov NCT00402142.
UR - http://www.scopus.com/inward/record.url?scp=79751500441&partnerID=8YFLogxK
U2 - 10.1093/infdis/jiq077
DO - 10.1093/infdis/jiq077
M3 - Article
C2 - 21233310
AN - SCOPUS:79751500441
SN - 0022-1899
VL - 203
SP - 473
EP - 478
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 4
ER -