| Literature DB >> 21679735 |
Cristina Gil1, Núria Climent, Felipe García, Carmen Hurtado, Sara Nieto-Márquez, Agathe León, M Teresa García, Cristina Rovira, Laia Miralles, Judith Dalmau, Tomás Pumarola, Manel Almela, Javier Martinez-Picado, Jeffrey D Lifson, Laura Zamora, José M Miró, Christian Brander, Bonaventura Clotet, Teresa Gallart, José M Gatell.
Abstract
This study provides a detailed description and characterization of the preparation of individualized lots of autologous heat inactivated HIV-1 virions used as immunogen in a clinical trial designed to test an autologous dendritic-cell-based therapeutic HIV-1 vaccine (Clinical Trial DCV-2, NCT00402142). For each participant, ex vivo isolation and expansion of primary virus were performed by co-culturing CD4-enriched PBMCs from the HIV-1-infected patient with PBMC from HIV-seronegative unrelated healthy volunteer donors. The viral supernatants were heat-inactivated and concentrated to obtain 1 mL of autologous immunogen, which was used to load autologous dendritic cells of each patient. High sequence homology was found between the inactivated virus immunogen and the HIV-1 circulating in plasma at the time of HIV-1 isolation. Immunogens contained up to 10⁹ HIV-1 RNA copies/mL showed considerably reduced infectivity after heat inactivation (median of 5.6 log₁₀), and were free of specified adventitious agents. The production of individualized lots of immunogen based on autologous inactivated HIV-1 virus fulfilling clinical-grade good manufacturing practice proved to be feasible, consistent with predetermined specifications, and safe for use in a clinical trial designed to test autologous dendritic cell-based therapeutic HIV-1 vaccine.Entities:
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Year: 2011 PMID: 21679735 DOI: 10.1016/j.vaccine.2011.05.096
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641