Recent advances in delivery systems for anti-HIV1 therapy
- 1 January 2007
- journal article
- review article
- Published by Taylor & Francis in Journal of Drug Targeting
- Vol. 15 (1), 21-36
- https://doi.org/10.1080/10611860600942178
Abstract
In the last years, different non-biological and biological carrier systems have been developed for anti-HIV1 therapy. Liposomes are excellent potential anti-HIV1 carriers that have been tested with drugs, antisense oligonucleotides, ribozymes and therapeutic genes. Nanoparticles and low-density lipoproteins (LDLs) are cell-specific transporters of drugs against macrophage-specific infections such as HIV1. Through a process of protein transduction, cell-permeable peptides of natural origin or designed artificially allow the delivery of drugs and genetic material inside the cell. Erythrocyte ghosts and bacterial ghosts are a promising delivery system for therapeutic peptides and HIV vaccines. Of interest are the advances made in the field of HIV gene therapy by the use of autologous haematopoietic stem cells and viral vectors for HIV vaccines. Although important milestones have been reached in the development of carrier systems for the treatment of HIV, especially in the field of gene therapy, further clinical trials are required so that the efficiency and safety of these new systems can be guaranteed in HIV patients.Keywords
This publication has 145 references indexed in Scilit:
- Protein transduction technology offers a novel therapeutic approach for diabetesJournal of Hepato-Biliary-Pancreatic Surgery, 2006
- Gene-Based Immunotherapy for Human Immunodeficiency Virus Infection and Acquired Immunodeficiency SyndromeHuman Gene Therapy, 2006
- Long-Term Inhibition of HIV-1 Infection in Primary Hematopoietic Cells by Lentiviral Vector Delivery of a Triple Combination of Anti-HIV shRNA, Anti-CCR5 Ribozyme, and a Nucleolar-Localizing TAR DecoyMolecular Therapy, 2005
- High‐Dose Recombinant Canarypox Vaccine Expressing HIV‐1 Protein, in Seronegative Human SubjectsThe Journal of Infectious Diseases, 2005
- Efficient lentiviral vector-mediated control of HIV-1 replication in CD4 lymphocytes from diverse HIV+ infected patients grouped according to CD4 count and viral loadMolecular Therapy, 2004
- Intracellular tracking of protamine/antisense oligonucleotide nanoparticles and their inhibitory effect on HIV-1 transactivationJournal of Controlled Release, 2004
- Attempts to use liposomes and RBC ghosts as vectors in drug and antisense therapy of virus infectionResearch in Virology, 1997
- Efficient Transfer of Synthetic Ribozymes into Cells Using Hemagglutinating Virus of Japan (HVJ)-Cationic LiposomesPublished by Elsevier ,1997
- Azidothymidine Homodinucleotide-Loaded Erythrocytes as Bioreactors for Slow Delivery of the Antiretroviral Drug AzidothymidineBiochemical and Biophysical Research Communications, 1996
- FIV infection of macrophages: in vitro and in vivo inhibition by dideoxycytidine 5′-triphosphateVeterinary Immunology and Immunopathology, 1995