Abstract
Even in the era of highly active antiretroviral therapy (HAART), gene therapy (GT) can remain a promising approach for suppressing HIV infection, especially if complemented with other forms of pharmacological and immunological intervention. A large number of vectors and targets have been studied. Here we discuss the potential of genetically treated, antigen-specific immunocompetent cells for adoptive autologous immunotherapy of HIV infection. Cellular therapies with gene-modified CD8 and CD4 lymphocytes are aimed at reconstituting the antigen-specific repertoires that may be deranged as a consequence of HIV infection. Even if complete eradication of HIV from the reservoirs cannot be achieved, reconstitution of cellular immunity specific for opportunistic pathogens and for HIV itself is a desirable option to control progression of HIV infection and AIDS pathogenesis better.
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Acknowledgements
This work was supported by grants to G Palù (National Health Institute, Rome, AIDS Project N.40B.72, Fondazione Cassa di Risparmio di Padova e Rovigo, MURST, CNR Target Project on Biotechnology), to C Parolin (National Health Institute, Rome, AIDS Project N.30C.57) and to F Manca (National Health Institute, Rome, AIDS Project N.40A.0.64 and Tuberculois Project 99/D/T; National Research Council, Rome – Biotechnology Project 1999; European Union Contracts – CA BHH4-CT9720, FAIR CT97-3046, QLRT-1999-31041, QLK2-1999-01040, QLK2-CT1999-01321). The authors thank M Guida for artwork.
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Palù, G., Pira, G., Gennari, F. et al. Genetically modified immunocompetent cells in HIV infection. Gene Ther 8, 1593–1600 (2001). https://doi.org/10.1038/sj.gt.3301569
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DOI: https://doi.org/10.1038/sj.gt.3301569


