Abstract
Alpha-lipoic acid, a naturally occurring disulfide-compound that acts as a cellular coenzyme, inhibits replication of HIV-1 in cultured lymphoid T-cells. Alpha-lipoic acid was added 16 hours after infection of the T-cell lines Jurkat, SupT1 and Molt-4 with HTLV IIIB and HIV-1 Wal (a wild type HIV-1 isolate). We observed a dose dependent inhibition of HIV-1-replication in CPE (Cytopathic effect) formation, reverse transcriptase activity and plaque formation on CD4-transformed HeLa-cells. An over 90% reduction of reverse transcriptase activity could be achieved with 70 micrograms alpha-lipoic acid/ml, a complete reduction of plaque-forming units at concentrations of greater than or equal to 35 micrograms alpha-lipoic acid/ml. An augmentation of the antiviral activity was seen by combination of zidovudine and low dose of alpha-lipoic acid (7 micrograms/ml). Trypan blue staining revealed no toxic effects of alpha-lipoic acids on peripheral blood mono-nuclear cells and T-cell lines even in concentrations of greater than or equal to 70 micrograms/ml. Therefore, we propose the inclusion of alpha-lipoic acid into chemotherapy trials in combination with zidovudine.
MeSH Terms
Cells, Cultured
Cytopathogenic Effect, Viral/drug effects
HIV/drug effects
HIV Reverse Transcriptase
HIV-1/drug effects
RNA-Directed DNA Polymerase/metabolism
T-Lymphocytes
Thioctic Acid/pharmacology
Viral Plaque Assay
Virus Replication/drug effects
Zidovudine/pharmacology
Chemicals
Zidovudine
Thioctic Acid
HIV Reverse Transcriptase
RNA-Directed DNA Polymerase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Baur A
Institut für Klinische und Molekulare Virologie der Universität Erlangen-Nürnberg.
Harrer T
Peukert M
Jahn G
Kalden J R
Fleckenstein B
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