Dual Activity of Phosphorothioate CpG Oligodeoxynucleotides on HIV
Autor: | Eleni Koutsilieri, Anett Ullrich, Stefan Lamla, Ulf Dittmer, Carsten Scheller, Axel Rethwilm |
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Rok vydání: | 2006 |
Předmět: |
CpG Oligodeoxynucleotide
General Neuroscience T cell TLR9 hemic and immune systems respiratory system Biology Virology Molecular biology General Biochemistry Genetics and Molecular Biology Virus medicine.anatomical_structure Immune system History and Philosophy of Science CpG site Viral replication Complementary DNA medicine |
Zdroj: | Annals of the New York Academy of Sciences. 1091:540-547 |
ISSN: | 1749-6632 0077-8923 |
DOI: | 10.1196/annals.1378.095 |
Popis: | CpG oligodeoxynucleotides (CpG ODNs) bind to toll-like receptor-9 (TLR-9) and activate immune cells with antigen-presenting activity, including B cells and dendritic cells. Here we show that treatment of the latently human immunodeficiency virus (HIV)-infected T cell line ACH-2 with the CpG ODNs 2006 or 2040 triggers activation of viral gene expression, demonstrating that CpG-signaling activity can also be found in T cells. The CpG ODNs g12AAC and g12GTC had no effect on virus reactivation. In contrast to the stimulating effects on viral gene expression in latently infected cells, CpG ODNs potently suppressed HIV replication in productively infected MT4 T cells or PBLs. Inhibition of virus replication was not related to the CpG motif but similarly occurred with non-CpG phosphorothioate (PTO)-ODNs. Thus, virus inhibition was likely caused by the PTO backbone of the CpG ODNs, probably by interfering with events prior to integration of the viral cDNA into the host genome. The ability of CpG PTO-ODNs to trigger reactivation of latent HIV in combination with their antiviral activity on productive infection makes this substance class an interesting candidate for further test to asses their potential as supplements in HIV therapy. |
Databáze: | OpenAIRE |
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