Cited by 19T-cell and Retrovirus StudiesHIV/AIDS drug development and treatmentHIV Research and Treatment

Protective effect of the acyclic nucleoside phosphonate tenofovir toward human T-cell leukemia/lymphotropic virus type 1 infection of human peripheral blood mononuclear cells in vitro

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Balestrieri, Emanuela, Sciortino, Maria Teresa, Mastino, Antonio, Macchi, Beatrice·2005·Antiviral Research

Abstract

9-(R)-[(2-Phosphonomethoxy)propyls]adenine (tenofovir), is an acyclic nucleoside phosphonate known to inhibit HIV replication in vitro and to reduce viremia in HIV-infected patients. Here we have investigated whether tenofovir is able to protect peripheral blood mononuclear cells (PBMCs) from healthy donors against human T-cell leukemia/lymphotropic virus type 1 (HTLV-1) infection in vitro. PBMCs were pre-treated with tenofovir and infected by exposure to an irradiated cell line chronically harbouring HTLV-1. Measurements of viral DNA, as well as viral gene and protein expression, at 4 weeks after infection, revealed that tenofovir at concentrations of 1 microM and higher completely protected PBMCs against HTLV-1; lower concentrations did not fully prevent HTLV-1 infection of the cultures. Nevertheless, in the long term, cell growth of infected PBMCs was inhibited in vitro even by 0.1 microM tenofovir. In addition, tenofovir directly inhibited HTLV-1 reverse transcriptase activity, in a cell-free assay that utilizes a crude preparation from HTLV-1 viral particles as a source of the enzyme. The selectivity index of tenofovir for HTLV-1, was about four times higher than that of azidothymidine. Taken together our results strongly encourage further studies to investigate the real impact of tenofovir towards HTLV-1 infection.

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Crossref · 10.1016/j.antiviral.2005.09.001

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  • Tenofovir demonstrated long-term inhibition of HTLV-1 infection in PBMCs at concentrations as low as 0.1 μM.

    “The acyclic nucleoside phosphonate tenofovir has also demonstrated long-term inhibition of HTLV-1 infection in PBMCs in concentrations as low as 0.1 µM [180].”

    From Current State of Therapeutics for HTLV-1 (2024) · cites this paper as [180]

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Authors
Balestrieri, E., Sciortino, M. T., Mastino, A., & Macchi, B.
Affiliations
  • University of Rome Tor Vergata (IT)
  • University of Messina (IT)
Corresponding author
Macchi, Beatrice
Venue
Antiviral Research
Publisher
Elsevier BV
Published
2005-12
Volume
68
Issue
3
Pages
154-162
ISSN
0166-3542 (ISSN-L)
OpenAlex
W2116626387
Cited by
19
References
0
Citations by year
2025: 2 · 2024: 2 · 2022: 1 · 2020: 2 · 2018: 3 · 2017: 1 · 2013: 3
FWCI
0.36
Type
journal article
Language
en
Open access
Locations
  • Antiviral Research (publishedVersion)
  • PubMed (publishedVersion)
  • Cineca Institutional Research Information System (Tor Vergata University) (submittedVersion, cc-by)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and Retrovirus Studies
  • Health Sciences › Medicine › Infectious Diseases › HIV/AIDS drug development and treatment
  • Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
Keywords
tenofovir, HTLV-1, acyclic nucleoside phosphonates, antiviral defense, peripheral blood mononuclear cells, reverse transcriptase inhibition, viral DNA replication, selectivity index, zidovudine
MeSH terms
Tenofovir, Adenine, DNA, Viral, Humans, Leukocytes, Mononuclear, Human T-lymphotropic virus 1, Leukemia, T-Cell, Anti-HIV Agents, Organophosphonates

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