Cited by 54T-cell and Retrovirus StudiesHIV/AIDS drug development and treatmentHIV Research and Treatment

Integrase Inhibitors Effective against Human T-Cell Leukemia Virus Type 1

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Seegulam, Muhammad Esa, Ratner, Lee·2011·Antimicrobial Agents and Chemotherapy

Abstract

Drugs targeting the viral enzyme integrase have been in use for several years as part of the treatment regimen for patients with human immunodeficiency virus type 1 (HIV-1), and similar classes of compounds have been shown to inhibit human T-cell leukemia virus type 1 (HTLV-1) integration in vitro. The current study shows that the clinically approved HIV-1 integrase inhibitor, raltegravir, as well as the more recent diketo acid derivative, MK-2048, are active inhibitors of HTLV-1 infection in vitro. These agents were effective in inhibiting cell-free and cell-to-cell transmission of HTLV-1 in lymphoid and nonlymphoid cells. The drugs also inhibited HTLV-1 immortalization of human peripheral blood mononuclear cells. A novel adaptation of the Alu assay for viral integration was used to show that the drugs inhibit viral integration without affecting reverse transcription. These data support the administration of raltegravir and other integrase inhibitors as treatments for patients with HTLV-1-associated diseases.

Integrity signals

Registry

Crossref · 10.1128/aac.01413-10

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2 of 2 references verified0 citation errors · 0 not checkable

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  • Neither study observed significant changes in HTLV-1 PVL beyond the course of therapy.

    “Ultimately, neither study observed significant changes in HTLV-1 PVL beyond the course of therapy.”

    From Current State of Therapeutics for HTLV-1 (2024) · cites this paper as [188]

  • Studies have characterised Raltegravir's effects in treating HTLV-1, with reports of a transient reduction in PVL in patients and inhibition of transmission and immortalisation in isolated human PBMCs.

    “Studies have characterised its effects in treating HTLV-1, with reports of a transient reduction in PVL in patients [160] and inhibition of transmission and immortalisation in isolated human PBMCs [188].”

    From Current State of Therapeutics for HTLV-1 (2024) · cites this paper as [188]

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Authors
Seegulam, M. E., & Ratner, L.
Affiliations
Washington University in St. Louis (US)
Venue
Antimicrobial Agents and Chemotherapy
Published
2011-05
Volume
55
Issue
5
Pages
2011-2017
ISSN
  • 0066-4804 (ISSN-L)
  • 1098-6596
OpenAlex
W2096894434
Cited by
54
References
2
Citations by year
2024: 5 · 2023: 5 · 2022: 3 · 2021: 3 · 2020: 6 · 2019: 7 · 2018: 3 · 2016: 4 · 2015: 5 · 2014: 2 · 2013: 2 · 2012: 5
FWCI
1.84
Type
journal article
Language
en
Open access
Locations
  • Antimicrobial Agents and Chemotherapy (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Digital Commons@Becker (Washington University School of Medicine) (submittedVersion)
Funders
National Cancer Institute (CA 10073, R01CA063417, P50CA094056, CA-94056, CA 63417)
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
integrase inhibitors, HTLV-1, raltegravir, viral integration, cell-to-cell transmission, cell-free transmission, reverse transcription, antiviral therapy
MeSH terms
Raltegravir Potassium, Cell Line, Cells, Cultured, Enzyme-Linked Immunosorbent Assay, Humans, Pyrrolidinones, Human T-lymphotropic virus 1, Virus Integration, HIV Integrase Inhibitors

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