Cited by 117T-cell and Retrovirus StudiesHIV Research and TreatmentInfectious Diseases and Tuberculosis

The DOI matches its Crossref record; 33 of the 35 references it cites were found in a registry or an index.

Zidovudine plus lamivudine in Human T-Lymphotropic Virus type-I-associated myelopathy: a randomised trial

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Abstract

BACKGROUND: No therapies have been proven to persistently improve the outcome of HTLV-I-associated myelopathy. Clinical benefit has been reported with zidovudine and with lamivudine in observational studies. We therefore conducted a randomised, double blind, placebo controlled study of six months combination therapy with these nucleoside analogues in sixteen patients. RESULTS: Primary outcomes were change in HTLV-I proviral load in PBMCs and clinical measures. Secondary endpoints were changes in T-cell subsets and markers of activation and proliferation. Six patients discontinued zidovudine. No significant changes in pain, bladder function, disability score, gait, proviral load or markers of T-cell activation or proliferation were seen between the two arms. Active therapy was associated with an unexplained decrease in CD8 and non-T lymphocyte counts. CONCLUSION: Failure to detect clinical improvement may have been due irreversible nerve damage in these patients with a long clinical history and future studies should target patients presenting earlier. The lack of virological effect but may reflect a lack of activity of these nucleoside analogues against HTLV-I RT in vivo, inadequate intracellular concentrations of the active moiety or the contribution of new cell infection to maintaining proviral load at this stage of infection may be relatively small masking the effects of RT inhibition.

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Crossref · 10.1186/1742-4690-3-63

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Figure 1 Changes in timed 13 meter walk observed during the study period.
Figure 1 Changes in timed 13 meter walk observed during the study period.CC BY · PubMed Central

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Metadata

Authors
Taylor, G. P., Goon, P., Furukawa, Y., Green, H., Barfield, A., Mosley, A., Nose, H., Babiker, A., Rudge, P., Usuku, K., Osame, M., Bangham, C. R., & Weber, J. N.
Affiliations
  • Imperial College London (GB)
  • Kagoshima University (JP)
  • Medical Research Council (GB)
  • National Hospital for Neurology and Neurosurgery (GB)
Corresponding author
Taylor, Graham P
Venue
Retrovirology
Published
2006-09-19
Volume
3
Issue
1
Pages
63-63
ISSN
1742-4690 (ISSN-L)
OpenAlex
W2154664865
Cited by
117
References
35
Citations by year
2026: 2 · 2025: 4 · 2024: 4 · 2023: 4 · 2022: 1 · 2021: 2 · 2020: 8 · 2019: 8 · 2018: 6 · 2017: 5 · 2016: 9 · 2015: 11 · 2014: 8 · 2013: 10 · 2012: 6
FWCI
2.15
Type
journal article
Language
en
Open access
Locations
  • Retrovirology (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • UCL Discovery (University College London) (submittedVersion)
  • Spiral (Imperial College London) (submittedVersion, cc-by)
Funders
  • GlaxoSmithKline
  • Medical Research Council
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and Retrovirus Studies
  • Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
  • Health Sciences › Medicine › Infectious Diseases › Infectious Diseases and Tuberculosis
Keywords
tropical spastic paraparesis, zidovudine, lamivudine, nucleoside reverse transcriptase inhibitors, highly active antiretroviral therapy, T cell activation, CD8+ T cell depletion, treatment discontinuation, nerve injury
MeSH terms
Aged, Double-Blind Method, Drug Therapy, Combination, Female, Humans, Male, Middle Aged, Placebos, Zidovudine, Paraparesis, Tropical Spastic, Lamivudine, Anti-HIV Agents, Viral Load, Cell Proliferation

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