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Increased seroreactivity to HERV-K10 peptides in patients with HTLV myelopathy
BACKGROUND: Previously, we had shown that persons infected with human T-cell lymphoma leukemia virus 1 or 2 (HTLV-1 or 2) had an increased prevalence of antibodies to a peptide in the Pol protein of the retrovirus HERV-K10, homologous to a peptide in HTLV gp21 envelope protein. The prevalence rate w...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878045/ https://www.ncbi.nlm.nih.gov/pubmed/24365054 http://dx.doi.org/10.1186/1743-422X-10-360 |
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author | Perzova, Raisa Graziano, Elliot Sanghi, Swathi Welch, Caitlin Benz, Patricia Abbott, Lynn Lalone, Danielle Glaser, Jordan Loughran, Thomas Sheremata, William Poiesz, Bernard J |
author_facet | Perzova, Raisa Graziano, Elliot Sanghi, Swathi Welch, Caitlin Benz, Patricia Abbott, Lynn Lalone, Danielle Glaser, Jordan Loughran, Thomas Sheremata, William Poiesz, Bernard J |
author_sort | Perzova, Raisa |
collection | PubMed |
description | BACKGROUND: Previously, we had shown that persons infected with human T-cell lymphoma leukemia virus 1 or 2 (HTLV-1 or 2) had an increased prevalence of antibodies to a peptide in the Pol protein of the retrovirus HERV-K10, homologous to a peptide in HTLV gp21 envelope protein. The prevalence rate was higher in those with myelopathy vs. non-myelopathy. We have now extended our observations to a cohort restricted to North America in whom the diagnosis of HTLV myelopathy was rigorously confirmed to also test for reactivity to another HERV-K10 peptide homologous to the HTLV p24 Gag protein. METHODS: Sera from 100 volunteer blood donors (VBD), 53 patients with large granular lymphocytic leukemia (LGLL), 74 subjects with HTLV-1 or 2 infection (58 non-myelopathy and 16 myelopathy) and 83 patients with multiple sclerosis (MS) were evaluated in ELISA assays using the above peptides. RESULTS: The HTLV myelopathy patients had a statistically significant increased prevalence of antibodies to both HERV-K10 peptides (87.5%) vs. the VBD (0%), LGLL patients (0%), MS patients (4.8%), and the HTLV positive non-myelopathy subjects (5.2%). CONCLUSION: The data suggest that immuno-cross-reactivity to HERV-K10 peptides and/or transactivation of HERV-K10 expression by the HTLV Tax protein may be involved in the pathogenesis of HTLV-associated myelopathy/tropical spastic paraparesis and spastic ataxia. |
format | Online Article Text |
id | pubmed-3878045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38780452014-01-03 Increased seroreactivity to HERV-K10 peptides in patients with HTLV myelopathy Perzova, Raisa Graziano, Elliot Sanghi, Swathi Welch, Caitlin Benz, Patricia Abbott, Lynn Lalone, Danielle Glaser, Jordan Loughran, Thomas Sheremata, William Poiesz, Bernard J Virol J Research BACKGROUND: Previously, we had shown that persons infected with human T-cell lymphoma leukemia virus 1 or 2 (HTLV-1 or 2) had an increased prevalence of antibodies to a peptide in the Pol protein of the retrovirus HERV-K10, homologous to a peptide in HTLV gp21 envelope protein. The prevalence rate was higher in those with myelopathy vs. non-myelopathy. We have now extended our observations to a cohort restricted to North America in whom the diagnosis of HTLV myelopathy was rigorously confirmed to also test for reactivity to another HERV-K10 peptide homologous to the HTLV p24 Gag protein. METHODS: Sera from 100 volunteer blood donors (VBD), 53 patients with large granular lymphocytic leukemia (LGLL), 74 subjects with HTLV-1 or 2 infection (58 non-myelopathy and 16 myelopathy) and 83 patients with multiple sclerosis (MS) were evaluated in ELISA assays using the above peptides. RESULTS: The HTLV myelopathy patients had a statistically significant increased prevalence of antibodies to both HERV-K10 peptides (87.5%) vs. the VBD (0%), LGLL patients (0%), MS patients (4.8%), and the HTLV positive non-myelopathy subjects (5.2%). CONCLUSION: The data suggest that immuno-cross-reactivity to HERV-K10 peptides and/or transactivation of HERV-K10 expression by the HTLV Tax protein may be involved in the pathogenesis of HTLV-associated myelopathy/tropical spastic paraparesis and spastic ataxia. BioMed Central 2013-12-23 /pmc/articles/PMC3878045/ /pubmed/24365054 http://dx.doi.org/10.1186/1743-422X-10-360 Text en Copyright © 2013 Perzova et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Perzova, Raisa Graziano, Elliot Sanghi, Swathi Welch, Caitlin Benz, Patricia Abbott, Lynn Lalone, Danielle Glaser, Jordan Loughran, Thomas Sheremata, William Poiesz, Bernard J Increased seroreactivity to HERV-K10 peptides in patients with HTLV myelopathy |
title | Increased seroreactivity to HERV-K10 peptides in patients with HTLV myelopathy |
title_full | Increased seroreactivity to HERV-K10 peptides in patients with HTLV myelopathy |
title_fullStr | Increased seroreactivity to HERV-K10 peptides in patients with HTLV myelopathy |
title_full_unstemmed | Increased seroreactivity to HERV-K10 peptides in patients with HTLV myelopathy |
title_short | Increased seroreactivity to HERV-K10 peptides in patients with HTLV myelopathy |
title_sort | increased seroreactivity to herv-k10 peptides in patients with htlv myelopathy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878045/ https://www.ncbi.nlm.nih.gov/pubmed/24365054 http://dx.doi.org/10.1186/1743-422X-10-360 |
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