Cargando…

Absence of human T-cell lymphotropic virus type I and human foamy virus in thymoma

The cause of thymoma, a rare malignancy of thymic epithelial cells, is unknown. Recent studies have reported the detection of DNA from human T-cell lymphotropic virus type I (HTLV-I) and human foamy virus (HFV) in small numbers of thymoma tumours, suggesting an aetiologic role for these retroviruses...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, H, Loehrer, P J, Hisada, M, Henley, J, Whitby, D, Engels, E A
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409482/
https://www.ncbi.nlm.nih.gov/pubmed/15150553
http://dx.doi.org/10.1038/sj.bjc.6601841
_version_ 1782155775644270592
author Li, H
Loehrer, P J
Hisada, M
Henley, J
Whitby, D
Engels, E A
author_facet Li, H
Loehrer, P J
Hisada, M
Henley, J
Whitby, D
Engels, E A
author_sort Li, H
collection PubMed
description The cause of thymoma, a rare malignancy of thymic epithelial cells, is unknown. Recent studies have reported the detection of DNA from human T-cell lymphotropic virus type I (HTLV-I) and human foamy virus (HFV) in small numbers of thymoma tumours, suggesting an aetiologic role for these retroviruses. In the present study, we evaluated 21 US thymoma patients and 20 patients with other cancers for evidence of infection with these viruses. We used the polymerase chain reaction to attempt to amplify viral DNA from tumour tissues, using primers from the pol and tax (HTLV-I) and gag and bel1 (HFV) regions. In these experiments, we did not detect HTLV-I or HFV DNA sequences in any thymoma or control tissues, despite adequate sensitivity of our assays (one HTLV-I copy per 25 000 cells, one HFV copy per 7500 cells). Additionally, none of 14 thymoma patients evaluated serologically for HTLV I/II infection was positive by enzyme-linked immunoassay (ELISA), while five (36%) had indeterminate Western blot reactivity. In comparison, one of 20 US blood donors was HTLV-I/II ELISA positive, and nine (45%) donors, including the ELISA-positive donor, had indeterminate Western blot reactivity. Western blot patterns varied across individuals and consisted mostly of weak reactivity. In conclusion, we did not find evidence for the presence of HTLV-I or HFV in US thymoma patients.
format Text
id pubmed-2409482
institution National Center for Biotechnology Information
language English
publishDate 2004
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-24094822009-09-10 Absence of human T-cell lymphotropic virus type I and human foamy virus in thymoma Li, H Loehrer, P J Hisada, M Henley, J Whitby, D Engels, E A Br J Cancer Molecular and Cellular Pathology The cause of thymoma, a rare malignancy of thymic epithelial cells, is unknown. Recent studies have reported the detection of DNA from human T-cell lymphotropic virus type I (HTLV-I) and human foamy virus (HFV) in small numbers of thymoma tumours, suggesting an aetiologic role for these retroviruses. In the present study, we evaluated 21 US thymoma patients and 20 patients with other cancers for evidence of infection with these viruses. We used the polymerase chain reaction to attempt to amplify viral DNA from tumour tissues, using primers from the pol and tax (HTLV-I) and gag and bel1 (HFV) regions. In these experiments, we did not detect HTLV-I or HFV DNA sequences in any thymoma or control tissues, despite adequate sensitivity of our assays (one HTLV-I copy per 25 000 cells, one HFV copy per 7500 cells). Additionally, none of 14 thymoma patients evaluated serologically for HTLV I/II infection was positive by enzyme-linked immunoassay (ELISA), while five (36%) had indeterminate Western blot reactivity. In comparison, one of 20 US blood donors was HTLV-I/II ELISA positive, and nine (45%) donors, including the ELISA-positive donor, had indeterminate Western blot reactivity. Western blot patterns varied across individuals and consisted mostly of weak reactivity. In conclusion, we did not find evidence for the presence of HTLV-I or HFV in US thymoma patients. Nature Publishing Group 2004-06-01 2004-05-04 /pmc/articles/PMC2409482/ /pubmed/15150553 http://dx.doi.org/10.1038/sj.bjc.6601841 Text en Copyright © 2004 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular and Cellular Pathology
Li, H
Loehrer, P J
Hisada, M
Henley, J
Whitby, D
Engels, E A
Absence of human T-cell lymphotropic virus type I and human foamy virus in thymoma
title Absence of human T-cell lymphotropic virus type I and human foamy virus in thymoma
title_full Absence of human T-cell lymphotropic virus type I and human foamy virus in thymoma
title_fullStr Absence of human T-cell lymphotropic virus type I and human foamy virus in thymoma
title_full_unstemmed Absence of human T-cell lymphotropic virus type I and human foamy virus in thymoma
title_short Absence of human T-cell lymphotropic virus type I and human foamy virus in thymoma
title_sort absence of human t-cell lymphotropic virus type i and human foamy virus in thymoma
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409482/
https://www.ncbi.nlm.nih.gov/pubmed/15150553
http://dx.doi.org/10.1038/sj.bjc.6601841
work_keys_str_mv AT lih absenceofhumantcelllymphotropicvirustypeiandhumanfoamyvirusinthymoma
AT loehrerpj absenceofhumantcelllymphotropicvirustypeiandhumanfoamyvirusinthymoma
AT hisadam absenceofhumantcelllymphotropicvirustypeiandhumanfoamyvirusinthymoma
AT henleyj absenceofhumantcelllymphotropicvirustypeiandhumanfoamyvirusinthymoma
AT whitbyd absenceofhumantcelllymphotropicvirustypeiandhumanfoamyvirusinthymoma
AT engelsea absenceofhumantcelllymphotropicvirustypeiandhumanfoamyvirusinthymoma