2013
DOI: 10.1038/jid.2012.371
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No Evidence for Viral Sequences in Mycosis Fungoides and Sézary Syndrome Skin Lesions: A High-Throughput Sequencing Approach

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Cited by 15 publications
(15 citation statements)
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References 14 publications
(15 reference statements)
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“…Because directly carcinogenic viruses actively express oncogenes in tumour cells, sequencing a tumour transcriptome to a sufficient depth should detect viral transcript if present. Together with other SS studies, we can conclude that the possibility of MF or SS being caused by a directly oncogenic virus is exceedingly low, but – owing to some limitations of DTS, such as failure to detect a novel virus lacking homology to known species – not zero. Additionally, viral sequences erroneously characterized as human, such as the endogenous retroviruses, which comprise ~ 10% of the human genome, could be falsely subtracted during DTS.…”
Section: Gene Expression Analysis Identifies Infectious Disease Pathwmentioning
confidence: 66%
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“…Because directly carcinogenic viruses actively express oncogenes in tumour cells, sequencing a tumour transcriptome to a sufficient depth should detect viral transcript if present. Together with other SS studies, we can conclude that the possibility of MF or SS being caused by a directly oncogenic virus is exceedingly low, but – owing to some limitations of DTS, such as failure to detect a novel virus lacking homology to known species – not zero. Additionally, viral sequences erroneously characterized as human, such as the endogenous retroviruses, which comprise ~ 10% of the human genome, could be falsely subtracted during DTS.…”
Section: Gene Expression Analysis Identifies Infectious Disease Pathwmentioning
confidence: 66%
“…Presently, none of the recent studies looking for evidence of HTLV‐1 in CTCL were able to identify this sequence . Because studies utilizing digital transcriptome subtraction techniques did not detect clonally integrated HTLV‐1 into the host genome, we can conclude with a high degree of certainty that HTLV‐1 is not a directly oncogenic virus in CTCL pathogenesis. However, it does not exclude a possibility that concurrent infection with HTLV‐1 could contribute to a chronic antigen stimulation model, which has long been proffered …”
Section: Gene Expression Analysis Identifies Infectious Disease Pathwmentioning
confidence: 80%
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“…Since MF, the most common form of CTCL, clinically resembles the smoldering form of adult T-cell lymphoma/leukemia, caused by human T-cell leukaemia/lymphoma virus I (HTLV-I) and since CTCL patients also have antibodies cross-reacting with HTLV-I and/or human immunodeficiency virus type 1 (HIV-1) core proteins [15,16] exogenous retroviruses were extensively sought for as an etiologic agent. However, neither replicating retroviruses nor any other viruses have been found in CTCL [17-22]. …”
Section: Introductionmentioning
confidence: 99%
“…High molecular weight DNA of the eight patients were then pooled for library construction and HTS was subcontracted to DNA Vision (Charleroi, Belgium) on a HiSeq 2000 instrument (Illumina Inc, San Diego, CA, U.S.A.), generating approximately 120 million reads. Sequences were trimmed and analysed as described previously: overlapping reads were assembled to obtain contiguous sequences (contigs). Nonoverlapping reads (singletons) were also kept for the analysis.…”
Section: Viral Contiguous Sequences (Contigs; Genomic Sequences Obtaimentioning
confidence: 99%