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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1992-10-13
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pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S44624,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S44625,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S72766,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S72767,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S72768,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S72769,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S72771,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X63096,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X63097,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X63098
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pubmed:abstractText |
The human T-cell lymphotropic virus type I (HTLV-I) is causally associated with adult T-cell leukemia, but its role in mycosis fungoides (MF) has remained enigmatic. The virus is suspect because a small percentage of patients with MF have antibodies to it, the cells of others harbor deleted HTLV-I proviral sequences, and particles resembling HTLV-I emerge in cultured blood lymphocytes obtained from most patients. An alternative possibility is that disparate lymphotropic retroviruses may infect or affect a population of epidermotropic lymphocytes, leading to the same outcome, ie, MF. In studies designed to identify the particles detected in lymphocyte cultures of nine patients with a diagnosis of skin involvement characteristic of MF, this concept has gained support. While the cells of four patients provided evidence of HTLV-I infection, molecular hybridization with HTLV-II-specific pol probes showed HTLV-II in the cells of another patient. The 103-bp fragment amplified by the HTLV-II-specific probe was sequenced and proved to have greater than 90% homology with the same fragment amplified from cells known to be infected with HTLV-II. A role for HTLV-II in MF has not been suggested heretofore. Therefore, HTLV-I, HTLV-II, and their incomplete forms may be found in cells of MF patients, suggesting new theories regarding the pathogenesis of this disease.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
0006-4971
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
15
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pubmed:volume |
80
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1537-45
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1520878-Base Sequence,
pubmed-meshheading:1520878-DNA, Viral,
pubmed-meshheading:1520878-Female,
pubmed-meshheading:1520878-Human T-lymphotropic virus 1,
pubmed-meshheading:1520878-Human T-lymphotropic virus 2,
pubmed-meshheading:1520878-Humans,
pubmed-meshheading:1520878-Lymphocytes,
pubmed-meshheading:1520878-Middle Aged,
pubmed-meshheading:1520878-Molecular Sequence Data,
pubmed-meshheading:1520878-Mycosis Fungoides,
pubmed-meshheading:1520878-Sequence Homology, Nucleic Acid
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pubmed:year |
1992
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pubmed:articleTitle |
Human lymphotropic retroviruses associated with mycosis fungoides: evidence that human T-cell lymphotropic virus type II (HTLV-II) as well as HTLV-I may play a role in the disease.
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pubmed:affiliation |
Department of Medicine, New York University Medical Center, New York 10016.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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