pubmed-article:10365395 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10365395 | lifeskim:mentions | umls-concept:C0042776 | lld:lifeskim |
pubmed-article:10365395 | lifeskim:mentions | umls-concept:C0020094 | lld:lifeskim |
pubmed-article:10365395 | lifeskim:mentions | umls-concept:C0023418 | lld:lifeskim |
pubmed-article:10365395 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
pubmed-article:10365395 | lifeskim:mentions | umls-concept:C0017263 | lld:lifeskim |
pubmed-article:10365395 | lifeskim:mentions | umls-concept:C1817908 | lld:lifeskim |
pubmed-article:10365395 | pubmed:issue | 1384 | lld:pubmed |
pubmed-article:10365395 | pubmed:dateCreated | 1999-6-28 | lld:pubmed |
pubmed-article:10365395 | pubmed:abstractText | About 1% of people infected with the human T-cell leukaemia virus, type 1 (HTLV-I) develop a disabling chronic inflammatory disease of the central nervous system known as HTLV-I-associated myelopathy/tropical spastic paraparesis (HAM/TSP). Patients with HAM/TSP have a vigorous immune response to HTLV-I, and it has been widely suggested that this immune response, particularly the HTLV-I-specific cytotoxic T-lymphocyte (CTL) response, causes the tissue damage that is seen in HAM/TSP. In this paper we summarize recent evidence that a strong CTL response to HTLV-I does in fact protect against HAM/TSP by reducing the proviral load of HTLV-I. We conclude that HTLV-I is persistently replicating at a high level, despite the relative constancy of its genome sequence. These results imply that antiretroviral drugs could reduce the risk of HAM/TSP by reducing the viral load, and that an effective anti-HTLV-I vaccine should elicit a strong CTL response to the virus. The dynamic nature of the infection also has implications for the epidemiology and the evolution of HTLV-I. | lld:pubmed |
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pubmed-article:10365395 | pubmed:language | eng | lld:pubmed |
pubmed-article:10365395 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10365395 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:10365395 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10365395 | pubmed:month | Apr | lld:pubmed |
pubmed-article:10365395 | pubmed:issn | 0962-8436 | lld:pubmed |
pubmed-article:10365395 | pubmed:author | pubmed-author:OsameMM | lld:pubmed |
pubmed-article:10365395 | pubmed:author | pubmed-author:HallS ESE | lld:pubmed |
pubmed-article:10365395 | pubmed:author | pubmed-author:BanghamC RCR | lld:pubmed |
pubmed-article:10365395 | pubmed:author | pubmed-author:NowakM AMA | lld:pubmed |
pubmed-article:10365395 | pubmed:author | pubmed-author:UsukuKK | lld:pubmed |
pubmed-article:10365395 | pubmed:author | pubmed-author:JefferyK JKJ | lld:pubmed |
pubmed-article:10365395 | pubmed:author | pubmed-author:WodarzDD | lld:pubmed |
pubmed-article:10365395 | pubmed:author | pubmed-author:VineA MAM | lld:pubmed |
pubmed-article:10365395 | pubmed:author | pubmed-author:WitkoverAA | lld:pubmed |
pubmed-article:10365395 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10365395 | pubmed:day | 29 | lld:pubmed |
pubmed-article:10365395 | pubmed:volume | 354 | lld:pubmed |
pubmed-article:10365395 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10365395 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10365395 | pubmed:pagination | 691-700 | lld:pubmed |
pubmed-article:10365395 | pubmed:dateRevised | 2010-8-25 | lld:pubmed |
pubmed-article:10365395 | pubmed:meshHeading | pubmed-meshheading:10365395... | lld:pubmed |