pubmed-article:11090168 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11090168 | lifeskim:mentions | umls-concept:C0029347 | lld:lifeskim |
pubmed-article:11090168 | lifeskim:mentions | umls-concept:C0521346 | lld:lifeskim |
pubmed-article:11090168 | lifeskim:mentions | umls-concept:C0025260 | lld:lifeskim |
pubmed-article:11090168 | lifeskim:mentions | umls-concept:C1332717 | lld:lifeskim |
pubmed-article:11090168 | lifeskim:mentions | umls-concept:C1706438 | lld:lifeskim |
pubmed-article:11090168 | lifeskim:mentions | umls-concept:C0085358 | lld:lifeskim |
pubmed-article:11090168 | lifeskim:mentions | umls-concept:C1545588 | lld:lifeskim |
pubmed-article:11090168 | lifeskim:mentions | umls-concept:C1413244 | lld:lifeskim |
pubmed-article:11090168 | lifeskim:mentions | umls-concept:C2698600 | lld:lifeskim |
pubmed-article:11090168 | lifeskim:mentions | umls-concept:C0805586 | lld:lifeskim |
pubmed-article:11090168 | lifeskim:mentions | umls-concept:C1704240 | lld:lifeskim |
pubmed-article:11090168 | pubmed:issue | 24 | lld:pubmed |
pubmed-article:11090168 | pubmed:dateCreated | 2001-1-11 | lld:pubmed |
pubmed-article:11090168 | pubmed:abstractText | The recall of CD8(+) T-cell memory established by infecting H-2(b) mice with an H1N1 influenza A virus provided a measure of protection against an extremely virulent H7N7 virus. The numbers of CD8(+) effector and memory T cells specific for the shared, immunodominant D(b)NP(366) epitope were greatly increased subsequent to the H7N7 challenge, and though lung titers remained as high as those in naive controls for 5 days or more, the virus was cleared more rapidly. Expanding the CD8(+) memory T-cell pool (<0.5 to >10%) by sequential priming with two different influenza A viruses (H3N2-->H1N1) gave much better protection. Though the H7N7 virus initially grew to equivalent titers in the lungs of naive and double-primed mice, the replicative phase was substantially controlled within 3 days. This tertiary H7N7 challenge caused little increase in the magnitude of the CD8(+) D(b)NP(366)(+) T-cell pool, and only a portion of the memory population in the lymphoid tissue could be shown to proliferate. The great majority of the CD8(+) D(b)NP(366)(+) set that localized to the infected respiratory tract had, however, cycled at least once, though recent cell division was shown not to be a prerequisite for T-cell extravasation. The selective induction of CD8(+) T-cell memory can thus greatly limit the damage caused by a virulent influenza A virus, with the extent of protection being directly related to the number of available responders. Furthermore, a large pool of CD8(+) memory T cells may be only partially utilized to deal with a potentially lethal influenza infection. | lld:pubmed |
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pubmed-article:11090168 | pubmed:language | eng | lld:pubmed |
pubmed-article:11090168 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11090168 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:11090168 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11090168 | pubmed:month | Dec | lld:pubmed |
pubmed-article:11090168 | pubmed:issn | 0022-538X | lld:pubmed |
pubmed-article:11090168 | pubmed:author | pubmed-author:DohertyP CPC | lld:pubmed |
pubmed-article:11090168 | pubmed:author | pubmed-author:ChristensenJ... | lld:pubmed |
pubmed-article:11090168 | pubmed:author | pubmed-author:RiberdyJ MJM | lld:pubmed |
pubmed-article:11090168 | pubmed:author | pubmed-author:BranumK CKC | lld:pubmed |
pubmed-article:11090168 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11090168 | pubmed:volume | 74 | lld:pubmed |
pubmed-article:11090168 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11090168 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11090168 | pubmed:pagination | 11690-6 | lld:pubmed |
pubmed-article:11090168 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:11090168 | pubmed:year | 2000 | lld:pubmed |
pubmed-article:11090168 | pubmed:articleTitle | Profound protection against respiratory challenge with a lethal H7N7 influenza A virus by increasing the magnitude of CD8(+) T-cell memory. | lld:pubmed |
pubmed-article:11090168 | pubmed:affiliation | Department of Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA. | lld:pubmed |
pubmed-article:11090168 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11090168 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:11090168 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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