pubmed-article:15351492 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:15351492 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
pubmed-article:15351492 | lifeskim:mentions | umls-concept:C0442118 | lld:lifeskim |
pubmed-article:15351492 | lifeskim:mentions | umls-concept:C0042210 | lld:lifeskim |
pubmed-article:15351492 | lifeskim:mentions | umls-concept:C2076600 | lld:lifeskim |
pubmed-article:15351492 | lifeskim:mentions | umls-concept:C0027964 | lld:lifeskim |
pubmed-article:15351492 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:15351492 | pubmed:dateCreated | 2004-9-7 | lld:pubmed |
pubmed-article:15351492 | pubmed:abstractText | Live, cold-adapted, temperature-sensitive (ca/ts) Russian influenza A vaccines are prepared in eggs by a 6:2 gene reassortment of the ca/ts donor strain A/Leningrad/134/17/57 (H2N2) (Len/17) with a current wild-type (wt) influenza A strain contributing hemagglutinin (HA) and neuraminidase (NA) genes. However, egg-derived reassortant vaccines are potentially more problematic to manufacture in large quantities than vaccines from cell-based procedures. To compare egg- and cell culture-derived reassortant vaccines, we prepared in Madin Darby canine kidney (MDCK) cells two cloned, ca/ts reassortants (25M/1, 39E/2) derived from Len/17 and a wt reference strain A/New Caledonia/20/99 (H1N1) (NC/wt). Both 25M/1 and 39E/2 reassortants preserved the ca/ts phenotype and mutations described for internal genes of the A/Len/17 parent. When compared to a commercial, egg-derived ca/ts Russian A/17/NC/99/145 (H1N1) New Caledonia vaccine (NC/145), the MDCK-derived reassortant 39E/2 vaccine conferred similar levels of protection in ferrets challenged i.n. with 7 x 10(10) pfu of NC/wt. In a dose-ranging study, the protective vaccine dose for 50% of ferrets (PD50) was less than 1.2 x 10(4) pfu for the 25M/1 vaccine derived by recombination and amplification in MDCK cells. Clonal isolates of ca/ts influenza A/New Caledonia/20/99 (H1N1) obtained by recombination and amplification entirely in MDCK cells can be highly protective i.n. vaccines. | lld:pubmed |
pubmed-article:15351492 | pubmed:language | eng | lld:pubmed |
pubmed-article:15351492 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15351492 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:15351492 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15351492 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15351492 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15351492 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15351492 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:15351492 | pubmed:month | Oct | lld:pubmed |
pubmed-article:15351492 | pubmed:issn | 0168-1702 | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:YouilRimaR | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:MR GRG | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:KiselevaIrina... | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:ShawAlanA | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:SzymkowiakChr... | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:KwanWan-SangW... | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:RudenkoLarisa... | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:PalkerThomasT | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:JohnstonKimbe... | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:TonerTimothyT | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:RubinBorisB | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:PetrukhinLuba... | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:WlochowskiJoa... | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:MonteiroJuani... | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:KraiouchkineN... | lld:pubmed |
pubmed-article:15351492 | pubmed:author | pubmed-author:DiStefanoDani... | lld:pubmed |
pubmed-article:15351492 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:15351492 | pubmed:volume | 105 | lld:pubmed |
pubmed-article:15351492 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:15351492 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:15351492 | pubmed:pagination | 183-94 | lld:pubmed |
pubmed-article:15351492 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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pubmed-article:15351492 | pubmed:year | 2004 | lld:pubmed |
pubmed-article:15351492 | pubmed:articleTitle | Protective efficacy of intranasal cold-adapted influenza A/New Caledonia/20/99 (H1N1) vaccines comprised of egg- or cell culture-derived reassortants. | lld:pubmed |
pubmed-article:15351492 | pubmed:affiliation | Department of Virus and Cell Biology, Vaccine and Biologics Research, Merck Research Laboratories, Merck and Co., Inc., 770 Sumneytown Pike, WP16-101, West Point, PA 19486, USA. tom_palker@merck.com | lld:pubmed |
pubmed-article:15351492 | pubmed:publicationType | Journal Article | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15351492 | lld:pubmed |