| pubmed-article:10816541 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10816541 | lifeskim:mentions | umls-concept:C0026946 | lld:lifeskim |
| pubmed-article:10816541 | lifeskim:mentions | umls-concept:C0001554 | lld:lifeskim |
| pubmed-article:10816541 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
| pubmed-article:10816541 | lifeskim:mentions | umls-concept:C0014264 | lld:lifeskim |
| pubmed-article:10816541 | lifeskim:mentions | umls-concept:C0023810 | lld:lifeskim |
| pubmed-article:10816541 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:10816541 | lifeskim:mentions | umls-concept:C1704410 | lld:lifeskim |
| pubmed-article:10816541 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:10816541 | pubmed:dateCreated | 2000-6-23 | lld:pubmed |
| pubmed-article:10816541 | pubmed:abstractText | Lipopolysaccharide (LPS) pretreatment of mice resulted in a significantly enhanced survival after disseminated Cryptococcus neoformans infection. The survival was associated with reduced fungal burden in tissues. LPS-pretreated mice had lower levels of cytokines in blood, spleen, and lungs and higher levels in brain. Pentoxifylline abolished the beneficial effect of LPS pretreatment. | lld:pubmed |
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| pubmed-article:10816541 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:10816541 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:10816541 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10816541 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:10816541 | pubmed:issn | 0019-9567 | lld:pubmed |
| pubmed-article:10816541 | pubmed:author | pubmed-author:CavaillonJ... | lld:pubmed |
| pubmed-article:10816541 | pubmed:author | pubmed-author:LortholaryOO | lld:pubmed |
| pubmed-article:10816541 | pubmed:author | pubmed-author:FittingCC | lld:pubmed |
| pubmed-article:10816541 | pubmed:author | pubmed-author:DromerFF | lld:pubmed |
| pubmed-article:10816541 | pubmed:author | pubmed-author:RayhaneNN | lld:pubmed |
| pubmed-article:10816541 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10816541 | pubmed:volume | 68 | lld:pubmed |
| pubmed-article:10816541 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10816541 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10816541 | pubmed:pagination | 3748-53 | lld:pubmed |
| pubmed-article:10816541 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:10816541 | pubmed:year | 2000 | lld:pubmed |
| pubmed-article:10816541 | pubmed:articleTitle | Administration of endotoxin associated with lipopolysaccharide tolerance protects mice against fungal infection. | lld:pubmed |
| pubmed-article:10816541 | pubmed:affiliation | Unité d'Immuno-Allergie, Institut Pasteur, 75015 Paris, France. | lld:pubmed |
| pubmed-article:10816541 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:10816541 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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