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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3 Suppl
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pubmed:dateCreated |
1999-6-15
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pubmed:abstractText |
The murine Leishmania major model has proven fertile ground for the elucidation of CD4+ T cell effector subset differentiation in vivo. The availability of a highly susceptible inbred strain, BALB/c, that develops progressive disease due to the aberrant differentiation of Th2, as opposed to protective Th1, responses, has allowed the identification of both T cell intrinsic as well as T cell extrinsic properties that combine to mediate disease outcome. The intrinsic T cell phenotype relates to the capacity of BALB/c-derived CD4+ T cells to acquire the potential to secrete IL-4 more readily than cells from other strains of mice. The extrinsic T cell phenotype relates to the creation of a T cell repertoire capable of recognizing the immunodominant parasite antigen. Together, the two traits confer the aberrant response seen in susceptible mice challenged with L. major.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
1148-5493
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
102-6
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:9831197-Animals,
pubmed-meshheading:9831197-Cytokines,
pubmed-meshheading:9831197-Disease Models, Animal,
pubmed-meshheading:9831197-Disease Susceptibility,
pubmed-meshheading:9831197-Leishmania major,
pubmed-meshheading:9831197-Leishmaniasis, Cutaneous,
pubmed-meshheading:9831197-Mice,
pubmed-meshheading:9831197-Mice, Inbred BALB C
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pubmed:year |
1998
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pubmed:articleTitle |
Disease susceptibility and development of the cytokine repertoire in the murine Leishmania major model.
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pubmed:affiliation |
Department of Medicine, University of California San Francisco, 94143-0654, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Review,
Research Support, Non-U.S. Gov't
|