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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1996-1-26
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pubmed:abstractText |
In this review we have summarized the main data concerning Leishmania-macrophage interactions, with particular emphasis on receptors involved in adhesion, activating or deactivating cytokines and toxic molecules responsible for parasite killing. At present it is also known that a different T helper (Th)1- or Th2-cell response may be critical for the outcome of Leishmania infection in human and in murine models. Therefore, we have mentioned the recent studies on cytokines, such as IL-2, which are able to cause the switch from a Th2, disease-promoting immune response, to a Th1, protective response. In fact, in the light of these findings, these molecules may be used in the future for immunotherapeutical or immunoprophylactic purposes.
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pubmed:language |
ita
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
|
pubmed:issn |
0048-2951
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
37
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5-15
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:8532367-Animals,
pubmed-meshheading:8532367-Arginine,
pubmed-meshheading:8532367-Cell Adhesion,
pubmed-meshheading:8532367-Cytokines,
pubmed-meshheading:8532367-Host-Parasite Interactions,
pubmed-meshheading:8532367-Humans,
pubmed-meshheading:8532367-Leishmania,
pubmed-meshheading:8532367-Leishmaniasis,
pubmed-meshheading:8532367-Macrophages,
pubmed-meshheading:8532367-Mice,
pubmed-meshheading:8532367-Nitric Oxide,
pubmed-meshheading:8532367-Nitric Oxide Synthase,
pubmed-meshheading:8532367-T-Lymphocytes, Helper-Inducer
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pubmed:year |
1995
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pubmed:articleTitle |
[Leishmania-macrophage interactions: role of cytokines and molecules co-involved in killing].
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pubmed:affiliation |
Istituto di Malattie Infettive e Parassitarie degli Animali, Università di Bari.
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pubmed:publicationType |
Journal Article,
English Abstract,
Review,
Research Support, Non-U.S. Gov't
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