Source:http://linkedlifedata.com/resource/pubmed/id/10631573
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2000-2-15
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pubmed:abstractText |
Cell-mediated immune responses are essential for host control of intracellular infections. Toxoplasma gondii is a protozoan parasite that infects multiple vertebrate species and invades multiple cell types. Upon initial encounter with the immune system, the parasite rapidly induces production of the type-1 promoting cytokine IL-12 most likely from a subpopulation of dendritic cells. NK and T cells are then activated and triggered to synthesize IFN-gamma, the major mediator of host resistance during the acute and chronic phases of infection. During the acute phase, a concomitant IL-10 response dampens the systemic type-1 cytokine production and prevents lethal immunopathology. Cytokine (IFN-gamma und TNF-alpha) rather than cytotoxicity-based effector functions are more critical for protective immunity both during the acute and chronic phases of T. gondii infection. Both hemopoietic and non-hemopoietic cellular elements act as IFN-gamma and TNF-dependent effectors of host resistance. Type II iNOS-derived nitric oxide (NO) is required mainly for hemopoietic cell-derived effector cell activity in the central nervous system (CNS) during the chronic phase of infection. Nevertheless, in both the acute and chronic stages, IFN-gamma-dependent but iNOS-independent mechanism(s) play a major function in parasite control and their identification remains an important challenge for this field.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-10,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-12,
http://linkedlifedata.com/resource/pubmed/chemical/NOS2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase Type II,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0171-2985
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
201
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
240-7
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pubmed:dateRevised |
2011-10-27
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pubmed:meshHeading |
pubmed-meshheading:10631573-Acute Disease,
pubmed-meshheading:10631573-Animals,
pubmed-meshheading:10631573-Chronic Disease,
pubmed-meshheading:10631573-Dendritic Cells,
pubmed-meshheading:10631573-Humans,
pubmed-meshheading:10631573-Immunity, Cellular,
pubmed-meshheading:10631573-Interferon-gamma,
pubmed-meshheading:10631573-Interleukin-10,
pubmed-meshheading:10631573-Interleukin-12,
pubmed-meshheading:10631573-Killer Cells, Natural,
pubmed-meshheading:10631573-Lymphocyte Subsets,
pubmed-meshheading:10631573-Nitric Oxide Synthase,
pubmed-meshheading:10631573-Nitric Oxide Synthase Type II,
pubmed-meshheading:10631573-T-Lymphocytes,
pubmed-meshheading:10631573-Toxoplasma,
pubmed-meshheading:10631573-Toxoplasmosis,
pubmed-meshheading:10631573-Toxoplasmosis, Animal,
pubmed-meshheading:10631573-Tumor Necrosis Factor-alpha
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pubmed:year |
1999
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pubmed:articleTitle |
Cell-mediated immunity to Toxoplasma gondii: initiation, regulation and effector function.
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pubmed:affiliation |
Immunobiology Section, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
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pubmed:publicationType |
Journal Article,
Review
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