Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2006-10-25
pubmed:abstractText
Infection with Leishmania sp. is particularly suitable for the study of immunoregulatory mechanisms associated with host susceptibility or resistance. The clinical spectrum of this infection results from parasite virulence factors and host immune responses, some of which acting in a host protective manner while others exacerbate the disease. In the mouse model, factors governing resistance to Leishmania major infection mainly depends on the IFN-gamma activation of the leishmanicidal function of macrophages, and the Fas/ FasL-dependent T-cell cytotoxicity against infected macrophages. On the other hand, the immunological factors of susceptibility involve: I) the early upregulation of IL-4 production induced by the LACK antigen, II) the upregulation of IL-2 production, III) the high production of TGF-beta as macrophage deactivating factor, and IV) the production of IL-10 by the L. major infected macrophages, inhibited their microbicidal activity.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD95, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Protozoan, http://linkedlifedata.com/resource/pubmed/chemical/Cytokines, http://linkedlifedata.com/resource/pubmed/chemical/Fas Ligand Protein, http://linkedlifedata.com/resource/pubmed/chemical/Fasl protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-13, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4, http://linkedlifedata.com/resource/pubmed/chemical/LACK antigen, Leishmania, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide, http://linkedlifedata.com/resource/pubmed/chemical/Protozoan Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta
pubmed:status
MEDLINE
pubmed:issn
0187-4640
pubmed:author
pubmed:issnType
Print
pubmed:volume
43
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
135-42
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:17061500-Animals, pubmed-meshheading:17061500-Antigens, CD95, pubmed-meshheading:17061500-Antigens, Protozoan, pubmed-meshheading:17061500-Cytokines, pubmed-meshheading:17061500-Disease Susceptibility, pubmed-meshheading:17061500-Fas Ligand Protein, pubmed-meshheading:17061500-Immune Tolerance, pubmed-meshheading:17061500-Immunity, Innate, pubmed-meshheading:17061500-Interferon-gamma, pubmed-meshheading:17061500-Interleukin-13, pubmed-meshheading:17061500-Interleukin-2, pubmed-meshheading:17061500-Interleukin-4, pubmed-meshheading:17061500-Leishmania major, pubmed-meshheading:17061500-Leishmaniasis, Cutaneous, pubmed-meshheading:17061500-Macrophages, pubmed-meshheading:17061500-Macrophages, Peritoneal, pubmed-meshheading:17061500-Mice, pubmed-meshheading:17061500-Mice, Inbred BALB C, pubmed-meshheading:17061500-Mice, Inbred C57BL, pubmed-meshheading:17061500-Nitric Oxide, pubmed-meshheading:17061500-Protozoan Proteins, pubmed-meshheading:17061500-Th1 Cells, pubmed-meshheading:17061500-Transforming Growth Factor beta
pubmed:articleTitle
Immunological factors governing resistance and susceptibility of mice to Leishmania major infection.
pubmed:affiliation
Departamento de Inmunología, Escuela Nacional de Ciencias Biológicas, IPN, México DF. faguilar@bios.encb.ipn.mx
pubmed:publicationType
Journal Article, Review, Research Support, Non-U.S. Gov't