Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2000-2-14
pubmed:abstractText
In Sudan, post kala-azar dermal leishmaniasis (PKDL) caused by Leishmania donovani develops in half of the patients treated for visceral leishmaniasis (kala-azar). In most patients lesions heal spontaneously, but in others symptoms are severe and persist for years. This study examined the immunological response in lesions of PKDL patients by immunohistochemistry and compared the findings with results obtained using peripheral blood mononuclear cells (PBMCs). In all lesions, parasites or parasite antigen were present and provoked the formation of an inflammatory infiltrate consisting of a mixture of macrophages, lymphocytes, and plasma cells. In patients who had high interferon-gamma (IFNgamma) responses to Leishmania antigen in vitro, compact epithelioid granulomas were formed. The inflammatory cells were mainly CD3(+) and interleukin-10 (IL10) was the most prominent cytokine in the lesions. However, IFNgamma was found in all and IL4 in most lesions, in varying amounts. PBMCs from all patients responded to Leishmania antigen by IFNgamma production or proliferation. The results indicate that PKDL develops as a result of an influx of immunocompetent cells into skin, which harbours parasites. The inflammatory response to the parasites is complex. It involves several cell types and cytokines, of which some are antagonistic. It is conceivable that the balance between these cytokines determines the outcome of the disease.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0022-3417
pubmed:author
pubmed:copyrightInfo
Copyright 1999 John Wiley & Sons, Ltd.
pubmed:issnType
Print
pubmed:volume
189
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
615-22
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:10629566-Adolescent, pubmed-meshheading:10629566-Adult, pubmed-meshheading:10629566-Animals, pubmed-meshheading:10629566-Antigens, Protozoan, pubmed-meshheading:10629566-Case-Control Studies, pubmed-meshheading:10629566-Cell Division, pubmed-meshheading:10629566-Cells, Cultured, pubmed-meshheading:10629566-Child, pubmed-meshheading:10629566-Cytokines, pubmed-meshheading:10629566-Female, pubmed-meshheading:10629566-Flow Cytometry, pubmed-meshheading:10629566-Humans, pubmed-meshheading:10629566-Immunohistochemistry, pubmed-meshheading:10629566-Interferon-gamma, pubmed-meshheading:10629566-Interleukin-10, pubmed-meshheading:10629566-Interleukin-4, pubmed-meshheading:10629566-Leishmania donovani, pubmed-meshheading:10629566-Leishmaniasis, Cutaneous, pubmed-meshheading:10629566-Leishmaniasis, Visceral, pubmed-meshheading:10629566-Male, pubmed-meshheading:10629566-Statistics, Nonparametric, pubmed-meshheading:10629566-T-Lymphocytes
pubmed:year
1999
pubmed:articleTitle
Immunopathology of post kala-azar dermal leishmaniasis (PKDL): T-cell phenotypes and cytokine profile.
pubmed:affiliation
Centre for Medical Parasitology, Institute of Medical Microbiology and Immunology, University of Copenhagen, Denmark. aicmp@biobase.dk
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't