Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1996-12-6
pubmed:abstractText
Specific T cell hyporesponsiveness and depressed antibody production is a key feature of human infection with the filarial nematodes, Brugia malayi and Wuchereria bancrofti. Despite this immune suppression, responses indicative of Th2 subset activation are present, including unusually high levels of specific IgG4. We tested the possibility that infection with filarial nematodes causes a reduction in the co-stimulatory or antigen-presenting capacity of macrophages resulting in a failure to activate specific T cells. Adherent peritoneal exudate cells (PEC) from mice implanted with adult B. Malayi were used to present antigen to the conalbumin-specific T cell clone, D10.G4. Proliferation of the D10 cells at even background levels was completely blocked by the presence of implant-derived adherent PEC. However, cytokine production by these cells in response to antigen was intact, and thus PEC from implanted mice are capable of functionally processing and presenting antigen. The elicitation of a suppressive cell population was specific for live adults as cells from mice implanted with dead adult parasites effectively stimulated D10 proliferation. The block in cellular proliferation is not due to the production of factors typically associated with macrophage suppression such as nitric oxide, prostaglandins or catalase. These observations are consistent with the T cell hyporesponsiveness seen in human cases of patent Brugia infection and may provide a murine model for the immune suppression seen in lymphatic filariasis.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0953-8178
pubmed:author
pubmed:issnType
Print
pubmed:volume
8
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
143-51
pubmed:dateRevised
2009-9-29
pubmed:meshHeading
pubmed-meshheading:8671598-Adult, pubmed-meshheading:8671598-Animals, pubmed-meshheading:8671598-Antigen Presentation, pubmed-meshheading:8671598-Brugia malayi, pubmed-meshheading:8671598-Cytokines, pubmed-meshheading:8671598-Female, pubmed-meshheading:8671598-Filariasis, pubmed-meshheading:8671598-Humans, pubmed-meshheading:8671598-Hydrogen Peroxide, pubmed-meshheading:8671598-Interferon-gamma, pubmed-meshheading:8671598-Lymphocyte Activation, pubmed-meshheading:8671598-Macrophage Activation, pubmed-meshheading:8671598-Male, pubmed-meshheading:8671598-Mice, pubmed-meshheading:8671598-Mice, Inbred CBA, pubmed-meshheading:8671598-Nitric Oxide, pubmed-meshheading:8671598-Peritoneal Cavity, pubmed-meshheading:8671598-Prostaglandins, pubmed-meshheading:8671598-T-Lymphocytes, pubmed-meshheading:8671598-Transforming Growth Factor beta
pubmed:year
1996
pubmed:articleTitle
APC from mice harbouring the filarial nematode, Brugia malayi, prevent cellular proliferation but not cytokine production.
pubmed:affiliation
Institute of Cell, Animal and Population Biology, Ashworth Laboratories, University of Edinburgh, Edinburgh EH9 3JT, UK.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't