Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2003-2-7
pubmed:abstractText
Interaction of chemokines with their specific receptors results in tight control of leukocyte migration and positioning. CCR8 is a chemokine receptor expressed mainly in CD4(+) single-positive thymocytes and Th2 cells. We generated CCR8-deficient mice (CCR8(-/-)) to study the in vivo role of this receptor, and describe in this study the CCR8(-/-) mouse response in OVA-induced allergic airway disease using several models, including an adoptive transfer model and receptor-blocking experiments. All CCR8(-/-) mice developed a pathological response similar to that of wild-type animals with respect to bronchoalveolar lavage cell composition, peripheral blood and bone marrow eosinophilia, lung infiltrates, and Th2 cytokine levels in lung and serum. The results contrast with a recent report using one of the OVA-induced asthma models studied here. Similar immune responses were also observed in CCR8(-/-) and wild-type animals in a different model of ragweed allergen-induced peritoneal eosinophilic inflammation, with an equivalent number of eosinophils and analogous increased levels of Th2 cytokines in peritoneum and peripheral blood. Our results show that allergic diseases course without critical CCR8 participation, and suggest that further work is needed to unravel the in vivo role of CCR8 in Th2-mediated pathologies.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
170
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2138-46
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:12574386-Adoptive Transfer, pubmed-meshheading:12574386-Allergens, pubmed-meshheading:12574386-Animals, pubmed-meshheading:12574386-Antibodies, Monoclonal, pubmed-meshheading:12574386-Chemokines, CC, pubmed-meshheading:12574386-Crosses, Genetic, pubmed-meshheading:12574386-Disease Models, Animal, pubmed-meshheading:12574386-Eosinophilia, pubmed-meshheading:12574386-Female, pubmed-meshheading:12574386-Injections, Intraperitoneal, pubmed-meshheading:12574386-Male, pubmed-meshheading:12574386-Mice, pubmed-meshheading:12574386-Mice, Inbred C57BL, pubmed-meshheading:12574386-Mice, Knockout, pubmed-meshheading:12574386-Ovalbumin, pubmed-meshheading:12574386-Peritonitis, pubmed-meshheading:12574386-Receptors, CCR8, pubmed-meshheading:12574386-Receptors, Chemokine, pubmed-meshheading:12574386-Recombination, Genetic, pubmed-meshheading:12574386-Respiratory Hypersensitivity, pubmed-meshheading:12574386-Th2 Cells, pubmed-meshheading:12574386-Time Factors
pubmed:year
2003
pubmed:articleTitle
Absence of CCR8 does not impair the response to ovalbumin-induced allergic airway disease.
pubmed:affiliation
Departamento de Inmunología y Oncología, Centro Nacional de Biotecnología/Consejo Superior de Investigaciones Cientificas, Universidad Autónoma de Madrid, Cantoblanco, 28040-Madrid, Spain.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't