| http://purl.uniprot.org/citations/16210591 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/16210591 | http://www.w3.org/2000/01/rdf-schema#comment | "The 4-1BB receptor acts as a costimulator in CD8(+) T cell activation. Agonistic stimulation through this molecule by treatment with anti-4-1BB Abs has been demonstrated to inhibit various experimentally induced diseases in animals. However, the effect of anti-4-1BB Abs on experimental allergic diseases has not been reported. We investigated the effect of anti-4-1BB Abs on the development and progression of experimental allergic conjunctivitis in mice. To examine the effects of Abs during the induction or effector phase, actively immunized mice or passively immunized mice by splenocyte transfer were treated with agonistic anti-4-1BB Abs, blocking anti-4-1BB ligand Abs, or normal rat IgG. Eosinophil infiltration into the conjunctiva was significantly reduced in wild-type mice by the anti-4-1BB Ab treatment during either induction or effector phase. Th2 cytokine production by splenocytes and total serum IgE were significantly reduced by the anti-4-1BB Ab treatment, while IFN-gamma production was increased. The anti-4-1BB Ab treatment induced a relative increase of CD8-positive cell numbers in the spleens. Moreover, inhibition of eosinophil infiltration by the treatment with anti-4-1BB Abs was also noted in actively immunized IFN-gamma knockout mice. Taken altogether, in vivo treatment with agonistic anti-4-1BB Abs in either induction or effector phase inhibits the development of experimental allergic conjunctivitis, and this inhibition is likely to be mediated by suppression of Th2 immune responses rather than up-regulation of IFN-gamma."xsd:string |
| http://purl.uniprot.org/citations/16210591 | http://purl.org/dc/terms/identifier | "doi:10.4049/jimmunol.175.8.4897"xsd:string |
| http://purl.uniprot.org/citations/16210591 | http://purl.uniprot.org/core/author | "Ueno H."xsd:string |
| http://purl.uniprot.org/citations/16210591 | http://purl.uniprot.org/core/author | "Yamaguchi T."xsd:string |
| http://purl.uniprot.org/citations/16210591 | http://purl.uniprot.org/core/author | "Fukushima A."xsd:string |
| http://purl.uniprot.org/citations/16210591 | http://purl.uniprot.org/core/author | "Yagita H."xsd:string |
| http://purl.uniprot.org/citations/16210591 | http://purl.uniprot.org/core/author | "Ishida W."xsd:string |
| http://purl.uniprot.org/citations/16210591 | http://purl.uniprot.org/core/author | "Mittler R.S."xsd:string |
| http://purl.uniprot.org/citations/16210591 | http://purl.uniprot.org/core/author | "Fukata K."xsd:string |
| http://purl.uniprot.org/citations/16210591 | http://purl.uniprot.org/core/date | "2005"xsd:gYear |
| http://purl.uniprot.org/citations/16210591 | http://purl.uniprot.org/core/name | "J Immunol"xsd:string |
| http://purl.uniprot.org/citations/16210591 | http://purl.uniprot.org/core/pages | "4897-4903"xsd:string |
| http://purl.uniprot.org/citations/16210591 | http://purl.uniprot.org/core/title | "Engagement of 4-1BB inhibits the development of experimental allergic conjunctivitis in mice."xsd:string |
| http://purl.uniprot.org/citations/16210591 | http://purl.uniprot.org/core/volume | "175"xsd:string |
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