| authorizations: |
registration not required
|
| accessURL: |
http://www.iedb.org/reference/1031398 |
| landingPage: |
http://www.iedb.org/assay/3198098 |
| type: |
Literature
|
| publicationVenue: |
Proc Natl Acad Sci U S A
|
| dates: |
2017
|
| study type: | t cell assays |
| subject species: | Gallus gallus |
| fullName: |
Novalia Pishesha
Angelina M Bilate
Marsha C Wibowo
Nai-Jia Huang
Zeyang Li
Rhogerry Dhesycka
Djenet Bousbaine
Hojun Li
Heide C Patterson
Stephanie K Dougan
Takeshi Maruyama
Harvey F Lodish
Hidde L Ploegh
|
| method: |
in vivo assay
|
| name: |
Engineered erythrocytes covalently linked to antigenic peptides can protect against autoimmune disease.
|
| description: |
In mice that received epitope-RBC, the transferred T cells showed only modest expansion, compared with mice receiving an equivalent number of unmodified RBCs or epitope peptide. Upon in vitro restimulation with epitope, the T cells produced fewer proinflammatory cytokines, TNF-alpha, and IFN-gamma, than OT-I T cells from mice that received OT-I peptide alone. These cells also failed to respond to ovalbumin. These cells displayed characteristics of nonresponsive (tolerant) cells. The epitope was synthesized with GGGK(biotin)KKFR on the N-terminus.
|
| name: |
iedb
|
| homePage: |
http://www.iedb.org |