http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102258773-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4873cd720f7e169a6f1bd1ed6b41c31a
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K39-39
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K39-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K19-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 2011-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_72d257042432cdb0f005ec8c5ae6e7d9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_08b167f1c503e0832290c6be41cfa0dd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5cdf9b79b9edcd4589854c4d55da1f95
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_93980165846dc9f2096c55e27184b41b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e013c658df91745801ce9c284892c69e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_614ac5f9000deb1b911caf50a6fc3eab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aeb1061d3e338c76b81159fce338cc88
publicationDate 2013-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102258773-B
titleOfInvention Mesylate protein kinase receptor EphA2 dominant epitope compound and preparation method and application thereof
abstract The invention discloses a mesylate protein kinase receptor EphA2 dominant epitope compound and a preparation method and application thereof in preparing a therapeutic vaccine for tumor. The compound is prepared from EphA258-66 epitope fusion peptide, EphA2550-558 epitope fusion peptide and EphA2253-261 epitope fusion peptide in mol ratio of 1:1:1 and an LIGHT gene recombinant eukaryotic expression vector; the EphA258-66/550-558/253-261 epitope fusion peptides are respectively prepared from EphA258-66/550-558/253-261 epitopes and a transmembrane sequence HIV-Tat49-57, an endoplasmic reticulum retention signal sequence KDEL and a linker sequence AAY; the combination of the three EphA2 dominant epitopes can effectively overcome the deficiency of a single epitope on immune effect; the three epitope fusion peptides can enter the kytoplasm under the guide action of the transmembrane sequence, target the endoplasmic reticulum under the action of the endoplasmic reticulum retention signal sequence, and efficiently enter an MHC-I (major histocompatibility complex-class I) antigen presenting route; and the LIGHT gene recombinant eukaryotic expression vector can express LIGHT protein in vivoand play a role of a molecular adjuvant to promote the immune response of epitope specific T cells.
priorityDate 2011-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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