2011 Fiscal Year Final Research Report
Developing T-cell based immunotherapy using ubiquitously expressing tumor-associated antigen, Aurora-A kinase and FAK
Project/Area Number |
21590424
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Experimental pathology
|
Research Institution | Asahikawa Medical College |
Principal Investigator |
|
Project Period (FY) |
2009 – 2011
|
Keywords | CD4 ヘルパーT 細胞 / 腫瘍抗原 / ペプチド / HLA |
Research Abstract |
Focal adhesion kinase (FAK) and Aurora kinase A (Aurora-A) are ubiquitously expressed kinase involved in cancer progression and with poor prognosis that are found overexpressed in various types of cancer. To validate FAK and Aurora-A as a TAA recognized by CD4 helper T lymphocytes (HTL), we have combined the use of predictive peptide/MHC class II binding algorithms with in vitro vaccination of CD4 T lymphocytes from healthy individuals and cancer patients. Synthetic peptides correspond to potential HTL epitopes induced HTL responses that directly recognized FAK/Aurora-A-expressing tumor cells and autologous dendritic cells pulsed with these TAA-expressing tumor cell lysates in an HLA class II-restricted manner. Moreover, since the FAK/Aurora-A peptides were recognized by cancer patient's CD4 T cells, the T helper peptide epitopes might be used for designing T cell-based immunotherapy for FAK/Aurora-A-expressing cancers.
|
-
-
[Journal Article] Characterization of human CD4 helper T cellresponses against Aurora kinase A2010
Author(s)
Kobayashi H, Azumi M, Hayashi S, Sato K, Aoki N, Kimura S, Kakizaki H, NagatoT, Harabuchi Y, Tateno M, Celis E
-
Journal Title
CancerImmunol Immunother
Volume: 59(7)
Pages: 1029-39
DOI
-
-
-
-
-