Distinct but overlapping T helper epitopes in the 37-58 region of SSX-2
Details
Serval ID
serval:BIB_4FDC597DC998
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Distinct but overlapping T helper epitopes in the 37-58 region of SSX-2
Journal
Clinical Immunology
ISSN
1521-6616 (Print)
Publication state
Published
Issued date
01/2005
Volume
114
Number
1
Pages
70-8
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Jan
Research Support, Non-U.S. Gov't --- Old month value: Jan
Abstract
Because of their specific expression in tumors of different histological types, the products of the SSX genes are important candidate targets for development of cancer vaccines. We have previously identified two immunodominant SSX-2-derived T cell epitopes recognized by HLA-A2-restricted CD8+ T cells (SSX-2 41-49) and HLA-DR11-restricted CD4+ T cells (SSX-2 45-59), respectively. In this study, we report the identification of an HLA-DR3-restricted epitope mapping to the 37-51 region of SSX-2, overlapping both previously identified epitopes. As about one fifth of individuals from several major ethnic groups express HLA-DR3, the identification of this epitope significantly increases the percent of patients that are expected to mount specific CD4+ T cell responses following vaccination with peptides in this region of SSX-2. Retrieval of multiple overlapping epitopes in a defined region of SSX-2 protein suggests the presence of a "hot spot" for T cell recognition that may prove sufficient for the induction of immune responses.
Keywords
Alleles
Amino Acid Sequence
CD4-Positive T-Lymphocytes/*immunology
Cells, Cultured
Epitope Mapping
Epitopes, T-Lymphocyte/*chemistry/genetics
HLA-DR Antigens/immunology
HLA-DR3 Antigen/immunology
Humans
Melanoma/immunology
Molecular Sequence Data
Neoplasm Proteins/immunology
Peptide Fragments/*immunology
Repressor Proteins/*immunology
T-Lymphocytes, Helper-Inducer/immunology
Pubmed
Web of science
Create date
28/01/2008 11:13
Last modification date
20/08/2019 14:05