An immunodominant SSX-2-derived epitope recognized by CD4+ T cells in association with HLA-DR

Détails

ID Serval
serval:BIB_E82E81398C61
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
An immunodominant SSX-2-derived epitope recognized by CD4+ T cells in association with HLA-DR
Périodique
Journal of Clinical Investigation
Auteur⸱e⸱s
Ayyoub  M., Hesdorffer  C. S., Montes  M., Merlo  A., Speiser  D., Rimoldi  D., Cerottini  J. C., Ritter  G., Scanlan  M., Old  L. J., Valmori  D.
ISSN
0021-9738 (Print)
Statut éditorial
Publié
Date de publication
04/2004
Volume
113
Numéro
8
Pages
1225-33
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Apr
Résumé
Ectopic gene expression in tumors versus normal somatic tissues provides opportunities for the specific immunotargeting of cancer cells. SSX gene products are expressed in tumors of different histological types and can be recognized by tumor-reactive CTLs from cancer patients. Here, we report the identification of an SSX-2-derived immunodominant T cell epitope recognized by CD4(+) T cells from melanoma patients in association with HLA-DR. The epitope maps to the 37-58 region of the protein, encompassing the sequence of the previously defined HLA-A2-restricted immunodominant epitope SSX-2(41-49). SSX-2(37-58)-specific CD4(+) T cells were detected among circulating lymphocytes from the majority of melanoma patients analyzed and among tumor-infiltrating lymphocytes, but not in healthy donors. Together, our data suggest a dominant role of the 37-58 sequence in the induction of cellular CD4(+) T cell responses against SSX antigens and will be instrumental for both the onset and the monitoring of upcoming cancer-vaccine trials using SSX-derived immunogens.
Mots-clé
Amino Acid Sequence CD4-Positive T-Lymphocytes/*immunology Cancer Vaccines/*immunology *Epitopes, T-Lymphocyte HLA-DR Antigens/*immunology Humans *Immunodominant Epitopes Melanoma/immunology Molecular Sequence Data Neoplasm Proteins/*immunology Peptide Fragments/immunology Repressor Proteins/*immunology
Pubmed
Web of science
Open Access
Oui
Création de la notice
28/01/2008 12:13
Dernière modification de la notice
20/08/2019 17:11
Données d'usage