Author/Authors :
Toyoshima، نويسنده , , Takeshi and Kumamaru، نويسنده , , Wataru and Hayashida، نويسنده , , Jun-nosuke and Moriyama، نويسنده , , Masahumi and Kitamura، نويسنده , , Ryoji and Tanaka، نويسنده , , Hideaki and Yamada، نويسنده , , Akira and Itoh، نويسنده , , Kyogo and Nakamura، نويسنده , , Seiji، نويسنده ,
Abstract :
The aim of this study was to clarify candidate peptides for peptide-based specific immunotherapy of patients with oral squamous cell carcinoma (SCC). Thirteen peptides were examined for in vitro induction of peptide-specific CD8+ T lymphocyte (CD8+TL) activity in peripheral blood mononuclear cells from 35 patients with oral SCC. A correlation between the induction ability of CD8+TL and in vivo immune response of host was carried out immunohistochemically in 23 patients. Peptide-specific activities of CD8+TL for at least one peptide were detectable in 21/35 patients (60.0%). The potent peptides were SART-1690 in 9/35 (25.7%), SART-293, and ART475 in 7/35 (20.0%), respectively. In the 9 patients with SART-1690-specific activity, the whole of activities was significantly inducible for more number of other peptides compared to that in 26 patients without the activity (P = 0.035). Cellular responses in 7 patients with SART-1690-specific activity were significantly stronger than those in 16 patients without the activity (P = 0.027). Furthermore, the number of CD3+ T cells around the SCC was also significantly different between the 2 groups of patients (P = 0.041). In conclusion, SART-1690, SART-293, and ART475 could be applicable as peptide-based specific immunotherapies for the majority of patients with oral SCC.
Keywords :
Peptide-based specific immunotherapy , Tumor-associated antigenic peptides , Peptide-specific CD8+ T lymphocyte (CD8+TL) , Oral squamous cell carcinoma (SCC)