In vitro induction of specific CD8+ T lymphocytes by tumor-associated antigenic peptides in patients with oral squamous cell carcinoma

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 mononucle...

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Veröffentlicht in:Cancer letters 2012-09, Vol.322 (1), p.86-91
Hauptverfasser: Toyoshima, Takeshi, Kumamaru, Wataru, Hayashida, Jun-nosuke, Moriyama, Masahumi, Kitamura, Ryoji, Tanaka, Hideaki, Yamada, Akira, Itoh, Kyogo, Nakamura, Seiji
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Sprache:eng
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Zusammenfassung: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.
ISSN:0304-3835
1872-7980
DOI:10.1016/j.canlet.2012.02.016