Comparative study on the immunogenicity between an HLA-A24-restricted cytotoxic T-cell epitope derived from survivin and that from its splice variant survivin-2B in oral cancer patients.
Comparative study on the immunogenicity between an HLA-A24-restricted cytotoxic T-cell epitope derived from survivin and that from its splice variant survivin-2B in oral cancer patients.
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DOI:
10.1186/1479-5876-7-1
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发表时间:
2009-01-06
影响因子:
7.4
通讯作者:
Sato N
中科院分区:
文献类型:
--
作者:
Kobayashi J;Torigoe T;Hirohashi Y;Idenoue S;Miyazaki A;Yamaguchi A;Hiratsuka H;Sato N
We previously reported an HLA-A24-restricted cytotoxic T-cell epitope, Survivin-2B80-88, derived from a splice variant of survivin, survivin-2B. In this report, we show a novel HLA-A24-restricted T-cell epitope, Survivin-C58, derived from a wild type survivin, and compared their immunogenicity in oral cancer patients. By stimulating peripheral blood lymphocytes of HLA-A24-positive cancer patients with Survivin-C58 peptide in vitro, the peptide-specific CTLs were induced. In order to compare the immunogenic potential between C58 peptide and 2B80-88 peptide, peripheral blood T-cells from thirteen HLA-A24-positive oral cancer patients were stimulated with either or both of these two peptides. Survivin-2B80-88 peptide-specific CTLs were induced from four patients, and C58 peptide-specific CTLs were induced from three out of eight patients with over stage II progression. The CTLs exerted cytotoxicity against HLA-A24-positive tumor cells. In contrast, CTL induction failed from a healthy volunteer and all four patients with cancer stage I. It was indicated that a splicing variant-derived peptide and wild type survivin-derived peptide might have a comparable potency of CTL induction, and survivin targeting immunotherapy using survivin-2B80-88 and C58 peptide cocktail should be suitable for HLA-A24+ oral cancer patients.
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影响因子:
11.5
作者:
Idenoue, S;Hirohashi, Y;Sato, N
通讯作者:
Sato, N
影响因子:
6.4
作者:
Rosato, Antonio;Pivetta, Michela;Zanovello, Paola
通讯作者:
Zanovello, Paola
影响因子:
11.2
作者:
Asanuma, H;Torigoe, T;Sato, N
通讯作者:
Sato, N
影响因子:
8
作者:
Caldas, H;Jiang, YY;Altura, RA
通讯作者:
Altura, RA
影响因子:
4.4
作者:
Sato, Y;Nabeta, Y;Sato, N
通讯作者:
Sato, N