| Literature DB >> 28895362 |
Shuo Wang1, Hongxia Fan2, Yang Li3, Huaguo Zheng3, Xin Li3, Changfei Li3, Lizhao Chen3, Ying Ju3, Songdong Meng3,4.
Abstract
Cancer stem cells are currently under intensive investigation due to their capabilities for tumor initiation, self-renewal, and resistance to chemotherapy. CD133 is implicated in stemness and the malignancy of tumor cells. Here, we explored heat shock protein gp96 adjuvanted CD133 epitope vaccine against leukemia. We screened and identified three H2-Kd-restricted cytotoxic T lymphocyte (CTL) epitopes derived from CD133, CD133₄₁₉₋₄₂₈, CD133₇₀₂₋₇₁₀ and CD133₇₆₀₋₇₆₉. The immunogenicity and antitumor activity of the epitope vaccine using heat shock protein gp96 as adjuvant were further determined in CD133⁺ leukemia xenograft mice. Finally, we demonstrate that adoptive transfer of epitope-specific CTLs led to suppression of leukemia growth. Our data therefore provide the basis for designing a CD133 epitope vaccine to activate specific CTLs against CD133⁺ leukemia and other cancers.Entities:
Keywords: CD133; CTL; epitope; gp96; leukemia
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Year: 2017 PMID: 28895362 DOI: 10.13345/j.cjb.160481
Source DB: PubMed Journal: Sheng Wu Gong Cheng Xue Bao ISSN: 1000-3061