免疫原性
佐剂
抗原
CD8型
细胞毒性T细胞
表位
肿瘤抗原
癌症疫苗
免疫学
免疫系统
主要组织相容性复合体
生物
癌症研究
免疫疗法
体外
生物化学
作者
Eugene Maraskovsky,Sigrid Sjölander,Debbie Drane,Max Schnurr,Thuy T. Le,Luis Mateo,Thomas Luft,Kelly‐Anne Masterman,Tsin-Yee Tai,Qiyuan Chen,Simon Green,Anders Sjölander,Martin J. Pearse,François A. Lemonnier,Weisan Chen,Jonathan Cebon,Andreas Suhrbier
标识
DOI:10.1158/1078-0432.ccr-03-0245
摘要
Abstract NY-ESO-1 is a 180 amino-acid human tumor antigen expressed by many different tumor types and belongs to the family of “cancer-testis” antigens. In humans, NY-ESO-1 is one of the most immunogenic tumor antigens and NY-ESO-1 peptides have been shown to induce NY-ESO-1-specific CD8+ CTLs capable of altering the natural course of NY-ESO-1-expressing tumors in cancer patients. Here we describe the preclinical immunogenicity and efficacy of NY-ESO-1 protein formulated with the ISCOMATRIX adjuvant (NY-ESO-1 vaccine). In vitro, the NY-ESO-1 vaccine was readily taken up by human monocyte-derived dendritic cells, and on maturation, these human monocyte-derived dendritic cells efficiently cross-presented HLA-A2-restricted epitopes to NY-ESO-1-specific CD8+ T cells. In addition, epitopes of NY-ESO-1 protein were also presented on MHC class II molecules to NY-ESO-1-specific CD4+ T cells. The NY-ESO-1 vaccine induced strong NY-ESO-1-specific IFN-γ and IgG2a responses in C57BL/6 mice. Furthermore, the NY-ESO-1 vaccine induced NY-ESO-1-specific CD8+ CTLs in HLA-A2 transgenic mice that were capable of lysing human HLA-A2+ NY-ESO-1+ tumor cells. Finally, C57BL/6 mice, immunized with the NY-ESO-1 vaccine, were protected against challenge with a B16 melanoma cell line expressing NY-ESO-1. These data illustrate that the NY-ESO-1 vaccine represents a potent therapeutic anticancer vaccine.
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