Kobayashi H, Lu J, Celis E
Department of Immunology and Cancer Center, Mayo Clinic and Mayo Graduate School, Rochester, Minnesota 55905, USA.
Cancer Res. 2001 Oct 15;61(20):7577-84.
The melanocyte-associated antigen gp100 constitutes one of the most attractive targets for T-cell-based immunotherapy against malignant melanoma. Although several MHC class I-restricted epitopes have been identified for CTLs, thus far, only one MHC class II T helper epitope (restricted by HLA-DR4) has been described in the literature. Using an algorithm to identify promiscuous helper T-cell epitopes, here we describe three additional MHC class II-restricted epitopes from gp100. Whereas one T helper epitope, gp100(175-189), was restricted by the HLA-DR53 and DQw6 alleles, the T-cell responses to two other epitopes, gp100(74-89) and gp100(576-590), were restricted by HLA-DR7. Most interestingly, the newly identified helper T lymphocyte epitopes encompass or lie proximal to previously described CTL epitopes for this tumor-associated antigen. Together with the previously described HLA-DR4-restricted epitope, these T helper epitopes offer coverage for the majority of the human population. Moreover, the use of peptide vaccines containing both CTLs and T helper epitopes could offer therapeutic advantages over current approaches that focus solely on eliciting antitumor CTL responses.
黑色素细胞相关抗原gp100是基于T细胞的恶性黑色素瘤免疫治疗中最具吸引力的靶点之一。尽管已经为细胞毒性T淋巴细胞(CTL)鉴定了几种MHC I类限制性表位,但迄今为止,文献中仅描述了一种MHC II类辅助性T细胞表位(受HLA - DR4限制)。我们使用一种算法来鉴定通用辅助性T细胞表位,在此描述了来自gp100的另外三种MHC II类限制性表位。其中一个辅助性T细胞表位gp100(175 - 189)受HLA - DR53和DQw6等位基因限制,而对另外两个表位gp100(74 - 89)和gp100(576 - 590)的T细胞反应受HLA - DR7限制。最有趣的是,新鉴定的辅助性T淋巴细胞表位包含或紧邻此前针对该肿瘤相关抗原描述的CTL表位。连同此前描述的受HLA - DR4限制的表位,这些辅助性T细胞表位覆盖了大多数人群。此外,使用包含CTL表位和辅助性T细胞表位的肽疫苗可能比目前仅专注于引发抗肿瘤CTL反应的方法具有治疗优势。