Suppr超能文献

[对特异性细胞毒性T淋巴细胞识别的肿瘤排斥抗原肽的分析]

[Analysis of tumor rejection antigen peptides recognized by specific CTL].

作者信息

Uenaka A, Nakayama E

机构信息

Department of Parasitology and Immunology, Okayama University Medical School.

出版信息

Nihon Rinsho. 1996 Jan;54(1):242-9.

PMID:8587197
Abstract

Tumor rejection antigens, recognized by cytotoxic T lymphocytes (CTL), have been identified in several tumors. In malignant melanoma MAGE-1 and -3 antigen peptides, recognized by specific CTL, were defined. Tyrosinase, gp100 and Melan A/MART-1, normally expressed in the melanosome, were also shown to be recognized by specific CTL. In murine tumors, three antigenic peptides were identified. These are P1A in mastocytoma P815, MUT1 in murine lung carcinoma (3LL) derived from connexin 37, and pRL1 in murine leukemia RL male 1 derived from c-akt proto-oncogene. Analysis of the tumor rejection antigen peptides will elucidate the molecular nature of the tumor rejection antigen and facilitate their therapeutic use as tumor vaccine.

摘要

细胞毒性T淋巴细胞(CTL)识别的肿瘤排斥抗原已在多种肿瘤中得到鉴定。在恶性黑色素瘤中,已确定了可被特异性CTL识别的MAGE-1和-3抗原肽。通常在黑素小体中表达的酪氨酸酶、gp100和Melan A/MART-1也被证明可被特异性CTL识别。在鼠类肿瘤中,鉴定出了三种抗原肽。它们分别是肥大细胞瘤P815中的P1A、源自连接蛋白37的鼠肺癌(3LL)中的MUT1,以及源自c-akt原癌基因的鼠白血病RL male 1中的pRL1。对肿瘤排斥抗原肽的分析将阐明肿瘤排斥抗原的分子本质,并促进其作为肿瘤疫苗的治疗应用。

相似文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验