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鉴定EBNA1中被CD4(+) T细胞识别的HLA-DP3限制性肽段。

Identification of HLA-DP3-restricted peptides from EBNA1 recognized by CD4(+) T cells.

作者信息

Voo Kui Shin, Fu Tihui, Heslop Helen E, Brenner Malcolm K, Rooney Cliona M, Wang Rong-Fu

机构信息

The Center for Cell and Gene Therapy, Department of Immunology, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Cancer Res. 2002 Dec 15;62(24):7195-9.

Abstract

The EBV-encoded nuclear antigen 1 (EBNA1) is required for the maintenance and replication of the viral episome in EBV-transformed human B-lymphoblastoid cell lines. It is expressed in all EBV-associated tumors, making it a potentially important target for immunotherapy. However, this promise has not been realized, because an endogenously processed MHC class I-restricted T-cell epitope remains to be identified, and relatively little is known about MHC class II-restricted helper epitopes in the molecule. In this report, we identify a T-cell peptide derived from EBNA1 that is recognized by CD4(+) T cells. More importantly, EBNA1-specific, HLA-DP3-restricted CD4(+) T cells are capable of recognizing MHC class II-matched Burkitt's lymphoma cells, autologous peripheral blood mononuclear cells loaded with the purified EBNA1 protein, as well as target cells transfected with Ii-EBNA1 cDNA. These new findings demonstrate that EBNA1 is processed endogenously and presented to T cells by MHC class II molecules, and, hence, may be useful to incorporate into cancer vaccines to enhance antitumor immunity against EBV-associated tumors.

摘要

EB病毒编码的核抗原1(EBNA1)是EB病毒转化的人B淋巴母细胞系中病毒附加体维持和复制所必需的。它在所有EB病毒相关肿瘤中均有表达,使其成为免疫治疗的一个潜在重要靶点。然而,这一前景尚未实现,因为内源性加工的MHC I类限制性T细胞表位仍有待确定,而且关于该分子中MHC II类限制性辅助表位的了解相对较少。在本报告中,我们鉴定出一种源自EBNA1的T细胞肽,它可被CD4(+) T细胞识别。更重要的是,EBNA1特异性、HLA-DP3限制性CD4(+) T细胞能够识别MHC II类匹配的伯基特淋巴瘤细胞、负载纯化EBNA1蛋白的自体外周血单个核细胞以及用Ii-EBNA1 cDNA转染的靶细胞。这些新发现表明EBNA1可被内源性加工并由MHC II类分子呈递给T细胞,因此,将其纳入癌症疫苗中可能有助于增强针对EB病毒相关肿瘤的抗肿瘤免疫力。

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