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热激蛋白gp96免疫学功能及在主动免疫治疗肿瘤和传染病中的应用
引用本文:徐亚星,王赛锋,张小俊,孟颂东.热激蛋白gp96免疫学功能及在主动免疫治疗肿瘤和传染病中的应用[J].生物工程学报,2012,28(3):261-266.
作者姓名:徐亚星  王赛锋  张小俊  孟颂东
作者单位:中国科学院微生物研究所 中国科学院病原微生物与免疫学重点实验室,北京 100101;中国科学院微生物研究所 中国科学院病原微生物与免疫学重点实验室,北京 100101;中国科学院微生物研究所 中国科学院病原微生物与免疫学重点实验室,北京 100101;中国科学院微生物研究所 中国科学院病原微生物与免疫学重点实验室,北京 100101
基金项目:国家自然科学基金 (Nos. 30970146, 91029724, 81021003) 资助。
摘    要:热激蛋白gp96可特异性结合来源于肿瘤和病毒的抗原肽,与抗原呈递细胞表面CD91等受体作用进入胞内,并在内质网中将结合的抗原通过抗原呈递链呈递给MHCI类分子,激活特异性T细胞。同时,与细胞表面Toll样受体(TLR)TLR2、TLR4等相互作用,激活天然免疫。近期研究发现调节性T细胞(Treg)对gp96免疫功能有显著抑制作用,随着对影响gp96免疫功能的免疫抑制机制的深入了解,以及利用汉逊酵母表达有免疫活性的全长gp96蛋白体系的建立,gp96将在治疗肿瘤及传染性疾病中发挥更大的作用。

关 键 词:gp96  T细胞  调节性T细胞  肿瘤  传染病
收稿时间:2011/12/7 0:00:00

Immune activity of heat shock protein gp96 and its application in active immunotherapy for tumor and infectious diseases
Yaxing Xu,Saifeng Wang,Xiaojun Zhang and Songdong Meng.Immune activity of heat shock protein gp96 and its application in active immunotherapy for tumor and infectious diseases[J].Chinese Journal of Biotechnology,2012,28(3):261-266.
Authors:Yaxing Xu  Saifeng Wang  Xiaojun Zhang and Songdong Meng
Institution:CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China;CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China;CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China;CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China
Abstract:Heat-shock protein gp96 associates with antigenic peptides derived from tumor and virus. Exogenous gp96-peptide complexes are taken up by antigen-presenting cells through interaction with its receptor CD91 on the cell surface, and cross-present antigenic peptides to MHC class I molecules by a peptide relay line in the endoplasmic reticulum for specific T-cell activation. Meanwhile, gp96 has been shown to initiate innate immune responses through interaction with toll-like receptor 2 and toll-like receptor 4. Recent studies have shown a gp96-mediated immune balance between CTL and Tregs. With the further understanding of counteracting immunosuppressive mechanisms in gp96-induced cellular immune responses, and establishment of high level production of recombinant gp96 by the yeast, gp96 appears to be a promising candidate for designing effective therapeutic vaccines against tumor and infectious diseases.
Keywords:gp96  T cell  regulatory T cell (Treg)  tumor  infectious diseases
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