Cross-reactivity of autoreactive T cells with MBP and viral antigens in patients with MS

被引:31
作者
Cheng, Weizhi [1 ]
Ma, Yanhui [1 ]
Gong, Fang [1 ]
Hu, Chaoying [1 ]
Qian, Liu [1 ]
Huang, Qiuyu [1 ]
Yu, Qiwen [1 ]
Zhang, Jiying [1 ]
Chen, Shengdi [2 ]
Liu, Zhengguo [3 ]
Chen, Xuehua [2 ]
Zhou, Tong [2 ]
Zhang, Dongqing [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Inst Immunol, Shanghai 200025, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Shanghai 200025, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Xinhua Hosp, Shanghai 200092, Peoples R China
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2012年 / 17卷
基金
中国国家自然科学基金;
关键词
Molecular mimicry; Multiple sclerosis; Human hepersvirus-6; Epstein-barr virus; Autoreactive T cell; CD8(+) T cell; MYELIN BASIC-PROTEIN; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; MULTIPLE-SCLEROSIS; IMMUNE-RESPONSES; CDR3; SEQUENCE; MODEL; HUMAN-HERPESVIRUS-6; EXPRESSION; PEPTIDES;
D O I
10.2741/4010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we detected the viral DNA of Human Herpes Virus 6 (HHV-6) in the sera and cell-free cerebrospinal fluid (CSF) of Chinese multiple sclerosis (MS) patients. The results revealed that the copy numbers of serum HHV-6 viral DNA were higher in MS than in normal subjects (NS) or in other neurologic diseases (OND). We also found that in the MS subjects, most T cells recognizing myelin basic protein (MBP) were cross-reactive and could be activated by a synthetic peptide corresponding to residues of HHV-6 or EBV. The estimated precursor frequency of these cross-reactive T cells recognizing both peptides, MBP and HHV-6 or EBV, was significantly elevated in MS compared with that in controls. More significant was the presence of CD8(+) cytotoxic cross-reactive T cells, as they could directly induce injury to oligodendrocytes that are known to express both MBP and MHC class I molecules. The study provides important evidence for understanding the potential role of HHV-6 or EBV infection in the pathogenesis of MS.
引用
收藏
页码:1648 / 1658
页数:11
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