Lovett-Racke A E, Martin R, McFarland H F, Racke M K, Utz U
Neuroimmunology Branch, National Institute of Neurologic Diseases and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
J Neuroimmunol. 1997 Sep;78(1-2):162-71. doi: 10.1016/s0165-5728(97)00097-0.
This study analyzed the stability of the myelin basic protein (MBP)-specific T-cell receptor (TCR) repertoire during the course of multiple sclerosis (MS) in three patients who were monitored for three years by gadolinium-enhanced magnetic resonance imaging. Bulk-culture T-cell lines (TCLs) were generated from 3-4 time points for each patient, including times of active and quiescent disease. TCR analysis of these TCLs indicated that both the V alpha and V beta usage was similar over time for each patient. Sequencing of TCRs demonstrated conserved complementarity-determining region 3 (CDR3) sequences within TCLs that expressed the same V alpha segment over time, although the J alpha usage was different for each TCR. This indicates that the population of MBP-reactive T-cells is changing during the course of MS, but that host and/or environmental factors may be selecting T-cells with particular MHC/peptide binding domains.
本研究分析了三名接受钆增强磁共振成像监测三年的多发性硬化症(MS)患者病程中髓鞘碱性蛋白(MBP)特异性T细胞受体(TCR)库的稳定性。从每位患者的3 - 4个时间点(包括疾病活动期和静止期)获取样本建立大量培养T细胞系(TCLs)。对这些TCLs进行TCR分析表明,每位患者随着时间推移Vα和Vβ的使用情况相似。TCR测序显示,随着时间推移,表达相同Vα片段的TCLs内互补决定区3(CDR3)序列保守,尽管每个TCR的Jα使用情况不同。这表明在MS病程中,MBP反应性T细胞群体在发生变化,但宿主和/或环境因素可能在选择具有特定MHC/肽结合域的T细胞。