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作 者:Hanjie Li Congting Ye Guoli Ji Jiahuai Han
机构地区:[1]State Key Laboratory of Cellular Stress Biology and School of Life Sciences,Xiamen University,Xiamen,Fujian 361005,China [2]Department of Automation,Xiamen University,Xiamen,Fujian 361005,China
出 处:《Cell Research》2012年第1期33-42,共10页细胞研究(英文版)
基 金:This work was supported by the National Basic Research Pro- gram of China (973 Program; 2009CB522200), the National Natu- ral Science Foundation of China (30830092, 30921005, 91029304, 81061160512, 61174161), Sino-Swiss International Collaboration Grant (2009DFA32760), the Science Planning Program of Fujian Province (2009J1010), the Specialized Research Fund for the Doc- toral Program of Higher Education of China (20090121110022), and the Fundamental Research Funds for the Central Univer- sities of Xiamen University (2011121047, 201112G018 and CXB2011035).
摘 要:Historically, sharing T cell receptors (TCRs) between individuals has been speculated to be impossible, consider- ing the dramatic discrepancy between the potential enormity of the TCR repertoire and the limited number of T cells generated in each individual. However, public T cell response, in which multiple individuals share identical TCRs in responding to a same antigenic epitope, has been extensively observed in a variety of immune responses across many species. Public T cell responses enable individuals within a population to generate similar antigen-specific TCRs against certain ubiquitous pathogens, leading to favorable biological outcomes. However, the relatively concentrated feature of TCR repertoire may limit T cell response in a population to some other pathogens. It could be a great ben- efit for human health if public T cell responses can be manipulated. Therefore, the mechanistic insight of public TCR generation is important to know. Recently, high-throughput DNA sequencing has revolutionized the study of immune receptor repertoires, which allows a much better understanding of the factors that determine the overlap of TCR repertoire among individuals. Here, we summarize the current knowledge on public T-cell response and discuss fu- ture challenges in this field.
关 键 词:public T cell response convergent recombination recombinatorial biases thymic selection
分 类 号:S852.4[农业科学—基础兽医学] TM54[农业科学—兽医学]
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