2017 Fiscal Year Final Research Report
Functional analysis of senescence-Associated T cells (SA-T)
Project/Area Number |
26460066
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Biological pharmacy
|
Research Institution | Keio University (2015-2017) Kyoto University (2014) |
Principal Investigator |
INOUE Joe 慶應義塾大学, 政策・メディア研究科(藤沢), 特任准教授 (00433714)
|
Project Period (FY) |
2014-04-01 – 2018-03-31
|
Keywords | 免疫老化 / 自己免疫疾患 / 胚中心 |
Outline of Final Research Achievements |
Our group has found and identified senescence-associated T cells (SA-T) which increase with age. In this study, the functions of SA-T in aged mice and various disease model mice were analyzed. Increase of SA-T and increase of germinal center reaction were confirmed in aged mice, and auto-antibody increased in some individuals. Similarly, NZB / W-F1 mouse, an autoimmune disease model mouse, showed an increase in SA-T, an increase in germinal center reaction and auto-antibody production from young age as compared with wild type mouse. Interestingly, analysis of mice lacking B cells revealed that there was almost no SA-T despite being an aged individual.
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Free Research Field |
免疫学
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