Publication | Open Access
High Frequency of Herpesvirus-Specific Clonotypes in the Human T Cell Repertoire Can Remain Stable over Decades with Minimal Turnover
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Citations
14
References
2012
Year
Viral ReplicationAdaptive Immune SystemT-regulatory CellImmunologyImmunodominancePathologyHigh FrequencyImmunotherapyViral PersistenceEpstein-barr VirusHuman RetrovirusHematologyViral GeneticsNeurovirologyVirologyAutoimmunityT Cell ImmunityMinimal TurnoverChronic Viral InfectionCell BiologyT Cell ExpansionsHerpesvirus-specific ClonotypesPathogenesisMinimal InflationHerpesvirusesAdult T-cell Leukemia-lymphomaMedicine
High-throughput T cell receptor sequencing on sequentially banked blood samples from healthy individuals has shown that high-frequency clonotypes can remain relatively stable for up to 18 years, with minimal inflation, deflation, or turnover. These populations included T cell expansions specific for Epstein-Barr virus. Thus, in spite of exposure to a barrage of microorganisms over the course of life, the dominant clonotypes in the mature peripheral T cell repertoire can alter surprisingly little.
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