| Literature DB >> 31924652 |
Annette Ko1, Masashi Watanabe2, Thomas Nguyen1, Alvin Shi3, Achouak Achour1, Baojun Zhang4, Xiaoping Sun1, Qun Wang4, Yuan Zhuang4, Nan-Ping Weng5, Richard J Hodes6.
Abstract
Thymic regulatory T cells (tTreg) are critical in the maintenance of normal T cell immunity and tolerance. The role of TCR in tTreg selection remains incompletely understood. In this study, we assessed TCRα and TCRβ sequences of mouse tTreg and thymic conventional CD4+ T cells (Tconv) by high-throughput sequencing. We identified αβ TCR sequences that were unique to either tTreg or Tconv and found that these were distinct as recognized by machine learning algorithm and by preferentially used amino acid trimers in αβ CDR3 of tTreg. In addition, a proportion of αβ TCR sequences expressed by tTreg were also found in Tconv, and machine learning classified the great majority of these shared αβ TCR sequences as characteristic of Tconv and not tTreg. These findings identify two populations of tTreg, one in which the regulatory T cell fate is associated with unique properties of the TCR and another with TCR properties characteristic of Tconv for which tTreg fate is determined by factors beyond TCR sequence.Entities:
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Year: 2020 PMID: 31924652 PMCID: PMC7002224 DOI: 10.4049/jimmunol.1901006
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422