Analyses of the TCR repertoire of MHC class II-restricted innate CD4+ Tcells

  • Byung Hyun Kang
  • , Hye Sook Min
  • , You Jeong Lee
  • , Bomi Choi
  • , Eun Ji Kim
  • , Jonghoon Lee
  • , Jeong Rae Kim
  • , Kwang Hyun Cho
  • , Tae Jin Kim
  • , Kyeong Cheon Jung
  • , Seong Hoe Park

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Analysis of the T-cell receptor (TCR) repertoire of innate CD4+ T cells selected by major histocompatibility complex (MHC) class II-dependent thymocyte–thymocyte (T-T) interaction (T-T CD4+ T cells) is essential for predicting the characteristics of the antigens that bind to these T cells and for distinguishing T-T CD4+ T cells from other types of innate T cells. Using the TCRmini Tg mouse model, we show that the repertoire of TCRα chains in T-T CD4+ T cells was extremely diverse, in contrast to the repertoires previously described for other types of innate T cells. The TCRα chain sequences significantly overlapped between T-T CD4+ T cells and conventional CD4+ T cells in the thymus and spleen. However, the diversity of the TCRα repertoire of T-T CD4+ T cells seemed to be restricted compared with that of conventional CD4+ T cells. Interestingly, the frequency of the parental OT-II TCRα chains was significantly reduced in the process of T-T interaction. This diverse and shifted repertoire in T-T CD4+ T cells has biological relevance in terms of defense against diverse pathogens and a possible regulatory role during peripheral T-T interaction.

Original languageEnglish
Article numbere154
JournalExperimental and Molecular Medicine
Volume47
Issue number3
DOIs
StatePublished - Mar 2015

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