Literature DB >> 32875554

Preselection TCR repertoire predicts CD4+ and CD8+ T-cell differentiation state.

Xianliang Hou1,2, Wenbiao Chen1, Xujun Zhang1, Guangyu Wang2, Jianing Chen1, Ping Zeng1, Xuyan Fu1, Qiong Zhang1, Xiangdong Liu3, Hongyan Diao1.   

Abstract

T cells must display diversity regarding both the cell state and T-cell receptor (TCR) repertoire to provide effective immunity against pathogens; however, the generation and evolution of cellular T-cell heterogeneity in the adaptive immune system remains unclear. In the present study, a combination of multiplex PCR and immune repertoire sequencing (IR-seq) was used for a standardized analysis of the TCR β-chain repertoire of CD4+ naive, CD4+ memory, CD8+ naive and CD8+ memory T cells. We showed that the T-cell subsets could be distinguished from each another with regard to the TCR β-chain (TCR-β) diversity, CDR3 length distribution and TRBV usage, which could be observed both in the preselection and in the post-selection repertoire. Moreover, the Dβ-Jβ and Vβ-Dβ combination patterns at the initial recombination step, template-independent insertion of nucleotides and inter-subset overlap were consistent between the pre- and post-selection repertoires, with a remarkably positive correlation. Taken together, these results support differentiation of the CD4+ and CD8+ T-cell subsets prior to thymic selection, and these differences survived both positive and negative selection. In conclusion, these findings provide deeper insight into the generation and evolution of TCR repertoire generation.
© 2020 John Wiley & Sons Ltd.

Entities:  

Keywords:  T-cell receptor; cell subsets; deep sequencing

Mesh:

Substances:

Year:  2020        PMID: 32875554      PMCID: PMC7692249          DOI: 10.1111/imm.13256

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  24 in total

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Journal:  Front Immunol       Date:  2019-02-26       Impact factor: 7.561

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