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High-throughput T cell receptor sequencing identifies clonally expanded CD8+ T cell populations in alopecia areata.


ABSTRACT: Alopecia areata (AA) is an autoimmune disease in which cytotoxic T cells specifically target growing hair follicles. We used high-throughput TCR sequencing in the C3H/HeJ mouse model of AA and in human AA patients to gain insight into pathogenic T cell populations and their dynamics, which revealed clonal CD8+ T cell expansions in lesional skin. In the C3H/HeJ model, we observed interindividual sharing of TCR? chain protein sequences, which strongly supports a model of antigenic drive in AA. The overlap between the lesional TCR repertoire and a population of CD8+NKG2D+ T cells in skin-draining lymph nodes identified this subset as pathogenic effectors. In AA patients, treatment with the oral JAK inhibitor tofacitinib resulted in a decrease in clonally expanded CD8+ T cells in the scalp but also revealed that many expanded lesional T cell clones do not completely disappear from either skin or blood during treatment with tofacitinib, which may explain in part the relapse of disease after stopping treatment.

SUBMITTER: de Jong A 

PROVIDER: S-EPMC6237451 | biostudies-literature | 2018 Oct

REPOSITORIES: biostudies-literature

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High-throughput T cell receptor sequencing identifies clonally expanded CD8+ T cell populations in alopecia areata.

de Jong Annemieke A   Jabbari Ali A   Dai Zhenpeng Z   Xing Luzhou L   Lee Dustin D   Li Mei Mei MM   Duvic Madeleine M   Hordinsky Maria M   Norris David A DA   Price Vera V   Mackay-Wiggan Julian J   Clynes Raphael R   Christiano Angela M AM  

JCI insight 20181004 19


Alopecia areata (AA) is an autoimmune disease in which cytotoxic T cells specifically target growing hair follicles. We used high-throughput TCR sequencing in the C3H/HeJ mouse model of AA and in human AA patients to gain insight into pathogenic T cell populations and their dynamics, which revealed clonal CD8+ T cell expansions in lesional skin. In the C3H/HeJ model, we observed interindividual sharing of TCRβ chain protein sequences, which strongly supports a model of antigenic drive in AA. The  ...[more]

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