A preliminary study of peripheral T-cell subsets in porokeratosis patients with or variants.

BACKGROUND

Porokeratosis (PK) is considered a skin-specific autoinflammatory keratinization disease. Intriguingly, four causative genes of PK are in turn arranged in mevalonate pathway, with variants being the commonest followed by variants in a cohort of Chinese patients. Evidence indicates that mevalonate metabolites induce trained immunity in human monocytes and regulate T cells at multiple levels. Of note, γδT cells are dually regulated by intracellular and extracellular mevalonate metabolism.

AIMS

To identify the possible differences in T-cell between or variants from PK patients.

MATERIALS & METHODS: Targeted exome sequencing and exonic CNV screening were performed in 26 patients with PK. Sanger sequencing was used to validate all identified variants. Among them, 22 patients were identified with or variants. PBMCs from 22 PK patients and 27 normal controls (NCs) were analysed by flow cytometry for the frequencies of T cells subsets, including IFN-γ-, and TNF-α-producing T cells.

RESULTS

There were 14 mutations identified in the 26 PK patients, including 6 novel mutations (: c.118_226+1337dup, c.388_392delGATATinsC, c.613A>T, c.768G>C, and : c.250C>T, c.988T>G). In contrast to NCs, significantly decreased frequencies of CD8 and Vγ9Vδ2 T cells were observed in the PK patients with variants. Moreover, it was found that dysregulated secretion of pro-inflammatory cytokines by T cells in both PK patients with and variants.

CONCLUSIONS

Our findings enriched the Human Gene Mutation Databases and showed probable differences in peripheral T cells subsets between PK patients and controls.