Transcriptomic response of peripheral blood mononuclear cells to secukinumab in epidermolytic ichthyosis

Author:

Hou Ping-Chen1,Hong Yi-Kai123,Lin Yu-Chen12,Yang Min-Chia14,Hsu Chung-Ting5,McGrath John A16ORCID,Hsu Chao-Kai127ORCID

Affiliation:

1. Department of Dermatology

2. International Center for Wound Repair and Regeneration (iWRR), National Cheng Kung University , Tainan , Taiwan

3. Department of Dermatology, Feinberg School of Medicine, Northwestern University , Chicago, IL , USA

4. Education Center, National Cheng Kung University Hospital

5. Division of Neonatology, Department of Pediatrics, Taichung Veterans General Hospital , Taichung , Taiwan

6. St John’s Institute of Dermatology, School of Basic and Medical Biosciences, King’s College London , London , UK

7. Institute of Clinical Medicine, College of Medicine

Abstract

Epidermolytic ichthyosis (EI) is a subtype of ichthyosis, characterized by generalized blistering and erythroderma since birth followed by scaling and palmoplantar keratoderma. Several major orphan forms of ichthyosis have been linked to T helper (Th)17 signalling upregulation. Anecdotal reports also described the beneficial role of Th17-targeted agents in ichthyosis. However, the therapeutic efficacy and the transcriptomic changes caused by secukinumab in EI have rarely been discussed. We present a patient treated with secukinumab for 1 year and evaluated the transcriptomic alterations in peripheral blood after treatment, which revealed that interleukin-1 signalling and Toll-like receptor 2 cascade may underpin the inflammatory and hyperkeratotic footprint in EI.

Funder

International Center for Wound Repair

National Cheng Kung University Hospital

Publisher

Oxford University Press (OUP)

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