PRURISEQ: Transcriptomic Landscape of T Lymphocytes of Atopic Dermatitis, Atopic Prurigo Nodularis (of Besnier) and Non-atopic Prurigo Nodularis (of Hyde) Using Single Cell RNA-sequencing

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04681300
Collaborator
(none)
20
5.4

Study Details

Study Description

Brief Summary

Prurigo nodularis (PN) is a skin condition characterized by symmetrically distributed widespread, pruritic nodules that occurs in patients with chronic pruritus. There are 2 subtypes of PN depending on the association with an atopic dermatitis (AD) : atopic PN (Besnier) and non-atopic PN (Hyde). There are no approved therapies, and treatment options currently used have limited efficacy and their long-term use carries the risk of potential severe toxic effects.

The mechanisms triggering PN are still unknown. However, recent findings suggest a major role for the Th2 inflammatory pathway.

Beyond advancing the basic understanding of PN pathophysiology, our study might also pave the way for developing novel Th2-targeted therapeutic strategies for PN and AD. The primary objective of this study is to characterize the transcriptional profile of the T lymphocytes isolated from skin samples from patients with PN. This study will allow a gain a deeper understanding of the pathophysiologic mechanism of PN, a better classification of its subtypes, as well as their physiopathologic link with AD. Moreover, it will help shape new effective and safe therapeutic approaches in these diseases which are important for optimal therapeutic management.

Condition or Disease Intervention/Treatment Phase
  • Other: Skin biopsy
  • Other: Plastic surgery remnants

Study Design

Study Type:
Observational
Anticipated Enrollment :
20 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Transcriptomic Landscape of T Lymphocytes of Atopic Dermatitis, Atopic Prurigo Nodularis (of Besnier) and Non-atopic Prurigo Nodularis (of Hyde) Using Single Cell RNA-sequencing
Anticipated Study Start Date :
Feb 1, 2021
Anticipated Primary Completion Date :
Jul 15, 2021
Anticipated Study Completion Date :
Jul 15, 2021

Arms and Interventions

Arm Intervention/Treatment
Patients with atopic Prurigo nodularis , non-atopic Prurigo nodularis or atopic dermatitis

Other: Skin biopsy
a skin sample will be taken using a 4 mm punch biopsy in lesional skin

Patients with plastic surgery interventions

Other: Plastic surgery remnants
healthy skin from plastic surgery interventions

Outcome Measures

Primary Outcome Measures

  1. Transcriptional profile of the T lymphocytes [at inclusion]

Secondary Outcome Measures

  1. Inflammatory pathways [at inclusion]

  2. Molecular differences [at inclusion]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • More than 18 years of age

  • Signature of the written contentment

  • Clinical diagnostic of PN defined by the following: a minimum of 20 PN lesions, in total on both legs, and/or both arms; an average worst itch score of ≥7. Atopic PN will be defined as PN associating clinical sings or history of AD according to Hanifin et Rajka criteria. Non-Atopic PN will be defined as PN non-associated with clinical sings or history of AD according to Hanifin et Rajka criteria.

  • or confirmed diagnosis of AD according to Hanifin et Rajka criteria without associated PN.

  • Washout period for topical treatments (> 1 week) ans systemic treatments (> 1 month).

  • Indication and absence of contraindication to performing a skin biopsy as part of the treatment

Inclusion criteria for healthy controls:
  • more than 18 years of age

  • Signature of the written contentment

  • Hospitalised in the plastic surgery department of Saint-Louis Hospital.

  • No associated inflammatory or tumoral skin condition

  • No contraindication for biopsy

Exclusion criteria :
  • Presence of inflammatory or tumoral skin morbidities other than PN and atopic dermatitis

  • Treatment induced pruritus

  • Pruritus secondary to other medical conditions such as bullous dermatosis, renal insufficiency, infectious diseases, …)

  • AD under biologic therapy

  • Patient under guardianship or conservatorship

  • No health insurance coverage

  • Patient under State Medical Assistance (AME)

  • Pregnancy or breastfeeding

  • Persons deprived of their liberty by a judicial or administrative decision

  • People undergoing psychiatric care making their consent impossible

  • Adults who are the subject of a legal protection measure or unable to express their consent

  • Patients unable to read and write

Exclusion criteria for healthy controls:
  • Inflammatory or tumoral medical condition

  • Biological therapy for any other medical condition

  • Associated inflammatory or tumoral skin condition

  • Pregnancy or breastfeeding

  • Persons deprived of their liberty by a judicial or administrative decision

  • People undergoing psychiatric care making their consent impossible

  • Adults who are the subject of a legal protection measure or unable to express their consent

  • Patients unable to read and write

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assistance Publique - Hôpitaux de Paris

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT04681300
Other Study ID Numbers:
  • APHP200325
First Posted:
Dec 23, 2020
Last Update Posted:
Feb 9, 2021
Last Verified:
Dec 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 9, 2021