HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Transcriptomes of MPO-Deficient Patients with Generalized Pustular Psoriasis Reveals Expansion of CD4+ Cytotoxic T Cells and an Involvement of the Complement System.

Abstract
Generalized pustular psoriasis is a severe psoriatic subtype characterized by epidermal neutrophil infiltration. Although variants in IL36RN and MPO have been shown to affect immune cells, a systematic analysis of neutrophils and PBMC subsets and their differential gene expression dependent on MPO genotypes was not performed yet. We assessed the transcriptomes of MPO-deficient patients using single-cell RNA sequencing of PBMCs and RNA sequencing of neutrophils in a stable disease state. Cell-type annotation by multimodal reference mapping of single-cell RNA-sequencing data was verified by flow cytometry of surface and intracellular markers; the proportions of CD4+ cytotoxic T lymphocytes and other CD4+ effector cells were increased in generalized pustular psoriasis, whereas the frequencies of naïve CD4+ T cells were significantly lower. The expression of FGFBP2 marking CD4+ cytotoxic T lymphocytes and CD8+ effector memory T cells was elevated in patients with generalized pustular psoriasis with disease-contributing variants compared with that in noncarriers (P = 0.0015). In neutrophils, differentially expressed genes were significantly enriched in genes of the classical complement activation pathway. Future studies assessing affected cell types and pathways will show their contribution to generalized pustular psoriasis's pathogenesis and indicate whether findings can be transferred to the acute epidermal situation and whether depletion or inactivation of CD4+ cytotoxic T lymphocytes may be a reasonable therapeutic approach.
AuthorsStefan Haskamp, Benjamin Frey, Ina Becker, Anja Schulz-Kuhnt, Imke Atreya, Carola Berking, David Pauli, Arif B Ekici, Johannes Berges, Rotraut Mößner, Dagmar Wilsmann-Theis, Michael Sticherling, Steffen Uebe, Philipp Kirchner, Ulrike Hüffmeier
JournalThe Journal of investigative dermatology (J Invest Dermatol) Vol. 142 Issue 8 Pg. 2149-2158.e10 (08 2022) ISSN: 1523-1747 [Electronic] United States
PMID34973310 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.
Chemical References
  • Peroxidase
Topics
  • Acute Disease
  • CD4-Positive T-Lymphocytes (pathology)
  • Chronic Disease
  • Humans
  • Leukocytes, Mononuclear (pathology)
  • Peroxidase (deficiency)
  • Psoriasis (pathology)
  • Skin Diseases, Vesiculobullous (pathology)
  • T-Lymphocytes, Cytotoxic
  • Transcriptome

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: