Publication Summary

DUCRAY

Effective inhibition of Th17/Th22 pathway in 2D and 3D human models of psoriasis by celastrol enriched plant cell culture extract

T. Nguyen, F. Lestienne, A. Cousy, V. Mengeaud, N. Castex-Rizzi
Journal of the European Academy of Dermatology and Venereology
2020

Objective

Evaluate the immunomodulatory effect of Celastrol in in vitro models of psoriatic inflammation.

Celastrol is a triterpene produced in vitro from Tripterygium Wilfordii plant cell culture (patented technique developed by the Pierre Fabre Research Center's biotechnology unit).

  

Methodology

Preincubation of human CD4+ T lymphocytes (hCD4), normal human keratinocytes (NHEK), micro-epidermis and reconstructed human epidermis (RHE) with Celastrol and reference controls

 

Evaluation Criteria

Quantification of psoriasis biomarkers by enzyme-linked immunosorbent assay (ELISA)

Results

 

  • CD4+ T LYMPHOCYTES

 

Celastrol inhibits IL-17A and IL-22 cytokine production in a dose-dependent manner

Lymphocytes T CD4+ humains stimulés par des anticorps anti-CD3 et anti-CD28
Human CD4* T lymphocytes stimulated by anti-CD3 and anti-CD28 antibodies
  • RECONSTRUCTED HUMAN EPIDERMIS:

Celastrol inhibits the production of the pro-inflammatory mediator IL-8

Epiderme humain reconstruit incubé avec du Célastrol (TW)  ou un contrôle avant stimulation et quantification
Reconstructed human epidermis incubated with Celastrol (TW) or a control before stimulation and quantification

Conclusion

Celastrol modulates TH17/TH22 inflammation by acting on 2 targets: T lymphocytes and keratinocytes.

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