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Development of Stem Cell-derived Antigen-specific Regulatory T Cells Against Autoimmunity
Published on: November 8, 2016
Anti-cytokine therapies for psoriasis
Kristine E Nograles1, James G Krueger
1Laboratory for Investigative Dermatology, The Rockefeller University, New York, NY, USA.
Abstract:
Current approaches for the treatment of psoriasis with anti-cytokine therapies involve the blockade of TNF-α, or the p40 sub-unit of IL-12 and IL-23. However, the field is currently evolving to test more selective antagonists, such as anti-IL-23p19, IL-17 and other inflammatory cytokines. Here we discuss our current understanding of dendritic cell and T cell subsets that are relevant in psoriasis, and the pharmacologic strategies that temper their activity in this disease.
Insights
Current psoriasis treatments target TNF-α, IL-12, and IL-23. Emerging therapies focus on selective blockade of cytokines like IL-23p19 and IL-17, targeting key immune cells involved in the disease.
Area of Science:
- Immunology
- Dermatology
- Pharmacology
Background:
- Psoriasis treatment currently relies on anti-cytokine therapies targeting TNF-α, IL-12, and IL-23.
- The therapeutic landscape is shifting towards more selective antagonists.
Purpose of the Study:
- To review current understanding of dendritic cell and T cell subsets in psoriasis.
- To discuss evolving pharmacologic strategies targeting these immune cells.
Main Methods:
- Review of current literature on psoriasis pathogenesis and treatment.
- Analysis of dendritic cell and T cell subsets involved in psoriasis.
- Discussion of emerging anti-cytokine therapies.
Main Results:
- Existing therapies block TNF-α, IL-12 p40, or IL-23 p40.
- Newer strategies target IL-23p19 and IL-17.
- Dendritic cells and T cell subsets play critical roles in psoriasis.
Conclusions:
- Selective cytokine blockade represents the next frontier in psoriasis treatment.
- Targeting specific immune cell pathways offers potential for improved efficacy and safety.
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