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Updated: May 10, 2026

Isolation and Th17 Differentiation of Naïve CD4 T Lymphocytes
Published on: September 26, 2013
IL-17 targeted therapies for psoriasis
Andrea Chiricozzi1, James G Krueger
1The Rockefeller University, Laboratory for Investigative Dermatology , 1230 York Avenue, New York City, NY 10065, USA. chiricozziandrea@gmail.com
New biologic therapies targeting interleukin-17A (IL-17A) show significant promise for treating psoriasis. Blocking IL-17A effectively reduces disease severity, indicating its crucial role in this chronic inflammatory skin condition.
Area of Science:
- Immunodermatology
- Inflammatory skin diseases
- Cytokine signaling
Background:
- Psoriasis is a chronic inflammatory skin disease with incompletely understood pathogenesis.
- Immune responses involving cytokines like IL-17A are implicated in psoriasis development.
- Genetic and environmental factors contribute to the immune dysregulation seen in psoriasis.
Purpose of the Study:
- To review the role of IL-17A in psoriasis pathogenesis.
- To discuss the development and efficacy of IL-17-targeted therapies.
- To evaluate the potential impact of IL-17 blockade on psoriasis comorbidities.
Main Methods:
- Review of emerging evidence on IL-17A's role in psoriasis.
- Analysis of Phase II and III clinical trial data for IL-17 inhibitors (secukinumab, ixekizumab, brodalumab).
- Assessment of therapeutic efficacy and safety profiles of anti-IL-17 agents.
Main Results:
- IL-17A is confirmed as a central mediator in psoriasis pathogenesis.
- Phase II trials demonstrated marked improvement in psoriasis severity with IL-17 blockade.
- Agents targeting IL-17 or its receptor show significant efficacy in clinical studies.
Conclusions:
- Anti-IL-17 agents are poised to become key therapeutics for psoriasis.
- These therapies may positively influence psoriasis comorbidities such as cardiovascular disease and arthritis.
- Targeting the IL-17 pathway offers a promising therapeutic strategy for managing psoriasis and its associated conditions.
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