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Published on: March 8, 2024
Interleukin 22 and 6 serum concentrations decrease under long-term biologic therapy in psoriasis.
Irmina Olejniczak-Staruch1, Joanna Narbutt2, Igor Bednarski2
1Department of Dermatology and Venereology, Medical University of Lodz, Lodz, Poland.
Long-term biologic therapy for psoriasis significantly reduces serum levels of IL-6 and IL-22, key inflammatory markers. These cytokine changes indicate treatment effectiveness, complementing clinical improvements in skin lesions.
Area of Science:
- Dermatology
- Immunology
- Pharmacology
Background:
- Psoriasis affects 2% of the global population, characterized by chronic inflammation and cytokine overexpression.
- Existing data on antipsoriatic therapy's impact on cytokine levels are inconsistent and short-term.
- Understanding long-term cytokine changes is crucial for effective psoriasis management.
Purpose of the Study:
- To assess the long-term effects of biologic therapies on IL-6 and IL-22 serum concentrations in psoriasis patients.
- To evaluate the influence of TNF-α blockers (adalimumab, etanercept, infliximab) and an IL-12/23 inhibitor (ustekinumab).
Main Methods:
- Serum IL-6 and IL-22 levels were measured in 42 psoriasis patients over 36 months of biologic therapy.
- Psoriasis Activity and Severity Index (PASI) was assessed concurrently.
- A control group of 30 healthy volunteers was included for comparison.
Main Results:
- Mean PASI scores significantly decreased throughout the observation period.
- Serum IL-6 concentrations showed a significant reduction across all treatment groups (p < 0.05).
- IL-22 levels significantly decreased with adalimumab and infliximab, but not etanercept or ustekinumab.
Conclusions:
- Serum IL-6 and IL-22 may serve as accurate biomarkers for response to antipsoriatic biologic therapy.
- Biologic therapy offers sustained clinical improvement in psoriasis, marked by reduced skin lesions and lower pro-inflammatory cytokine levels.
- While not directly correlated with PASI, cytokine levels reflect therapeutic efficacy.
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