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Updated: Aug 10, 2026

Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture
Published on: April 8, 2016
Cytokines in skin lesions of psoriasis
A J Gearing1, N J Fincham, C R Bird
1National Institute for Biological Standards and Control (NIBSC), Potters Bar, Herts, UK.
Insights
Psoriatic lesions show elevated levels of biologically active interleukin-8 (IL-8), a neutrophil attractant. Other tested cytokines were not significantly elevated or biologically active in psoriatic skin, suggesting IL-8
Area of Science:
- Immunology
- Dermatology
- Biochemistry
Background:
- Psoriasis is a chronic inflammatory skin disease.
- Cytokines play a crucial role in immune responses and inflammation.
- Understanding cytokine profiles in psoriatic lesions is vital for disease pathogenesis research.
Purpose of the Study:
- To compare cytokine levels in psoriatic lesions versus normal skin.
- To identify specific cytokines involved in the pathogenesis of psoriasis.
Main Methods:
- Aqueous extracts of stratum corneum from psoriatic lesions and normal heel skin were analyzed.
- Immunoassays and biological activity tests were used to quantify cytokine levels.
- Specific neutralizing antiserum was employed to identify chemoattractants.
Main Results:
- Normal heel skin showed high levels of interleukin-1 alpha (IL-1 alpha) and beta, with only IL-1 alpha being biologically active.
- Psoriatic lesions had significantly reduced IL-1 levels.
- A neutrophil chemoattractant, identified as interleukin-8 (IL-8), was elevated in psoriatic lesions.
- Tumor necrosis factor alpha/beta and interferon alpha/gamma were detected by immunoassay but lacked biological activity in lesions.
- Interleukins 2, 4, 6, and GM-CSF were undetectable in all samples.
Conclusions:
- Interleukin-8 (IL-8) is the primary biologically active cytokine elevated in psoriatic lesions.
- IL-8 may play a significant role in the pathogenesis of psoriasis.
- Further research into IL-8's role could lead to targeted therapies.
Abstract:
Cytokine levels were compared in aqueous extracts of stratum corneum from psoriatic lesions and normal heel. Samples from heel contained high levels of interleukin-1 alpha (IL-1 alpha) and beta measured in immunoassays, although only the IL-1 alpha was biologically active. No other cytokines could be detected in heel samples. Interleukin-1 (IL-1) levels were dramatically reduced in lesional samples. A neutrophil chemoattractant was found in all lesional extracts, and was demonstrated to be mainly interleukin-8 (IL-8) using a specific neutralizing antiserum. Tumor necrosis factor alpha (TNF-alpha) and beta (TNF-beta), and interferon alpha (IFN-alpha) and gamma (IFN-gamma) were detected in lesional extracts using immunoassays, however, no equivalent biological activities could be detected. Interleukins 2 (IL-2), 4 (IL-4), and 6 (IL-6), granulocyte and granulocyte/macrophage colony stimulating factor (GM-CSF), could not be detected in any samples. IL-8 is therefore the only biologically active cytokine shown in this study to be elevated in psoriatic lesional extracts, and may therefore play a role in the pathogenesis of the disease.
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