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Updated: Aug 16, 2025

Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture
Published on: April 8, 2016
Skin TARC/CCL17 increase precedes the development of childhood atopic dermatitis
Anne-Sofie Halling1, Maria Rasmussen Rinnov2, Iben Frier Ruge1
1Department of Dermatology and Venereology, Bispebjerg Hospital, University of Copenhagen, Copenhagen, Denmark; Department of Dermatology and Allergy, Herlev and Gentofte Hospital, University of Copenhagen, Hellerup, Denmark.
Insights
Skin biomarkers collected at two months can predict atopic dermatitis (AD) risk. Elevated immune markers and low filaggrin degradation products at this early stage indicate future AD development.
Area of Science:
- Dermatology
- Immunology
- Pediatrics
Background:
- Predicting atopic dermatitis (AD) onset in infancy is crucial for prevention trials.
- Identifying infants at high risk for AD using early biomarkers remains challenging.
Purpose of the Study:
- To investigate if skin biomarkers collected in infancy can predict the development of AD within the first two years of life.
- To assess the utility of noninvasive skin biomarkers for identifying infants at risk for AD.
Main Methods:
- Enrolled 450 infants (300 term, 150 preterm) and collected skin tape strips at birth and two months.
- Analyzed biomarkers related to immune and barrier functions.
- Utilized Cox regression to calculate hazard ratios (HR) for AD risk.
Main Results:
- Skin biomarkers at birth did not predict AD. Elevated thymus- and activation-regulated chemokine/C-C motif chemokine ligand 17 (TARC/CCL17) at two months increased AD risk (HR: 2.11).
- Interleukin-8 (IL-8) and IL-18 predicted moderate-to-severe AD. Low filaggrin degradation products also increased AD risk (HR: 2.04).
- Biomarker levels at two months predicted AD onset at other sites and months later.
Conclusions:
- Noninvasively collected skin biomarkers reflecting barrier and immune pathways can precede the clinical onset of atopic dermatitis.
- These findings support the use of early-life skin biomarkers for predicting AD risk and informing prevention strategies.
Background:
It is unknown whether skin biomarkers collected in infancy can predict the onset of atopic dermatitis (AD) and be used in future prevention trials to identify children at risk.
Objectives:
This study sought to examine whether skin biomarkers can predict AD during the first 2 years of life.
Methods:
This study enrolled 300 term and 150 preterm children at birth and followed for AD until the age of 2 years. Skin tape strips were collected at 0 to 3 days and 2 months of age and analyzed for selected immune and barrier biomarkers. Hazard ratio (HR) with 95% confidence interval (CI) using Cox regression was calculated for the risk of AD.
Results:
The 2-year prevalence of AD was 34.6% (99 of 286) and 21.2% (25 of 118) among term and preterm children, respectively. Skin biomarkers collected at birth did not predict AD. Elevated thymus- and activation-regulated chemokine/C-C motif chemokine ligand 17 -levels collected at 2 months of age increased the overall risk of AD (HR: 2.11; 95% CI: 1.36-3.26; P = .0008) and moderate-to-severe AD (HR: 4.97; 95% CI: 2.09-11.80; P = .0003). IL-8 and IL-18 predicted moderate-to-severe AD. Low filaggrin degradation product levels increased the risk of AD (HR: 2.04; 95% CI: 1.32-3.15; P = .001). Elevated biomarker levels at 2 months predicted AD at other skin sites and many months after collection.
Conclusions:
This study showed that noninvasively collected skin biomarkers of barrier and immune pathways can precede the onset of AD.
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