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Breaking the Barrier: CD8+ T cells in Atopic Dermatitis and Psoriasis Vulgaris

Breaking the Barrier: CD8+ T cells in Atopic Dermatitis and Psoriasis Vulgaris - CD8+ T cells in Atopic Dermatitis and Psoriasis Vulgaris

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON32531
Enrollment
36
Registered
2008-12-09
Start date
2009-04-08
Completion date
Unknown
Last updated
2024-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

atopic dermatitis eczema

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Atopic dermatitis patients: - Adult (18-70 years of age) male or female patients diagnosed with atopic dermatitis - Positive APT to house dust mite allergen - Biopsy location (~4 cm2) should not be treated with topical steroids for at least 1 week - No use of oral antihistamines in the 2 weeks prior to inclusion;Psoriasis vulgaris patients: - Adult (18-70 years of age) male or female patients diagnosed with psoriasis vulgaris - Biopsy location (~4 cm2) should not be treated with topical steroids for at least 1 week;Healthy controls: - Adult (18-70 years of age) male or female volunteers without a history of skin diseases - Biopsy location (~4 cm2) should not be treated with topical steroids for at least 1 week - No history of asthma and/or hay fever

Exclusion criteria

Exclusion criteria: - Use of systemic immunosuppressive drugs (i.e., cyclosporin, prednisolone, methotrexate, neotigason, fumaric acid) in the 6 weeks prior to inclusion - Exposure of biopsy location to (extraordinary) UV sunlight (i.e. UV-therapy, sunny holiday) in the weeks prior to inclusion - (Secondary) skin infection

Design outcomes

Primary

MeasureTime frame
We will determine the percentage of CD8+ IL-13-producing skin resident T cells in acute and chronic AD using the APT as an in vivo model. Results will be compared to data from lesional and non-lesional AD, PV skin and healthy control skin.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)