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Unable to isolate sufficient cells from the skin biopsy to perform study related experiments
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| Name | Class |
|---|---|
| Doris Duke Charitable Foundation | OTHER |
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Ultra-violet light B (UVB) therapy has been used by dermatologists to treat psoriasis for decades. Only a few studies have begun to dissect the mechanism of how NB-UVB therapy causes lesion resolution. Results from this study will aid in identifying other diseases that may be treated successfully with NB-UVB. If we can identify the mechanism of action of this therapy, this may give us additional new therapeutic targets for psoriasis and other diseases. Our overall hypothesis is that UVB induces changes that will indicate a mechanism of action of this therapy in psoriasis.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| NB-UVB | Other | Regular, monitored NB-UVB treatment. Patients will be treated 3 times per week, and a full course of therapy is 12 weeks. NB-UVB dosing is increased by 5-20% increments in exposure time, depending on response of the patient. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| NB-UVB | Procedure | UVB light will be administered to the entire body except for the genitals in men and eyelids, which will be shielded.NB-UVB dosing is increased by 5-20% increments in exposure time, depending on response of the patient. |
| Measure | Description | Time Frame |
|---|---|---|
| The primary outcome is genomic analysis of lesional skin biopsies, in a time course experiment,by microarray and RT-PCR. | End of study |
| Measure | Description | Time Frame |
|---|---|---|
| cell counts of leukocytes populations in skin biopsies including (but not limited to) myeloid dendritic cells (CD11c and CD1c/BDCA-1), plasmacytoid dendritic cells (BDCA-2/CD123), macrophages (CD163), and T cells (CD3, CD4, CD8, Foxp3, RORγ). | End of study | |
| Effects of NB-UVB on NL skin will be determined by comparison of microarray analysis of NL skin biopsies throughout treatment. |
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Inclusion Criteria:
Exclusion Criteria:
Subjects who do not meet the above criteria, or who meet any of the following criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Michelle Lowes, MD, PhD | Rockefeller University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Rockefeller University | New York | New York | 10065 | United States |
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| End of study |
| To determine if there is a set of genes that can predict response, expressed in circulating PBMCs, we will perform microarray on baseline PBMCs, and compare the gene sets for responders and non-responders (discriminant analysis). | End of study |
| To evaluate if treatment causes an altered ratio of Th17:Tregs in the circulation and skin, we will perform intracellular cytokine staining by flow cytometry on peripheral blood and from the shave biopsy. | Before and after treatment |