{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Xlsx":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PAD000045/Sampledata.xlsx"],"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PAD000045/checksum.txt"],"Other":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PAD000045/PLASMA.1.3k.HybNorm.MedNorm.Cal.20151030.adat","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PAD000045/Novartis.ATI013.27Aug2020.HybNormPlateScaleCalMedNorm.adat"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"labhead_mail":["r.m.luiten@amsterdamumc.nl"],"submitter":["Wouter Ouwerkerk"],"technology_type":["SomaScan affinity proteomics","Mass Spectrometry","Affinity proteomics"],"disease":["Vitiligo"],"software":["Not available"],"submitter_keywords":[""],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PAD000045"],"tissue":["Blood Plasma","Skin"],"sample_protocol":["Skin punch biopsies, of four-millimeter diameter, were collected from the border of a vitiligo lesion at baseline and 3-months after start of therapy (adjacent to the pre-treatment biopsies at the same lesion). These biopsies were dissociated into single cells through enzymatic digestion, by using the Whole Skin Dissociation Kit and mechanical dissociation with the gentleMACSTM Dissociator (both Miltenyi Biotec, Germany). Subsequently, a 70 μm cell strainer was used for filtering and collecting the cells. A suction blister (1 cm diameter) was raised at the border of a lesion and in a non-lesional control area in the same skin region (with similar type of skin) at Baseline. After 3 months of treatment, another suction blister was raised at a predefined area from the original border of the same lesion. From each blister, approximately 400 μL fluid was harvested. The blister fluid was used to study the skin interstitial fluid for its cellular composition or soluble factors before and after therapy in parallel to the skin biopsy analyses.Peripheral blood samples were obtained from all patients at baseline and 3-months. Peripheral Blood. Mononuclear Cells (PBMC) were purified from the peripheral blood by Ficol density gradient centrifugation (Axis-Shield density gradient media, Fresenius Kabi Norge AS, Halden, Norway)."],"repository":["Pride"],"modification":["Not available"],"quantification_method":[""],"data_protocol":["The proteomics data from blister fluid and blood plasma at baseline and upon treatment was analyzed by SomaLogic technology. Proteomics data was normalized according to the SomaLogic Hyb normalization - median signal normalization procedure. The data was quality controlled and assembled with lab sample data and clinical data to obtain about 4550 log2 transformed human protein quantities per sample."],"omics_type":["Proteomics"],"labhead":["Rosalie Luiten"],"instrument_platform":[""],"submission_type":["AFFINITY"],"labhead_affiliation":["LED, dept dermatology, amsterdamumc, Amsterdam, The netherlands"],"species":["Homo Sapiens (human)"],"publication":["40848929 Ouwerkerk W, Narayan VS, Chielie S, van Uden NOP, Schneider MA, Hillenbrand R, Gaulis S, Kjellerup RB, Loesche C, Hanser M, McNamara E, Bekkenk MW, Wolkerstorfer A, Luiten RM. Immune and Biological Changes during Treatment in Patients with Nonsegmental Vitiligo and their Relation to Repigmentation. J Invest Dermatol. 2026 146(3):699-710 10.1016/j.jid.2025.07.029"],"submitter_mail":["w.ouwerkerk@amsterdamumc.nl"],"submitter_affiliation":["Dept Dermatology, amsterdam UMC"],"submitter_country":["Netherlands"],"doi":["10.6019/PAD000045"],"pubmed_abstract":["The treatment of nonsegmental vitiligo remains challenging and poorly understood. The aim of this study was to evaluate protein differences in lesional and nonlesional skin and changes of cellular and proteomic markers early in treatment in lesional skin and blood in relation to clinical response. This prospective exploratory study was conducted in 30 patients with nonsegmental vitiligo, 11 starting with standard-of-care topical therapy and 19 starting in combination with narrow-band UVB phototherapy. We identified 53 proteins that differed between blister fluids from lesional and nonlesional skin before treatment. After 3 months of therapy, CD3<sup>+</sup>, CD8<sup>+</sup> T, and tissue-resident memory (CD69<sup>+</sup>CD103<sup>-</sup>) cell populations decreased in skin biopsies, together with changes in 47 blister fluid proteins. Percentages of circulating follicular T helper type 17, CD336<sup>+</sup>Nk<sup>bright</sup>, type 1 regulatory T (Tr1), and IL-10-secreting Tr1 cells decreased in blood. Decreases in tissue-resident memory, Tr1, and IL-10-secreting Tr1 cells and fatty acid-binding protein 4 were associated with repigmentation, measured by Vitiligo Extent Score at baseline and 6 months. Differences in lesional and nonlesional skin prior to treatment do not reflect changes in lesional skin early in therapy nor associations with clinical repigmentation response. We found an association between decreasing fatty acid-binding protein 4 and tissue-resident memory cells in the skin and IL-10-secreting Tr1 cells in the blood and repigmentation response to treatment of vitiligo."],"pubmed_title":["Immune and Biological Changes during Treatment in Patients with Nonsegmental Vitiligo and their Relation to Repigmentation."],"pubmed_authors":["Ouwerkerk Wouter W, Narayan Vidhya S VS, Chielie Saskia S, van Uden Nathalie O P NOP, Schneider Martin A MA, Hillenbrand Rainer R, Gaulis Swann S, Kjellerup Rasmus B RB, Loesche Christian C, Hanser Malika M, McNamara Elizabeth E, Bekkenk Marcel W MW, Wolkerstorfer Albert A, Luiten Rosalie M RM"],"additional_accession":[]},"is_claimable":false,"name":"Early clinical and biomarker responses after treatment in patients with non-segmental vitiligo.","description":"This study was a prospective cohort study in patients with non-segmental vitiligo receiving SoCtreatment. Standard of care treatment involved a potent topical corticosteroid, such as Fluticasonepropionate (FP) cream, used alone or in combination with NB-UVB phototherapy treatment, based ondisease severity per the investigator’s evaluation. For this study, as per institutional guidelines, FP creamwas the first choice for SoC treatment; however, if FP cream was not available, then potent topicalcorticosteroids such as Mometasone furoate (i.e. Elocon, Mometason) or betametasone valerate (i.e.Betnelan, betamethason) were prescribed. Calcineurin inhibitors were used for the face according to theSoC instead of steroids. Study participation did not affect SoC treatment. The study was conducted atthe Netherlands Institute for Pigment Disorders (NIPD), Department of Dermatology, AmsterdamUniversity Medical Center (AMC), University of Amsterdam, The 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