Psoriatic Arthritis Leukopak
About:LeukoCore Psoriatic Arthritis Leukopak contains concentrated immune cells from donors with clinically confirmed psoriatic arthritis, collected via apheresis. Psoriatic arthritis is a seronegative, IL-23/IL-17-driven spondyloarthritis rather than an autoantibody-mediated disease. Ideal for Th17 and innate-like lymphocyte immunophenotyping, rare-subset sorting, IL-17/IL-23 functional assays, and single-cell studies. Matched healthy controls available.
About Psoriatic Arthritis Leukopak
High-Yield LeukoCore Psoriatic Arthritis Leukopaks for Immune-Mediated Inflammatory Disease Research
LeukoCore Psoriatic Arthritis Leukopak biospecimens are collected from IRB-consented donors clinically diagnosed with psoriatic arthritis through IRB-approved apheresis procedures, then processed and shipped within 24 hours of collection. Each leukopak contains large quantities of peripheral blood mononuclear cells (PBMCs). Psoriatic arthritis is a seronegative, immune-mediated inflammatory disease of the IL-23/IL-17 axis – it is not autoantibody-driven – and high-yield leukocyte material supports the cellular immunology that this mechanism demands.
Psoriatic Arthritis Immunology and Why a Leukopak
- Psoriatic arthritis belongs to the seronegative spondyloarthritis family. Rheumatoid factor and anti-citrullinated protein antibodies are characteristically absent, so the rheumatoid arthritis autoantibody framework does not apply and should not be imported.
- The central pathogenic pathway runs from IL-23 through Th17 and related innate-like lymphocyte populations to IL-17A, IL-17F, and IL-22, with TNF contributing throughout. This is validated by the efficacy of IL-17, IL-23, and TNF inhibitors in the disease.
- Characteristic lesions include enthesitis at tendon and ligament insertions, dactylitis, nail disease, and both bone erosion and new bone formation – a combination of destructive and proliferative change that distinguishes it from rheumatoid arthritis.
- HLA-B27 is associated particularly with axial involvement, while HLA-C*06:02 associates with the cutaneous psoriasis phenotype, and the two patterns can be used to stratify donors.
- Innate-like and tissue-homing lymphocyte subsets – including gamma-delta T cells, mucosal-associated invariant T cells, and CCR6+ Th17 populations – are present at low frequency in blood, which is precisely why apheresis-scale material is required to isolate and study them.
- Leukopaks deliver the cell numbers needed for multi-arm functional assays, rare-subset sorting, and single-cell studies that cannot be powered from a standard venous draw.
Donor Stratification Available
- Disease pattern: peripheral oligoarticular or polyarticular versus axial involvement
- Presence of enthesitis, dactylitis, and nail psoriasis
- Concomitant cutaneous psoriasis and its severity where documented
- Treatment exposure: bDMARD-naive, anti-TNF, anti-IL-17, anti-IL-23/IL-12-23, or JAK inhibitor treated; conventional DMARD background
- Disease activity at collection and disease duration
- HLA-B27 status where typing is available; age band and sex
- Matched healthy controls available
Product Features
- Research Use Only (RUO) human leukopaks
- Clinically confirmed psoriatic arthritis donors
- High cell yield for large-scale studies
- Processed and shipped within 24 hours of collection
- Fresh or cryopreserved options available
- IRB-approved and ethically sourced
- Infectious disease testing
- HLA-A typing
- Screen donors with LeukoLot™
De-identified Donor Data
- Verified psoriatic arthritis diagnosis from healthcare providers
- Donor demographics: age, sex assigned at birth, race/ethnicity
- Self-reported medication history and allergies
- Relevant clinical data, including disease pattern, activity, and treatment history where documented
Applications
- Immunophenotyping of Th17, Tc17, gamma-delta T-cell, and MAIT populations by spectral or conventional flow cytometry
- Cell sorting of rare tissue-homing and innate-like lymphocyte subsets
- IL-23/IL-17 axis functional assays, including stimulation and cytokine release profiling
- Ex vivo drug screening and mechanism-of-action work for IL-17, IL-23, TNF, and JAK-targeted agents
- Single-cell RNA sequencing, CITE-seq, and TCR repertoire analysis
- Osteoclast differentiation assays from donor-derived monocytes to model bone erosion
- Biomarker discovery and validation for treatment response and disease activity
- Large matched cell lot banking for multi-site or longitudinal spondyloarthritis studies
Other Psoriatic Arthritis Specimen Types
- Psoriatic Arthritis PBMC
- Psoriatic Arthritis Plasma
- Psoriatic Arthritis Serum
- Psoriatic Arthritis Whole Blood
- Psoriatic Arthritis Synovial Fluid
- Psoriatic Arthritis Skin Punch Biopsy
- Psoriatic Arthritis Bulk Plasma
Compliance and Quality Assurance
- Collected under IRB oversight with donor e-consent (21 CFR Part 11 compliant)
- HIPAA-compliant handling of donor information
- Rigorous donor screening and documentation
Ordering & Customization
Psoriatic Arthritis Leukopak is available fresh or cryopreserved. For pricing, international shipping, or regulatory documentation, please contact learnmore@sanguinebio.com to confirm regional compliance and shipping availability. Need a different condition, or want to check current availability across our full inventory? Visit our human leukopak page to browse other disease-state options and live stock status.
Donor Metadata
- Verified diagnosis and clinical history
- Demographic data: age, sex assigned at birth, race/ethnicity
- Medication and treatment background when available
Compliance and Quality Assurance
- IRB-approved collections and standardized procedures
- 21 CFR Part 11-compliant e-consent system
- HIPAA-compliant data management
Ordering & Customization
Human Leukopak are available in customizable aliquot sizes. For international orders or documentation needs, please contact learnmore@sanguinebio.com to confirm requirements and availability. We also work with multiple ordering platforms and distributors, learn more here.
Protocols & Documentation
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Leukopak Cryopreservation
Standard operating procedure for cryopreserving leukopak units with controlled freezing and post-thaw viability targets.
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Leukopak Thawing
Validated thawing workflow for cryopreserved leukopaks to maximize recovery while maintaining sterility and chain of custody.
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Choosing the Right PBMC Configuration
Reference guide comparing PBMC formats, cryopreservation states, and study-fit recommendations for your application.
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Informed Consent Form (ICF)
Available upon request — confirms donor consent for research use and downstream commercialization.
Leukopak
Where can I find your complete catalog?
You can find our full product catalog here.
How long can samples be stored?
Storage depends on sample type but often cryopreserved samples stored in liquid nitrogen can be stored for years.
What customization options are available?
Extensive customization is available. To discuss your project request a quote or email us at learnmore@sanguinebio.com.
Do you offer prospective collections?
Sanguine offers flexible prospective collection services tailored to fit your research. For more information and to request a quote, please see: our prospective biospecimen collection services page.
What is the turnaround time for custom collections?
Timelines depend on condition, sample type, and I/E criteria but we often start collection within 2 weeks of signed agreement.
Do you have samples in stock?
YES - we have in-stock inventory. You can also email us at learnmore@sanguinebio.com as we continually get new samples in our inventory.
What does unique donor mean?
Each sample from a different individual - Unique donor means each sample comes from a different person, ensuring biological diversity in your study.
Are samples collected under IRB-approved protocols?
YES - "IRB-approved collection protocols" and IRB approval documentation available upon request. Sanguine utilizes two internationally-recognized IRBs (Advarra and WCG IRB) for review and approval.
Frequently Asked Questions
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9 In Stock View InventoryNeed a custom Leukopak cohort?
Our scientific team can scope prospective collections with donor-specific I/E criteria, typically starting within 2 weeks of agreement.