Sjogren’s Syndrome Plasma
About:Sjogren's Syndrome Plasma from IRB-consented donors with clinically confirmed Sjogren's syndrome, processed within one day of collection. Supports anti-Ro/SSA and anti-La/SSB autoantibody assay work, BAFF and CXCL13 B-cell axis markers, type I interferon signature profiling, immunoglobulin and free light chain quantification, and complement-based lymphoma risk research. Donors can be stratified by autoantibody profile, primary versus secondary disease, ESSDAI activity and extraglandular involvement. Bulk plasma is available.
About Sjogren’s Syndrome Plasma
Sjogren’s Syndrome Plasma for Autoimmune and Autoantibody Research
Sjogren’s Syndrome Plasma is collected from IRB-consented donors clinically diagnosed with Sjogren’s syndrome and processed within one day of collection to preserve labile analytes such as cytokines, proteins and metabolites. Sjogren’s syndrome is a systemic autoimmune disease in which lymphocytic infiltration of the salivary and lacrimal glands produces dryness of the mouth and eyes, accompanied by autoantibody production and a type I interferon-driven inflammatory response. Bulk plasma is available for higher-volume programs.
What Sjogren’s Syndrome Plasma Reveals
- Sjogren’s syndrome is defined serologically by anti-Ro/SSA autoantibodies, directed against Ro52/TRIM21 and Ro60, frequently with anti-La/SSB, ANA and rheumatoid factor. These autoantibodies are a genuine feature of the disease rather than a template phrase, and plasma from characterised donors supports assay development against each specificity.
- Polyclonal B-cell hyperactivity is a hallmark, producing hypergammaglobulinaemia and elevated free light chains. Plasma is the practical matrix for quantifying total and subclass immunoglobulins, free light chains and beta-2 microglobulin as measures of that B-cell drive.
- The B-cell survival factor BAFF and the B-cell chemoattractant CXCL13 are elevated in Sjogren’s syndrome and reflect the ectopic lymphoid organisation seen in affected glands. Both are measurable in plasma and both sit on pathways being targeted therapeutically.
- A type I interferon signature is well documented, and interferon-inducible chemokines such as CXCL10 are measurable in plasma, giving a systemic readout of a pathway central to disease biology.
- Sjogren’s syndrome carries a materially increased risk of B-cell lymphoma, particularly mucosa-associated lymphoid tissue lymphoma of the parotid. Persistently low C4 and cryoglobulinaemia are recognised risk markers, and complement components are best preserved in citrate or EDTA plasma rather than in serum, where clotting consumes them.
- Disease extends well beyond sicca symptoms to fatigue, arthralgia, interstitial lung disease, peripheral neuropathy and cutaneous vasculitis, so plasma from donors annotated by extraglandular involvement supports linking circulating markers to specific systemic domains.
Donor Stratification Available
- Autoantibody profile where documented: anti-Ro/SSA (Ro52 and Ro60), anti-La/SSB, ANA pattern and titre, rheumatoid factor
- Primary Sjogren’s syndrome versus secondary disease with rheumatoid arthritis, SLE or systemic sclerosis
- Disease activity where documented, including ESSDAI, and patient-reported symptom burden by ESSPRI
- Laboratory features where documented: hypergammaglobulinaemia, low C4, cryoglobulinaemia, and labial gland biopsy focus score
- Extraglandular involvement: articular, pulmonary, neurological, cutaneous vasculitis, or renal; and history of lymphoproliferative disease
- Treatment status including hydroxychloroquine, corticosteroid, immunosuppressant or B-cell directed therapy; matched healthy controls available
Product Features
- Research Use Only (RUO)
- Plasma collected from clinically confirmed Sjogren’s syndrome donors
- Processed within one day of collection
- Anticoagulant selection (EDTA, citrate, heparin) available on request
- IRB-approved protocols and informed consent
- Custom aliquot volumes available upon request; volumes reported per lot
De-identified Donor Data
- Verified Sjogren’s syndrome diagnosis
- Demographic data: age, sex assigned at birth, race/ethnicity
- Donor-reported medications, allergies, and comorbidities
- Additional Sjogren’s syndrome-specific metadata available on request
Applications
- Anti-Ro/SSA and anti-La/SSB autoantibody assay development and validation
- BAFF, CXCL13 and B-cell axis biomarker research
- Type I interferon signature and interferon-inducible chemokine profiling
- Immunoglobulin, free light chain and complement quantification
- Lymphoma risk marker research, including low C4 and cryoglobulinaemia
- Plasma proteomics and metabolomics
- Disease activity and treatment-response biomarker discovery
- Therapeutic target validation and pharmacodynamic assay development
Other Sjogren’s Syndrome Specimen Types
- Sjogren’s Syndrome Serum
- Sjogren’s Syndrome Whole Blood
- Sjogren’s Syndrome PBMC
- Sjogren’s Syndrome Leukopak
- Sjogren’s Syndrome Bulk Plasma
- Sjogren’s Syndrome CD19+ B Cells
- Primary Sjogren’s Syndrome Plasma
- Secondary Sjogren’s Syndrome Plasma
Compliance and Quality Assurance
- IRB-approved and HIPAA-compliant protocols
- Electronic informed consent with 21 CFR Part 11 – compliant e-signatures
- Documentation support available for regulatory review
Ordering & Customization
Sjogren’s syndrome plasma is available in standard and custom volumes. For pricing, current availability, or a quote on a stratified donor cohort, email learnmore@sanguinebio.com. For international orders or documentation requirements, please contact us to ensure compatibility with your country’s regulations. To browse other disease states in this specimen type, visit our human plasma page.
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 Plasma 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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Download
Plasma Isolation
Protocol for plasma separation from anticoagulated whole blood, including processing, storage, and traceability requirements.
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Informed Consent Form (ICF)
Available upon request — confirms donor consent for research use and downstream commercialization.
Plasma
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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216 In Stock View InventoryNeed a custom Plasma cohort?
Our scientific team can scope prospective collections with donor-specific I/E criteria, typically starting within 2 weeks of agreement.