Multiple Sclerosis PBMC
About:Cryopreserved PBMC from clinically confirmed multiple sclerosis donors, processed within 24 hours and stored in CryoStor CS10. The target compartment for nearly every MS disease-modifying therapy: supports myelin-reactive T-cell assays, memory B-cell and anti-CD20 pharmacodynamics, integrin and S1P trafficking studies, and Treg function work. Stratifiable by disease course, EDSS and DMT.
About Multiple Sclerosis PBMC
Multiple Sclerosis PBMC for Neuroimmunology and Autoimmunity Research
Multiple Sclerosis (MS) Human PBMC are sourced from IRB-consented donors clinically diagnosed with MS, processed within 24 hours of collection and cryopreserved in CryoStor® CS10. MS is an autoimmune disease of the central nervous system in which lymphocytes cross the blood-brain barrier and drive demyelination and axonal loss. Because the pathogenic cells originate in and traffic through the blood, cryopreserved peripheral blood mononuclear cells are the workhorse specimen for MS immunology and drug development.
Why PBMC for Multiple Sclerosis
Nearly every approved disease-modifying therapy in MS acts on a peripheral blood leukocyte — by depleting it, sequestering it, or blocking its migration. That makes PBMC not merely a convenient surrogate but the actual target compartment.
- Myelin-reactive T cells — CD4+ Th1 and Th17 cells reactive to myelin antigens are central to MS pathogenesis, and PBMC support antigen-specific stimulation, proliferation and cytokine recall assays that cannot be done in serum or plasma.
- B cells are pathogenic, not incidental — the striking efficacy of anti-CD20 therapy established B cells as central to MS. PBMC allow memory B-cell phenotyping, depletion pharmacodynamics and repopulation kinetics to be measured directly.
- Lymphocyte trafficking mechanisms — natalizumab blocks alpha-4 integrin (VLA-4) and S1P receptor modulators trap lymphocytes in lymph nodes; both mechanisms are assayed on intact PBMC through adhesion, migration and receptor-expression readouts.
- Regulatory T-cell function — impaired regulatory T-cell suppressive capacity is a recurring finding in MS and requires live, functional cells to test.
- CD8+ T cells and tissue-resident phenotypes — CD8+ T cells dominate MS lesions, so circulating CD8 differentiation and clonality are informative, particularly alongside TCR sequencing.
- Epstein-Barr virus biology — the strong epidemiologic link between EBV infection and MS is investigated using EBV-specific T-cell and B-cell responses, which requires viable PBMC for antigen recall assays.
Donor Stratification Available
- Disease course: relapsing-remitting, secondary progressive, or primary progressive MS
- Clinical state at collection: active relapse versus clinical remission
- Disability level: EDSS score where recorded, and disease duration since diagnosis
- Disease-modifying therapy: treatment-naive, interferon beta, glatiramer acetate, dimethyl fumarate, S1P modulator, natalizumab, anti-CD20 therapy, or cladribine
- Recent corticosteroid exposure and time since last dose, which materially affects immune phenotype
- Matched healthy controls available, age- and sex-matched on request
Product Features
- Research Use Only (RUO), cryopreserved PBMCs
- Clinically confirmed MS donors
- Available in cell counts ranging from 5 million to 2 billion
- Processed within 24 hours of collection
- Stored using CryoStor® CS10 freezing media
- Viability and recovery reported per lot
- IRB-approved protocols and electronic informed consent
- Screen LeukoLot™ available prior to bulk orders
De-identified Donor Data
- Verified MS diagnosis, including disease course where available
- Donor demographics: age, sex assigned at birth, race/ethnicity
- Self-reported allergies, medications and infectious disease history
- EDSS, relapse history and treatment history where recorded
- Additional MS-specific data available upon request
Applications
- Antigen-specific T-cell stimulation, proliferation and cytokine recall assays
- Deep immunophenotyping of T-cell, B-cell and monocyte compartments
- Memory B-cell and anti-CD20 pharmacodynamic and repopulation research
- Lymphocyte adhesion, migration and integrin blockade assays
- Regulatory T-cell functional suppression studies
- TCR and BCR repertoire sequencing
- Single-cell RNA-seq and CITE-seq of the MS immune compartment
- Drug screening, mechanism-of-action and biomarker discovery for disease-modifying therapies
Other Multiple Sclerosis Specimen Types
- Multiple Sclerosis Serum
- Multiple Sclerosis Plasma
- Multiple Sclerosis Whole Blood
- Multiple Sclerosis Leukopak
- Multiple Sclerosis Cerebrospinal Fluid
- Relapsing-Remitting MS PBMC and Secondary Progressive MS PBMC
Compliance and Quality Assurance
- IRB-approved collections and protocols
- 21 CFR Part 11 – compliant e-consent system
- HIPAA-compliant donor data protection
Ordering & Customization
Multiple Sclerosis PBMC samples are shipped on dry ice and available in custom aliquots. For pricing, availability or a specific stratification request, email learnmore@sanguinebio.com; please also contact us for international orders or regulatory documentation needs. To browse availability across all disease states, visit our human PBMC 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 PBMC 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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PBMC Isolation from Whole Blood
Standard operating procedure for isolating peripheral blood mononuclear cells from whole blood using density-gradient separation.
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Immune Cell Isolation
Guidelines for isolating immune cell populations with validated enrichment steps, purity checkpoints, and documentation.
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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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Thawing Cryopreserved PBMC
Validated thawing protocol to recover viable cryopreserved PBMCs while minimizing activation and loss of function.
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Informed Consent Form (ICF)
Available upon request — confirms donor consent for research use and downstream commercialization.
PBMC
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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806 In Stock View InventoryNeed a custom PBMC cohort?
Our scientific team can scope prospective collections with donor-specific I/E criteria, typically starting within 2 weeks of agreement.