Multiple Sclerosis PBMC
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.
| Lot # | Condition | Cell Count (M) | Race/Ethnicity | Age | Gender | Country of Collection | Medications | Vials | Price | Action |
|---|---|---|---|---|---|---|---|---|---|---|
| 75352 | Multiple Sclerosis | 50M | Caucasian | 46 | Female | United States |
Trazadone 150 mg PRN Albuterol PRN Magnesium 500mg QN Metoprolol 25mg ER QD Xanax 0.5 mg qd PRN Flexeral 10mg PRN Vumerity Vitamin D3 2,000 IC Normethadone Black cohosh supplement menopause
|
46 | $1,109.00 | |
| 76047 | Multiple Sclerosis | 50M | Caucasian | 57 | Female | United States |
copaxone 30mg injection QD Gabapentin 600mg BID Linzess QD Minocycline QD Prozac Lithium SPRAVATO
|
78 | $1,109.00 | |
| 76047 | Multiple Sclerosis | 10M | Caucasian | 57 | Female | United States |
copaxone 30mg injection QD Gabapentin 600mg BID Linzess QD Minocycline QD Prozac Lithium SPRAVATO
|
12 | $530.00 | |
| 76047 | Multiple Sclerosis | 50M | Caucasian | 57 | Female | United States |
copaxone 30mg injection QD Gabapentin 600mg BID Linzess QD Minocycline QD Prozac Lithium SPRAVATO
|
1 | $1,109.00 | |
| 75571 | Multiple Sclerosis | 50M | Caucasian | 55 | Female | United States |
Flexeril 10 mg QD Vit D 10,000 IU's po QD B-12 QM Zofran PRN Bcomplex QD Klonopin .5 PRN Nurtec 75mg PRN
|
59 | $1,109.00 | |
| 75571 | Multiple Sclerosis | 10M | Caucasian | 55 | Female | United States |
Flexeril 10 mg QD Vit D 10,000 IU's po QD B-12 QM Zofran PRN Bcomplex QD Klonopin .5 PRN Nurtec 75mg PRN
|
12 | $530.00 | |
| 75352 | Multiple Sclerosis | 10M | Caucasian | 46 | Female | United States |
Trazadone 150 mg PRN Albuterol PRN Magnesium 500mg QN Metoprolol 25mg ER QD Xanax 0.5 mg qd PRN Flexeral 10mg PRN Vumerity Vitamin D3 2,000 IC Normethadone Black cohosh supplement menopause
|
12 | $530.00 | |
| 74781 | Multiple Sclerosis | 50M | Asian/Pacific Islander | 31 | Male | United States |
No medications
|
42 | $1,109.00 | |
| 74781 | Multiple Sclerosis | 10M | Asian/Pacific Islander | 31 | Male | United States |
No medications
|
12 | $530.00 | |
| 73966 | Multiple Sclerosis | 50M | Caucasian | 59 | Male | United States |
Levothyroxine 88 mcg once daily Baclofen pump 7.6 mcg an hour or 181.3 mcg a day Ocrevus Advil 200 mg once a night
|
91 | $1,109.00 |
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.
Protocols & Documentation
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Download
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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Download
Immune Cell Isolation
Guidelines for isolating immune cell populations with validated enrichment steps, purity checkpoints, and documentation.
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Download
Choosing the Right PBMC Configuration
Reference guide comparing PBMC formats, cryopreservation states, and study-fit recommendations for your application.
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Download
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
Frequently Asked Questions
1 Answer
YES – All collections are conducted under IRB-approved protocols and electronic informed consent. Sanguine utilizes Advarra and WCG IRB for oversight.
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YES – all our products are research use only (RUO).
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You can find our full product catalog here.
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Storage depends on sample type but often cryopreserved samples stored in liquid nitrogen can be stored for years.
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Extensive customization is available. To discuss your project request a quote or email us at learnmore@sanguinebio.com.
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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.
1 Answer
Timelines depend on condition, sample type, and I/E criteria but we often start collection within 2 weeks of signed agreement.
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YES – we have in-stock inventory. You can also email us at learnmore@sanguinebio.com as we continually get new samples in our inventory.
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Each sample from a different individual – Unique donor means each sample comes from a different person, ensuring biological diversity in your study.
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YES – Unique donors can be specified and guaranteed based on your requirements.
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For information about sample quality, please see: Quality and Compliance
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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.
Ask a Question
Need a custom PBMC cohort?
Our scientific team can scope prospective collections with donor-specific I/E criteria, typically starting within 2 weeks of agreement.