Type 1 Diabetes Leukopak
LeukoCore Type 1 Diabetes Leukopak — apheresis-collected concentrated immune cells from IRB-consented T1D donors with HLA-A typing. Built for yield-limited work: rare autoreactive T cell detection, regulatory T cell isolation, TCR repertoire sequencing, and cell therapy feasibility studies.
| Lot # | Condition | Bag Size | Race/Ethnicity | Age | Gender | Country of Collection | Medications | Vials | Price | Action |
|---|---|---|---|---|---|---|---|---|---|---|
| 56980 | Diabetes Type I | Asian/Pacific Islander | 34 | Male | United States |
GLARGINE 24 UNITS/24 LANTIS INSULIN 8UNITS/18UNITS/15UNITS MILD DIABETIC RETINOPATHY
|
1 | |||
| 55922 | Diabetes Type I | Half Bag | Hispanic/Latino | 46 | Male | United States |
Atorvastatin 40mg qd, Losartan 50mg qd, Pantoprazole 20mg bid, Humalog with Insulin pump
|
1 | $10,500.00 | |
| 59332 | Diabetes Type I | Full Bag | Hispanic/Latino | 34 | Male | United States |
Himalogue pump - based on 1 for every 7 carts None
|
1 | $15,225.00 | |
| 57651 | Diabetes Type I | Half Bag | Caucasian | 36 | Female | United States |
Humalog/40units / QD, TRESIBA 16 U IN MORN/10 AT NIGHT
|
1 | $10,500.00 | |
| 59332 | Diabetes Type I | Full Bag | Hispanic/Latino | 34 | Male | United States |
Himalogue pump - based on 1 for every 7 carts None
|
3 | $15,225.00 |
High-Yield LeukoCore Type 1 Diabetes Leukopak for Autoimmune Immunology Research
LeukoCore Type 1 Diabetes Leukopak biospecimens are collected from IRB-consented donors clinically diagnosed with type 1 diabetes (T1D) through IRB-approved apheresis procedures. Each leukopak contains large quantities of peripheral blood mononuclear cells (PBMCs), making it suited to studies that require high input cell numbers.
Why a Leukopak for Type 1 Diabetes Research
T1D is a T cell–mediated autoimmune disease in which cytotoxic lymphocytes destroy insulin-producing pancreatic beta cells. The central experimental problem is that the cells responsible are extremely rare in circulation, and a standard blood draw simply does not contain enough of them. A leukopak solves the numbers problem.
- Autoreactive T cells are rare — CD8 T cells recognising beta-cell antigens such as preproinsulin circulate at very low frequency, so tetramer or multimer-based detection and functional assays require the cell numbers only apheresis provides
- Regulatory T cell isolation at scale — defective regulatory T cell control of autoreactive responses is a core feature of T1D, and Treg purification for phenotyping, suppression assays, or expansion feasibility work is yield-limited
- HLA class II restriction shapes the response — T1D risk is strongly associated with HLA-DR and HLA-DQ haplotypes, and antigen-specific work depends on matching donor HLA type to the reagents used
- Antigen-specific readouts need replicates — low-frequency responses require large-input, multi-replicate assay designs to achieve statistical confidence, which single-tube draws cannot support
- Cell therapy and tolerance-induction feasibility — engineered regulatory T cell and antigen-specific tolerance approaches are assessed for manufacturing feasibility at scales only leukopaks reach
- One donor, many assays — a single apheresis collection allows immunophenotyping, functional assays, and multi-omics on the same donor material, eliminating inter-donor variability as a confounder
Donor Stratification Available
- Disease duration — new-onset within the first year versus long-standing disease
- Islet autoantibody profile — GAD65, IA-2, ZnT8, and insulin autoantibody status where measured
- Residual beta-cell function — C-peptide detectable versus undetectable where measured
- HLA type — HLA-A typing included; extended class II typing available on request
- Glycaemic control and treatment modality — HbA1c where recorded; injection, pump, or automated insulin delivery
- Age at onset — paediatric versus adult onset; coexisting autoimmune disease where documented
- Matched healthy controls available — demographically matched healthy donor leukopaks
Product Features
- Research Use Only (RUO) human leukopaks
- Clinically confirmed T1D donors
- High cell yield for large-scale studies
- Processed and shipped within 24 hours of collection
- Fresh or cryopreserved options available
- Cell yield and viability reported per lot
- IRB-approved and ethically sourced
- Infectious disease testing
- HLA-A typing
- Screen donors with LeukoLot™
De-identified Donor Data
- Verified T1D diagnosis from healthcare providers
- Donor demographics: age, sex assigned at birth, race/ethnicity
- Self-reported medication history and allergies
- Relevant clinical data including age at onset and disease duration (if available)
Applications
- Antigen-specific autoreactive T cell detection by tetramer or multimer staining
- Regulatory T cell isolation, phenotyping, and suppression assays
- Immune cell characterisation and deep immunophenotyping in T1D
- Cell-based assays, cytokine profiling, and functional readouts at scale
- Multi-omics studies including single-cell and TCR repertoire sequencing
- HLA-restricted antigen presentation research
- Cell therapy and tolerance-induction feasibility studies
- Therapeutic development, screening, and mechanism-of-action work
Other Type 1 Diabetes Specimen Types
Matched material from the same T1D donor pool is available as type 1 diabetes serum, plasma, whole blood, and PBMC. Isolated subsets are available as CD4+ T cells, CD8+ T cells, and CD19+ B cells.
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
Type 1 Diabetes Leukopak samples are available fresh or cryopreserved. For pricing, or to check current availability across our full leukopak inventory, visit our human leukopak page to browse other disease-state options and live stock status. For international shipping or regulatory documentation, please contact learnmore@sanguinebio.com to confirm regional compliance and shipping availability.
Protocols & Documentation
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Download
Leukopak Cryopreservation
Standard operating procedure for cryopreserving leukopak units with controlled freezing and post-thaw viability targets.
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Download
Leukopak Thawing
Validated thawing workflow for cryopreserved leukopaks to maximize recovery while maintaining sterility and chain of custody.
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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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Informed Consent Form (ICF)
Available upon request — confirms donor consent for research use and downstream commercialization.
Leukopak
Frequently Asked Questions
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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.
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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 Leukopak cohort?
Our scientific team can scope prospective collections with donor-specific I/E criteria, typically starting within 2 weeks of agreement.