Rheumatoid Arthritis Leukopak

LeukoCore Rheumatoid Arthritis Leukopak for Autoimmune and Immunology Research

LeukoCore Rheumatoid Arthritis Leukopak biospecimens are collected from IRB-consented donors clinically diagnosed with rheumatoid arthritis (RA) through IRB-approved apheresis procedures. Rheumatoid arthritis is a genuinely autoimmune disease: loss of tolerance to citrullinated self-proteins gives rise to anti-citrullinated protein antibodies (ACPA) and rheumatoid factor, and the resulting synovial inflammation destroys cartilage and bone. Each leukopak contains large quantities of peripheral blood mononuclear cells, supporting cell-intensive work in autoimmunity, B cell biology and bone destruction.

Why a Leukopak for Rheumatoid Arthritis Research

  • ACPA and rheumatoid factor are produced by autoreactive B cells and plasmablasts that circulate at low frequency. Isolating and characterising antigen-specific B cells requires the cell numbers only apheresis can deliver.
  • The strongest genetic risk in RA lies in the HLA-DRB1 shared epitope, which shapes presentation of citrullinated peptides to CD4+ T cells. Leukopaks provide enough CD4 T cells for antigen-specific and tetramer-based work in HLA-typed donors.
  • Peripheral helper T cells and other B cell-helping T populations described in RA are rare subsets; recovering them in usable numbers for functional assays is a practical argument for leukopak rather than venipuncture collection.
  • Bone erosion in RA is mediated by RANKL-driven osteoclasts differentiated from the monocyte lineage. A single leukopak supplies enough monocytes to generate osteoclasts in vitro and study erosive potential in patient-derived cells.
  • RA is the disease in which TNF, IL-6 receptor, JAK, CD20 and CD28-costimulation blockade are all clinically established. Leukopak-scale material allows several mechanism-of-action readouts to be run in parallel on one donor rather than split across cohorts.
  • High cell yields support engineered cell approaches — including regulatory T cell expansion and CAR-based tolerance strategies — that are increasingly explored in autoimmune disease.

Donor Stratification Available

  • Serology: ACPA-positive, rheumatoid factor-positive, dual-positive, or seronegative RA
  • Disease activity by DAS28 or CDAI where recorded
  • Treatment status: biologic-naive, on methotrexate or other conventional synthetic DMARD, on TNF inhibitor, on IL-6 receptor inhibitor, on JAK inhibitor, on rituximab or abatacept, or in washout
  • Disease duration: early versus established RA
  • Erosive versus non-erosive disease where radiographic status is reported
  • Extra-articular involvement and comorbidity, including interstitial lung disease
  • Matched healthy controls available

Product Features

  • Research Use Only (RUO) human leukopaks
  • Clinically confirmed RA 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 RA diagnosis from healthcare providers
  • Donor demographics: age, sex assigned at birth, race/ethnicity
  • Self-reported medication history and allergies
  • Serology and disease activity where available
  • Relevant clinical data

Applications

  • Autoreactive and antigen-specific B cell isolation and repertoire analysis
  • CD4+ T cell subset isolation, including B cell-helping and peripheral helper populations
  • Monocyte-derived osteoclast differentiation and bone resorption assays
  • Mechanism-of-action studies for TNF, IL-6R, JAK, CD20 and costimulation-directed therapeutics
  • Regulatory T cell expansion and engineered cell therapy development
  • Cytokine profiling and cell-based functional assays
  • Multi-omics studies including single-cell RNA sequencing and immune repertoire sequencing
  • Immunophenotyping of seropositive versus seronegative RA

Other Rheumatoid Arthritis Specimen Types

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

Rheumatoid Arthritis Leukopak is available fresh or cryopreserved. For pricing, current availability, or to discuss a serology-stratified cohort, contact learnmore@sanguinebio.com. Need a different condition, or want 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 us to confirm regional compliance and shipping availability.

Protocols & Documentation

  • Leukopak Cryopreservation

    Standard operating procedure for cryopreserving leukopak units with controlled freezing and post-thaw viability targets.

    Download
  • 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

Frequently Asked Questions

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Are samples IRB approved?

1 Answer

YES – All collections are conducted under IRB-approved protocols and electronic informed consent. Sanguine utilizes Advarra and WCG IRB for oversight.

YES – all our products are research use only (RUO).

Storage depends on sample type but often cryopreserved samples stored in liquid nitrogen can be stored for years.

Extensive customization is available. To discuss your project request a quote or email us at learnmore@sanguinebio.com.

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.

Timelines depend on condition, sample type, and I/E criteria but we often start collection within 2 weeks of signed agreement.

YES – we have in-stock inventory. You can also email us at learnmore@sanguinebio.com as we continually get new samples in our inventory.

Each sample from a different individual – Unique donor means each sample comes from a different person, ensuring biological diversity in your study.

YES – Unique donors can be specified and guaranteed based on your requirements.

For information about sample quality, please see: Quality and Compliance

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.

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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.

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