Inflammatory Bowel Disease Plasma

Inflammatory Bowel Disease Plasma for Immune-Mediated Inflammatory Disease Research

Inflammatory Bowel Disease Plasma is collected from IRB-consented donors clinically diagnosed with inflammatory bowel disease (IBD) and processed within one day of collection to preserve cytokines, proteins and metabolites. IBD — comprising Crohn’s disease and ulcerative colitis — is a chronic immune-mediated inflammatory disease of the gastrointestinal tract in which a dysregulated mucosal immune response to the gut microbiota, on a permissive genetic background and with a compromised epithelial barrier, drives relapsing inflammation. Plasma is acellular and is supplied for soluble-analyte work rather than cell-based assays.

Mucosal Immune Dysregulation and Why Plasma

  • TNF and IL-23/IL-17 axis signalling is central to IBD pathogenesis and is the target of the anti-TNF and anti-IL-23/IL-12 biologics that dominate current therapy, making these cytokines the highest-value plasma analytes.
  • Gut-homing and leukocyte trafficking: the alpha4beta7 integrin-MAdCAM-1 axis and sphingosine-1-phosphate receptor signalling direct lymphocytes to the intestine and are targeted by vedolizumab and S1P modulators; soluble trafficking-related markers are measurable in plasma.
  • Epithelial barrier dysfunction generates circulating permeability and epithelial-damage markers, providing a non-invasive window on mucosal integrity.
  • Systemic inflammatory burden: CRP and other acute-phase reactants, IL-6, and neutrophil-derived mediators track disease activity and support flare-prediction research.
  • Therapeutic drug monitoring and immunogenicity: biologic drug levels and anti-drug antibodies are measured in circulation, and this cohort supports assay development for that purpose.
  • Fibrosis and stricturing biology in Crohn’s disease can be studied through extracellular matrix turnover markers in the same aliquot.

Donor Stratification Available

  • Disease subtype: Crohn’s disease versus ulcerative colitis, and IBD-unclassified where documented
  • Disease activity at collection: active flare versus clinical remission
  • Disease location and extent: ileal, colonic or ileocolonic Crohn’s; proctitis, left-sided or extensive colitis
  • Behaviour: inflammatory, stricturing, or penetrating/fistulising Crohn’s disease
  • Treatment status: anti-TNF biologic, anti-IL-23/IL-12 biologic, anti-integrin biologic, JAK inhibitor, S1P modulator, thiopurine, corticosteroid, 5-ASA, or treatment-naive
  • Surgical history, including prior resection or ostomy
  • Extraintestinal manifestations and comorbidities such as primary sclerosing cholangitis, spondyloarthritis, or hidradenitis suppurativa
  • Matched healthy controls available

Product Features

  • Research Use Only (RUO)
  • Plasma collected from clinically confirmed inflammatory bowel disease donors
  • Processed within one day of collection
  • Anticoagulant selection available on request
  • IRB-approved protocols and informed consent
  • Custom aliquot volumes available upon request

De-identified Donor Data

  • Verified inflammatory bowel disease diagnosis, with subtype where documented
  • Demographic data: age, sex assigned at birth, race/ethnicity
  • Donor-reported medications, allergies, and comorbidities
  • Disease activity and treatment context reported per lot where captured
  • Additional IBD-specific metadata available on request

Applications

  • TNF-alpha, IL-6, IL-23 and IL-17 pathway cytokine profiling
  • Disease activity and flare-prediction biomarker discovery and validation
  • Gut permeability and epithelial damage marker measurement
  • Acute-phase reactant and systemic inflammation characterisation
  • Biologic drug level and anti-drug antibody assay development
  • Extracellular matrix turnover and intestinal fibrosis marker research
  • Plasma proteomic and metabolomic discovery, including microbiota-derived metabolites
  • Crohn’s versus ulcerative colitis differential biomarker studies and therapeutic response research

Other Inflammatory Bowel Disease Specimen Types

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

Inflammatory bowel disease plasma is available in standard and custom volumes. For pricing, international orders, or documentation requirements, please email learnmore@sanguinebio.com to ensure compatibility with your country’s regulations. To compare collection formats or check wider availability, visit our human plasma page.

Protocols & Documentation

  • Plasma Isolation

    Protocol for plasma separation from anticoagulated whole blood, including processing, storage, and traceability requirements.

    Download
  • Informed Consent Form (ICF)

    Available upon request — confirms donor consent for research use and downstream commercialization.

Plasma

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 Plasma 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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