Lyme Disease Plasma
Lyme Disease Plasma from IRB-consented donors diagnosed with Lyme disease. Because two-tier serology is insensitive early and antibodies persist after cure, plasma-based host-response, proteomic, metabolomic and direct-detection approaches are where the research need sits. Donors can be stratified by disease stage, objective manifestations, serostatus, antibiotic treatment timing, persistent post-treatment symptoms and tick-borne co-infection status, with matched healthy controls available.
Lyme Disease Plasma for Infectious Disease and Host Response Research
Lyme Disease Plasma is collected from IRB-consented donors diagnosed with Lyme disease and processed under standardised SOPs. Lyme disease is an infectious disease caused by Borrelia burgdorferi sensu lato, transmitted by Ixodes ticks, and the clinical picture reflects the host immune response to that infection and to its dissemination. These samples support research into the host response, biomarker discovery and therapeutic development, including persistent symptoms after treatment.
What Lyme Disease Plasma Reveals
- Lyme disease progresses through recognised stages: early localised infection with erythema migrans, early disseminated disease with manifestations such as multiple skin lesions, cranial neuropathy or carditis, and late disease presenting most often as Lyme arthritis or neuroborreliosis. Plasma from stage-annotated donors is what allows host-response markers to be mapped onto that progression.
- Standard diagnosis relies on two-tier antibody testing, which is insensitive in the first weeks of infection because seroconversion has not yet occurred. That diagnostic gap is the main reason disease-state plasma is valuable: direct-detection and host-response approaches are being developed specifically to fill it.
- B. burgdorferi is present in blood at very low abundance and localises to tissue, so pathogen nucleic acid detection in plasma is technically demanding. Work in this area depends on well-characterised patient plasma rather than spiked controls.
- Antibody responses persist for months to years after successful antibiotic treatment, so serology cannot establish cure. Plasma-based cytokine, chemokine, proteomic and metabolomic signatures are therefore being investigated as treatment-response and resolution markers.
- A subset of patients report persistent symptoms after standard antibiotic therapy. The mechanism remains unresolved, and longitudinally characterised plasma from these donors is central to work on immune activation signatures in that population.
- Tick-borne co-infections including Anaplasma phagocytophilum and Babesia microti share the same vector and can confound host-response interpretation, so co-infection status is a meaningful stratification variable rather than an afterthought.
Donor Stratification Available
- Disease stage: early localised with erythema migrans, early disseminated, or late Lyme disease
- Objective manifestations where documented: Lyme arthritis, neuroborreliosis, carditis, or cutaneous only
- Serostatus by two-tier testing where documented, including IgM and IgG immunoblot results
- Treatment status and timing: pre-treatment, on antibiotics, or post-treatment with interval since completion
- Persistent symptoms after treatment versus symptom resolution
- Geographic region of exposure and documented tick-borne co-infection status; matched healthy controls available
Product Features
- Plasma isolated from clinically confirmed Lyme disease donors
- Research Use Only (RUO)
- Rigorous donor screening and sample quality checks
- Anticoagulant selection available on request
- Standard and custom volumes; volumes reported per lot
- Matched serum, whole blood and PBMC from the same donors available on request
De-identified Donor Data
- Age, sex, race, medication, diagnosis method, disease severity and stage
- Optional: comorbidities, lab values, and clinical history
- Treatment history and symptom duration available on request
Applications
- Cytokine and chemokine profiling of the host response to Borrelia infection
- Plasma proteomic and metabolomic signature discovery for early diagnosis
- Direct-detection assay development, including low-abundance nucleic acid and antigen approaches
- Serology and immunoassay development, including matched-matrix comparability work
- Treatment-response and resolution biomarker research
- Persistent post-treatment symptom research and immune activation profiling
- Tick-borne co-infection differential marker studies
- Disease-state control matrix for infectious disease immunoassay qualification
Other Lyme Disease Specimen Types
- Lyme Disease Serum
- Lyme Disease Whole Blood
- Lyme Disease PBMC
- Lyme Disease Leukopak
- Lyme Disease Bulk Plasma
Quality and Compliance
- IRB-approved protocols
- Informed donor consent
- Standardized collection and processing SOPs
- HIPAA-compliant donor data protection
Ordering & Customization
Lyme disease plasma is available in both standard and custom volumes to meet your research needs. For pricing, current availability, or a quote on a stratified donor cohort, contact learnmore@sanguinebio.com.
International Orders: For international shipments or country-specific documentation requirements, please contact us at learnmore@sanguinebio.com to ensure compliance with your local regulations. To browse other disease states in this specimen type, visit our human plasma page.
Protocols & Documentation
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Download
Plasma Isolation
Protocol for plasma separation from anticoagulated whole blood, including processing, storage, and traceability requirements.
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Informed Consent Form (ICF)
Available upon request — confirms donor consent for research use and downstream commercialization.
Plasma
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 Plasma cohort?
Our scientific team can scope prospective collections with donor-specific I/E criteria, typically starting within 2 weeks of agreement.