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Flow Cytometric Immune Monitoring of B. Afzelii-Specific T Lymphocytes

Flow Cytometric Immune Monitoring of B. Afzelii-Specific T Lymphocytes

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07703787
Acronym
LyTLymICS-AIM
Enrollment
20
Registered
2026-07-14
Start date
2026-09-01
Completion date
2029-03-01
Last updated
2026-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lyme Borreliosis, Lyme Disease

Brief summary

Lyme borreliosis diagnosis currently relies on clinical assessment and detection of Borrelia-specific antibodies. However, serology does not allow reliable assessment of active infection. Evaluation of the cellular immune response through Borrelia-specific T lymphocyte monitoring may provide complementary diagnostic and prognostic information. This study aims to assess Borrelia afzelii-specific T-cell responses using multiparameter flow cytometry after stimulation with standardized peptide pools. This approach enables the characterization of CD4+ and CD8+ T cells, including polyfunctional immune responses. The diagnostic and prognostic value of this immunomonitoring strategy will be evaluated in patients with acrodermatitis chronica atrophicans, a late manifestation of Lyme borreliosis associated with B. afzelii.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age ≥ 18 years * Subject informed of the results of the prior medical examination * Subject informed about the objectives, procedures, and potential risks of the study * Subject affiliated with a health insurance/social security scheme (beneficiary or dependent) * Subject having provided dated and signed informed consent * Lyme borreliosis/acrordermatitis chronica atrophicans (ACA) group: Subject presenting clinical and biological criteria or Borrelia identification confirming chronic atrophic acrodermatitis, with appropriate antibiotic treatment initiated less than 18 months ago or untreated • Control group: Healthy subject with no history of Lyme disease and negative Lyme serology

Exclusion criteria

* Body weight \< 50 kg * Pregnancy or breastfeeding * Diabetes mellitus * Immunodeficiency or ongoing immunosuppressive treatment (including oral corticosteroids) * Contraindication to local anesthesia with lidocaine, with or without adrenaline * Inability to provide informed consent (emergency situation, inability to understand study information, …) * Participation in another clinical trial * Legal protection measures (guardianship, curatorship, or legal safeguard)

Design outcomes

Primary

MeasureTime frameDescription
Characterization of Borrelia afzelii-specific T-cell immune responses by multiparameter flow cytometryAt study inclusion (baseline visit)Descriptive analysis of antigen-specific T-cell responses after stimulation with Borrelia afzelii peptide pools using intracellular cytokine staining (ICS) and activation-induced marker (AIM) assays. Outcomes will include the polyfunctionality index of antigen-specific T cells, comparison of ICS and AIM responses, number of positive peptide pools, and magnitude of antigen-specific CD4+ and CD8+ T-cell responses.

Countries

France

Contacts

CONTACTSarah HUSTACHE
dpidrci@chru-strasbourg.fr+33 3 88 11 54 15

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 15, 2026