K05
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The following general criteria must be met for inclusion in the study: - Capacity to provide informed consent - Patients with periodontitis as well as individuals without a diagnosis of periodontitis, provided all other inclusion criteria are met, and no exclusion criteria apply. Additionally, the following criteria must be checked and satisfied immediately before blood collection: - Puncture site: Free from lesions or infections - Presence of a signed informed consent form for participation in the study
Exclusion criteria
Exclusion criteria: - Existing cytopenias (leukocytes 2 kg, diabetic metabolic state, pulmonary exacerbation, or loss of lung function (FEV1 > 10%) in the past 3 months - No fever
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The identification of functional antibodies from the sera of periodontitis patients with a long-standing history and/or progressive form of periodontitis (Grade C) involves titration of blood sera against potent virulence factors of the key periodontal pathogen Porphyromonas gingivalis (PA strain), followed by the establishment of various immunological assays utilizing sera from patients with particularly high titers. Isolation of B cells from sera exhibiting particularly inhibitory antibodies, followed by subsequent antibody production. In vitro testing of the generated antibodies. | — |
Secondary
| Measure | Time frame |
|---|---|
| New insights into the relationships between immunological processes and clinical parameters | — |
Countries
Germany
Contacts
Abteilung für zahnerhaltung & Parodontologie // Klinik für Zahn- Mund- und Kieferheilkunde