Characterization of Antibacterial Antibodies in Patients With Cystic Fibrosis
Identification and Characterization of Antibacterial Antibodies in Sera of Patients With Cystic Fibrosis
University Hospital of Cologne
75 participants
Oct 1, 2020
OBSERVATIONAL
Conditions
Summary
Most of the cystic fibrosis (CF) patients are or have been pulmonary colonized with bacteria such as Pseudomonas aeruginosa or Staphylococcus aureus. Aim of this study is to detect virulence factor neutralizing antibodies in the sera of the study population followed by B cell repertoire analyses to design B cell-derived neutralizing monoclonal antibodies. The functionality of neutralizing antibodies rests on inhibition of virulence factors by binding of crucial epitopes rather than merely the induction of opsonization. Focusing on patients with bacterial colonization/chronic infections or a history of an acute infection in the past, will increase the likelihood for identification of serum with neutralizing activity as in vivo antigen contact is a prerequisite for antibody development and maturation. Since virulence factors are essential for infection, dissemination and tissue damage, inhibition of these factors by developed neutralizing antibodies might contribute to a favorable outcome of life-threatening infections.
Eligibility
Inclusion Criteria8
- Age ≥ 18 years
- Ability to give consent
- Normal vital signs including:
- Blood pressure systolic value 150 - 100 mmHg, diastolic value < 90 mmHg
- Respiratory rate < 20/min
- Oxygen saturation >92%
- Heart rate 50 - 110/min
- Body temperature <38°C
Exclusion Criteria5
- Cytopenia (leukocytes < 1.500/µl, thrombocytes < 50.000/µl, Hemoglobin < 12 g/dl)
- Heart disease or pulmonary hypertension
- Body weight <50 kg (exclusion of blood sampling for B cell isolation)
- Blood donation, larger blood loss and/or major surgery in the last 8 (male) or 12 (female) weeks
- Any decline of the general state of health in the last 3 month including weight loss > 2kg, pulmonal exacerbation or increased impairment of pulmonary function (FEV1 < 50%)
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
Screening: Blood sampling of 15 ml whole blood B cell isolation: Blood sampling of max. 400 ml whole blood or 6% of the total blood volume (♀ 65 ∓ 10 ml/kg; ♂ 77 ∓ 10 ml/kg)
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT04700358