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RecruitingNCT07436780OLYMPEUpdated Sep 24, 2026

B Lymphocyte Populations in the Pulmonary Microenvironment of Patients Under Mechanical Ventilation With or Without VAP (Ventilator-Associated Pneumonia)

An observational study in Ventilator-associated Pneumonia, sponsored by University Hospital, Limoges. Recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-24.

Sponsored by University Hospital, Limoges · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
75
Ages
18 Years and older
Sex
All
01

Study summary

Diagnosis of VAP relies on a set of non-specific clinical, biological, and imaging criteria.

Understanding host-pathogen interactions and the mechanisms of deregulations leading to infection of pulmonary tissue appears essential.

The aim is to qualitatively describe the B lymphocyte populations present in the pulmonary microenvironment of patients admitted to intensive care and requiring invasive mechanical ventilation

Read the detailed description

The study of the immune system and host-pathogen interactions is the subject of extensive research to improve the understanding of pathophysiology, leading to more precise diagnostic criteria, and considering preventive or curative treatments while limiting the use of anti-infective molecules. Understanding host-pathogen interactions and the mechanisms of deregulations leading to infection of pulmonary tissue seems essential. The study of T lymphocyte populations has already been the focus of numerous investigations. However, regarding the humoral immune response, B lymphocyte populations and their roles have so far been little explored in this context. Nevertheless, the presence of B lymphocytes in pulmonary tissue has been proven, particularly in infectious, postinfectious, or postvaccination contexts, but currently, there are no published studies regarding the B lymphocytes role in the pathophysiology of VAP (Ventilator-Associated Pneumonia).

Respiratory samples (endotracheal aspirates) will be collected from patients under mechanical ventilation on the day of intubation (D0), the day before extubation (Dext), and the day of VAP diagnosis (DVAP) for patients who will develop it. The samples will be stored and then analyzed by flow cytometry.

02

Conditions studied

  • Ventilator-associated Pneumonia

Keywords

  • ventilator-associated pneumonia
  • Intensive care medicine
  • host-pathogen interaction
  • humoral immunity
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients of Limoges University Hospital admitted to emergency room

Inclusion criteria

  • Adult patients (≥18 years old), admitted to intensive care under mechanical ventilation for an estimated duration of at least 5 days.

Exclusion criteria

Exclusion Criteria:

  • Patients admitted for an infectious pneumonia or presenting with acute respiratory distress syndrome (ARDS). Patients in aplasia (leukocytes \< 0.5 gigal/L).
04

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
75 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Ventilator Associated Pneumonia (VAP)

    Patient who developped Ventilator Associated Pneumonia (VAP) under mechanical ventilation

  • Without Ventilator Associated Pneumonia

    Patient who did not develop Ventilator Associated Pneumonia (VAP) under mechanical ventilation

05

What researchers measure

Primary outcomes

  1. Qualitative description of B lymphocyte populations by flow cytometry analysis with specific antibodies

    To qualitatively describe the B lymphocyte populations in the endotracheal aspirates of patients admitted to intensive care and requiring invasive mechanical ventilation. B lymphocyte subpopulations will be described using a flow cytometry method using antibodies targeting the following markers: CD93, CD62L, CD14, CXCR4, CD32, CD27, CD38, CD138, CD3, CD10, CD19, CD20, kappa light chains, lambda light chains.

    Time frame: At the inclusion (T1), at diagnosis (T2 on the day of VAP diagnosis for patient who will develop it, on average 72 hours after the inclusion), at the end of the study (T3 on the day before extubation, on average 5 days after the inclusion)

Secondary outcomes

  1. Quantitative description of B lymphocyte populations by flow cytometry analysis with specific antibodies

    To quantitatively describe the B lymphocyte populations in the endotracheal aspirates of patients admitted to intensive care, requiring invasive mechanical ventilation, and presenting ventilator associated pneumonia (VAP). B lymphocyte subpopulations will be described using a flow cytometry method using antibodies targeting the following markers: CD93, CD62L, CD14, CXCR4, CD32, CD27, CD38, CD138, CD3, CD10, CD19, CD20, kappa light chains, lambda light chains

    Time frame: At the inclusion (T1), at diagnosis (T2 on the day of VAP diagnosis for patient who will develop it, on average 72 hours after the inclusion), at the end of the study (T3 on the day before extubation, on average 5 days after the inclusion)

06

Study locations

1 of 1 sites recruiting
  • CHU Limoges
    Limoges, 87042, France
    Recruiting
07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07436780
Lead sponsor
University Hospital, Limoges
Responsible party
Sponsor
First posted
Feb 27, 2026
Start date
Jan 12, 2026
Primary completion
Jul 11, 2027 (estimated)
Completion
Jul 11, 2027 (estimated)
Last update
Sep 24, 2026

Study contacts

Safirah Akowanou
Contact
safirah.akowanou@chu-limoges.fr
+33555058755
Abdeslam BEN TALEB
Contact
abdeslam.bentaleb@chu-limoges.fr
+33555058616
Julien VAIDIE, Dr
principal investigator · University Hospital, Limoges

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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