Actively Recruiting
The Role of CXCR4-expressing Neutrophils in Influenza-related Acute Respiratory Distress Syndrome
Led by University Hospital, Bordeaux · Updated on 2024-12-27
90
Participants Needed
2
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Influenza remains a major global health threat, causing over 650,000 deaths annually without significant advances in patient care despite decades of research. Severe influenza can lead to acute lung injury due to a disrupted immune response, where neutrophils play a role in both fighting infection and disease tolerance. This study focuses on a specific subgroup of neutrophils that express CXCR4, which may be linked to worsening lung infections. Researchers aim to compare the levels of these CXCR4-expressing neutrophils in the blood and lung fluid of influenza patients who survive versus those who do not. Participants will undergo blood sampling and bronchoalveolar lavage (BAL) within 24 hours and again on day 3 after ICU admission to collect neutrophils. These cells will be isolated and analyzed through immunostaining and flow cytometry to measure the percentage of CXCR4-expressing neutrophils. Additionally, extra blood tubes and lung fluid samples will be collected during treatment for detailed study. The mortality rates of participants will be assessed at 28 and 90 days after inclusion. During the study, participants will be closely monitored with blood and lung fluid tests to evaluate immune cell behavior. Researchers will collect clinical data and mortality outcomes to understand the relationship between CXCR4-expressing neutrophils and disease severity. The study's findings aim to shed light on immune mechanisms in influenza-related acute respiratory distress syndrome and may help guide future therapies. Participant involvement will last at least 90 days, covering initial ICU admission through follow-up assessments.
CONDITIONS
Official Title
The Role of Cxcr4Hi neutrOPhils in InflueNza
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient aged 18 yo or above.
- Acute respiratory distress syndrome as defined by the Berlin classification.
- Invasive mechanical ventilation for less than 24 hours.
- Cause of ARDS: Influenza infection proven by polymerase chain reaction OR Bacterial infection (tracheal aspirate with more than 105 CFU/mL and BAL with more than 104 CFU/mL) OR Pancreatitis according to the 2013 Working Group IAP/APA Acute Pancreatitis Guidelines OR Peritonitis according to the 2018 SFAR guidelines.
- Health insurance.
- Written informed consent from legal relative or representative.
You will not qualify if you...
- Neutropenia (< 500/mm3).
- Neutrophils qualitative defect.
- Patient included in an interventional research assessing an immunomodulatory or antiviral drug.
- Acquired ImmunoDeficiency Syndrome.
- Contraindication to BAL: Severe bronshospasm, Out-of-control shock, Intracranial high pressure, Refractory hypoxemia (PaO2/FiO2 < 60 mmHg).
- Legal restriction: prisoners, pregnancy, legal protection.
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Trial Site Locations
Total: 2 locations
1
Hopital Pellegrin
Bordeaux, France, 33000
Actively Recruiting
2
Hopital Haut-Lévêque
Pessac, France, 33604
Not Yet Recruiting
Research Team
R
Renaud PREVEL, Dr
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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