Official Title
C5a Receptor Expression in Circulating Myeloid Cells in ARDS Secondary to COVID-19
Brief Summary

The pathophysiology of ARDS is linked to an uncontrolled inflammatory response at the level of alveolo-capillary membrane, mediated by neutrophils and mononuclear cells. The complement system and anaphylatoxin C5a have shown central role in the recruitment of these pro-inflammatory cells and more broadly in the genesis of cytokinic storm syndrome. C5a acts via receptors C5aR and C5L2. This is a preliminary study aimed at studying the expression of the C5a receptor on myeloid cells in peripheral blood of patients with ARDS secondary to COVID-19. This study has of primary objective to show there is an overexpression of the C5a receptor in patients with ARDS secondary to COVID-19 compared to control patients (patients with COVID-19 without respiratory distress and healthy volunteers). The medium-term objective is to develop a clinical trial to test the effectiveness of anti-C5aR antibody in this condition.

Detailed Description

The pathophysiology of ARDS is linked to an uncontrolled inflammatory response at the level
of alveolo-capillary membrane, mediated by neutrophils and mononuclear cells. The complement
system and anaphylatoxin C5a have shown central role in the recruitment of these
pro-inflammatory cells and more broadly in the genesis of cytokinic storm syndrome. C5a acts
via receptors C5aR and C5L2.

This is a preliminary study aimed at studying the expression of the C5a receptor on myeloid
cells in peripheral blood of patients with ARDS secondary to COVID-19.

This study has of primary objective to show there is an overexpression of the C5a receptor in
patients with ARDS secondary to COVID-19 compared to control patients (patients with COVID-19
without respiratory distress and healthy volunteers).

The medium-term objective is to develop a clinical trial to test the effectiveness of
anti-C5aR antibody in this condition.

Unknown status
COVID-19

Other: draw blood

40 mL blood sample will be taken within the first three days of hospitalization, a second sample will be taken between the 5th and 10th day of hospitalization and a third sample will be taken on the 10th day of hospitalization or the day of discharge if earlier.

Eligibility Criteria

Inclusion Criteria:

For patients in resuscitation unit with ARDS linked to COVID-19:

- Patient under invasive mechanical ventilation

- PaO2 / FiO2 <300

- PCR SARS-CoV-2 positive in a pharyngeal or respiratory sample

For control patients with COVID-19 without ARDS

- Oxygen flow always less than 5 L / min

- PCR SARS-CoV-2 positive in a pharyngeal or respiratory sample

- No passage in resuscitation unit

- Favorable evolution

Exclusion Criteria:

- Minors

- Patient deprived of liberty

- Patient's refusal to participate at study

- Patient for whom therapeutic limitation measures such as non-admission to intensive
care have been issued

- Medullar aplasia

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
France
Locations

Assistance Publique Hôpitaux de Marseille
Marseille, France

Investigator: Julien CARVELLI
Contact: 04 13 42 95 35
Julien.CARVELLI@ap-hm.fr

Investigator:

Contacts

Julien JC CARVELLI, MD
04 13 42 95 35 - +33
Julien.CARVELLI@ap-hm.fr

Kahéna KA AMICHI
04 91 38 19 66 - +33
Kahena.AMICHI@ap-hm.fr

Emilie EGP GARRIDO-PRADALIE, Study Director
Assistance Publique Hôpitaux de Marseille

Innate Pharma
NCT Number
Keywords
Covid-19
ARDS
C5a receptors
MeSH Terms
COVID-19