Official Title
Study of the Kinetics of the Immune Response During the Intensive Care Unit Stay in Adult Patients Infected With SARS-CoV-2: Multicentric Non Interventional Study
Brief Summary

Infection with the SARS-CoV-2 coronavirus (COVID-19) has recently been identified as apandemic due to the speed and global scale of its transmission. In Auvergne-Rhône-Alpesregion (AURA), the epidemic began in February 2020 and the number of infected people isstill important. Between 15 and 20% of COVID-19 patients develop an acute respiratorydistress syndrome (ARDS) leading to their hospitalization in intensive care. Theirclinical progression can be rapidly harmful with the development of severe ARDSassociated with an increased risk of death.Preliminary data on the immune response of COVID-19 patients describe the induction of amoderate inflammatory response and the occurrence of major progressive lymphopenia overtime associated with potential immunosuppression. Up to 50% of secondary infections arereported in deceased COVID-19 patients. However, no prospective study has exhaustivelydescribed the kinetics of the immune response of COVID-19 patients in intensive care.The precise description of the immune response over time in adult patients with a proveninfection with the SARS-CoV-2 virus and the study of the relation between this responseand the increased risk of organ failure (severe ARDS), death or nosocomial infection willallow us to better understand the pathophysiology of the immune response induced byCOVID-19 in order to (i) identify new therapeutic strategies targeting the host responsein patients in intensive care (ii) to develop biological markers to stratify patients forfuture clinical trials evaluating these immunoadjuvant treatments in COVID-19.

Unknown status
Intensive Care Unit
SARS-CoV-2

Biological: Collection of blood samples in order to create a biocollection

Blood samples will be collected at admission in intensive care, at Day 3, Day 7, Day 12
and Day 20 during their hospitalization. Clinical data from routine care will be
collected. Vital status will be assessed at Day 28 and Day 90.

Eligibility Criteria

Inclusion Criteria:

1. Man or woman aged 18 or over,

2. Hospitalization in intensive care for Sars-Cov-2 pneumopathy,

3. First hospitalization in intensive care unit,

4. Positive diagnosis of SARS-CoV2 infection carried out by PCR or by another approved
method in at least one respiratory sample,

5. Sampling in the first 24 hours after admission to intensive care unit (D0 / D1)
feasible,

6. Patient or next of kin who has been informed of the terms of the study and has not
objected to participating.

Exclusion Criteria:

1. Pregnant or lactating woman,

2. Person placed under legal protection,

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

Hôpital Pierre Wertheimer
Bron, France

Hôpital Gabriel Montpied
Clermont-Ferrand, France

Centre hospitalier universitaire de Grenoble Alpes
Grenoble, France

Hôpital Edouard Herriot
Lyon, France

Hôpital Edouard Herriot
Lyon, France

Hôpial de la Croix Rousse
Lyon, France

Hôpital Lyon Sud
Pierre-Bénite, France

CH de St Etienne
Saint-Étienne, France

Contacts

Fabienne VENET
4 72 11 97 46 - +33
fabienne.venet@chu-lyon.fr

Marie GROUSSAUD
4 72 35 71 70 - +33
marie.groussaud@chu-lyon.fr

Fabienne VENET, Principal Investigator
Hospices Civils de Lyon

NCT Number