Immunological Profiling of Patients With COVID-19 in Respiratory Distress
NCT ID: NCT04351711
Last Updated: 2025-12-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
120 participants
OBSERVATIONAL
2020-04-09
2022-12-12
Brief Summary
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Detailed Description
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However, this initial replication causes a cytokine storm involving inflammatory cytokines. The intensity of this cytokine storm is correlated with the severity of COVID-19 cases.
Pulmonary involvement, which is the main cause of death in SARS-CoV infections, has been attributed to local inflammation, with infiltration of CD8 + T cells, polymorphonuclear cells, monocytes and macrophages, infiltration proportional to the severity of respiratory failure as well as increased vascular permeability.
SARS-CoV also induces T cell apoptosis. This pro-apoptotic effect could contribute to the lymphopenia observed in 37 to 63% of COVID-19 cases, which is predictive of severe forms.
Thus the pulmonary involvement could be partly caused by immunopathological mechanisms.
Immunological disturbances associated with respiratory failure need to be better defined. Recently, we measured a panel of soluble and membrane markers allowing to characterize T CD4 +, T CD8 +, B, monocytic, NK, endothelial activation as well as inflammation in a sample made up of 150 volunteers from a general population providing a control population.
The study investigators aim to use this panel to define the immune activation state of patients infected with SARS-CoV-2 hospitalized for respiratory distress. In addition, the investigators will identify the soluble factors linked to the immune activation overproduced by the peripheral blood mononuclear cells (PBMC) of these patients. Finally, the investigators want to characterize the transcriptome of the main circulating immune sub-populations. These parameters will be compared with those of patients infected with SARS-CoV-2 hospitalized before experiencing respiratory distress.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Patients SARS-CoV-2 with respiratory failure
Patients in intensive care
Immunological profiling
The immune activation phenotype will be assessed using a standardized panel of soluble and membrane immune activation markers
Patients SARS-CoV-2 without respiratory failure
Patients hospitalized in normal hospital wards
Immunological profiling
The immune activation phenotype will be assessed using a standardized panel of soluble and membrane immune activation markers
HEALTHY VOLUNTEERS
HEALTHY VOLUNTEERS
Immunological profiling
The immune activation phenotype will be assessed using a standardized panel of soluble and membrane immune activation markers
NON-COVID-19 PATIENTS
Patient hospitalized at the CHU of Nîmes for an infection by a virus other than SARS-CoV-2
Immunological profiling
The immune activation phenotype will be assessed using a standardized panel of soluble and membrane immune activation markers
PAUCISYMPTOMATIC SARS-COV-2+ PATIENTS
Patient positive for SARS-CoV-2 by RT-PCR at the CHU of Nîmes and presenting at most moderate clinical signs without respiratory insufficiency (O2 saturation greater than or equal to 96%) during the confinement period
Immunological profiling
The immune activation phenotype will be assessed using a standardized panel of soluble and membrane immune activation markers
convalescent patients
Additional 1-year follow-up visit
Immunological profiling
The immune activation phenotype will be assessed using a standardized panel of soluble and membrane immune activation markers
Immunological profiling
The immune activation phenotype will be assessed using a standardized panel of soluble and membrane immune activation markers
Interventions
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Immunological profiling
The immune activation phenotype will be assessed using a standardized panel of soluble and membrane immune activation markers
Immunological profiling
The immune activation phenotype will be assessed using a standardized panel of soluble and membrane immune activation markers
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Patient hospitalized in respiratory resuscitation or in the service of Infectious and Tropical Diseases of the CHU de Nîmes with infection by SARS-CoV-2, confirmed by RT-PCR or by an antigen test.
Exclusion Criteria
* The patient is under safeguard of justice
* Patient already under ventilation transferred from another center
18 Years
ALL
Yes
Sponsors
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Institute of Human Genetics, Montpellier
UNKNOWN
Centre Hospitalier Universitaire de Nīmes
OTHER
Responsible Party
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Principal Investigators
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Pierre Corbeau
Role: PRINCIPAL_INVESTIGATOR
CHU Nimes
Locations
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CHU de Nimes
Nîmes, , France
Countries
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References
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Andre S, Picard M, Cezar R, Roux-Dalvai F, Alleaume-Butaux A, Soundaramourty C, Cruz AS, Mendes-Frias A, Gotti C, Leclercq M, Nicolas A, Tauzin A, Carvalho A, Capela C, Pedrosa J, Castro AG, Kundura L, Loubet P, Sotto A, Muller L, Lefrant JY, Roger C, Claret PG, Duvnjak S, Tran TA, Racine G, Zghidi-Abouzid O, Nioche P, Silvestre R, Droit A, Mammano F, Corbeau P, Estaquier J. T cell apoptosis characterizes severe Covid-19 disease. Cell Death Differ. 2022 Aug;29(8):1486-1499. doi: 10.1038/s41418-022-00936-x. Epub 2022 Jan 22.
Other Identifiers
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2020-A00875-34
Identifier Type: OTHER
Identifier Source: secondary_id
NIMAO/2020-01/PC-01
Identifier Type: -
Identifier Source: org_study_id
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