Immunological Profiling of Patients With COVID-19 in Respiratory Distress

NCT ID: NCT04351711

Last Updated: 2025-12-10

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

120 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-04-09

Study Completion Date

2022-12-12

Brief Summary

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The study investigators hypothesize that the pneumonia arising in patients with COVID-19 is largely of immunopathological origin. The investigators will therefore seek to define the immune activation phenotype of patients in respiratory distress and to see if this immune signature is predictive of mortality. Finally, the investigators will look for overproduced inflammatory mediators to identify potential therapeutic targets.

Detailed Description

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SARS-CoV inhibits the viral detection systems and the signaling pathways of type I interferons (IFN-I). The weakness of the initial interferon response is predictive of the severity of future lung disease. The effectiveness of this escape strategy seems to allow these coronaviruses to replicate in the human body without triggering an effective innate immune response. This could explain the contagiousness of asymptomatic infected people.

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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SARS-CoV-2 Covid-19

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients SARS-CoV-2 with respiratory failure

Patients in intensive care

Immunological profiling

Intervention Type OTHER

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

Intervention Type OTHER

The immune activation phenotype will be assessed using a standardized panel of soluble and membrane immune activation markers

HEALTHY VOLUNTEERS

HEALTHY VOLUNTEERS

Immunological profiling

Intervention Type OTHER

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

Intervention Type OTHER

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

Intervention Type OTHER

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

Intervention Type OTHER

The immune activation phenotype will be assessed using a standardized panel of soluble and membrane immune activation markers

Immunological profiling

Intervention Type OTHER

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

Intervention Type OTHER

Immunological profiling

The immune activation phenotype will be assessed using a standardized panel of soluble and membrane immune activation markers

Intervention Type OTHER

Other Intervention Names

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Additional 1-year follow-up visit for 30 convalescent patients

Eligibility Criteria

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Inclusion Criteria

* The patient must be a member or beneficiary of a health insurance plan
* 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 subject is in a period of exclusion determined by a previous study
* The patient is under safeguard of justice
* Patient already under ventilation transferred from another center
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Institute of Human Genetics, Montpellier

UNKNOWN

Sponsor Role collaborator

Centre Hospitalier Universitaire de Nīmes

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pierre Corbeau

Role: PRINCIPAL_INVESTIGATOR

CHU Nimes

Locations

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CHU de Nimes

Nîmes, , France

Site Status

Countries

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France

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.

Reference Type RESULT
PMID: 35066575 (View on PubMed)

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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