Immune Profiling of COVID19-patients Admitted to ICU

• Conditions: COVID-19
• Interventions: Other: No intervention

• Registration Number: NCT04473131
• Lead Sponsor: Hamad Medical Corporation

Brief Summary

SARS-CoV-2 is the novel coronavirus responsible for COVID-19, coronavirus disease 2019. This new coronavirus was first detected in Wuhan, China in late December 2019. According to WHO, the incidence rate of COVID-19 is prominent among adults and elderly people, reaching so far \>2 million cases globally. Meanwhile, confirmed death cases reached \>126 thousands of reported cases in 185 countries and still increasing. We anticipate that immunological differences among COVID19-infected patients might be a reason behind the variation of patient outcomes. Therefore, we intend to investigate cellular and humoral immune responses of COVID19-positive patients, and we claim to discover new indicators of patients' prognosis. Our target population includes three categories of patients staying at ICU, HMC (COVID19-positive vs. COVID19-negative vs. healthy control). Throughout their ICU stay, multiple blood samples will be screened for leukocytes surface markers, leukocytes' production of certain molecules, and circulating cytokines/chemokines/checkpoint inhibitors. Their plasma/serum will be used as well for immune proteomics, metabolomics, and other serological tests. Such parameters can provide the more comprehensive status of COVID19-infected patients at infection onset, during treatment intake, and at recovery or relapse stage. Following analysis, the main prospective outcome of this study is to identify the most reflective markers of COVID19-positive patients' outcomes.

Detailed Description

Not available

Study Timeline

• Study Start: 2020-04-27
• Status Verified: 2020-07
• Study First Submitted: 2020-07-15
• Study First Submitted QC: 2020-07-15
• Last Update Submitted: 2020-07-15
• Study First Posted: 2020-07-16
• Last Update Posted: 2020-07-16
• Primary Completion: 2022-06
• Study Completion: 2022-06

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

• Admitted to ICU for suspicious COVID-19
• Signed consent form

Exclusion Criteria

• Immuno-compromised or immuno-deficient patients
• Diagnosed with any immunological disorders, cancer, and onco-hematological diseases at the inclusion date
• Patients under treatment or treated within 5 years before inclusion or at the end of chemotherapy within the 6 months prior to inclusion date
• Patients under any immune-suppressive medications, antibody therapy, corticosteroids, bone marrow transplant under the last 6 months of inclusion
• Unsigned consent form

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
COVID-19 positive	No intervention	Inclusion criteria: 1. Male or female aged over 18 years 2. Admitted patients to ICU with a suspicious COVID19 infection 3. Tested positive for SARS-CoV-2 Exclusion criteria: 1. Burn and trauma 2. Any immunological diseases, or immunosuppressive medications 3. Other immune-related conditions (cancer, hematological malignancies, bone marrow diseases or transplant) Sample collection time points: 4 to 5 (day 1-3, day 7, day 14, day 21, discharge day from ICU -between day 30-60- if possible)
Heathy volunteers	No intervention	Inclusion criteria: 1. Male or female aged over 18 years 2. Normal clinical examination Exclusion criteria: 1. Person with an infectious syndrome during the last 90 days 2. Extreme physical stress within the last week 3. Person receiving within the last 90 days, a treatment based on: antivirals; antibiotics; antiparasitics; antifungals; non-steroidal anti-inflammatory drugs; immunosuppressive therapy; corticosteroids; therapeutic antibodies; chemotherapy 4. Person with history of: innate or acquired immune deficiency; hematological disease; solid tumor; severe chronic disease; surgery or hospitalization within the last 2 years; pregnancy within the last year; participation to a phase I clinical assay during the last year; participation to a phase I clinical assay during the last year; pregnant or breastfeeding women; a person with restricted liberty or under legal protection Sample collection time points: 1 (day of blood sample donation)
COVID-19 negative	No intervention	Inclusion criteria: 1. Male or female aged over 18 years 2. Admitted patients to ICU 3. Tested negative for SARS-CoV-2 Exclusion criteria: 1. Burn and trauma 2. Any immunological diseases, or immunosuppressive medications 3. Other immune-related conditions (cancer, hematological malignancies, bone marrow diseases or transplant) Sample collection time points: 4 to 5 (day 1-3, day 7, day 14, day 21, discharge day from ICU -between day 30-60- if possible)

Primary Outcome Measures

Name	Time	Method
To correlate patients' immune profile to disease severity and patient's outcome	4 to 6 months	A correlative analysis of the immune cells and cytokines levels with the COVID-19 severity and with the patient's outcome following their stay at the ICU. An attempt to identify markers associated with the disease severity and predictive measures to the patient's outcome.
To create an immune profile for each COVID19-positive patient during their ICU stay	8 to 12 months	A descriptive analysis of the innate and adaptive immune cells (phenotypically and functionally), along with circulating pro- and anti-inflammatory cytokines, and the dynamic change of immune cells and cytokines throughout the first 4 weeks of the COVID-19 infection.

Trial Locations

Locations (1)

Hamad Medical Corporation; 🇶🇦 Doha, Qatar