Calprotectin, a Biomarker of COVID-19 Severity (CALPRO)

Assistance Publique - Hôpitaux de Paris

Status: Not yet enrolling

Conditions: Severe/Moderate Coronavirus; Old Age; Myelodysplastic Syndromes; Chronic Myelomonocytic Leukemia

Treatments: Biological: Blood samples

Study type: Interventional

Funder types: Other

Identifiers

NCT04953312

2021-A00674-37 (Other Identifier)

APHP210522

Details and patient eligibility

About

The purpose of this study is to provide new insights into the pathophysiology of emergency hematopoiesis detected in severe COVID-19 patients. The investigators aim to explore the ability of calprotectin to induce an immunosuppressive myeloid program at the hematopoietic stem and progenitor cell (HSPC) level, and to identify the receptor(s) involved in this effect. Since patients with a hematological malignancy demonstrate a very high propensity to develop a severe COVID-19, the investigators will explore how HSPCs collected from patients with a myeloid malignancy respond to calprotectin.

Full description

Emergency myelopoiesis in response to SARS-CoV-2 infection produce immunosuppressive myeloid cells with accumulation of immature granulocytes and loss of non-classical monocytes. Excessive release of calprotectin, the dimer of S100A8/A9 alarmins, by immature granulocytes and activated monocytes reflects this situation. A role of calprotectin has been previously described in the initiation and progression of chronic hematological malignancies such as myelodysplastic syndromes.

To provide a rationale for the targeting of alarmin-driven signaling pathways and limit the pathogenic inflammatory response to SARS-CoV-2 infection, the role of calprotectin in the production of immunosuppressive cells from the bone marrow hematopoietic stem and progenitors cells needs to be investigated in patients with severe COVID-19 in comparison with patients with chronic myeloid malignancies (such as chronic myelomonocytic leukemia and myelodysplastic syndromes) and with age-mached healthy controls.

A comprehensive and integrated multiomics approach will be used to decipher the features of immunosuppressive cells and identify therapeutic targets in deregulated pathways.

Enrollment: 55 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

Criteria for all groups:

• Adults ≥ 18 years

• Dated and signed inform consent *

  • * : written informed consent of relative (trusted person, close family) in case of emergency procedure, by default emergency inclusion notified in medical file and pursuance consent sought.

• Affiliation with a social security scheme

Criteria for control group:

• Age-matched healthy donors

Criteria for chronic myeloid malignancies:

• A diagnosis of low or high-risk myelodysplastic syndromes according to the WHO 2016 classification
• A diagnosis of dysplastic or proliferative chronic myelomonocytic leukemia according to WHO 2016

Criteria for COVID-19 patients:

• Patients with a recent diagnosis (<7 days since first symptoms) of moderate or severe COVID-19

Exclusion criteria

• Pregnant women
• Minor patient or major under protection
• Patients with COVID-19 infection and active cancer or a history of cancer within the last 6 months
• Patients with COVID-19 and severe comorbidities including cardiovascular or respiratory diseases, unbalanced diabetes, obesity (IMC >29)
• Patient on AME (state medical aid)

Trial design

Primary purpose: Diagnostic

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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55 participants in 3 patient groups

COVID-19 patients (group 1)

Experimental group

Description:

Patients with a recent diagnosis (\<7 days since first symptoms) of moderate or severe COVID-19

Treatment:

Biological: Blood samples

Chronic myeloid malignancies (group 2)

Experimental group

Description:

Adults with chronic myeloid malignancies including myelodysplastic syndromes with low risk MDS ; high risk MDS according to IPSS-R or with dysplastic or proliferative chronic myelomonocytic leukemia according to WHO2016

Treatment:

Biological: Blood samples

Control group (group 3)

Other group

Description:

Age-matched healthy donors

Treatment:

Biological: Blood samples