Plasma Exchange in Covid-19 Patients With Anti-interferon Autoantibodies

• Status: Recruiting
• Trial end date: 2022-03-22
• Target enrollment: 0
• Participant gender: All

Summary

COVID-19 associated mortality remains high despite the advances in therapeutics such as dexamethasone. The severity of COVID-19 results from direct viral cytotoxicity, and the inflammatory response, which is associated with a hypercoagulable state, contribute to lethal hypoxemic pneumonia. During the SARS-CoV-2 replication phase, infected cells secrete chemokines and die by activating the immune system locally. A local inflammatory loop induces tissue destruction, which activates the immune system's circulating cells, leading to another amplifying loop called the cytokine storm. In these phenomena, the integrity of the interferon pathway plays a significant role.

Specific impairment of the interferon pathway has been identified in a subset of patients and is associated with high Covid-19 severity. This subset of patients presents preexisting autoimmune disease mediated by autoantibodies directed against IFN. It represents 10.2% (101/987) of patients admitted in ICU with COVID-19 pneumonia, and the observed mortality in this subgroup is 40%.

The investigators hypothesized that plasma exchanges (PE) would eliminate these autoantibodies while acting on other mechanisms of the pathogenesis of severe COVID-19, such as cytokine storm or hypercoagulability(7).

The EPIC trial aims to demonstrate the efficacy of plasma exchange in the subpopulation of patients with anti-interferon autoantibodies and severe COVID-19 hospitalized in intensive care and on oxygen therapy, high flow or not, receiving non-ventilation or invasive ventilation, on D28 survival.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Centre Hospitalier St Anne

Criteria

Inclusion Criteria:

1. SARS-CoV-2 infection proven by PCR.

2. Positive detection of anti-interferon antibodies.

3. Patient, family or deferred consent (emergency clause).

4. Affiliation to a social security scheme (or exemption from affiliation). Inclusions are possible also for protected patient (under guardianship and tutornship).

Exclusion Criteria:

1. Pregnant women, parturients and nursing mothers

2. Minor patient

3. Participation in another interventional trial in progress, with the objective, even secondary, of reducing mortality

4. Indication to EPT for another associated pathology

5. Contra-indication to EPT, known allergy to albumin 5%.

6. Persons under court protection,

7. Disturbance of the haemostasis balance (PT<50%, APTT>1.5 and fibrinogen <1g/L)

8. Patient presenting a hemorrhagic diathesis (intracranial or digestive bleeding or threatening the functional prognosis)

9. Any progressive and advanced pathology whose life expectancy is less than one month

10. Bacterial or viral infectious disease (HIV) explaining most of the aggravation