Official Title
Blood Innate Biomarkers as Predictors of COVID-19 Disease Progression in Recently Infected Chronic Haemodialysis Patients
Brief Summary

SARS-CoV-2 induces over-production of inflammatory cytokines, and especially interleukin-6 (IL-6). The apparently strong association between blood levels of inflammaory cytokines and SARS-CoV-2 disease severity has led clinicians to evaluate the administration of steroids or anti-IL-6 antagonists in severely ill patients. As of this day, biomarkers capable of predicting clinical disease progression in Covid-19 patients with mild-to-moderate symptoms have not yet been formally identified. Identifying such markers and evaluating their predictive value may be exploited to guide patient care management, and as such forms the core objective of this proposal. Because of strong inter-individual variations in the ability of innate immune cells to produce cytokines, the hypothesis the investigators formulate and intend to test is that innate IL-6 responsiveness varies between recently infected Covid-19 patients and could predict disease outcome. To test this hypothesis, the investigators propose to follow recently infected chronic haemodialysis patients with moderate Covid-19 symptoms. These patients stand a higher risk to progress to severe disease. The investigators plan to collect a blood sample in these patients using a system whereby ex vivo cytokine production is initiated in the very same blood collection tube without prior separation and centrifugation, thus reducing labour and operator bias. After incubation with or without known innate immune stimuli, the cell-free phase from each collection-culture tube will be assayed for IL-6 content. Associations between IL-6 content and disease outcome (encephalopathy, transfer to acute care or death) will be determined in 115 Covid-19 chronic haemodialysis patients with moderate symptoms followed in 9 centers.

Unknown status
COVID-19 by SARS-CoV-2 Infection

Other: blood sample

a blood sample is taken on Covid-19 chronic haemodialysis patients with moderate symptoms

Eligibility Criteria

Inclusion Criteria:

- Patients with end-stage chronic renal disease requiring haemodialysis support;

- SARS-CoV-2 positive (RT-PCR);

- COVID-19 symptoms at least once over a 8-day period preceding inclusion;

- Hospitalized or outpatients in one of the study centers: CHU de Nice, CHU de
Strasbourg, Hôpital Necker (APHP), Hôpital Kremlin Bicêtre (APHP), Hôpital
Pitié-Salpétriêre (APHP), Hospices Civils de Lyon, CHU de Saint-Etienne, CHU de
Montpellier, Hôpital La Conception (APHM);

- Age > 18 years;

- Free and informed consent.

Exclusion Criteria:

- Age > 85 years ;

- Peritoneal dialysis;

- Onset of symptoms (fever and/or cough) for more than 8 days;

- Acute respiraytory distress despite oxygen therapy, 02 ≥ 4L/min, arterial pressure <
85/55 mmHg or hemodynamic instability at time of inclusion, encephalopathy with
Glasgow coma scale < 14;

- Treatment with non-steroids anti-inflammatory agents within the laste 14 days
preceding onset of symptoms;

- Active bacterial or fungal infection documented at inclusion;

- Pregnancy;

- Under guardianship or curatorship;

- Non-affiliated person with Social Security.

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: 85 Years
Countries
France
Locations

CHU de nice
Nice, Alpes-Maritimes, France

Investigator: SICARD Antoine
Contact: +33492037918
sicard.a@chu-nice.fr

Investigator: SICARD Antoine

Contacts

SICARD Antoine, Ph
+33492037918
sicard.a@chu-nice.fr

BEN HASSEN-DAKHLAOUI NADIA CHU Nice +33492037918
BEN HASSEN-DAKHLAOUI NADIA CHU Nice

sicard antoine, ph, Principal Investigator
Néphrologie, CHU de Nice

Centre Hospitalier Universitaire de Nice
NCT Number
MeSH Terms
COVID-19
Disease Progression