Waeckel, Louis
Venet, Fabienne
Gossez, Morgane
Monard, Céline
Rimmelé, Thomas
Monneret, Guillaume
Funding for this research was provided by:
Hospices Civils de Lyon (-)
Article History
Received: 21 January 2020
Accepted: 30 March 2020
First Online: 7 April 2020
Ethics approval and consent to participate
: This project was approved by our Institutional Review Board for ethics (“Comité de Protection des Personnes Sud-Est II”, number 11236).This study is registered at the French Ministry of Research and Teaching (#DC-2008-509), at the Commission Nationale de l’Informatique et des Libertés, and on clinicaltrials.gov (NCT02803346). Oral information and non-opposition to inclusion in the study were mandatory and recorded in patients’ clinical files. Peripheral blood from healthy volunteers was provided by the “Etablissement Français du Sang” from Lyon. According to EFS standardized procedures for blood donation and to provisions of the articles R.1243–49 and following ones of the French public health code, a written non-opposition to the use of donated blood for research purposes was obtained from HV. The blood donors’ personal data were anonymized before transfer to our research laboratory.
: Not applicable.
: The authors declare they have no conflict of interest.