Bidar, Frank
Hamada, Sarah
Gossez, Morgane
Coudereau, Remy
Lopez, Jonathan
Cazalis, Marie-Angelique
Tardiveau, Claire
Brengel-Pesce, Karen
Mommert, Marine
Buisson, Marielle
Conti, Filippo
Rimmelé, Thomas
Lukaszewicz, Anne-Claire
Argaud, Laurent
Cour, Martin
Monneret, Guillaume
Venet, Fabienne http://orcid.org/0000-0003-0462-4235
,
Pescarmona, Remi
Garnier, Lorna
Lombard, Christine
Perret, Magali
Villard, Marine
Viel, Sébastien
Cheynet, Valérie
Cerrato, Elisabeth
Peronnet, Estelle
Llitjos, Jean-François
Itah, Laetitia
Boussaha, Inesse
Poitevin-Later, Françoise
Malcus, Christophe
Godignon, Marine
Wallet, Florent
Delignette, Marie-Charlotte
Dailler, Frederic
Simon, Marie
Dargent, Auguste
Bertrand, Pierre-Jean
Stevic, Neven
Provent, Marion
Bignet, Laurie
Cerro, Valérie
Richard, Jean-Christophe
Bitker, Laurent
Mezidi, Mehdi
Baboi, Loredana
Clinical trials referenced in this document:
Documents that mention this clinical trial
Recombinant human interleukin-7 reverses T cell exhaustion ex vivo in critically ill COVID-19 patients
https://doi.org/10.1186/s13613-022-00982-1
Funding for this research was provided by:
hospices civils de lyon
Article History
Received: 6 September 2021
Accepted: 13 January 2022
First Online: 5 March 2022
Change Date: 1 April 2022
Change Type: Correction
Change Details: A Correction to this paper has been published:
Change Details: https://doi.org/10.1186/s13613-022-01007-7
Declarations
:
: This project was part of an ongoing prospective observational clinical study (RICO, REA-IMMUNO-COVID) performed in line with the principles of the Declaration of Helsinki. It was approved by ethics committee (Comité de Protection des Personnes Ile de France 1-N°IRB / IORG #: IORG0009918) under agreement number 2020-A01079-30. This clinical study was registered at ClinicalTrials.gov (NCT04392401). The committee waived the need for written informed consent because the study was observational, with a low risk to patients, and no specific procedure, other than routine blood sampling, was required. Oral information and non-opposition to inclusion in the study were mandatory and were systematically obtained before any blood sample was drawn. This was recorded in patients’ clinical files. If a patient was unable to consent directly, non-opposition was obtained from the patient’s legally authorized representative and reconfirmed from the patient at the earliest opportunity.
: All authors have read the manuscript and have consented for its publication.
: The authors declare no competing financial interests in relation to the work. MAC, KBP and MM are bioMérieux’s employees. This private company had no role in the study design, result analysis and decision to publish this study.