key: cord-0826870-o5mpqetz
authors: Kreutmair, Stefanie; Unger, Susanne; Núñez, Nicolás Gonzalo; Ingelfinger, Florian; Alberti, Chiara; De Feo, Donatella; Krishnarajah, Sinduya; Kauffmann, Manuel; Friebel, Ekaterina; Babaei, Sepideh; Gaborit, Benjamin; Lutz, Mirjam; Jurado, Nicole Puertas; Malek, Nisar P.; Goepel, Siri; Rosenberger, Peter; Häberle, Helene A.; Ayoub, Ikram; Al-Hajj, Sally; Nilsson, Jakob; Claassen, Manfred; Liblau, Roland; Martin-Blondel, Guillaume; Bitzer, Michael; Roquilly, Antoine; Becher, Burkhard
title: Distinct immunological signatures discriminate severe COVID-19 from non-SARS-CoV-2-driven critical pneumonia
date: 2022-02-08
journal: Immunity
DOI: 10.1016/j.immuni.2022.01.015
sha: 8272ac72daea207a7698e00b54814e6c3b634442
doc_id: 826870
cord_uid: o5mpqetz

nan

(Immunity 54, 1578 -1593 July 13, 2021) In our original article, the FlowSOM-generated CD3 + CD56 + CD4 À CD8 À T cell cluster was named NKT cells. CD3 + CD56 + cells do not exclusively describe NKT cells, but rather a heterogeneous collection of unconventional T cells. As we had not included iNKT-specific CD1d tetramers loaded with a-galactosylceramide in our panels, to be more precise, we corrected the term NKT cells with CD56 + T cells throughout the text and in the listed figures, as well as Tables S1, S3, and S4 and the graphical abstract. This error does not affect the overall conclusions of the paper. Additionally, to more appropriately reflect this change, reference Zhang et al., 2020a has been replaced with Notarbartolo et al., 2021 .The authors apologize for any confusion caused. 

Integrated longitudinal immunophenotypic, transcriptional and repertoire analyses delineate immune responses in COVID-19 patients