Mature neutrophils and a NF-κB-to-IFN transition determine the unifying disease recovery dynamics in COVID-19

Cell Reports Medicine - Tập 3 - Trang 100652 - 2022
Amit Frishberg1,2,3, Emma Kooistra4,5, Melanie Nuesch-Germano6, Tal Pecht6, Neta Milman3, Nico Reusch6, Stefanie Warnat-Herresthal1,6, Niklas Bruse4,5, Kristian Händler7, Heidi Theis7, Michael Kraut7, Esther van Rijssen8, Bram van Cranenbroek8, Hans JPM. Koenen8, Hidde Heesakkers4, Mark van den Boogaard4, Marieke Zegers4, Peter Pickkers4,5, Matthias Becker7, Anna C. Aschenbrenner1,6,9,7
1Systems Medicine, Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Bonn, Germany
2Institute of Computational Biology, Helmholtz Center Munich, 85764, Neuherberg, Germany
3Department of Immunology, Faculty of Medicine, Technion, Israel Institute of Technology, Haifa, Israel
4Department of Intensive Care Medicine, Radboud University Medical Center, Nijmegen, The Netherlands
5Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands
6Genomics and Immunoregulation, Life & Medical Sciences (LIMES) Institute, University of Bonn, Bonn, Germany
7Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), PRECISE Platform for Genomics and Epigenomics at DZNE and University of Bonn, Bonn, Germany
8Laboratory for Medical Immunology, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, Netherlands
9Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, The Netherlands

Tài liệu tham khảo

Silvin, 2020, Elevated calprotectin and abnormal myeloid cell subsets discriminate severe from mild COVID-19, Cell, 182, 1401, 10.1016/j.cell.2020.08.002 Schulte-Schrepping, 2020, Severe COVID-19 is marked by a dysregulated myeloid cell compartment, Cell, 182, 1419, 10.1016/j.cell.2020.08.001 Aschenbrenner, 2021, Disease severity-specific neutrophil signatures in blood transcriptomes stratify COVID-19 patients, Genome. Med., 13, 7, 10.1186/s13073-020-00823-5 Stephenson, 2021, Single-cell multi-omics analysis of the immune response in COVID-19, Nat. Med., 27, 904, 10.1038/s41591-021-01329-2 Su, 2020, Multi-Omics resolves a sharp disease-state shift between mild and moderate COVID-19, Cell, 183, 1479, 10.1016/j.cell.2020.10.037 Georg, 2022, Complement activation induces excessive T cell cytotoxicity in severe COVID-19, Cell, 185, 493, 10.1016/j.cell.2021.12.040 Wen, 2020, Author Correction: immune cell profiling of COVID-19 patients in the recovery stage by single-cell sequencing, Cell. Discov., 6, 41, 10.1038/s41421-020-00187-5 Zheng, 2020, Longitudinal transcriptome analyses show robust T cell immunity during recovery from COVID-19, Signal Transduct. Target. Ther., 5, 294, 10.1038/s41392-020-00457-4 Bernardes, 2020, Longitudinal multi-omics analyses identify responses of megakaryocytes, erythroid cells, and plasmablasts as hallmarks of severe COVID-19, Immunity, 53, 1296, 10.1016/j.immuni.2020.11.017 Frishberg, 2021, Multiple trajectory alignment reconstructs disease dynamics for discovery and clinical benefit, BioRxiv Warnat-Herresthal, 2021, Swarm Learning for decentralized and confidential clinical machine learning, Nature, 594, 265, 10.1038/s41586-021-03583-3 Bergamaschi, 2021, Longitudinal analysis reveals that delayed bystander CD8+ T cell activation and early immune pathology distinguish severe COVID-19 from mild disease, Immunity, 54, 1257, 10.1016/j.immuni.2021.05.010 Zanella, 2021, Time course of risk factors associated with mortality of 1260 critically ill patients with COVID-19 admitted to 24 Italian intensive care units, Intensive. Care. Med., 47, 995 Kooistra, 2021, Body mass index and mortality in coronavirus disease 2019 and other diseases: a cohort study in 35,506 ICU patients, Crit. Care. Med., 50, e1, 10.1097/CCM.0000000000005216 Ali, 2020, Elevated level of C-reactive protein may be an early marker to predict risk for severity of COVID-19, J. Med. Virol., 92, 2409, 10.1002/jmv.26097 Liu, 2021, The chronic kidney disease and acute kidney injury involvement in COVID-19 pandemic: a systematic review and meta-analysis, PLoS One., 16, e0244779, 10.1371/journal.pone.0244779 Sabaka, 2021, Role of interleukin 6 as a predictive factor for a severe course of Covid-19: retrospective data analysis of patients from a long-term care facility during Covid-19 outbreak, BMC. Infect. Dis., 21, 308, 10.1186/s12879-021-05945-8 Meizlish, 2021, A neutrophil activation signature predicts critical illness and mortality in COVID-19, Blood. Adv., 5, 1164, 10.1182/bloodadvances.2020003568 Zheng, 2021, Multi-cohort analysis of host immune response identifies conserved protective and detrimental modules associated with severity across viruses, Immunity, 54, 753, 10.1016/j.immuni.2021.03.002 Andres-Terre, 2015, Integrated, multi-cohort analysis identifies conserved transcriptional signatures across multiple respiratory viruses, Immunity, 43, 1199, 10.1016/j.immuni.2015.11.003 Karami, 2021, Weighted gene co-expression network analysis combined with machine learning validation to identify key modules and hub genes associated with SARS-CoV-2 infection, J. Clin. Med., 10, 3567, 10.3390/jcm10163567 Martonik, 2021, The role of Th17 response in COVID-19, Cells, 10, 1550, 10.3390/cells10061550 Pacha, 2020, COVID-19: a case for inhibiting IL-17?, Nat. Rev. Immunol., 20, 345, 10.1038/s41577-020-0328-z Hennighausen, 2020, Activation of the SARS-CoV-2 receptor Ace2 through JAK/STAT-Dependent enhancers during pregnancy, Cell. Rep., 32, 108199, 10.1016/j.celrep.2020.108199 Saeed, 2021, Coronavirus disease 2019 and cardiovascular complications: focused clinical review, J. Hypertens., 39, 1282, 10.1097/HJH.0000000000002819 Lee, 2021, Lymphopenia as a biological predictor of outcomes in COVID-19 patients: a nationwide cohort study, Cancers, 13, 471, 10.3390/cancers13030471 Liu, 2020, Lymphopenia predicted illness severity and recovery in patients with COVID-19: a single-center, retrospective study, PLoS. One, 15, e0241659, 10.1371/journal.pone.0241659 Garrafa, 2021, Early prediction of in-hospital death of COVID-19 patients: a machine-learning model based on age, blood analyses, and chest x-ray score, Elife, 10, e70640, 10.7554/eLife.70640 Chen, 2020, Longitudinal hematologic and immunologic variations associated with the progression of COVID-19 patients in China, J. Allergy Clin. Immunol., 146, 89, 10.1016/j.jaci.2020.05.003 Frishberg, 2019, Cell composition analysis of bulk genomics using single-cell data, Nat. Methods, 16, 327, 10.1038/s41592-019-0355-5 Reusch, 2021, Neutrophils in COVID-19, Front. Immunol., 12, 652470, 10.3389/fimmu.2021.652470 Hazeldine, 2021, Neutrophils and COVID-19: active participants and rational therapeutic targets, Front. Immunol., 12, 680134, 10.3389/fimmu.2021.680134 Shen-Orr, 2013, Computational deconvolution: extracting cell type-specific information from heterogeneous samples, Curr. Opin. Immunol., 25, 571, 10.1016/j.coi.2013.09.015 Anft, 2020, COVID-19-Induced ARDS is associated with decreased frequency of activated memory/effector T cells expressing CD11a++, Mol. Ther., 28, 2691, 10.1016/j.ymthe.2020.10.001 Xi, 2019, GSDMD is required for effector CD8+ T cell responses to lung cancer cells, Int. Immunopharmacol., 74, 105713, 10.1016/j.intimp.2019.105713 Cruikshank, 2008, lnterleukin-16: the ins and outs of regulating T-cell activation, Crit. Rev. Immunol., 28, 467, 10.1615/CritRevImmunol.v28.i6.10 Lechuga, 2021, SARS-CoV-2 proteins bind to hemoglobin and its metabolites, Int. J. Mol. Sci., 22, 9035, 10.3390/ijms22169035 Choi, 2017, THEMIS enhances TCR signaling and enables positive selection by selective inhibition of the phosphatase SHP-1, Nat. Immunol., 18, 433, 10.1038/ni.3692 Zhang, 2013, Loss of β-arrestin 2 exacerbates experimental autoimmune encephalomyelitis with reduced number of Foxp3+ CD4+ regulatory T cells, Immunology, 140, 430, 10.1111/imm.12152 Lu, 2018, Human Semaphorin-4A drives Th2 responses by binding to receptor ILT-4, Nat. Commun., 9, 742, 10.1038/s41467-018-03128-9 Nelms, 1999, The IL-4 receptor: signaling mechanisms and biologic functions, Annu. Rev. Immunol., 17, 701, 10.1146/annurev.immunol.17.1.701 Huang, 2021, The predicting roles of carcinoembryonic antigen and its underlying mechanism in the progression of coronavirus disease 2019, Crit. Care., 25, 234, 10.1186/s13054-021-03661-y Krämer, 2021, Early IFN-α signatures and persistent dysfunction are distinguishing features of NK cells in severe COVID-19, Immunity, 54, 2650, 10.1016/j.immuni.2021.09.002 Hadjadj, 2020, Impaired type I interferon activity and inflammatory responses in severe COVID-19 patients, Science, 369, 718, 10.1126/science.abc6027 Ruetsch, 2021, Functional exhaustion of type I and II interferons production in severe COVID-19 patients, Front. Med., 7, 603961, 10.3389/fmed.2020.603961 Geense, 2017, MONITOR-IC study, a mixed methods prospective multicentre controlled cohort study assessing 5-year outcomes of ICU survivors and related healthcare costs: a study protocol, BMJ. Open., 7, e018006, 10.1136/bmjopen-2017-018006 Rockwood, 2005, A global clinical measure of fitness and frailty in elderly people, CMAJ (Can. Med. Assoc. J.), 173, 489, 10.1503/cmaj.050051 Geense, 2020, Changes in frailty among ICU survivors and associated factors: results of a one-year prospective cohort study using the Dutch Clinical Frailty Scale, J. Crit. Care., 55, 184, 10.1016/j.jcrc.2019.10.016 Muscedere, 2017, The impact of frailty on intensive care unit outcomes: a systematic review and meta-analysis, Intensive Care Med., 43, 1105, 10.1007/s00134-017-4867-0 Ware, 1992, The MOS 36-ltem short-form health survey (SF-36), Med. Care., 30, 473, 10.1097/00005650-199206000-00002 Aguirre-Gamboa, 2016, Differential effects of environmental and genetic factors on T and B cell immune traits, Cell. Rep., 17, 2474, 10.1016/j.celrep.2016.10.053 Velten, 2022, Identifying temporal and spatial patterns of variation from multimodal data using MEFISTO, Nat. Methods, 19, 179, 10.1038/s41592-021-01343-9 Hao, 2021, Integrated analysis of multimodal single-cell data, Cell, 184, 3573, 10.1016/j.cell.2021.04.048