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A proteomic survival predictor for COVID-19 patients in intensive care

['Vadim Demichev', 'Charité Universitätsmedizin Berlin', 'Department Of Biochemistry', 'Berlin', 'The Francis Crick Institute', 'Molecular Biology Of Metabolism Laboratory', 'London', 'United Kingdom', 'The University Of Cambridge', 'Cambridge Centre For Proteomics']

Date: 2022-01 

Abstract Global healthcare systems are challenged by the COVID-19 pandemic. There is a need to optimize allocation of treatment and resources in intensive care, as clinically established risk assessments such as SOFA and APACHE II scores show only limited performance for predicting the survival of severely ill COVID-19 patients. Additional tools are also needed to monitor treatment, including experimental therapies in clinical trials. Comprehensively capturing human physiology, we speculated that proteomics in combination with new data-driven analysis strategies could produce a new generation of prognostic discriminators. We studied two independent cohorts of patients with severe COVID-19 who required intensive care and invasive mechanical ventilation. SOFA score, Charlson comorbidity index, and APACHE II score showed limited performance in predicting the COVID-19 outcome. Instead, the quantification of 321 plasma protein groups at 349 timepoints in 50 critically ill patients receiving invasive mechanical ventilation revealed 14 proteins that showed trajectories different between survivors and non-survivors. A predictor trained on proteomic measurements obtained at the first time point at maximum treatment level (i.e. WHO grade 7), which was weeks before the outcome, achieved accurate classification of survivors (AUROC 0.81). We tested the established predictor on an independent validation cohort (AUROC 1.0). The majority of proteins with high relevance in the prediction model belong to the coagulation system and complement cascade. Our study demonstrates that plasma proteomics can give rise to prognostic predictors substantially outperforming current prognostic markers in intensive care.

Author summary Healthcare systems around the world are struggling to accommodate high numbers of the most severely ill patients with COVID-19. Moreover, the pandemic creates a pressing need to accelerate clinical trials investigating potential new therapeutics. While various biomarkers can discriminate and predict the future course of disease for patients of different disease severity, prognosis remains difficult for patient groups with similar disease severity, e.g. patients requiring intensive care. Established risk assessments in intensive care medicine such as the SOFA or APACHE II show only limited reliability in predicting future disease outcomes for COVID-19. In this study we hypothesized that the plasma proteome, which reflects the complete set of proteins that are expressed by an organism and are present in the blood, and which is known to comprehensively capture the host response to COVID-19, can be leveraged to allow for prediction of survival in the most critically ill patients with COVID-19. Here, we found 14 proteins, which over time changed in opposite directions for patients who survive compared to patients who do not survive on intensive care. Using a machine learning model which combines the measurements of multiple proteins, we were able to accurately predict survival in critically ill patients with COVID-19 from single blood samples, weeks before the outcome, substantially outperforming established risk predictors.

Citation: Demichev V, Tober-Lau P, Nazarenko T, Lemke O, Kaur Aulakh S, Whitwell HJ, et al. (2022) A proteomic survival predictor for COVID-19 patients in intensive care. PLOS Digit Health 1(1): e0000007. https://doi.org/10.1371/journal.pdig.0000007 Editor: Reinhard Bauer, Universitatsklinikum Jena, GERMANY Received: June 11, 2021; Accepted: November 18, 2021; Published: January 18, 2022 Copyright: © 2022 Demichev et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Data Availability: The protein quantities table along with the associated metadata are provided in supplementary materials. All scripts used to train and assess the machine learning models are likewise provided (S1 Data.zip). The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium (http://proteomecentral.proteomexchange.org) via the PRIDE partner repository with the dataset identifier PXD029009. All scripts used to train and assess the machine learning models as well as the respective input proteomics data are provided in supplementary materials (S1 Data.zip). Funding: This work was supported by the Berlin University Alliance (501_Massenspektrometrie, 501_Linklab, 112_PreEP_Corona_Ralser), by UKRI/NIHR through the UK Coronavirus Immunology Consortium (UK-CIC), the BMBF/DLR Projektträger (01KI20160A, 01ZX1604B, 01KI20337, 01KX2021), Charité-BIH Centrum für Therapieforschung (BIH_PA_covid-19_Ralser), the BBSRC (BB/N015215/1, BB/N015282/1), the Francis Crick Institute, which receives its core funding from Cancer Research UK (FC001134), the UK Medical Research Council (FC001134), and the Wellcome Trust (FC001134 and IA 200829/Z/16/Z), as well as the European Research Council (SyG 951475 to M.R.). The work was further supported by the Ministry of Education and Research (BMBF), as part of the National Research Node ‘Mass spectrometry in Systems Medicine (MSCoresys), under grant agreements 031L0220A and 161L0221. The study was further supported by the German Federal Ministry of Education and Research (NaFoUniMedCovid19 – NUM -NAPKON, NUM-COVIM, FKZ: 01KX2021 and PROVID—FKZ: 01KI20160A) to Florian Kurth, Leif E. Sander, Martin Witzenrath, Norbert Suttorp and Stefan Hippenstiel. Leif Erik Sander is supported by the German Research Foundation (DFG, SFB-TR84 114933180) and by the Berlin Institute of Health (BIH), which receives funding from the Ministry of Education and Research (BMBF). Martin Witzenrath is supported by grants from the German Research Foundation, SFB-TR84 C06 and C09, by the German Ministry of Education and Research (BMBF) in the framework of the CAPSyS (01ZX1304B), CAPSyS-COVID (01ZX1604B), SYMPATH (01ZX1906A) and PROVID project (01KI20160A) and by the Berlin Institute of Health (CM-COVID). Stefan Hippenstiel is supported by the German Research Foundation (DFG, SFB-TR84 A04 and B06), and the BMBF (PROVID, and project 01KI2082). Norbert Suttorp is supported by grants from the German Research Foundation, SFB-TR84 C09 und Z02, by the German Ministry of Education and Research (BMBF) in the framework of the PROGRESS 01KI07114. The study was further supported by Wellcome Trust (200829/Z/16/Z). The Generation Scotland study received core support from the Chief Scientist Office of the Scottish Government Health Directorates (CZD/16/6) and the Scottish Funding Council (HR03006), and is now supported by the Wellcome Trust (216767/Z/19/Z). Archie Campbell is funded by HDR UK and the Wellcome Trust (216767/Z/19/Z). Caroline Hayward is supported by an MRC University Unit Programme Grant (MC_UU_00007/10) (QTL in Health and Disease). Riccardo Marioni is supported by an Alzheimer’s Research UK project grant (ARUK-PG2017B-10). HJ. Whitwell, JF. Timms, A. Zaikin and T. Nazarenko are supported by a Medical Research Council grant (MR/R02524X/1) and HJ. Whitwell, A. Zaikin and O. Blyuss by the Ministry of Science and Higher Education agreement No. 075-15-2020-808. HJ. Whitwell is supported by the National Institute for Health Research (NIHR) Imperial Biomedical Research Centre (BRC). J. Timms is supported by the National Institute for Health Research (NIHR) UCLH/UCL Biomedical Research Centre. Mirja Mittermaier is a participant in the BIH-Charité Digital Clinician Scientist Program funded by the Charité – Universitätsmedizin Berlin, the Berlin Institute of Health, and the German Research Foundation (DFG). Markus A. Keller is supported by the Austrian Science Funds (FWF; P33333) and the Austrian Research Promotion Agency (FFG, #878654). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Competing interests: The authors declare no competing interests. Author John F. Timms was unable to confirm their authorship contributions. On their behalf, the corresponding author has reported their contributions to the best of their knowledge.

Introduction The COVID-19 pandemic has brought health systems around the globe to the brink of collapse. Capacities for intensive care treatment of patients with organ failure have reached their limits in many regions with intense SARS-CoV-2 transmission and were often central to political decisions regarding restrictions on public life, e.g. through contact restrictions or lock-downs. The global impact of the pandemic increases the pressures to devise new clinical approval strategies so that potential therapeutics can be identified and tested faster, at higher accuracy, and in clinical trials with smaller sample sizes [1]. Various models for classification of disease severity and for prediction of clinical trajectories and outcome have been developed for COVID-19, based on laboratory measurements, clinical scores, imaging, and omics technologies [2–5]. These pointed to the importance of specific immune cells, inflammatory and antiviral cytokines and chemokines, as well as the coagulation cascade in COVID-19 disease progression [5–13]. They predict the risk of the future need for mechanical ventilation in the heterogeneous group of patients at early time points, e.g. at admission to the hospital, when clinical parameters and biomarkers differ substantially between mildly affected and severely ill patients [2–5,14]. Treatment decisions within the most severely ill patients, for instance whether a patient should be treated with extracorporeal membrane oxygenation (ECMO), have a major impact on resources. Currently, such decisions are often based primarily on the patient’s age, comorbidities, and established intensive care prognosis models, such as the Sequential Organ Failure Assessment (SOFA) or Acute Physiology and Chronic Health Evaluation (APACHE II), which assess the patient on the basis of a combination of established clinical and laboratory risk parameters [15,16]. However, the predictive values of both SOFA and APACHE II for the most critical forms of COVID-19 are limited [17–19], creating a diagnostic gap and imminent need for reliable predictors, specifically validated in severely ill COVID-19 patients, to guide and tailor efforts in treating these critically ill patients. Moreover, the lack of reliable predictors increases the challenge of interpreting the results of early phase clinical trials, which typically enroll low numbers of patients. Indeed, testing for the success of a clinical intervention requires classification of divergent clinical trajectories within more homogeneous groups, such as WHO grade 7 patients. At least in COVID-19, this is hampered by the fact that molecular signatures within a group of patients with comparable disease severity are considerably more similar when compared to the differences between mild and severe patients [6,7,14]. Plasma proteomics holds the promise of integrating the genetic background of an individual with their life history, physiological, nutritional, and demographic parameters, and hence, have the potential to form the foundation of a new generation of predictors [20–24]. Among the spectrum of proteomic technologies available, mass spectrometry has the appeal that once markers are identified, they allow for the direct generation of targeted panel assays measurable by selective reaction monitoring (SRM), simplifying their implementation into clinical routine. Recently, new mass spectrometry based proteomic technologies have been developed to increase throughput and measurement precision, so that the path from discovery to application is simplified [6,25–28]. We studied proteomes of two well characterized cohorts of the most severely ill patients with COVID-19 in two independent health care centers (Charité–Universitätsmedizin Berlin, Germany, and Medical University of Innsbruck, Austria) who gave informed consent to deep clinical and molecular phenotyping [14,19,29]. Using a recently published dataset from our group [14], we specifically assessed whether proteomic measurements can be used to predict the outcome (death vs. survival) of severe COVID-19 from time series data, as well as from samples taken at key clinical decision points. We found 14 protein concentration trajectories that, over the timeline of disease progression, distinguish survivors from non-survivors. Moreover, a machine learning (ML) model, based on parenclitic networks, generated accurate prognosis on single time point samples that were collected once the patient reached the maximum treatment level. Emphasizing the prognostic potential of the proteome, this sample was, in median, taken 39 days before outcome. The ML predictor trained on these samples substantially outperformed established clinical risk scores and predicted the outcome among a group of severely ill patients with similar clinical presentation with high accuracy.

Discussion The prognostic value of several biomarkers (e.g. CRP, IL-6, ferritin) and clinical scores for predicting disease progression in COVID-19 at early disease stages, e.g. at hospital admission, is now well established [35,36]. For the comparatively homogeneous subgroup of severely ill patients already requiring mechanical ventilation and additional organ support, prediction of future disease trajectories and outcome (survival or death) is by far more challenging, and only limited data exist [17,37,38]. Moreover, clinical severity scores are often not validated for unconscious patients, and laboratory measurements are frequently confounded by intensive care treatment. Outcome of ICU patients may further be critically determined by resource constraints, the varying level of experience with organ replacement therapies or the rates of superinfection, rendering prediction complex [38]. On the other hand, patients in intensive care units, and particularly those in need of special organ replacement therapies such as ECMO, require a disproportionately large share of resources compared to other patients, so decisions to initiate such therapies should be based on the best information and assessment possible. Prognostic tools in critically ill patients are hence of crucial importance to guide and tailor the treatment efforts. This is particularly true in a situation when health care systems are overstrained. Another key potential for the use of outcome predictors is clinical trial monitoring, where measurements of prognostic molecular signatures over time can be used to evaluate experimental therapies on an individual, time-resolved basis. Moreover, an accurate outcome predictor would allow us to test whether a given treatment changes the predicted trajectory of an individual patient. Previously, we and others investigated plasma proteome alterations in COVID-19 [6–8,10,12,14], which show a remarkable ability to classify the severity of disease. For instance, our investigations showed that the host response in the early inflammatory phase creates a strong signature in the plasma proteome, and is critical as well as predictive about the future disease progression in severe COVID-19 [14]. New proteomic platform technologies have significantly gained precision and throughput compared to their predecessors, rendering the application of multivariate regression models more effective and bringing them increasingly close to routine clinical use [6]. Importantly, even without platform technologies, biomarkers identified in proteomic profiles can be translated into clinical use, e.g. by using standard techniques such as selective reaction monitoring (SRM) for the quantification of protein panels, or enzyme linked immunosorbent assays (ELISA) for the sensitive quantification of individual biomarkers. Here, we show that an increase in specific inflammatory and acute phase proteins over time (e.g., SAA1;SAA2, CRP, ITIH3, LRG1, SERPINA1, and LBP) is associated with the risk of death from COVID-19, while an increase of kallikrein (KLKB1), kallistatin (SERPINA4), thrombin (F2), apolipoprotein C3 (APOC3), GPLD1, and the protease inhibitor A2M, is associated with survival. Interestingly, we and others have found all of these proteins to also be differentially expressed depending on disease severity in COVID-19 [6,7,10,12,14]. Moreover, there is substantial overlap with a panel of proteins predictive of mortality in COVID-19 identified by Völlmy et al. [39]. Hence, despite only a subset of proteins that are differentially concentrated depending on disease severity predict outcome, and the fact that typical single-centre ICU studies are conducted on small numbers of patients, this result indicates a high congruence and reproducibility of plasma proteome signatures across studies. SAA1;SAA2, CRP, ITIH3, SERPINA1 are acute phase proteins that are also dysregulated in other inflammatory states including sepsis [40]. Increased LRG1 and LBP as well as decreased A2M [40,41] are indicators of an ongoing immune response, complementing the general pro-inflammatory signature of these predictive proteins. APOC3 and GPLD1 are involved in lipid metabolism, which has been shown to be dysregulated in bacterial pneumonia, thereby associated with unfavorable outcomes [42]. Kallikrein is involved in the blood coagulation system, fibrinolysis, and the complement cascade, three systems known to be dysregulated in COVID-19 [43–45]. It mediates the cleavage of kininogen to bradykinin and des-Arg9-bradykinin, a potent vasoactive peptide which is counter-regulated by ACE2, the cell entry receptor for SARS-CoV-2. Since the loss of ACE2 in COVID-19 supposedly leads to an imbalance of bradykinins, inhibition of the kallikrein-kinin system has been discussed as a treatment strategy in COVID-19 [46–48]. This hypothesis is not supported by our data, which indicate improved prognosis with increasing kallikrein levels. Kallikrein is counterbalanced by kallistatin, which equally increased over time in survivors in our study population, thereby potentially equilibrating the increase in the kinin-kallikrein system. Kallistatin is known for pleiotropic effects in vascular repair, endothelial function, and inflammation [49] and possesses protective properties in acute lung injury. According to our data kallistatin should be considered as a potential candidate for clinical testing in critical COVID-19 [50]. While prognostic assessments based on repeated measurements over time allow for treatment monitoring, including evaluation of experimental therapies in clinical trials, prognostic measurements from single time points are particularly valuable for timely patient management and resource allocation. We therefore employed a machine learning model to integrate proteomic measurements from the first time point at WHO grade 7, i.e. invasive mechanical ventilation and additional organ support therapy, in order to derive prognosis of outcome. We achieve high prognostic values, both in the exploratory cohort, as well as in a fully independent cohort. The results are currently based on a comparatively small number of patients with adverse outcome. Given the naturally small sample sizes of ICU cohorts and the exploratory character of our study, findings will have to be validated in larger cohorts, before further steps can be undertaken to translate our findings into clinical practice in the future. The panel of proteins identified in our study should also be assessed for other conditions such as non-COVID-19 ARDS. The majority of proteins with the highest relevance for the machine learning predictor were components of the coagulation system and the complement cascade (S2 Table). Both systems are known to be crucial for treatment and disease courses for severely ill COVID-19 patients [9,10]. This is particularly well illustrated by recent data from a multi-platform clinical trial indicating that a substantial proportion of patients with severe COVID-19 develop thromboembolic events despite therapeutic anticoagulation [51,52]. The protein with the highest relevance in our model is Fetuin-A (AHSG), which is known to be strongly downregulated in severe COVID-19 [10,14]. Of note, genetic polymorphisms associated with higher AHSG plasma concentrations were found to be protective in SARS-CoV-1 infection [53]. One important function of AHSG is regulation of inflammation through deactivation of macrophages [54], and there is emerging evidence that macrophages play a key role in pulmonary inflammation and dysfunction in COVID-19 [11,55–57]. A number of proteins identified as outcome predictors have also been shown to be differentially expressed in sepsis, including SAA1, CRP, SERPINA1, KLKB1, and A2M [40], indicating a general inflammatory signature rather than specific markers of COVID-19. In summary, we have leveraged the power of the proteome to address a problematic diagnostic gap in the prognosis of the most critical form of COVID-19, that is not covered by established clinical assessments, such as the SOFA or APACHE II scores. We show that the proteome accurately predicts survival in critically ill patients with COVID-19, from samples that were collected 39 days in median before the outcome. The findings warrant further prospective assessment of proteomic predictors and the described models in larger cohorts. The majority of proteins with high relevance in the model are components of the coagulation system and complement cascade, highlighting their critical role in progression and outcome of most severe COVID-19.

Methods Charité patient cohort and clinical data Patients included in this analysis are a sub-cohort of the PA-COVID-19 study conducted at Charité—Universitätsmedizin Berlin, a prospective observational cohort study on the pathophysiology of COVID-19 as described previously [14,19,29]. All patients with PCR-confirmed SARS-CoV-2 infection that progressed to critical disease (WHO grade 7, i.e. invasive mechanical ventilation and additional organ support), were eligible for inclusion. Exclusion criteria included refusal to provide informed consent by the patient or a legal representative, and any condition prohibiting serial biosampling. Patients were treated according to current clinical guidelines. Patients for whom limitation of therapy was decided according to the patient’s wish were excluded from analysis. This includes three cases, for whom limitation of therapy was decided at a later time point according to the patient’s presumed wish and predictably unfavorable outcome. All other patients received maximum intensive care treatment including organ replacement therapies at the discretion of the responsible physicians. One patient (ID 135), who was still hospitalized and clinically improving 5 months after admission, was classified as a survivor. One patient still in critical condition 5 months after admission was excluded due to uncertain outcome. Biosampling of EDTA plasma for proteome measurement was performed up to 3 times per week after inclusion. Disease severity was assessed according to the WHO ordinal scale for clinical improvement (World Health Organisation 2020). Clinical data were captured in secuTrial (interActive Systems GmbH, Berlin, Germany). Pseudonymized data exported from secuTrial were processed using JMP Pro 15 (SAS Institute Inc., Cary, NC, USA). Innsbruck Patient cohort and clinical data Serum samples from patients admitted to the intensive care unit at the Department of Medicine, University Hospital of Innsbruck with PCR-confirmed severe COVID-19 were collected within the first days (median 7.5, IQR 5–12) after admission, and written informed consent was obtained. Patients were treated according to national guidelines. The study was approved by the local ethics research committee EK-Nr. 1107/2020, and EK-Nr. 1103/2020 for follow-up. Statistical analysis and multiple-testing correction Statistical testing on proteomic and diagnostic data was performed in the R environment for statistical computing, version 3.6.0 [58], as described previously [14]. Briefly, all protein measurements were first log2-transformed and only protein groups matched to at least three different peptides were considered. Quantities of gene products corresponding to open reading frames IGxx (i.e. different types of immunoglobulin chains) were summed together to generate quantities representative of the overall levels of immunoglobulin classes (IGHVs, IGLVs, etc). Imputation of missing data was not performed. Significance testing for equal medians was performed using the Mann-Whitney U test, as implemented in the “wilcox.test” function of the “stats” R package. A non-parametric test was chosen here to minimise the influence of outliers on the calculated p-values. Multiple-testing correction was performed using the Benjamini-Hochberg false discovery rate controlling procedure [59], implemented in the “p.adjust” function of the “stats” R package. Adjusted p-values below 0.05 were considered significant. Identifying omics trajectories that are predictive of survival at the peak period of the disease For each omics feature, the difference between its log2-levels at the last and the first sampling timepoints during the peak period of the disease was considered. This period was defined as the time when the patient was receiving the most intensive treatment during their stay in hospital, that is the time when the patient was at WHO grade 6 or 7. The distribution of this difference between survivors and non-survivors was compared using the Mann-Whitney U test. Only non-DNI patients with known outcome were included. Prediction of survival The first time point measured at the WHO grade 7 was selected per patient, to train the survival predictor. This ensured that ‘future’ information, encoded in the later time points, was not used for predictor training. To reduce the feature space used as input for the machine learning model, we limited it to the quantities of 57 proteins which are FDA-approved biomarkers with MRM assays available [32] and which were quantified with at least three different peptides in this study. Missing values were imputed using minimal value imputation, and the data were standardized. Machine learning was carried out using the parenclitic networks approach [33,34]. Briefly, during training, for each pair of features, a radial SVM classifier is trained (using the svm() function from the “e1071” R package with default settings). For each sample, a network is then built, wherein vertices correspond to features and the edge weight is the death probability as predicted by the SVM classifier. Maximum, mean and standard deviation of the edge weights, as well as the numbers of edges with weights greater than 0.5 (i.e. fatal outcome is predicted) and nodes with at least one such edge are calculated. A LASSO classification model (alpha = 0.01) is then constructed on these 5 features using the glmnet() function of the “glmnet” [60] R package with default settings. For the assessment of the classifier performance (Charité cohort), a cross-validation method was applied in the following way: the prediction was made for each sample by excluding (withholding) it from the dataset along with two other samples (chosen randomly with the constraint that out of 3 samples one corresponds to a non-survivor and two to survivors), training the classifier on the remaining (independent) samples and then generating predictions for the withheld samples using the trained model. Such a leave-3-out partition was generated randomly 50 times and the predictions for each sample were averaged. The partitioning strategy ensured that the evaluation of the predictive performance would not be affected by any potential overfitting, no matter how significant. For the assessment of the performance on an independent dataset (Innsbruck cohort), the classifier was trained on all the Charité samples and used to estimate the probabilities of fatal outcome on the Innsbruck cohort. The source code is provided in supplementary materials. The ‘relevance’ scores for proteins in the parenclitic model were calculated as Kleinberg’s authority centrality scores for the respective vertices in the “generalizing network”. This network was generated by (i) replacing edge weights greater than 0.5 with 1.0 and weights less than 0.5 with 0.0 in the networks corresponding to non-survivors and (ii) averaging the resulting networks. For survival prediction using support vector machines (SVM), the same data and the same selection of proteins as for the parenclitic network model was applied. The SVM was built in Python 3.8.5 using the SVC() function with an rbf-kernel and a gamma value of 0.005 as implemented in scikit-learn 0.23.2 [61]. To circumvent class-imbalances, balanced class-weights were assumed. For benchmarking the model a stratified 10-fold cross-validation was performed. The data were scaled to zero mean and unit variance based on the training data. The reported results for the Charité-cohort are based on the data that were withheld when constructing the model in each cross-validation step. For validating the model, a model was trained on all samples of the Charité-cohort and validated using the independent Innsbruck-cohort. p-Values were calculated using the Mann-Whitney U test as implemented in SciPy 1.5.2 [62]. AUC values and confidence intervals were obtained using the roc() function of the pROC R package. We followed the guidelines for transparent reporting of multivariable prediction models for individual prognosis or diagnosis (TRIPOD) as proposed by the EQUATOR network [63]. Study approval The study was approved by the ethics committee of Charité—Universitätsmedizin Berlin (EA2/066/20) and conducted in accordance with the Declaration of Helsinki and guidelines of Good Clinical Practice (ICH 1996). Written informed consent was obtained from all patients or legal representatives according to regulations set by the ethics committee of Charité—Universitätsmedizin Berlin. The study is registered in the German and the WHO international registry for clinical studies (DRKS00021688).

Acknowledgments We thank Jan-David Manntz (Beckman, Germany) for help with the Biomek i7, Robert Lane, Jean-Baptiste Vincedent and Nick Morrice (SCIEX) for help with the TripleTOF 6600. PA-COVID-19 Study group, Charité–Universitätsmedizin Berlin Malte Kleinschmidt, Katrin M. Heim, Belén Millet, Lil Meyer-Arndt, Nils B. Müller, Ralf H. Hübner, Tim Andermann, Jan M. Doehn, Bastian Opitz, Birgit Sawitzki, Daniel Grund, Peter Radünzel, Mariana Schürmann, Thomas Zoller, Fridolin Steinbeis, Florian Alius, Philipp Knape, Astrid Breitbart, Yaosi Li, Felix Bremer, Panagiotis Pergantis, Susanne Fieberg, Anne Wetzel, Moritz Müller-Plathe, Timur Özkan, Carola Misgeld, Dirk Schürmann, Bettina Temmesfeld-Wollbrück, Britta Stier, Martin Möckel, Jan A. Graaw, Victor Wegener, Marc Kastrup, Felix Balzer, Daniel Wendisch, Sophia Brumhard, Sascha S. Haenel, Philipp Georg, Claudia Conrad, Kai-Uwe Eckardt, Lukas Lehner, Jan M. Kruse, Carolin Ferse, Roland Körner, Andreas Edel, Steffen Weber-Carstens, Alexander Krannich, Saskia Zvorc, Linna Li, Uwe Behrens, Sein Schmidt, Maria Rönnefarth, Christina Pley, Claudia Fink, Chantip Dang-Heine, Robert Röhle, Emma Lieker, Christian Wollboldt, Yinan Wu, Georg Schwanitz, Constanze Lüttke, Denise Treue, Michael Hummel, Victor M. Corman, Christian Drosten, Christof von Kalle

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