Next Article in Journal
Cell Count Differentials by Cytomorphology and Next-Generation Flow Cytometry in Bone Marrow Aspirate: An Evidence-Based Approach
Next Article in Special Issue
The Diagnostic Value of Cerebrospinal Fluid Lactate for Detection of Sepsis in Community-Acquired Bacterial Meningitis
Previous Article in Journal
Classification of Breast Lesions on DCE-MRI Data Using a Fine-Tuned MobileNet
Previous Article in Special Issue
Predicting Bacteremia among Septic Patients Based on ED Information by Machine Learning Methods: A Comparative Study
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Diagnostics
Volume 13
Issue 6
10.3390/diagnostics13061069
diagnostics-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Infection with SARS-CoV-2 Is Associated with Elevated Levels of IP-10, MCP-1, and IL-13 in Sepsis Patients

by
Tanja Eichhorn
1,
Silke Huber
2,
René Weiss
1,
Marie Ebeyer-Masotta
1,
Lucia Lauková
1,
Robert Emprechtinger
3,
Rosa Bellmann-Weiler
4,
Ingo Lorenz
5,
Judith Martini
6,
Markus Pirklbauer
7,
Dorothea Orth-Höller
8,
Reinhard Würzner
2 and
Viktoria Weber
1,*
1
Department for Biomedical Research, University for Continuing Education Krems, 3500 Krems, Austria
2
Institute of Hygiene and Medical Microbiology, Medical University of Innsbruck, 6020 Innsbruck, Austria
3
Faculty of Health and Medicine, University for Continuing Education Krems, 3500 Krems, Austria
4
Department of Internal Medicine II, Medical University of Innsbruck, 6020 Innsbruck, Austria
5
Department of General and Surgical Critical Care Medicine, Medical University of Innsbruck, 6020 Innsbruck, Austria
6
Department of Anaesthesia and Intensive Care Medicine, Medical University of Innsbruck, 6020 Innsbruck, Austria
7
Department of Internal Medicine IV-Nephrology and Hypertension, Medical University Innsbruck, 6020 Innsbruck, Austria
8
MB-LAB Clinical Microbiology Laboratory, 6020 Innsbruck, Austria
*
Author to whom correspondence should be addressed.
Diagnostics 2023, 13(6), 1069; https://doi.org/10.3390/diagnostics13061069
Submission received: 21 February 2023 / Revised: 7 March 2023 / Accepted: 9 March 2023 / Published: 11 March 2023
(This article belongs to the Special Issue Prediction and Diagnosis of Sepsis)
Browse Figures
Versions Notes

Abstract

:
Immunothrombosis, an excessive inflammatory response with simultaneous overactivation of the coagulation system, is a central pathomechanism in sepsis and COVID-19. It is associated with cellular activation, vascular damage, and microvascular thrombosis, which can lead to multiple organ failure and death. Here, we characterized factors related to immunothrombosis in plasma samples from 78 sepsis patients. In the course of routine clinical testing, SARS-CoV-2 was detected in 14 of these patients. Viral infection was associated with a higher mortality. Both, COVID-19 negative and COVID-19 positive sepsis patients showed increased levels of effectors of immunothrombosis, including platelet factor 4, D-dimer, nucleosomes, citrullinated histone H3, high mobility group box-1 protein, as well as phosphatidylserine-expressing platelet-derived extracellular vesicles, compared to healthy controls (n = 25). Using a 27-plex cytokine bead array, we found that Interleukin (IL)-1ra, IL-6, IL-8, IL-13, tumor necrosis factor (TNF)-α, interferon inducible protein (IP)-10, monocyte chemotactic protein (MCP)-1, macrophage inflammatory protein (MIP)-1α, and granulocyte-colony stimulating factor (G-CSF) were elevated in both, COVID-19 negative and COVID-19 positive sepsis patients, as compared to healthy controls. SARS-CoV-2 infection was associated with elevated levels of IP-10, MCP-1, and IL-13, while all other mediators widely overlapped between COVID-19 negative and COVID-19 positive patients.

1. Introduction

Sepsis is a life-threatening systemic inflammatory syndrome triggered by an inadequate host response to infection [1]. COVID-19, caused by the severe acute respiratory syndrome coronavirus SARS-CoV-2, shares many pathophysiological and clinical features with sepsis, including coagulopathy and vascular microthrombosis, as well as multiple organ failure [2,3,4], which accounts for most of the deaths in COVID-19 [5].
The thrombotic events associated with sepsis are best described as immunothrombosis, a simultaneous overactivation of the innate immune system and coagulation [6,7,8]. Dysregulated complement activation enhances neutrophil activation and recruitment to the lungs, and induces tissue factor (TF) expression on neutrophils, monocytes, and endothelial cells, resulting in microvascular thrombosis and endothelial dysfunction [2]. The release of neutrophil extracellular traps (NETs), decondensed DNA associated with neutrophil elastase, antimicrobial peptides, histones, and high mobility group box-1 protein (HMGB-1) further promotes thrombosis and tissue damage [9]. NETs trigger coagulation via both, the intrinsic (FXII activation) [10] and the extrinsic (TF exposure) pathways [11].
Next to neutrophils, platelets are the main effectors of immunothrombosis [12,13,14]. Platelet activation triggers the release of platelet factor 4 (PF4, CXCL4), supporting monocyte and neutrophil recruitment [15]. Activated platelets secrete HMGB-1 and promote NETosis [16,17], and enhanced aggregate formation of activated platelets with monocytes and neutrophils has been linked to thrombotic complications in severe COVID-19 [9,18,19,20]. Activated platelets are a major source of circulating extracellular vesicles (EVs) [21,22], which expose phosphatidylserine and serve as a catalytic surface for thrombin generation [23,24].
Here, we analyzed a panel of 47 parameters related to immunothrombosis in sepsis patients and found that patients with confirmed SARS-CoV-2 infection had higher levels of IP-10, MCP-1, and IL-13.

2. Materials and Methods

2.1. Patients and Sample Collection

Between October 2019 and July 2021, 78 sepsis patients with suspected bloodstream infection and a sequential organ failure assessment (SOFA) score > 2 hospitalized at the Department of Internal Medicine or the Department of Operative Medicine, both Medical University of Innsbruck, Austria, were enrolled in this study. Collection of EDTA-anticoagulated whole blood using an aspiration-based blood collection system (S-Monovette®, Sarstedt, Goetzis, Austria) was performed during routine venipuncture for blood culture testing. Whole blood was centrifuged (2000× g, 15 min, 22 °C) within 4 h to obtain platelet-poor plasma and stored in aliquots at −80 °C until further analysis. Of the 78 sepsis patients, 14 were additionally diagnosed with COVID-19 using the cobas® SARS-CoV-2 Qualitative RT-PCR Test (Roche, Mannheim, Germany) for the detection of the target E gene (pan-Sarbecovirus) and the SARS-CoV-2 specific target orf1a/b gene. The control group (n = 25) consisted of healthy individuals from whom EDTA-anticoagulated blood was collected after written consent and directly processed.

2.2. Data Collection

Clinical data collected from the electronic medical record included the date of sampling, gender, age, ward, the result of routine blood culture (BC), clinical diagnosis, death within one month after sampling, antimicrobial treatment, puncture site, C-reactive protein (CRP), procalcitonin (PCT), red blood cell, white blood cell, monocyte, neutrophil, lymphocyte, and platelet counts, as well as neutrophil-to-lymphocyte ratio (NLR). The 14 COVID-19 patients were classified according to the WHO severity criteria (moderate, n = 6; severe, n = 5; critical, n = 3) [25].

2.3. Blood Culture

Routine blood culture testing was performed on the wards by inoculating at least one set of BACTEC™ Plus Aerobic/F and BACTEC™ Lytic/10 Anaerobic/F culture bottles (both BD Diagnostics, Vienna, Austria) with the patient’s whole blood. Culture bottles were immediately transported to the routine microbiological laboratory and incubated at 37 °C using the BACTEC FX Packaged continuous BC monitoring system (BD Diagnostics) until growth or for 5 days post-inoculation. Positive BCs were further used for pathogen identification after cultivation on agar plates using matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF MS) based on the reference Biotyper library v4.1 (both Bruker Daltonik, Bremen, Germany) and antimicrobial susceptibility testing (AST). Disk diffusion was used for the latter and was performed in accordance with the current EUCAST guidelines at the time point of sampling [26].

2.4. Coagulation-Related Parameters

In addition to platelet counts, plasma concentrations of PF4 and D-dimer were quantified by ELISA (R&D Systems, Minneapolis, MN, and Technozym, Vienna, Austria, respectively). The cell death detection ELISA (Roche, Mannheim, Germany) was used to quantify nucleosomes in plasma. Results are indicated as arbitrary units (AU), which represent the ratio of the maximum measured absorbance and the absorbance of the individual samples. Citrullinated histone H3 and HMGB-1 were quantified by ELISA (Cayman Chemical, Ann Arbor, MI, and IBL International, Hamburg, Germany).

2.5. Characterization of Extracellular Vesicles

EVs were characterized using a CytoFLEX LX flow cytometer (Beckman Coulter, Brea, CA, USA) equipped with 405 nm, 488 nm, 561 nm, and 631 nm lasers. For staining, samples were diluted 1:100 in sterile-filtered Annexin V (Anx5) binding buffer (0.1 μm Minisart syringe filter, Sartorius Stedim Biotech, Goettingen, Germany). Aliquots (100 μL) of the diluted samples were incubated for 15 min at room temperature in the dark with APC-conjugated Anx5 (BD Biosciences, San Jose, CA, USA) as a marker for EVs exposing phosphatidylserine in combination with PE-conjugated anti-hCXCL4 (R&D Systems) and PC7-conjugated anti-CD41 or with FITC-conjugated anti-CRP (Abcam, Cambridge, UK). All fluorochrome conjugates and the respective antibody clones are listed in Supplementary Table S1. To remove potential precipitates, fluorochrome conjugates were centrifuged at 18,600× g for 10 min at 4 °C prior to use. Stained samples were diluted 1:5 in sterile-filtered Anx5 binding buffer (BD Biosciences) prior to analysis. Calibration of the flow cytometer was performed with fluorescent silica beads (1 μm, 0.5 μm, 0.1 μm; excitation/emission 485/510 nm; Kisker Biotech, Steinfurt, Germany). The triggering signal for EVs was set to the violet side scatter (405 nm), and the EV gate was set below the 1 µm bead cloud (Supplementary Figure S1) as previously described [27,28]. Acquisition was performed for 2 min at a flow rate of 10 µL/min. Data were analyzed using the Kaluza Software (Beckman Coulter, version 2.1). EVs were identified as Anx5+ events in the EV gate.

2.6. Quantification of C5b-9

Levels of the C5b-9 (terminal complement complex, TCC) were measured using an in-house sandwich ELISA as previously described [29]. Briefly, 96-well medium-binding microplates (Greiner Bio-One, St. Gallen, Switzerland) were coated with a monoclonal anti-human C9 neoantigen antibody (Hycult Biotech, Uden, The Netherlands). Following sample incubation, a custom-made biotinylated polyclonal anti-human C7 antibody [30] and avidin-alkaline phosphatase (Millipore, Sigma, Merck KGaA, Darmstadt, Germany) were used to detect bound C5b-9. Zymosan-activated human serum was used as standard.

2.7. Quantification of Cytokines, Chemokines, and Growth Factors

A set of 27 cytokines, chemokines, and growth factors were analyzed by bead array (Bio-Plex Pro human cytokine 27-plex; Bio-Rad, Hercules, CA, USA), including interleukin (IL)-1β, IL-1 receptor antagonist (IL-1ra), IL-2, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-12p70, IL-13, IL-15, IL-17A, interferon-gamma (IFN-γ), tumor necrosis factor-alpha (TNF-α), eosinophil chemotactic protein (eotaxin), interferon-gamma inducible protein-10 (IP-10), monocyte chemotactic protein-1 (MCP-1), macrophage inflammatory protein-1 alpha and beta (MIP-1α, MIP-1β), regulated on activation, normal T-cell expressed and secreted (RANTES), basic fibroblast growth factor (FGF), granulocyte colony-stimulating factor (G-CSF), granulocyte-macrophage colony-stimulating factor (GM-CSF), platelet-derived growth factor (PDGF), as well as vascular endothelial growth factor (VEGF). Plasma samples were diluted 1:4 with sample diluent and analyzed according to the instructions of the manufacturer using the Bio-Plex 200 System and the Bio-Plex Manager software version 5.0 (Bio-Rad).

2.8. Statistical Analysis

Statistical analysis was carried out using R (version 4.1.3). We reported the bias-corrected and accelerated (BCa) bootstrap 95% confidence intervals (CI) of the median. If the bootstrapping confidence interval returned the warning “extreme order statistics used as endpoints”, we used the percentage bootstrap confidence interval. Calculation of confidence intervals was performed by nonparametric bootstrapping using the boot package with 100,000 iterations [31,32]. Correlation analysis was performed using the Spearman correlation test and heat map analyses of the correlation coefficients were performed.

3. Results

3.1. Patient Characteristics

Samples from 78 sepsis patients were analyzed in this study. Fourteen of these patients were diagnosed with COVID-19 during routine clinical testing in the course of the pandemic, with mean Ct values of 27.9 for the orf1a/b gene and 28.3 for the E gene. Twenty-five healthy individuals served as controls. The patient characteristics are summarized in Table 1. The in-hospital mortality was 11% for COVID-19 negative and 43% for COVID-19 positive patients. Bacteremia was confirmed by blood culture in 9 of the 78 sepsis patients (COVID-19 negative, n = 8; COVID-19 positive, n = 1). The panel of identified pathogens included Staphylococcus aureus (n = 4), Pseudomonas aeruginosa (n = 2), Escherichia coli (n = 2), Klebsiella pneumoniae (n = 1), Streptococcus pneumoniae (n = 1), Enterobacter cloacae (n = 1), and Staphylococcus epidermidis (n = 1). Hereby, two patients suffered from co-infections with up to three different pathogens, and Pseudomonas aeruginosa was isolated from one COVID-19 positive patient. Blood culture-positive patients exhibited higher PCT levels than blood culture-negative patients, 16.78 (CI 1.61–71.46) µg/L vs. 0.42 (CI 0.2–0.54) µg/L, respectively. The profiles of inflammatory mediators for COVID-19 positive and negative patients are summarized in Table 2. The parameters presented in Table 2 were grouped into factors related to coagulation and complement activation (Figure 1), as well as cytokines, chemokines, and growth factors (Figure 2). Mediator profiles of blood culture-negative and blood culture-positive patients are summarized in Supplementary Table S2, and mediator profiles of survivors and non-survivors are compiled in Supplementary Table S3. Spearman correlation coefficients for all parameters are summarized in Supplementary Figures S2 and S3.

3.2. Coagulation- and Complement-Related Parameters

Coagulation- and complement-related parameters included platelet counts, PF4, D-dimer, nucleosomes, citrullinated histone H3, HMGB-1, EV counts, as well as the terminal complement complex C5b-9. EVs were further analyzed regarding their platelet origin (CD41+) and their association with CRP (CRP+). Both patient groups showed a trend towards lower platelet counts, however, the confidence intervals for both groups overlapped with the control group. D-dimer was elevated in both patient groups. PF4 was increased in COVID-19 negative patients, while the confidence intervals overlapped with the control for COVID-19 positive patients.
We also measured markers of NET formation and observed increased nucleosome and citrullinated histone H3 levels in both patient groups. Likewise, HMGB-1, a known inducer of NET formation, as well as C5b-9 were elevated in both patient groups.
EVs shed from the plasma membrane expose phosphatidylserine and thereby provide a catalytic surface mediating thrombin generation [23,24]. Both, total EV counts and platelet-derived EVs were elevated in COVID-19 positive and COVID-19 negative patients (Figure 1). Both groups showed elevated levels of CRP+ EVs, with 55% (CI 46–61%) and 62% (CI 40–68%) CRP+ EVs in COVID-19 negative and COVID-19 positive patients, respectively, confirming previous results [33], while only 4% (CI 2–4%) of all EVs were associated with CRP in healthy controls. Percentages of CRP+ EVs correlated with CRP levels in both patient groups (Supplementary Figures S2 and S3).

3.3. Cytokines, Chemokines, and Growth Factors

COVID-19 positive and COVID-19 negative patients had increased levels of IL-1ra, IL-6, IL-8, IL-13, TNF-α, IP-10, MCP-1, MIP-1α, and G-CSF (Figure 2). FGF was elevated in COVID-19 positive, but not in COVID-19 negative sepsis patients. IP-10, MCP-1, and IL-13 were higher for COVID-19 positive than for COVID-19 negative patients. Both patient groups exhibited lower levels of IL-9 and IL-17 as compared to healthy donors. Mediator levels were not different for survivors and non-survivors (Supplementary Table S3).

4. Discussion

Blood culture confirmed bacterial infection in 11.5% of the 78 sepsis patients included in our study (13% of the COVID-19 negative and 7% of the COVID-19 positive sepsis patients). Viral co-infection was associated with a higher prevalence of ICU admission and a higher mortality. Our data confirm recent meta-analyses reporting bacterial co-infections in 7–8% of COVID-19 patients, most frequently in those with critical illness [34,35]. The close connection between bacterial and viral infection is highlighted by recent work on mechanisms leading to gut dysbiosis in COVID-19, showing that SARS-CoV-2 can induce dysbiosis by triggering intestinal inflammation, by dysregulating the angiotensin-converting enzyme 2 (ACE2), which is essential for amino acid metabolism, and by infection of intestinal bacteria [36,37].
The dysregulated immune response in COVID-19 is associated with an enhanced release of inflammatory mediators [38,39,40,41,42,43]. Several studies, however, have challenged the concept of a cytokine storm that would differentiate COVID-19 from sepsis [44,45,46,47]. In line with previous studies, our data suggest that inflammatory mediator profiles in sepsis patients who tested positive for SARS-CoV-2 do not substantially differ from those of critically ill patients suffering from sepsis or acute respiratory distress syndrome [48]. We found increased levels of IL-1ra, IL-6, IL-8, IL-13, TNF-α, IP-10, MCP-1, MIP-1α, and G-CSF in both, COVID-19 negative and COVID-19 positive sepsis patients, as compared to healthy controls. Three out of the 27 factors included in the cytokine bead array, IP-10, MCP-1, and IL-13, were higher in COVID-19 positive than in COVID-19 negative sepsis patients. The chemokine IP-10 is mainly released by lymphocytes, neutrophils, and endothelial cells in response to IFNs and lipopolysaccharide to mediate the recruitment of immune cells [49]. Elevated IP-10 levels, which increased with disease progression, have been described in sepsis patients [50]. Elevation of IP-10 was also observed in COVID-19, where several studies demonstrated an association of IP-10 with increased viral titers and disease severity [39,51]. Along with IP-10, MCP-1 has been associated with disease progression in COVID-19 patients in previous studies, as well [39,52,53]. Consistent with our findings, Donlan and co-workers detected significantly increased IL-13 levels in COVID-19 patients [54]. IL-13 is a type-2 cytokine for the recruitment of eosinophils and M2 macrophages to the lung and is implicated in smooth muscle cell proliferation as well as in mucus production and fibrosis [55]. Its elevation has been closely related to respiratory failure requiring mechanical ventilation, while its blockade showed the potential to ameliorate disease severity [54].
The inflammatory responses in sepsis and in COVID-19 are highly dynamic, resulting in pronounced heterogeneity of patient cohorts. Under this aspect, it is essential to consider that most studies, including ours, are limited to the analysis of single time points rather than providing time courses. Therefore, they can only yield snapshots of the dynamic inflammatory response. From this point of view, a recent prospective study by Loftus and co-workers is particularly valuable. They compared inflammatory and immunosuppressive profiles of 30 critically ill patients with SARS-CoV-2 infection with ten critically ill bacterial sepsis patients at five-time points over a period of 21 days. According to this study, bacterial sepsis was rather associated with early, severe inflammation and profound immunosuppression, while SARS-CoV-2 patients had less severe early inflammation, but persistent immunosuppression, making them particularly vulnerable to secondary infection [56].
The activation and interaction of platelets, neutrophils, and monocytes are major drivers of immunothrombosis. Elevated levels of PF4 have been linked to enhanced platelet activation [57,58,59] and to a hypercoagulable state associated with increased D-dimer levels in sepsis and COVID-19 [9,18,60]. Our data support these observations, since both, COVID-19 negative and COVID-19 positive sepsis patients had increased PF4 and D-dimer levels compared to healthy individuals. However, we could not confirm previous findings [46,61] on distinct D-dimer levels among sepsis and COVID-19 patients.
Activated neutrophils exacerbate immunothrombosis by releasing NETs, DNA fibers decorated with antimicrobial peptides and histones. Exaggerated NET formation has been correlated with disease severity and poor clinical outcome in sepsis as well as COVID-19 [9,62,63,64,65]. NETosis is induced by a range of proinflammatory mediators, including IL-1β and IL-8, while the increased generation of reactive oxygen species is a crucial intracellular process triggering NETosis. Platelet activation represents another route of NET generation, and platelets enhance NETosis by interacting with neutrophils through TLR4, PF4, and extracellular vesicle-dependent processes. NET-associated histones induce further platelet activation and contribute to vascular damage due to their cytotoxicity.
We determined nucleosomes and citrullinated histone H3 as markers of NET formation. Both were elevated in COVID-19 positive and COVID-19 negative sepsis patients, supporting previous findings by Traby and co-workers, who reported elevated levels of citrullinated histone H3, D-dimer, CRP, IL-6, as well as an increased neutrophil-to-lymphocyte ratio in COVID-19 patients [60].
Extracellular vesicles are increasingly considered as amplifiers of immunothrombosis, particularly the subset of EVs exposing phosphatidylserine on their surface, which propagates thrombin generation [23,24]. In line with previous studies [60,66], we observed elevated levels of phosphatidylserine-exposing EVs in COVID-19 negative as well as COVID-19 positive sepsis patients, the majority of which were platelet-derived. While the levels of platelet-derived EVs did not differ between COVID-19 negative and COVID-19 positive sepsis patients, the concentration of CRP+ EVs was higher in COVID-19 positive sepsis patients. The association of CRP with EVs may further support inflammation, as there is increasing evidence that functionally inert pentameric CRP dissociates to pro-inflammatory monomeric CRP upon binding to phosphocholine-enriched membranes [67].

5. Conclusions

Our study provides evidence that the profiles of inflammatory mediators largely overlap between COVID-19 negative and COVID-19 positive sepsis patients. Our data support the notion that activated platelets and platelet-derived EVs are potential mediators of immunothrombosis in sepsis and COVID-19.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/diagnostics13061069/s1, Figure S1: Calibration and controls for the flow cytometric characterization of extracellular vesicles.; Figure S2: Spearman-based correlation plot of all inflammatory mediators analyzed in COVID-19 negative sepsis patients.; Figure S3: Spearman-based correlation plot of all inflammatory mediators analyzed in COVID-19 positive sepsis patients.; Table S1: Antibodies and fluorochrome conjugates used for flow cytometric characterization of extracellular vesicles.; Table S2: Mediator profiles in sepsis patients with unknown and confirmed bacteremia.; Table S3: Inflammatory mediator profiles in survivors and non-survivors.

Author Contributions

Conceptualization, T.E. and V.W.; Data curation, T.E., S.H., R.W. (René Weiss), D.O.-H. and R.W. (Reinhard Würzner); Formal analysis, R.E.; Funding acquisition, T.E. and V.W.; Investigation, T.E., S.H., R.W. (René Weiss), M.E.-M. and L.L.; Methodology, T.E., S.H., R.W. (René Weiss) and M.E.-M.; Resources, R.B.-W., I.L., J.M., M.P., D.O.-H. and R.W. (Reinhard Würzner); Supervision, V.W.; Visualization, R.E.; Writing—original draft, T.E. and V.W.; Writing—review & editing, S.H., R.W. (René Weiss), M.E.-M., L.L., R.E., R.B.-W., I.L., J.M., M.P., D.O.-H. and R.W. (Reinhard Würzner). All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Lower Austrian Society for Research Funding Organization, grant number K3-F-744/005-2019 and by the Austrian Research Promotion Agency (FFG; Bridge), grant number 871243. Furthermore, this research was supported by the Austrian Science Fund (FWF), grant number W-1253 (HOROS) and Land Tirol. APC and Open Access was funded by FWF, HOROS W-1253.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki. The collection of blood samples from patients and from healthy individuals was approved by the Ethics Committee of the Medical University of Innsbruck (ECS1021/2019, date of approval: 1 May 2019; ECS1166/2018, date of approval: 14 November 2018, respectively).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

All authors confirm that all relevant data are included in the article. Additional statistical data are available from the corresponding author upon request.

Acknowledgments

The authors are indebted to the nurses and technicians at the intensive care unit and the central laboratory of the Medical University of Innsbruck.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Singer, M.; Deutschman, C.S.; Seymour, C.W.; Shankar-Hari, M.; Annane, D.; Bauer, M.; Bellomo, R.; Bernard, G.R.; Chiche, J.D.; Coopersmith, C.M.; et al. The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3). JAMA 2016, 315, 801–810. [Google Scholar] [CrossRef] [PubMed]
  2. Bonaventura, A.; Vecchie, A.; Dagna, L.; Martinod, K.; Dixon, D.L.; Van Tassell, B.W.; Dentali, F.; Montecucco, F.; Massberg, S.; Levi, M.; et al. Endothelial dysfunction and immunothrombosis as key pathogenic mechanisms in COVID-19. Nat. Rev. Immunol. 2021, 21, 319–329. [Google Scholar] [CrossRef] [PubMed]
  3. Iba, T.; Levy, J.H.; Levi, M.; Connors, J.M.; Thachil, J. Coagulopathy of Coronavirus Disease 2019. Crit. Care Med. 2020, 48, 1358–1364. [Google Scholar] [CrossRef] [PubMed]
  4. Olwal, C.O.; Nganyewo, N.N.; Tapela, K.; Djomkam Zune, A.L.; Owoicho, O.; Bediako, Y.; Duodu, S. Parallels in Sepsis and COVID-19 Conditions: Implications for Managing Severe COVID-19. Front. Immunol. 2021, 12, 602848. [Google Scholar] [CrossRef]
  5. Remmelink, M.; De Mendonca, R.; D’Haene, N.; De Clercq, S.; Verocq, C.; Lebrun, L.; Lavis, P.; Racu, M.L.; Trepant, A.L.; Maris, C.; et al. Unspecific post-mortem findings despite multiorgan viral spread in COVID-19 patients. Crit. Care 2020, 24, 495. [Google Scholar] [CrossRef]
  6. Engelmann, B.; Massberg, S. Thrombosis as an intravascular effector of innate immunity. Nat. Rev. Immunol. 2013, 13, 34–45. [Google Scholar] [CrossRef]
  7. Ackermann, M.; Verleden, S.E.; Kuehnel, M.; Haverich, A.; Welte, T.; Laenger, F.; Vanstapel, A.; Werlein, C.; Stark, H.; Tzankov, A.; et al. Pulmonary Vascular Endothelialitis, Thrombosis, and Angiogenesis in COVID-19. N. Engl. J. Med. 2020, 383, 120–128. [Google Scholar] [CrossRef]
  8. Skendros, P.; Mitsios, A.; Chrysanthopoulou, A.; Mastellos, D.C.; Metallidis, S.; Rafailidis, P.; Ntinopoulou, M.; Sertaridou, E.; Tsironidou, V.; Tsigalou, C.; et al. Complement and tissue factor-enriched neutrophil extracellular traps are key drivers in COVID-19 immunothrombosis. J. Clin. Investig. 2020, 130, 6151–6157. [Google Scholar] [CrossRef]
  9. Middleton, E.A.; He, X.Y.; Denorme, F.; Campbell, R.A.; Ng, D.; Salvatore, S.P.; Mostyka, M.; Baxter-Stoltzfus, A.; Borczuk, A.C.; Loda, M.; et al. Neutrophil extracellular traps contribute to immunothrombosis in COVID-19 acute respiratory distress syndrome. Blood 2020, 136, 1169–1179. [Google Scholar] [CrossRef]
  10. Gould, T.J.; Vu, T.T.; Swystun, L.L.; Dwivedi, D.J.; Mai, S.H.; Weitz, J.I.; Liaw, P.C. Neutrophil extracellular traps promote thrombin generation through platelet-dependent and platelet-independent mechanisms. Arterioscler. Thromb. Vasc. Biol. 2014, 34, 1977–1984. [Google Scholar] [CrossRef] [Green Version]
  11. Kambas, K.; Chrysanthopoulou, A.; Vassilopoulos, D.; Apostolidou, E.; Skendros, P.; Girod, A.; Arelaki, S.; Froudarakis, M.; Nakopoulou, L.; Giatromanolaki, A.; et al. Tissue factor expression in neutrophil extracellular traps and neutrophil derived microparticles in antineutrophil cytoplasmic antibody associated vasculitis may promote thromboinflammation and the thrombophilic state associated with the disease. Ann. Rheum. Dis. 2014, 73, 1854–1863. [Google Scholar] [CrossRef] [Green Version]
  12. Foley, J.H.; Conway, E.M. Cross Talk Pathways Between Coagulation and Inflammation. Circ. Res. 2016, 118, 1392–1408. [Google Scholar] [CrossRef]
  13. Martinod, K.; Deppermann, C. Immunothrombosis and thromboinflammation in host defense and disease. Platelets 2021, 32, 314–324. [Google Scholar] [CrossRef]
  14. Ebeyer-Masotta, M.; Eichhorn, T.; Weiss, R.; Laukova, L.; Weber, V. Activated Platelets and Platelet-Derived Extracellular Vesicles Mediate COVID-19-Associated Immunothrombosis. Front. Cell Dev. Biol. 2022, 10, 914891. [Google Scholar] [CrossRef]
  15. Slungaard, A. Platelet factor 4: A chemokine enigma. Int. J. Biochem. Cell Biol. 2005, 37, 1162–1167. [Google Scholar] [CrossRef]
  16. Vogel, S.; Bodenstein, R.; Chen, Q.; Feil, S.; Feil, R.; Rheinlaender, J.; Schaffer, T.E.; Bohn, E.; Frick, J.S.; Borst, O.; et al. Platelet-derived HMGB1 is a critical mediator of thrombosis. J. Clin. Investig. 2015, 125, 4638–4654. [Google Scholar] [CrossRef] [Green Version]
  17. Maugeri, N.; Campana, L.; Gavina, M.; Covino, C.; De Metrio, M.; Panciroli, C.; Maiuri, L.; Maseri, A.; D′Angelo, A.; Bianchi, M.E.; et al. Activated platelets present high mobility group box 1 to neutrophils, inducing autophagy and promoting the extrusion of neutrophil extracellular traps. J. Thromb. Haemost. 2014, 12, 2074–2088. [Google Scholar] [CrossRef]
  18. Hottz, E.D.; Azevedo-Quintanilha, I.G.; Palhinha, L.; Teixeira, L.; Barreto, E.A.; Pao, C.R.R.; Righy, C.; Franco, S.; Souza, T.M.L.; Kurtz, P.; et al. Platelet activation and platelet-monocyte aggregate formation trigger tissue factor expression in patients with severe COVID-19. Blood 2020, 136, 1330–1341. [Google Scholar] [CrossRef]
  19. Manne, B.K.; Denorme, F.; Middleton, E.A.; Portier, I.; Rowley, J.W.; Stubben, C.; Petrey, A.C.; Tolley, N.D.; Guo, L.; Cody, M.; et al. Platelet gene expression and function in patients with COVID-19. Blood 2020, 136, 1317–1329. [Google Scholar] [CrossRef]
  20. McDonald, B.; Urrutia, R.; Yipp, B.G.; Jenne, C.N.; Kubes, P. Intravascular neutrophil extracellular traps capture bacteria from the bloodstream during sepsis. Cell Host Microbe 2012, 12, 324–333. [Google Scholar] [CrossRef] [Green Version]
  21. Puhm, F.; Flamand, L.; Boilard, E. Platelet extracellular vesicles in COVID-19: Potential markers and makers. J. Leukoc. Biol. 2022, 111, 63–74. [Google Scholar] [CrossRef] [PubMed]
  22. Kerris, E.W.J.; Hoptay, C.; Calderon, T.; Freishtat, R.J. Platelets and platelet extracellular vesicles in hemostasis and sepsis. J. Investig. Med. 2020, 68, 813–820. [Google Scholar] [CrossRef] [PubMed]
  23. Tripisciano, C.; Weiss, R.; Eichhorn, T.; Spittler, A.; Heuser, T.; Fischer, M.B.; Weber, V. Different Potential of Extracellular Vesicles to Support Thrombin Generation: Contributions of Phosphatidylserine, Tissue Factor, and Cellular Origin. Sci. Rep. 2017, 7, 6522. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Owens, A.P., 3rd; Mackman, N. Microparticles in hemostasis and thrombosis. Circ. Res. 2011, 108, 1284–1297. [Google Scholar] [CrossRef]
  25. World Health Organization. Clinical Management of COVID-19. Living Guideline. 2021. Available online: https://www.who.int/teams/health-care-readiness/covid-19 (accessed on 5 April 2022).
  26. EUCAST Disk Diffusion – Manual v 2.0 to v 7.0. Available online: https://www.eucast.org/ast_of_bacteria/previous_versions_of_documents/ (accessed on 21 July 2021).
  27. George, S.K.; Laukova, L.; Weiss, R.; Semak, V.; Fendl, B.; Weiss, V.U.; Steinberger, S.; Allmaier, G.; Tripisciano, C.; Weber, V. Comparative Analysis of Platelet-Derived Extracellular Vesicles Using Flow Cytometry and Nanoparticle Tracking Analysis. Int. J. Mol. Sci. 2021, 22, 3839. [Google Scholar] [CrossRef]
  28. Ebeyer-Masotta, M.; Eichhorn, T.; Weiss, R.; Semak, V.; Laukova, L.; Fischer, M.B.; Weber, V. Heparin-Functionalized Adsorbents Eliminate Central Effectors of Immunothrombosis, including Platelet Factor 4, High-Mobility Group Box 1 Protein and Histones. Int. J. Mol. Sci. 2022, 23, 1823. [Google Scholar] [CrossRef]
  29. Huber, S.; Massri, M.; Grasse, M.; Fleischer, V.; Kellnerova, S.; Harpf, V.; Knabl, L.; Knabl, L., Sr.; Heiner, T.; Kummann, M.; et al. Systemic Inflammation and Complement Activation Parameters Predict Clinical Outcome of Severe SARS-CoV-2 Infections. Viruses 2021, 13, 2376. [Google Scholar] [CrossRef]
  30. Wurzner, R.; Nitze, R.; Gotze, O. C7*9, a new frequent C7 allele detected by an allotype-specific monoclonal antibody. Complement. Inflamm. 1990, 7, 290–297. [Google Scholar] [CrossRef]
  31. Canty, A.R.; Ripley, B.D. boot: Bootstrap R (S-Plus) Functions. R package version 1.3-28. Available online: https://cran.r-project.org/web/packages/boot/index.html (accessed on 30 November 2022).
  32. Davison, A.C.; Hinkley, D.V. Bootstrap Methods and Their Applications; Cambridge University Press: Cambridge, UK, 1997. [Google Scholar]
  33. Fendl, B.; Weiss, R.; Eichhorn, T.; Linsberger, I.; Afonyushkin, T.; Puhm, F.; Binder, C.J.; Fischer, M.B.; Weber, V. Extracellular vesicles are associated with C-reactive protein in sepsis. Sci. Rep. 2021, 11, 6996. [Google Scholar] [CrossRef]
  34. Langford, B.J.; So, M.; Raybardhan, S.; Leung, V.; Westwood, D.; MacFadden, D.R.; Soucy, J.R.; Daneman, N. Bacterial co-infection and secondary infection in patients with COVID-19: A living rapid review and meta-analysis. Clin. Microbiol. Infect. 2020, 26, 1622–1629. [Google Scholar] [CrossRef]
  35. Musuuza, J.S.; Watson, L.; Parmasad, V.; Putman-Buehler, N.; Christensen, L.; Safdar, N. Prevalence and outcomes of co-infection and superinfection with SARS-CoV-2 and other pathogens: A systematic review and meta-analysis. PLoS ONE 2021, 16, e0251170. [Google Scholar] [CrossRef]
  36. Clerbaux, L.A.; Fillipovska, J.; Muñoz, A.; Petrillo, M.; Coecke, S.; Amorim, M.J.; Grenga, L. Mechanisms Leading to Gut Dysbiosis in COVID-19: Current Evidence and Uncertainties Based on Adverse Outcome Pathways. J. Clin. Med. 2022, 11, 5400. [Google Scholar] [CrossRef]
  37. Gang, J.; Wang, H.; Xue, X.; Zhang, S. Microbiota and COVID-19: Long-term and complex influencing factors. Front. Microbiol. 2022, 13, 963488. [Google Scholar] [CrossRef]
  38. Petrey, A.C.; Qeadan, F.; Middleton, E.A.; Pinchuk, I.V.; Campbell, R.A.; Beswick, E.J. Cytokine release syndrome in COVID-19: Innate immune, vascular, and platelet pathogenic factors differ in severity of disease and sex. J. Leukoc. Biol. 2021, 109, 55–66. [Google Scholar] [CrossRef]
  39. Huang, C.; Wang, Y.; Li, X.; Ren, L.; Zhao, J.; Hu, Y.; Zhang, L.; Fan, G.; Xu, J.; Gu, X.; et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet 2020, 395, 497–506. [Google Scholar] [CrossRef] [Green Version]
  40. Del Valle, D.M.; Kim-Schulze, S.; Huang, H.H.; Beckmann, N.D.; Nirenberg, S.; Wang, B.; Lavin, Y.; Swartz, T.H.; Madduri, D.; Stock, A.; et al. An inflammatory cytokine signature predicts COVID-19 severity and survival. Nat. Med. 2020, 26, 1636–1643. [Google Scholar] [CrossRef]
  41. Jarczak, D.; Nierhaus, A. Cytokine Storm-Definition, Causes, and Implications. Int. J. Mol. Sci. 2022, 23, 11740. [Google Scholar] [CrossRef]
  42. Osuchowski, M.F.; Winkler, M.S.; Skirecki, T.; Cajander, S.; Shankar-Hari, M.; Lachmann, G.; Monneret, G.; Venet, F.; Bauer, M.; Brunkhorst, F.M.; et al. The COVID-19 puzzle: Deciphering pathophysiology and phenotypes of a new disease entity. Lancet Respir. Med. 2021, 9, 622–642. [Google Scholar] [CrossRef]
  43. Chi, Y.; Ge, Y.; Wu, B.; Zhang, W.; Wu, T.; Wen, T.; Liu, J.; Guo, X.; Huang, C.; Jiao, Y.; et al. Serum Cytokine and Chemokine Profile in Relation to the Severity of Coronavirus Disease 2019 in China. J. Infect. Dis. 2020, 222, 746–754. [Google Scholar] [CrossRef]
  44. Monneret, G.; Benlyamani, I.; Gossez, M.; Bermejo-Martin, J.F.; Martin-Fernandez, M.; Sesques, P.; Wallet, F.; Venet, F. COVID-19: What type of cytokine storm are we dealing with? J. Med. Virol. 2021, 93, 197–198. [Google Scholar] [CrossRef]
  45. Kox, M.; Waalders, N.J.B.; Kooistra, E.J.; Gerretsen, J.; Pickkers, P. Cytokine Levels in Critically Ill Patients With COVID-19 and Other Conditions. JAMA 2020, 324, 1565–1567. [Google Scholar] [CrossRef] [PubMed]
  46. Leisman, D.E.; Ronner, L.; Pinotti, R.; Taylor, M.D.; Sinha, P.; Calfee, C.S.; Hirayama, A.V.; Mastroiani, F.; Turtle, C.J.; Harhay, M.O.; et al. Cytokine elevation in severe and critical COVID-19: A rapid systematic review, meta-analysis, and comparison with other inflammatory syndromes. Lancet Respir. Med. 2020, 8, 1233–1244. [Google Scholar] [CrossRef] [PubMed]
  47. Stolarski, A.E.; Kim, J.; Zhang, Q.; Remick, D.G. Cytokine Drizzle-The Rationale for Abandoning “Cytokine Storm”. Shock 2021, 56, 667–672. [Google Scholar] [CrossRef] [PubMed]
  48. Wilson, J.G.; Simpson, L.J.; Ferreira, A.M.; Rustagi, A.; Roque, J.; Asuni, A.; Ranganath, T.; Grant, P.M.; Subramanian, A.; Rosenberg-Hasson, Y.; et al. Cytokine profile in plasma of severe COVID-19 does not differ from ARDS and sepsis. JCI Insight 2020, 5, e140289. [Google Scholar] [CrossRef]
  49. Dufour, J.H.; Dziejman, M.; Liu, M.T.; Leung, J.H.; Lane, T.E.; Luster, A.D. IFN-gamma-inducible protein 10 (IP-10; CXCL10)-deficient mice reveal a role for IP-10 in effector T cell generation and trafficking. J. Immunol. 2002, 168, 3195–3204. [Google Scholar] [CrossRef] [Green Version]
  50. Punyadeera, C.; Schneider, E.M.; Schaffer, D.; Hsu, H.Y.; Joos, T.O.; Kriebel, F.; Weiss, M.; Verhaegh, W.F. A biomarker panel to discriminate between systemic inflammatory response syndrome and sepsis and sepsis severity. J. Emerg. Trauma Shock 2010, 3, 26–35. [Google Scholar] [CrossRef] [Green Version]
  51. Liu, Y.; Zhang, C.; Huang, F.; Yang, Y.; Wang, F.; Yuan, J.; Zhang, Z.; Qin, Y.; Li, X.; Zhao, D.; et al. Elevated plasma levels of selective cytokines in COVID-19 patients reflect viral load and lung injury. Natl. Sci. Rev. 2020, 7, 1003–1011. [Google Scholar] [CrossRef] [Green Version]
  52. Tegethoff, S.A.; Danziger, G.; Kuhn, D.; Kimmer, C.; Adams, T.; Heintz, L.; Metz, C.; Reifenrath, K.; Angresius, R.; Mang, S.; et al. TNF-related apoptosis-inducing ligand, interferon gamma-induced protein 10, and C-reactive protein in predicting the progression of SARS-CoV-2 infection: A prospective cohort study. Int. J. Infect. Dis. 2022, 122, 178–187. [Google Scholar] [CrossRef]
  53. Chen, Y.; Wang, J.; Liu, C.; Su, L.; Zhang, D.; Fan, J.; Yang, Y.; Xiao, M.; Xie, J.; Xu, Y.; et al. IP-10 and MCP-1 as biomarkers associated with disease severity of COVID-19. Mol. Med. 2020, 26, 97. [Google Scholar] [CrossRef]
  54. Donlan, A.N.; Sutherland, T.E.; Marie, C.; Preissner, S.; Bradley, B.T.; Carpenter, R.M.; Sturek, J.M.; Ma, J.Z.; Moreau, G.B.; Donowitz, J.R.; et al. IL-13 is a driver of COVID-19 severity. JCI Insight 2021, 6, e150107. [Google Scholar] [CrossRef]
  55. Marone, G.; Granata, F.; Pucino, V.; Pecoraro, A.; Heffler, E.; Loffredo, S.; Scadding, G.W.; Varricchi, G. The Intriguing Role of Interleukin 13 in the Pathophysiology of Asthma. Front. Pharmacol. 2019, 10, 1387. [Google Scholar] [CrossRef] [Green Version]
  56. Loftus, T.J.; Ungaro, R.; Dirain, M.; Efron, P.A.; Mazer, M.B.; Remy, K.E.; Hotchkiss, R.S.; Zhong, L.; Bacher, R.; Starostik, P.; et al. Overlapping but Disparate Inflammatory and Immunosuppressive Responses to SARS-CoV-2 and Bacterial Sepsis: An Immunological Time Course Analysis. Front. Immunol. 2021, 12, 792448. [Google Scholar] [CrossRef]
  57. Maharaj, S.; Chang, S. Anti-PF4/heparin antibodies are increased in hospitalized patients with bacterial sepsis. Thromb. Res. 2018, 171, 111–113. [Google Scholar] [CrossRef]
  58. Comer, S.P.; Cullivan, S.; Szklanna, P.B.; Weiss, L.; Cullen, S.; Kelliher, S.; Smolenski, A.; Murphy, C.; Altaie, H.; Curran, J.; et al. COVID-19 induces a hyperactive phenotype in circulating platelets. PLoS Biol. 2021, 19, e3001109. [Google Scholar] [CrossRef]
  59. Wegrzyn, G.; Walborn, A.; Rondina, M.; Fareed, J.; Hoppensteadt, D. Biomarkers of Platelet Activation and Their Prognostic Value in Patients with Sepsis-Associated Disseminated Intravascular Coagulopathy. Clin. Appl. Thromb. Hemost. 2021, 27, 1076029620943300. [Google Scholar] [CrossRef]
  60. Traby, L.; Kollars, M.; Kussmann, M.; Karer, M.; Sinkovec, H.; Lobmeyr, E.; Hermann, A.; Staudinger, T.; Schellongowski, P.; Rossler, B.; et al. Extracellular Vesicles and Citrullinated Histone H3 in Coronavirus Disease 2019 Patients. Thromb. Haemost. 2022, 122, 113–122. [Google Scholar] [CrossRef]
  61. Bouck, E.G.; Denorme, F.; Holle, L.A.; Middelton, E.A.; Blair, A.M.; de Laat, B.; Schiffman, J.D.; Yost, C.C.; Rondina, M.T.; Wolberg, A.S.; et al. COVID-19 and Sepsis Are Associated With Different Abnormalities in Plasma Procoagulant and Fibrinolytic Activity. Arterioscler. Thromb. Vasc. Biol. 2021, 41, 401–414. [Google Scholar] [CrossRef]
  62. Leppkes, M.; Knopf, J.; Naschberger, E.; Lindemann, A.; Singh, J.; Herrmann, I.; Sturzl, M.; Staats, L.; Mahajan, A.; Schauer, C.; et al. Vascular occlusion by neutrophil extracellular traps in COVID-19. EBioMedicine 2020, 58, 102925. [Google Scholar] [CrossRef]
  63. Ng, H.; Havervall, S.; Rosell, A.; Aguilera, K.; Parv, K.; von Meijenfeldt, F.A.; Lisman, T.; Mackman, N.; Thalin, C.; Phillipson, M. Circulating Markers of Neutrophil Extracellular Traps Are of Prognostic Value in Patients With COVID-19. Arterioscler. Thromb. Vasc. Biol. 2021, 41, 988–994. [Google Scholar] [CrossRef]
  64. Yokoyama, Y.; Ito, T.; Yasuda, T.; Furubeppu, H.; Kamikokuryo, C.; Yamada, S.; Maruyama, I.; Kakihana, Y. Circulating histone H3 levels in septic patients are associated with coagulopathy, multiple organ failure, and death: A single-center observational study. Thromb. J. 2019, 17, 1. [Google Scholar] [CrossRef]
  65. Maruchi, Y.; Tsuda, M.; Mori, H.; Takenaka, N.; Gocho, T.; Huq, M.A.; Takeyama, N. Plasma myeloperoxidase-conjugated DNA level predicts outcomes and organ dysfunction in patients with septic shock. Crit. Care 2018, 22, 176. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. Reid, V.L.; Webster, N.R. Role of microparticles in sepsis. Br. J. Anaesth. 2012, 109, 503–513. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  67. Dix, C.; Zeller, J.; Stevens, H.; Eisenhardt, S.U.; Shing, K.; Nero, T.L.; Morton, C.J.; Parker, M.W.; Peter, K.; McFadyen, J.D. C-reactive protein, immunothrombosis and venous thromboembolism. Front. Immunol. 2022, 13, 1002652. [Google Scholar] [CrossRef] [PubMed]
Diagnostics 13 01069 g001 550
Figure 1. Levels of coagulation- and complement-related parameters in sepsis patients (Sepsis − COVID-19), sepsis patients diagnosed with COVID-19 (Sepsis + COVID-19), and healthy controls. The x represents the median of the measurements. (PF4, platelet factor 4; cit H3, citrullinated histone H3; HMGB-1, high mobility group box-1 protein; EVs, extracellular vesicles; CRP, C-reactive protein; C5b-9, terminal complement complex).
Figure 1. Levels of coagulation- and complement-related parameters in sepsis patients (Sepsis − COVID-19), sepsis patients diagnosed with COVID-19 (Sepsis + COVID-19), and healthy controls. The x represents the median of the measurements. (PF4, platelet factor 4; cit H3, citrullinated histone H3; HMGB-1, high mobility group box-1 protein; EVs, extracellular vesicles; CRP, C-reactive protein; C5b-9, terminal complement complex).
Diagnostics 13 01069 g001
Diagnostics 13 01069 g002 550
Figure 2. Profiles of cytokines, chemokines, and growth factors in sepsis patients without (Sepsis − COVID-19) and with COVID-19 (Sepsis + COVID-19), and healthy controls. The x represents the median of the measurements.
Figure 2. Profiles of cytokines, chemokines, and growth factors in sepsis patients without (Sepsis − COVID-19) and with COVID-19 (Sepsis + COVID-19), and healthy controls. The x represents the median of the measurements.
Diagnostics 13 01069 g002
Table
Table 1. Patient characteristics at baseline.
Table 1. Patient characteristics at baseline.
CharacteristicsControls
(n = 25)		Sepsis − COVID-19
(n = 64)		Sepsis + COVID-19
(n = 14)
Age, years34.9 ± 11.7 63.6 ± 18.768.8 ± 17.3
Male10 (40%)41 (64%)11 (79%)
Female15 (60%)23 (36%)3 (21%)
ICU admissionn.a.14 (22%)5 (36%)
Mortalityn.a.7 (11%)6 (43%)
Positive blood culturen.a.8 (13%)1 (7%)
CRP [mg/dL]n.a.9.78 (6.31; 12.08)11.31 (5.67; 15.11)
PCT [µg/L]n.a.0.54 (0.31; 3.18)0.56 (0.16; 1.14)
Red blood cells [× 1012/L]n.a.3.42 (3.16; 3.57)3.45 (3.11; 3.97)
White blood cells [× 109/L]n.a.9.05 (7.55; 11.2)8.35 (6.15; 13.65)
Monocytes [× 109/L]n.a.0.69 (0.48; 0.83)0.38 (0.22; 0.64)
Neutrophils [× 109/L]n.a.9.4 (4.85; 11)9.85 (4.85; 13.6)
Lymphocytes [× 109/L]n.a.1.03 (0.69; 1.16)0.98 (0.36; 1.62)
Neutrophil-to-lymphocyte ratio (NLR)n.a.7.16 (5.53; 11.25)16.32 (1.74; 36.36)
Platelets [× 109/L]257 (222; 303) a 212 (166; 232)170 (132; 274)
Comorbidities, n (%)
Infectious/parasitic diseasesn.a.19 (30)4 (29)
Neoplasmsn.a.4 (6)5 (36)
Blood/blood forming organ diseasesn.a.9 (14)3 (21)
Immune system diseasesn.a.3 (5)0 (0)
Endocrine/nutritional/metabolic diseasesn.a.24 (38)6 (43)
Mental/behavioral/neurodevelopmental disordersn.a.9 (14)2 (14)
Nervous system diseases n.a.3 (5)4 (29)
Visual system diseasesn.a.1 (2)1 (7)
Circulatory system diseasesn.a.34 (53)10 (71)
Respiratory system diseasesn.a.25 (39)13 (93)
Digestive system diseasesn.a.11 (17)5 (36)
Skin diseasesn.a.4 (6)1 (7)
Musculoskeletal/connective tissue diseasesn.a.5 (8)0 (0)
Genitourinary system diseasesn.a.29 (45)6 (43)
Other symptoms, signs, or clinical findingsn.a.4 (6)6 (43)
Injury/poisoning/consequences of external causesn.a.5 (8)1 (7)
Factors influencing health status/contact with health servicesn.a.10 (16)2 (14)
Data are represented as mean ± standard deviation and counts (percentage). Laboratory parameters are reported as median (lower; upper confidence interval). a n = 10; n.a., not applicable; ICU, intensive care unit; CRP, C-reactive protein; PCT, procalcitonin.
Table
Table 2. Mediator profiles for controls, sepsis patients, and sepsis patients diagnosed with COVID-19.
Table 2. Mediator profiles for controls, sepsis patients, and sepsis patients diagnosed with COVID-19.
Parameter Controls
(n = 25)		Sepsis − COVID-19
(n = 64)		Sepsis + COVID-19
(n = 14)
PF4[ng/mL]558 (394; 587)820 (688; 1330)1260 (544; 2657)
D-dimer[ng/mL]227 (189; 253)471 (380; 617)378 (278; 485)
nucleosomes[AU]0.01 (0.01; 0.02)0.09 (0.05; 0.11)0.11 (0.04; 0.15)
cit H3[ng/mL]1 (0.78; 1.32)2.14 (1.62; 3.06)2.27 (1.32; 3.04)
HMGB-1[ng/mL]1.01 (0.35; 1.25)3.22 (2.63; 5.69)7.16 (3.74; 8.01)
C5b-9[µg/mL]0.68 (0.63; 0.76)1.36 (1.2; 1.44)1.52 (1.29; 1.74)
EVs [counts/µL]53,500 (45,000; 66,000)132,250 (100,250; 188,500)311,000 (151,000; 630,000)
CD41+ EVs[counts/µL]9000 (5940; 10,440)28,945 (23,090; 57,195)73,085 (39,790; 198,860)
CD41+ EVs[% of total EVs]15 (11; 18)27 (18; 34)31 (23; 35.5)
CRP+ EVs[counts/µL]2000 (1500; 4000)71,660 (52,500; 88,500)106750 (85,000; 263,500)
CRP+ EVs[% of total EVs]4 (2; 4)55 (46; 61)62 (40; 67.5)
IL-1β[pg/mL]0.92 (0.72; 1.32)1.88 (1.28; 1.88)2.16 (0.96; 2.84)
IL-1ra[pg/mL]251 (164; 379)1010 (431; 1353)1495 (866; 2805)
IL-2[pg/mL]1.7 (n.a.; n.a.)1.93 (1.7; 2.16)1.7 (1.7; 1.73)
IL-4[pg/mL]3.36 (2.6; 3.56)3.02 (2.56; 3.58)3.18 (2.08; 3.84)
IL-5[pg/mL]5.34 (n.a.; n.a.)5.34 (n.a.; n.a.)5.34 (n.a.; n.a.)
IL-6[pg/mL]0.42 (n.a.; n.a.)28.6 (20.12; 50.04)34.34 (12.32; 115)
IL-7[pg/mL]2.6 (n.a.; n.a.)10.86 (5.36; 12.64)12.64 (2.6; 17.68)
IL-8[pg/mL]2.76 (1.56; 4.64)15.44 (13.56; 21.84)15 (7.68; 22.3)
IL-9[pg/mL]557 (493; 591)383 (353; 402)402 (303; 440)
IL-10[pg/mL]0.81 (n.a.; n.a.)2.84 (1.84; 3.48)4.28 (0.81; 9.12)
IL-12[pg/mL]1.87 (n.a.; n.a.)1.87 (n.a.; n.a.)1.87 (1.83; 2.96)
IL-13[pg/mL]0.96 (0.44; 1.2)2.08 (1.32; 2.56)3.72 (2.76; 4.26)
IL-15[pg/mL]18.02 (n.a.; n.a.)18.02 (n.a.; n.a.)18.02 (n.a.; n.a.)
IL-17[pg/mL]11.24 (7.32; 11.48)2.67 (n.a.; n.a.)2.67 (2.67; 2.67)
IFN-γ[pg/mL]4.8 (3.48; 6.04)5.28 (3.84; 5.62)6.48 (5.58; 8.34)
TNF-α[pg/mL]32.72 (30.56; 34.84)82.92 (74.44; 93.96)52.38 (48.24; 85.52)
eotaxin[pg/mL]42.12 (30.32; 49.12)44.48 (36; 53.92)56.58 (45.76; 61.08)
IP-10[pg/mL]297 (202; 354)846 (614; 1400)5806 (2593; 8493)
MCP-1[pg/mL]23.2 (16.4; 25.52)34.22 (24.12; 44.64)98.24 (41.52; 184)
MIP-1α[pg/mL]1.28 (1.01; 1.28)5.42 (4.24; 6.6)3.2 (2.08; 7.42)
MIP-1β[pg/mL]248 (233; 271)207 (188; 220)212 (177; 251)
RANTES[pg/mL]7742 (4249; 9806)3940 (2989; 5182)5319 (2357; 8911)
FGF[pg/mL]21.2 (15.4; 22.04)26.24 (16.16; 27.12)30.66 (26.48; 33.28)
G-CSF[pg/mL]45.68 (31.6; 57.56)174 (148; 237)213 (90; 340)
GM-CSF[pg/mL]0.44 (n.a.; n.a.)0.44 (n.a.; n.a.)0.44 (n.a.; n.a.)
PDGF-bb[pg/mL]258 (164; 330)343 (222; 461)573 (329; 996)
VEGF[pg/mL]4.22 (n.a.; n.a.)4.22 (n.a.; n.a.)4.22 (n.a.; n.a.)
Data are represented as median (lower; upper confidence interval). n.a., not applicable as confidence intervals could not be calculated due to low variations.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Eichhorn, T.; Huber, S.; Weiss, R.; Ebeyer-Masotta, M.; Lauková, L.; Emprechtinger, R.; Bellmann-Weiler, R.; Lorenz, I.; Martini, J.; Pirklbauer, M.; et al. Infection with SARS-CoV-2 Is Associated with Elevated Levels of IP-10, MCP-1, and IL-13 in Sepsis Patients. Diagnostics 2023, 13, 1069. https://doi.org/10.3390/diagnostics13061069

AMA Style

Eichhorn T, Huber S, Weiss R, Ebeyer-Masotta M, Lauková L, Emprechtinger R, Bellmann-Weiler R, Lorenz I, Martini J, Pirklbauer M, et al. Infection with SARS-CoV-2 Is Associated with Elevated Levels of IP-10, MCP-1, and IL-13 in Sepsis Patients. Diagnostics. 2023; 13(6):1069. https://doi.org/10.3390/diagnostics13061069

Chicago/Turabian Style

Eichhorn, Tanja, Silke Huber, René Weiss, Marie Ebeyer-Masotta, Lucia Lauková, Robert Emprechtinger, Rosa Bellmann-Weiler, Ingo Lorenz, Judith Martini, Markus Pirklbauer, and et al. 2023. "Infection with SARS-CoV-2 Is Associated with Elevated Levels of IP-10, MCP-1, and IL-13 in Sepsis Patients" Diagnostics 13, no. 6: 1069. https://doi.org/10.3390/diagnostics13061069

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop