key: cord-0722309-hpjhalle
authors: deKay, Joanne T.; Emery, Ivette F.; Rud, Jonathan; Eldridge, Ashley; Lord, Christine; Gagnon, David J.; May, Teresa L.; Herrera, Victoria L. M.; Ruiz-Opazo, Nelson; Riker, Richard R.; Sawyer, Douglas B.; Ryzhov, Sergey; Seder, David B.
title: DEspR(high) neutrophils are associated with critical illness in COVID-19
date: 2021-11-17
journal: Sci Rep
DOI: 10.1038/s41598-021-01943-7
sha: 512ec15cbbc9fa8d5c20227fa991d105fa1f1fd9
doc_id: 722309
cord_uid: hpjhalle

SARS-CoV-2 infection results in a spectrum of outcomes from no symptoms to widely varying degrees of illness to death. A better understanding of the immune response to SARS-CoV-2 infection and subsequent, often excessive, inflammation may inform treatment decisions and reveal opportunities for therapy. We studied immune cell subpopulations and their associations with clinical parameters in a cohort of 26 patients with COVID-19. Following informed consent, we collected blood samples from hospitalized patients with COVID-19 within 72 h of admission. Flow cytometry was used to analyze white blood cell subpopulations. Plasma levels of cytokines and chemokines were measured using ELISA. Neutrophils undergoing neutrophil extracellular traps (NET) formation were evaluated in blood smears. We examined the immunophenotype of patients with COVID-19 in comparison to that of SARS-CoV-2 negative controls. A novel subset of pro-inflammatory neutrophils expressing a high level of dual endothelin-1 and VEGF signal peptide-activated receptor (DEspR) at the cell surface was found to be associated with elevated circulating CCL23, increased NETosis, and critical-severity COVID-19 illness. The potential to target this subpopulation of neutrophils to reduce secondary tissue damage caused by SARS-CoV-2 infection warrants further investigation.

www.nature.com/scientificreports/ endogenous ligand that binds DEspR within the range of low nanomolar concentrations 20 . Both endothelin-1 and Ca 2+ intracellular signaling play an important role in activating innate immunity 21, 22 . However, the role of DEspR in the regulation of myeloid cells, and specifically in neutrophils, has not been described.

The goals of this study were to characterize the expression of DEspR in subpopulations of immune cells in patients with COVID-19 and healthy donors and to determine the associations between the number of immune cells expressing a high level of DEspR (DEspR high ), inflammatory factors, and the severity and clinical features of COVID-19.

Study subjects. A convenience sample of 26 patients with COVID-19 and 12 control samples were analyzed. Among our COVID-19 study group, 6 patients (23%) were characterized by mild illness, 9 subjects (35%) had a severe illness, and 11 subjects (42%) were classified with a critical illness.

There were no differences in age or sex between study subjects and controls. A comparison of the demographics and clinical characteristics of COVID-19 and control subjects is provided in Table 1 .

To determine the cell surface expression of DEspR on circulating immune cells, we used flow cytometric analysis. Gates for cells expressing a high level of DEspR within major subpopulations of SSC high neutrophils, SSC intermediate monocytes, and SSC low lymphocytes were set up using isotype IgG's as shown in Fig. 1A . The majority of cells with a high level of DEspR at their surface are characterized by high intracellular granularity (SSC high ), which allowed us to identify these cells as neutrophils. These cells were found in both healthy subjects and COVID-19 patients. However, the number of DEspR high neutrophils was increased in COVID-19 patients compared to controls (Fig. 1B) . The analysis also revealed the accumulation of DEspR high cells in the blood of critically ill COVID-19 patients (Fig. 1C ).

DEspR high neutrophils express CD10 and elevated levels of CD14. To better characterize the antigenic phenotype of cells with high expression of DEspR, we performed the analysis of markers associated with neutrophils maturation and activation, CD10 and CD16, in the subpopulation of total neutrophils and subset of DEspR high neutrophils. High level expression of CD16 was found on the surface of more than ninety percent of cells in the total subpopulation of SSC high neutrophils in both control subjects and patients with COVID-19 ( Fig. 2A) . The majority of neutrophils from the control subjects were also characterized by the expression of CD10, whereas neutrophils from patients with COVID-19 did not express CD10, a marker associated with neutrophils maturation 23 , on their surfaces (Fig. 2B) .

We also determined the percentage of CD16 and CD10 positive cells in the subset of DEspR high neutrophils. Similar to the subpopulation of total neutrophils, the majority of DEspR high neutrophils expressed CD16 (Fig. 2C) .

Although not statistically significant, this subset of DEspR high neutrophils demonstrated a trend toward a higher percentage of CD10 expressing cells compared to total neutrophils in control subjects (Fig. 2D ). The high percentage of neutrophils that express CD10 within the subset of DEspR high neutrophils indicated their more mature state compared to total neutrophils in COVID-19 patients. There was a difference in the maturation state of DEspR high neutrophils between control and COVID-19 subjects. A trend toward a lower percentage of CD10 positive neutrophils and a significantly higher percentage of CD10 negative neutrophils were found in the subset of DEspR high neutrophils in patients with COVID-19 compared to control subjects (Fig. 2E ). www.nature.com/scientificreports/ CD14 is associated with pro-inflammatory activation of neutrophils 24, 25 . DEspR high neutrophils were characterized by significantly higher expression of CD14 compared to total neutrophils in both groups of study subjects (Fig. 2F ). No differences were found in the level of CD14 on the surface of total and DEspR high neutrophils between control and COVID-19. There was no difference in the cell surface expression of CD16 between total and DEspR high neutrophils or neutrophils in the groups of control subjects and patients with COVID-19 (Fig. 2G ).

Lack of association between the number of DEspR high neutrophils and lymphocyte count in COVID-19. Our data demonstrate that the neutrophil-to-lymphocyte ratio (NLR) is significantly increased in patients with COVID-19 compared to control (Fig. 3A) . We also found a positive correlation between the number of DEspR high neutrophils and NLR in COVID-19 (Fig. 3B ). Because neutrophils possess immunosuppressive properties 26 , we separately examined the potential relationship between both DEspR high neutrophils and lymphocytes in the circulation.

The number of CD3 lymphocytes and major subsets of CD4 and CD8 T cells were significantly decreased in COVID-19 compared to control subjects, indicating enhanced systemic immunosuppression ( Fig. 3C-E) . However, no associations were found between the number of DEspR high neutrophils and the total number of T cells and CD4 lymphocytes (Fig. 3F ,G). Although not statistically significant, a trend toward a weak positive association was found between DEspR high neutrophils and CD8 T cells in patients with COVID-19 (Fig. 3H ).

Circulating CCL23 is increased in COVID-19. In parallel with the flow cytometric analysis of DEspR high neutrophils, we determined the level of cytokines and chemokines that contribute to the activation and recruitment of neutrophils. As shown in Fig. 4 , the level of CCL23 was significantly increased in patients with COVID-19 compared to control subjects. No differences were found between the two groups in the levels of IL-6, IL-8, CXCL2, CCL2, or CCL4.

DEspR high neutrophils are associated with increased CCL23. To determine the potential relationship between DEspR high neutrophils and other measured parameters in relation to disease severity, a hierarchical clustering analysis in a group of patients with COVID-19 was performed. As shown in Fig. 5A , the majority of lymphocyte subpopulations, CCL2, and CCL4, were clustered with mild illness. As expected, DespR high neutrophils were clustered within the group of critically ill patients with COVID-19. In addition, we found that CCL23 is also associated with a critical illness (Fig. 5B) , and that CCL23 is significantly increased in non-survivors (Fig. 5C) .

A positive correlation was found between the number of DEspR high neutrophils, but not the total number of neutrophils, and the level of CCL23 (Fig. 5D,E) , indicating there may be a direct relationship between these two factors in the development of critical COVID-19. In addition, our analysis revealed positive correlations between the number of NETosing neutrophils and the number of both DEspR high and the total subpopulation of neutrophils (Fig. 5F ,G). 

This study demonstrates the presence of a newly defined subset of neutrophils characterized by high cell surface expression of DEspR in human blood. The number of these DEspR high neutrophils is increased in patients with COVID-19 and correlates with disease severity. Elevated expression of CD10 and CD14, markers of maturation and activation, may indicate the high pro-inflammatory potential of these neutrophils. An association was seen between the number of DEspR high neutrophils, NETosing neutrophils, the blood plasma level of CCL23, and critical illness in COVID-19. Accumulating evidence suggests that neutrophils are major players in the development of hyperinflammation associated with poor outcomes in patients with SARS-CoV-2 infection 27 . Neutrophils may contribute to disease progression via several mechanisms, including immunosuppression 28 , production of pro-inflammatory factors 29 , and activation of coagulation and thrombosis 30 . Recently it has been recognized that circulating neutrophils are a heterogeneous population of cells 31 . A subset of mature CD10-expressing neutrophils is characterized by the ability to suppress T lymphocytes 23 , which may contribute to systemic immunosuppression and prevent effective viral clearance 32 . It has also been shown that decreased lymphocyte count is associated with severe and critical conditions in COVID-19 33, 34 . Clustering analysis of data generated in our study demonstrated an association between immunosuppressive factors such as soluble CD73 35 , CD10 positive neutrophils 23 and IL-8 36 , and severe COVID-19. We also found that DEspR high neutrophils are characterized by the high expression of CD10. Our Mann-Whitney test. (F,G) Expression of (F) CD14 and (G) CD16 on total and DEspR high neutrophils in control and COVID-19 subjects. The expression is represented by the mean fluorescence intensity that corresponds to the level of cell surface CD14 and CD16. ΔMFI was calculated by subtracting the mean fluorescence intensity of isotype controls from the mean fluorescent intensity of specific antibodies. Two-way ANOVA with Tukey multiple comparisons test; P values are indicated. www.nature.com/scientificreports/ analysis revealed a positive correlation between DEspR high neutrophils and NLR and a significantly decreased number of lymphocytes in patients with COVID-19. In addition, we found differential clustering of DEspR high neutrophils to the group of critically ill patients compared to lymphocyte clustering in the group of patients with mild COVID-19 disease, pointing toward potential immunosuppressive properties of neutrophils expressing a high level of DEspR. No correlations, however, were found between DEspR high neutrophils and different subsets of circulating CD3 lymphocytes in the current study. Thus, our data indicate that DEspR high neutrophils are unlikely to be involved in the regulation of systemic lymphocyte trafficking or suppression. Further studies are warranted to determine the direct effect of DEspR high neutrophils on lymphocyte activation locally in inflamed tissue. While the majority of DEspR high neutrophils express CD10 in both study groups, the percent of CD10 negative neutrophils within the DEspR high subset is higher in patients with COVID-19 compared to control, reflecting the increased mobilization of immature neutrophils from the bone marrow in COVID-19. This also indicates that the upregulation of DEspR expression on neutrophils is not dependent on their maturation and is initiated www.nature.com/scientificreports/ in the peripheral circulation. This should result in their accumulation in the blood, however, the overall percent of DEspR high neutrophils is low. One possible explanation is related to the egress of DEspR high neutrophils out of the bloodstream due to their migration into tissues. It has been shown previously that endothelin-1, a DEspR ligand, enhances the adhesion of neutrophils to endothelial cells [37] [38] [39] and promotes the recruitment of neutrophils into inflamed tissue [40] [41] [42] .

Another important observation from this study is related to the high expression of CD14 on DEspR high neutrophils. CD14 is a coreceptor for toll-like receptors 43, 44 . Upon pro-inflammatory activation, the cell surface expression of CD14 is increased 45 and promotes synthesis and secretion of pro-inflammatory factors, such as tumor necrosis factor-alpha 46 . CD14 is involved in the activation of both monocytes and neutrophils in vasculitis 47, 48 , one of the common cardiovascular complications in COVID-19 49 . While high expression of CD14 is associated with activation of neutrophils, our data demonstrate that DEspR high neutrophils also express a high level of CD16 comparable to the level of expression found on most neutrophils in the blood. A high level of CD16 expression is usually found on resting, non-activated neutrophils 50 . Apoptotic neutrophils, subsets of immature or activated neutrophils, are characterized by a significant reduction in the cell surface expression of CD16 50 . The high levels of CD14 expression on DEspR high neutrophils may indicate their enhanced pro-inflammatory potential compared to the overall neutrophil population.

Chemokines are critical factors in the recruitment of immune cells to the area of inflammation 51 . Our study demonstrated elevated levels of circulating CCL23 in patients with COVID-19. CCL23 is a potent chemoattractant for the peripheral blood mononuclear cells, including monocytes, dendritic cells, and resting lymphocytes 52, 53 . Both monocytes and neutrophils produce CCL23 in response to a variety of toll-like receptor ligands 54 . However, in contrast to the majority of cytokines and chemokines secreted at a significantly higher level from monocytes, www.nature.com/scientificreports/ neutrophils produce high levels of CCL23. Furthermore, toll-like receptor ligands induce early neutrophils response compared to delayed upregulation and secretion of CCL23 in monocytes 54 . Neutrophils may represent a major source of CCL23 considering the significant increase in the number of neutrophils during the systemic inflammatory response. The expression of CCL23 by brain tissue-infiltrating neutrophils after a stroke has been reported 55 . Our analysis revealed a positive correlation between the number of DEspR high neutrophils, but not total neutrophils, and the level of circulating CCL23 in patients with COVID-19. Both DEspR high neutrophils and CCL23 were significantly increased in critically ill patients with COVID-19. Given a high expression of CD14 that promotes toll-like receptor signaling, it is plausible that DEspR high neutrophils produce CCL23 to further promote inflammation. This is supported by our data showing that a high level of CCL23 is associated with poor outcomes in patients with COVID-19. However, further studies are required to determine the potential role of DEspR high neutrophils in CCL23 secretion. Neutrophil extracellular traps (NET) propagate inflammation and microvascular thrombosis in patients with COVID-19 56 . Our data reveal a positive correlation between the number of DEspR high neutrophils and NETosing neutrophils in the peripheral circulation of patients with COVID-19, indicating potential involvement of DEspR in the regulation of NET. NETosing neutrophils may induce the secretion of endothelin-1 from endothelial cells 57 , suggesting the presence of an amplification loop that may further promote both NETosis and inflammatory activation of endothelial cells via mechanisms involving the generation of DEspR high neutrophils.

This study included a broad population of patients with COVID-19, and the sample size of subgroups was small, so important variability of individuals within the categories of mild, moderate, and severe disease may either be lost or exaggerated. Most patients were receiving corticosteroids, which may modulate the cellular immune response and could affect the behavior or activation status of lymphocytes and neutrophils; the effect on DEspR expression in vivo is unknown. Critically ill patients also received sedatives, analgesics, and sometimes neuromuscular blocking agents, all of which may affect the inflammatory response 58, 59 . Because the study was conducted over 5 months of intensive COVID-19 research and evolving clinical standards, care of early and later patients may have varied somewhat, potentially affecting the immunoinflammatory response. Nonetheless, this study is among the first to characterize a newly identified subset of DEspR high neutrophils in COVID-19, and ultimately its inclusion of healthy controls and patients with the full spectrum of severity of COVID-19 is a strength. Furthermore, the population studied reflects a "real-world" cohort with corresponding complexity and variability, making the strength of our findings even more relevant and clinically important.

In summary, the systemic inflammatory response in patients with COVID-19 is associated with an accumulation of neutrophils expressing a high level of DEspR at the cell surface. Antigenic immunophenotype identifies DEspR high neutrophils as mature neutrophils with high pro-inflammatory properties. A high number of circulating DEspR high neutrophils is associated with an increased level of CCL23 and NETosing neutrophils in critically ill COVID-19 patients, identifying DEspR high neutrophils as an intermediate biomarker to track in clinical trials of therapies for COVID-19 and a new potential therapeutic target for the prevention of immune cell-driven hyperinflammation.

Patients. The study and our informed consent process were approved by the Maine Medical Center Institutional Review Board. Informed consent was obtained from the patient or their legally authorized representative (LAR) using a secure electronic consent form (to prevent disease transmission), either in-person (with the patient) or by telephone (with the LAR). All methods were performed in accordance with the relevant guidelines and regulations. A convenience sample included hospitalized patients that provided informed consent between July and December 2020 within 72 h of being hospitalized with PCR-confirmed SARS-CoV-2 infection (realtime RT-PCR test, NorDx Laboratories, Portland, ME). We excluded patients under 18 years of age, those representing a vulnerable population, and those with hemoglobin < 8 g/dL.

The severity of COVID-19 disease was defined using the following criteria from the US Center for Disease Control (CDC) 60 , (1) mild illness individuals who have any signs and symptoms of COVID-19 (e.g., fever, cough, sore throat, malaise, headache, muscle pain) without shortness of breath, dyspnea, or abnormal chest imaging, (2) severe illness individuals who have respiratory frequency > 30 breaths per minute, SpO2 < 94% on room air at sea level (or, for patients with chronic hypoxemia, a decrease from baseline of > 3%), a ratio of arterial partial pressure of oxygen to fraction of inspired oxygen (PaO2/FiO2) < 300 mmHg, or lung infiltrates > 50%, and (3) critical illness individuals who have respiratory failure, septic shock, and/or multiple organ dysfunction.

Blood samples were additionally obtained from asymptomatic and SARS-CoV-2 negative subjects to serve as a control population. Pertinent demographic and clinical data were collected from the electronic medical record for all study participants.

Patients received an evolving standard of care during their hospitalization. This included the antiviral drug remdesivir 61 and the synthetic adrenocortical glucocorticoid dexamethasone 62 ; many also received systemic anticoagulation 63 , and antibiotics for community-acquired pneumonia 64 until it was determined they did not have a concurrent bacterial infection. Our cohort included a few patients who were asymptomatic but determined to have a SARS-CoV-2 infection on administrative testing, although most had a severe or critical disease. Mechanically ventilated patients received lung-protective ventilation according to international clinical practice guidelines 65 , proning for refractory hypoxemia 66 , and standard evidence-based critical care therapies (e.g., neuromuscular blocking agents, sedation, and analgesia) 67 . Patients may also have received renal replacement therapy (i.e., intermittent hemodialysis or continuous veno-venous hemofiltration) or underwent venovenous extracorporeal membrane oxygenation, as indicated. www.nature.com/scientificreports/ Blood sample collection. Subjects underwent phlebotomy on the day of enrollment. Venous blood (8.5 mL) was collected from COVID-19 and control subjects using BD Vacutainer ACD tubes. Blood aliquots (50 μL) for flow cytometric analysis underwent erythrocyte lysis with ammonium chloride lysing solution (150 mmol/L NH 4 Cl, 10 mmol/L NaHCO 3 , and 1 mmol/L EDTA, pH 7.4). Blood smears were prepared and fixed in cold 100% methanol; slides were stored at − 20 °C until shipment on dry ice for third-party NETosis analysis. Platelet-free plasma (PFP) was prepared at room temperature using 2-step centrifugation, each at 2000×g for 20 min. After processing, plasma was stored at − 80 °C until further analysis. No more than one freeze/thaw cycle was allowed for PFP samples to prevent protein degradation.

Flow cytometric analysis. After red blood cell lysis, white blood cells (WBC, 10 6 cells/mL) were treated with whole molecule mouse and human IgGs to prevent nonspecific binding, followed by incubation with relevant antibodies for 25 min at 4 °C. Cells were washed once with ten volumes of cold PBS/0.5% BSA/2 mM EDTA before data acquisition.

Subpopulations of WBC were analyzed using the following antibodies: CD3 (UCHT1), CD4 (OKT4), CD8a (HIT8a), CD10 (HI10a), CD14 (HCD14), CD16 (3G8), CD26 (BA5b), CD38 (HIT2), CD45 (HI30), CD73 (AD2), HLA-DR (LN2430) (all purchased from BioLegend). Human anti-human/mouse DEspR antibody (NCTX-01) was provided by NControl Therapeutics (Medfield, MA). Human IgG4-S228P isotype control was obtained from Syd Labs (Southborough, MA). Both anti-DEspR and isotype IgGs were conjugated with Alexa Fluor 647 using Molecular Probes ® Alexa Fluor ® Antibody Labeling Kits (ThermoFisher Scientific). Subpopulations of cells were defined as follows: side scatter (SSC) high /CD16 high /CD14 low/− /HLA-DR negative neutrophils, SSC intermediate / CD14 high /HLA-DR positive monocytes, SSC low /CD14 negative lymphocytes. Subsets of CD4 and CD8 T cells coexpressing CD73 and CD26 were determined within the subpopulation of CD3 positive cells.

The total number of WBC was determined using TruCount™ Tubes (BD Biosciences). Viable and non-viable cells were distinguished using 4′,6-diamidino-2-phenylindole (DAPI) to detect dead nucleated cells. Data acquisition was performed on a MacsQuant Analyzer 10 (Miltenyi Biotec, Inc), and the data were analyzed using 

performed as a contract research service at Nikon Imaging Laboratory (Cambridge, MA) as follows. Slides were imaged with a Nikon Ti2-E Widefield microscope equipped with a Plan Apo λ 20× objective and Spectra LED light source and controlled by NIS-Elements. An automated JOBS routine in NIS-Elements was used to image 100 evenly spaced positions along with an entire slide. At each position, automatic focus adjustment with the Perfect Focus System (PFS) was followed by sequential imaging with the 395 (Blue), 470 (Green), and 555 (Red) nm LED light to detect DAPI (nuclei), Alexa Fluor 488 (CD11b) and Alexa Fluor 568 (DEspR, hu6g8), respectively. A General Analysis 3 algorithm was used to process image stacks to segment the nuclei, measure circularity, and quantify signal intensity. Generated CSV files were imported to Excel for scoring. Cells were separated into non-NETosing (Circularity > 0.8) and NETosing (Circularity < 0.8) groups. Scoring of CD11b and DEspR expression was based on the mean signal intensities of the respective fluorophore stainings relative to background fluorescence. Boolean operations were used to count the number of cells in each subgroup as graded by the three markers (Yes/No NETosis, +/− CD11b, +/− DEspR). Statistical analysis. Data in this study are expressed as mean value and standard error for normal distribution or as median and interquartile range if the distribution is skewed. Comparisons between two groups were performed using Mann-Whitney tests. Comparisons between more than two groups were performed using Kruskal-Wallis test with Dunn's multiple-comparisons test, or two-way ANOVA with Tukey multiple comparisons test. Correlation analysis was performed using a Spearman (skewed distribution) correlation. ClustVis v2.0 was used to compute hierarchical clustering and heat map on measured clinical and laboratory parameters 68 . P < 0.05 was considered significant.

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We are grateful to David Groft and the NorDx lab, Dr. Anne Breggia, Sue LaPierre, and the MMC BioBank, a Core Facility, for subject recruitment; Divya Guthikonda and Meghan P. Searight for providing logistical support during sample transportation. We would like to thank our research subjects and their families for their contribution to this project and to offer condolences to the families of those that did not survive.

Victoria L. M. Herrera and Nelson Ruiz-Opazo are co-inventors on Boston University patents on DEspR; coscientific founders of NControl Therapeutics, Inc., with the option to license DEspR intellectual property from Boston University. All other co-authors have no competing interests.

Correspondence and requests for materials should be addressed to S.R. or D.B.S.Reprints and permissions information is available at www.nature.com/reprints.Publisher's note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.