Recent studies have provided insights into the pathogenesis of coronavirus disease 2019 (COVID-19)1,2,3,4. However, the longitudinal immunological correlates of disease outcome remain unclear. Here we serially analysed immune responses in 113 patients with moderate or severe COVID-19. Immune profiling revealed an overall increase in innate cell lineages, with a concomitant reduction in T cell number. An early elevation in cytokine levels was associated with worse disease outcomes. Following an early increase in cytokines, patients with moderate COVID-19 displayed a progressive reduction in type 1 (antiviral) and type 3 (antifungal) responses. By contrast, patients with severe COVID-19 maintained these elevated responses throughout the course of the disease. Moreover, severe COVID-19 was accompanied by an increase in multiple type 2 (anti-helminths) effectors, including interleukin-5 (IL-5), IL-13, immunoglobulin E and eosinophils. Unsupervised clustering analysis identified four immune signatures, representing growth factors (A), type-2/3 cytokines (B), mixed type-1/2/3 cytokines (C), and chemokines (D) that correlated with three distinct disease trajectories. The immune profiles of patients who recovered from moderate COVID-19 were enriched in tissue reparative growth factor signature A, whereas the profiles of those with who developed severe disease had elevated levels of all four signatures. Thus, we have identified a maladapted immune response profile associated with severe COVID-19 and poor clinical outcome, as well as early immune signatures that correlate with divergent disease trajectories.
COVID-19 is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a highly infectious virus that exploits angiotensin-converting enzyme 2 (ACE2)5,6 as a cell entry receptor. The clinical presentation of COVID-19 involves a broad range of symptoms and disease trajectories. Understanding the nature of the immune response that leads to recovery over severe disease is key to developing effective treatments for COVID-19. Coronaviruses, including Severe Acute Respiratory Syndrome (SARS-CoV) and Middle Eastern Respiratory Syndrome (MERS), typically induce strong inflammatory responses and associated lymphopenia7,8. Studies of patients with COVID-19 have reported increases in inflammatory monocytes and neutrophils, and a sharp decrease in lymphocytes1,2,3,4, and an inflammatory milieu containing IL-1β, IL-6, and TNF (previously known as TNFα) in severe disease1,2,4,9,10. Despite these analyses, the dynamics of the immune response during the course of SARS-CoV-2 infection and its association with clinical trajectory remain unclear.
Immune responses against pathogens are divided roughly into three types11,12,13. Type 1 immunity, characterized by responses that depend on the transcription factor T-bet (also known as TBX21) and expression of interferon-γ (IFNγ), is generated against intracellular pathogens such as viruses. In type 1 immunity, pathogen clearance is mediated through effector cells including group 1 innate lymphocytes (ILC1), natural killer (NK) cells, cytotoxic T lymphocytes, and T helper 1 (TH1) cells. Type 2 immunity, which relies on the GATA3 transcription factor, mediates defence against helminths through effector molecules such as IL-4, IL-5, IL-13, and IgE that work to expel these pathogens through the concerted action of epithelial cells, mast cells, eosinophils, and basophils. Type 3 immunity, which is orchestrated by the RORγt-induced cytokines IL-17 and IL-22 secreted by ILC3 and TH17 cells, is mounted against fungi and extracellular bacteria to elicit neutrophil-dependent clearance. We have focused on the longitudinal analysis of these three types of immune response in patients with COVID-19 and identified correlations between distinct immune phenotypes and disease course.
Immunological features of COVID-19
One hundred and thirteen patients with COVID-19 who were admitted to Yale New Haven Hospital (YNHH) between 18 March 2020 and 27 May 2020 were recruited to the Yale IMPACT (Implementing Medical and Public Health Action Against Coronavirus CT) study. We assessed viral RNA load (quantified by quantitative PCR with reverse transcription (RT–qPCR) using nasopharyngeal swabs); levels of plasma cytokines and chemokines; and leukocyte profiles (by flow cytometry using freshly isolated peripheral blood mononuclear cells; PBMCs). We performed 253 collections and follow-up measurements on the patient cohort with a range of one to seven longitudinal time-points that occurred 3–51 days after the onset of symptoms. In parallel, we enrolled 108 volunteer healthcare workers (HCWs), whose samples served as healthy controls (SARS-CoV-2-negative by RT–qPCR and serology).
Basic demographic information stratified by disease severity is provided in Extended Data Table 1 and detailed in Supplementary Table 1. Patients who had been admitted to YNHH were stratified into moderate and severe disease groups on the basis of supplemental oxygen requirements and admission to the intensive care unit (ICU) (Fig. 1a). Among our cohort, patients who developed moderate or severe disease did not differ significantly with respect to age or sex. Body mass index (BMI) was generally higher among patients with severe disease, and extremes in BMI correlated with an increased relative risk (RR) of mortality (RR BMI ≥ 35: 1.62 (95% confidence interval (CI) 0.81–3.22)) (Extended Data Table 1, Extended Data Fig. 1a, b). Exposure to select therapeutic regimens of interest was assessed in patients with moderate or severe disease (Extended Data Fig. 1c.) Initial presenting symptoms demonstrated a preponderance of headache (54.55%), fever (64.47%), cough (74.03%), and dyspnoea (67.09%) with no significant difference in symptom presentation between patients with moderate disease and those who developed severe disease. Finally, mortality was significantly higher in patients who were admitted to the ICU than in those who were not (27.27% versus 3.75%; P < 0.001) (Extended Data Table 1).
We analysed PBMC and plasma samples from patients with moderate or severe COVID-19 and healthy HCW donors (Fig. 1a, gating strategy in Extended Data Fig. 9) by flow cytometry and ELISA to quantify leukocytes and soluble mediators, respectively. An unsupervised heat map constructed from the main innate and adaptive circulating immune cell types revealed marked changes in patients with COVID-19 compared to uninfected HCWs (Fig. 1b). As reported1,2,3,4, patients with COVID-19 presented with marked reductions in the number and frequency of both CD4+ and CD8+ T cells, even after normalizing for age as a possible confounder (Extended Data Fig. 1d). Granulocytes, such as neutrophils and eosinophils, are normally excluded from the PBMC fraction following density gradient separation. However, low-density granulocytes are found in the PBMC layer of peripheral blood collected from patients with inflammatory diseases14. In patients with COVID-19, increases in monocytes, low-density neutrophils and eosinophils correlated with the severity of disease (Fig. 2c, Extended Data Fig. 2a, b). In addition, patients showed increased activation of T cells and a reduction in expression of the human leukocyte antigen DR isotype (HLA-DR) by circulating monocytes1 (Extended Data Fig. 2c). A complete overview of PBMC subsets is presented in Extended Data Fig. 2.
To gain insights into key differences in cytokines, chemokines, and additional immune markers between patients with moderate and severe disease, we correlated the measurements of these soluble proteins across all sample collection time-points. (Fig. 1d). We observed a ‘core COVID-19 signature’ that was shared by both moderate and severe disease groups and was defined by the following inflammatory cytokines, which correlated positively with each other: IL-1α, IL-1β, IL-17A, IL-12 p70, and IFNα (Fig. 1d). In patients with severe disease, we observed an additional inflammatory cluster defined by thrombopoietin (TPO), IL-33, IL-16, IL-21, IL-23, IFNλ, eotaxin and eotaxin 3 (Fig. 1d). Most of the cytokines linked to cytokine release syndrome (CRS), such as IL-1α, IL-1β, IL-6, IL-10, IL-18 and TNF, showed increased positive associations in patients with severe disease (Fig. 1d–f, Extended Data Fig. 3). These data highlight broad inflammatory changes, involving concomitant release of type 1, type 2 and type 3 cytokines, in patients with severe COVID-19.
Longitudinal immune profiling of COVID-19
Our data presented above, as well as previous single-cell transcriptome and flow-cytometry-based studies2,4,15,16,17, depicted overt innate and adaptive immune activation in patients with severe COVID-19. Longitudinal cytokine correlations, measured in terms of days from symptom onset (DfSO), indicated that major differences in immune phenotypes between moderate and severe disease were apparent after day 10 of infection (Fig. 2a). In the first 10 DfSO, patients with severe or moderate disease displayed similar correlation intensity and markers, including the overall core COVID-19 signature described above (Fig. 2a). After day 10 these markers declined steadily in patients with moderate disease. By contrast, patients with severe COVID-19 maintained elevated levels of these core signature makers. Notably, additional correlations between cytokines emerged in patients with severe disease following day 10 (Fig. 2a). These analyses strongly support the observation (Fig. 1) that TPO and IFNα associate strongly with IFNλ, IL-9, IL-18, IL-21, IL-23, and IL-33 (Fig. 2a). These observations indicate sharp differences in the expression of inflammatory markers along disease progression between patients who exhibit moderate versus severe symptoms of COVID-19.
Temporal analyses of PBMCs and soluble proteins in plasma, either by linear regression or grouped intervals, supported distinct courses in disease. IFNα levels were sustained at higher levels in patients with severe disease, but these declined in patients with moderate disease (Fig. 2b). Plasma levels of IFNλ increased during the first week of symptoms in patients with severe disease, and remained elevated in later phases (Fig. 2b). In addition, inflammasome-induced cytokines, such as IL-1β and IL-18, were also higher in patients with severe disease than in patients with moderate disease at most time-points analysed (Fig. 2c). IL-1 receptor antagonist (IL-1Ra), which is induced by IL-1R signalling as a negative feedback regulator18, was also increased in patients with severe COVID-19 from day 10 of disease onset (Extended Data Fig. 4).
With respect to type 1 immunity, there was an increased number of monocytes at approximately 14 DfSO in patients with severe but not moderate COVID-19 (Fig. 2d). The innate cytokine IL-12, a key inducer of type-1 immunity11,12, displayed a similar pattern to IFNγ—increasing over time in patients with severe disease but declining steadily in those with moderate disease (Fig. 2d). Intracellular cytokine staining showed that CD4+ and CD8+ T cells from patients with moderate disease secreted comparable amounts of IFNγ to those from patients with severe disease. Together with the severe T cell depletion seen in patients with severe disease (Fig. 1), our data suggest that secretion of IFNγ by non-T cells (ILC1, NK cells), or non-circulating T cells in tissues was the primary contributor to the enhanced levels observed in patients with severe disease (Extended Data Fig. 5).
Type-2 immune markers continued to increase over time in patients with severe COVID-19, as indicated by the strong correlations observed at late time points for these patients (Fig. 2a). Eosinophils and levels of eotaxin-2 increased in patients with severe disease and remained higher than in patients with moderate disease (Fig. 2e). Type 2 innate immune cytokines, including thymic stromal lymphopoietin (TSLP) and IL-33, did not show significant differences between patients with severe and moderate disease (Fig. 2e). Levels of hallmark type 2 cytokines, including IL-5 (associated with eosinophilia) and IL-13 (Fig. 2e), were higher in patients with severe disease than in those with moderate disease. By contrast, IL-4 levels were not significantly different. However, IL-4, similar to IL-5 and IL-13, showed an upward trend over the course of disease in patients with severe COVID-19 (Fig. 2e). The type 2 antibody isotype IgE was also higher in patients with severe diasease and continued to increase during the disease course (Fig. 2e).
IL-6, which is linked to CRS, was elevated in patients with severe disease19. Circulating neutrophils did not show a significant increase in our longitudinal analysis (Fig. 2f), although patients with severe disease showed hallmarks of type 3 responses, including increased plasma IL-17A and IL-22, as well as secretion of IL-17 by circulating CD4 T cells as assessed by intracellular cytokine staining (Fig. 2f, Extended Data Fig. 5). These data identify broad elevations of type 1, type 2 and type 3 signatures in severe cases of COVID-19, with differences in their kinetics and magnitudes between patients with severe and moderate disease.
Viral load correlates with elevated cytokines
We next measured viral load kinetics using serial nasopharyngeal swabs. Although there was no significant difference in viral RNA load between patients with moderate and severe disease at any specific time point analysed, patients with moderate disease showed a steady decline in viral load over the course of disease, whereas those with severe disease did not (Fig. 3a). Regardless of whether patients exhibited moderate or severe disease, viral load correlated significantly with the levels of IFNα, IFNγ, TNF and tumour necrosis factor-related apoptosis-inducing ligand (TRAIL) (Fig. 3b). In addition, several chemokines responsible for monocyte recruitment correlated significantly with viral load only in patients with severe disease (Extended Data Fig. 6a, b). These data indicate that nasopharyngeal viral load correlates with plasma levels of interferons and cytokines.
Early cytokine profile marks disease outcomes
Next, we investigated whether specific early cytokine responses are associated with severe COVID-19. To this end, we conducted an unsupervised clustering analysis using baseline measurements collected before 12 DfSO (Fig. 3c). Three main clusters with correlation to distinct disease outcomes emerged. These were characterized by four distinct immune signatures. Signature A contained several stromal growth factors, including epidermal growth factor (EGF), platelet-derived growth factor (PDGF) and vascular endothelial growth factor (VEGF), that are mediators of wound healing and tissue repair20, as well as IL-7, a key growth factor for lymphocytes. Signature B consisted of eotaxin 3, IL-33 and TSLP, along with IL-21, IL-23 and IL-17F, thus representing type 2 and type 3 immune effectors. Signature C comprised a mixture of all immunotypes, including type 1 (IFNγ, IL-12 p70, IL-15, IL-2 and TNF), type 2 (IL-4, IL-5 and IL-13), and type 3 cytokines (IL-1α, IL-1β, IL-17A, IL-17E and IL-22). Finally, signature D contained a number of chemokines involved in leukocyte trafficking, including CCL1, CCL2, CCL5, CCL8, CCL15, CCL21, CCL22, CCL27, CXCL9, CXCL10, CXCL13, and SDF1.
Cluster 1 primarily comprised patients with moderate disease who experienced low occurrences of coagulopathy, shorter lengths of hospital stay, and no mortality (Fig. 3c, d). The main characteristics in this cluster were low levels of inflammatory markers and similar or increased levels of parameters in signature A, which contains tissue reparative growth factors (Fig. 3c). Clusters 2 and 3 were characterized by a rise in inflammatory markers, and patients belonging to these clusters had a higher incidences of coagulopathy and mortality, which was more pronounced in cluster 3 (Fig. 3c, d). Patients in cluster 2 showed higher levels of markers in signatures C and D, which included IFNα, IL-1Ra and several hallmark type 1, type 2 and type 3 cytokines, than patients in cluster 1, but lower expression of markers in signatures B, C and D than those in cluster 3 (Fig. 3c, d). Patients in cluster 3 showed higher expression of markers in signatures B, C and D than those in other clusters. Cluster 3 showed particular enrichment in expression of markers in signature B, including several innate cytokines such as IFNλ, TGFα, TSLP, IL-16, IL-23 and IL-33, and markers linked to coagulopathy, such as TPO (Fig. 3c, d).
We next ranked these parameters obtained at early time points as predictors of severe disease outcomes (Fig. 3e, Extended Data Fig. 6c). In both cases, plasma inflammatory markers were strongly associated with severe disease outcomes. For example, high levels of type I IFN (IFNα) before the first 12 DfSO correlated with longer hospital stays and death (Fig. 3e, Extended Data Fig. 6c). Moreover, patients who ultimately died of COVID-19 exhibited significantly elevated levels of IFNα, IFNλ and IL-1Ra, as well as chemokines associated with monocytes and T cell recruitment and survival such as CCL1, CLL2, macrophage colony stimulating factor (M-CSF), IL-2, IL-16 and CCL21, within the first 12 DfSO (Fig. 3e, Extended Data Fig. 6c). These analyses identify specific immunological markers that appear early in the disease and correlate strongly with poor outcomes and death.
Retrospective analysis of immune correlates
To further evaluate potential drivers of severe COVID-19 outcome in an unbiased manner, we performed unsupervised clustering analysis that included all patients and all time points using cytokines and chemokines (Fig. 4a). Notably, three main clusters of patients emerged and the distribution of patients in early time-point clusters identified in Fig. 3c matched the distribution for the all-time point analysis (Fig. 4a) in 96% of cases. Cluster 1 primarily comprised patients with moderate disease who showed improving clinical signs (Fig. 4a–d, Extended Data Fig. 7). This cluster contained only two deceased patients. Cluster 1 was characterized by low levels of inflammatory markers as well as similar or increased expression of markers in signature A′ (Fig. 4a–d), which mostly matched the signature A markers described in Fig. 3c. Clusters 2 and 3 contained patients with coagulopathy and worsened clinical progression, including most of the deceased patients (Fig. 4a–d, Extended Data Fig. 7).
Clusters 2 and 3 were driven by a set of inflammatory markers that fell into signatures B′, C′ and D′ to some extent, which overlapped highly with the ‘core signature’ cytokines and chemokines identified in Fig. 1 as well as with signatures B and C identified in Fig. 3c. These include type 1 immunity markers, including IL-12, chemokines linked to monocyte recruitment and IFNγ; type 2 responses, such as TSLP, chemokines linked to eosinophil recruitment, IL-4, IL-5 and IL-13; and type-3 responses, including IL-23, IL-17A and IL-22. In addition, most CRS- and inflammasome-associated cytokines were enriched in these clusters, including IL-1α, IL-1β, IL-6, IL-18 and TNF (Fig. 4a). These findings were consistent with generalized estimating equations that identified relationships between the risk of death and cytokines or immune cell populations over time (Extended Data Fig. 8). Together, these results identify groups of inflammatory and potentially protective markers that correlated with COVID-19 trajectories. The immune signatures that correlate with recovery (cluster 1) and the immune signatures that correlate with worsening diseases (cluster 2 < cluster 3) were remarkably similar whether we took a prospective (Fig. 3) or retrospective (Fig. 4) approach.
Our longitudinal analyses of patients admitted to YNHH with COVID-19 revealed key temporal features of viral load and immune responses that distinguish disease trajectories during hospitalization. Unsupervised clustering revealed three distinct profiles that influenced the evolution and severity of COVID-19. Cluster 1, characterized by low expression of proinflammatory cytokines and enrichment in tissue repair genes, followed a disease trajectory that remained moderate and led to eventual recovery. Clusters 2 and 3 were characterized by highly elevated proinflammatory cytokines (cluster 3 being more intense), worse disease, and death. Thus, in addition to the known CRS-related pro-inflammatory cytokines, we propose these four signatures of immune response profiles that more accurately divide patients into distinct COVID-19 disease courses.
Although nasopharyngeal viral RNA levels were not significantly different between patients with moderate and severe disease at the specific time points, linear regression analyses showed a slower decline of viral loads in patients who were admitted to the ICU. Viral load was highly correlated with IFNα, IFNγ and TNF, suggesting that viral load may drive these cytokines and that interferons may not successfully control the viral replication. Moreover, many interferons, cytokines, and chemokines were elevated early in disease for patients who ultimately died of COVID-19. This finding suggests possible pathological roles associated with these host defence factors, as previous reported for patients infected with SARS-CoV-121.
Our comprehensive analysis of soluble plasma factors revealed broad misfiring of immune effectors in patients with COVID-19, with early predictive markers and distinct dynamics between types of immune responses among moderate and severe disease outcomes. These results suggest that late-stage pathology in COVID-19 may be driven primarily by host immune responses to SARS-CoV-2 and highlights the need for combination therapy to block other cytokines highly represented by these clusters, including inflammasome-dependent cytokines and type 2 cytokines. We observed a correlation with cytokines linked to the inflammasome pathway, which partially overlap with CRS, including IL-1β and IL-18. Indeed, it is plausible that inflammasome activation, along with a sepsis-like CRS, triggers the vascular insults and tissue pathology that are observed in patients with severe COVID-1922.
Overall, our analyses provide a comprehensive examination of the diverse inflammatory dynamics during COVID-19 and possible contributions of distinct sets of inflammatory mediators to disease progression. This raises the possibility that early immunological interventions that target inflammatory markers that are predictive of worse disease outcome would be more beneficial than those that block late-appearing cytokines. Our disease trajectory analyses provide bases for more targeted treatment of patients with COVID-19 based on early cytokine markers, as well as therapies designed to enhance tissue repair and promote disease tolerance.
This study was approved by Yale Human Research Protection Program Institutional Review Boards (FWA00002571, protocol ID 2000027690). Informed consent was obtained from all enrolled patients and healthcare workers.
One-hundred and thirty-five patients admitted to YNHH with COVID-19 between 18 March 2020and 5 May 2020 were included in this study. No statistical methods were used to predetermine sample size. Nasopharyngeal swabs were collected as described23, approximately every four days, for SARS-CoV-2 RT–qPCR analysis where clinically feasible. Paired whole blood for flow cytometry analysis was collected simultaneously in sodium heparin-coated vacutainers and kept on gentle agitation until processing. All blood was processed on the day of collection. Patients were scored for COVID-19 disease severity through review of electronic medical records (EMR) at each longitudinal time point. Scores were assigned by a clinical infectious disease physician according to a custom-developed disease severity scale. Moderate disease status (clinical score 1–3) was defined as: SARS-CoV-2 infection requiring hospitalization without supplementary oxygen (1); infection requiring non-invasive supplementary oxygen (<3 l/min to maintain SpO2 >92%) (2); and infection requiring non-invasive supplementary oxygen (>3 l/min to maintain SpO2 >92%, or >2 l/min to maintain SpO2 >92% and had a high-sensitivity C-reactive protein (CRP) >70) and received tocilizumab). Severe disease status (clinical score 4 or 5) was defined as infection meeting all criteria for clinical score 3 and also requiring admission to the ICU and >6 l/min supplementary oxygen to maintain SpO2 >92% (4); or infection requiring invasive mechanical ventilation or extracorporeal membrane oxygenation (ECMO) in addition to glucocorticoid or vasopressor administration (5). Clinical score 6 was assigned for deceased patients. Of note, the use of tocilizumab can increase circulating levels of IL-6 by inhibiting IL-6Rα-mediated degradation. Analysis of our cohort indicate higher plasma levels of IL-6 in patients with either moderate or severe disease who received tocilizumab treatment (Extended Data Fig. 1d).
For all patients, days from symptom onset were estimated as follows: (1) highest priority was given to explicit onset dates provided by patients; (2) next highest priority was given to the earliest reported symptom by a patient; and (3) in the absence of direct information regarding symptom onset, we estimated a date through manual assessment of the electronic medical record (EMRs) by an independent clinician. Demographic information was aggregated through a systematic and retrospective review of patient EMRs and was used to construct Extended Data Table 1. Symptom onset and aetiology were recorded through standardized interviews with patients or patient surrogates upon enrollment in our study, or alternatively through manual EMR review if no interview was possible owing to clinical status. The clinical data were collected using EPIC EHR and REDCap 9.3.6 software. At the time of sample acquisition and processing, investigators were unaware of the patients’ conditions. Blood acquisition was performed and recorded by a separate team. Information about patients’ conditions was not available until after processing and analysis of raw data by flow cytometry and ELISA. A clinical team, separate from the experimental team, performed chart reviews to determine relevant statistics. Cytokines and FACS analyses were performed blinded. Patients’ clinical information and clinical score coding were revealed only after data collection.
Viral RNA measurements
RNA concentrations were measured from nasopharyngeal samples by RT–qPCR as previously described23. In brief, total nucleic acid was extracted from 300 μl of viral transport medium (nasopharyngeal swab) using the MagMAX Viral/Pathogen Nucleic Acid Isolation kit (ThermoFisher Scientific) with a modified protocol and eluted into 75 μl elution buffer.
To detect SARS-CoV-2 RNA, we tested 5 μl RNA 371 template as previously described24, using the US CDC real-time RT–qPCR primer/probe sets for 2019-nCoV_N1, 2019-nCoV_N2, and the human RNase P (RP) as an extraction control. Virus RNA copies were quantified using a tenfold dilution standard curve of RNA transcripts that we previously generated24. The lower limit of detection for SARS-CoV-2 genomes assayed by qPCR in nasopharyngeal specimens was established as described24. In addition to a technical detection threshold, we also used a clinical referral threshold (detection limit) to either: (1) refer asymptomatic HCWs for diagnostic testing at a CLIA-approved laboratory; or (2) cross-validate results from a CLIA-approved laboratory for SARS-CoV-2 qPCR-positive individuals upon study enrollment. Individuals above the technical detection threshold, but below the clinical referral threshold, were considered SARS-CoV-2 positive for the purposes of our research.
Isolation of patient plasma
Plasma samples were collected after centrifugation of whole blood at 400g for 10 min at room temperature (RT) without brake. The undiluted serum was then transferred to 15-ml polypropylene conical tubes, and aliquoted and stored at −80 °C for subsequent analysis.
Cytokine and chemokine measurements
Patient serum was isolated as before and aliquots were stored at −80 °C. Sera were shipped to Eve Technologies (Calgary, Alberta, Canada) on dry ice, and levels of cytokines and chemokines were measured using the Human Cytokine Array/Chemokine Array 71-403 Plex Panel (HD71). All samples were measured upon the first thaw.
Isolation of PBMCs
PBMCs were isolated from heparinized whole blood using Histopaque (Sigma-Aldrich, #10771-500ML) density gradient centrifugation in a biosafety level 2+ facility. After isolation of undiluted serum, blood was diluted 1:1 in room temperature PBS, layered over Histopaque in a SepMate tube (StemCell Technologies; #85460) and centrifuged for 10 min at 1,200g. The PBMC layer was isolated according to the manufacturer’s instructions. Cells were washed twice with PBS before counting. Pelleted cells were briefly treated with ACK lysis buffer for 2 min and then counted. Percentage viability was estimated using standard Trypan blue staining and an automated cell counter (Thermo-Fisher, #AMQAX1000).
Antibody clones and vendors were as follows: BB515 anti-hHLA-DR (G46-6) (1:400) (BD Biosciences), BV785 anti-hCD16 (3G8) (1:100) (BioLegend), PE-Cy7 anti-hCD14 (HCD14) (1:300) (BioLegend), BV605 anti-hCD3 (UCHT1) (1:300) (BioLegend), BV711 anti-hCD19 (SJ25C1) (1:300) (BD Biosciences), AlexaFluor647 anti-hCD1c (L161) (1:150) (BioLegend), biotin anti-hCD141 (M80) (1:150) (BioLegend), PE-Dazzle594 anti-hCD56 (HCD56) (1:300) (BioLegend), PE anti-hCD304 (12C2) (1:300) (BioLegend), APCFire750 anti-hCD11b (ICRF44) (1:100) (BioLegend), PerCP/Cy5.5 anti-hCD66b (G10F5) (1:200) (BD Biosciences), BV785 anti-hCD4 (SK3) (1:200) (BioLegend), APCFire750 or PE-Cy7 or BV711 anti-hCD8 (SK1) (1:200) (BioLegend), BV421 anti-hCCR7 (G043H7) (1:50) (BioLegend), AlexaFluor 700 anti-hCD45RA (HI100) (1:200) (BD Biosciences), PE anti-hPD1 (EH12.2H7) (1:200) (BioLegend), APC anti-hTIM3 (F38-2E2) (1:50) (BioLegend), BV711 anti-hCD38 (HIT2) (1:200) (BioLegend), BB700 anti-hCXCR5 (RF8B2) (1:50) (BD Biosciences), PE-Cy7 anti-hCD127 (HIL-7R-M21) (1:50) (BioLegend), PE-CF594 anti-hCD25 (BC96) (1:200) (BD Biosciences), BV711 anti-hCD127 (HIL-7R-M21) (1:50) (BD Biosciences), BV421 anti-hIL17a (N49-653) (1:100) (BD Biosciences), AlexaFluor 700 anti-hTNFa (MAb11) (1:100) (BioLegend), PE or APC/Fire750 anti-hIFNy (4S.B3) (1:60) (BioLegend), FITC anti-hGranzymeB (GB11) (1:200) (BioLegend), AlexaFluor 647 anti-hIL-4 (8D4-8) (1:100) (BioLegend), BB700 anti-hCD183/CXCR3 (1C6/CXCR3) (1:100) (BD Biosciences), PE-Cy7 anti-hIL-6 (MQ2-13A5) (1:50) (BioLegend), PE anti-hIL-2 (5344.111) (1:50) (BD Biosciences), BV785 anti-hCD19 (SJ25C1) (1:300) (BioLegend), BV421 anti-hCD138 (MI15) (1:300) (BioLegend), AlexaFluor700 anti-hCD20 (2H7) (1:200) (BioLegend), AlexaFluor 647 anti-hCD27 (M-T271) (1:350) (BioLegend), PE/Dazzle594 anti-hIgD (IA6-2) (1:400) (BioLegend), PE-Cy7 anti-hCD86 (IT2.2) (1:100) (BioLegend), APC/Fire750 anti-hIgM (MHM-88) (1:250) (BioLegend), BV605 anti-hCD24 (ML5) (1:200) (BioLegend), BV421 anti-hCD10 (HI10a) (1:200) (BioLegend), BV421 anti-CDh15 (SSEA-1) (1:200) (BioLegend), AlexaFluor 700 Streptavidin (1:300) (ThermoFisher), BV605 Streptavidin (1:300) (BioLegend). In brief, freshly isolated PBMCs were plated at 1–2 × 106 cells per well in a 96-well U-bottom plate. Cells were resuspended in Live/Dead Fixable Aqua (ThermoFisher) for 20 min at 4 °C. Following a wash, cells were blocked with Human TruStan FcX (BioLegend) for 10 min at RT. Cocktails of desired staining antibodies were added directly to this mixture for 30 min at RT. For secondary stains, cells were first washed and supernatant aspirated; then to each cell pellet a cocktail of secondary markers was added for 30 min at 4 °C. Prior to analysis, cells were washed and resuspended in 100 μl 4% PFA for 30 min at 4 °C. For intracellular cytokine staining following stimulation, cells were resuspended in 200 μl cRPMI (RPMI-1640 supplemented with 10% FBS, 2 mM l-glutamine, 100 U/ml penicillin, and 100 mg/ml streptomycin, 1 mM sodium pyruvate, and 50 μM 2-mercaptoethanol) and stored at 4 °C overnight. Subsequently, these cells were washed and stimulated with 1× Cell Stimulation Cocktail (eBioscience) in 200 μl cRPMI for 1 h at 37 °C. Fifty microlitres of 5× Stimulation Cocktail (plus protein transport 442 inhibitor) (eBioscience) was added for an additional 4 h of incubation at 37 °C. Following stimulation, cells were washed and resuspended in 100 μl 4% PFA for 30 min at 4 °C. To quantify intracellular cytokines, these samples were permeabilized with 1× permeabilization buffer from the FOXP3/Transcription Factor Staining Buffer Set (eBioscience) for 10 min at 4 °C. All subsequent staining cocktails were made in this buffer. Permeabilized cells were then washed and resuspended in a cocktail containing Human TruStan FcX (BioLegend) for 10 min at 4 °C. Finally, intracellular staining cocktails were added directly to each sample for 1 h at 4 °C. Following this incubation, cells were washed and prepared for analysis on an Attune NXT (ThermoFisher). Data were analysed using FlowJo software version 10.6 software (Tree Star). The specific sets of markers used to identify each subset of cells are summarized in Extended Data Fig. 9.
Patients and their analysed features were clustered using the K-means algorithm. Heat maps were created using the ComplexHeatmap package25. The optimum number of clusters was determined by using the silhouette coefficient analysis, available with the NBClust and factoextra packages26. Before data visualization, each feature was scaled and centred. Multiple group comparisons were analysed by running both parametric (ANOVA) and non-parametric (Kruskal–Wallis) statistical tests with Dunn’s and Tukey’s post hoc tests. Mutual information analyses were performed using the Caret R package and visualized using ggplot2. Multiple correlation analysis was performed by computing Spearman’s coefficients with the Hmisc package for R and visualized with corrplot by only showing correlations with P < 0.05. For generalized linear models (GLM), we calculated the incident risk ratio (IRR) by conducting a Poisson regression with a log link and robust variance estimation; this value approximates the risk ratio estimated by a log-linear model. For generalized estimating equation (GEE) models, we calculated the incidence risk ratio (IRR) in the same way as for non-GEE GLM models, assuming an independent correlation structure. All models controlled for participant sex and age.
Further information on research design is available in the Nature Research Reporting Summary linked to this paper.
Giamarellos-Bourboulis, E. J. et al. Complex immune dysregulation in COVID-19 patients with severe respiratory failure. Cell Host Microbe 27, 992–1000.e3 (2020).
Zhou, Z. et al. heightened innate immune responses in the respiratory tract of COVID-19 patients. Cell Host Microbe 27, 883–890.e2 (2020).
Huang, C. et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet 395, 497–506 (2020).
Mathew, D. et al. Deep immune profiling of COVID-19 patients reveals distinct immunotypes with therapeutic implications. Science https://doi.org/10.1126/science.abc8511 (2020).
Hoffmann, M. et al. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell 181, 271–280.e8 (2020).
Yan, R. et al. Structural basis for the recognition of SARS-CoV-2 by full-length human ACE2. Science 367, 1444–1448 (2020).
Chen, J. & Subbarao, K. The Immunobiology of SARS. Annu. Rev. Immunol. 25, 443–472 (2007).
Jose, R. J. & Manuel, A. COVID-19 cytokine storm: the interplay between inflammation and coagulation. Lancet Respir. Med. 8, e46–e47 (2020).
Chen, G. et al. Clinical and immunological features of severe and moderate coronavirus disease 2019. J. Clin. Invest. 130, 2620–2629 (2020).
Chen, N. et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet 395, 507–513 (2020).
Annunziato, F., Romagnani, C. & Romagnani, S. The 3 major types of innate and adaptive cell-mediated effector immunity. J. Allergy Clin. Immunol. 135, 626–635 (2015).
Iwasaki, A. & Medzhitov, R. Control of adaptive immunity by the innate immune system. Nat. Immunol. 16, 343–353 (2015).
O’Shea, J. J. & Paul, W. E. Mechanisms underlying lineage commitment and plasticity of helper CD4+ T cells. Science 327, 1098–1102 (2010).
Ostendorf, L. et al. Low-density granulocytes are a novel immunopathological feature in both multiple sclerosis and neuromyelitis optica spectrum disorder. Front. Immunol. 10, 2725 (2019).
Kalfaoglu, B., Almeida-Santos, J., Adele Tye, C., Satou, Y. & Ono, M. T-cell hyperactivation and paralysis in severe COVID-19 infection revealed by single-cell analysis. Preprint at https://www.biorxiv.org/content/10.1101/2020.05.26.115923v2 (2020).
Blanco-Melo, D. et al. Imbalanced host response to SARS-CoV-2 drives development of COVID-19. Cell 181, 1036–1045.e1039 (2020).
Kuri-Cervantes, L. et al. Comprehensive mapping of immune perturbations associated with severe COVID-19. Sci. Immunol. 15, eabd7114 (2020).
Gabay, C., Lamacchia, C. & Palmer, G. IL-1 pathways in inflammation and human diseases. Nat. Rev. Rheumatol. 6, 232–241 (2010).
Wang, D. et al. The regulation of the Treg/Th17 balance by mesenchymal stem cells in human systemic lupus erythematosus. Cell. Mol. Immunol. 14, 423–431 (2017).
Duffield, J. S., Lupher, M., Thannickal, V. J. & Wynn, T. A. Host responses in tissue repair and fibrosis. Annu. Rev. Pathol. 8, 241–276 (2013).
Cameron, M. J. et al. Interferon-mediated immunopathological events are associated with atypical innate and adaptive immune responses in patients with severe acute respiratory syndrome. J. Virol. 81, 8692–8706 (2007).
Yap, J. K. Y., Moriyama, M. & Iwasaki, A. Inflammasomes and pyroptosis as therapeutic targets for COVID-19. J. Immunol. 205, 307–312 (2020).
Wyllie, A. L. et al. Saliva is more sensitive for SARS-CoV-2 detection in COVID-19 patients than nasopharyngeal swabs. Preprint at https://www.medrxiv.org/content/10.1101/2020.04.16.20067835v1 (2020).
Vogels, C. B. F. et al. Analytical sensitivity and efficiency comparisons of SARS-COV-2 qRT-PCR primer-probe sets. Nat. Microbiol. https://doi.org/10.1038/s41564-020-0761-6 (2020).
Gu, Z., Eils, R. & Schlesner, M. Complex heatmaps reveal patterns and correlations in multidimensional genomic data. Bioinformatics 32, 2847–2849 (2016).
Charrad, M., Ghazzali, N., Boiteau, V. & Niknafs, A. NbClust: An R package for determining the relevant number of clusters in a data set. J. Stat. Softw. 61, 1–36 (2014).
We thank M. Linehan for technical and logistical assistance, and A. Wang, A. Ring, C. Wilen and D. Mucida for discussions. This work was supported by the Women’s Health Research at Yale Pilot Project Program (A.I.), Fast Grant from Emergent Ventures at the Mercatus Center, Mathers Foundation, and the Ludwig Family Foundation, the Department of Internal Medicine at the Yale School of Medicine, Yale School of Public Health and the Beatrice Kleinberg Neuwirth Fund. IMPACT received support from the Yale COVID-19 Research Resource Fund. A.I. is an Investigator of the Howard Hughes Medical Institute. C.L. is a Pew Latin American Fellow. P.W. is supported by Gruber Foundation and the NSF. B.I. is supported by NIAID 2T32AI007517-16. C.B.F.V. is supported by NOW Rubicon 019.181EN.004.
The authors declare no competing interests.
Peer review information Nature thanks Petter Brodin, Malik Peiris and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.
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Extended data figures and tables
a, b, Aggregated ages (a) and BMIs (b) were collected for patients with moderate, severe, and fatal COVID-19 and relative frequency histograms generated for comparison across disease sub-groups. Gaussian and lognormal distributions were fit through least squares regression and compared for goodness of fit through differential Akaike information criterion (AICc) comparison. All distributions were best described by a Gaussian model except for age in the ‛severe’ disease category, which was best modelled by a lognormal distribution. c, Proportion of patients admitted to YNHH receiving hydroxycholorquine (HCQ), tocilizumab (Toci), methylprednisolone (Solu-medrol), and remdesivir (Rem) are shown, stratified by disease severity. d, Medication and age adjustments for IL-6 and T cell count.
a, b, Immune cell subsets of interest, plotted as a concentration of millions of cells per millilitre of blood (a) or as a percentage of a parent population (b). c, Phenotyping to TCR-activated T cells, cytokine-secreting T cells, and HLA-DR expression within monocytes and neutrophils. Each dot represents a separate time point per subject (HCW, n = 49; Moderate, n = 114; Severe, n = 41). For all boxplots, the centre is drawn through the median of the measurement, and the lower and upper bounds of the box correspond to the first and third percentile. Whiskers beyond these points denote 1.5 × the interquartile range. P values were determined by two-sided, Wilcoxon rank-sum test.
a, Quantification of cytokines in the periphery plotted as log10-transformed concentrations. Each dot represents a separate time point per subject (HCW, n = 47; Moderate, n = 124; Severe, n = 45). For all boxplots, the centre is drawn through the median of the measurement, while the lower and upper bounds of the box correspond to the first and third percentile. Whiskers beyond these points denote 1.5 × the interquartile range. P values were determined by two-sided, Wilcoxon rank-sum test.
a, Quantification of cytokines plotted as log10-transformed concentration over time according to the days of symptom onset for patients with moderate disease (n = 112) or severe disease (n = 39). The dotted green line represents the mean measurement from uninfected HCWs. Regression lines are indicated by the dark blue (moderate) or red (severe) solid lines. Associated, Pearson’s correlation coefficients and linear regression significance are in pink (moderate) or dark blue (severe). 95% confidence intervals for the regression lines are denoted by the pink (moderate) or dark blue (severe) filled areas.
a, b, CD4+ (a) and CD8+ (b) T cell populations of interest, plotted as a percentage of parent populations, over time according to the days following symptom onset for patients with moderate disease (n = 118) or severe disease (n = 41). Each dot represents a distinct patient and time point arranged by intervals of five days until 25 days. Dark blue or pink lines pass through the mean of each measurement at the specified time interval; error bars at this intersection denote s.e.m. The dotted green line represents the mean measurement from uninfected HCWs.
a, Quantification of log10-transformed cytokine concentrations plotted continuously with NP viral load (expressed as log10 genomic equivalents (GE)/ml) per within an individual patient and time point. Regression lines are indicated by the dark blue (moderate) or red (severe) solid lines for patients with moderate disease (n = 112) or severe disease (n = 39), respectively. Associated Pearson’s correlation coefficients, and linear regression significance are in pink (moderate) or dark blue (severe). 95% confidence intervals for the regression lines are denoted by the pink (moderate) or dark blue (severe) filled areas. b, Correlation map of highly correlated cytokines with NP viral load in patients with moderate (blue) or severe disease (red). Pearson’s correlation coefficients are indicated in grey, connecting the central node, NP viral load, with peripheral nodes; P values for each correlation are indicated above each peripheral node. c, Length of hospital stay plotted per patient against an individual’s baseline plasma cytokine measurements (<12 days from symptom onset), which were grouped according to high or low expression (>0.5 log10-transformed difference): IFNa2 (Hi:12, Lo:13), TNFa (Hi:6, Lo:4), IL4 (Hi:7, Lo:11), IL4 (Hi:8, Lo:6), IL1RA (Hi:8, Lo:7), IL1b (Hi:11, Lo:5), IL6 (Hi:8, Lo:7), IL18 (Hi:5, Lo:5). d, Baseline plasma cytokine measurements for each patient who was either discharged from the hospital (n = 83) or expired during treatment for COVID-19 (n = 11). For all boxplots, the centre is drawn through the median of the measurement, while the lower and upper bounds of the box correspond to the first and third percentile. Whiskers beyond these points denote 1.5 × the interquartile range. P values were determined by two-sided, Wilcoxon rank-sum test.
Extended Data Fig. 7 Distribution of days from symptom onset stratified by collection time point and select cluster clinical data.
a, Correlation of days from symptom onset and samples collection time points. Violin plots comparing the distributions of days from symptom for each patient ordered by sequential IMPACT study time points (1–8). Study time points 7 and 8 are represented by discrete points for the single patient collected at each. Violin plots display median values (solid line) and associated quartiles (dashed lines). T1–8 (time point 1 to 8). b–h, Aggregated clinical data for patients in clusters 1–3. Displayed are laboratory values at time of admission to YNHH (“admit”); last recorded values from duration of admission (“last”); maximum recorded values from duration of admission (“max”); minimum recorded values from duration of admission (“min”); and average recorded values for duration of admission (“mean”). Scatter plots show cluster means with s.e.m. plotted above and below. Clusters were subsequently compared using ordinary two-way ANVOA and post hoc pairwise comparisons are identified where significant (adjusted P values displayed, Tukey’s method for multiple comparisons).
Forest plots comparing the risk of death among ill patients. Each effect estimate represents an individual regression estimate with a Poisson family, log link, and robust variance estimation; each model accounts for repeated measures within one individual through the use of generalized estimating equations (GEE). Measurements are divided into three time-periods: 0–11 days after symptom onset, 12–19 days after symptom onset, and ≥20 days after symptom onset. If an individual had more than one measurement of a biomarker during any particular time period, we used the average of all values. Each model controls for participant age and gender.
Gating strategies are shown for the key cell populations described in Figs. 1b, c, 2d–f, and in Extended Data Figures. a, Leukocyte gating strategy to identify lymphocytes, granulocytes, monocytes, pDCs, and cDCs in Figs. 1b, c, 2d–f and Extended Data Fig. 2a. b, T cell surface staining gating strategy to identify CD4 and CD8 T cells, TCR-activated T cells, terminally-differentiated T cells, and additional subsets as shown in Extended Data Fig. 2b. c, Intracellular T cell gating strategy to identify CD4 and/or CD8 T cells secreting TNF, IFNγ, IL-6, IL-2, granzyme B, IL-4, and/or IL-17 in Extended Data Figs. 2c, 5a, b.
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Lucas, C., Wong, P., Klein, J. et al. Longitudinal analyses reveal immunological misfiring in severe COVID-19. Nature 584, 463–469 (2020). https://doi.org/10.1038/s41586-020-2588-y
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