key: cord-1036765-8i90jk7y
authors: O'Riordan, Caroline E.; Purvis, Gareth S. D.; Collotta, Debora; Krieg, Nadine; Wissuwa, Bianka; Sheikh, Madeeha H.; Ferreira Alves, Gustavo; Mohammad, Shireen; Callender, Lauren A.; Coldewey, Sina M.; Collino, Massimo; Greaves, David R.; Thiemermann, Christoph
title: X-Linked Immunodeficient Mice With No Functional Bruton's Tyrosine Kinase Are Protected From Sepsis-Induced Multiple Organ Failure
date: 2020-10-07
journal: Front Immunol
DOI: 10.3389/fimmu.2020.581758
sha: 27cef0cf6a3a136d683a8634380a88a787a2749b
doc_id: 1036765
cord_uid: 8i90jk7y

We previously reported the Bruton's tyrosine kinase (BTK) inhibitors ibrutinib and acalabrutinib improve outcomes in a mouse model of polymicrobial sepsis. Now we show that genetic deficiency of the BTK gene alone in Xid mice confers protection against cardiac, renal, and liver injury in polymicrobial sepsis and reduces hyperimmune stimulation (“cytokine storm”) induced by an overwhelming bacterial infection. Protection is due in part to enhanced bacterial phagocytosis in vivo, changes in lipid metabolism and decreased activation of NF-κB and the NLRP3 inflammasome. The inactivation of BTK leads to reduced innate immune cell recruitment and a phenotypic switch from M1 to M2 macrophages, aiding in the resolution of sepsis. We have also found that BTK expression in humans is increased in the blood of septic non-survivors, while lower expression is associated with survival from sepsis. Importantly no further reduction in organ damage, cytokine production, or changes in plasma metabolites is seen in Xid mice treated with the BTK inhibitor ibrutinib, demonstrating that the protective effects of BTK inhibitors in polymicrobial sepsis are mediated solely by inhibition of BTK and not by off-target effects of this class of drugs.

Sepsis is a common and life-threatening condition caused by a dysregulated host response to an infection, either bacterial, fungal, or viral (1) . Sepsis is a major public health problem leading to multiple organ dysfunction and death. Globally there are 50 million cases of sepsis resulting in the death of 11 million people every year representing 20% of all deaths worldwide (2) . Despite intensive, supportive care, and current treatments (antibiotic therapy and fluid resuscitation), no targeted therapies have proven effective at reducing mortality (3, 4) . There is an urgent need for the development of pharmacological treatments for sepsis-induced organ dysfunction (5) .

Bruton's tyrosine kinase (BTK) is well-known as a critical component of the B-cell antigen receptor (BCR) signaling pathway (6) . BTK is also involved in the activation of the toll-like receptor (TLR) signaling pathways (by binding to the TIR domain of TLR4 and TLR's adaptor molecules MyD88, and Mal) and the NLRP3 inflammasome (by binding to the ASC component) (7) (8) (9) . Activation of both the TLR signaling pathway and the NLRP3 inflammasome play a pivotal role in the pathophysiology of sepsis (10, 11) . The expression of BTK is not restricted to B cells, as BTK is also expressed in cells of myeloid lineage, including macrophages and neutrophils (12, 13) , activation of which contributes to the pathophysiology of sepsis.

We have recently shown that the BTK inhibitors ibrutinib (first generation) and acalabrutinib (more selective, second generation) attenuate the systemic inflammation ("cytokine storm") and the multiple organ failure caused by sepsis in mice (14) . Ibrutinib is already approved for the use in chronic lymphatic leukemia, mantle cell lymphoma, Waldenstrom macroglobulinemia, and graft vs. host disease (15) and acalabrutinib in mantle cell lymphoma (16) . The recent COVID-19 pandemic has driven the search for drugs that can be repurposed to either reduce virus load and/or the cytokine storm in patients with severe COVID-19 infections. It has been found that BTK activation and IL-6 production is increased in COVID-19 patients and the effects of acalabrutinib are currently being evaluated in these patients (17) . Roschewski et al. (17) showed that some severe COVID-19 patients receiving acalabrutinib had improved oxygenation and reduced CRP and plasma IL-6, suggesting that BTK inhibitors could be repurposed for diseases involving excessive inflammation.

Although we have proposed that the inhibition of BTK is the key driver of the observed beneficial effects of BTK inhibitors in sepsis, it is possible that some of the well-known off-target effects of these compounds account for or, at least, contribute to the beneficial effects observed (14) . For instance, we identified that both ibrutinib and acalabrutinib strongly inhibit five different kinases: BTK, Bmx, ErbB4, RIPK2, and TEC. Our discovery that acalabrutinib and ibrutinib reduce inflammation and organ dysfunction in sepsis has triggered three important questions: (1) Does inhibition of BTK activity alone account for the observed beneficial effects? And (2) Does inhibition of systemic inflammation reduce the host response to infection and ultimately cause increased harm? (3) What effect does BTK inactivation have on the metabolomic profile of septic mice? Interest in metabolomic profiling is growing, as the metabolome is the result of expression and function of a multitude of proteins and, hence, has been suggested to be a sensitive readout of drug responses (18, 19) . The present study was designed to address these questions by inducing polymicrobial sepsis in mice with X-linked immunodeficiency (Xid). Xid mice have a missense mutation within the BTK gene [arginine to cysteine at position 28 (R28C)] in the N-terminally located pleckstrin homology domain, resulting in expression of a BTK protein that is functionally inactive (20, 21) . Having developed a model of sepsis in Xid mice (and wild-type mice, CBA background), we have investigated the impact of impaired BTK function on organ dysfunction, systemic inflammation (cytokine storm), changes in plasma metabolites, and bacterial clearance.

The 

This study was carried out on twenty-three 10 week-old, male CBA mice (Charles River Laboratories UK Ltd., Kent, UK) and twenty-one 10 week-old, male CBA/CaHN-Btk xid /J (Xid) mice (from Jackson laboratory), weighing 25-30 g and kept under standard laboratory conditions. Six mice were housed together (in each cage) with access to a chow diet and water ad libitum. They were subjected to a 12 h light and dark cycle with a temperature maintained at 19-23 • C. Group sizes for each experiment were calculated following power calculations based on previous studies (14) .

Cecal ligation and puncture (CLP) was performed in 10 weekold male CBA (wild type) or Xid mice as previously described (14, 22) . Mice were randomly assigned to undergo CLP or shamoperated surgery, the surgeon was blinded to the genotype of the mouse. Briefly, mice were anesthetised with isoflurane (2% delivered in O 2 ) and the cecum was fully ligated below the ileocecal valve. A double puncture was made with a 18G needle into the cecum and a small amount of feces was squeezed out after which the cecum was returned to its anatomical position, then the laparotomy was closed. All animals received fluids (5 ml/kg saline into abdomen before closure and 10 ml/kg saline s.c., immediately after surgery), antibiotics (Imipenem/Cilastatin; 20 mg/kg dissolved in 7.5 ml/kg of saline s.c.), and analgesics (buprenorphine; 0.05 mg/kg i.p.) at 6 and 18 h after surgery. Sham-operated mice underwent the same procedure, but without CLP. At 1 h after CLP, WT or Xid mice received 30 mg/kg ibrutinib (Selleck Chemicals) intravenously.

A clinical score for monitoring the health of experimental mice was used to evaluate the symptoms consistent with murine sepsis. The maximum score of six comprised the presence of the following signs: lethargy, piloerection, tremors, periorbital exudates, respiratory distress, and diarrhea. Mice with a clinical score >3 were defined as exhibiting severe sepsis, against a moderate sepsis for a score ≤3. Animals were culled at 24 h after the onset of sepsis (CLP).

At 24 h post CLP, mice were anesthetised (0.5-2% isoflurane in O 2 ); body temperature was maintained at 37 • C and heart rate was maintained at 450 bpm. Then, cardiac function was assessed by M-mode and B-mode echocardiography using the VisualSonics Vevo 3100 echocardiographic system and a MX550D transducer. The following parameters were measured: left ventricular ejection fraction, fractional shortening, fractional area change, cardiac output, stroke volume, and myocardial performance index, as described previously (14) .

After 24 h, mice were sacrificed by terminal cardiac puncture, where terminal blood samples were immediately decanted into 1.3 ml serum gel tubes (Sarstedt, Nürnbrecht, Germany). Blood was allowed to coagulate for at least 10 min at room temperature, then samples were centrifuged at 9,000 rpm for 3 min to separate the serum. Then 100 µl of serum was snap frozen in liquid nitrogen and sent to an independent veterinary testing laboratory (MRC Harwell Institute, Oxford, UK) to evaluate the following biomarkers in a blinded fashion: Urea and creatinine (as markers of renal dysfunction), alanine aminotransferase (ALT), aspartate transaminase (AST) (markers of hepatocellular injury), and lactate dehydrogenase (LDH) (marker of cell injury).

Peritoneal lavage exudate was collected by injecting 5 ml of 2 mM of EDTA in PBS into the peritoneal cavity. After gentle massaging, ∼4 ml of exudate was removed with an 18G needle. Cells were washed in FACS buffer (0.05 % BSA, 2 mM EDTA in PBS pH 7.4) and then blocked using anti-CD16/32 (Biolegend) for 10 min at 4 • C. Peritoneal cells were analyzed using anti-CD45 (clone 30-F11; BioLegend), anti-CD11b (clone M1/70; BioLegend), anti-F4/80 (clone BM8; BioLegend), anti-Ly6G (clone 1A8; BioLegend), anti-CD206 (clone C068C2; BioLegend), and anti-MHCII (clone. M5/114.15.2; BioLegend) antibodies. Absolute cell count was calculated by the addition of counting beads (BioLegend). Data were acquired using BD LSR II Fortessa (Becton Dickinson) and analyzed using FlowJo analysis software (version 10.6, Treestar Inc.). The gating strategy is depicted in Figure S1 .

The principle of multiplex flow immunoassay technology has been reviewed previously (23, 24) . Cytokines, chemokines, and a growth factor were determined in serum by Bio-Plex Pro Mouse 

Accurate evaluation of the number of bacteria in peritoneal lavage fluid and blood samples was performed by flow cytometry using the SYTO BC bacteria counting kit (Thermo Fischer Scientific).

Peritoneal lavage exudate containing neutrophils and macrophages was obtained 24 h after CLP as described above. pHrodo TM red E. Coli bioparticles TM (Thermo Fischer Scientific) were resuspended in live cell imagining solution (BioLegend) at 10 mg/ml and 10 µL of bioparticles were opsonised with 20 µL of fresh serum for 1 h at 37 • C under gentle agitation, after which they were washed and resuspended in 10 µL of live cell imagining solution. 1 × 10 6 cells of peritoneal exudate were collected by centrifugation (300 g × 5 min) and resuspended in 890 µL of live cell imaging solution, after which 100 µl of fresh serum and 10 µL of optimized bioparticles were added and incubated for 45 min at 37 • C under gentle agitation in the dark. Cells were washed and then blocked using anti-CD16/32 (Biolegend) for 10 min at 4 • C followed by staining with surface markers anti-CD11b (clone M1/70; BioLegend), anti-Ly6G (clone 1A8; BioLegend), and anti-F4/80 (clone BM8; BioLegend) for 30 min at 4 • C. 10,000 CD11b + cells were collected by Amnis R ImageStream R X Mk II Imaging Flow Cytometer (Luminex) at a magnification of x40 and analyzed by IDEAS software for each experimental sample. Neutrophils were identified as (CD11b + , Ly6G + , F4/80 − ) and macrophages were identified as (CD11b + , Ly6G − , F4/80 + ). This equated to ∼7,000 neutrophils and 2,000 macrophages for both WT and Xid mice to undergo phagocytosis analysis via IDEAS software. 

Immunoblot analyses of cardiac tissue samples were carried out using a semi-quantitative western blotting analysis. The antibody used were: 1:1,000 rabbit anti-Ser 176/180 -IKKα/β, 1:1,000 rabbit anti-total IKKα/β, mouse anti-Ser 32/36 -IκBα, mouse anti-total IκBα, rabbit anti-Tyr 223 -BTK, rabbit anti-total BTK, rabbit anti-Tyr 1217 PLCγ, rabbit anti-total PLCγ (from Cell Signaling), 1:5,000 rabbit anti NLRP3 inflammasome (from Abcam), mouse anti-caspase 1 (p20) (from Adipogen). The apex of the heart was taken and homogenized. Proteins were then extracted as previously described (25) and concentrations were quantified by bicinchoninic acid (BCA) protein assay (Thermo Fisher Scientific Rockford, IL). Proteins were separated by 8% sodium dodecyl sulfate (SDS)-PAGE and transferred to polyvinylidene fluoride membranes. Membranes were blocked in 10% milk solution with TBS-Tween and then incubated with the primary antibody overnight at 4 • C. The next day the secondary antibody was added for 30 min at room temperature and visualized using the ECL detection system. Tubulin was used as loading control. The immunoreactive bands were analyzed by the Bio-Rad Image Lab Software TM 6.0.1 and results were normalized to the sham bands.

Original data was obtained from the gene expression omnibus under dataset number GDS4971 which was published by Parnell et al. (26) . RNA isolated from whole-blood samples of survivors (n = 26) and non-survivors (n = 9) of sepsis as well as healthy participants (n = 18) over the course of 5 days was assayed on the Illumina HT-12 gene expression microarray consisting of 48,804 probes. The dataset was analyzed for expression of BTK gene in these three groups. The figure was generated using R software (ver 4.0.2), gene expression is quantile normalization and log transformation of the data was applied. Significance was determined by a one-way ANOVA followed by a Bonferroni post hoc-test.

Metabolites were analyzed by liquid chromatography coupled to triple quadrupole mass spectrometry (LC-MS/MS) using an ultra-high-performance liquid chromatography (UHPLC) system (Nexera LC-40 series) and the triple quadrupole mass spectrometer LCMS-8050, both from Shimadzu Deutschland GmbH (Duisburg, Germany). Samples were analyzed with a method for sphingosine-1-phosphate and sphingosine and the supplied method packages "primary metabolites, " "phospholipids, " and "lipid mediators" according to the manufacturer's protocols (Shimadzu Deutschland GmbH, Duisburg, Germany) with the following modifications: 20 µL of serum sample were precipitated by addition of 200 µL of methanol (LCMS-grade) in vials. Prior to processing, the methanol was spiked with internal standard (IS) solution in a final concentration of 45.45 nM. The supernatant was taken for analysis after 4 days of incubation at −80 • C and subsequent centrifugation at 14,000 rcf for 10 min at 4 • C. Primary metabolites were analyzed using the HPLC Column Discovery R HS F5, 3 µm, 150 × 2.1 mm from Sigma-Aldrich Chemie GmbH (Munich, Germany). For phospholipids and lipid mediators, the 2.1 × 150 mm 2.6 µm particle size C8 Kinetex LC Column (Phenomenex Inc., Torrance, USA) was used. Sphingosine-1-phosphate and sphingosine were separated using a MultoHigh 100 RP 18-3µ 60 × 2 mm column (Chromatographie Service GmbH, Langerwehe, Germany) with intermittent runs for equilibration. Mass spectrometric detection was performed by multiple reactions monitoring (MRM) after injection of 10 µl sample, unless stated otherwise. Further information on HPLC programs and solvents (Table S1), LCMS-8050 settings (Table S2) , and recorded mass transitions of identified significantly changed analytes (Tables S3-S6) are listed in the Supplement. Metabolome primary data were analyzed and further processed with LabSolutions 5.91 and LabSolutions Insight 3.10 (Shimadzu Deutschland GmbH, Duisburg, Germany).

Statistical differences were determined using a one-way ANOVA, followed by Bonferroni post hoc-test or unpaired Student's t-test as appropriate (GraphPad Prism 8.0; significant when P < 0.05).

Results are expressed as mean ± SEM of n observations, where n represents the number of animals studied.

Metabolome data were determined by calculating area ratios for each analyte by dividing peak area of each analyte by peak area of the related IS. Data analysis for metabolome data was performed as follows: Readings below detection level were set to half of detection level for each analyte separately. Metabolome data was log2 transformed and normalized by subtracting median metabolite abundance per sample from all abundances of each sample. Normalization was carried out separately for primary metabolites, phospholipids, and lipid mediators. Z scores were calculated using mean and standard deviation of all samples. Contrasts were analyzed pairwise between selected sample groups by unpaired t-tests. P-values were Benjamini Hochberg adjusted (27) . Analytes with adjusted P-values below 0.05 were considered significantly different. For a first exploratory overview a principal component analysis (PCA) was carried out using the normalized and scaled metabolome data. Data analysis was carried out using R version 3.4.4 (28) .

When compared to sham-operated mice, WT mice subjected to cecal ligation and puncture (CLP) showed clinical signs of severe sepsis (80%; score >3). In contrast, all Xid mice subjected to CLP had a score of ≤3 indicating only moderate sepsis ( Figure 1A ). All mice in the WT-CLP group which received ibrutinib had a score of ≤3 indicating moderate sepsis and all mice in the Xid-CLP + ibrutinib group had a score ≤3. When compared to sham-operated mice, WT mice subjected to CLP experienced hypothermia (a rectal temperature of <30 • C) at 24 h after the onset of CLP, whereas the rectal temperature of Xid-CLP, WT-CLP + ibrutinib and Xid-CLP + ibrutinib remained at 37 • C ( Figure 1B) . A reduction in temperature to <30 • C or a change of 5 • C over time in each animal has been reported to predict death in mice with CLP (29) . As mortality of animals is not an acceptable routine endpoint in the UK, we used the reduction in rectal temperature <30 • C as a surrogate marker for mortality. Using this surrogate marker, we would predict the mortality of WT-CLP mice to be 90% (confirming that our model is a model of severe sepsis), while the predicted mortality of Xid-CLP mice would be 0% (e.g., 100% predicted survival; Figure 1C ). WT-CLP mice receiving ibrutinib had a predicted mortality of 15%, whereas Xid-CLP mice receiving ibrutinib had a predicted mortality of 0%. When compared to shamoperated mice, WT mice subjected to CLP showed a decrease in heart rate, whereas the heart rate of Xid-CLP remained similar to that of sham-operated animals ( Figure 1D) . When compared to WT-CLP mice, the administration of ibrutinib 1 h after CLP attenuated the decline in heart rate in WT mice. Mice in the Xid-CLP + ibrutinib group had a similar heart rate to mice in the Xid-CLP group. Xid-CLP mice receiving (P) AST (U/L). The following groups were studied WT sham (n = 5), Xid sham (n = 5), WT-CLP (n = 10), Xid-CLP (n = 10), WT-CLP + ibrutinib (n = 8), and Xid-CLP + ibrutinib (n = 6). Data are expressed as mean ± SEM and analyzed by one-way ANOVA with a Bonferroni post hoc-test. *P < 0.05, **P < 0.01, ***P < 0.001, and ****P < 0.0001 vs. WT-CLP.

ibrutinib had a higher heart rate than WT-CLP mice treated with ibrutinib.

Cardiac function was assessed in vivo by echocardiography. Figure 1E shows representative M-mode images in the short axis in sham-operated mice, CLP mice, and CLP + ibrutinib mice of both genotypes. When compared to sham-operated mice, WT mice subjected to CLP showed a reduction in ejection fraction (EF), fractional shortening (FS), fractional area change (FAC), cardiac output (CO), stroke volume (SV), and an increase in myocardial performance index (MPI), indicating severe global, systolic cardiac dysfunction. In contrast, Xid mice subjected to CLP had only a very minor cardiac dysfunction and all indices of cardiac performance (EF, FS, FAC, CO, SV, and MPI) were significantly improved from those measured in WT-CLP ( Figures 1F-K) . Thus, the degree of cardiac dysfunction caused by CLP in Xid mice is significantly reduced when compared to that observed in WT-mice. When compared to WT-CLP mice (CBA background) treatment of WT-mice with ibrutinib 1 h after CLP attenuated the sepsis-induced cardiac dysfunction.

In contrast, administration of ibrutinib to Xid-CLP mice had no effect on cardiac function ( Figures 1F-K) , indicating that the addition of ibrutinib in Xid mice with CLP results in no beneficial or deleterious effects due to off target actions of the drug.

Kidney dysfunction and hepatocellular injury was assessed by measuring serum creatinine, urea, ALT, AST, and LDH. When compared to sham-operated mice, WT mice subjected to CLP had significant renal dysfunction (rise in urea and creatinine), hepatocellular injury (rise in ALT and AST) and cell injury (rise in LDH). In contrast, in Xid mice subjected to CLP, the degree of kidney dysfunction, hepatocellular injury and cell injury was significantly reduced when compared to WT-CLP mice (Figures 1L-P) . When compared to WT-CLP, treatment of WT-CLP mice with ibrutinib (1 h after CLP) significantly attenuated the rise of plasma/serum urea, creatinine, ALT, AST, and LDH. In contrast, administration of ibrutinib in Xid-CLP mice had no significant effect on organ dysfunction (as this was prevented in Xid-mice). No significant difference was observed between WT-CLP + ibrutinib and Xid-CLP + ibrutinib for any of the parameters of organ dysfunction measured.

Using a multiplex array, we analyzed 31 cytokines and chemokines in the serum of all animals. When compared to sham-operated mice, WT mice subjected to CLP sepsis showed a significant increase in the serum levels of pro-inflammatory cytokines TNF-α, IL-6, and IL-1β, the anti-inflammatory cytokine IL-10, neutrophils chemoattractant chemokines (KC & ENA-78), monocyte chemoattractant chemokines (MCP-1, MIP-1α, and MIP-1β) and G-CSF. In contrast, the levels of these cytokines and chemokines in the serum of Xid-CLP were significantly reduced when compared to WT-CLP mice (Figures 2A-J) . When compared to WT-CLP, treatment of WT-CLP mice with ibrutinib (1 h after CLP) significantly attenuated the rise in cytokines and chemokines.

In contrast, administration of ibrutinib in Xid-CLP-mice had no significant effect on the production of cytokines and chemokines (as this was prevented in Xid-mice). No significant difference was observed between WT-CLP + ibrutinib and Xid-CLP + ibrutinib for any cytokines and chemokines. The alterations of a further 21 cytokines and chemokines can be seen in Figure 2K and absolute values in Table S7 .

We also evaluated the cell composition and phenotype in the peritoneal exudates of all animals by flow cytometry gating strategy seen in Figure S1 . When compared to shamoperated mice, WT mice subjected to CLP showed a significant increase in neutrophils and macrophages into the peritoneum. In contrast, Xid-CLP mice exhibited a significant reduction in the number of infiltrating neutrophils and macrophages when compared to WT-CLP mice (Figures 3A-C) . Upon further analysis of the subsets of macrophages, we found that the macrophages obtained from WT-CLP mice are predominately of the pro-inflammatory M1 phenotype (60% M1 and 40% M2), while the macrophages of Xid-CLP are of the pro-resolving (anti-inflammatory) M2 phenotype (40% M1 and 60% M2) (Figures 3D,E) .

In order to determine the mechanism that accounts for the improved outcome of BTK deficient mice, we investigated bacterial clearance in vivo in WT and Xid-mice at 24 h after the onset of CLP, as the survival of sepsis is dependent on the ability to clear bacteria. When compared to shamoperated mice, WT mice subjected to CLP exhibited elevated peritoneal and blood bacteria counts (Figures 4A-D) . However, Xid-CLP mice had significantly fewer bacteria in the peritoneal cavity and blood than WT-CLP mice, showing that Xid-mice clear bacteria more efficiently than WT mice. Clearance of bacteria is secondary to phagocytosis of bacteria in neutrophils and macrophages. Xid mice subjected to CLP presented with a reduced number of infiltrating immune cells, but also reduced bacterial counts at 24 h post CLP. This raises the question as to how fewer infiltrating immune cells are able to clear more bacteria? To address this question, we investigated whether Xid neutrophils and macrophages have increased phagocytic ability in vivo. We found that the percentage of neutrophils and macrophages, which are phagocytosing bacteria, are similar in WT-CLP and Xid-CLP mice. However, neutrophils and macrophages of Xid-CLP mice contain more bacteria per immune cell than WT-CLP mice, showing a 100% increase in phagocytic ability of both neutrophils and macrophages (Figures 4E-L) . Collectively, this data clearly demonstrates that Xid mice with a deficiency in BTK show enhanced phagocytosis in vivo resulting in improved clearance of bacteria during a septic episode.

BTK, NF-κB, and NLRP3 Inflammasome Are Not Activated in Xid Mice After Polymicrobial Sepsis

To understand the signaling mechanism associated with the observed cardiac dysfunction in CLP-sepsis, we investigated the effect of BTK deficiency in Xid mice on the activation of key signaling pathways of inflammation: BTK, NF-κB, and NLRP3 inflammasome activation (Figure 5) . When compared to sham-operated mice, WT mice subjected to CLP showed an increase of BTK activation as demonstrated by significant increases in the phosphorylation of cardiac BTK at Tyr 223 and the phosphorylation of PLCγ at Tyr 1217 . No activation of BTK was detected in Xid mice, even after CLP injury and the phosphorylation of cardiac BTK at Tyr 223 and the phosphorylation of PLCγ at Tyr 1217 in Xid-CLP mice were similar to that of sham-operated animals (Figures 5A,B) . NF-κB activation plays a key role in the pathophysiology of sepsis. When compared to sham-operated mice, WT-CLP mice exhibit a significant increase in NF-κB activation as demonstrated by significant increases in the phosphorylation of IKKα/β at Ser 176/180 and the phosphorylation of IκBα at Ser 32/36 . When compared to WT-CLP mice, Xid-CLP mice the phosphorylation of IKKα/β at Ser 176/180 and IκBα at Ser 32/36 was significantly reduced, indicating that the degree of activation of NF-κB caused by sepsis in the heart was significantly lower in Xid-mice than in WT-mice (Figures 5C,D) .

When compared to sham-operated mice, WT mice subjected to CLP showed an increase in the activation of the NLRP3 inflammasome, demonstrated by an increase in the expression of the NLRP3 inflammasome and cleavage of pro-caspase-1 to caspase-1 in the heart (Figures 5E,F) as well as an increase the production of IL-1β in serum ( Figure 2C) . In contrast, Xid-CLP mice showed reduced activation of NLRP3 inflammasome as demonstrated by a decrease in the expression of the NLRP3 inflammasome, cleavage of pro-caspase-1 to caspase-1 (Figures 5E,F) and IL-1β when compared to WT-CLP mice ( Figure 2C ). 

Using a targeted metabolomic approach, we detected 240 analytes in murine plasma. A two-dimensional principal component analysis (PCA) of all detected analytes (Figure 6) , revealed a clear distinction between the two sham-operated mice groups (WT sham and Xid sham), the WT-CLP mice group and the three treated and/or Xid CLP-induced mice groups (Xid CLP, WT CLP + Ibrutinib, and Xid CLP + Ibrutinib). The first principal component explained about 36% of total variation among the six mice groups and separated the sham-operated mice from the CLP-induced mice groups. The second principal component explained about 13% of total variation of all metabolites and achieved the same effect as PC2, but further it separated the CLP-induced WT mice group from the three mice groups Xid CLP, WT CLP + ibrutinib, and Xid CLP + ibrutinib. Significant changes in analytes were identified and analyzed via hierarchical clustered z score heatmaps and their significant log2-fold changes of selected group comparisons were shown in log2-fold change heatmaps (Figures S2-S5) . The heatmaps illustrate 55 significant primary metabolites (Figure S2) , 138 significant phospholipids . Each column in a z score heatmap represented the mean value of all animals in a group, each column in a log2-fold change heatmap represented a groupwise comparison and each row defined an analyte. Analytes were hierarchically clustered using Ward's minimum variance method (76) and an euclidian distance between log2-fold changes. Dendrograms provide information about distances between clusters. AA, arachidonic acid; AEA, arachidonoylethanolamide; DHA, docosahexaenoic acid; DOPA, dihydroxyphenylalanine; EPA, eicosapentaenoic acid; LPE, lysophosphatidylethanolamine; LPG, lysophosphatidylglycerol; LPS, lysophosphatidylserine; lyso-PAF, lyso-platelet activating factor; OEA, oleoylethanolamine; PE, phosphatidylethanolamine; PI, phosphatidylinositol; PS, phosphatidylserine; TDCA, taurodeoxycholic acid.

and their derivatives (Figures S3,S4) , and 6 significant lipid mediators ( Figure S5) . Figure 7 shows a sorting of 24 analytes that were significantly restored in the three mice groups Xid-CLP, WT-CLP + ibrutinib, and Xid-CLP + ibrutinib to the initial levels of both sham-operated groups compared to the WT-CLP mice group. The ibrutinib treatment or the BTK inactivation or the combination of both restored 7 significant decreased and 17 significant increased analytes in CLP-induced WT-mice. The decreased analytes belonged predominantly to the lipid mediator's docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA), lyso-platelet activating factor (lyso-PAF), and oleoylethanolamine (OEA). The bile acid taurodeoxycholic acid (TDCA), the phosphatidylinositol (PI) (34:2) and the primary metabolite niacinamide were also reduced. The increased analytes included five primary metabolites (dihydroxyphenylalanine (DOPA), creatine, carnosine, nicotinic acid, cytosine), four lysophosphatidylserines, five phosphatidylserines, one lysophosphatidylethanolamine, one lysophaphatidylglycerol and one phosphytidylethanolamine.

Sorting by analytes that were only significantly restored in Xid-CLP ( Figure S6) showed five analytes. One analyte was increased, the primary metabolite kynurenine, and four analytes were decreased in the WT-CLP group and this included the primary metabolite uridine and one the phospholipids phosphatidylserine, phosphatidylethanolamine, and phosphatidylinositol. Twenty-three analytes showed the sorting by significantly restored analytes in the mice groups Xid CLP and Xid CLP + Ibrutinib ( Figure S7) . The levels of 10 analytes (cGMP, creatinine, ursodeoxycholic acid (UDCA), deoxycholic acid (DCA), adenine, one lysophosphatidylserine, one lysophosphatidylglycerol, three lysophosphatidylethanolamines) were upregulated and 13 analytes (one sphingomyelin, six phosphatidylcholines, three phosphatidylethanolamines, two phosphatidylserines, one phosphatidylinositol) were downregulated in CLPinduced wildtype mice. Analytes that were only restored in the mice group WT-CLP + ibrutinib could not be determined. The heatmap with analytes that were significantly restored in the mice groups WT-CLP + ibrutinib and Xid-CLP + ibrutinib ( Figure S8 ) showed one increased primary metabolite (cholesterol) and three decreased phospholipids (two phosphatidylserines and one lysophosphatidylserine).

Parnell et al. (26) collected whole blood of patients confirmed with sepsis (and healthy participants) over a 5 day time course with the first day of collection being within the initial 24 h of admission to the ICU. RNA was extracted from whole blood and gene expression was analyzed by microarray. Three groups were collected, healthy participants, septic survivors and septic non-survivors. Dataset is available on the gene expression omnibus under GDS4791. We reanalysed this dataset for BTK expression in these three groups and found that at day 1 there is no significant differences in gene expression between healthy, septic survivors, and septic non-survivors (Figures 8A,B) . However, over the course of 5 days BTK expression increases in septic non-survivors and a significant difference between non-survivors and healthy participants as well as a significant difference between non-survivors and survivors is observed at day 5 ( Figure 8C) . There was no significant difference in BTK expression between septic survivors and healthy volunteers (Figures 8A-C) .

Sepsis is the overwhelming host response to infection (bacterial, fungal, or viral) leading to shock and multiple organ dysfunction. We have previously reported that BTK inhibitors (ibrutinib, acalabrutinib) significantly attenuate sepsis-induced cardiac dysfunction and reduced inflammatory cytokine production, but BTK inhibitors have many off target effects (14) . In the present study we investigated whether the beneficial effects are exclusively due to inhibition of BTK and how a reduction in systemic inflammation due to BTK loss of function mutation affects bacterial clearance in vivo. We addressed these questions by conducting a model of polymicrobial sepsis in Xid mice (which have a missense mutation in the BTK gene, resulting in BTK to be functionally impaired). We report here for the first time that Xid mice are protected from sepsis-induced multiple organ dysfunction (cardiac, renal, and hepatocellular) due to increased bacterial clearance and suppression of systemic inflammation (cytokine storm) (please see Figure 9 for schematic diagram of the role of BTK in the pathophysiology of sepsis).

Sepsis results in multiple organ failure including cardiac dysfunction, renal dysfunction and hepatocellular injury. We report here for the first time that Xid mice subjected to sepsis are protected from developing cardiac dysfunction, hepatocellular injury, and renal dysfunction. Most notably, ibrutinib significantly reduced sepsis-induced multiple organ failure in WT-mice but had no further beneficial effect in Xidmice subjected to CLP-indicating that the observed beneficial effect of ibrutinib in WT-mice can solely be explained by inhibition of BTK-activity. We have previously reported that inhibition of BTK by ibrutinib or acalabrutinib attenuate sepsisinduced cardiac and renal dysfunction in C57Bl/6 mice (14) and additionally we have now shown that delayed administration of ibrutinib in WT-CLP (CBA background) also attenuates sepsis-induced cardiac dysfunction, renal dysfunction, and hepatocellular injury, confirming that BTK inhibitors work in two different genetic backgrounds of mice. Furthermore, in this study we find that administration of ibrutinib (which inhibits a significant number of kinases in addition to BTK, more than acalabrutinib) in Xid-CLP mice neither results in further beneficial effects nor any adverse effects on cardiac, renal, or liver (dys)function. Inhibition of BTK reduces disease severity in animal models of sepsis-induced lung injury (30, 31) , warm liver ischemia and reperfusion (32) and spontaneous lupus nephritis (33) . Thus, we here provide evidence that inhibition of BTK alone is sufficient to prevent sepsis-induced multiple organ injury.

We then investigated the mechanism(s) by which inactivation of BTK protects mice against sepsis-induced multiple organ failure. In septic patients, an essential treatment is early source control (removal of infection), which is associated with improved outcomes (34) . We found that CLP in Xid mice results in a reduction of the number of bacteria in both peritoneum and blood (at 24 h after onset of CLP) when compared to WT-CLP mice. This may well be due to an increase in bacterial phagocytosis in Xid mice. Macrophages obtained from FIGURE 9 | Schematic diagram representing the role of Bruton's tyrosine kinase (BTK) in the pathophysiology of sepsis. LPS is released from Gram-negative bacteria which activate the TLR4 signaling pathway and the release of PepG from Gram-positive bacteria activate the TLR2 signaling pathway. BTK is involved in the activation of TLR4 and TLR2 by binding to MyD88 and TRIF thus activating their representative signaling cascades. The activation of the MyD88 signaling pathway, leads to the activation of NF-κB and the production of pro-inflammatory cytokines. Additionally, BTK activates the NLRP3 inflammasome by binding to the ASC component of the inflammasome. Once active the NLRP3 inflammasome cleaves pro-IL-1β to active IL-1β. The production of chemokines from NF-κB activation results in the recruitment of neutrophils and macrophages. Excessive inflammation from the cytokine storm and innate immune cells results in multiple organ failure/injury. The use of BTK inhibitors such as ibrutinib or acalabrutinib supress sepsis-induced inflammation and thus multiple-organ failure/injury.

Xid-mice do not show defects in in phagocytosis (35, 36) and we found that the percentage of phagocytosing cells are similar in both WT and Xid mice. We discovered, however, that macrophages obtained from Xid-mice with sepsis had taken up a significantly larger number of bacteria. This was also true for neutrophils from Xid-mice. We believe that the increase in phagocytosis by macrophages and neutrophils from Xid-mice in vivo could explain the observed increase in clearance of bacteria in peritoneum and blood. Beguem et al. (37) found that monocytes from healthy volunteers stimulated with LPS and treated with evobrutinib resulted in an increased rate of phagocytosis in vitro due to a switch of macrophages from the pro-inflammatory M1 to the pro-resolving M2 phenotype and this was associated with reduced secretion of TNF-α. In addition, Xid mice infected with Francisella tularensis showed enhanced bacterial clearance from the lung and spleen, which correlated with a significant improvement of survival when compared to wild-type controls (38) .

This raises the question of the underlying mechanisms that enables or drives increased phagocytosis in Xid-mice? Neither inhibition of BTK activity with ibrutinib nor inactivation of BTK in Xid mice affects monocyte FcγR-mediated phagocytosis, but it does supress FcγR-mediated cytokine production. The decrease of calcium flux due to BTK inhibition also does not affect phagocytosis, but does decrease cytokine production (35) . BTK inhibition results in the polarization to M2 macrophages [which have greater phagocytic ability (39) ], demonstrated by increased expression of CD206. CD206 is involved in phagocytosis of a number of bacterial strains. For example, monocyte-derived macrophages that express high levels of CD206 phagocytosed 78% of E. coli, while monocyte-derived macrophages that express low levels of CD206 only phagocytosed 30% of E. coli (40) . Excessive activation of neutrophils is known to decrease survival and enhance susceptibility to subsequent bacterial infections (41) . One mechanism that may contribute to the pathology of sepsis is the release of neutrophil extracellular traps as they contain the beneficial antimicrobial nuclear proteins but also damaging citrullinated histones, elastase, myeloperoxidase and MMP-3 (42, 43) . The release of neutrophil extracellular traps results in ineffective phagocytosis (44) . Florence et al. (31) showed that BTK was increased in the lung neutrophils and inhibiting BTK protected mice against lethal influenza by reducing the release of neutrophil extracellular traps. The decrease of neutrophil extracellular traps was also observed in human peripheral blood neutrophils incubated with influenza and BTK inhibitor (31) . However, the exact molecular mechanisms underlying this phenomenon are yet to be elucidated. Future studies are required to increase our understanding as to how Xid macrophages and neutrophils phagocytose more bacteria per immune cell.

Infiltration of the Peritoneum With Innate Immune Cells BTK plays a fundamental role in signaling and function of B cells, but BTK is also highly expressed in myeloid cells such as macrophages and neutrophils (9) and inactivation of BTK results in reduced cell-mediated inflammatory responses (45, 46) . We report here that Xid-CLP mice have reduced infiltrating innate immune cells (macrophages and neutrophils) in the peritoneum (site of infection). We propose that this may lead to a reduction of the formation of cytokines/chemokines in the serum and, hence, will prevent the cytokines storm.

Macrophages play an important role in the two phases of sepsis (early pro-inflammatory phase and the later antiinflammatory phase), as they can have either pro-inflammatory or anti-inflammatory properties. Initially, M1 macrophages (proinflammatory) activate inflammation by secreting TNF-α, IL-1β, IL-6, and IL-12 to promote the removal of the pathogen, then M2 macrophages repair tissue and resolve inflammation by secreting cytokines including IL-10 (47, 48) . If the M1 macrophage-driven pro-inflammatory response cannot be controlled, the resultant cytokine storm can be a key driver of the severity of sepsis leading to organ failure and death (49) . From our experiments we conclude that a loss of function or inhibition of BTK drives the switch from the pro-inflammatory M1 phenotype to proresolving M2 phenotype in response to LPS (50) . Here we report that macrophages obtained from septic Xid-mice have a pro-resolving M2 phenotype, whereas macrophages obtained from septic WT-mice have the M1 phenotype. Most notably, macrophages of the M2 phenotype have a greater phagocytotic function resulting in increased clearance of apoptotic cells and an acceleration of resolution (39) . Indeed, M2 macrophages protect against sepsis-induced lung injury (51) and sepsis-induced acute kidney injury (52) . Transplantation of M2 macrophages has been suggested as a potential therapeutic approach for sepsis-induced lung injury (51) .

BTK plays a pivotal role in the activation of TLRs and, hence, the signaling steps leading to the activation of NF-κB (7) , which plays a key role in the pathophysiology of septic cardiomyopathy (53) . Here we report that Xid mice subjected to polymicrobial sepsis have a reduced activation of BTK and NF-κB (measured as phosphorylation of IKKα/β and IκBα) in the heart. We have previously reported that BTK inhibitors ibrutinib or acalabrutinib reduce the activation of cardiac BTK and NF-κB in mice subjected to sepsis (14) . Furthermore, we have shown that inhibition of NF-κB activation with an inhibitor of IKK also attenuates the cardiac dysfunction associated with polymicrobial sepsis (53) . Purvis et al. (46) showed that ibrutinib treatment attenuated the activation of NF-κB and gene expression of cytokines in the diabetic kidney and liver. Thus, we propose that an impairment in the activation of BTK in Xid mice leads to reduced activation of NF-κB in the heart, which contributes to or accounts for the observed reduction in organ injury and dysfunction observed in Xid-mice with sepsis.

Activation of NF-κB leads to an increase in the production of cytokines and chemokines such as the pro-inflammatory cytokines TNF-α, IL-6, IL-1β, and the anti-inflammatory cytokine IL-10, neutrophils chemoattractant chemokines (KC & ENA-78), monocyte chemoattractant chemokines (MCP-1, MIP-1α, and MIP-1β) and G-CSF, all of which contribute to the systemic inflammation and organ dysfunction associated with sepsis (54) . Out of all these cytokines, the ones increased most in our model of murine sepsis were IL-6, KC, and MCP-1. The levels of IL-8 and monocyte chemoattractant protein-1 (MCP-1) are associated with early 48 h and 28 day mortality in sepsis patients (55) . Most notably, we report that in Xid-mice subjected to CLP-sepsis, all of these cytokines and chemokines are markedly reduced. WT-CLP mice treated with ibrutinib also show reduced production of sepsis-associated cytokines and chemokines and no difference is observed with the addition of ibrutinib to Xid-CLP mice. Thus, an impairment of BTK activation in Xid-mice prevents NF-κB and NLRP3-dependent, systemic inflammation (cytokine storm) resulting in a reduction in organ injury/dysfunction.

BTK is also involved in the assembly/activation of the NLRP3 inflammasome in both mice and humans (8, 56) . The activation of the NLRP3 inflammasome also plays a role in the pathophysiology of sepsis and septic cardiomyopathy (57) . Pharmacological inhibition of NLRP3 activation with MCC950 (NLRP3 inflammasome inhibitor) reduced the neurological and cognitive impairment in septic animals (58) . It has also been reported that genetic deficiency of NLRP3 promotes resolution of inflammation in polymicrobial sepsis (59) . We report here that the activation of the NLRP3 inflammasome (measured as NLRP3 activation, caspase-1 activation and IL-1β release) was largely reduced in Xid-mice subjected to CLP when compared to WTmice with sepsis. We previously reported that BTK inhibitors (ibrutinib or acalabrutinib) inhibit the activation of the NLRP3 inflammasome and production of IL-1β in septic animals (14) . Purvis et al. (46) showed that ibrutinib treatment also attenuated the activation NLRP3 inflammasome in the diabetic kidney and liver. Thus, we propose that prevention of the activation of the NLRP3 inflammasome secondary to reduced activation of BTK importantly contributes to the reduction in inflammation and organ dysfunction observed in septic Xid-mice.

PCA showed that 49% of the total variance of all metabolites formed three well separable clusters. The metabolomic profiles of CLP-induced WT mice formed one cluster and was clearly distinguishable from a second cluster (WT sham-operated and Xid sham-operated) and a third cluster consisting of the three groups Xid-CLP, WT-CLP + ibrutinib, and Xid-CLP + ibrutinib. The common clustering of the latter three groups supports the assumption that the inhibition of BTK alone is responsible for the partial restoration of dysregulated metabolites in sepsis.

Host defense toward bacterial infection is a complex interplay of several mechanisms including inflammation, coagulation, immune activation, hypoxia, and metabolic reprogramming. Specifically, the regulation and impact of the metabolic changes is known to play an important role in the pathophysiology of sepsis (60) . We demonstrated in this study that deregulated members of lipid mediators, phospholipids, primary metabolites and bile acids in CLP-induced WT-mice were restored by ibrutinib (in WT-mice) and/or by inactivation of the BTK gene (Xidmice). The elevated and reduced plasma levels of some restored metabolites in the WT CLP group were already shown. For example, an increased metabolism of the lipid mediators AA and EPA could be found in plasma of sepsis patients (61) . In addition, two other lipid mediators, OEA and lyso-PAF, were decreased in CLP-induced WT mice. Platelet-activating factor (PAF) is a proinflammatory mediator in systemic inflammation and its known to be upregulated in sepsis (62) . Degradation of the immediate precursor lyso-PAF is probably a result of its increased transformation to PAF (63) . The decreased levels of the lipid-amide OEA are probably a compensatory mechanism in sepsis-related weight loss and disturbed energy balance, because OEA is a modulator in food consumption and weight management and actually leads to satiation or meal termination (64) . Even the restoration of the reduced bile acid TDCA and the elevated amino acid DOPA seems to be a positive regulatory mechanism. TDCA ameliorates systemic inflammation, normalizes blood pressure, prevents kidney injury, and prolongs survival in a mouse sepsis model (65) . DOPA has anti-neuro inflammation effects and improved neuroplasticity in septic mice (66) . The plasma of the WT-CLP group showed also increased levels of isoforms of the phospholipids species lysophaphatidylserine and PS, probably due to their procoagulant activity in sepsis (67, 68) . Some primary metabolites were also enhanced in septic mice and restored by ibrutinib administration and BTK inactivation such as the dysregulated precursors (cytosine, niacinamide, nicotinic acid) of nucleotide or nicotinate and nicotinamide metabolism (69, 70) . The restoration also included the loss of carnosine to plasma due to skeletal muscle wasting in sepsis (71) and the elevated levels of creatine presumably because of the known higher activity of creatine kinase to catalyze the urgently required ATP in developing sepsis (72) . This data of restored metabolites demonstrates that Xid mice with a deficiency in BTK have a similar metabolomic profile in sepsis than WT-CLP-mice treated with ibrutinib.

In addition, the data in Figures S5,S6 reveal that Xid mice restored metabolites 7 times more than ibrutinib-treated mice ( Figure S7) . Many of the additionally restored metabolites in Xid mice are known to be deregulated in sepsis such as adenine (73) creatinine (74) , and kynurenine (75) . An explanation for the different magnitude of restored metabolites in Xid mice in comparison with ibrutinib-treated mice could be the different number of inhibited kinases. Thus, the Xid mice seem to benefit from the inhibition of only one kinase, namely BTK, which in addition to reducing cytokine storm restores the sepsis-related dysregulation of specific metabolites.

Currently the expression and/or activation of BTK in septic patients has not been reported. There are datasets available on the GEO and we reanalysed microarray data (GDS4971) of the time course of gene expression in healthy, septic survivors, and septic non-survivors published by Parnell et al. (26) . Interestingly, our analysis revealed an increase in expression of BTK in septic non-survivors, whereas BTK expression in septic survivors does not increase and is not different from healthy volunteers. Thus, increases in BTK expression in septic patients correlate with mortality, while lower levels of BTK expression are associated with survival from sepsis. There were no clear differences between cytokine expression of TNF-α, IL-6, MCP-1, CXCL1 in the three groups, expression of BTK was a better predictor of mortality rather than with the expression of any one cytokine. We have previously shown in septic mouse hearts that activation of BTK correlates with cardiac dysfunction (14) . BTK activation also increases in whole blood of COVID-19 patients which, like septic patients, also present with excessive systemic inflammation (cytokine storm) (17) .

We have shown that Xid-mice subjected to CLP have increased bacterial clearance and reduced systemic inflammation (secondary to reduced activation of the NLRP3 inflammasome and NF-κB) and cardiac (organ) dysfunction. There is good evidence that mortality of patients with sepsis increases with an increase in the number of organs failing (SOFA scores). In the UK survival studies in septic models are not routinely conducted due to ethical reasons. Thus, we were unable to investigate the survival of Xid mice undergoing sepsis. It has been reported that a reduction in temperature <30 • C or a change of temperature of 5 • C over time predicts mortality in animals with sepsis (29) . Using this more humane surrogate marker, we found that Xid mice with sepsis have a predicted mortality of 0% (100% survival), while WT-mice with sepsis would have a predicted mortality of 90% (10% survival). We found that ibrutinib does not affect predicted mortality in Xid-CLP resulting in a predicted mortality of 0% (100% survival) and that delayed administration of ibrutinib in WT-CLP mice led to a predicated mortality of 15% (85% survival). It would be useful to confirm the impact of an impairment in BTK function in Xid-mice on outcome (mortality) in a more long-term sepsis model.

We report here for the first time that genetic inactivation of BTK is responsible for conferring protection against multiple organ failure in a clinically relevant model of sepsis. Most importantly we have shown that the inactivation of BTK in Xid mice results in an increase of bacterial phagocytosis in macrophages and neutrophils, thus, increasing bacterial clearance in both peritoneum and blood. Inactivation of BTK also results in a phenotypic switch of macrophages from M1 to the M2 phenotype, which aids in the resolution of sepsis. The suppression of the immune system by inactivated BTK leads to reduced activation of NF-κB and the NLRP3 inflammasome, therefore, preventing the induction of the cytokine storm. Metabolomic analysis revealed a dysregulation of metabolites in WT septic mice. Most notably, we found that inactivation of BTK in Xid-mice or administration of ibrutinib in WT mice is responsible for the (partial) restoration of dysregulated metabolites in sepsis. As the administration of ibrutinib to Xid-CLP mice did not result in any additional (beneficial) effects on the alterations in organ dysfunction, cytokine/chemokines formation and changes in metabolites caused by sepsis, our data strongly suggest that BTK inactivation is responsible for the observed effects of ibrutinib. Lastly, we have found that BTK expression in humans is increased in the blood of septic non-survivors, while lower expression is associated with survival from sepsis. Taken together our work suggests that BTK inhibitors maybe repurposed for the use in sepsis (or other conditions associated with excessive local or systemic inflammation including COVID-19) due to their ability to reduce systemic inflammation (cytokine storm), their ability to enhance the phagocytosis of macrophages and switch macrophages from the pro-inflammatory M1 to the antiinflammatory M2 phenotype.

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

The animal study was reviewed and approved by The Animal Welfare Ethics Review Boards of Queen Mary University of 

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We would like to thank Hira Bahadur Ale for their technical assistance on the Amnis R ImageStream R X Mk II Imaging Flow Cytometer. We thank Dominik Driesch (BioControl Jena GmbH, Jena, Germany) for statistical advice with respect to metabolome analysis.

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu. 2020.581758/full#supplementary-material