key: cord-0031712-wl4t79no
authors: Wohlsein, Jan C.; Meurer, Marita; Neßler, Jasmin; Wohlsein, Peter; von Köckritz-Blickwede, Maren; Baumgärtner, Wolfgang; Tipold, Andrea
title: Detection of Extracellular Traps in Canine Steroid-Responsive Meningitis-Arteritis
date: 2022-05-03
journal: Front Vet Sci
DOI: 10.3389/fvets.2022.863579
sha: c9c5710ec15db00881c4303f3d00461a36ae4f59
doc_id: 31712
cord_uid: wl4t79no

Extracellular traps (ETs) are DNA networks formed by immune cells to fight infectious diseases by catching and attacking pathogenic microorganisms. Uncontrolled ET formation or impaired ET clearance can cause tissue and organ damage. Steroid-responsive meningitis-arteritis (SRMA) represents an immune-mediated, presumably non-infectious, purulent leptomeningitis and fibrinoid-necrotizing arteritis and periarteritis of young-adult dogs. Chronic and recurrent cases of SRMA are characterized by lymphohistiocytic inflammatory cell infiltration in the meninges and perivascular tissue. This study aimed to identify extracellular traps in dogs with SRMA, a model for immune-mediated diseases in the central nervous system (CNS). Hematoxylin and eosin-stained samples of two young dogs with chronic, recurrent SRMA were examined by light microscopy for characteristic lesions and consecutive slices of affected tissues were stained for detection of ETs by immunofluorescence microscopy using antibodies against DNA–histone-1 complexes, myeloperoxidase, and citrullinated histone H3. Histology revealed purulent and lymphohistiocytic leptomeningitis (n = 2/2) with meningeal periarteritis (n = 2/2) and periadrenal located lymphohistiocytic periarteritis (n = 1). Extracellular DNA networks and inflammatory cell infiltrates of macrophages, neutrophil granulocytes, and lymphocytes were detected in the subarachnoid space of the leptomeninx (n = 2/2) and perivascularly in meningeal (n = 2/2) as well as periadrenal vessels (n = 1/1). In summary, extracellular DNA fibers and attached ET markers are detectable in affected perivascular and meningeal tissues of dogs suffering from SRMA. The proof of principle could be confirmed that ETs are present in canine, inflammatory, and non-infectious CNS diseases and possibly play a role in the pathogenesis of SRMA.

Several immune cells of the innate immune system, including neutrophils, eosinophils, monocytes, mast cells, and basophils, are capable of producing extracellular DNA traps (ETs) (1) (2) (3) (4) (5) .

Extracellular trap formation can be differentiated in three pathways: suicidal, vital, and mitochondrial mechanisms (1, 2, (6) (7) (8) (9) (10) (11) . The term ETosis was created to define this distinct cell death apart from necrosis and apoptosis describing the suicidal pathway of ET formation (6, 12) . This particular cell death involves the resolution of nuclear membrane, decondensation of chromatin, and mixing with granule components followed by release of ETs after permeabilization of the cell membrane (1, 6) . ET-related proteins and components such as myeloperoxidase (MPO), citrullinated histone H3 (H3Cit), and DNA-histone complexes were used with antibody-based techniques to co-stain these specific ET markers (13) .

The view on ETosis and suicidal ET formation had to be renewed after a groundbreaking discovery in 2012. Pilsczek et al. (7) described viable neutrophils performing phagocytosis and migration after the release of ETs during an acute infection with Staphylococcus aureus. The term ET formation was expanded and divided up in suicidal and vital way of ET release (7, 10, 11) . Suicidal ET formation is reactive oxygen dependent and pursues after 3-8 h, whereas vital ET formation is reactive oxygen independent and performed in 5-60 min (6, 7, 14) . The third way of ET formation due to mitochondrial DNA release by viable cells is not entirely understood (9) . In this study, the term ET formation is used to resume all the different ways of creating extracellular DNA traps regardless of the cell origin and type of ET metabolism.

These extracellular DNA formations are composed of a scaffold of decondensed chromatin fibers equipped with granule proteins [e.g., myeloperoxidase (MPO) and neutrophil elastase (NE)], nuclear proteins [e.g., citrullinated histone H3 (H3Cit)], and antimicrobial enzymes forming web-like structures (1, 13, 15, 16) . Beyond phagocytosis, degranulation, and creation of reactive oxygen species, ET formation is a genuine extracellular strategy especially of neutrophils to kill, disarm, and entrap invading pathogens (1, 17, 18) .

Recently, study shifted from infectious to non-infectious diseases investigating potential impact and therapeutic opportunities of extracellular trap release and degradation. On one hand, ET formation is another effective antimicrobial mechanism of the innate immune system combating different pathogens; on the other hand, excessive ET expression, unregulated ET release, and insufficient ET clearance can cause detrimental effects and lead to or are associated with ET-related pathologies ["ETopathies" (19, 20) ]: endothelial or epithelial tissue damage (21) (22) (23) , pancreatitis (24, 25) , autoimmune diseases (26, 27) , thrombosis (16) , vasculitis (28) , and cancer (29, 30) .

In dogs, neutrophil extracellular traps (NETs) were recently described in infectious diseases such as parasitic infections with Toxoplasma gondii, Trypanosoma cruzi, and Dirofilaria immitis (31) (32) (33) and bacterial infections such as pyometra caused by Escherichia coli and Streptococcus species (34) and NETs were isolated from pleural and abdominal effusions in septic dogs (35) . However, the influence on the pathogenesis and prognosis of ET formation in canine non-infectious diseases, especially in the CNS, still has to be elucidated. NETs have an impact on the immune system in canine immune-mediated hemolytic anemia (36) (37) (38) , on clot formation and canine immunothrombosis (16, 39) .

Steroid-responsive meningitis-arteritis (SRMA) is an immune-mediated, systemic, inflammatory, and presumably non-infectious disorder predominantly in young-adult and medium-to-large-sized dogs (40) . The disease affects typically 6 to 18 month-old dogs with a possible range of 3 months to 9 years (40) (41) (42) . SRMA can occur in any dog breed, but is overrepresented in Bernese mountain dogs, Boxers, Beagles (43, 44) , Nova Scotia Duck Tolling Retrievers, Weimaraners, and Petit Basset Griffon Vendéens (45) . A German study showed a sex predisposition for male individuals (46) , but other studies do not show significant difference in sex distribution of this disease (47, 48) . The assembly of signalment, clinical signs, and laboratory findings of CSF and blood analysis associated with a quick clinical improvement after application of immunosuppressive therapy with glucocorticosteroids and an exclusion of an infectious etiology lead to the antemortem diagnosis of SRMA (40, (48) (49) (50) .

The typical, acute form of SRMA is characterized by recurrent fever, cervical hyperesthesia, neck rigidity, stiff gait, reluctance to move, and depression. Laboratory findings of the acute form include a moderate-to-severe, non-degenerative neutrophilic pleocytosis of the cerebrospinal fluid (CSF) and blood profiles show a neutrophilic leukocytosis with left shift (44, 51) . Furthermore, elevated immunoglobulin A levels in serum and CSF serve as diagnostic tool (44, 52) . Levels of acute phase proteins such as C-reactive protein, serum amyloid A, haptoglobin (53), or neutrophil gelatinase-associated lipocalin (54) are elevated in the acute disease episode compared to non-inflammatory neurological diseases. Especially, CRP is used as a remission and therapy monitoring marker (55) . Pathohistologically, the acute form is represented by a multifocal to generalized fibrinoid-necrotizing vasculitis with thrombosis and purulent leptomeningitis preferentially in the meninges of the cervical spinal cord (40, 43, (56) (57) (58) .

The atypical, chronic, and protracted form of SRMA is observed primarily due to relapses and inadequate, immunosuppressive treatment. CSF analysis predominantly reveals mononuclear cells (44) and non-suppurative, mononuclear cell infiltrates in the meninges and perivascular tissue dominate pathohistological findings (58) .

Steroid-responsive meningitis-arteritis offers ideal circumstances for the possible detection of ETs for the first time in canine central nervous system (CNS) tissue representing an immune-mediated, inflammatory, and non-infectious neuronal disorder mainly driven by a neutrophil immune response (40, 44) . ET detection in the acute phase of Kawasaki disease of children, which causes a comparable vasculitis with consecutive inducing tissue damage-like SRMA, was successful (59) (60) (61) . Consequently, we hypothesized that ETs take part in the etiopathogenesis of SRMA and a successful detection of ETs in the commonly affected tissues of meninges and vessels seems promising. This study should be a proof of principle that ETs can be detected in histologically confirmed cases of SRMA. Based on confirmation of extracellular DNA traps, corresponding clinical studies, new diagnostic, and treatment strategies could be developed.

From the archive of the Department of Pathology, two dogs were selected for this study. The inclusion criteria were signalment, reported clinical signs, pathohistological findings such as purulent or lymphohistiocytic leptomeningitis with associated arteritis or periarteritis, and no detectable pathogens with special staining such as periodic acid-Schiff-reaction, Gram's staining, Ziehl-Neelsen's staining, or Grocott's silver impregnation method. Retrospective study revealed that no further microbiological or virologic examination was conducted on serum or CSF samples of these dogs to exclude a pathogenetic etiology.

Routinely processed formalin-fixed and paraffin-embedded (FFPE) tissues of the affected dogs were selected from the block archive of the Department of Pathology for further histopathologic and immunofluorescent examination.

Regions of affected tissue of the cervical spinal cord with associated leptomeningeal vessels and peripheral, particularly periadrenal vessels were embedded in paraffin and cut at 2-4 µm for H&E and immunofluorescence staining. H&E staining of the affected tissue was performed by automated dying in Leica ST4040 (Leica, Wetzlar, Germany) with 0.1% hematoxylin (Roth, Karlsruhe, Germany) and 1% eosin (Roth, Karlsruhe, Germany). The presence of vascular and meningeal lesions was evaluated qualitatively by a board certified veterinary pathologist [the European College of Veterinary Pathologists (ECVP)] with special emphasis on neutrophilic and inflammatory cell invasion in the vascular walls or meninges. The H&E slides were examined microscopically on an Olympus BX53 (Olympus, Tokyo, Japan) light microscope. Pictures were edited with ImageJ software (version 1.53, National Institutes of Health, USA).

For ET detection, unstained, native paraffin slides of affected tissues of the spinal cord, brain, and periadrenal arteries were analyzed. Co-staining of DNA-histone-1 complexes and MPO or H3Cit was performed according to the following protocol as previously described (62, 63) with the following changes.

After permeabilization for 10 min (0.1% Triton X-100) and blocking for 20 min (blocking buffer for co-staining of DNA-histone-1 complexes and MPO: 5% bovine serum albumin, 5% goat serum, 2% cold water fish gelatin, 0.05% Tween-20, and 0.05% Triton X-100; blocking buffer for costaining of DNA-histone-1 complexes and H3Cit: 10% fetal calf serum, 2% bovine serum albumin, 0.05% Tween-20, and 0.1% Triton X-100), samples were incubated overnight at 4 • C using the following first antibodies, diluted in respective blocking buffer: mouse monoclonal IgG2a anti-DNA/histone (Millipore MAB3864, Billerica, Massachusetts, USA; 0.55 mg/ml; 1:100) and rabbit antihuman myeloperoxidase (Dako, A0398, 3.3 mg/ml, 1:300) or rabbit antihuman H3Cit (citrulline R2 + R8 + R17) antibody (Abcam, ab5103, Cambridge, UK, 1 mg/ml, 1:31.6). For isotype control, murine IgG2a (from murine myeloma M5409, Sigma Aldrich, Munich, Germany, 0.2 mg/ml, 1:36.4) and rabbit immunoglobulin G (IgG) (from rabbit serum I5006, Sigma Aldrich, Munich, Germany, 1.16 mg/ml, 1:108.75 for staining of DNA-histone-1 complex and MPO 1:36.7 for staining of DNA-histone-1 complex and H3Cit) were used. The secondary staining was performed for 1 h in the dark at room temperature using a goat anti-rabbit Alexa 633conjugated antibody (Invitrogen, Carlsbad, California, USA, 2 mg/ml, 1:500) and a goat anti-mouse Alexa 488-conjugated antibody (Invitrogen, Carlsbad, California, USA, 2 mg/ml, 1:500). Counterstaining of DNA was performed with aqueous Hoechst 33342 (Sigma B-2261, St. Louis, Missouri, USA, 0.5 mg/ml, 1:1,000) for 10 min. At the end, all the samples were processed with the TrueVIEW Autofluorescence Quenching Kit (Vector laboratories, San Francisco, California, USA) following the manufacturer's instructions and covered with Mounting Medium of the TrueVIEW Autofluorescence Quenching Kit (Vector laboratories, San Francisco, California, USA).

Serial cuts of histopathologically altered tissues were stained and analyzed, whether ET formation or ET markers were detectable. Neutrophils and macrophages infiltrating the subarachnoid space, meningeal arteries, and extraneural perivascular tissue of SRMA-affected dogs are capable of releasing extracellular DNA fibers consisting of ET-markers such as DNA-histone-1 complexes, attached MPO, or H3Cit, which is a typical and strong evidence of ET formation (1, (64) (65) (66) .

Extracellular trap formation was semiquantitatively analyzed in the meninges of the spinal cord and affected vessels. The amount of ET formation was counted in five 400 µm × 400 µm fields (0.16 µm 2 ) of affected tissues of each dog and compared to each other ( Table 1) .

The stained samples were examined microscopically on a Leica TCS SP5 AOBS confocal inverted-base fluorescence microscope with HCX PL APO 40 × 0.75-1.25 oil immersion objectives with an Argon 405 and 633 nm laser (Leica, Wetzlar, Germany). The settings were adjusted using isotype control antibodies in separate preparations. Pictures were edited with ImageJ software (version 1.53, National Institutes of Health, USA).

Two dogs were included with histological lesions indicative of acute and chronic SRMA. The first dog was an 11 months old, male Bernese mountain dog. Anamnestically, this dog had recurrent episodes of pyrexia up to 41 • C and lameness. Laboratory findings revealed moderate leukocytosis of 25,000/µl (Figures 3A, 4A) and semiquantitatively more affected than the meninges of the Bernese mountain dog ( Figure 1A ).

and elevated protein content of the CSF [positive Pandyreaktion (+)]. Initial treatment was started with doxycycline and prednisolone for an unknown period and clinical signs were ameliorating. 3 weeks after terminating the medication, the dog relapsed and showed similar clinical signs with episodes of fever and leukocytosis of 28,000/µl. Another treatment with prednisolone was initiated and the dog was anesthetized for further diagnostics, but developed cardiorespiratory arrest. After unsuccessful resuscitation, it was sent to the Department of Pathology for necropsy. Necropsy revealed only agonal gross changes. Pathohistological evaluation of the cervical spinal cord revealed infiltration of neutrophils, macrophages, lymphocytes, and plasma cells resulting in a moderate diffuse, purulent, and lymphohistiocytic leptomeningitis ( Figure 1A) . Extraneural findings showed moderate infiltrations of lymphocytes, macrophages, and plasma cells causing a subacute to chronic, diffuse lymphohistiocytic, periadrenal periarteritis (Figure 2A) . The second dog was a 5-month-old, female, Petit Basset Griffon Vendéen, which was euthanized because of a pleural effusion causing dyspnea and additional acute kidney injury (urea in the aqueous humor: 180 mg/dl). The history revealed undulating fever episodes of unknown origin and relapsing episodes of forelimb lameness. No treatment strategies were attached to the submission report of this dog. Anamnestically, another littermate was affected with comparable clinical signs. Necropsy revealed diffuse subdural hemorrhage expanding from the cerebellum throughout the dural tube. A circumferential dark red mass was located in the precardiac mediastinum (4 cm × 4 cm × 3 cm). In the thoracic cavity, there was a hemothorax, consisting of partially clotted 300 ml in the left and 100 ml in the right pleural cavity. Pathohistologically the leptomeninx of the cervical spinal cord was moderately-to-severely infiltrated with neutrophils, macrophages, lymphocytes, and plasma cells showing a severe, subacute, multifocal, lymphohistiocytic leptomeningitis accompanied with severe subarachnoid hemorrhage with erythrophagocytosis ( Figure 3A) . Cervical meningeal arteries revealed mild periarterial infiltration of lymphocytes, macrophages, and few neutrophils resulting in a moderate, acute, diffuse, lymphohistiocytic periarteritis with an intraluminal thrombus formation and meningeal hemorrhage ( Figure 4A) .

Both the dogs showed features of chronic-active and acute neural and extraneural histopathologic lesions that are characteristically observed in undulating clinical courses of SRMA (44, 67) . The severity of meningeal inflammatory infiltration of the Bernese mountain dog was lower than of the Petit Basset Griffon Vendéen.

As a next step, we used fluorescence microscopy to visualize formation of ETs in the biopsies. Since the major backbone of ETs is DNA, DNA intercalating dyes are widely used to stain ETs based on the electrostatic interactions of these dyes, e.g., 4 ′ , 6-diamidino-2-phenylindole (DAPI) with DNA (13). However, this method cannot discriminate between DNA derived from ET-releasing cells vs. necrosis. Furthermore, it has to be considered that some granule components such as antimicrobial peptides block the visualization of ETs by DNA-intercalating dyes (68) . Therefore, antibody-based techniques that stain ET-specific markers such as DNA-histone complexes in combination with cell-specific proteins that are frequently found associated with ETs such as myeloperoxidase are needed to confirm release of ETs by immunofluorescence microscopy (13, (68) (69) (70) .

Using this technique, the lymphohistiocytic, periadrenal periarteritis of the Bernese mountain dog showed mild presence of DNA-histone-1 complex positive web-like structures and moderate, extracellular MPO signal surrounding infiltrating macrophages. ET formation appeared perivascularly and intraluminally, but was not to be found in the vascular walls (Figures 2B,C; Table 1 ). These ET detections were similar to histopathological findings, which showed only perivascular inflammatory cell infiltration. Meningeal lesions occurred in contrast to perivascular lesions with mild infiltration of neutrophils next to macrophages and lymphocytes. Mild-tomoderate detection of extracellular DNA-histone-1 complexes and MPO as ET markers could visualized in the meninges of the spinal cord around infiltrating neutrophils (Figures 1B,C) . To sum up pathohistological as well as immunofluorescent findings, ET formation could present in the meninges and extraneural arteries of this dog. Extracellular trap markers in terms of extracellular DNAhistone-1 complexes and MPO were also positive in the meninges of the Petit Basset Griffon Vendéen. Infiltrating neutrophils, macrophages, and lymphocytes causing a purulent to lymphohistiocytic leptomeningitis are forming ETs proven by DNA-histone-1 complex, MPO, and H3Cit signals in this affected area (Figures 3B,C, 4B,C) . Summarizing pathohistological and immunofluorescent findings of this dog, ETs were present at the time of death in damaged meninges and meningeal arteries. Respective isotype control images did not show any signal intensity at DNA-histone-1 complex, MPO, or H3Cit settings.

In this study, we could proof our hypothesis that ET formation and ET markers of two representative dogs suffering from SRMA are detectable and visualizable in typical affected tissues such as meninges of the cervical spinal cord and neural, as well as extraneural vessels. To the best of the author's knowledge, this is the first study confirming the presence of extracellular DNA formations composed of DNA-histone-1 complexes, MPO, or H3Cit in the CNS of dogs and especially affected with SRMA.

ET formation was present in acute and chronic-active lesions of recurrent, waxing-waning disease periods of both the dogs, implicating that this mechanism of the immune system seems to play a certain role in the pathogenesis of SRMA.

As hallmark of the pathogenesis of SRMA, neutrophils conquer the subarachnoid space causing a neutrophil pleocytosis of the CSF (44) . The detailed mechanism of this immune compartmentalization is not fully understood. Neutrophil recruitment to vascular wall adhesion is mediated by CD11a upregulation (51) and a possible factor of the blood-brain barrier disruption is caused by releasing matrix metalloproteinases-2 and−9 (MMP-2/-9) (71). Khandpur et al. (27) positively correlate the amount of netting neutrophils and production of interleukin-17 (IL-17). These findings could be supported by Freundt-Revilla et al. (72) that production of IL-17 ensures neutrophil granulocyte recruitment in the CNS compartment and disruption of the blood-brain barrier in dogs with SRMA. IL-17 production in dogs with SRMA can lead to increased NET formation and may facilitate the leukocyte extravasation of neutrophils by disrupting the blood-brain barrier.

We hypothesize that ET formation interdigitates with the current detailed knowledge of immunologic dysregulation causing SRMA (43) . Recently, it was shown that ET formation promotes vasculopathies (73) and externalization of ETassociated proteins such as histones and MPO leads to vascular barrier injury (23, 74, 75) . Especially, histones are described in small-vascular angiopathies to drive vascular damage and vascular wall necrosis (23, 74, 75) . The positive evidence of H3Cit in the meningeal arteries could be another explanation to the invasion and compartmentalization of neutrophils in the subarachnoid space with associated hemorrhage and frequently detected fibrinoid-necrotizing arteritis in SRMA (43) .

Furthermore, histones as major proinflammatory components of extracellular released DNA traps may drive and perpetuate the innate immune response and maintain persistent sterile inflammation in SRMA through interaction with Toll-like receptor (TLR) 4 (76) (77) (78) . Being part of pattern recognition receptors (PRRs), TLRs play a crucial role of the innate immune system and stimulating the adaptive immune response (79) . They are able to recognize foreign, pathogen-associated molecular patterns (PAMPs) in infectious diseases, as well as host-derived damage-associated molecular patterns (DAMPs) The upregulation of this PRR on immune cells mediating the pathogenesis of SRMA such as neutrophils and macrophages illuminates chronic inflammation and autoimmunity and may be attributed due to higher levels of H3Cit (82, 83) .

In addition, higher concentration of intrathecal produced extracellular heat shock protein 70 (eHSP70) as representative example of the DAMP family may interact with TLR4 (84) . Continuous activation of neutrophils releasing their ETs due to interaction with DAMPs such as citrullinated histones or other host-derived self-antigens such as eHSP70 can lead to a vicious circle of autoimmunity and supporting the theory of existing autoantigenic triggers (14, 85) . Based on these findings, the hypothesis of an existing self-antigen or environmental trigger acting according to the hit-and-run principle must be requested.

Furthermore, the externalization of ETs is the source of major autoantigens for autoantibody formation and is supposed to be pathogenic in several autoimmune-derived diseases (86) . Until now, autoantibodies against endogenous CNS tissue only serve as "epiphenomenon" of SRMA (40, 87) . If the presence of these major autoantigenetic in terms of ET-associated structures drive and maintain immunologic processes in meninges and vessels of these dogs, the complex pathogenesis of SRMA could be well explained.

Histopathological and immunofluorescent findings (Figures 1-4) of acute and chronic lesions in both the dogs represented by mainly lymphohistiocytic, as well as neutrophils invading meninges or perivascular spaces could be explained with prolonged activation of macrophages and neutrophils generating ETs or an impaired self-clearance of ETs. Remnants of ETs could serve as constant trigger in terms of DAMPs for immune cells maintaining CNS and vascular inflammation resulting in continuous invasion of neutrophils in this already chronic process. Both the dogs showed similar pathohistologic lesions of chronic active inflammation at the time of death with different amount of ET formation ( Table 1 ). In general, the meninges of the Petit Basset Griffon Vendéen were infiltrated more severely than in the Bernese mountain dog. This could be explained by a more acute and severe clinical course of the Petit Basset Griffon Vendéen in contrast to the Bernese mountain dog. Another explanation could be the different pharmacological influence of variably administered antiinflammatory drugs. Primarily perivascular detection of ETs was present in affected arteries.

Generating histological samples in the future will be very unlikely because clinical diagnosis, treatment management, and awareness of this disease reduced the mortality of SRMA in the last decades (44, 46, 88) . Therefore, prospective clinical studies could confirm antemortem evidence of ETs in dogs measuring ET markers and correlating ET inducers in clinical accessible samples of serum and CSF such as H3Cit and cell-free DNA. Visualization or stimulation assays of ETs released by isolated nucleated cells in CSF samples in acute diseased, treated, and relapsed dogs with SRMA offer another possibility supporting the results of this study. Comparing ET markers to dogs with other inflammatory as well as non-inflammatory CNS diseases of infectious and non-infectious origin is necessary to probably underline and distinguish the final role of ETs in the pathogenesis of SRMA.

Treatment of autoimmune and immune-mediated diseases in veterinary medicine is lacking of specific therapeutic options such as the usage of recombinant monoclonal antibodies, intracellular pathway modulating, or receptor-targeting drugs (89) . Also, steroid therapy is associated with many undesirable side effects and 30% of human patients are identified as "non-responders" or resistant to glucocorticoid application (88, 89) . Specific ETtargeting therapeutics options with fewer side effects such as DNases (90) exist in human medicine and urge to be tested in veterinary medicine. SRMA represents an ideal large animal model of suppurative, non-infectious meningitis with proven ET formation to evaluate and develop new therapeutics in future research studies in a translational context (81) . Based on this pilot study of ET formation in the CNS of dogs, clinical studies will be performed investigating the influence on canine neuropathies.

In conclusion, ETs are detectable in tissue samples of necropsied SRMA cases. This study represents the first trial to proof of principle of ET visualization in canine central nervous system tissue. The detection of ETs in SRMA gains new possibilities to explore the existence and etiopathogenetic influence of this host mechanism of immune cells in infectious and non-infectious canine neuropathies. To give an outlook, a magnitude of study is required concerning clinical importance of innovative diagnostics tools as remission and therapy marker and the development of specific, ET-targeting therapeutic options with fewer side effects than conventional glucocorticoid therapy.

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

AT, WB, MvK-B, and JN conceived, designed, and supervised the study. JW and MM performed all the experiments, analyzed the data, and performed immunofluorescence staining and microscopy. JW drafted the manuscript. 

Special thanks to the laboratory technicians of the Department of Pathology Julia Baskas and Carolin Schütz for supplying slides for H&E and immunofluorescence staining.

Neutrophil extracellular traps kill bacteria

Catapultlike release of mitochondrial DNA by eosinophils contributes to antibacterial defense

Identification of macrophage extracellular trap-like structures in mammary gland adipose tissue: a preliminary study

Phagocytosis-independent antimicrobial activity of mast cells by means of extracellular trap formation

NADPH oxidase-independent formation of extracellular DNA traps by basophils

Novel cell death program leads to neutrophil extracellular traps

A novel mechanism of rapid nuclear neutrophil extracellular trap formation in response to staphylococcus aureus

The immune system throws its traps: cells and their extracellular traps in disease and protection

Viable neutrophils release mitochondrial DNA to form neutrophil extracellular traps

Infectioninduced NETosis is a dynamic process involving neutrophil multitasking in vivo

NETosis: how vital is it? Blood

ETosis: a novel cell death pathway

How neutrophil extracellular traps become visible

Neutrophil extracellular traps in immunity and disease

Neutrophil extracellular traps in the second decade

Neutrophil-extracellular traps, cellfree DNA, and immunothrombosis in companion animals: a review

Neutrophil extracellular traps: is immunity the second function of chromatin?

NETopathies? unraveling the dark side of old diseases through neutrophils

An emerging role for neutrophil extracellular traps in non-infectious disease

Neutrophil extracellular traps directly induce epithelial and endothelial cell death: a predominant role of histones

Proteins derived from neutrophil extracellular traps may serve as self-antigens and mediate organ damage in autoimmune diseases

Citrullinated histone 3 causes endothelial barrier dysfunction

Neutrophil extracellular traps induce trypsin activation, inflammation, and tissue damage in mice with severe acute pancreatitis

]and the pH regulate the capacity of neutrophils to form nets

Netting neutrophils are major inducers of type I IFN production in pediatric systemic lupus erythematosus

NETs are a source of citrullinated autoantigens and stimulate inflammatory responses in rheumatoid arthritis

Netting neutrophils in autoimmune small-vessel vasculitis

Cancers predispose neutrophils to release extracellular DNA traps that contribute to cancer-associated thrombosis

Author correction: neutrophils support lung colonization of metastasis-initiating breast cancer cells

Toxoplasma gondii triggers neutrophil extracellular traps release in dogs

Extracellular trap formation in response to trypanosoma cruzi infection in granulocytes isolated from dogs and common opossums, natural reservoir hosts

Dirofilaria immitis microfilariae and third-stage larvae induce canine netosis resulting in different types of neutrophil extracellular traps

Bacteria causing pyometra in bitch and queen induce neutrophil extracellular traps

novel approach to identifying and quantifying neutrophil extracellular trap formation in septic dogs using immunofluorescence microscopy

Cell-free DNA and dnase activity in dogs with immune-mediated hemolytic anemia

Dogs cast nets too: canine neutrophil extracellular traps in health and immunemediated hemolytic anemia

Neutrophil extracellular traps in plasma from dogs with immune-mediated hemolytic anemia

Canine neutrophil extracellular traps enhance clot formation and delay lysis

An update on steroid responsive meningitis-arteritis

Long-term treatment of dogs with steroid-responsive meningitis-arteritis: clinical, laboratory and therapeutic results

Polyarteritis in a colony of beagles

Veterinary Neuranatomy and Clinical Neurology

Steroid responsive meningitis-arteritis in dogs: long-term study of 32 cases

Steril-eitrige meningitis-arteriitis (SRMA) bei drei wurfgeschwistern der rasse petit basset griffon vendéen

Steroid-responsive meningitis-arteritis in dogs in germany: are there epidemiological or clinical factors influencing recurrence rate?

Harcourt-Brown TR. The impact of demographic, social, and environmental factors on the development of steroid-responsive meningitis-arteritis (SRMA) in the United Kingdom

Steroid responsive meningitis-arteritis: a prospective study of potential disease markers, prednisolone treatment, and longterm outcome in 20 dogs

Screening diagnostics to identify triggers in 21 cases of steroid-responsive meningitis-arteritis

Clinical reasoning in canine cervical hyperaesthesia: which presenting features are important?

Selective CD11a upregulation on neutrophils in the acute phase of steroid-responsive meningitisarteritis in dogs

Determination of immunoglobulin a concentrations in the serum and cerebrospinal fluid of dogs: an estimation of its diagnostic value in canine steroid-responsive meningitis-arteritis

Concentrations of acute-phase proteins in dogs with steroid responsive meningitis-arteritis

Measurement of neutrophil gelatinase-associated lipocalin concentration in canine cerebrospinal fluid and serum and its involvement in neuroinflammation

Biomarkers of noninfectious inflammatory CNS diseases in dogs: where are we now? part 2 -steroid responsive meningitis-arteritis

Canine meningitis. a changing emphasis

Neuroimmunological studies in steroid-responsive meningitis-arteritis in dogs

Veterinary Neuropathology: Essentials of Theory and Practice

Immunologic abnormalities in canine juvenile polyarteritis syndrome: a naturally occurring animal model of kawasaki disease

Enhanced formation of neutrophil extracellular traps in kawasaki disease

Neutrophil extracellular trap from kawasaki disease alter the biologic responses of pbmc

Neutrophil extracellular trap formation in the Streptococcus suis-infected cerebrospinal fluid compartment

Degraded neutrophil extracellular traps promote the growth of Actinobacillus pleuropneumoniae

Histone hypercitrullination mediates chromatin decondensation and neutrophil extracellular trap formation

PAD4 mediated histone hypercitrullination induces heterochromatin decondensation and chromatin unfolding to form neutrophil extracellular trap-like structures

Thrombosis: tangled up in nets

Pathologic features of naturally occurring juvenile polyarteritis in beagle dogs

The antimicrobial peptide LL-37 facilitates the formation of neutrophil extracellular traps

Induction and quantification of neutrophil extracellular traps

Diverse stimuli engage different neutrophil extracellular trap pathways

Marked MMP−2 transcriptional up-regulation in mononuclear leukocytes invading the subarachnoidal space in aseptic suppurative steroidresponsive meningitis-arteritis in dogs

Th17-skewed immune response and cluster of differentiation 40 ligand expression in canine steroid-responsive meningitis-arteritis, a large animal model for neutrophilic meningitis

Neutrophil extracellular traps in vasculitis, friend or foe?

Neutrophilmediated vascular barrier injury: role of neutrophil extracellular traps

Neutrophil extracellular trap-related extracellular histones cause vascular necrosis in severe gn

Damage-associated molecular pattern-activated neutrophil extracellular trap exacerbates sterile inflammatory liver injury

DNA, and citrullination promote neutrophil extracellular trap inflammation by regulating the localization and activation of TLR4

Platelet TLR4 activates neutrophil extracellular traps to ensnare bacteria in septic blood

Toll-like receptors

Janeway's Immunobiology

Toll-like receptors 4 and 9 are responsible for the maintenance of the inflammatory reaction in canine steroid-responsive meningitis-arteritis, a large animal model for neutrophilic meningitis

The role of innate immunity in the induction of autoimmunity

Toll-like receptors in systemic autoimmune disease

Extracellular hsp70 release in canine steroid responsive meningitis-arteritis

Damps and nets in sepsis

Neutrophil extracellular traps (nets) take the central stage in driving autoimmune responses

Autoantibodies against structures of the central nervous system in steroid responsive meningitis-arteriitis in dogs

Relapses in dogs with steroidresponsive meningitis-arteritis

Immunomodulatory drugs and their application to the management of canine immune-mediated disease

Consideration of dornase alfa for the treatment of severe COVID-19 acute respiratory distress syndrome

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fvets. 2022.863579/full#supplementary-material