Open Access

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

  • Jessica Freundt-Revilla1, 6Email author,
  • Arianna Maiolini1,
  • Regina Carlson1,
  • Martin Beyerbach2,
  • Kai Rentmeister3,
  • Thomas Flegel4,
  • Andrea Fischer5 and
  • Andrea Tipold1, 6
Journal of Neuroinflammation201714:20

DOI: 10.1186/s12974-016-0784-3

Received: 28 July 2016

Accepted: 26 December 2016

Published: 23 January 2017

Abstract

Background

Steroid-responsive meningitis-arteritis (SRMA) is an immune-mediated disorder characterized by neutrophilic pleocytosis and an arteritis particularly in the cervical leptomeninges. Previous studies of the disease have shown increased levels of IL-6 and TGF-ß1 in cerebrospinal fluid (CSF). In the presence of these cytokines, naive CD4+ cells differentiate into Th17 lymphocytes which synthesize interleukin 17 (IL-17). It has been shown that IL-17 plays an active role in autoimmune diseases, it induces and mediates inflammatory responses and has an important role in recruitment of neutrophils. The hypothesis of a Th17-skewed immune response in SRMA should be supported by evaluating IL-17 and CD40L, inducing the vasculitis.

Methods

An enzyme-linked immunosorbent assay (ELISA) was performed to measure IL-17 and CD40L in serum and CSF from a total of 79 dogs. Measurements of patients suffering from SRMA in the acute state (SRMA A) were compared with levels of patients under treatment with steroids (SRMA T), recurrence of the disease (SRMA R), other neurological disorders, and healthy dogs, using the two-part test. Additionally, secretion of IL-17 and interferon gamma (IFN-γ) from the peripheral blood mononuclear cells (PBMCs) was confirmed by an enzyme-linked immunospot (ELISpot) assay.

Results

Significant higher levels of IL-17 were found in CSF of dogs with SRMA A compared with SRMA T, other neurological disorders and healthy dogs (p < 0.0001). In addition, levels of CD40L in CSF in dogs with SRMA A and SRMA R were significantly higher than in those with SRMA T (p = 0.0004) and healthy controls (p = 0.014). Furthermore, CSF concentrations of IL-17 and CD40L showed a strong positive correlation among each other (rSpear = 0.6601; p < 0.0001) and with the degree of pleocytosis (rSpear = 0.8842; p < 0.0001 and rSpear = 0.6649; p < 0.0001, respectively). IL-17 synthesis from PBMCs in SRMA patients was confirmed; however, IL-17 is mainly intrathecally produced.

Conclusions

These results imply that Th17 cells are inducing the autoimmune response in SRMA and are involved in the severe neutrophilic pleocytosis and disruption of the blood-brain barrier (BBB). CD-40L intrathecal synthesis might be involved in the striking vasculitis. The investigation of the role of IL-17 in SRMA might elucidate important pathomechanism and open new therapeutic strategies.

Keywords

Steroid-responsive meningitis-arteritis (SRMA) Interleukin-17 (IL-17) Cluster of differentiation 40 ligand (CD40L) Interferon gamma (IFN-γ) Cerebrospinal fluid (CSF) Serum Canine

Background

Steroid-responsive meningitis-arteritis (SRMA) is the most frequently diagnosed meningitis in canines [1]. It is a systemic immune-mediated disorder [2] characterized by systemic inflammatory lesions of the vessels, but particularly in the cervical leptomeninges [3, 4] and in a recognized large animal model for neutrophilic meningitis [5]. This disorder affects typically young adult dogs [6], can occur in any breed, although beagles, boxers, Bernese mountain dogs [3, 7], Weimaraners, Nova Scotia duck tolling retrievers [2], and Petit Basset Griffon Vendéen [8] are over-represented.

Two different forms of SRMA are recognized, a typical acute form and a protracted atypical form [7]. In the acute one, common clinical signs include fever, reluctance to move, stiff gait, cervical rigidity, and pain [3]; the analysis of cerebrospinal fluid (CSF) reveals a marked polymorphonuclear pleocytosis and elevated protein [7]. The protracted form may be observed following relapses and neurological deficits like reduced menace response, anisocoria, strabismus, and variable degrees of paresis and ataxia might occur; CSF analysis at this stage reveals mononuclear or mixed cell populations [7].

The etiology of SRMA remains unknown, even a genetic predisposition was described in Nova Scotia duck tolling retrievers [9]. Up to now, no infectious agents eliciting the disease have been consistently detected [4, 6, 7, 1012]. Several studies [1317] confirmed an immune-mediated disease. Furthermore, high concentrations of immunoglobulin A (IgA) have been found both intrathecally and systemically in dogs affected with SRMA [13, 18].

A predominance of T helper lymphocytes (CD4+) in the peripheral blood [15] with a prominent Th2-mediated immune response in dogs suffering from SRMA was shown [17]. Furthermore, increased levels of interleukin 6 (IL-6) and transforming growth factor beta 1 (TGF-ß1) have been found in CSF. A combined intrathecal increase of these proteins could induce CD4+ progenitors to differentiate to the recently discovered third T helper subset (Th17) and enhance the autoimmune response in SRMA [14].

Interleukin 17 (IL-17) synthesizing cells are known to be involved in the pathogenesis of several autoimmune diseases [1922]. IL-17 is a pro-inflammatory cytokine secreted primarily not only by activated T cells [23] but also by neutrophils [24], eosinophils [25], and monocytes [26] and acts on the IL-17 receptor (IL-17R) [27]. Furthermore, IL-17 has a role, coordinating local tissue inflammation through the induced release of pro-inflammatory and neutrophil-mobilizing cytokines [28, 29]. It has been shown to disrupt tight junctions between the endothelial cells of the blood-brain barrier in humans [30]. These mechanisms might explain an influence of IL 17 on the massive invasion of neutrophils into the subarachnoidal space in dogs affected with SRMA.

The CD40 Ligand or CD154 is primarily expressed on the surface of activated CD4+ T cells [31]. However, activated T cells not only express CD40L on their membranes, but a soluble, biologically active form of CD40L also interacts with the CD40 receptor [32] expressed mainly by B cells but also by many other cells [31]. The vascular endothelial cells express the CD40 receptor, and its interaction with CD40L leads to endothelial cell activation and leukocyte adhesion [33].

In the current study, we hypothesized the following: (1) that a Th17-skewed immune response is involved in the inflammatory reaction in SRMA and should be confirmed by evaluating IL-17 systemically, intrathecally, and at the cellular level; (2) that a dysregulated expression of CD40L is presumably involved in the pathogenesis of SRMA. Upon confirmation of a Th17-skewed immune response, new treatment strategies directly influencing this cell population could be evaluated in this model.

Methods

Serum and cerebrospinal fluid samples

Ninety-eight serum and 98 CSF samples were collected between 2005 and 2015, aliquoted and stored at −20 °C until determination of IL-17 and CD40L concentrations by a sandwich enzyme-linked immunosorbent assay (ELISA) was performed. Samples were taken from client-owned patients and controls derived from healthy university-owned beagles of the University of Veterinary Medicine Hannover, Germany. This study was conducted in accordance with the ethical guidelines of the University of Veterinary Medicine Hannover and was approved by the authorities of Lower Saxony (Animal experiment number 33.9-42502-05-14A453). CSF samples were collected by suboccipital puncture of the dogs under general anaesthesia, and serum samples were obtained by puncture of the cephalic or saphenous peripheral vein. All control dogs had routine CSF parameters in physiological ranges relating to the cell count (0–3 cells/μl), glucose (60–80% of the blood glucose concentration), and protein (less than 25 mg/dl) [34]. CSF samples with severe blood contamination were excluded, and in ten inflammatory CSF samples, a slightly elevated erythrocyte count was detected reflecting the vasculitis in SRMA [35]. Clinical and neurological examinations in all the healthy control dogs revealed no pathological findings. Client-owned patients were divided into four groups: SRMA in the acute stage (SRMA A), SRMA showing relapses of the disease (SRMA R), SRMA under treatment with glucocorticosteroids (SRMA T), and miscellaneous (neoplasia, intervertebral disc herniation (IVDH), fever of unknown origin, and meningoencephalitis of unknown origin (MUO).

SRMA in the acute stage was defined by occurrence of cervical rigidity and pain, fever, and polymorphonuclear pleocytosis in the CSF. IgA content in serum and CSF was determined to support diagnosis of SRMA as previously described [7]. Other possible causes of neck pain, elevated body temperature and/or pleocytosis were ruled out. Patients in the SRMA A group were not pre-treated with glucocorticosteroids prior to CSF puncture. Clinical signs, previous/ongoing treatment and CSF parameters for the three stages of the disease (SRMA acute, SRMA relapse and SRMA under treatment) at the time of sampling were considered as previously described [14].

EDTA blood samples

Fresh ethylenediaminetetraacetic acid (EDTA) blood samples were prospectively collected from 18 healthy university-owned beagles and 96 client-owned patients suffering from different neurological disorders between 2014 and 2015 at the Department of Small Animal Medicine and Surgery, University of Veterinary Medicine Hannover, Germany. The diagnosis of the neurological disorder was performed by a resident or a diplomate of the European College of Veterinary Neurology (ECVN). Diagnoses were based on clinical signs, neurological examination, complete blood cell count, blood chemistry, CSF analysis, different imaging techniques, electrophysiology, surgery, and/or histopathology when needed. EDTA blood was immediately processed after sampling for isolation of the peripheral blood mononuclear cells (PBMCs), which were subsequently used for the ELISpot assays.

PBMCs isolation and freezing

The mononuclear cell fraction was separated by density gradient centrifugation, using Histopaque®-1.199 (N° 11191, Sigma-Aldrich®, Saint Louis, USA) and Pancoll human 1.077 (N° P04-60500, Pan Biotec™) as described before [36]. Isolated PBMCs were washed three times with phosphate-buffered saline (PBS buffer: 8.00 g NaCl, 0.20 g KCl, 1.15 g Na2HPO4, 0.20 g KH2PO4, in 1000-ml ultrapure water, pH 7.4). When the cell pellet was contaminated with erythrocytes, hypotonic lysis was performed using purified water and double-concentrated PBS. Subsequently, the number of viable cells was determined by staining with Tryptan blue solution 0.4% (N° T6146, Sigma-Aldrich®, Saint Louis, USA) in PBS. The cells were resuspended and diluted to a concentration of 40 × 106 cells/ml in an ice-cold Roswell Park Memorial Institute 1640 medium with l-glutamine phenol red (RPMI 1640 Medium, 21875-034, Gibco®) and 15% serum replacement-1 (S0638, Sigma-Aldrich®, Saint Louis, USA). The following steps were performed on ice: 0.5 ml of cell suspension was dispensed in labelled cryovials and ice-cold RPMI 1640 medium with l-glutamine, 15% serum replacement-1, and 20% dimethyl sulfoxide (DMSO, Sigma-Aldrich®, Saint Louis, USA) was added slowly to obtain a final cell suspension of 20 × 106 cells/ml. Finally, the cryovials were placed immediately in a freezing container (N°5100-0001, Fisher Scientific GmbH, Schwerte, Germany) and stored at −90 °C. After >24 h the cryovials containing the cell suspension were stored at −150 °C until further analysis.

Determination of IL-17 and CD40L concentrations in CSF and serum

Both proteins were measured in CSF and serum samples using sandwich enzyme-linked immunosorbent assay commercial kits to detect canine IL-17 (SEA063Ca, Cloud-Clone Corp., Houston, USA) and canine CD40L (SEA119Ca, Cloud-Clone Corp., Houston, USA), following the manufacturer’s protocols. Briefly, CSF, serum samples, and standards of the tested proteins were diluted to the desired dilutions. Samples were diluted in 0.01 mol/L PBS, pH 7.0–7.2. Final dilution for most SRMA A and SRMA R samples was of 1:8 for IL-17 in CSF as most of these samples exceeded the maximal detectable value. Standard or samples were added in duplicates (100 μl per well) in 96-well pre-coated plates and incubated for 2 h at 37 °C. Subsequently, the liquid of each well was removed followed by incubation with 100 μl per well of detection agent A (biotin-conjugated antibody specific to canine IL-17 or canine CD-40L) for 1 hour at 37 °C. After washing three times, the remaining wash buffer was removed by decanting and 100 μl per well of detection agent B (avidin conjugated to horseradish peroxidase) were added to each well and incubated for 30 min at 37 °C. After adequate washing steps, 90-μl/well TMB chromogenic substrate (3.3′.5.5′ Tetramethylbenzidine) was added and incubated for 25 min at 37 °C. After adding 50-μl stop solution containing sulphuric acid, the plates were measured using a microplate reader (Synergy 2 Multi-mode microplate reader, BioTek Instruments Inc., Bad Friedrichshall, Germany) spectrophotometrically at a wavelength of 450 nm ± 10 nm.

All samples were tested in duplicates and the mean value was calculated. The minimum detectable value for IL-17 was 7.8 pg/ml and for CD40L 0.156 ng/ml, lower values were considered negative (0 pg/ml and 0 ng/ml, respectively). Samples resulting in measurements exceeding the maximal detectable value for IL-17 (500 pg/ml) or CD40L (10 ng/ml) were diluted and measured again.

Determination of IL-17 and IFN-γ-producing PBMCs

Quantitative determination of the frequency of PBMCs releasing canine IL-17 and/or interferon gamma (IFN-γ) was performed using a commercially available dual-Color enzyme-linked immunoSpot (ELISpot) assay (N° ELD6555, R&D Systems®, Inc., Minneapolis, USA), following the manufacturer’s instructions. Briefly, all reagents were brought to room temperature except for the detection antibody concentrate and the dilution buffer. Cells to be analysed were thawed and washed with RPMI 1640 medium once the number of viable cells was determined and two different dilutions were made for each sample (2.5 × 105 cells/ml and 5 × 105 cells/ml) in RPMI 1640 medium containing l-glutamine, 15% serum replacement-1, and 4-μg/ml concanavalin A (N° C5275, Sigma-Aldrich®, St. Louis, USA) for stimulation. Simultaneously, all wells from a 96-well PVDF (polyvinylidine fluoride) membrane-backed microplate coated with a monoclonal antibody specific for canine IFN-γ and a monoclonal antibody specific for canine IL-17 were filled with 200-μl RPMI 1640 medium containing l-glutamine and incubated for 20 min at room temperature. When the cells were ready to be plated, the medium of each well was removed and 100 μl of appropriate controls and PBMCs in stimulation medium were added to each well. All samples and controls were assayed in triplicate. The cells were stimulated overnight at 37 °C in a 5% CO2 incubator. After incubation, the wells were washed four times with wash buffer (300 μl pro well) to remove the cells and culture medium and 100-μl detection antibody mixture (containing biotinylated polyclonal antibody specific for canine IFN-γ and horseradish peroxidase-conjugated polyclonal antibody specific for canine IL-17) was added to each well and incubated at 4 °C overnight. After incubation, the liquid of each well was removed by aspiration and washing was performed four times with wash buffer. One hundred microliter streptavidin-AP (streptavidin conjugated to alkaline phosphatase) was added to each well and incubated for 2 h at room temperature. After adequate washing steps, 100 μl of BCIP/NBT chromogen [5-bromo-4-chloro-3′indolylphosphate p-toluidine salt (BCIP) and nitro blue tetrazolium chloride (NBT)] were added to each well and incubated for 1 h protected from light at room temperature. BCIP/NBT chromogen was discarded and plates were rinsed once with deionized water. After removal of water was completed, 100 μl AEC (3-amino-9-ethylcarbazole) chromogen in stabilizing buffer (0.1% H2O2 in acetate buffer) were added to each well incubating for 20 min protected from light at room temperature. After decanting and rinsing with deionized water, excess of water and plate underdrain were removed. Finally, microplates were dried completely at room temperature for 90 min before analysis.

An ELISpot puncher (Eli.Punch, A.EL.VIS GmbH, Hannover, Germany) was used to remove the 96-well bottoms, and counting of spots was performed using an ELISpot scanner and Analysis Software (Eli.Scan, A.EL.VIS GmbH, Hannover, Germany). All samples were tested in triplicates for both dilutions (2.5 × 105 cells/ml and 5 × 105 cells/ml). Since the wells from the 5 × 105 cells/ml dilution showed a high density of the spots and the 2.5 × 105 cells/ml dilution showed better defined, distinct, separated, clear spots, only this dilution was further analysed. Red spots (IL-17-producing PBMCs) and black spots (IFN-γ-producing PBMCs) were counted separately, and the settings used were brightness: 75% and region of interest (ROI): 66% (Fig. 1). Results are expressed in number of spot-forming cells (SFC) per number of cells in each well. Finally, the means from the well triplicates were calculated.
https://static-content.springer.com/image/art%3A10.1186%2Fs12974-016-0784-3/MediaObjects/12974_2016_784_Fig1_HTML.gif
Fig. 1

IL-17 and IFN-γ spot-forming cells. a Scan of a 96-well PVDF-backed ELISpot microplate. Positive and negative controls are shown vertically in duplicates (A1-D3) and sample wells horizontally in triplicates (E1-H12). b Red spots (IL-17-producing PBMCs) and black spots (IFN-γ-producing PBMCs) are presented in a zoomed well (C10). Brightness: 75% and region of interest (ROI): 66%

Statistical analysis

Statistical evaluation to test for significant differences of IL-17 and CD40L concentrations in CSF and serum, and IL-17- and IFN-γ-producing PBMCs, among the different groups, was performed using SAS® software Version 9.3 (SAS Inst. Inc. Cary, NC, USA). Graphics from the statistical data obtained were made by using GraphPad software (GraphPad Prism®, version 5, La Jolla, CA, USA).

Statistical analysis of IL-17 and CD40L concentrations in CSF and serum

In the statistical analyses, IL-17 and CD40L values under the detection limits were treated like zeros and will be referred to as “zero values” hereinafter. All groups were compared pairwise using the two-part test [37, 38]. This test combines the comparison of the percentages of zeros using Fisher’s exact test and Wilcoxon’s two-sample test of the values above the detection limits (non-zero values). When not only zero values were present in one or both groups but also values greater than zero in both groups, then the two-part test was used. However, if there were only zeros in a group, only the Fisher exact test was used. Furthermore, the two-part test was not necessary for the analysis of CD40L in serum, since no zeros were present in this variable. Therefore, the Wilcoxon test alone was performed for this analysis given that the non-zero values were not normally distributed. Results are given as medians, minimal and maximal values of the non-zero values, and percentages of zero values. Additionally, Spearman’s rank correlation coefficients (rSpear) were calculated to determine correlations between IL-17 and CD40L and between white blood cell count in CSF and both proteins. A comparisonwise error rate of 5% was applied in the analysis of the data, differences between groups and correlation coefficients were claimed as significant if the corresponding p values were lesser than 0.05.

Given the prolonged period of storage of some serum and CSF samples, linear regression analyses separated by groups were performed to look for significant linear regression coefficients of IL-17 and CD40L through the years where the samples were collected. No significant correlations between the concentration of the proteins analysed and the years of sampling were found in any of the groups (p > 0.05).

Statistical analysis of IL-17 and IFN-γ-producing PBMCs

Since these variables were not normally distributed within the groups, all groups were compared pairwise using the Wilcoxon two-sample test. Medians of the means were compared and values of p < 0.05 were considered significant.

Results

Serum and CSF samples

Serum and/or CSF were collected and analysed from 79 dogs in total. In some dogs with SRMA, samples were taken twice, in the acute phase (SRMA A) and during treatment (SRMA T).

From the total of 98 CSF and serum samples, 89 were paired CSF and serum samples. In some cases, both proteins could not be measured because the material was not sufficient (Table 1).
Table 1

Number of CSF and serum samples analysed for IL-17 and CD40L in each group

Groups

IL-17

CD40L

CSF

Serum

CSF

Serum

SRMA A

30

30

31

31

SRMA R

6

6

6

6

SRMA T

26

27

26

28

Healthy

12

14

14

14

Miscellaneous

8

9

8

8

Total

82

86

85

87

IL-17, interleukin-17, CD40L cluster of differentiation 40 ligand, CSF cerebrospinal fluid, SRM A steroid-responsive meningitis-arteritis in acute stage, SRMA R recurrence of SRMA, SRMA T SRMA patients under treatment

Among the patients with SRMA, 16 different breeds and mixed-bred dogs were included. The most common breeds were boxer (25%), Bernese mountain dogs (16.7%), beagles (16.7%), and mixed breeds (10.4%). Most dogs diagnosed with SRMA in the acute phase of the disease were <1 year (55.2%), 34.48% were between 1- and 2-years old, and 10.3% were between 2- and 3-years old.

CSF and serum concentrations of IL-17

The highest concentrations of IL-17 were found in CSF samples of patients with SRMA A (median 901.77 pg/mL; range 70.73–2967.14 pg/mL; percentage of zeros 0%), followed by those with SRMA R (median 533.01 pg/mL; range 97.52–1771.87; percentage of zeros 0%). Concentrations of IL-17 CSF samples “SRMA A” differed significantly from other groups, SRMA T (p < 0.0001), healthy dogs (p < 0.0001), and miscellaneous (p = 0.0005). However, there was no difference to values measured in samples from dogs with relapses (SRMA R), a group also displaying significant differences with SRMA T (p = 0.0004), healthy dogs (p = 0.0051), and miscellaneous (p = 0.0415).

Similarly, the highest values of IL-17 in serum were found in dogs with SRMA A (median 45.95 pg/mL; range 12.18–251.53 pg/mL; percentage of zeros 50%), followed by serum samples of dogs with SRMA R (median 43.30 pg/mL; range 12.52–126.74 pg/mL; percentage of zeros 16.67%). Significantly higher values were found in SRMA A when compared with the group “miscellaneous” (p = 0.0445). Furthermore, statistically significant differences were found between the groups “SRMA R” and “healthy” (median 32.34 pg/mL; range 9.40–87.46 pg/mL; percentage of zeros 14.29%) when compared with SRMA T (p = 0.0166 and p = 0.0021, respectively) and miscellaneous (p = 0.0268 and p = 0.0022, respectively).

IL-17 concentrations in CSF and serum, in addition to percentage of zeros (values under the detection limits), are summarized in Table 2. Significant differences among groups are shown in Fig. 2.
Table 2

Concentrations of IL-17 and CD40L in CSF and serum samples analysed

Groups

 

IL-17 (pg/mL)

CD40L (ng/mL)

CSF

Serum

CSF

Serum

SRMA A

Median

901.77

45.95

0.51

1.37

Range

(70.73–2967.14)

(12.18–251.53)

(0.16–1.95)

(0.25–3.10)

Percentage of zeros

0%

50%

50%

SRMA R

Median

533.01

43.30

0.22

1.37

Range

(97.52–1771.87)

(12.52–126.74)

(0.17–0.91)

(0.76–3.06)

Percentage of zeros

0%

16.67%

33.33%

SRMA T

Median

29.67

21.04

0

1.29

Range

(12.47–78.86)

(8.10–32.92)

(0–0)

(0.29–6.39)

Percentage of zeros

38.46%

59.26%

100%

Healthy

Median

30.90

32.34

0.17

1.70

Range

(15.45–172.17)

(9.40–87.46)

(0.17–0.17)

(0.38–5.75)

Percentage of zeros

8.33%

14.29%

92.86%

Miscellaneous

Median

53.54

10.98

0.63

1.08

Range

(13.64–221.82)

(8.65–13.30)

(0.63–0.63)

(0.48–5.80)

Percentage of zeros

30%

69.23%

72.73%

Median and range (minimum-maximum) of values above the detection limits and percentage of zeros for each group

IL-17 interleukin-17, CD40L cluster of differentiation 40 ligand, CSF cerebrospinal fluid, SRMA A steroid-responsive meningitis-arteritis in acute stage, SRMA R recurrence of SRMA, SRMA T SRMA patients under treatment

https://static-content.springer.com/image/art%3A10.1186%2Fs12974-016-0784-3/MediaObjects/12974_2016_784_Fig2_HTML.gif
Fig. 2

Concentration of IL-17 (a, b) and CD40L (c, d) in CSF and serum samples and percentage of zeros. Boxes contain values from the first to the third quartile, lines inside the box indicate median values, endpoints of vertical lines represent minimum and maximum values, and • represent outliners. Number sign represents percentage of zero values. Asterisks indicate statistically significant differences from the SRMA A group (****p < 0.0001, ***p < 0.005), plus indicate statistically significant differences from the SRMA R group (+++ p < 0.005, ++ p < 0.01, + p < 0.05) and circles indicate statistically significant differences from the healthy group (oo p < 0.01). IL-17: interleukin-17, CD40L: cluster of differentiation 40 ligand, CSF: cerebrospinal fluid, SRMA: steroid-responsive meningitis-arteritis, SRMA A: acute stage of SRMA, SRMA R: recurrence of SRMA, SRMA T: SRMA patients under treatment

CSF and serum concentrations of CD40L

CD40L concentrations in CSF were overall very low; a high number of values were found under the detection limit. These values are described as “zero” values and are expressed as percentage for each group.

The lowest values were found in the SRMA T group, followed by the healthy group. Measurable CD40L concentrations and lower percentage of zeros were found in the SRMA A and SRMA R groups. Statistically significant differences occurred between the SRMA A (median 0.51 ng/mL; percentage of zeros 50%) and the SRMA R (median 0.22 ng/mL; percentage of zeros 33.33%) groups when compared with the SRMA T (p < 0.0001 and p = 0.0005, respectively) and healthy dogs (p = 0.0042 and p = 0.0145, respectively). CD40L concentrations in serum of all the groups examined did not differ significantly, all values were above the detection limit.

CD40L concentrations in CSF and serum as well as the percentage of zeros are summarized in Table 2. Significant differences among groups are displayed in Fig. 2.

Correlation analysis

CSF concentrations of IL-17 and CD40L showed a strong positive correlation among each other (rSpear = 0.6601; p < 0.0001) and with the degree of pleocytosis in all groups (rSpear = 0.8842; p < 0.0001 and rSpear = 0.6649; p < 0.0001, respectively). In SRMA A and SRMA R, correlations between IL-17 levels in CSF and degree of pleocytosis were rSpear = 0.7574 (p < 0.0001) and rSpear = 0.8857 (p = 0.0188), respectively.

Blood samples for PBMCs used for determination of IL-17 and IFN-γ by ELISpot

After complete diagnostic workup was made, the patients were divided in seven groups. The number of PBMCs samples used for determination of IL-17 and IFN-γ are shown in Table 3.
Table 3

Number of IL-17 and IFN-γ spot-forming cells (median and range)

Groups

 

IL-17

IFN-γ

SRMA A (n = 18)

Median

12.83

43.83

Range

(3.33–34.67)

(1.67–315.00)

SRMA T (n = 9)

Median

13.00

25.33

Range

(1.00–95.33)

(5.33–169.67)

Healthy (n = 16)

Median

4.34

291.50

Range

(0.67–14.00)

(77.67–695.00)

Idiopathic epilepsy (n = 10)

Median

28.33

109.17

Range

(2.33–66.00)

(35.33–350.00)

MUO (n = 8)

Median

13.50

87.50

Range

(3.33–74.67)

(20.33–296.67)

IVDH (n = 7)

Median

7.67

61.00

Range

(5.67–44.67)

(12.00–215.33)

Miscellaneous (n = 8)

Median

6.84

42.50

Range

(1.67–33.00)

(14.00–369.00)

SFCs spot-forming cells, IL-17 interleukin-17, IFN-γ Interferon gamma, SRMA A steroid-responsive meningitis-arteritis in acute stage, SRMA T SRMA patients under treatment, MUO meningoencephalitis of unknown origin, IVDH intervertebral disc herniation

Number of PBMCs secreting IL-17 and IFN-γ

The lowest values were found in the healthy group (median 4.34 SFCs; range 0.67–14.00 SFCs), which differed significantly from SRMA A (p = 0.0007), SRMA T (p = 0.0134), idiopathic epilepsy (p = 0.0006), MUO (p = 0.0106), and intervertebral disc herniation (IVDH) (p = 0.0266). The number of IL-17-producing PBMCs in the epilepsy group and in cases with MUO varied widely.

IFN-γ was mostly produced by PBMCs of the healthy group (median 291.50 SFCs; range 77.67–695.00 SFCs). Significant differences were found between this group and all the other groups: SRMA A (p < 0.0001), SRMA T (p = 0.0005), idiopathic epilepsy (p = 0.0057), MUO (p = 0.0077), IVDH (p = 0.0029), and miscellaneous (p = 0.0053).

The number of IL-17 and IFN-γ SFCs are summarized in Table 3. Significant differences between groups are displayed in Fig. 3.
https://static-content.springer.com/image/art%3A10.1186%2Fs12974-016-0784-3/MediaObjects/12974_2016_784_Fig3_HTML.gif
Fig. 3

IL-17 (a) and IFN-γ (b) spot-forming cells. Boxes contain values from the first to the third quartile, lines inside the box indicate median values, and endpoints of vertical lines represent minimum and maximum values, and • represent outliners. Circles indicate statistically significant differences from the healthy group (oooo p < 0.0001, ooo p < 0.005, oo p < 0.01, o p < 0.05). Number sign indicates statistically significant differences between idiopathic epilepsy (#p < 0.05) and other groups. SFCs: spot-forming cells, IL-17: interleukin-17, IFN-γ: interferon gamma, SRMA A: steroid-responsive meningitis-arteritis in acute stage, SRMA T: SRMA patients under treatment, MUO: meningoencephalitis of unknown origin, IVDH: intervertebral disc herniation

Discussion

In the current study, we could support the hypothesis that SRMA is associated with a Th17-skewed immune response. Increased intrathecal levels of IL-17 and CD40L in patients with SRMA in the acute stage and during relapses were detected. Furthermore, IL-17 CSF levels showed a strong positive correlation with the degree of pleocytosis (rSpear = 0.8842; p < 0.0001) suggesting that IL17 might be involved in the massive migration of neutrophils in the CSF and the induction of vascular damage.

SRMA is a primary immune-mediated meningeal disorder [3], but despite extensive research, the exact etiopathogenesis remains unknown. The treatment of choice are long-term glucocorticosteroids and when dogs in the acute stage of the disease are treated promptly, the prognosis is fair to good [2, 6]. Nevertheless, a recent study showed relapses in about 30% of the cases where a lasting improvement is not achieved [39] or the required dosage of glucocorticosteroids may lead to severe side effects. Autoimmune diseases, both in canines and humans, urge the development of new treatment strategies with a specific mechanism of action to avoid potentially serious side effects. In depth understanding and characterization of the cytokine profile leading to a dysregulation of the immune system in autoimmune inflammatory disorders allows implementation of novel therapeutic approaches based on specific cytokine modulation. To date, no studies have been performed on the recently discovered IL-17-producing T cell subset (Th17) in SRMA patients. However, IL-17-producing cells have an important role in the development of several autoimmune diseases in humans such as systemic lupus erythematosus [40], rheumatoid arthritis [41], bronchial allergy [21], inflammatory bowel disease [20], multiple sclerosis [42], and Kawasaki disease [43] and also in experimental models such as collagen-induced arthritis [19] and experimental autoimmune encephalomyelitis (EAE) [22]. The extrapolation of findings in experimental rodent models for human inflammatory diseases is very limited. SRMA as a naturally occurring animal model for human meningitis and vasculitides of unknown origin including Kawasaki Syndrome [14, 15, 44, 45] might overcome this limitation. Recently, IL-17-producing cells were found in inflamed tissues of several chronic idiopathic disorders in dogs including inflammatory bowel disease, gingivitis, chronic idiopathic rhinitis, and chronic dermatoses [46]. Increased levels of IL-17 were found in dog brain tissues with granulomatous meningoencephalomyelitis (GME) [47]. Additionally, in the current study, we could show increased values of IL 17 and CD40L in serum and CSF of dogs with SRMA, most probably having a role in the massive invasion of neutrophils to the subarachnoidal space and being involved in the development of the striking vasculitis.

IL-17 is upregulated both systemically and intrathecally in patients suffering from SMRA in the acute phase and during relapses. IL-17 was measurable in all CSF samples belonging to these two groups in contrast to the control groups. Furthermore, most measurements in CSF samples of SRMA A (median 901.77 pg/mL) and SRMA R (median 533.01 pg/mL) groups exceeded the maximal detectable value for IL-17 (500 pg/mL) of the ELISA kit and had to be diluted to obtain readable values. Patients in the SRMA A and SRMA R groups displayed a neutrophilic pleocytosis. In line with the known ability of IL-17 to induce neutrophil recruitment into sites of inflammation, the groups that displayed the highest CSF IL-17 levels showed also the highest numbers of neutrophils. Furthermore, the CSF concentrations of IL-17 showed a strong positive correlation with the degree of pleocytosis (rSpear = 0.8842; p < 0.0001).

Strikingly, IL-17 values measured in CSF exceeded 20 times the amount of IL-17 detected in the serum of patients in the SRMA A group and more than 10 times of patients in the SRMA R group supporting the hypothesis that IL17 is produced intrathecally and not a spill over through a damaged blood-brain barrier. Although vascular lesions may be present in the coronary arteries and other organs [45, 48, 49], the vasculitis in SRMA patients is accentuated in the subarachnoidal space of the cervical meninges [7, 15]. All CSF samples in our patients were collected from the cisterna magna near to the main lesions in SRMA. Circulating cytokines reach high concentrations at the site of release, but after dilution in the blood, much lower concentrations can be found peripherally [50] as observed in the current study.

SRMA-affected dogs have higher number of helper CD4+ T cells than cytotoxic CD8+ T cells in the peripheral blood [15]. This predominance of T helper (Th) lymphocytes indicates that in SRMA patients a humoral immune response is present, occurring typically to eliminate extracellular pathogens or in autoimmune diseases [15]. Naive CD4+ T cells differentiate into different subsets with distinct effector functions when activated in a specific cytokine environment [51]. Initially, Th differentiation was proposed to be divided in two subpopulations based on their cytokine expression profiles: Th1 and Th2 [52]. Th1 synthesize IFN-γ and mediate protection against intracellular pathogens [51]. In former studies, this cytokine was only detected in low levels in SRMA [17], we confirmed this finding in the current study, demonstrating low IFN-γ spot-forming cells in dogs with SRMA. Th2 cells synthesize IL-4, IL-13, and IL-25, moderate the clearance of extracellular pathogens [51], and were found to occur in SRMA [17]. However, the paradigm of two Th subpopulations was challenged following the discovery of a third subset of Th cells, known as Th17 cells [53], which synthesize IL-17 and are potent inducers of autoimmunity and tissue inflammation [51]. Th17 cells require both TGF-ß1 and IL-6 for their development [54, 55]. In humans, IL-23 is essential for the maturation of inflammatory Th17 cells [22]. It has been shown that IL-6-deficient mice fail to develop a Th17 response and are resistant to the development of EAE [55, 56] and collagen-induced arthritis [57]. In recent studies, increased levels of IL-6 and TGF-ß1 were described in CSF of canines suffering from SRMA. A combined intrathecal increase of these proteins could induce CD4+ progenitors to differentiate into Th17 subset and enhance the autoimmune response [14]. Additionally, dendritic cells activated by Toll-like receptor (TLR) 4 and TLR9, produce IL-23, which subsequently can activate CD4+ T cells shifting towards Th17 differentiation under the effect of IL-6 and TGF-ß1 [5]. In SRMA, such an influence of Toll-like receptors was already shown [5] and furthermore supports the hypothesis of a Th17-skewed immune response in the described disease.

IL-17 has been designated IL-17A to indicate that it is the founding member of the IL-17 cytokine family consisting of IL-17A-F members [27, 58] playing an active role in inflammatory responses and in autoimmune diseases [29]. IL-17 is a pro-inflammatory cytokine secreted primarily by activated T cells [23, 24, 29, 30, 58, 59], although it is also produced by neutrophils [24], eosinophils [25], and monocytes [26]. IL-17 acts on the IL-17 receptor (IL-17R) expressed on the cells of all the tissues examined to date [27]. The activation of IL-17R results generally in the induction of other pro-inflammatory cytokines [27]. IL-17 induces the release of IL-6 and other cytokines that trigger an inflammatory reaction characterized by neutrophil influx [21] and promotes granulopoiesis [28]. Experimental studies showed that overexpression of IL-17 in the joint space of mice with collagen-induced arthritis leads to increased neutrophil recruitment [60]. Interestingly, the mechanisms by which IL-17 disrupts the tight junctions between the endothelial cells of the blood-brain barrier (BBB) were recently demonstrated and the ability of Th17 cells to transmigrate efficiently across the BBB was proven [30]. Expression of IL-17 and IL-22 receptors on the endothelial cells of the BBB results in the binding of Th17 cells to the BBB tight junctions which causes its disruption and allows Th17 cells to transmigrate across the BBB [61]. Furthermore, IL-17 enhances inflammatory cytokine production by microglia and even its synthesis by microglia and astrocytes has been proven [62]. Altogether, these mechanisms might explain the striking increase of IL-17 intrathecally and its influence on the massive invasion of neutrophils into the subarachnoidal space in dogs affected with SRMA.

Patients in the SRMA T group were under long-term treatment with prednisolone as previously described [35] and did not show any clinical signs at the time of sampling and had CSF parameters in physiological ranges. IL-17 levels in these patients were both low in CSF (median 29.67 pg/mL) and in serum (median 21.04 pg/mL). Glucocorticoids are known to induce lymphocyte apoptosis and alter leukocyte migration and redistribution. The most important immunosuppressive effect of glucocorticosteroids is on T cell activation by inhibition of the genes that encode for cytokine production [63]. The mechanisms of action of glucocorticoids are, however, unspecific and are associated with potentially serious side effects [63, 64]. In SRMA, management of the clinical signs and a complete remission is often achieved with long-term treatment with prednisolone [2]. In refractory cases, other immunosuppressive drugs are used in combination with glucocorticoids [2, 39]. However, in approximately 30% of the patients a lasting improvement is not achieved, relapses are persistent [39], and unacceptable side effects appear [64]. In humans, up to 30% of patients treated for inflammatory diseases develop glucocorticoid resistance [64]. Hence, novel therapeutic strategies targeting specific aspects of the immune response are practiced in human medicine. Current medical trials aimed to neutralize IL-17 or IL-23 have shown to be highly effective in humans in the treatment of psoriasis and show promising initial results in ankylosing spondylitis and multiple sclerosis [65]. These innovating therapies are now appearing in companion animal medicine [66] and should be considered in inflammatory autoimmune diseases like SRMA.

In the second part of our study, increased levels of soluble CD40L in CSF of dogs with SRMA A (median 0.51; range 0.16–1.95 ng/mL) and SRMA R (median 0.22; range 0.17–0.91 ng/mL) were found when compared with all other groups. Interestingly, CD40L was not measurable in any CSF sample of the SRMA T group and only in one sample of the healthy (0.17 ng/mL) and one of the miscellaneous (0.67 ng/mL in meningoencephalitis of unknown origin) groups. To our knowledge, serum and CSF values of CD40L have not been previously evaluated in canines, and hence no reference values have been established. It was unexpected to find no differences in the expression of CD40L in serum among any of the groups.

The CD40 ligand or CD154 is a transmembrane glycoprotein from the tumor necrosis factor α (TNF α) family primarily expressed on the surface of activated CD4+ T cells which interacts with the CD40 receptor expressed principally in B cells but also in other cells [31]. Activated T cells not only express CD40L in their membranes but also produce a soluble form of CD40L, which is biologically active and interacts also with the CD40 receptor [32]. The CD40 receptor is expressed by the vascular endothelial cells and its activation by CD40L leads to leukocyte adhesion [33].

Our results showed increased levels of CD40L in CSF in dogs in the acute stage and during relapses of SRMA. High levels of soluble CD40L can regulate CNS inflammation at the BBB [67]. Recently, increased expression of CD40L in CD4+ T cells as well as soluble CD40L was found in patients with Kawasaki disease and the levels correlated with coronary artery lesions [68].

The third part of our study aimed to confirm IL-17 secretion by PBMCs at the single cellular level by ELISpot assays. The development of novel tools allows us to study cell-mediated immunity in a more sensitive and precise manner. Since its development in 1983 [69], the ELISpot assays have been employed in the identification of cytokine-producing cells at the single-cell level allowing the visualization and quantification of the secretory products of individually activated cells. The dual ELISpot allows simultaneous detection of two cytokines. We performed ELISpot assays to detect IL-17 (indicating a Th17 response) and IFN-γ (indicating a Th1 response) in PBMCs after cryopreservation. Previous studies in humans have shown full functionality after cryopreservation of PBMCs [70]. Our results proved IL-17 and IFN-γ production of activated and responsive PBMCs after cryopreservation in canines. IL-17 is produced by PBMCs and not only by neutrophils occurring in high numbers in CSF samples of dogs with SRMA.

Given the systemic nature of SRMA [17, 71], PBMCs were isolated and IL-17 production was evaluated at a single-cell level by an ELISpot assay. Although, a higher number of IL-17 SFCs were found in the SRMA A group than in the healthy group, an increased production of IL-17 in PBMCs was also found in all the other groups when compared with the healthy controls. Intriguingly, single patients of the group with idiopathic epilepsy showed more spot-forming cells as found in all other diseases. Interictal increased levels of IL-17 in CSF and serum have been found in humans with three types of epilepsy (temporal lobe epilepsy, extra-temporal lobe epilepsy, and idiopathic generalized epilepsy) [72]. Another group found a significant correlation among increased IL-17 levels and seizure frequency, IL-17 is known to facilitate Th17 migration across the BBB [73]. Another explanation could be the presence of single cases with immune-mediated diseases among our idiopathic epilepsy group. In humans, some seizure disorders once thought to be idiopathic now seem to be immune-mediated [74] and occurrence of autoantibodies to different neuronal structures were found [7476]. Nonetheless, we have clearly demonstrated the IL-17 production at the single-cell level in the peripheral blood in SRMA patients and compared it to positive and negative controls.

Finally, IFN-γ spot-forming cells in SRMA patients in the acute as well as those under treatment remained low. Previous studies demonstrated a downregulation of IFN-γ mRNA expression by means of reverse transcriptase real-time polymerase chain reaction in dogs with SRMA in the acute phase [17]; our findings confirmed low IFN-γ expression at the protein level compared to healthy dogs excluding a Th1 response and further supporting a Th17 response.

The current study is, to our knowledge, the first one to demonstrate IL-17 expression in canine CSF and its involvement in the pathogenesis in SRMA patients. Our findings follow up the already known roles of cytokines involved in the pathogenesis of SRMA [77] and give a clear direction for future treatment approaches.

Conclusions

The described results imply that Th17 cells are inducing the autoimmune response in SRMA and are involved in the development of the severe neutrophilic pleocytosis and disruption of the BBB. The investigation of the role of IL-17 and CD40L in SRMA adds to the knowledge of pathophysiological mechanisms in SRMA and opens the discussion about new therapeutic strategies in this valuable naturally occurring large animal model.

Abbreviations

BBB: 

Blood-brain barrier

CD: 

Cluster of differentiation

CD40L: 

Cluster of differentiation 40 ligand

CNS: 

Central nervous system

CSF: 

Cerebrospinal fluid

EAE: 

Experimental autoimmune encephalomyelitis

EDTA: 

Ethylenediaminetetraacetic acid

ELISA: 

Enzyme-linked immunosorbent assay

ELISpot: 

Enzyme-linked immunospot assay

IE: 

Idiopathic epilepsy

IFN-γ: 

Interferon gamma

IgA: 

Immunoglobulin A

IL: 

Interleukin

IVDH: 

Intervertebral disc herniation

MRI: 

Magnetic resonance imaging

MUO: 

Meningoencephalitis of unknown origin

PBMCs: 

Peripheral blood mononuclear cells

PBS: 

Phosphate-buffered

rSpear: 

Spearman’s rank correlation coefficient

SFCs: 

Spot-forming cells

SRMA: 

Steroid-responsive meningitis-arteritis

TGF-ß1

Transforming growth factor beta 1

Th17: 

T helper 17

Declarations

Acknowledgements

The authors would like to thank the staff of the Department of Small Animal Medicine and Surgery, University of Veterinary Medicine, Hannover, Germany for helping examining the dogs and collecting the samples. The authors are also grateful to Dorothea Dijkstra, PhD from the Department of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School and Prof. Dr. med. Heinfried Radeke form the Institute of Pharmacology and Toxicology, Clinic of the Goethe University Frankfurt Main for their excellent technical assistance.

Funding

The authors received no financial support for the research, authorship, and/or publication of this article. Jessica Freundt-Revilla received financial support from the German Academic Exchange Service (DAAD, Germany).

Availability of data and materials

Data supporting the conclusions of this article are presented in the manuscript.

Authors’ contributions

AT conceived, designed, and supervised the study. JFR performed the experiments, analyzed the data, and drafted the manuscript. AM in part conceived and designed the study. RC conceived in part the study, gave substantial contributions to the acquisition, analysis, and interpretation of the data. MB gave substantial contribution to the statistical analysis. KR, TF, and AF contributed with the clinical evaluation of patients and collection of samples. All authors contributed to the critical revision of the manuscript for important intellectual content and have read and approved the final version.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not applicable.

Ethics approval and consent to participate

This study was conducted in accordance with the ethical guidelines of the University of Veterinary Medicine Hannover and was approved by the authorities of Lower Saxony (animal experiment number 33.9-42502-05-14A453).

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Small Animal Medicine and Surgery, University of Veterinary Medicine
(2)
Institute for Biometry, Epidemiology and Information Processing, University of Veterinary Medicine
(3)
Tierärztliche Praxis für Neurologie
(4)
Department of Small Animal Medicine, University of Leipzig
(5)
Clinic of Small Animal Medicine, Centre for Clinical Veterinary Medicine, LMU Munich
(6)
Center for Systems Neuroscience

References

  1. Meric SM. Canine meningitis. A changing emphasis. J Vet Intern Med. 1988;2(1):26–35.View ArticlePubMedGoogle Scholar
  2. Tipold A, Schatzberg SJ. An update on steroid responsive meningitis-arteritis. J Small Anim Pract. 2010;51(3):150–4.View ArticlePubMedGoogle Scholar
  3. De Lahunta A, Glass E. Small Animal Spinal Cord Disease. In: Veterinary Neuroanatomy and Clinical Neurology. 3 edn. Edited by Saunders WB. St. Louis: Elsevier Science; 2009. p. 243-84.
  4. Harcourt R. Polyarteritis in a colony of beagles. Vet Rec. 1978;102:519–22.View ArticlePubMedGoogle Scholar
  5. Maiolini A, Carlson R, Tipold A. 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. J Neuroinflammation. 2012;9:226.View ArticlePubMedPubMed CentralGoogle Scholar
  6. Cizinauskas S, Jaggy A, Tipold A. Long-term treatment of dogs with steroid-responsive meningitis-arteritis: clinical, laboratory and therapeutic results. J Small Anim Pract. 2000;41(7):295–301.View ArticlePubMedGoogle Scholar
  7. Tipold A, Jaggy A. Steroid responsive meningitis-arteritis in dogs: long-term study of 32 cases. J Small Anim Pract. 1994;35(6):311–6.View ArticleGoogle Scholar
  8. Vos J, Rentmeister K, Maiolini A, Tipold A. Steril-eitrige Meningitis-Arteriitis (SRMA) bei drei Wurfgeschwistern der Rasse Petit Basset Griffon Vendéen. Kleintierpraxis. 2012;57:185–91.Google Scholar
  9. Wilbe M, Jokinen P, Truve K, Seppala EH, Karlsson EK, Biagi T, Hughes A, Bannasch D, Andersson G, Hansson-Hamlin H, et al. Genome-wide association mapping identifies multiple loci for a canine SLE-related disease complex. Nat Genet. 2010;42(3):250–4.View ArticlePubMedGoogle Scholar
  10. Meric SM, Perman V, Hardy RM. Corticosteroid-responsive meningitis in ten dogs. J Am Anim Hosp Assoc. 1985;22:677–84.Google Scholar
  11. Rose JH, Harcourt-Brown TR. Screening diagnostics to identify triggers in 21 cases of steroid-responsive meningitis-arteritis. J Small Anim Pract. 2013;54(11):575–8.View ArticlePubMedGoogle Scholar
  12. Lazzerini K, Tipold A, Kornberg M, Silaghi C, Mietze A, Lubke-Becker A, Balling A, Pfeffer M, Wieler LH, Pfister K, et al. Testing for vector-transmitted microorganisms in dogs with meningitis and meningoencephalitis of unknown aetiology. J Vet Med Res. 2015;2(1):1014.Google Scholar
  13. Maiolini A, Carlson R, Schwartz M, Gandini G, Tipold A. 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. Vet J. 2012;19(2):219–24.View ArticleGoogle Scholar
  14. Maiolini A, Otten M, Hewicker-Trautwein M, Carlson R, Tipold A. Interleukin-6, vascular endothelial growth factor and transforming growth factor beta 1 in canine steroid responsive meningitis-arteritis. BMC Vet Res. 2013;9:23.View ArticlePubMedPubMed CentralGoogle Scholar
  15. Schwartz M, Moore PF, Tipold A. Disproportionally strong increase of B cells in inflammatory cerebrospinal fluid of dogs with steroid-responsive meningitis-arteritis. Vet Immunol Immunopathol. 2008;125(3-4):274–83.View ArticlePubMedGoogle Scholar
  16. Schwartz M, Carlson R, Tipold A. Selective CD11a upregulation on neutrophils in the acute phase of steroid-responsive meningitis-arteritis in dogs. Vet Immunol Immunopathol. 2008;126(3-4):248–55.View ArticlePubMedGoogle Scholar
  17. Schwartz M, Puff C, Stein VM, Baumgartner W, Tipold A. Pathogenetic factors for excessive IgA production: Th2-dominated immune response in canine steroid-responsive meningitis-arteritis. Vet J. 2011;187(2):260–6.View ArticlePubMedGoogle Scholar
  18. Tipold A, Pfister H, Zurbriggen A, Vandevelde M. Intrathecal synthesis of major immunoglobulin classes in inflammatory diseases of the canine CNS. Vet Immunol Immunopathol. 1994;42(2):149–59.View ArticlePubMedGoogle Scholar
  19. Lubberts E, Koenders MI, Oppers-Walgreen B, van den Bersselaar L, Coenen-de Roo CJ, Joosten LA, van den Berg WB. Treatment with a neutralizing anti-murine interleukin-17 antibody after the onset of collagen-induced arthritis reduces joint inflammation, cartilage destruction, and bone erosion. Arthritis Rheum. 2004;50(2):650–9.View ArticlePubMedGoogle Scholar
  20. Zhang Z, Zheng M, Bindas J, Schwarzenberger P, Kolls JK. Critical role of IL-17 receptor signaling in acute TNBS-induced colitis. Inflamm Bowel Dis. 2006;12(5):382–8.View ArticlePubMedGoogle Scholar
  21. Hellings PW, Kasran A, Liu Z, Vandekerckhove P, Wuyts A, Overbergh L, Mathieu C, Ceuppens JL. Interleukin-17 orchestrates the granulocyte influx into airways after allergen inhalation in a mouse model of allergic asthma. Am J Respir Cell Mol Biol. 2003;28(1):42–50.View ArticlePubMedGoogle Scholar
  22. Cua DJ, Sherlock J, Chen Y, Murphy CA, Joyce B, Seymour B, Lucian L, To W, Kwan S, Churakova T, et al. Interleukin-23 rather than interleukin-12 is the critical cytokine for autoimmune inflammation of the brain. Nature. 2003;421(6924):744–8.View ArticlePubMedGoogle Scholar
  23. Yao Z, Painter SL, Fanslow WC, Ulrich D, Macduff BM, Spriggs MK, Armitage RJ. Human IL-17: a novel cytokine derived from T cells. J Immunol. 1995;155(12):5483–6.PubMedGoogle Scholar
  24. Ferretti S, Bonneau O, Dubois GR, Jones CE, Trifilieff A. IL-17, produced by lymphocytes and neutrophils, is necessary for lipopolysaccharide-induced airway neutrophilia: IL-15 as a possible trigger. J Immunol. 2003;170(4):2106–12.View ArticlePubMedGoogle Scholar
  25. Molet S, Hamid Q, Davoine F, Nutku E, Taha R, Page N, Olivenstein R, Elias J, Chakir J. IL-17 is increased in asthmatic airways and induces human bronchial fibroblasts to produce cytokines. J Allergy Clin Immunol. 2001;108(3):430–8.View ArticlePubMedGoogle Scholar
  26. Zhou Q, Desta T, Fenton M, Graves DT, Amar S. Cytokine profiling of macrophages exposed to Porphyromonas gingivalis, its lipopolysaccharide, or its FimA protein. Infect Immun. 2005;73(2):935–43.View ArticlePubMedPubMed CentralGoogle Scholar
  27. Moseley TA, Haudenschild DR, Rose L, Reddi AH. Interleukin-17 family and IL-17 receptors. Cytokine Growth Factor Rev. 2003;14(2):155–74.View ArticlePubMedGoogle Scholar
  28. Chen Y, Thai P, Zhao YH, Ho YS, DeSouza MM, Wu R. Stimulation of airway mucin gene expression by interleukin (IL)-17 through IL-6 paracrine/autocrine loop. J Biol Chem. 2003;278(19):17036–43.View ArticlePubMedGoogle Scholar
  29. Kolls JK, Linden A. Interleukin-17 family members and inflammation. Immunity. 2004;21(4):467–76.View ArticlePubMedGoogle Scholar
  30. Kebir H, Kreymborg K, Ifergan I, Dodelet-Devillers A, Cayrol R, Bernard M, Giuliani F, Arbour N, Becher B, Prat A. Human TH17 lymphocytes promote blood-brain barrier disruption and central nervous system inflammation. Nat Med. 2007;13(10):1173–5.View ArticlePubMedPubMed CentralGoogle Scholar
  31. Cron RQ. CD154 transcriptional regulation in primary human CD4 T cells. Immunol Res. 2003;27(2-3):185–202.View ArticlePubMedGoogle Scholar
  32. Graf D, Muller S, Korthauer U, van Kooten C, Weise C, Kroczek RA. A soluble form of TRAP (CD40 ligand) is rapidly released after T cell activation. Eur J Immunol. 1995;25(6):1749–54.View ArticlePubMedGoogle Scholar
  33. Hollenbaugh D, Mischel-Petty N, Edwards CP, Simon JC, Denfeld RW, Kiener PA, Aruffo A. Expression of functional CD40 by vascular endothelial cells. J Exp Med. 1995;182(1):33–40.View ArticlePubMedGoogle Scholar
  34. Tipold A. Cerebrospipal fluid. In: Braund KG editor. Clinical Neurology in Small Animals- Localization, Diagnosis and Treatment. International Veterinary Information Service: International Veterinary Information Service; 2003. http://www.ivis.org.
  35. Tipold A. Steroid-responsive meningitis-arteritis in dogs. In: B J, editor. Kirk's Current Veterinary Therapy XIII: Small Animal Practice. Philadelphia: Saunders; 2000.Google Scholar
  36. Boyum A. Isolation of mononuclear cells and granulocytes from human blood. Isolation of monuclear cells by one centrifugation, and of granulocytes by combining centrifugation and sedimentation at 1 g. Scand J Clin Lab Invest Suppl. 1968;97:77–89.PubMedGoogle Scholar
  37. Lachenbruch PA. Comparisons of two-part models with competitors. Stat Med. 2001;20(8):1215–34.View ArticlePubMedGoogle Scholar
  38. Lachenbruch PA. Analysis of data with excess zeros. Stat Methods Med Res. 2002;11(4):297–302.View ArticlePubMedGoogle Scholar
  39. Biedermann E, Tipold A, Flegel T. Relapses in dogs with steroid-responsive meningitis-arteritis. J Small Anim Pract. 2016;57(2):91–5.View ArticlePubMedGoogle Scholar
  40. Shah K, Lee WW, Lee SH, Kim SH, Kang SW, Craft J, Kang I. Dysregulated balance of Th17 and Th1 cells in systemic lupus erythematosus. Arthritis Res Ther. 2010;12(2):R53.View ArticlePubMedPubMed CentralGoogle Scholar
  41. Chabaud M, Durand JM, Buchs N, Fossiez F, Page G, Frappart L, Miossec P. Human interleukin-17: a T cell-derived proinflammatory cytokine produced by the rheumatoid synovium. Arthritis Rheum. 1999;42(5):963–70.View ArticlePubMedGoogle Scholar
  42. Brucklacher-Waldert V, Stuerner K, Kolster M, Wolthausen J, Tolosa E. Phenotypical and functional characterization of T helper 17 cells in multiple sclerosis. Brain. 2009;132(Pt 12):3329–41.View ArticlePubMedGoogle Scholar
  43. Guo MM, Tseng WN, Ko CH, Pan HM, Hsieh KS, Kuo HC. Th17- and Treg-related cytokine and mRNA expression are associated with acute and resolving Kawasaki disease. Allergy. 2015;70(3):310–8.View ArticlePubMedGoogle Scholar
  44. Burns JC, Felsburg PJ, Wilson H, Rosen FS, Glickman LT. Canine pain syndrome is a model for the study of Kawasaki disease. Perspect Biol Med. 1991;35(1):68–73.View ArticlePubMedGoogle Scholar
  45. Snyder PW, Kazacos EA, Scott-Moncrieff JC, HogenEsch H, Carlton WW, Glickman LT, Felsburg PJ. Pathologic features of naturally occurring juvenile polyarteritis in beagle dogs. Vet Pathol. 1995;32(4):337–45.View ArticlePubMedGoogle Scholar
  46. Kol A, Walker NJ, Nordstrom M, Borjesson DL. Th17 pathway as a target for multipotent stromal cell therapy in dogs: implications for translational research. PLoS One. 2016;11(2):e0148568.View ArticlePubMedPubMed CentralGoogle Scholar
  47. Park ES, Uchida K, Nakayama H. Th1-, Th2-, and Th17-related cytokine and chemokine receptor mRNA and protein expression in the brain tissues, T cells, and macrophages of dogs with necrotizing and granulomatous meningoencephalitis. Vet Pathol. 2013;50(6):1127–34.View ArticlePubMedGoogle Scholar
  48. Hayes TJ, Roberts GKS, Halliwell WH. An idiopathic febrile necrotizing arteritis syndrome in the dog: beagle pain syndrome. Toxicol Pathol. 1989;18:219–23.Google Scholar
  49. Scott-Moncrieff JC, Snyder PW, Glickman LT, Davis EL, Felsburg PJ. Systemic necrotizing vasculitis in nine young beagles. J Am Vet Med Assoc. 1992;201(10):1553–8.PubMedGoogle Scholar
  50. Rentzos M, Rombos A, Nikolaou C, Zoga M, Zouvelou V, Dimitrakopoulos A, Alexakis T, Tsoutsou A, Samakovli A, Michalopoulou M, et al. Interleukin-17 and interleukin-23 are elevated in serum and cerebrospinal fluid of patients with ALS: a reflection of Th17 cells activation? Acta Neurol Scand. 2010;122(6):425–9.View ArticlePubMedGoogle Scholar
  51. Bettelli E, Korn T, Oukka M, Kuchroo VK. Induction and effector functions of T(H)17 cells. Nature. 2008;453(7198):1051–7.View ArticlePubMedGoogle Scholar
  52. Mosmann TR, Coffman RL. TH1 and TH2 cells: different patterns of lymphokine secretion lead to different functional properties. Annu Rev Immunol. 1989;7:145–73.View ArticlePubMedGoogle Scholar
  53. Langrish CL, Chen Y, Blumenschein WM, Mattson J, Basham B, Sedgwick JD, McClanahan T, Kastelein RA, Cua DJ. IL-23 drives a pathogenic T cell population that induces autoimmune inflammation. J Exp Med. 2005;201(2):233–40.View ArticlePubMedPubMed CentralGoogle Scholar
  54. Mangan PR, Harrington LE, O'Quinn DB, Helms WS, Bullard DC, Elson CO, Hatton RD, Wahl SM, Schoeb TR, Weaver CT. Transforming growth factor-beta induces development of the T(H)17 lineage. Nature. 2006;441(7090):231–4.View ArticlePubMedGoogle Scholar
  55. Bettelli E, Carrier Y, Gao W, Korn T, Strom TB, Oukka M, Weiner HL, Kuchroo VK. Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells. Nature. 2006;441(7090):235–8.View ArticlePubMedGoogle Scholar
  56. Korn T, Bettelli E, Gao W, Awasthi A, Jager A, Strom TB, Oukka M, Kuchroo VK. IL-21 initiates an alternative pathway to induce proinflammatory T(H)17 cells. Nature. 2007;448(7152):484–7.View ArticlePubMedPubMed CentralGoogle Scholar
  57. Alonzi T, Fattori E, Lazzaro D, Costa P, Probert L, Kollias G, De Benedetti F, Poli V, Ciliberto G. Interleukin 6 is required for the development of collagen-induced arthritis. J Exp Med. 1998;187(4):461–8.View ArticlePubMedPubMed CentralGoogle Scholar
  58. Korn T, Bettelli E, Oukka M, Kuchroo VK. IL-17 and Th17 cells. Annu Rev Immunol. 2009;27:485–517.View ArticlePubMedGoogle Scholar
  59. Vojdani A, Lambert J. The role of Th17 in neuroimmune disorders: target for CAM therapy. Part I. Evid Based Complement Alternat Med. 2011;2011:927294.PubMedPubMed CentralGoogle Scholar
  60. Lubberts E, Joosten LA, Oppers B, van den Bersselaar L, Coenen-de Roo CJ, Kolls JK, Schwarzenberger P, van de Loo FA, van den Berg WB. IL-1-independent role of IL-17 in synovial inflammation and joint destruction during collagen-induced arthritis. J Immunol. 2001;167(2):1004–13.View ArticlePubMedGoogle Scholar
  61. Vojdani A, Lambert J. The role of Th17 in neuroimmune disorders: target for CAM therapy. Part II. Evid Based Complement Alternat Med. 2011;2011:984965.PubMedPubMed CentralGoogle Scholar
  62. Kawanokuchi J, Shimizu K, Nitta A, Yamada K, Mizuno T, Takeuchi H, Suzumura A. Production and functions of IL-17 in microglia. J Neuroimmunol. 2008;194(1-2):54–61.View ArticlePubMedGoogle Scholar
  63. Meier CA. Mechanisms of immunosuppression by glucocorticoids. Eur J Endocrinol. 1996;134(1):50.View ArticlePubMedGoogle Scholar
  64. Whitley NT, Day MJ. Immunomodulatory drugs and their application to the management of canine immune-mediated disease. J Small Anim Pract. 2011;52(2):70–85.View ArticlePubMedGoogle Scholar
  65. Gaffen SL, Jain R, Garg AV, Cua DJ. The IL-23-IL-17 immune axis: from mechanisms to therapeutic testing. Nat Rev Immunol. 2014;14(9):585–600.View ArticlePubMedPubMed CentralGoogle Scholar
  66. Yasukawa K, Saito S, Kubo T, Shibasaki Y, Yamaoka K, Hachimura H, Kuyama T, Amimoto A, Kumata T, Kitahara Y, et al. Low-dose recombinant canine interferon-gamma for treatment of canine atopic dermatitis: an open randomized comparative trial of two doses. Vet Dermatol. 2010;21(1):42–9.View ArticlePubMedGoogle Scholar
  67. Ramirez SH, Fan S, Dykstra H, Reichenbach N, Del Valle L, Potula R, Phipps RP, Maggirwar SB, Persidsky Y. Dyad of CD40/CD40 ligand fosters neuroinflammation at the blood-brain barrier and is regulated via JNK signaling: implications for HIV-1 encephalitis. J Neurosci. 2010;30(28):9454–64.View ArticlePubMedPubMed CentralGoogle Scholar
  68. Wang CL, Wu YT, Liu CA, Lin MW, Lee CJ, Huang LT, Yang KD. Expression of CD40 ligand on CD4+ T-cells and platelets correlated to the coronary artery lesion and disease progress in Kawasaki disease. Pediatrics. 2003;111(2):E140–7.View ArticlePubMedGoogle Scholar
  69. Czerkinsky CC, Nilsson LA, Nygren H, Ouchterlony O, Tarkowski A. A solid-phase enzyme-linked immunospot (ELISPOT) assay for enumeration of specific antibody-secreting cells. J Immunol Methods. 1983;65(1-2):109–21.View ArticlePubMedGoogle Scholar
  70. Kreher CR, Dittrich MT, Guerkov R, Boehm BO, Tary-Lehmann M. CD4+ and CD8+ cells in cryopreserved human PBMC maintain full functionality in cytokine ELISPOT assays. J Immunol Methods. 2003;278(1-2):79–93.View ArticlePubMedGoogle Scholar
  71. Bathen-Noethen A, Carlson R, Menzel D, Mischke R, Tipold A. Concentrations of acute-phase proteins in dogs with steroid responsive meningitis-arteritis. J Vet Intern Med. 2008;22(5):1149–56.View ArticlePubMedGoogle Scholar
  72. Wang Y, Wang D, Guo D. Interictal cytokine levels were correlated to seizure severity of epileptic patients: a retrospective study on 1218 epileptic patients. J Transl Med. 2015;13:378.View ArticlePubMedPubMed CentralGoogle Scholar
  73. Mao LY, Ding J, Peng WF, Ma Y, Zhang YH, Fan W, Wang X. Interictal interleukin-17A levels are elevated and correlate with seizure severity of epilepsy patients. Epilepsia. 2013;54(9):e142–5.View ArticlePubMedGoogle Scholar
  74. Lancaster E, Lai M, Peng X, Hughes E, Constantinescu R, Raizer J, Friedman D, Skeen MB, Grisold W, Kimura A, et al. Antibodies to the GABA(B) receptor in limbic encephalitis with seizures: case series and characterisation of the antigen. Lancet Neurol. 2010;9(1):67–76.View ArticlePubMedGoogle Scholar
  75. Dalmau J, Gleichman AJ, Hughes EG, Rossi JE, Peng X, Lai M, Dessain SK, Rosenfeld MR, Balice-Gordon R, Lynch DR. Anti-NMDA-receptor encephalitis: case series and analysis of the effects of antibodies. Lancet Neurol. 2008;7(12):1091–8.View ArticlePubMedPubMed CentralGoogle Scholar
  76. McKnight K, Jiang Y, Hart Y, Cavey A, Wroe S, Blank M, Shoenfeld Y, Vincent A, Palace J, Lang B. Serum antibodies in epilepsy and seizure-associated disorders. Neurology. 2005;65(11):1730–6.View ArticlePubMedGoogle Scholar
  77. Spitzbarth I, Baumgartner W, Beineke A. The role of pro- and anti-inflammatory cytokines in the pathogenesis of spontaneous canine CNS diseases. Vet Immunol Immunopathol. 2012;147(1-2):6–24.View ArticlePubMedGoogle Scholar

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