Objectives Clinical evidence suggests that neurological lesions can protect from arthritis. Acute cerebral ischaemia induces severe immunosuppression, resulting in enhanced susceptibility to infections. We aimed to determine if stroke-induced immunosuppression can ameliorate arthritis and to delineate the immunological mechanisms involved.
Methods Unilateral cerebral ischaemia was induced in mice by occlusion of one middle cerebral artery (MCAO) at different time points after induction of G6PI-induced arthritis in mice. Clinical and histological signs of arthritis were assessed. Regulatory T cells were specifically depleted by injection of diphtheria toxin into transgenic DEREG mice. Immunological correlates of MCAO were determined by flow cytometry and serological methods.
Results MCAO reduced the clinical and histological signs of arthritis significantly. To be effective, stroke had to be induced during the induction phase or the early clinical stage of arthritis. MCAO induced a global loss of leucocytes. Despite the reduced absolute number of lymphocytes, the functional differentiation of T helper cells into Th1/17 cells and the production of autoantibodies were unimpaired. Depletion experiments showed that regulatory T cells were dispensable for the protective effect of MCAO.
Conclusions MCAO ameliorates arthritis. The correlate of protection from arthritis is not the reduction of a particular pathogenic leucocyte subset or the preferential expansion or emergence of a protective cell population but the global reduction of leucocytes during arthritis.
- T Cells
This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
Statistics from Altmetric.com
The immune system and the nervous system communicate continually.1 Neurotransmitters modulate innate and adaptive immune responses while cytokines modulate body temperature, mood and sleep. Acute cerebral ischaemia induces severe immunosuppression,2–6 resulting in enhanced susceptibility to respiratory and urinary tract infections, which are the leading cause of death in stroke patients.4 ,6–8 Stroke-induced tissue destruction and disruption of the blood–brain barrier also result in the release of CNS autoantigens and their presentation to T-lymphocytes under proinflammatory immunogenic conditions.4 ,6 ,9 It has, therefore, been suggested that stroke-induced immunosuppression protects from stroke-induced autoimmune responses against CNS autoantigens.4 Autoimmune responses are essential in the pathogenesis of rheumatic diseases such as rheumatoid arthritis and spondyloarthropathies.10 ,11 Clinical evidence suggests that ischaemic, traumatic or postinfectious damage to the nervous system can protect from or ameliorate arthritis.12–17 However, the underlying mechanisms have remained enigmatic.
The aims of this study were to examine if stroke-induced immunosuppression can ameliorate arthritis and to delineate the immunological mechanisms involved.
Materials and methods
Mice and induction of glucose-6-phosphate isomerase-induced arthritis
DBA/1 and DBA/1 DEREG mice were bred and underwent experiments at the animal facility of the University Hospital Jena. All animal studies were approved by the appropriate authorities (reg. No. 02-006/08). Arthritis was induced by subcutaneous immunisation with 200 µg of recombinant human G6PI in complete Freund's adjuvant (Sigma-Aldrich, Taufkirchen, Germany) and evaluated clinically as described.18 Depletion of regulatory T cells (Treg) was performed in DBA/1 DEREG mice19 by intraperitoneal application of 0.5 µg of diphtheria toxin 48 and 24 h before and 4 and 5 d after G6PI immunisation. This resulted in reliable transient depletion of Treg cells (data not shown). For experiments analysing the time point of middle cerebral artery occlusion (MCAO) performance on arthritis severity, DBA/1 or non-depleted DBA/1 DEREG mice were used.
Histopathological assessment of glucose-6-phosphate isomerase-induced arthritis
Haematoxylin-eosin-stained sections of fixed and decalcified joints were evaluated by a pathologist. Inflammation and cartilage and bone destruction were graded as described before.20
Middle cerebral artery occlusion
MCAO was performed under isoflurane anaesthesia. A nylon monofilament coated with silicone (Heraeus Kulzer, Hanau, Germany) was introduced into the common carotid artery and moved to the origin of the middle cerebral artery (MCA) to block perfusion. The filament was left in this position for 60 min. In sham-operated animals, it was immediately withdrawn 4–5 mm to prevent brain ischaemia. After MCAO, mice were kept in heated cages, and 3 d before surgery Enrofloxacin (25 mg/mL; Bayer HealthCare, Leverkusen, Germany) was added to the drinking water.
Enzyme-linked immunosorbent assay (ELISA)
Single-cell suspensions were prepared from spleens and lymph nodes (LN) (inguinal, axillary, paraaortic) and cultured in medium alone or with 25 µg huG6PI or 2 µg plate-bound anti-CD3 and 2 µg anti-CD28. Supernatants were harvested and concentrations of IFN-γ, TNF-α, IL-4, IL-5, IL-6 and IL-17 were measured by sandwich ELISAs (eBiosciences, Frankfurt, Germany) using recombinant cytokines (Peprotech, Hamburg, Germany) as standard. G6PI-specific antibody serum concentrations were determined as previously described.21
Single-cell suspensions from draining LN were prepared 9 d after immunisation and cultured with medium alone or 25 μg/mL G6PI for 72 h. [3H]-thymidine (0.5 µCi/well; Hartmann Analytic) per well was added for the last 18 h. Cells were harvested, and incorporation of radiolabelled thymidine was measured using a microplate scintillation luminescence counter (Canberra-Packard, Rüsselsheim, Germany). The stimulation index (SI) was calculated as described.22
Flow cytometric analysis of cell populations and cytokine production
Single-cell suspensions from spleen and draining LN were prepared 9 d after immunisation and cultured with anti-CD16/32 (2.4G2) and rat IgG to prevent unspecific binding, followed by fluorochrome-conjugated antibodies directed against B220 (RA3-6B2), CD3, CD4, CD8, Gr-1, CD11b (all from eBioscience) or CD11c (M1/70).
Analysis of G6PI-specific cytokine-producing T cells was performed after culturing for 6 h with 25 µg/mL G6PI or medium alone as described.23–25 Data were acquired using a LSRII flow cytometer (Becton Dickinson, Heidelberg, Germany) and analysed using FlowJo V.8.1.1 software (Tree Star, Ashland, Oregon, USA). Gates for CD154 were set using unstimulated control samples.
Statistical differences between groups were evaluated using the non-parametric Mann–Whitney U test. Statistical significance was accepted for p values of less than 0.05 (*p<0.05; **p<0.01; ***p<0.001). All calculations were performed using the SPSS software V.16.0 (SPSS Inc, Chicago, Illinois, USA). Data are presented as arithmetic mean and SE of the mean.
Temporary occlusion of the middle cerebral artery (MCAO) induced substantial necrosis in the parietal lobe supplied by this vessel. Ischaemia was observable macroscopically in the left hemisphere, whereas the contralateral hemisphere was not affected (figure 1A). Histological sections revealed disbandment of cortical structures in the ischaemic brain areas (figure 1B) and extensive necrosis (figure 1C).
MCAO ameliorates arthritis
To evaluate the effects of stroke-induced immunosuppression at different stages of arthritis pathogenesis, stroke was induced at various time points after G6PI immunisation. MCAO 3 days before G6PI immunisation (d-3) had no effect on incidence or severity of arthritis (figure 2A). MCAO 3 days after immunisation with antigen in CFA resulted in an unacceptably high mortality rate (data not shown). In contrast, MCAO 6 days after immunisation (d6) ameliorated the course of arthritis significantly (figure 2B). MCAO 10 days after G6PI immunisation, when clinical signs of arthritis were already clearly visible, also reduced arthritis severity (figure 2C). Stroke induction at later time points (d12, d15) had only minor effects on arthritis (data not shown). Thus, stroke ameliorates the clinical course of arthritis when MCAO is performed in the induction phase or during the early clinical stage of G6PI-induced arthritis.
Mice that had undergone MCAO or sham surgery 6 days after G6PI immunisation were examined histopathologically 16 d after G6PI immunisation. Paws from animals with experimental stroke had diminished signs of acute and chronic inflammation. They also had less cartilage and bone destruction compared with animals of the sham group, confirming the clinical scoring (figure 2D).
MCAO induces a profound and prolonged loss of leucocytes
To determine the immunological correlates of protection, we examined the effect of stroke on the number of leucocytes within the secondary lymphoid organs. At day 16 after G6PI immunisation (10 d after MCAO), when arthritis severity was maximal in control mice, we found significantly reduced cell numbers in LN and spleens of MCAO mice (figure 3A). Flow cytometric analyses revealed that the reduction of cell numbers was not caused by the loss of a particular cell population. The numbers of B220+ B cells, CD3+CD4+ T helper cells, CD3+CD8+ cytotoxic T cells, as well as macrophages (CD11b+), dendritic cells (CD11c+) and neutrophil granulocytes (Gr-1+), were all reduced significantly by 45–75% (figure 3B). Thus, amelioration of arthritis was associated with a massive and prolonged global loss of leucocytes. Adoptive transfer of 107 unseparated cells from LN and spleens from G6PI-immunised mice 2 days after MCAO did not reconstitute disease development (data not shown).
MCAO does not affect autoantibody production
Autoantibodies against G6PI are necessary but not sufficient for induction of G6PI-induced arthritis.18 ,21 ,26 ,27 Sixteen days after G6PI immunisation, titres of G6PI-specific IgG1, IgG2a, IgG2b, IgG3 and IgM antibodies were slightly but not significantly reduced in the MCAO group (figure 4A). Therefore, stroke-induced dampening of the humoral immune response does not explain the reduced arthritis severity in MCAO mice.
Cytokine production is similar in MCAO and control mice
Sixteen days after G6PI immunisation (10 d after MCAO), proliferation in response to G6PI was similar in cells from the draining LN of MCAO or sham-operated mice (figure 4B). Concentrations of IL-6, IL-17, IFN-γ and TNF-α in the supernatants of LN cells were similar in both groups in response to stimulation with G6PI or anti-CD3/CD28 (figure 4C). Concentrations of IL-4 and IL-5 were near the detection limit in both groups.
Functional differentiation of G6PI-specific Th cells is unimpaired after MCAO
TNF-α, IL-17 and IFN-γ are key cytokines in the pathogenesis of G6PI-induced arthritis.18 ,28 ,29 We analysed the G6PI-specific Th cell cytokine production 10 d after immunisation in mice that had undergone MCAO or sham surgery at d6 after G6PI immunisation. The number of LN and spleen cells did not differ between MCAO and sham animals at this time point (figure 5A). We used polychromatic flow cytometry to analyse the functional differentiation of G6PI-specific Th cells 10 d after immunisation. We found no difference in the numbers of total CD4+ Th cells or G6PI-specific CD4+CD154+ cells in MCAO and sham mice (figure 5B). The numbers of IFN-γ, TNF-α or IL-17-producing G6PI-specific T cells were also similar in control and MCAO mice (figure 5C). Thus, differentiation towards a Th1 or Th17 phenotype was unimpaired following stroke.
Treg cells are dispensable for stroke-induced immunosuppression
CD4+CD25+FoxP3+ regulatory T cells have been shown to be relevant for the prevention and down-modulation of experimental arthritis.25 ,31–34 An increased frequency of Treg cells was reported 4 days after experimental stroke.35 Moreover, Treg cells have been claimed as major modulators of postischaemic inflammatory brain damage.36 We employed DEREG mice, in which Foxp3+ regulatory T cells can be depleted by injecting diphtheria toxin,19 to examine the relevance of Treg cells for the MCAO-induced amelioration of arthritis. Depletion of regulatory T cells resulted in enhanced severity and chronicity of G6PI-induced arthritis (figure 6A), confirming our earlier findings.25 MCAO reduced clinical arthritis in Treg-cell-depleted DEREG mice significantly compared with sham-operated mice. Arthritis severity was significantly reduced in both DBA/1 DEREG mice and non-transgenic littermates upon MCAO without a difference between these groups. Treg cells and other cells produce the anti-inflammatory cytokine TGF-β. Serum concentrations of TGF-β can be modulated by the sympathetic nervous system (SNS).37 We, therefore, examined TGF-β serum concentrations 16 and 25 d after GPI immunisation. There was no difference between mice that had undergone MCAO 6 d after G6PI immunisation and sham-operated mice (data not shown). Thus, stroke-induced immunosuppression protects from arthritis even in the absence of Treg cells and independently of increased TGF-β production.
MCAO does not induce increased numbers of regulatory T cells in arthritic mice
We used green fluorescent protein (GFP) expression by Treg cells in the DEREG mouse strain19 to determine the frequency of Treg cells during the course of experimental arthritis. There was no difference between MCAO and sham-operated animals. Approximately 5% of CD4+ T cells were GFP+ Treg before day 15. When acute arthritis was already resolving 25 d postimmunisation, the frequency of Treg cells was 9.9% in the MCAO group and 12.7% in the sham group, respectively (figure 6B). Therefore, the resolution of arthritis was associated with an increase in Treg cells, but this increase was not further enhanced by MCAO.
Stroke-induced immunosuppression is a major pathogenic factor predisposing patients for morbidity and mortality through secondary infections, particularly pneumonia.2–4 6–8 Anecdotal clinical evidence has suggested that stroke or denervation can protect from arthritis.12–17 We show here that stroke-induced immunosuppression modulates the pathogenic immune responses that induce autoimmune arthritis.
The main ex vivo correlate of stroke-induced protection from arthritis was a global reduction in leucocyte numbers. Reduced lymphocyte numbers in secondary lymphatic organs5 ,6 ,7 ,35 ,39 ,40 and the peripheral blood39 are characteristics of stroke in murine models. Several studies have demonstrated that this lymphocyte loss was due to apoptosis.7 ,35 ,39 Offner et al35 reported a reduction in splenic cell yield already 22 h after stroke. This differs from our findings: we did not find dramatically reduced cell numbers in spleen and LN 4 d after MCAO; instead we found a massive reduction in leucocyte numbers 10 d after MCAO. Moreover, we found an approximately twofold reduction in spleen cell numbers, whereas Offner et al35 reported an approximately fivefold reduction. These differences are explicable by several factors. First, we induced MCAO 6 d after immunisation with G6PI in CFA, that is, during an ongoing immune response when T-lymphocytes and B-lymphocytes proliferated in the draining LN and spleen. In contrast, Offner et al analysed unimmunised mice after MCAO. The ongoing activation and proliferation is likely to influence both the cells’ susceptibility to stroke-induced apoptosis and the time needed to replenish the lymphocyte pool. Second, we studied DBA/1 mice, whereas Offner et al used C57BL/6 mice. Mouse strains differ in their susceptibility to stroke-induced immunosuppression.41 In addition to global leucocyte numbers, we also analysed the antigen-specific immune responses to G6PI, the autoantigen inciting the arthritogenic immune responses in G6PI-induced arthritis.18 ,30 There are several novel aspects in the current study of stroke-induced immunosuppression. B cell numbers were significantly reduced in mice in which arthritis was ameliorated after MCAO. In contrast, G6PI-specific antibody titres were not reduced in these animals, reflecting the fact that most of the antibody production had occurred prior to the stroke-induced B cell loss and confirming our earlier findings that antibodies are not sufficient to induce G6PI-induced arthritis.18 ,21
The published data on the influence of stroke on T-cell cytokine production is contradictory. One study reported an initial hyperinflammatory reaction characterised by an increased production of proinflammatory cytokines preceding the stroke-induced immunosuppression in mice.42 A Th1/Th2 shift following clinical43 or experimental39 stroke was reported, whereas another study found unimpaired production of TNF-α and IL-6 in T cells from stroke patients.44 One possible explanation for these contradictory findings is that global ELISAs were used in those studies. Using flow cytometry, antigen-specific Th cells can be identified by their expression of CD154 upon a brief ex vivo stimulation with their cognate antigen.21 ,23–25 ,29 ,45–47 Ten days after immunisation with G6PI, we found similar numbers of G6PI-specific CD4+CD154+ Th cells in the draining LN from control mice and mice that had undergone MCAO. Moreover, the number of cytokine-producing CD4+CD154+ G6PI-specific Th cells was similar in MCAO mice and controls. Therefore, the proliferation of antigen-specific Th cells and the acquisition of Th cell effector functions are unaltered after MCAO.
CD4+CD25+FoxP3+ regulatory T cells maintain immune homeostasis by suppressing immune responses to self and non-self antigens.48 An increased frequency of Treg cells has been reported in patients for up to 3 weeks after stroke.49 Treg cell frequencies were also increased in unimmunised mice 96 h after MCAO.35 Due to the massive loss of lymphocytes, absolute Treg cell numbers were nevertheless strongly decreased in MCAO mice in that study.35 In contrast to these findings, we did not find an increase in Treg cells in MCAO mice. One important difference between our study and the earlier study35 is that we examined the consequences of MCAO in mice with an ongoing autoimmune response. We found increased Treg cell frequencies during the remission phase of arthritis both in MCAO and control mice. This increased Treg cell frequency was not further enhanced by MCAO. Whether Treg cells contribute to the systemic stroke-induced immunosuppression has not been analysed to date. Using a genetic model of Treg cell depletion, we found that Treg cells were dispensable for the arthritis-ameliorating effect of experimental stroke.
How does stroke mediate these immunomodulatory effects? Two immediate candidates are the hypothalamic–pituitary–adrenal axis and the SNS, both of which are known to be immunosuppressive and activated in response to stroke.39 An elegant experimental study showed that both SNS-blockade with Propranolol or application of the glucocorticoid receptor antagonist RU486 prevented the apoptosis-induced decrease in lymphocyte counts. Yet, only Propranolol but not RU486 prevented bacteraemia and pneumonia and improved survival in MCAO mice.39 Thus, activation of the SNS seems to be a major mechanism for stroke-induced immunosuppression. Confirming and extending these findings, we have found that chemical sympathectomy with 6-hydroxydopamine (6-OHDA) prevents G6PI-induced arthritis (Müller et al, manuscript in preparation).
Experimental stroke causes a global loss of leucocytes and ameliorates arthritis. The correlate of protection from arthritis is not the reduction of a particular, pathogenic leucocyte subset or the preferential expansion or emergence of a protective cell population but the global reduction of leucocytes during arthritis.
The authors thank Dr. Tim Sparwasser (Institute of Infection Immunology, TWINCORE, Hannover, Germany) for DEREG mice, Dipl. Ing. Ronald Naumann (MPI of Molecular Cell Biology and Genetics, Dresden, Germany) for speed-congenic back-cross of the DEREG mice onto the DBA/1 strain, Dr. Sylvia Heink (Institute of Immunology, University Hospital Jena, Jena, Germany) for help with mouse-typing and Dr. Andreas Meisel (Department of Neurology, Charité University Hospital Berlin, Germany) for introduction to the MCAO technique. We further thank Claudia Doering for technical assistance in histopathology and Annett Krause for organisational assistance.
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Files in this Data Supplement:
- Data supplement 1 - Online supplement
Handling editor Tore K Kvien
Contributors TK conceived of the concept. II performed experiments and analysed data. MG did and interpreted histopathological studies. IMI and TK designed the studies, interpreted data and drafted the manuscript. All authors read and approved the final manuscript.
Funding This work was supported by the BMBF (IMMUNOPAIN programme “Neuroimmune connections in inflammation and pain”, TP 6 “Neuro-Immunomodulation of Arthritis” (01EC1004B to TK). Federal Ministry of Education and Research.
Competing interests None.
Provenance and peer review Not commissioned; externally peer reviewed.