Introduction
Systemic lupus erythematosus (SLE) is a chronic inflammatory autoimmune disease characterized by multiple organ involvement, production of autoantibodies to nuclear components, and immune complex deposition [
1]. Lupus nephritis (LN) is regarded as one of the most severe organ manifestations of SLE, affecting approximately 35% to 50% of patients with lupus. Despite increased knowledge of pathogenesis and improved treatment regimens, LN remains a main cause of morbidity among patients with SLE [
2].
High-mobility group box 1 protein (HMGB1), a nuclear protein found in all mammalian cells, is known as a DNA-binding protein participating in chromatin structure and transcriptional regulation [
3,
4]. Extracellular HMGB1 has been identified as a proinflammatory mediator and, owing to its proinflammatory and immunostimulatory properties, has been proposed to contribute to the pathogenesis of multiple chronic inflammatory and autoimmune diseases [
5‐
8]. HMGB1 is actively secreted from activated immune cells such as macrophages and monocytes and is passively released from injured or necrotic cells. When translocated from the nucleus to the extracellular milieu, HMGB1 can act as an 'alarmin', a danger signal that can activate the immune system and has been demonstrated as a key factor in necrosis-induced inflammation [
9,
10]. Moreover, HMGB1 induces other cytokines such as tumor necrosis factor and interleukin-1 (IL-1), IL-6, and IL-8 and is an activator of endothelial cells leading to the upregulation of adhesion molecules [
11,
12].
Elevated serum levels of HMGB1 have been found in different inflammatory conditions such as sepsis [
13], rheumatoid arthritis [
14,
15], anti-neutrophilic cytoplasmatic antibody (ANCA)-associated vasculitis [
16], and chronic kidney disease [
17] as well as in SLE [
18‐
20]. Previous studies have shown increased HMGB1 expression in skin lesions of patients with SLE [
21], thus indicating that HMGB1 may be an important mediator of inflammation in target organs in lupus.
Interestingly, increased levels of HMGB1 were recently demonstrated in patients with active LN in comparison with patients with active non-renal disease [
22]. However, specified data on the severity of renal disease, histopathological findings, or tissue expression were not included in that study. The aim of this study was to investigate renal tissue expression and serum levels of HMGB1 in correlation not only with renal histopathological and clinical activity but also with response to therapy in order to further investigate its role in patients with LN.
Materials and methods
Patients
Thirty-five patients with SLE and biopsy-proven active LN during the period of 1996 to 2008 were included in this study. All patients fulfilled the 1982 American College of Rheumatology classification criteria for SLE [
23] and participated in a prospective control program for LN at the rheumatology clinic of Karolinska University Hospital in Stockholm, Sweden. Thirty of the 35 patients were female (86%) and five were men (14%), and the mean age was 34 years (range of 18 to 50). The patients were treated, in accordance with standard therapy for LN, with corticosteroids combined with cyclophosphamide (
n = 21), mycophenolate mofetil (
n = 8), or rituximab (
n = 5), and one patient was treated with azathioprin. After induction therapy for a mean duration of 8 months (range of 6 to 14), all patients underwent a second renal biopsy. At both biopsies, clinical data and blood and urinary samples were collected. Serum samples were frozen at -70°C for future analyses. As a control group for serum levels of HMGB1, blood samples from 48 healthy controls were used [
17]. The clinical characteristics of patients and nephritis data at baseline and follow-up are presented in Table
1.
Table 1
Clinical characteristics of all patients at baseline and follow-up
Creatinine, μmol/L | 92.3 (46.6) | 81.6 (42.6) |
Proteinuria, g/day | 2.0 (1.8) | 0.7 (0.8) |
C3, g/L | 0.53 (0.23) | 0.80 (0.23) |
C4, g/L | 0.09 (0.06) | 0.13 (0.07) |
C1q | 66.6% (41.0%) | 75.2% (29.5%) |
Anti-dsDNA-positivea | 83% | 44% |
Glomerular filtration rate | 80.7 (29.4) | 88.6 (26.4) |
U-erythrocytes > 1+ | 79% | 46% |
Renal histology, number | | |
Class I | 15 | 1 |
Class II | 12 | 13 |
Class III | 2 | 6 |
Class IV | 6 | 3 |
Class III/V | | 12 |
Class V | | |
Activity index | 5.7 (3.1) | 2.5 (2.3) |
Chronicity index | 1.8 (2.0) | 2.3 (2.3) |
Treatment, number | | |
Cyclophosphamide | 21 | |
Mycophenolate mofetil | 8 | |
Rituximab | 5 | |
Azathioprin | 1 | |
BILAG renal index, number | | |
A | 32 | 2 |
B | 3 | 18 |
C | | 7 |
D | | 8 |
Evaluation of renal function, histopathology, and renal activity
Renal evaluation at the time point of the first and second biopsies included urine analyses (dipslide procedure), urinary sediment assessment, and investigation of 24-hour urine albumin excretion. Renal function was determined by serum creatinine levels (expressed as micromoles per liter) and estimated glomerular filtration rate (GFR) by using the modification in diet in renal disease (MDRD) formula [
24].
Renal biopsies were performed by percutaneous ultrasonography-guided puncture. The renal tissue obtained was evaluated by light microscopy, immunofluorescence, and electron microscopy. The biopsies were graded according to the World Health Organization (WHO) classification of nephritis [
25] and additionally scored for activity and chronicity indices [
26]. Renal tissue from an unaffected part of a kidney that was nephrectomized owing to carcinoma was used as control. Evaluation of renal activity was estimated by using the British Isles lupus assessment group (BILAG) index [
27,
28]. Patients with renal BILAG C or D at follow-up were regarded as responders (as previously suggested [
29]).
Serology and complement measures
Assessments of serum IgG anti-double-stranded DNA (anti-dsDNA) antibodies were carried out by immunofluorescence microscopy by using Crithidiae luciliae as a source of antigen. Analyses of complement component C1q were performed by rocket electrophoresis by using rabbit anti-C1q as the antibody. Levels of C1q were expressed as the percentage of the levels of healthy blood donors (normal range of 76% to 136%). C3 (normal range of 0.67 to 1.43 g/L) and C4 (normal range of 0.12 to 0.32 g/L) levels were determined by nephelometry.
HMGB1 serum determination
HMGB1 was analyzed by Western blot in sera from 20 of the patients at baseline and at repeat biopsy by a method previously described [
17].
Immunohistochemical staining of renal biopsies
Immunohistochemical stainings of HMGB1 expression were performed on formaldehyde-fixed paraffin-embedded serial 4-μm sections of renal biopsies. Slides were deparaffinized in xylene and rehydrated with ethanol. Antigen retrieval treatment prior to staining was omitted to allow clearer visualization of extranuclear HMGB1. To block endogenous peroxidase activity, sections were treated with 3% H2O2 followed by a serum block with 2% human AB sera for 30 minutes and an avidin/biotin-blocking step (Vector Laboratories Inc., Burlingame, CA, USA). The slides were thereafter incubated overnight with an affinity-purified monoclonal mouse IgG2b anti-HMGB1 antibody (concentration of 10 μg/mL, 2G7; Critical Therapeutics Inc., Lexington, MA, USA). A biotin-labeled horse anti-mouse antibody (Vector Laboratories Inc.) containing 2% normal horse serum was used for detection. Stainings were developed by using a DAB kit (Vector Laboratories Inc.) in accordance with the instructions of the manufacturer. Sections were counterstained with Mayer's hematoxylin. Phosphate-buffered saline supplemented with 0.1% saponin was used in all subsequent washes and incubation steps in order to permeabilize the cells. In each assay, controls for specificity of the HMGB1 staining were included on the basis of parallel staining studies omitting the primary antibody, and a primary isotype-matched immunoglobulin of irrelevant antigen specificity (negative mouse IgG2b control; Dako Cytomatation, Glostrup, Denmark) was used. The specificities of extracellular and intracellular HMGB1 immunoreactivities were further verified by blocking experiments with preabsorption of the HMGB1-specific antibody with recombinant HMGB1 prior to staining.
Statistics
For comparisons of variables at baseline and at repeat biopsy, the non-parametric Wilcoxon matched pair test was used. For comparisons of variables between groups, the non-parametric Mann-Whitney test was used. Correlations were calculated by using Spearman's rank correlation. P values of less than 0.05 were considered statistically significant. Statistical evaluation was made with statistical software (STATISTICA 9; StatSoft, Inc., Tulsa, OK, USA).
Ethics
Informed consent was obtained from all subjects, and the study protocol was approved by the regional ethics committee in Stockholm.
Discussion
To the best of our knowledge, we are the first to demonstrate HMGB1 expression in affected renal tissue from LN patients, in whom we clearly show an increased expression in active disease as well as after immunosuppressive therapy. HMGB1 tissue stainings were predominantly found outlining the glomerular endothelium but also were expressed in the mesangium. In this study, we could also confirm the findings of elevated serum levels of HMGB1 in LN measured by Western blot, as recently shown by Abdulahad and colleagues [
22].
We found a clear tissue staining for HMGB1 in LN and this staining was absent in non-lupus control renal tissue. There was no distinct difference in expression of HMGB1 either in the proliferative glomerular lesions or in sites with infiltrates of inflammatory cells in comparison with less affected glomeruli, and the exact origin of the increased renal expression of HMGB1 is not fully clear. The staining outlining the glomerular endothelium could emanate from local extracellular release but also may reflect capture from circulating HMGB1. Thus, one may speculate that the findings of increased serum levels as well as tissue expression of HMGB1 reflect both systemic and local inflammation within the kidney. In glomeruli, the pronounced endothelial staining and the increased expression in the mesangium suggest a co-localization for HMGB1 and immune depositions in LN. However, further studies with other methodologies are required to address this issue.
Elevated HMGB1 expression has previously been demonstrated in lupus patients with cutaneous photoinduced inflammation, in whom cytoplasmatic and extracellular HMGB1 were detected in biopsies from the most clinically active skin lesions in comparison with inactive or non-lesional skin [
21]. That study also demonstrated that HMGB1 was still expressed in persisting dermal infiltrates in a proportion of healing lesions, thus suggesting that HMGB1 might be a mediator of both early and late inflammation and may participate in the inflammatory process over longer periods of time.
In a recent study by Bruchfeld and colleagues [
16], increased serum levels and renal tissue expression of HMGB1 were demonstrated in ANCA-associated vasculitis with renal involvement. In that study, high baseline serum levels of HMGB1 decreased significantly after treatment, and in contrast to our findings in LN, a more distinct histopathological response and a more distinct clinical response were demonstrated. These findings are consistent with other studies showing that patients with LN, even patients with quiescent clinical pictures, still may have histopathological inflammatory activity after induction treatment [
30,
31]. Of note, less than half of the patients in the present study were regarded as renal responders according to the definition used. Our observation that serum HMGB1 remained significantly elevated combined with persistent expression in renal tissue at follow-up may reflect an ongoing inflammatory activity in patients with LN despite immunosuppressive therapy. The findings in patients with vasculitis are of particular interest since LN with a focal segmental glomerular pattern (WHO class III), which had the highest HMGB1 levels in our study, has been considered to have features and possibly immune mechanisms similar to those of lesions of systemic vasculitis [
32] in comparison with the more widespread global pattern characterized by more pronounced immune depositions seen in patients with class IV. The difference observed in HMGB1 levels when focal and diffuse proliferative nephritis were compared may suggest differences in pathogenic mechanisms and deserves further studies.
In the study by Abdulahad and colleagues [
22], a correlation between serum HMGB1 and proteinuria was shown in active SLE patients having some degree of proteinuria but was not confirmed in our study on patients with active biopsy-proven LN only. The two study populations may not be fully comparable, however. Although we could confirm the finding of elevated HMGB1 levels in patients with LN as determined by Western blot, the methods used in the two studies may not be fully comparable (whole serum in the study by Abdulahad and colleagues [
22] in comparison with low molecular serum components in the present study). This methodological issue may have contributed to the discrepancies regarding circulating HMGB1 and disease activity between the two studies. Further studies would be of interest to determine the optimal method for HMGB1 determination in patients with LN.
Although HMGB1 levels have been shown to correlate inversely with renal function in patients with chronic kidney disease [
17], no such correlation was found in our study or in the previous study of patients with SLE [
22]. HMGB1 has been proposed to be involved in the pathogenesis of SLE, and several biological properties of HMGB1 are currently of major interest in SLE research [
8]. Inappropriate apoptosis is regarded as a key event in the pathogenesis of SLE. Nuclear autoantigens from not properly cleared apoptotic cells may be excessively presented to the immune system, resulting in loss of self-tolerance and generation of nuclear autoantibodies [
33]. HMGB1 released from apoptotic cells may therefore be of special interest in SLE. In primary apoptosis, there is almost no release of HMGB1; however, in conditions with inappropriate clearance of apoptotic material, apoptotic cells may undergo secondary necrosis leading to HMGB1 release [
34,
35]. HMGB1 has been demonstrated to bind to the chromatin of cells during apoptosis and to remain bound to nucleosomes when released from apoptotic cells. Furthermore, HMGB1-nuclesome complexes have recently been demonstrated to induce the production of proinflammatory cytokines from macrophages and dendritic cells and to induce anti-dsDNA and anti-histone IgG responses and therefore may play a central role in breaking tolerance against nuclear antigens [
36]. In that study, circulating HMGB1-nucleosome complexes were detected in serum from patients with SLE but not in healthy controls.
Previous studies have demonstrated high levels of anti-HMGB1 antibodies in patients with SLE [
22,
37]. This finding raises the possibility that the monoclonal anti-HMGB1 antibody used for tissue staining could have difficulties in binding to HMGB1 if the epitope was already occupied by deposited anti-HMGB1 antibodies. This could possibly contribute to underestimating the local renal expression of HMGB1 and, if so, could explain why there were no clear differences in HMGB1 expression in the most proliferative inflammatory lesions in comparison with less affected glomeruli.
Biomarkers available for assessing renal activity and classification, response to therapy, remission, and flares are insufficient in SLE and do not always reflect the actual inflammatory activity in the renal tissue [
30,
38]. Although renal biopsy is regarded as the 'gold standard' for assessing renal activity [
39], there is a need for new biomarkers for evaluation of disease activity in LN. In the present study, we were not able to determine whether serum levels of HMGB1 could be used for monitoring of renal disease activity
per se but found persistently elevated levels of serum as well as tissue expression, suggesting that HMGB1 is an important inflammatory mediator in LN. To determine whether a more pronounced reduction of HMBG1 levels can be achieved in a less active phase of LN, more long-term studies with sequential serum HMGB1 determination and repeat biopsies will be required, however.
As therapeutic targeting of HMGB1 has been found to be protective against tissue injury in various preclinical inflammatory disease models (reviewed in [
40]), HMGB1 blocking may be of future interest in the development of new treatment strategies in autoimmune disease and also in SLE. As our study was of limited size, additional extended studies will be required to study the role of HMGB1 as a biomarker for renal disease activity in patients with lupus.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
AZ participated in patient characterization, acquisition of data, statistical analyses, interpretation of results, and manuscript writing. KP participated in immunohistochemistry staining, interpretation of results, and manuscript writing. BS participated in evaluation of renal biopsies and interpretation of results of HMGB1 tissue staining. SC and KJT were responsible for serum HMGB1 measurement and interpretation of data. AB participated in interpretation of results and manuscript writing. IG participated in study design, interpretation of results, and manuscript writing. All authors were involved in revising the manuscript critically for content and read and approved the final manuscript.