Mice expressing HLA-DQ6α8β transgenes develop polychondritis spontaneously
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Relapsing polychondritis (RP) is a human autoimmune disease of unknown etiology in which cartilaginous sites are destroyed by cyclic inflammatory episodes beginning, most commonly, during the fourth or fifth decade of life. We have previously described collagen-induced polychondritis that closely mirrors RP occurring in young (6–8 weeks old) HLA-DQ6αβ8αβ transgenic Aβ0 mice, following immunization with heterologous type II collagen (CII).
We present evidence here that transgenic strains expressing the DQ6α8β transgene develop spontaneous polychondritis (SP) at the mouse equivalent of human middle age (4.5–6 months and 40–50 years old, respectively) and display polyarthritis, auricular chondritis and nasal chondritis – three of the most common sites affected in RP. Auricular chondritis in SP, like RP but unlike CII-induced polychondritis, exhibited a relapsing/remitting phenotype, requiring several inflammatory cycles before the cartilage is destroyed. Elevated serum levels of total IgG corresponded with the onset of disease in SP, as in RP and CII-induced polychondritis. No CII-specific immune response was detected in SP, however – more closely mirroring RP, in which as few as 30% of RP patients have been reported to have CII-specific IgG. CII-induced polychondritis displays a strong CII-specific immune response. SP also demonstrated a strong female preponderance, as some workers have reported in RP but has not observed in CII-induced polychondritis. These characteristics of SP allow for the examination of the immunopathogenesis of polychondritis in the absence of an overwhelming CII-specific immune response and the strong adjuvant-induced immunostimulatory influence in CII-induced polychondritis.
This spontaneous model of polychondritis provides a new and unique tool to investigate both the initiatory events as well as the immunopathogenic mechanisms occurring at cartilaginous sites during the cyclic inflammatory assaults of polychondritis.
KeywordsRelapse Polychondritis Human Autoimmune Disease Spontaneous Mouse pNpp Substrate Relapse Polychondritis Patient
bovine serum albumin
type II collagen
enzyme-linked immunosorbent assay
transforming growth factor beta.
Relapsing polychondritis (RP) is a human autoimmune disease of unknown etiology. RP is relatively rare, affecting 3.5–4/1,000,000 people, with a slight female preponderance . Typical onset occurs during mid-life years with a median age of diagnosis at 46.6 years, although cases have been reported in newborns and in individuals over the age of 80 . The most prominent manifestations of RP are auricular chondritis, polyarthritis and saddle nose deformation, with auricular chondritis being the most common presenting symptom [1, 2]. Any other cartilaginous tissue may also be affected in RP, including the eyes, the trachea and the respiratory tract [2, 3]. Other tissues can also be affected since some RP patients have demonstrated renal involvement and skin lesions [2, 4]. Autoantibodies specific for type II, type IX and type XI collagen and for matrilin-1 [5, 6, 7, 8] have all been detected in sera from RP patients, supporting RP as an autoimmune disease.
We have previously described a murine model of induced polychondritis that mimics many characteristics of RP [9, 10]. Young mice (6–8 weeks of age) expressing the HLA-DQ6α8β molecule, either the DQ6α8β transgenic (tg) or DQ6αβ8αβ tg strains, develop polychondritis following immunization with an emulsion of type II collagen (CII) and Complete Fruend's Adjuvant. Induced polychondritis is characterized by a single acute inflammatory event, by auricular chondritis or by polyarthritis, followed by the destruction of the cartilage in both the peripheral joints and ears, and by pannus formation. Neither of the parental strains, DQ6αβ tg mice or DQ8αβ tg mice, develop polychondritis, although DQ8αβ tg mice do develop collagen-induced arthritis [9, 10]. Hansson and colleagues  have also recently described a model of polychondritis, induced in DBA mice and in Lew congenic rats by immunization with bovine matrilin-1 in Complete Fruend's Adjuvant. In that model, there is inflammation of the trachea and respiratory tract, followed by their destruction; however, the ears, joints and other cartilaginous sites are not affected.
We present evidence that when mice expressing the DQ6α8β transgene and lacking both endogenous H2-A and H-2E expression, either DQ6αβ8αβ tg mice or DQ6α8β tg mice, reach middle age (between 4 and 6 months of age), they develop spontaneous polychondritis (SP), with inflammatory events occurring at the ears, the peripheral joints and the nose. Auricular chondritis in SP displayed a relapsing/remitting phenotype, more closely mirroring human RP than induced polychondritis. This model occurs in the absence of overt stimulation by an exogenous antigen such as CII, or adjuvant, or by artificially induced trauma to any of the sites of inflammation, and provides an excellent model that mirrors the human disease more closely than any previously described model of RP.
Materials and methods
The generation of mice expressing both HLA-DQ6αβ (DQA1*0103/DQB*0601) and HLA-DQ8αβ (DQA*0301/DQB*0302) transgenes in the absence of endogenous MHC class II expression (Aβ0) was previously described , and the mice were initially provided by Dr Chella David (Mayo Clinic, Rochester, MN, USA). Briefly, the transgenes were introduced into the H2f background crossed with Aβ0 mice, resulting in tg mice expressing the DQ transgene and lacking both H2-A and H2-E expression. All breeding occurred in laminar flow isolation hoods to maintain a relatively pathogen-free environment. Retired breeders and mice aged greater than 6 months were moved to clean conventional rooms in the Center for Biomedical Research. Mice were given rodent chow and water ad libitum. All studies were approved by the University of North Dakota Institutional Animal Care and Usage Committee. Mice were bled retro-orbitally; the blood was spun for 10 minutes at 12,000 × g and the serum was decanted for analysis of IgG specificity.
Total IgG levels
Total serum IgG levels were determined by ELISA as previously described . Briefly, serum from experimental mice was diluted fourfold, 1/1,000–1/64,0000, in coating buffer (1 M Na2CO3 + 1 M NaHCO3 + 1 M NaN3), and 200 μl was added to Nunc Maxisorb microtiter plates in duplicate and incubated at room temperature for 2 hours. Plates were washed three times with PBS/Tween as in CII antibody, and then 100 μl/well goat anti-mouse immunoglobulin (Sigma-Aldrich, St Louis, MO, USA) was added and plates were incubated for 2 hours at 37°C. Plates were washed three times with PBS/Tween, and then 200 μl/well pNpp substrate (Sigma-Aldrich) was added and incubated for 1 hour at 37°C to visualize the reaction. The colorimetric change of each well was determined at an optical density of 405 nm on a Thermomax Microplate Reader (Molecular Devices, Sunnyvale, CA, USA), and the data were analyzed using the SOFTmax analytical software program (Molecular Devices) and Microsoft Excel.
Type II collagen-specific antibody levels
One hundred microliters of collagen solution (Arthrogen-CIA® mouse type II collagen, 5 mg/ml) diluted in 1 × collagen dilution buffer as per the manufacturer's instructions (Chondrex, Redmond, WA, USA) was added to Nunc Maxisorb microtiter plates (NNI, Rochester, NY, USA) and incubated overnight at 4°C. Plates were washed three times with PBS/0.5% Tween 20, were blocked by adding 1% BSA in PBS (blocking buffer) for 2 hours at room temperature and were then washed again three times with PBS/Tween. Experimental serum was diluted fourfold, 1/1,000–1/64,000, in blocking buffer/Tween, and then 200 μl was added to the plates in duplicate.
Titration of a high-titer CII-specific IgG-positive control and a CII-negative serum control were run with each plate. Sera were incubated for 2 hours at 37°C and were washed three times with PBS/Tween. CII-specific mouse IgG was detected with peroxidase-conjugated goat anti-mouse IgG (Sigma-Aldrich) for 1 hour at 37°C. The plates were again washed three times with PBS/Tween and the reaction visualized with pNpp substrate (Sigma-Aldrich). The colorimetric change of each well was determined at an optical density of 405 nm on a Thermomax Microplate reader, and the data were analyzed using the SOFTmax analytical software program (Molecular Devices) and Microsoft Excel.
Detection of matrilin-1 antibodies
The presence of matrilin-1-specific IgG was determined in sera from representative SP mice, in sera from young and middle-aged naïve DQ6αβ8αβ tg mice and in sera from CII-immunized young DQ6αβ8αβ tg mice by western blot as previously described . Briefly, matrilin proteins were extracted from bovine epiphyseal cartilages, were resolved by SDS-PAGE and were transblotted to polyvinylidene difluoride membrane (BioRad, Richmond, CA, USA) for western blot analysis. The western blot analysis was performed with mouse serum diluted 1:100 and probed with an alkaline phosphatase-conjugated goat anti-mouse IgG Fc (Jackson ImmunoResearch, Avondale, PA, USA). The blots were developed using 5-Bromo-4-chloro-3-indolyl phosphate/nitroblue tetrazolium.
Outer ears displaying clinical chondritis or outer ears from undiseased normal controls were surgically removed from mice anesthetized with Isofluorane (Phoenix Pharmaceutical Inc., St Joseph, MO, USA) at various time points in the course of disease. Ears were embedded in paraffin, were sectioned, were mounted onto slides and were stained with hematoxylin and eosin. Front and hind limbs were removed and dissected from euthanized mice at the conclusion of the experiment. Joints were decalcified and embedded in paraffin. Sections were cut, mounted and stained with hematoxylin and eosin. Sections of both ears and joints were also stained with Safranin O or Toludine Blue to determine the presence of mast cells. All sections were assessed in a blinded fashion by Dr Maryann Sens (Department of Pathology, UNDSMHS, Grand Forks, ND, USA) for histopathological changes and for cellular infiltration.
Statistical analysis was carried out using the Mann–Whitney rank sum test for nonparametric tests. P < 0.05 was considered statistically significant unless otherwise noted.
Spontaneous onset of polychondritis
Summary of spontaneous polychondritis in DQ6α8β transgenic mouse strains
Incidence of spontaneous auricular chondritis (%)
Incidence of spontaneous arthritis (%)
DQ6αβ8αβ (n = 125)
DQ6α8β (n = 114)
Previous studies in human rheumatoid arthritis and RP patients and the collagen-induced arthritis models have shown antibody responses to a variety of collagens, particularly CII [5, 7], as well as cartilage matrix proteins such as matrilin-1 , especially during the acute phase of the disease. As CII-induced murine models of both RP and rheumatoid arthritis are dependent on both exogenous CII and adjuvant, it was of particular interest whether antibody levels were elevated in SP and what antibody specificities were present in the lack of the strong but artificial CII-specific response.
Few spontaneous models of arthritic disease have been observed [14, 15, 16], and none have as yet described all the manifestations necessary to be considered a spontaneous model of relapsing polychondritis – which is characterized not only by polyarthritis, but also by involvement of the ears, the nose and possibly the trachea. Hansson and colleagues have described a chondritic model in which matrilin-1 immunization induces involvement of the respiratory tract but in which peripheral joints and ears are unaffected .
We describe herein a model of spontaneous autoimmune polychondritis that occurs in mice expressing the DQ6α8β transgene without the exogenous stimulation by antigen or adjuvant and the possible interference those substances may add. The mean onset of disease occurs about 6 months of age. Although difficult to directly correlate mouse years with human years, this places the onset of disease approximately at middle age, or near the fourth or fifth decade of life in human years, matching the mean onset of RP in humans. There is a strong female preponderance, which correlates with some reports of human relapsing polychondritis  and autoimmune diseases in general. This would suggest that the gender-related factors that make females more prone to autoimmune responses may also be occurring in this newly identified model, and thus may be better understood. It is of note that enhanced female susceptibility is not observed in the CII-induced model of polychondritis or arthritis.
Human studies have shown that as many as two-thirds of RP patients do not develop antibodies to CII during the course of disease , correlating to the finding that there was not a CII-specific immune response during SP. There are, however, significant total IgG responses in both SP and RP, suggesting a role for antibodies in the pathogenesis of disease. In addition, there is an increased infiltration of mast cells into the synovium and ears during SP, which also correlates with other recent reports suggesting a pathogenic role for the elevated IgG through mast cells in RA and animal models of arthritis [18, 19, 20, 21]. We are currently investigating the contribution the mast cells infiltrating into the cartilaginous tissues have toward the pathogenesis of SP. In addition, a strong antibody response to matrilin-1 is observed during SP, raising the possibility that matrilin-1 may be the putative autoantigen in the initiation of SP. This would correspond with an antimatrilin-1 antibody response observed in human RP patients  and with the ability of heterologous matrilin-1 to induce a polychondritis-like disease in mice .
There has been significant interest in another putative autoantigen, the ubiquitous protein glucose-6-phosphate-isomerase (G6PI), because antibodies specific for G6PI have been found deposited in the joints of RA patients as well as in mouse models of RA . There have not, however, been any reports of auricular chondritis in K/B × N mice or of anti-G6PI antibodies in RP patients. Both DQ6α8β tg expressing strains displayed high titers of anti-G6PI IgG1 regardless of the presence of clinical disease (Bradley and Wooley, personal communication), suggesting that while the deposition of antibody complexes into the joint may contribute to the overall destruction of synovial or auricular tissue, it is most probably not the initial trigger in pathogenesis of autoimmune damage in SP.
Treatment with transforming growth factor beta (TGF-β) has been shown recently to provide some protective effect against collagen-induced arthritis in young, susceptible mice, although the effects are not long-lasting. In aging mice, however, treatment with TGF-β has been shown to block induction of arthritis altogether . DQ6α8β tg expressing mice displayed an overall increase in the levels of TGF-β, regardless of the presence of disease, as compared with controls (naïve B10.T(6R) mice), with many samples reading high and out of range (Bradley and Cafruny, personal communication). It is unclear how this finding correlates with the immunoregulatory role of TGF-β in arthritis. It is possible, however, that the elevated TGF-β levels represent an active attempt by these mouse strains to downregulate the vigorous (auto)immune response. Alternatively, the TGF-β serum levels may represent another form of dysregulation, such as the role of TGF-β-specific antibodies in lupus-like diseases .
Correlations have been made between the HLA genotype and the genetic predisposition to many autoimmune diseases, including rheumatoid arthritis (HLA-DR4, DQ8), insulin-dependent diabetes mellitus (DR4, DQ8), thyroiditis (DR3) and multiple sclerosis (DR4) . The occurrence of SP in a mouse expressing the DQ6α8β transgene and lacking endogenous MHC class II expression may provide insight into the potential contribution of mixed haplotype molecules to RP, and perhaps more generally to immune responses. It is of note that HLA-DR4 subtypes, some of which are linked with DQ8 due to linkage disequilibrium, have been associated with RP [2, 26]. This association is true of the DR4 subtypes linked with DQ8 and the subtypes not linked with DQ8, however, suggesting that the RP HLA-D association may be more complex than the allelic association. This may also suggest that one or more mixed haplotypes molecules (e.g. DQ6α8β) may be able to present the pathogenic epitopes responsible for polychondritis.
The SP model of RP described herein is a model lacking artificial stimulation or enhancement in which the immunopathogenic events underlying inflammation of the joints, the ears, the nose and perhaps other cartilaginous sites can be examined, including, but not limited to, the role of antibody and mast cells in RP and related diseases. In addition, this model should provide an excellent tool to evaluate therapeutic regimes for RP and other inflammatory autoimmune diseases. As SP occurs in strains of mice expressing the mixed haplotype DQ6α8β molecule, it may also provide insight into genetic susceptibility of diseases in which the allelic models of predisposition have not provided clarity.
The authors thank Dr Mary Ann Sens (UNDSMHS) for the histological analyses of polyarthritic and chondritic tissues, Dr Rachel Caspi (NIH-NEI) for performing the ocular examinations, Dr Paul Wooley (Wayne State Medical School) for performing the anti-G6PI analysis and Dr William A Cafruny (University of South Dakota School of Medicine) for assaying the TGF-β levels present in DQ6α8β tg expressing mice. They also thank the staff of UND's Center for Biomedical Research for their excellent care of the mice utilized in these studies. These studies were funded by a grant from the NIH-NIAMS.
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