Introduction
Rheumatoid arthritis (RA) is a highly inflammatory chronic polyarthritis that causes joint destruction, deformity, and loss of function. Sequelae include pain, disability, and increased mortality. A role for CD4
+ T cells in the pathogenesis of RA is inferred from the strong HLA-DR association as well as the large numbers of major histocompatability complex class II-positive cells found in close proximity to activated CD4
+ T cells in inflamed joints. Furthermore, immunisation of transgenic mice expressing RA-associated HLA-DR4/DR1 haplotypes with type II collagen results in arthritis [
1,
2] and reveals a single immunodominant epitope (amino acids 261 to 273) that overlaps the immunodominant epitope in DBA/1 mice with collagen-induced arthritis (CIA) (256 to 270) [
1,
3].
The identification of tumour necrosis factor-alpha (TNF-α) as a key mediator of inflammation in RA has led to the development of TNF-α-blocking biologics that control disease activity, but there remains a need for therapies capable of modulating the underlying immune response [
4].
Pre-clinical assessment of therapeutics for RA has relied largely on murine models of arthritis, particularly the CIA model, in which mice are immunised with heterologous type II collagen in complete Freund's adjuvant (CFA) [
5]. The development of CIA is strain-dependent, with H-2
q and H-2
r haplotypes showing the greatest degree of susceptibility. The DBA/1 strain (H-2
q) is the most commonly used strain for pre-clinical testing of potential anti-arthritic drugs and was successfully used to predict the beneficial effects of TNF-α blockade [
6,
7]. However, although CIA in DBA/1 mice has been extremely useful for testing drugs with anti-inflammatory properties, its usefulness for assessing T cell-targeted therapies is limited to some extent by the relatively acute nature of the disease.
A further limitation of the classic CIA model in DBA/1 mice is that most transgenic and knockout strains of mice are on a C57BL/6 (B6) background (H-2
b), which is regarded to be relatively resistant to arthritis induction when bovine type II collagen is used as an immunogen [
8,
9]. To circumvent this problem, genetically modified strains have generally been backcrossed for a minimum of eight generations onto the DBA/1 background, which introduces a delay of 1 to 2 years. However, it has been reported that, contrary to previous findings, B6 mice are indeed susceptible to arthritis induced by chicken type II collagen [
10‐
12], although many groups have been unable to induce arthritis in this strain in a reproducible manner [
8].
The primary aims of this project were to characterise CIA in the C57BL/6 mouse clinically and histologically and to analyse cellular and humoral immune responses to type II collagen during the course of the disease. We show that B6 mice develop a chronic form of CIA and that this model closely resembles human RA in terms of its disease course, histological findings, and in its response to commonly used anti-arthritic drugs. We also show that B6 mice develop a sustained T-cell response to chicken collagen as well as to autologous (mouse) collagen.
Materials and methods
Purification of type II collagen
Bovine collagen was purified from articular cartilage, and mouse and chicken collagens were purified from non-articular (sternal) cartilage. All collagens were prepared by pepsin digestion and salt fractionation according to established procedures [
13]. Lathyritic rat type II collagen (a gift from Lars Klareskog, formerly of Uppsala, Sweden) was prepared without pepsin.
Induction and assessment of arthritis
Ten- to 12-week-old male mice were used for all procedures, were housed in groups of 10, and were maintained at 21°C ± 2°C on a 12-hour light/dark cycle with food and water
ad libitum. All experimental procedures were approved by the local ethical review process committee and the UK Home Office. DBA/1 mice were bred at the Kennedy Institute of Rheumatology (London, UK) and B6 mice were purchased from Harlan UK (Bicester, Oxfordshire, UK). To reduce the risk of fighting amongst males, mice from different cages were not mixed beyond 6 weeks of age. All mice were immunised intradermally in two sites at the base of the tail with 200 μg of bovine, chicken, or mouse type II collagen in CFA as described previously [
13]. To prepare the CFA, 100 mg of desiccated killed
Mycobacterium tuberculosis H37Ra (BD Biosciences, Oxford, Oxfordshire, UK) was ground with a pestle and mortar to produce a fine powder and then suspended in 30 mL of incomplete Freund's adjuvant (BD Biosciences). It was observed that fighting amongst male mice reduced the incidence of arthritis. Hence, to reduce the risk of fighting, mice from different cages were not mixed beyond 6 weeks of age. Each experiment was performed on a minimum of two occasions.
For macroscopic assessment of arthritis, the thickness of each affected hind paw was measured daily with microcalipers (Kroeplin GmbH, Schlüchtern, Germany) and the diameter was expressed as an average for inflamed hind paws per mouse. Animals were also scored for clinical signs of arthritis [
13] as follows: 0 = normal, 1 = slight swelling and/or erythema, 2 = pronounced oedematous swelling, and 3 = joint rigidity. Each limb was graded thus, allowing a maximum score of 12 per mouse. After completion of the experiment, mice were sacrificed and hind paws were immersion-fixed in 10% (vol/vol) buffered formalin and decalcified with 5.5% EDTA (ethylenediaminetetraacetic acid) in buffered formalin.
For histological assessment of arthritis, arthritic mice were killed up to 2 weeks after disease onset (early arthritis, n = 8) or 6 to 8 weeks following onset (late arthritis, n = 8). Joints were decalcified and paraffin-embedded, and sections (10 μm) were stained (haematoxylin and eosin) for conventional histology. Joints were classified according to the presence or absence of inflammatory cell infiltrates (defined as focal accumulations of leukocytes). Histological analysis was performed in a blinded fashion by a trained histopathologist (AS) (N = 8 per point).
Analysis of antibody production
Anti-collagen antibody isotypes were assessed in the serum of mice with early or late arthritis. Enzyme-linked immunosorbent assay (ELISA) plates (Thermo Fisher Scientific, Rochester, NY, USA) were coated with 5 μg/mL of type II collagen dissolved in Tris buffer (0.05 M Tris, containing 0.2 M NaCl, pH 7.4), blocked with 2% bovine serum albumin, and then incubated with serial dilutions of test sera. A standard curve was created for each assay by including serial dilutions of a reference sample on each plate. The reference sample was arbitrarily assigned an antibody concentration of 1 AU/mL. Bound IgG1 or IgG2a/c was detected by incubation with horseradish peroxidase-conjugated sheep anti-mouse IgG1 (BD Biosciences), or an antibody that recognises both IgG2a and IgG2c (BD Biosciences), followed by TMB (3,3', 5,5'-tetramethylbenzidine) substrate. Optical density was measured at 450 nm. Antibody concentrations for each serum sample were obtained by reference to the standard curve (N = 8 per point).
Analysis of T-cell activity
Inguinal lymph nodes were excised from mice with early or late arthritis. Lymph node cells (LNCs) were cultured in RPMI 1640 containing foetal calf serum (10% vol/vol), 2-mercaptoethanol (20 μM), L-glutamine (1% wt/vol), penicillin (100 U/mL), and streptomycin (100 μg/mL) in the presence or absence of type II collagen or the synthetic collagen fragment CII256-270 (both at 50 μg/mL). After 48 hours, 100 μL of culture medium was carefully removed for measurement of cytokines and the remaining cells were pulsed with 1 μCi 3H thymidine per well for a further 18 hours. Cells were then harvested and plates were assessed for 3H thymidine incorporation. Each assay was performed on a minimum of three occasions. Secreted interferon-gamma (IFN-γ), interleukin (IL)-5, and IL-10 were measured in the culture supernatant by sandwich ELISA using capture and detection antibody pairs (BD Biosciences).
Drug therapy
The therapeutic responses of arthritic B6 and DBA/1 mice to intraperitoneal administration of dexamethasone (0.5 mg/kg daily), anti-TNF monoclonal antibody (mAb) (TN3-19.12; 300 μg every 3 days), methotrexate (0.75 mg/kg every 3 days), or indomethacin (2.5 mg/kg daily) were assessed. The therapeutic response was defined as the percentage reduction in clinical score following 10 days of therapy relative to mice treated with vehicle alone. Each experiment was performed twice.
Statistical analysis
Statistical analysis was performed by one-way analysis of variance followed by Dunnett multiple comparisons test, where appropriate.
Discussion
The model of CIA, a T cell- and cytokine-dependent disease, in DBA/1 mice has led to increased understanding of RA and has facilitated the development of novel biologics, such as TNF-blocking therapies [
16]. However, the apparent resistance of strains normally used to carry modified genes has impeded our ability to rapidly ask basic questions about disease pathogenesis, as a 1- to 2-year backcross to DBA/1 mice is needed. Our aim was to comprehensively assess the susceptibility of B6 mice to CIA and compare the disease with the 'classic' model in DBA/1 mice.
Our studies showed that chicken, and not bovine, CII was capable of inducing disease in B6 mice, with an incidence of 50% to 75%, an incidence similar to that previously described [
10‐
12]. This is in contrast to DBA/1 mice, in which bovine, mouse, and chicken CII all induced disease, with an incidence of 80% to 100%. This may account for reports of resistance to CIA in B6 mice, in which bovine CII was used for immunisation [
8]. Other confounding factors could include the quality of collagen preparation, or substrains of B6 mice, and it is important to note that our study was carried out with B6 mice purchased from Harlan UK, although we have obtained similar results with B6 mice from Charles River UK Ltd. (Margate, Kent, UK).
The phenotype of arthritis was milder in B6 mice than in DBA/1 mice, with less swelling and a more gradual increase in clinical score. Histological assessment of the hind paws from arthritic DBA/1 and B6 mice revealed that, in early arthritis (up to 2 weeks after onset), there was a similar degree of inflammatory cell infiltration in the two strains. In contrast, in late arthritis (6 to 8 weeks after onset), inflammatory cell infiltration was reduced in DBA/1 mice compared with B6 mice, although it remains to be established which cell types are present in the joints of B6 CIA.
Assessment of lymph node responses showed that in the B6 mouse, both early and late after immunisation, proliferation and IFN-γ production in response to collagen occurred. Also of note, a strong response was observed in B6 mice to mouse collagen, suggesting the autoimmune nature of the model. It must be noted that bovine and murine collagen did not induce arthritis in B6 mice.
The reason why chicken, and not mouse or bovine, CII is arthritogenic in B6 mice is presumably due to recognition by B6 T cells of a peptide of chicken CII in the context of H-2b class II molecules. This suggests that differences in the amino acid sequence between chicken and mouse/bovine CII are required to break tolerance and induce arthritis. It is intriguing that the T-cell response was greater and more sustained in B6 mice compared with DBA/1 mice, but the reasons for this are unknown. The number and activity of CD4+CD25+ regulatory T cells were found to be similar in the two strains (G. Criado, M. Medghalchi, R.O. Williams, unpublished observations). Therefore, we cannot attribute sustained T-cell responses to any obvious defect in regulatory T cells in B6 mice.
It has been proposed that pepsin (used to purify collagen) plays an important role in breaking T-cell tolerance to collagen and that much of the T-cell response in some strains of mice and rat is directed against pepsin or pepsin-modified epitopes of collagen [
14]. By showing equivalent responses to CII prepared with and without pepsin using lathyritic collagen [
14], we have shown that the T-cell response is not dependent on pepsin in this model, in contrast to rat strains, in which T-cell responses have been shown to be directed mainly against contaminating pepsin [
15]. However, we cannot exclude the possibility that pepsin contributes to the breaking of tolerance during immunisation, and we were unable to obtain lathyritic chicken type II collagen in order to test this hypothesis. However, the mycobacterial component of CFA provides many factors that are able to break tolerance via activation of Toll-like receptors.
The therapeutic profile of CIA in the B6 mouse was similar to that of RA, with a therapeutic action of methotrexate at a dose comparable to human therapy. This is in contrast to CIA in DBA/1 mice, in which methotrexate had no effect. One of the anti-inflammatory mechanisms of methotrexate is thought to be due to increased adenosine production [
17]. Adenosine acts via G-protein-coupled receptors to increase cAMP levels, which is known to reduce inflammation [
18]. It was recently reported that DBA/1 mice, but not B6 mice, are genetically resistant to the effects of methotrexate, due to defective adenosine accumulation [
19]. This is of particular significance as methotrexate is now regarded as the 'gold standard' small-molecular-weight drug for RA and is frequently used in combination with biologics, such as anti-TNF therapy [
20]. There is, therefore, an increasing need to model the anti-arthritic effects of methotrexate in combination with other therapies in order to optimise treatment regimens and to identify possible interactions. Likewise, indomethacin did not slow the disease progression of CIA in B6 mice, as in RA, but significantly reduced the disease severity of CIA in DBA/1 mice [
21].
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
JJI was the main investigator, carried out most of the experiments, and contributed to the preparation of the manuscript. GC carried out some experiments and contributed to the preparation of the manuscript. MM performed some experiments. MA performed cytokine ELISAs. AS analysed joint histology. MF contributed to the preparation of the manuscript. ROW was the principal investigator, designed the study, and contributed to the preparation of the manuscript. All authors read and approved the final manuscript.