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CD4+CD28− T cells exhibit autoreactive potential in autoimmune disorders, including rheumatoid arthritis (RA). It is not well known which costimulator functions as an alternative second signal in the activation of this subset after CD28 expression is downregulated. Tumor necrosis factor receptor superfamily member OX40 is a key costimulator in the activation of T cells. The aim of this study was to investigate the costimulatory effects of OX40 on CD4+CD28− T cells in autoimmune arthritis.
Clinical samples were collected from patients with RA and control subjects. Collagen-induced arthritis (CIA) was induced with collagen type II (CII) in DBA/1 mice. The CD4+CD28−OX40+ T-cell subset and its cytokine production were detected by flow cytometry. After T-cell purification, adoptive transfer was performed in CIA mice. The regulatory role of OX40 was determined by blocking experiments in vitro and in vivo.
OX40 and OX40L were abnormally expressed in patients with RA and CIA mice. Further analysis showed that CD4+CD28−OX40+ T cells accumulated in patients with RA and in animal models. These cells produced higher levels of proinflammatory cytokines and were closely correlated with the clinicopathological features of the affected individuals. Adoptive transfer of CII-specific CD4+CD28−OX40+ T cells remarkably aggravated arthritic development and joint pathology in CIA mice. Moreover, OX40 blockade significantly reduced the proinflammatory responses and ameliorated arthritis development.
OX40 acts as an alternative costimulator of CD4+CD28− T cells and plays a pathogenic role in autoimmune arthritic development, suggesting that it is a potential target for immunomodulatory therapy of RA.
The online version of this article (doi:10.1186/s13075-017-1261-9) contains supplementary material, which is available to authorized users.
Rheumatoid arthritis (RA) is a type of symmetric polyarticular arthritis, and T cell-mediated autoimmune responses to the articular synovium play a central role in the pathogenesis of RA [1, 2]. A marked accumulation of CD4+ T cells that lack CD28 expression is observed in patients with RA . CD4+CD28− T cells are autoreactive and could be regarded as effector memory T cells . T-cell activation requires antigen recognition along with a second signal delivered by interactions between the costimulatory receptor on T cells and its ligands on antigen-presenting cells (APCs) . Costimulatory molecules, including B7/CD28 and tumor necrosis factor (TNF)/tumor necrosis factor receptor (TNFR) superfamily members, are critical in antigen-specific T-cell responses. The absence of a second signal results in anergy and programmed cell death [6, 7]. However, loss of CD28 does not induce apoptosis in CD4+ T cells of patients with RA, suggesting that CD28-independent costimulatory pathways are involved in T-cell activation.
OX40 (CD134) and its ligand OX40L (CD252) are members of the TNF/TNFR superfamily. OX40 (TNFR superfamily member 4, TNFRSF4) is predominantly expressed by activated T cells, whereas the primary source of OX40L (TNF superfamily member 4, TNFSF4) is likely to be APCs. OX40 ligation augments the effector differentiation and the survival of memory T cells. The roles of OX40 and OX40L have been examined in most well-established autoimmune models [8, 9]. Although TNFSF4 polymorphisms were shown not to be linked with RA susceptibility , blockade of OX40/OX40L in collagen-induced arthritis (CIA) mice dramatically ameliorated disease severity [11, 12]. This indicates that OX40 signal plays a critical role in the development of autoimmune arthritis. As an enhancer of effector memory T cells, OX40 may not be an initiator, but may be an accelerator, in the pathogenesis of RA. Association of OX40 expression with arthritis development should be further investigated. Meanwhile, whether OX40 signal is involved in the activation of CD4+CD28− T cells in RA should be clarified.
In view of this, potential correlations were analyzed between the CD4+CD28−OX40+ T-cell subset and clinicopathological characteristics of affected individuals among patients with RA and CIA mice. After cell sorting, the arthritis-associated pathogenic role of CD4+CD28−OX40+ T cells was investigated. Moreover, using OX40 blockade in vitro and in vivo, we revealed regulatory roles of OX40/OX40L signaling in autoimmune arthritis.
A total of 71 patients with RA diagnosed according to the 2010 rheumatoid arthritis classification criteria were recruited . Additionally, 44 sex- and age-matched patients with osteoarthritis (OA) and 47 healthy volunteers healthy controls (HCs) were included as control subjects. All subjects were recruited from the Third Affiliated Hospital of Soochow University, Jiangsu, China. Disease activity was evaluated according to the 28-joint Disease Activity Score (DAS28). The level of disease activity could be interpreted as rheumatoid arthritis with low disease activity (Lo-RA), rheumatoid arthritis with moderate disease activity (Mo-RA), rheumatoid arthritis with high disease activity (Hi-RA), or rheumatoid arthritis with remission (Re-RA), according to the European League Against Rheumatism criteria . Disease stages included early and late RA on the basis of criteria for early RA . Nine patients with RA received methotrexate (MTX; Shanghai Sine Pharmaceutical Laboratories Co., Shanghai, China) therapy (10 mg/week for 20 weeks by oral administration). None of the patients had received immunosuppressive drugs within 1 year before the study period. Peripheral blood (PB) and synovial fluid (SF) samples were obtained from subjects after informed consent was provided according to a protocol approved by the local ethics committee of Soochow University. Sampling was completed in accordance with the guidelines of the local institutional review boards. Data about the patients and HCs are presented in supplementary figures and tables (Additional file 1: Table S1).
Male DBA/1 mice at 8–10 weeks of age were obtained from the Shanghai Laboratory Animal Center and were maintained in a specific pathogen-free animal facility at Soochow University. All animal experiments conducted in this study were approved by the University Committee on the Use of Live Animals in Teaching and Research at our institution. Male DBA/1 mice were immunized intradermally at the base of the tail with 200 μg of bovine collagen type II (CII; Chondrex, Redmond, WA, USA) dissolved in 100 μl of 0.05 M acetic acid and mixed with an equal volume of complete Freund’s adjuvant containing heat-killed Mycobacterium tuberculosis (H37Ra strain, 4 mg/ml; Chondrex). Three weeks later, animals were reimmunized with 200 μg of CII emulsified in incomplete Freund’s adjuvant (Chondrex). Mice were scored for clinical signs as follows (per paw): 0, paws with no swelling; 1, paws with swelling of finger joints or focal redness; 2, paws with mild swelling of the wrist or ankle joints; 3, paws with severe swelling of the entire paw; and 4, paws with deformity or ankylosis. CIA mice were grouped into acute collagen-induced arthritis (A-CIA) and chronic collagen-induced arthritis (C-CIA) stages according to the criteria described by Thornton et al. . On day 35 after the first immunization, dexamethasone (Dex; Tianjin Pharmaceutical Jiaozuo Co., Tianjin, China) was intraperitoneally injected for 7 days, including low dose (L-dose, 0.5 mg/kg/day), high dose (H-dose, 2 mg/kg/day), and a PBS control.
For PB samples, the fluorochrome-labeled monoclonal antibodies (mAbs) antihuman CD4, CD28, and OX40 were added to 80 μl of whole blood before erythrocyte lysis was performed. Synovial fluid mononuclear cells (SFMCs) were isolated after SF samples were treated with hyaluronidase (10 μg/ml; Sigma-Aldrich, St. Louis, MO, USA). The mAbs described above were added to 100-μl SFMC suspensions (2×106 cells/ml). For CIA mice, fluorochrome-labeled antimouse mAbs were added to 100-μl splenocyte suspensions (1×106 cells/ml). Cells were incubated and evaluated using a COULTER EPICS XL flow cytometer (Beckman Coulter, Brea, CA, USA). The gating strategy for the CD4+CD28−OX40+ T-cell subset is described in supplementary figures and tables (Additional file 1: Fig. S1). For intracellular staining, peripheral blood mononuclear cells (PBMCs; 3×106/well) were stimulated with phorbol 12-myristate 13-acetate (PMA, 50 ng/ml; eBioscience, San Diego, CA, USA) and ionomycin (1 μg/ml; eBioscience). Antihuman CD4, CD28, and OX40 mAbs were added before fixation and permeabilization, followed by the addition of phycoerythrin (PE)-cyanine 7 (Cy7)-conjugated antihuman interferon (IFN)-γ (clone 4S.B3; BioLegend, San Diego, CA, USA), interleukin (IL)-4 (clone MP4-25D2; BioLegend), or IL-17A (clone BL168; BioLegend) mAbs. Intracellular cytokine production was assessed using an FC 500 analyzer (Beckman Coulter). Information about all antibodies is provided in supplementary figures and tables (Additional file 1: Table S2).
On day 28 after the second immunization, CIA mice were killed, and mononuclear splenocytes were stimulated in vitro with CII (30 μg/ml) for 72 h. CD4+ T cells were selected from mononuclear splenocytes using CD4+ microbeads (Miltenyi Biotec, Bergisch Gladbach, Germany) to over 97% purity. After CD28 and OX40 antimouse mAbs were added, T-cell subsets were sorted using a FACSAria™ II cell sorter (BD Biosciences, Franklin Lakes, NJ, USA). Sorted T cells (1×106 cells in 200 μl of PBS) were injected intravenously into CIA mice on day 0 after the second immunization. After being fixed and decalcified, mouse ankles were embedded in paraffin and sectioned at 5-μm thickness before being stained with hematoxylin and eosin (H&E).
On day 28 after the second immunization, mononuclear splenocytes (1×105/well) of CIA mice were seeded onto 96-well tissue culture plates (Corning, Corning, NY, USA) in 10% FBS/RPMI 1640 medium and stimulated with CII (30 μg/ml) or anti-CD3 mAb (clone 145-2C11, 1 μg/ml; BioLegend) in the presence of antimouse OX40L mAb (clone RM134L; BioLegend). Rat immunoglobulin G (IgG) (clone RTK4530; BioLegend) was added as a control. After 72 h of incubation, cell proliferation was determined using a Cell Counting Kit-8 (CCK-8; Dojindo Laboratories, Mashikimachi, Japan). Supernatant cytokine levels were assessed using a mouse Th1/Th2/Th17 cytokine kit (BD Biosciences) according to the manufacturer’s instructions.
On days 1–4 after the second immunization, randomized mice were injected intraperitoneally with antimouse OX40L mAb (100 μg/mouse/day) or IgG as controls. In another experiment, mice with similar arthritis scores were treated with anti-OX40L mAb or IgG on days 14–17 after the second immunization. On days 28 and 39 after anti-OX40L mAb early treatment, mononuclear splenocytes (1×105/well) were stimulated with CII (30 μg/ml) for 72 h. Cell proliferation, supernatant cytokine levels, and intracellular staining were evaluated as described above. The PE-Cy7-conjugated antimouse mAbs used were as follows: IFN-γ (clone XMG1.2), IL-4 (clone 11B11), TNF-α (clone MP6-XT22), and IL-17A (clone TC11-18H10.1) (all from BioLegend).
All statistical analyses were performed using IBM SPSS Statistics for Windows version 20.0 software (IBM, Armonk, NY, USA). All quantitative data are presented as the mean±SD. Student’s t test or nonparametric Mann-Whitney U test was used for independent samples. A paired-samples t test or a nonparametric Wilcoxon signed-rank test was performed for paired samples. For multiple comparisons, one-way analysis of variance or the Kruskal-Wallis test was performed. A Spearman’s r value was calculated for correlation analyses. A P value less than 0.05 was considered to denote a significant difference.
Flow cytometric analysis demonstrated that OX40 expression on CD4+ T cells in PB samples was more frequent in patients with RA than in patients with OA or HCs (9.30±3.14% vs 7.55±3.26%, 6.90±2.64%, respectively, P=0.008) (Fig. 1a and b). Expression of OX40L on CD14+ monocytes (P=0.034) and CD19+ B cells (P<0.001) also increased significantly in PB samples of patients with RA (Fig. 1a and b). In animal models, we found that OX40 and OX40L expression in spleen samples of CIA mice increased significantly compared with normal control mice (NC) (all P<0.001) (Fig. 1c and andd).d). Furthermore, SF samples exhibited increased expression of OX40 and OX40L in patients with RA (all P<0.05) (Fig. 1e and andff).
Flow cytometric assessments of PB samples revealed a higher percentage of CD4+CD28− T cells in patients with RA than in patients with OA and HCs (P=0.021) (Fig. 2a). Further analysis showed that OX40 expression on CD4+CD28− T cells was significantly increased in PB samples from patients with RA compared with those from control subjects (10.14±3.98% vs 7.83±4.28%, 6.91±3.13%, respectively; P=0.006) (Fig. 2b). Meanwhile, OX40 expression on CD4+CD28+ T cells was also elevated in PB samples of patients with RA compared with that in control subjects (P=0.004) (Fig. 2c). Additionally, enrichment of CD4+CD28−, CD4+CD28−OX40+, and CD4+CD28+OX40+ T cells could be observed in SF samples from patients with RA (all P<0.05) (Fig. 2d and ande).e). However, the percentages of CD4+CD28−OX40+ and CD4+CD28+OX40+ T cells were comparable in both PB and SF samples of patients with RA (both P>0.05). Similar to patients with RA, a higher percentage of CD4+CD28−, CD4+CD28−OX40+, and CD4+CD28+OX40+ T-cell subsets could be observed in spleen samples of CIA mice than in NCs (all P<0.001) (Fig. 2f–h). Moreover, CD4+CD28− T cells displayed enhanced CD45RO expression compared with CD4+CD28+ T cells in PB samples of patients with RA (Fig. 2i). Intracellular staining revealed that PMA/ionomycin-stimulated CD4+CD28−OX40+ T cells produced more IFN-γ (P=0.026) and IL-4 (P=0.042) in PB samples of patients with RA than those in control subjects. For CD4+CD28−OX40− or CD4+CD28+OX40+ T cells, just IFN-γ (P=0.036) or IL-4 (P=0.044) secretion was increased in patients with RA, respectively. No significant difference was observed in cytokine production of CD4+CD28+OX40− T cells between patients with RA and control subjects (Fig. 2j).
The DAS28 was used to evaluate arthritic activity, which was positively correlated with the percentage of CD4+CD28−OX40+ T cells in PB samples of patients with RA (r=0.515, P<0.001) (Fig. 3a). Further analysis showed significant differences among the percentages of CD4+CD28−OX40+ T cells in PB samples of patients with Re-RA (5.94±2.24%), Lo-RA (9.68±2.31%, P=0.001), Mo-RA (11.14±3.12%, P<0.001), and Hi-RA (12.65±4.47%, P<0.001) (all vs Re-RA) (Fig. 3b). MTX significantly relieved arthritis activity and reduced the percentage of CD4+CD28−OX40+ T cells in PB samples of patients with RA (5.93±1.80% vs 7.74±2.54% posttherapy vs pretherapy, P=0.038) after 16 weeks of treatment. However, follow-up in the 32nd week showed that, with arthritis relapse, the percentage of this T-cell subset was higher than in the 16th week (8.10±1.62% vs 5.93±1.80%, P=0.008) (Fig. 3c). In different clinical stages, patients with Late-RA exhibited a higher percentage of CD4+CD28−OX40+ T cells in PB samples than patients with Early-RA (P=0.002) (Fig. 3d, left). Additionally, there was a significant difference in the percentage of this subset in PB samples between patients with rheumatoid arthritis with extraarticular manifestations (Extra-RA) and patients with rheumatoid arthritis with limited joint manifestations (Limited-RA) (P=0.036) (Fig. 3d, right). As an important clinical indicator, the levels of rheumatoid factor (RF) were positively correlated with the percentage of CD4+CD28−OX40+ T cells in PB samples of patients with RA (r=0.288, P=0.015) (Fig. 3e). In spleen samples of animal models, a positive correlation was found between arthritis scores and the percentages of the CD4+CD28−OX40+ T-cell subset (r=0.5354, P=0.0004) (Fig. 3f). During different phases of disease, the number of CD4+CD28−OX40+ T cells was increased in spleen samples of C-CIA mice compared with that in A-CIA mice (Fig. 3g). Both L-dose and H-dose Dex markedly alleviated arthritic development in CIA mice (supplementary figures and tables in Additional file 1: Fig. S2) and reduced the percentages of CD4+CD28−OX40+ T cells in spleen samples (Fig. 3h). Three weeks after low doses of Dex administration, the percentage of CD4+CD28−OX40+ T cells in spleen samples of CIA mice approximated that of the control levels (Fig. 3i).
Arthritic onset in CIA mice that received transfer with CD4+CD28−OX40+ T cells occurred much earlier, and the arthritis scores in these mice were much higher than those in control CIA mice (8.55±3.17 vs 3.48±2.12, P<0.001) (Fig. 4c). Meanwhile, arthritis onset and scores in CIA mice that received transfer with CD4+CD28−OX40− T cells also showed a significant difference from those in control CIA mice (6.57±2.47 vs 3.48±2.12, P<0.001) (Fig. 4a). Although CD4+CD28+OX40− or CD4+CD28+OX40+ T-cell transfer slightly accelerated early arthritic development in CIA mice, these scores did not reach significance compared with control CIA mice (P=0.718 and P=0.102, respectively) (Fig. 4b and andd).d). Furthermore, among the four T-cell subsets transferred to CIA mice, CD4+CD28−OX40+ T cells displayed the most significant pathogenic role in arthritis development compared with CD4+CD28−OX40− (P=0.011), CD4+CD28+OX40− (P<0.001), and CD4+CD28+OX40+ (P<0.001) T cells. Severe synovial and periarticular inflammation with abnormal narrowing of the joint space was observed in H&E staining of CIA mice transferred with CD4+CD28−OX40+ T cells. Similarly, micro-computed tomography revealed the most serious bone erosion in CIA mice that received transfers with CD4+CD28−OX40+ T cells compared with those in control CIA mice (Fig. 4e).
In splenocytes stimulated with CII, OX40L-blocking antibodies at 2.5 μg/ml (P=0.006), 5.0 μg/ml (P<0.001), and 10.0 μg/ml (P<0.001) displayed inhibitory effects on cell proliferation compared with IgG controls (Fig. 5a, left). Simultaneously, antibodies at 5.0 μg/ml (P=0.002) and 10.0 μg/ml (P<0.001) exhibited depressing effects on the proliferation of splenocytes activated by CD3 stimuli (Fig. 5a, right). Further studies showed that applying the blocking antibody at 5.0 μg/ml remarkably reduced the cytokine secretion of CII-stimulated splenocytes, including IFN-γ (26.86±8.88 pg/ml vs 41.96±11.23 pg/ml, P=0.021), IL-4 (10.65±2.85 pg/ml vs 18.67±5.75 pg/ml, P=0.005), and TNF-α (190.59±90.11 pg/ml vs 371.86±160.72 pg/ml, P=0.021) (all vs IgG controls). However, levels of IL-10 were elevated (P=0.046), and the secretion of IL-2, IL-6, and IL-17A were not significantly different from those in the IgG controls (all P>0.05) (Fig. 5b). Additionally, OX40 blockade showed similar effects on cytokine production in splenocytes stimulated with CD3 (Fig. 5c).
Early treatment starting on day 1 after the second immunization indicated that OX40 blockade in vivo delayed arthritis onset and reduced the arthritis scores of CIA mice compared with IgG controls (P=0.013) (Fig. 6a). Correspondingly, late treatment starting on day 14 after the second immunization also evidently alleviated arthritis development (P=0.008) (Fig. 6b). Further studies demonstrated that OX40 blockade in vivo reduced cell proliferation (P=0.037) (Fig. 6c) and cytokine secretion, including IFN-γ (P=0.025), IL-4 (P=0.025), and TNF-α (P=0.037), by CII-stimulated splenocytes (Fig. 6d). Accordingly, in vivo changes in IL-10, IL-2, IL-6, and IL-17A levels were consistent with the in vitro experiment (Fig. 6d). Intracellular staining showed that OX40 blockade in vivo significantly suppressed cytokine secretion by CD4+CD28−OX40+ T cells, including IFN-γ (59.38±11.78% vs 74.10±10.39%, P=0.028), TNF-α (76.88±8.77% vs 90.84±7.43%, P=0.028), and IL-4 (9.11±3.12% vs 16.01±3.89%, P=0.016) (all vs IgG controls). However, the levels of IL-17A were not significantly different (Fig. 6e). For CD4+CD28+OX40+ T cells, TNF-α and IL-4 were reduced by OX40 blockade (both P<0.05). With regard to CD4+CD28−OX40− and CD4+CD28+OX40− T cells, OX40 blockade had no impact on the secretion of IFN-γ, TNF-α, IL-4, and IL-17A compared with IgG controls (all P>0.05) (Fig. 6e).
Recently, the self-activation mechanisms of CD4+CD28− T cells have been explored, including allelic associations , cytokine production [18, 19], cell receptor stimulation [20, 21], and DNA methylation [22, 23]. However, in the absence of CD28, which costimulatory molecules mediate the second signal is not yet well known. Researchers in a recent study reported that OX40 expression was upregulated on CD4+CD28− T cells in patients with acute coronary syndrome and that the secretion of IFN-γ and TNF-α was suppressed by OX40 blockade . However, whether abnormal OX40 signaling is involved in the self-responses of CD4+CD28− T cells in patients with RA remains unclear. In this study, a CD4+CD28−OX40+ T-cell subset was established to be clinicopathologically significant, and its autoreactivation and pathogenicity were demonstrated in patients with RA and CIA mice. Additionally, the regulatory roles of OX40 signaling in CD4+CD28− T cells were verified in vitro and in vivo.
In accord with previous studies , abnormal expression of OX40 in patients with RA and CIA mice suggested that an OX40 costimulatory signal was involved in the pathological development of autoimmune arthritis. Further upregulated expression of OX40 in SF of patients with RA implied that OX40 signal may promote abnormal activation of autoreactive T cells after migration of CD4+ T into the inflammatory microenvironment. In patients with RA, enhanced OX40 expression was observed not only on CD4+CD28− but also on CD4+CD28+ T cells. OX40 expression levels did not depend on CD28 expression in RA, suggesting that OX40 costimulated T cells in a CD28-independent way. In addition, CD4+CD28− T cells with enhanced CD45RO expression suggested the characteristics of memory T cells, and this population is enriched in patients with RA, probably because of OX40 overexpression. Elevated levels of IFN-γ and IL-4 suggest that CD4+CD28−OX40+ T cells may be involved in Th1/Th2 responses and help to produce autoantibody, such as RF . However, CD4+CD28−OX40− may just function in a Th1 pathway, and for CD4+CD28+OX40+ T cells, a Th2 pathway may be involved. These results implied that CD4+CD28−OX40+ T cells were distinct from the other T-cell subsets and may exhibit specific characteristics in autoimmune arthritis. Upon OX40 costimulation, effector differentiation and long survival may emerge in memory CD4+CD28− T cells, which may increase disease activity and lead to a protracted course of disease, as described in another study . As a consequence of OX40 overexpression, CD4+CD28− T cells may differentiate diversely in response to multiple autoantigens, suggesting extraarticular manifestations, as mentioned in previous studies [3, 27]. Immunosuppressive agents regulate immune responses by changing the expression and function of costimulatory molecules [28, 29], and this regulatory role could be effectively reversed by OX40-mediated costimulatory signals . Reduced OX40 signals by MTX or Dex treatment may suppress the autoactivation of CD4+CD28− T cells and lead to arthritis remission. However, arthritis relapses after medicine withdrawal suggest that new specific approaches for therapy must be explored.
In adoptive transfer assays, although similar arthritis scores were observed on day 34 in the duration curves, CD4+CD28−OX40+ T cells demonstrated a more powerful pathogenic role than the CD4+CD28−OX40−, CD4+CD28+OX40−, and CD4+CD28+OX40+ T cells in both early (days 1–33) and late (days 35–64) arthritis. This finding indicates that, in early arthritis, activation of CD4+CD28−OX40+ T cells occurs in a short-lived effector- and autoantigen-dependent manner but probably acts in a long-lived memory- and autoantigen-independent fashion in late arthritis, in agreement with the OX40 properties described by Croft [8, 9]. Probably owing to natural killer cell or chemokine receptors expressed on CD4+CD28− T cells [20, 21], mice that received transfers with CD4+CD28−OX40− T cells exhibited deteriorated arthritis progression, especially in early arthritis. On one hand, this meant that, in early arthritis, additional mechanisms were involved in activation of CD4+CD28− T cells, except for OX40 costimulation, On the other hand, long-lived memory characteristics of OX40 [8, 9] may take effects in late arthritis. Autoantigen-specific CD4+CD28−OX40+ T cells resulted in persistent autoimmune injuries and protracted joint damage. However, the absence of OX40 markedly reduced the survival of memory T cells, and late arthritis development was alleviated in the mice that received transfers with CD4+CD28+OX40− T cells. Recent studies showed that OX40 costimulatory signals promoted differentiation of effector T lymphocytes in a CD28-independent way  and that “superstimulation” of combined CD28 and OX40 did not outperform CD28 by itself . Additionally, the presence of OX40 may neutralize costimulation of CD28 , which may impair arthritis pathogenic roles of CD4+CD28+OX40+ T cells. A distinct pathogenic role has been further confirmed on the basis of different characteristics of CD28− and CD28+ T cells . The robust pathogenicity of CD4+CD28− T cells may reflect OX40 characteristics of costimulating memory T cells in a CD28-independent manner, as described in a report by Demirci et al. .
In vitro different time points resulted in findings inconsistent with those of Yoshioka et al. , probably because of the diverse roles of OX40 in short-lived effector and long-lived memory cells [8, 9]. In our study, the blockade time point was day 28 after the second immunization, whereas in the study by Yoshioka et al., it was day 7. On day 7, OX40+ T cells may have occurred in the absence of short-lived effector responses, whereas OX40 memory characteristics may be generated on days 14–28. In vitro OX40 blockade on day 7 may have little effect. On the basis of in vitro studies, early treatment on days 1–4 in vivo showed results similar to those of the studies by Yoshioka et al.  and Gwyer Findlay et al. , probably owing to suppression of short-lived effector responses of OX40+ T cells. However, inconsistent with the findings of Yoshioka et al. , delayed treatment on days 14–17 also distinctly ameliorated arthritis symptoms, mainly owing to the different time points. On day 14 (blockade time point in our study), generation of memory T cells may be reduced by OX40 blockage, whereas short-lived effector responses resulting from OX40 may have faded on day 7 (blockade time point in study by Yoshioka et al.). Changes in cytokine levels further corroborated the findings in analysis of human samples. In the immunopathogenesis of RA, Th1 and Th2 responses are involved in different phases . As observed in transfer assays, Th1/Th2-polarized CD4+CD28−OX40+ T cells played central roles in all phases of autoimmune arthritis. However, CD4+CD28+OX40− and CD4+CD28+OX40+ T cells contributed to outcomes only in the early phases of the pathological process. For CD4+CD28−OX40− T cells, although early Th1 response aggravated arthritic development in an OX40-independent way, progression faded in late-phase arthritis.
A novel CD4+CD28−OX40+ T-cell subset was established to be clinicopathologically significant, suggesting that OX40 may act as a promising biomarker for RA. OX40 was characterized as an alternative costimulator for autoactivation of CD4+CD28− T cells in autoimmune arthritis, and OX40 blockade may represent an effective approach for immunomodulatory therapy.
This work was supported by the National Program on Key Basic Research Project (973 Program grant 2013CB530501), the National Natural Science Foundation of China (grants 31320103918, 30930085, 31170834, 81373184, and 81371387), and the Advanced Research Project of Suzhou University for the National Natural Science Foundation (grant SDY2012B25).
Supplementary data are available online.
XZ had full access to all data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. JJ and CL carried out the FACS and molecular analyses, performed the statistical analysis, and drafted the manuscript. ML and YS performed biomarker analysis and critically revised the paper. XH and QW performed the molecular studies and helped to draft the manuscript. MW, JW, and QF were involved in the conception of the study and contributed to study design and data interpretation as well as the drafting of the paper. All authors were involved in drafting or revising the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Available upon request.
The study protocol and consent form were approved by the institutional medical ethics review board of Soochow University. Signed informed consent was obtained from all patients before study enrollment.
Additional file 1:(614K, doc) Supplementary figures and tables. (DOC 614 kb)
Supplementary figures and tables. (DOC 614 kb)
Juean Jiang, Email: moc.621@naeujgnaij.
Cuiping Liu, Email: moc.621@0891gnipiucuil.
Mi Liu, Email: moc.qq@930955941.
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