Artemisinin and its derivatives were reported to possess strong regulatory effects on inflammation and autoimmune diseases. This study was designed to examine the therapeutic effects and underlying mechanisms of SM934, a water-soluble artemisinin analogue, on lupus-prone female NZB×NZW F1 mice.
NZB/W F1 mice were treated orally with SM934 for 3 or 6 months respectively to investigate the effect on clinical manifestations and immunological correlates. To further explore the mechanisms of SM934, ovalbumin (OVA)-immunized or interferon (IFN)-γ-elicited C57BL/6 mice were used. In vivo, treatment with SM934 for 3 or 6 months significantly delayed the progression of glomerulonephritis and increased the survival rate of NZB/W F1 mice. Clinical improvement was accompanied with decreased Th1-related anti-double-strand DNA (dsDNA) IgG2a and IgG3 Abs, serum interleukin (IL)-17, and increased Th2-related anti-dsDNA IgG1 Ab, serum IL-10 and IL-4. SM934 treatment also suppressed the accumulation of effector/memory T cells, induced the apoptosis of CD4+ T cells, while enhancing the development of regulatory T cells in NZB/W F1 mice. In addition, SM934 treatment promoted the IL-10 production of macrophages from NZB/W F1 mice, OVA-immunized C57BL/6 mice and IFN-γ-elicited C57BL/6 mice. In vitro, SM934 enhanced IL-10 production from primary macrophages stimulated with IFN-γ.
Citation: Hou L-F, He S-J, Li X, Wan C-P, Yang Y, Zhang X-H, et al. (2012) SM934 Treated Lupus-Prone NZB×NZW F1 Mice by Enhancing Macrophage Interleukin-10 Production and Suppressing Pathogenic T Cell Development. PLoS ONE 7(2): e32424. doi:10.1371/journal.pone.0032424
Editor: Amr H. Sawalha, University of Oklahoma and Oklahoma Medical Research Foundation, United States of America
Received: December 30, 2011; Accepted: January 26, 2012; Published: February 28, 2012
Copyright: © 2012 Hou et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by the grants of Science & Technology Commission of Shanghai Municipality, China (No. 08XD14053), and National Science & Technology Major Project “New Drug Creation and Manufacturing Program”, China (2009ZX09301-001, 2009ZX09102-019). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by abnormal accumulation of autoreactive T lymphocytes and production of autoantibody against self-antigen, which result in the development of immune complex-mediated glomerulonephritis and renal failure , . Female NZB/W F1 mice resemble human lupus closely. This strain of mice spontaneously develops severe autoimmune disease, especially the fatal immune complex-mediated glomerulonephritis, around 5 to 7 months of age, and approximately 50% die by 8 months and 90% die by 12 months of age , . It's well documented that activated/memory helper T cells (CD4+CD44+CD62L− effector T cells, Teff), especially IFN-γ-producing Th1 subset, are responsible for inciting human and murine lupus, in part through increased production of highly nephritogenic Th1-related Ig2a and IgG3 autoantibodies –. With the development of pathogenic helper T cells, CD4+Foxp3+ regulatory T cells (Treg) failed to maintain a competitive pool size in the peripheral lymphoid organs, finally resulting in a progressive imbalance of Treg and Teff –.
The recently defined IL-23/IL-17 axis, as well as the IL-12/IFN-γ axis, is emerging to be critical in many autoimmune diseases , . IL-23 can directly elicit IL-17 family cytokines from memory helper T cells and other innate immune cells , , especially the γδ T cells , . In addition to recruiting neutrophils, recent evidences also strongly suggest that IL-23/IL-17 axis can exert its function by orchestrating adaptive Th1 responses in inflammatory bowel disease , , delayed type hypersensitivity , , and intracellular bacterial infection . Currently, there are compelling evidences for a pathogenic role of IL-17 in human lupus patients and lupus-prone female MRL/lpr mice , . However, the definite IL-17-producing cells and pathogenic role of IL-17 in lupus are still uncertain.
Disease severity in human and murine lupus is also tightly correlated to IL-10 . It was reported that patients with lupus produced large amount of IL-10 , . Administration of anti-IL-10 mAb to human patients with active lupus  or NZB/W F1 mice  led to the amelioration of disease activity. However, there were also some reports supporting a protective role of IL-10 in SLE. For example, in MRL/lpr mice, deficiency of IL-10 resulted in exacerbated disease, demonstrated by enhanced Th1 cell development and increased mortality ; Over-expression of IL-10 in lupus-prone NZM2410 mice could ameliorate lupus diseases . Routinely, IL-10 is deemed a regulatory cytokine. IL-10 could inhibit IFN-γ production and proliferation of CD4+ T cells through its direct inhibitory effects on T cells or indirect inhibitory effects on antigen-presenting cells . Many cells produce IL-10, especially the myeloid cells, and IL-10 released from myeloid cells can maintain Foxp3 expression and suppressive function of Treg cells in a paracrine manner . Thus, the role of IL-10 remains controversial in SLE.
Multifactorial pathogenesis resulted in scarcity of therapeutic approaches for SLE. Artemisinin derivatives possess strong anti-inflammatory and immunosuppressive functions, and have shown significant therapeutic effects on SLE clinically and experimentally –. SM934, β-aminoarteether maleate, was synthesized from β-hydroxyarteether at Shanghai Institute of Materia Medica. Chemically, as the derivative of artemisinin, SM934 also contains the unique peroxide bridge, but has higher bioavailability. Recently, we demonstrated that in vitro SM934 could suppress the Th1 and Th17 polarization, but exerted no influence on Treg differentiation; In vivo, SM934 could significantly ameliorate lupus diseases in MRL/lpr mice through inhibiting the both of Th1 and Th17 responses, and elevating Treg percentage . In MRL/lpr mice, the lpr (lymphoproliferative) mutation of the fas gene impairs activation-induced cell death (AICD), which results in the abnormal accumulation of autoreactive T, B and double negative T lymphocytes (CD3+CD4−CD8−B220+ cells) . However, in NZB/W F1 mice, the fas gene is intact, which makes the pathogenesis of NZB/W F1 mice largely different from that of MRL/lpr mice. In this study, we explored the therapeutic effects and underlying mechanisms of SM934 on NZB/W F1 mice and demonstrated that SM934 could exert comprehensive therapeutic effects on NZB/W F1 mice both in short-term and long-term treatment. SM934 treatment could significantly increase Treg percentage and suppress the Th1 and Th17 responses in NZB/W F1 mice. Although our previous report suggested that SM934 could induce activated CD4+ T cells into apoptosis in vitro , it's hardly to present such effects of SM934 in vivo, for that, usually apoptotic cells will be phagocytized and cleared quickly. Herein, through flow cytometric staining surface B220 and western blot analysis of Bcl-2 protein expression in the CD4+ T cells, we firstly demonstrated that SM934 treatment could prompt the apoptosis of activated CD4+ T cells in vivo. Furthermore, the therapeutic effects of SM934 on NZB/W F1 mice were tightly linked to enhancing IL-10 production from macrophages, which was absent in MRL/lpr mice.
Collectively, the results of this study demonstrated the therapeutic effects of artemisinin derivative SM934 on female NZB/W F1 mice with established nephritis. SM934 treatment could correct pathogenic helper T cell commitment and enhance IL-10 production that might be beneficial for future lupus treatment.
Therapeutic effects of SM934 on female NZB/W F1 mice with three months oral administration
Female NZB/W F1 mice develop kidney inflammation gradually from about 5 months old on. Here, we used 6.5 months old female NZB/W F1 mice with ongoing kidney injury, which was demonstrated by about 26% of mice with severe proteinuria scored ≥3+. As shown in Figure 1A, with aging, vehicle treated mice progressively developed severe proteinuria, manifested by absolute urinary protein concentration (Up-panel) and percentage of severe proteinuria scored ≥3+ (Bottom-panel), and peaked nearly at the age of 8 months. SM934 treatment, both 10 and 3 mg/kg, could dramatically inhibit the progression and aggravation of proteinuria, as quickly as 2 (for 10 mg/kg) to 4 weeks (for 3 mg/kg) after treatment. Meanwhile, SM934 at the dose of 1 mg/kg also presented mild therapeutic effects. In addition, all three doses of SM934 could maintain the bodyweight of lupus-suffered mice during treatment, in which 10 and 3 mg/kg showed statistical significance at indicated time point (Figure 1B). At the end of 3 months of treatment, mice were sacrificed and examined for blood urea nitrogen (BUN). Results showed that SM934 (10 mg/kg) and prednisolone (PNS) treatment significantly decreased the BUN levels (Figure 1C). Accumulated survival rate showed that SM934 treatment, especially at the dose of 10 mg/kg, could significantly decrease the death rate (p<0.05, Figure 1D). Kidneys were examined to evaluate renal pathology and IgG deposition. Histological sections from vehicle treated mice exhibited severe renal damage, characterized by glomerular sclerosis, hyalinosis, increased mesangial matrix, diffused perivascular and interstitial mononuclear cell infiltration, tubular atrophy, and accumulation of proteinaceous casts in the tubules. Mice treated with SM934 (10 and 3 mg/kg) presented significantly less severe renal damage that showed marked amelioration in glomerular, perivascular injuries, and interstitial inflammatory cell infiltration and lesion (representative histopathological pictures in Figure 2, Left panel and detailed individual histological score was listed in Table S1).
Six and half months old female NZB/W F1 mice were orally treated with vehicle (saline), SM934 (10, 3, and 1 mg/kg, respectively), and PNS (2 mg/kg) for 3 months (n = 11 per group). (A) Up: levels of proteinuria; Bottom: frequencies of mice with severe proteinuria (urinary protein ≥3 mg/ml). (B) Body weight. (C) Serum levels of blood urea nitrogen (BUN) immediately measured at the end of experiment. (D) Cumulative survival rate during 3 months of treatment. a = P<0.05; b = P<0.01 versus vehicle.
Six and half months old female NZB/W F1 mice were orally treated with vehicle (saline), SM934 (10, 3, and 1 mg/kg, respectively), and PNS (2 mg/kg) for 3 months (n = 11 per group). Left, representative kidney sections stained with H&E (Original magnification×200); Right, representative immunofluorescence staining of IgG deposit in the kidney sections (Original magnification×100).
Renal cryostat sections were stained for detecting IgG deposition. The pronounced mesangial IgG deposits were shown in kidneys from vehicle treated mice. In contrast, mice treated with SM934 (10 and 3 mg/kg) showed remarkably diminished IgG deposition (representative immunofluorescence pictures in Figure 2, Right panel and detailed individual score was listed in Table S1).
Effects of SM934 treatment on the sera levels of autoantibodies and cytokines in female NZB/W F1 mice
Anti-dsDNA IgG autoantibodies, especially Th1-related IgG2a and IgG3 isotypes, are hallmarks of SLE and play important pathogenic roles in lupus nephritis –, . However, Th2-related IgG1 isotype might play a protective role in murine and human lupus through preferentially stimulating inhibitory FcγR , . The serum levels of anti-dsDNA antibodies were examined and shown in Figure 3A. Three months SM934 treatment, at the doses of 10 and 3 mg/kg, largely decreased total anti-dsDNA IgG Ab (p = 0.13 and p = 0.05, respectively), IgG2a isotype (both p<0.05) and IgG3 isotype (p = 0.12 and p = 0.09, respectively), but significantly increased the level of IgG1 isotype (p<0.01 and p = 0.09, respectively).
At the termination of 3 months treatment, sera of female NZB/W F1 mice were collected and examined for anti-dsDNA autoantibodies and cytokines. (A) Serum levels of anti-dsDNA total IgG, IgG1, IgG2a and IgG3 antibodies. Sera of 10 months old female NZB/W F1 mice were used as the standard control. (B) Serum levels of IL-10, IL-4, IL-17A and IFN-γ. Shown were mean ± SEM. * = P<0.05; ** = P<0.01 versus vehicle.
The serum levels of cytokines were shown in Figure 3B. SM934 treatment, at the doses of 10 and 3 mg/kg, significantly increased serum levels of IL-10 and IL-4 (p<0.05, respectively). At the dose of 10 mg/kg, SM934 significantly decreased the serum level of IL-17A (P<0.05). However, SM934 treatment exerted no influence on serum transforming growth factor-β (data not shown).
SM934 treatment prompted the apoptosis of CD4+ T cells
After 3 months of treatment, splenocytes were obtained to examine the immunologic correlates. Flow cytometry analysis showed that SM934 treatment did not influence the percentage of major cellular population in spleens including CD4+ T cells, CD8+ T cells, B cells, dendritic cells, and monocytes (Table S2). For that our previous study showed that in vitro SM934 could exclusively induce activated, not naïve, CD4+ T cell into apoptosis , we then examined the B220 expression on the surface of CD4+ T cells, which was reported to be the apoptotic marker for activated CD4+ T cells , . Dramatically, SM934 treatment significantly enhanced the accumulation of CD4+B220+ population in the spleen (Figure 4A and 4B). Furthermore, western blot analysis showed that SM934 treatment decreased the Bcl-2 protein level in purified CD4+ T cells (Figure 4C).
At the termination of 3 months treatment, female NZB/W F1 mice in vehicle and SM934 (10 mg/kg) treated groups were randomly and averagely divided into 3 sub-groups. Spleens of each sub-group were pooled together. (A) Representative staining of surface CD4 and B220 in splenocytes. (B) Statistical results of percentage of CD4+B220+ population in splenocytes. (C) CD4+ T cells were purified through magnetic negative selection and examined for Bcl-2 expression through western blot analysis. One blot was the mix of two equal splenic samples from treated groups. Shown are mean ± SD, n = 3 in each treated group. * = P<0.05 versus vehicle.
SM934 treatment induced the accumulation of regulatory T cells
Our previous study showed that, in vitro, SM934 will not influence the differentiation of Treg cells, but could favor the accumulation of Treg cell in the spleens of MRL/lpr mice in vivo. We then examined the FoxP3 expression in the splenocytes. Results showed that SM934 treatment significantly enhanced the accumulation of CD4+FoxP3+ Treg cells in the spleens, regarding both intracellular FoxP3 protein (Figure 5A and 5B) and FoxP3 mRNA levels (Figure 5C) in CD4+ T cells.
At the termination of 3 months treatment, female NZB/W F1 mice in vehicle and SM934 (10 mg/kg) treated groups were randomly and averagely divided into 3 sub-groups. Spleens of each sub-group were pooled together. (A) Surface CD4 and intracellular FoxP3 expressions in splenocytes. (B) Statistical results of percentage of CD4+FoxP3+ population in splenocytes. (C) Real-time PCR analysis of FoxP3 mRNA expression in purified CD4+ T cells. Shown are mean ± SD, n = 3 in each treated group. * = P<0.05 versus vehicle.
Effects of SM934 treatment on the balance of pro-inflammatory and anti-inflammatory cytokines
To confirm the influence of SM934 treatment on the development of pathogenic T cells, splenocytes were ex vivo stimulated with anti-CD3 mAb. Results showed that splenocytes of SM934 treated mice produced higher IL-10 and IL-4, and less IL-17 and IFN-γ, compared with vehicle treated ones (Figure 6A). To clarify the major cellular source of IL-10, splenocytes were directly stimulated with PMA and ionomycin and examined by intracellular staining and flow cytometric analysis. The result was shown in Figure 6B, SM934 treatment significantly enhanced CD11b+F4/80+ macrophages, but not CD11b+CD11c+, CD4+, CD8+, B220+ cells (data not shown), to produce IL-10. Furthermore, flow cytometric analysis showed that SM934 treatment reduced the accumulation of IFN-γ-producing CD4+ T cells (Figure 6C) and IL-17-producing CD3+ T cells in the spleens (Figure 6D, Up-panel). Through co-staining of different surface markers, we identified that SM934 treatment only decreased the percentage of IL-17+ population in CD3+γδ− T cells, but not in CD3+γδ+ T cells (Figure 6D, Bottom-panel).
At the termination of 3 months treatment, female NZB/W F1 mice in vehicle and SM934 (10 mg/kg) treated groups were randomly and averagely divided into 3 sub-groups. Spleens of each sub-group were pooled together and ex vivo stimulated. (A) Cytokine productions in splenocytes stimulated with anti-CD3 mAb for 24 hours. Shown are mean ± SD, n = 3 in each treated group. (B) Flow cytometric analysis showing intracellular IL-10 expression in CD11b+F4/80+ macrophages. (C) Flow cytometric analysis of CD3+IFN-γ+ cells in splenocytes. (D) UP-panel, flow cytometric analysis of CD3+IL-17+ cells in splenocytes; Bottom-panel, flow cytometric analysis of intracellular IL-17 associated with surface CD4 and TCRγδ expressions. For all flow cytometry plots, shown are representative one of 3 samples with similar pattern in each treated group. * = P<0.05, ** = P<0.01 versus vehicle.
SM934 treatment induced IL-10 production from macrophage in OVA-immunized mice
To further confirm the effect of SM934 that induced higher production of IL-10 in macrophages, OVA/CFA-immunized female C57BL/6 mice were treated with SM934 (10 mg/kg) or vehicle for 7 days. Then, the splenocytes were obtained and stimulated with or without OVA recall. Compared with splenocytes from vehicle treated mice, splenocytes from SM934 treated mice produced more IL-10 (Figure 7A). In addition, purified F4/80+ splenic macrophages from SM934 treated mice showed the suppressive effect on the proliferation of co-cultured CD4+ T cells purified from vehicle treated mice under OVA-recall stimulation (Figure 7B).
Naïve female C57BL/6 mice were immunized with OVA/CFA and treated with vehicle or SM934 (10 mg/kg) for consecutive 7 days (9 mice per treated group). At the termination of treatment, both groups were randomly and averagely divided into 3 sub-groups. Spleens of each sub-group were pooled together. (A) IL-10 production in splenocytes cultured with OVA recall for 24 hours. (B) OVA-induced proliferation in CD4+ T cells from vehicle treated mice co-cultured with macrophages from vehicle or SM934 treated mice for 72 hours. Bars showed the mean ± SD. ** = P<0.01, *** = P<0.001 versus corresponding medium or vehicle control with similar stimulatory condition.
SM934 induced IL-10 production from macrophage elicited by IFN-γ in vitro and in vivo
Enriched primary peritoneal macrophages obtained from naïve female C57BL/6 mice were in vitro stimulated with or without IFN-γ to further determine the effect of SM934. The results showed that SM934 (10 µM) could directly enhance IL-10 production and suppress IL-12/23p40 production in primary peritoneal macrophages with IFN-γ stimulation (Figure 8A).
(A) Peritoneal macrophages were isolated from naïve C57BL/6 mice and then were in vitro stimulated with mIFN-γ in the presence or absence of SM934 for 24 hours. IL-10 (UP-panel) and IL-12/23p40 (Bottom-panel) productions in the supernatants were examined by ELISA. (B) C57BL/6 mice were i.p. elicited with mIFN-γ and orally administrated with vehicle or SM934 (10 mg/kg) for 3 days. Then, peritoneal macrophages were cultured with medium for 24 hours and supernatant IL-10 (UP-panel) and IL-12/23p40 (Bottom-panel) were examined by ELISA. Bars showed the mean ± SD of 3 independent experiments. * = P<0.05, ** = P<0.01, *** = P<0.001 versus corresponding medium or vehicle control with similar stimulatory condition.
To further confirm the IL-10-inducing ability of SM934 on IFN-γ-stimulated macrophages, we i.p. challenged the mice with IFN-γ and treated them with SM934 for 3 days. As shown in Figure 8B, ex vivo, SM934 treatment also significantly enhanced IL-10 production and suppressed IL-12/23p40 production from peritoneal macrophages.
Long-term treatment of SM934 gained more valuable therapeutic effects on female NZB/W F1 mice
To examine the long-term therapeutic effects of SM934, 6.5 months old female NZB/W F1 mice were treated with SM934 for 6 months at the dose of 10 mg/kg. Results showed that, with aging, vehicle treated mice developed severe proteinuria accompanied with progressive bodyweight loss. Compared with vehicle group, SM934 treatment significantly suppressed the progressive elevation of proteinuria level (Figure 9A) and ameliorated the loss of bodyweight (Figure 9B) during 6 months treatment period. Accumulated survival rate showed that SM934 treatment significantly prolonged the lifespan (Figure 9C). After 5.5 months treatment (at the age of 12 months), all mice in vehicle group died, while nearly 50% in SM934 treated group was still alive even after 6 months treatment. At the termination of this 6 months treatment, all remained mice were humanely sacrificed, and kidneys were removed for histological evaluation. As shown in Figure 9D, SM934 treatment significantly alleviated the kidney lesions, especially for decreased glomerular mesangial proliferation, basement membrane proliferation, glomerular sclerosis, tubular dilatation, and perivascular injuries, but exerted minor influence on interstitial inflammatory (detailed histological score was listed in Table S3).
Six and half months old female NZB/W F1 mice were orally treated with vehicle, SM934 (10 mg/kg), and PNS (2 mg/kg) for 6 months (n = 12 per group). (A and B), The levels of proteinuria (A) and bodyweight (B) were measured every two weeks. (C) Cumulative survival rate during 6 months of treatment. (D) Histology of representative kidney sections stained with H&E (Original magnification×200). In A, B and C, a = P<0.05; b = P<0.01; c = P<0.001 versus vehicle.
In this study, we explored the therapeutic effects and mechanisms of SM934 on autoimmune syndrome in lupus-prone female NZB/W F1 mice. Results of this study showed that SM934 treatment could significantly reverse the imbalance of Th1/Th2-related anti-dsDNA autoantibodies level, correct the abnormal development of helper T cells, reduce the immune complex deposition, ameliorate the lethal renal injury, and thus prolong the lifespan of female NZB/W F1 mice. Remarkably, the therapeutic effects of SM934 were also tightly linked to the enhanced production of IL-10 from macrophages.
In murine lupus, IgG2a autoantibody selectively binds activatory FcγRIV, while IgG1 isotype preferentially engages inhibitory FcγRIIb , . IgG3 autoantibody is the most potent isotype to activate complement system in the kidney. In the current study, SM934 could significantly suppress the serum levels of IgG2a and IgG3 anti-dsDNA autoantibodies, while increase the IgG1 anti-dsDNA subclass, which might largely contribute to the disease alleviation. However, 10 mg/kg SM934 was less effective to suppress the total anti-dsDNA IgG antibody level than 3 mg/kg SM934 did, which might be resulted from the elevated IgG1 subclass. Despite the less potency in suppressing serum total anti-dsDNA autoantibody, 10 mg/kg SM934 exerted similar inhibitory effects with 3 mg/kg SM934 on IgG deposit in the kidneys. Such inconsistency between serum total anti-dsDNA autoantibody level and IgG deposit in the kidney seems to be acceptable, for that, recently, Hughes et al also reported this phenomenon in progesterone treated NZB/W F1 mice .
IL-17 was found to be an important pathogenic factor in murine and human lupus. In the current report, we also found that there was a high concentration of IL-17 in the serum, and that the therapeutic effects of SM934 were tightly linked with its inhibiting serum IL-17 in NZB/W F1 mice. However, the definite cellular source of IL-17 was still elusive in NZB/W F1 mice, considering that both Th17 cells and innate-like IL-17-producing γδ T cells were reported to be major IL-17 producers in many autoimmune diseases , . In this study, we found that most of IL-17+ cells in the spleen were CD3+TCRγδ− T cells, which suggested that Th17, rather than γδ T cells were major IL-17 producers at the later stage of disease. SM934 could significantly suppress the development of Th17 cells and decrease serum IL-17 level, but did not exert influence on IL-17+γδ T cells. Thus, this study supported that Th17 cells might play an important pathogenic role in lupus diseases.
This pharmacological study also argued the role of so-called pathogenic role of IL-10 in the pathogenesis of lupus. Some published work reported that, in lupus, pathogenic T cells were comprehensive activated and less sensitive to the suppression of Treg or IL-10 –. Recently, Yuan et al demonstrated that the response of monocytes from lupus patients were less sensitive to the suppression of IL-10 . Here, although we did not compare the sensitivity of Teff cells to Treg and IL-10 between vehicle and SM934 treated groups, we still presumed that simultaneously regulating balance of effector T, naïve T, and regulatory T cells and increasing IL-10 production should largely contribute to disease remission. In addition, from the current study and other reports, we propose that IL-10 still work as an immunosuppressive factor, whereas the final readout of the suppressive effects of IL-10 will be determined by the pathogenic status of other responsive cells.
In vivo, SM934 treatment could induce the accumulation of Treg cell in peripheral. However, this inducible effect was not likable to be direct. Our previous work showed that, in vitro, SM934 could suppress Th1 and Th17 cell differentiation, but exerted no suppressive influence on Treg cell differentiation. Certainly, in vitro, SM934 will not induce FoxP3 expression in CD4+ T cells. In vitro, we also compared the effects of SM934 on the proliferation of CD4+CD25− and CD4+CD25+ T cells isolated from naïve C57BL/6 mice, and finally found that SM934 suppressed the proliferation of both similarly (unpublished observations). Thus, we suggested that, in vivo, SM934 treatment induced the apoptosis of activated effector T cells, rather than preferably inducing Treg accumulation, then accelerated the replenishment of CD4+ T cell pool consisting of more naïve population.
Collectively, this study demonstrated that artemisinin derivative SM934 exerted valuable therapeutic effects on lupus-prone female NZB/W F1 mice and possessed the great potential for future lupus treatment. The therapeutic mechanism of SM934 might be attributed to its regulating development of helper T cell subsets and enhancing IL-10 production.
Materials and Methods
Female NZB/W F1 mice were purchased from the Jackson Laboratory. Female C57BL/6 mice were obtained from Shanghai Laboratory Animal Center of the Chinese Academy of Sciences, and were used at 7 to 10 weeks of age. All mice were housed under specific pathogen-free conditions. Experiments were carried out according to the National Institute of Healthy Guide for Care and Use of Laboratory Animals and were approved by the Institutional Animal Care and Use Committee at the Shanghai Institute of Materia Medica, Chinese Academy of Sciences (IACUC protocol # 2010-10-ZJP-01).
NZB/W F1 mice
Six and half months old female NZB/W F1 mice were orally treated with SM934 for 3 months or 6 months respectively. At the initiation of treatment, mice were randomly divided according to bodyweight and proteinuria level and were orally treated for consecutive 6 days every week. In 3 months treatment, mice were divided into 5 groups (n = 11 per group): vehicle control group (saline), positive control group (prednisolone, PNS, 2 mg/kg/day), and SM934 treated groups (10, 3, and 1 mg/kg/day respectively), and the bodyweight and proteinuria level were monitored weekly. In 6 months treatment, mice were divided into 3 groups (n = 12 per group): vehicle control group (saline), positive control group (prednisolone, PNS, 2 mg/kg/day), and SM934 treated group (10 mg/kg/day), and the bodyweight and proteinuria level were monitored biweekly. During the treatment, individuals were euthanized, then sera and kidneys were collected, if their urine protein concentration >10 mg/ml for consecutive two weeks accompanied by weight loss >20%. In this case, the last known values for urinary protein and bodyweight were carried forward. For investigations of effects of SM934 treatment on immunological correlates, 3 months treatment experiments were carried out.
OVA-immunized C57BL/6 mice
Naïve female C57BL/6 mice were immunized with emulsive OVA/CFA according to our previous method , then were treated with saline or SM934 (10 mg/kg/day) for 7 days.
IFN-γ elicited C57BL/6 mice
To investigate the effects of SM934 on IFN-γ-primed peritoneal macrophages in vivo, naïve female C57BL/6 mice were i.p. injected with 300 units of mIFN-γ according to the method described by Takeda et al , and simultaneously orally administrated with SM934 (10 mg/kg/day) for consecutive 3 days. Then, peritoneal exudative cells were collected.
Biochemical parameters, serum anti-dsDNA antibody detection, renal histopathology and immunofluorescence
All examinations and scoring were carried out according to our previous descriptions . Briefly, urinary protein concentrations were determined with Coomassie blue G dye binding assay. Urinary protein was scored according to the following criteria: 0/trace, <0.3 mg/ml; 1+, ≥0.3 mg/ml; 2+, ≥1 mg/ml; 3+, ≥3 mg/ml; 4+, ≥10 mg/ml; Blood urea nitrogen (BUN) concentration was determined by BUN test kit (Jianchen biotechnology, Nanjing, China) according to the manufacturer's instructions; For ELISA detection of serum anti-dsDNA IgG and isotypes, sera from aged female NZB/W F1 mice (10 months of age) was used as the standard. Titers of standard serum were defined as follows: total IgG, 1000 U/ml; IgG1, 170 U/ml; IgG2a, 340 U/ml; IgG3, 270 U/ml; Formalin-fixed kidney sections were embedded in paraffin and stained with hematoxylin and eosin (H&E), then were graded by two independent renal pathologists; Snap-frozen kidneys were used for immunofluorescence examination of IgG deposits.
Flow cytometric analysis
Surface marker and intracellular transcription factor staining was conducted and analyzed according to our previous methods . For intracellular cytokine staining, cells were incubated for 4 hours with phorbol 12-myristate 13-acetate (PMA, 50 ng/ml) and ionomycin (750 ng/ml) in the presence of Brefeldin A (BFA, 10 µg/ml). At the end of incubation, suspended cells were collected. Adherent cells were treated with 10 mM EDTA-PBS solution (pH = 7.2) for 5 minutes and then collected. Suspended and adherent cells were mixed together and blocked with FcγR blocker before extracellular staining for corresponding fluorescence-labeled surface antibodies. After surface staining, cells were fixed, permeabilized and stained for cytokines according to manufacturer's instruction (FoxP3 Staining Buffer set was used).
The following reagents were used: FITC- and PE-anti-mCD4 (GK1.5), FITC- and PE-anti-mCD3 (145-2C11), biotinylated- and FITC-anti-mTCRγδ (GL3), biotinylated-anti-mB220 (RA3-6B2), PE-anti-mCD8 (2.43), FITC- and PE-anti-mCD11c (HL-3), biotinylated- and PE-anti-mCD11b (M1/70), FITC-anti-mGr-1 (RB6-8C5), FITC-anti-mIFN-γ (XMG1.2), PE-anti-mIL-10 (JES5-16E3), PE-anti-mIL-17 (TC11-18H10), and PE-Rat IgG1 were all purchased from BD Pharmingen; FITC-anti-mF4/80 (BM8), PE-Cy5-anti-mouse/rat FoxP3 (FJK-16s), PE-Cy5- and PE-Rat IgG2a, PE-Rat IgG2b, and FoxP3 Staining Buffer Set were all purchased from eBioscience.
Splenic CD4+ T cell.
Purified polyclonal CD4+ T cells from splenocytes were enriched as described previously .
Splenic and peritoneal macrophage.
To isolate splenic F4/80+ macrophages, splenocytes were blocked with saturated anti-m-CD16/32 (2.4G2, purified in-house), then reacted with FITC-anti-m-F4/80 mAb. After extensive washing, cells were incubated with anti-FITC microbeads (Miltenyi Biotec, Bergisch Gladbach, Germany) and positively selected. To acquire highly purified resulted cells, two rounds of positive selection were conducted. Purity of resulted cells was determined by flow cytometry analysis, and was consistently >98%.
To isolate peritoneal macrophages, naive female C57BL/6 mice were elicited by i.p. injection of 0.5 ml of 3% thioglycollate medium (TG, Difco, Detroit, MI). Three days later, adherent peritoneal exudative cells were obtained by peritoneal lavage using ice-cold phosphate-buffered saline, seeded in dishes, and collected by removing the non-adherent cells after 2 hours incubation at 37°C. Peritoneal macrophages from mIFN-γ-elicited C57BL/6 mice were enriched using similar protocol with thioglycollate-elicited ones.
Cell stimulation and culture
Splenocytes from NZB/W F1 mice were cultured in 24-well flat-bottom plates coated with anti-CD3 mAb (145-2C11, 5 µg/ml) for 24 hours. Splenocytes of OVA-immunized mice were stimulated with OVA (100 µg/ml) for 24 hours. After incubation, supernatants were collected and stored at −20°C for ELISA assay.
Primary peritoneal macrophages were cultured in 48-well flat-bottom plates and stimulated without or with 50 unit/ml mIFN-γ in the absence or presence of SM934 for 24 hours. After incubation, supernatants were collected and stored at −20°C for ELISA assay.
Purified CD4+ T cells and F4/80+ macrophages were cultured together with the ratio of 4∶1 in 96-well flat-bottom plates in the presence or absence of OVA (100 µg/ml) for 72 hours. Cultures were pulsed with 0.5 µCi 3H thymidine per well for 8 hours before harvesting and assessed for 3H thymidine incorporation at 72 hours.
Total RNA was isolated using Trizol reagent (Invitrogen, Carlsbad, CA, USA), reverse transcribed, and polymerase chain reaction amplified using specific primers. Real-time PCR was performed with SYBR Green PCR Reagents (Qiagen, Valencia, CA, USA) and a Continuous Fluorescence Detection System (MJ Research, USA), according to the manufacturer's instructions. Relative quantitation of mRNA expression was calculated as the fold increase in expression by using the ΔΔCt method. The forward and reverse primers for FoxP3 and HPRT were as follows: FoxP3 forward 5′-CCC ATC CCC AGG AGT CTT G-3′, FoxP3 reverse: 5′-ACC ATG ACT AGG GGC ACT GTA-3′; HPRT forward: 5′-GTT GGA TAC AGG CCA GAC TTT GTT G-3′, HPRT reverse: 5′-GAG GGT AGG CTG GCC TAT AGG CT-3′.
ELISA for cytokines detection
Cytokines in sera or culture supernatants were assayed using the mouse IL-10, IL-12/23p40, TGF-β, IFN-γ, IL-2, IL-4, IL-17A ELISA kit (all from BD Pharmingen) according to the manufacturer's instructions.
Purified CD4+ T cells from mice of different groups were directly lysed in SDS sample buffer and boiled for 5 min at 100°C. Proteins were resolved by 10% SDS-polyacrylamide gel electrophoresis (PAGE), transferred to the nitrocellulose membrane (Amersham Pharmacia Biotech, Buckinghamshire, UK). The membranes were treated with 5% BSA-TBST buffer (TBS containing 0.1% Tween20) for 2 hours to block nonspecific binding, rinsed, and incubated with anti-BCL-2 (SC-492, Santa Cruz Biotechnology) or anti-GAPDH (Cell Signaling Technology). Signals were detected with HRP-conjugated anti-rabbit or anti-mouse IgG using the ECL system (Amersham Biosciences)
Data were analyzed using Student's t-test and one-way analysis of variance (ANOVA) with Newman-Keuls multiple comparisons on post-tests. Nonparametric data (histological score) were analyzed using Mann-Whitney U test. Survival rate for treated group was compared with control group by log-rank test followed by Bonferroni adjustment. P<0.05 was considered to be statistically significant.
Glomerular, tubular, vascular, interstitial damage, and glomerular IgG depositions were analyzed using a semiquantitative scoring system and scored by two pathologists.
* P<0.05, ** P<0.01 versus vehicle.
Glomerular, tubular, vascular, and interstitial damages were analyzed using a semiquantitative scoring system: −, no changes; ±, minimal changes; +, mild changes; ++, moderate changes; +++, marked changes.
Conceived and designed the experiments: JPZ YL LFH SJH. Performed the experiments: LFH SJH XL CPW XHZ YY PLH YZ FHZ. Analyzed the data: JPZ LFH SJH WT YFY. Contributed reagents/materials/analysis tools: YL. Wrote the paper: JPZ LFH SJH.
- 1. Crispin JC, Kyttaris VC, Terhorst C, Tsokos GC (2010) T cells as therapeutic targets in SLE. Nat Rev Rheumatol 6: 317–325.
- 2. Sanz I, Lee FE-H (2010) B cells as therapeutic targets in SLE. Nat Rev Rheumatol 6: 326–337.
- 3. Brian LK (1996) Systemic Lupus Erythematosus. Cell 85: 303–306.
- 4. Andrews BS, Eisenberg RA, Theofilopoulos AN, Izui S, Wilson CB, et al. (1978) Spontaneous murine lupus-like syndromes. Clinical and immunopathological manifestations in several strains. J Exp Med 148: 1198–1215.
- 5. Akahoshi M, Nakashima H, Tanaka Y, Kohsaka T, Nagano S, et al. (1999) Th1/Th2 balance of peripheral T helper cells in systemic lupus erythematosus. Arthritis Rheum 42: 1644–1648.
- 6. Masutani K, Akahoshi M, Tsuruya K, Tokumoto M, Ninomiya T, et al. (2001) Predominance of Th1 immune response in diffuse proliferative lupus nephritis. Arthritis Rheum 44: 2097–2106.
- 7. Peng SL, Moslehi J, Craft J (1997) Roles of interferon-gamma and interleukin-4 in murine lupus. J Clin Invest 99: 1936–1946.
- 8. Haas C, Ryffel B, Le Hir M (1998) IFN-gamma receptor deletion prevents autoantibody production and glomerulonephritis in lupus-prone (NZB×NZW)F1 mice. J Immunol 160: 3713–3718.
- 9. Miyara M, Amoura Z, Parizot C, Badoual C, Dorgham K, et al. (2005) Global natural regulatory T cell depletion in active systemic lupus erythematosus. J Immunol 175: 8392–8400.
- 10. Scalapino KJ, Tang Q, Bluestone JA, Bonyhadi ML, Daikh DI (2006) Suppression of disease in New Zealand Black/New Zealand White lupus-prone mice by adoptive transfer of ex vivo expanded regulatory T cells. J Immunol 177: 1451–1459.
- 11. Humrich JY, Morbach H, Undeutsch R, Enghard P, Rosenberger S, et al. (2010) Homeostatic imbalance of regulatory and effector T cells due to IL-2 deprivation amplifies murine lupus. Proc Natl Acad Sci U S A 107: 204–209.
- 12. Miossec P, Korn T, Kuchroo VK (2009) Interleukin-17 and type 17 helper T cells. N Engl J Med 361: 888–898.
- 13. Zhou L, Chong MM, Littman DR (2009) Plasticity of CD4+ T cell lineage differentiation. Immunity 30: 646–655.
- 14. Roark CL, Simonian PL, Fontenot AP, Born WK, O'Brien RL (2008) gammadelta T cells: an important source of IL-17. Curr Opin Immunol 20: 353–357.
- 15. Cua DJ, Tato CM (2010) Innate IL-17-producing cells: the sentinels of the immune system. Nat Rev Immunol 10: 479–489.
- 16. Feng T, Qin H, Wang L, Benveniste EN, Elson CO, et al. (2011) Th17 cells induce colitis and promote Th1 cell responses through IL-17 induction of innate IL-12 and IL-23 production. J Immunol 186: 6313–6318.
- 17. He D, Wu L, Kim HK, Li H, Elmets CA, et al. (2009) IL-17 and IFN-gamma mediate the elicitation of contact hypersensitivity responses by different mechanisms and both are required for optimal responses. J Immunol 183: 1463–1470.
- 18. Nakae S, Komiyama Y, Nambu A, Sudo K, Iwase M, et al. (2002) Antigen-specific T cell sensitization is impaired in IL-17-deficient mice, causing suppression of allergic cellular and humoral responses. Immunity 17: 375–387.
- 19. Lin Y, Ritchea S, Logar A, Slight S, Messmer M, et al. (2009) Interleukin-17 is required for T helper 1 cell immunity and host resistance to the intracellular pathogen Francisella tularensis. Immunity 31: 799–810.
- 20. Crispin JC, Tsokos GC (2010) Interleukin-17-producing T cells in lupus. Curr Opin Rheumatol 22: 499–503.
- 21. Garrett-Sinha LA, John S, Gaffen SL (2008) IL-17 and the Th17 lineage in systemic lupus erythematosus. Curr Opin Rheumatol 20: 519–525.
- 22. Llorente L, Richaud-Patin Y (2003) The role of interleukin-10 in systemic lupus erythematosus. J Autoimmun 20: 287–289.
- 23. Houssiau FA, Lefebvre C, Vanden Berghe M, Lambert M, Devogelaer JP, et al. (1995) Serum interleukin 10 titers in systemic lupus erythematosus reflect disease activity. Lupus 4: 393–395.
- 24. Park YB, Lee SK, Kim DS, Lee J, Lee CH, et al. (1998) Elevated interleukin-10 levels correlated with disease activity in systemic lupus erythematosus. Clin Exp Rheumatol 16: 283–288.
- 25. Llorente L, Richaud-Patin Y, Garcia-Padilla C, Claret E, Jakez-Ocampo J, et al. (2000) Clinical and biologic effects of anti-interleukin-10 monoclonal antibody administration in systemic lupus erythematosus. Arthritis Rheum 43: 1790–1800.
- 26. Ishida H, Muchamuel T, Sakaguchi S, Andrade S, Menon S, et al. (1994) Continuous administration of anti-interleukin 10 antibodies delays onset of autoimmunity in NZB/W F1 mice. J Exp Med 179: 305–310.
- 27. Yin Z, Bahtiyar G, Zhang N, Liu L, Zhu P, et al. (2002) IL-10 regulates murine lupus. J Immunol 169: 2148–2155.
- 28. Blenman KR, Duan B, Xu Z, Wan S, Atkinson MA, et al. (2006) IL-10 regulation of lupus in the NZM2410 murine model. Lab Invest 86: 1136–1148.
- 29. Moore KW, de Waal Malefyt R, Coffman RL, O'Garra A (2001) Interleukin-10 and the interleukin-10 receptor. Annu Rev Immunol 19: 683–765.
- 30. Murai M, Turovskaya O, Kim G, Madan R, Karp CL, et al. (2009) Interleukin 10 acts on regulatory T cells to maintain expression of the transcription factor Foxp3 and suppressive function in mice with colitis. Nat Immunol 10: 1178–1184.
- 31. Lu L (2002) [Study on effect of Cordyceps sinensis and artemisinin in preventing recurrence of lupus nephritis]. Zhongguo Zhong Xi Yi Jie He Za Zhi 22: 169–171.
- 32. Wang JX, Tang W, Shi LP, Wan J, Zhou R, et al. (2007) Investigation of the immunosuppressive activity of artemether on T-cell activation and proliferation. Br J Pharmacol 150: 652–661.
- 33. Wang JX, Tang W, Zhou R, Wan J, Shi LP, et al. (2008) The new water-soluble artemisinin derivative SM905 ameliorates collagen-induced arthritis by suppression of inflammatory and Th17 responses. Br J Pharmacol 153: 1303–1310.
- 34. Hou LF, He SJ, Wang JX, Yang Y, Zhu FH, et al. (2009) SM934, a water-soluble derivative of arteminisin, exerts immunosuppressive functions in vitro and in vivo. Int Immunopharmacol 9: 1509–1517.
- 35. Wang JX, Hou LF, Yang Y, Tang W, Li Y, et al. (2009) SM905, an artemisinin derivative, inhibited NO and pro-inflammatory cytokine production by suppressing MAPK and NF-kappaB pathways in RAW 264.7 macrophages. Acta Pharmacol Sin 30: 1428–1435.
- 36. Jin O, Zhang H, Gu Z, Zhao S, Xu T, et al. (2009) A pilot study of the therapeutic efficacy and mechanism of artesunate in the MRL/lpr murine model of systemic lupus erythematosus. Cell Mol Immunol 6: 461–467.
- 37. Wu X, Zhang W, Shi X, An P, Sun W, et al. (2010) Therapeutic effect of artemisinin on lupus nephritis mice and its mechanisms. Acta Biochim Biophys Sin (Shanghai) 42: 916–923.
- 38. Hou LF, He SJ, Li X, Yang Y, He PL, et al. (2011) Oral administration of artemisinin analog SM934 ameliorates lupus syndromes in MRL/lpr mice by inhibiting Th1 and Th17 cell responses. Arthritis Rheum 63: 2445–2455.
- 39. Reilly CM, Gilkeson GS (2002) Use of genetic knockouts to modulate disease expression in a murine model of lupus, MRL/lpr mice. Immunol Res 25: 143–153.
- 40. Kaneko Y, Nimmerjahn F, Madaio MP, Ravetch JV (2006) Pathology and protection in nephrotoxic nephritis is determined by selective engagement of specific Fc receptors. J Exp Med 203: 789–797.
- 41. Boross P, Arandhara VL, Martin-Ramirez J, Santiago-Raber ML, Carlucci F, et al. (2011) The inhibiting Fc receptor for IgG, Fcgamma RIIB, is a modifier of autoimmune susceptibility. J Immunol 187: 1304–1313.
- 42. Renno T, Attinger A, Rimoldi D, Hahne M, Tschopp J, et al. (1998) Expression of B220 on activated T cell blasts precedes apoptosis. Eur J Immunol 28: 540–547.
- 43. Renno T, Hahne M, Tschopp J, MacDonald HR (1996) Peripheral T cells undergoing superantigen-induced apoptosis in vivo express B220 and upregulate Fas and Fas ligand. J Exp Med 183: 431–437.
- 44. Hughes GC, Martin D, Zhang K, Hudkins KL, Alpers CE, et al. (2009) Decrease in glomerulonephritis and Th1-associated autoantibody production after progesterone treatment in NZB/NZW mice. Arthritis Rheum 60: 1775–1784.
- 45. Monk CR, Spachidou M, Rovis F, Leung E, Botto M, et al. (2005) MRL/Mp CD4+,CD25- T cells show reduced sensitivity to suppression by CD4+,CD25+ regulatory T cells in vitro: a novel defect of T cell regulation in systemic lupus erythematosus. Arthritis Rheum 52: 1180–1184.
- 46. Wang L, Tassiulas I, Park-Min KH, Reid AC, Gil-Henn H, et al. (2008) ‘Tuning’ of type I interferon-induced Jak-STAT1 signaling by calcium-dependent kinases in macrophages. Nat Immunol 9: 186–193.
- 47. Gergely P Jr, Niland B, Gonchoroff N, Pullmann R Jr, Phillips PE, et al. (2002) Persistent mitochondrial hyperpolarization, increased reactive oxygen intermediate production, and cytoplasmic alkalinization characterize altered IL-10 signaling in patients with systemic lupus erythematosus. J Immunol 169: 1092–1101.
- 48. Yuan W, DiMartino SJ, Redecha PB, Ivashkiv LB, Salmon JE (2011) Systemic lupus erythematosus monocytes are less responsive to interleukin-10 in the presence of immune complexes. Arthritis Rheum 63: 212–218.
- 49. Takeda K, Clausen BE, Kaisho T, Tsujimura T, Terada N, et al. (1999) Enhanced Th1 activity and development of chronic enterocolitis in mice devoid of Stat3 in macrophages and neutrophils. Immunity 10: 39–49.