The Efficacy and Safety of the Combination of Total Glucosides of Peony and Leflunomide for the Treatment of Rheumatoid Arthritis: A Systemic Review and Meta-Analysis

Feng, Zhitao; Xu, Juan; He, Guochao; Cao, Meiqun; Duan, Lihong; Chen, Liguo; Wu, Zhengzhi

doi:https://doi.org/10.1155/2016/9852793

Evidence-Based Complementary and Alternative Medicine

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Volume 2016 | Article ID 9852793 | https://doi.org/10.1155/2016/9852793

The Efficacy and Safety of the Combination of Total Glucosides of Peony and Leflunomide for the Treatment of Rheumatoid Arthritis: A Systemic Review and Meta-Analysis

Zhitao Feng,^1,2,3,4Juan Xu,^5,6Guochao He,⁷Meiqun Cao,^3,4Lihong Duan,^3,4Liguo Chen,¹and Zhengzhi Wu^2,3,4

Academic Editor: Agnieszka Najda

Received25 Nov 2015

Accepted29 Dec 2015

Published10 Apr 2016

Abstract

Objective. To evaluate the efficacy and safety of the total glucosides of peony (TGP) and leflunomide (LEF) for the treatment of rheumatoid arthritis (RA). Methods. Randomized controlled trials (RCTs) on the efficacy and safety of the combination of TGP and LEF versus LEF alone for the treatment of RA were retrieved by searching PubMed, EMBASE, Cochrane Library, the China National Knowledge Infrastructure database, and Wanfang database. Results. Eight RCTs including 643 RA patients were included in the present meta-analysis. The quality of included studies was poor. The levels of ESR (), CRP (), and RF () in RA patients who received the combination of TGP and LEF were significantly lower than RA patients who received LEF therapy alone. The pooled results suggest that the combination of TGP and LEF caused less abnormal liver function than LEF alone (). No significant difference in the gastrointestinal discomfort was identified between the combination of TGP and LEF and LEF alone groups (). Conclusion. The combination of TGP and LEF in treatment of RA presented the characteristics of notably decreasing the levels of laboratory indexes and higher safety in terms of liver function. However, this conclusion should be further investigated based on a larger sample size.

1. Introduction

Rheumatoid arthritis (RA) is a common chronic inflammatory disorder characterized by synovial inflammation and angiogenesis and cartilage and bone destruction [1, 2]. The estimated incidence of RA in the industrialized world is 1% [3]. RA may cause progressive disability and a number of systemic complications, such as pulmonary, cardiovascular, psychological, and skeletal diseases [4]. It has been reported that early and sufficient application of conventional disease modifying antirheumatic drugs (DMARDs), such as leflunomide (LEF), methotrexate, sulfasalazine, hydroxychloroquine, and glucocorticoids, can effectively inhibit inflammation and bone erosion in RA patients [5]. The European League Against Rheumatism (EULAR) and American College of Rheumatology (ACR) recommend the application of DMARDs as soon as the confirmation of RA diagnosis [6]. In addition, DMARDs-naïve patients should be treated with either conventional DMARD monotherapy or DMARD combination therapy [7, 8]. Numerous studies reported that the combination of two or multiple DMARDs was more effective than single DMARD for the treatment of RA [9, 10].

Total glucoside of peony (TGP) is a biologically active compound extracted from traditional Chinese medicine of peony. Paeoniflorin (90%) is the major component in TGP. Previous studies have reported that paeoniflorin/TGP had both anti-inflammatory and immune-regulatory effects [11–13]. TGP has been widely used for the treatment of autoimmune diseases, especially RA, by alleviating inflammation [14]. In addition, TGP was able to relieve inflammation reactions, reduce joint pain and swelling, and delay bone erosion and destruction [15]. LEF is an efficient DMARD widely used for the treatment of RA [16]. LEF exhibits predominant functions including immunomodulation, immunosuppression, and antiproliferation [17]. LEF can prevent the progress of RA by inhibiting inflammatory reactions, protecting cartilage and bone from destruction, and delaying radiologic progression [16].

Currently, several clinical studies reported that the combination of TGP and LEF significantly improved the symptoms and prevented the progression of RA compared with LEF alone. However, most of these results were from uncontrolled clinical trials or retrospective studies. In addition, the safety of the combination of TGP and LEF for the treatment of RA is not clear. In the present study, we conducted a meta-analysis to evaluate the efficacy and safety of the combination of TGP and LEF for the treatment of RA. Our results provide evidence for the application of the combination of TGP and LEF for the treatment of RA patients.

2. Materials and Methods

2.1. Search Strategy

We searched the following databases to identify appropriate trials: PubMed (1865 to December 2015), EMBASE (1947 to December 2015), Cochrane Library (1993 to December 2015), the China National Knowledge Infrastructure database (1979 to December 2015), and the Wanfang database (1982 to December 2015). The search terms were (rheumatoid arthritis OR RA) AND (total glucosides of peony OR TGP) AND (leflunomide) AND (randomized controlled trial). Manual search in the references from original studies was performed to identify additional trials.

2.2. Study Selection

Studies meeting the following criteria were selected. (i) Patients were diagnosed with RA, according to the 1987 guidelines by the American Rheumatology Association. (ii) Studies were performed as a RCT describing a correct randomization procedure. Trials that used inappropriate methods of randomization (e.g., open alternation) were excluded. (iii) RA patients were treated with the combination of TGP and LEF, while controls were treated with LEF alone. (iv) Clinical outcomes included at least one of the following parameters: therapeutic effects, erythrocyte sedimentation rate (ESR), rheumatoid factor (RF), C reactive protein (CRP), and side effects. (v) Intervention lasted for four weeks or longer.

2.3. Data Extraction

The relevant data was extracted by two independent reviewers (Zhitao Feng and Guochao He), including the study design, randomization, diagnostic criteria for RA, the first author’s name, year of publication, sample size, treatment duration, dose, outcomes, and adverse events (AE). Disagreements were resolved by consensus or arbitrated by the third investigator (Zhengzhi Wu).

2.4. Data Synthesis and Analysis

Statistical analyses were performed using Review Manager 5.2 software (Cochrane Collaboration, Oxford, UK). Dichotomous data and continuous outcomes were presented as odds ratios (ORs) and mean difference (MD), respectively, both with 95% confidence interval (CI). The Cochrane’s chi-square test and Higgins were used to assess heterogeneity [26]. A considerable level of heterogeneity was defined when the value was <0.10 or the value was >50%. A fixed-effect model was employed when no statistical heterogeneity was identified among studies; otherwise the random-effect model was used [27].

3. Results

3.1. Study Selection

A total of 74 studies were identified by searching in the databases mentioned above. Of these, 18 studies were deemed to be duplicated. 56 eligible studies were retrieved for detailed evaluation. After content review, 8 non-RCT studies, including one case report, 5 meeting abstracts, and 3 review articles, were excluded. In addition, 6 studies in which no RA patients were enrolled, 24 studies in which the combination of TGP and LEF or LEF alone was not applied, and one study without clinical outcomes of interest were also excluded from this meta-analysis. Finally, a total of 8 trials including 319 RA cases and 324 controls that meet our inclusion criteria were included in the present meta-analysis. The general procedure of study selection was detailed in Figure 1.

3.2. Study Characteristics

The included studies have been published between 2006 and 2015. All the eight RCTs were conducted in China and published in Chinese with randomization procedure and single center. The participant numbers in the individual studies varied from 38 to 100. The duration of the interventions (the combination of TGP and LEF or LEF alone) in the included studies varied from 4 to 24 weeks, except one study in which the treatment duration was not described [19]. Four studies described the therapeutic effects that were evaluated on the basis of four classes of outcomes including “cure,” “significant effective,” “effective,” and “ineffective” [19, 21, 23, 25]. Six trials reported the AEs in detail [18, 19, 21, 22, 24, 25]. In addition, six trials mentioned the ESR [18–20, 22, 23, 25]; four trials referred to RF [18, 19, 23, 25]; and three trials analyzed CRP [18, 22, 25]. The characteristics of the included RCTs were shown in Table 1.

3.3. Risk of Bias Assessment

The risk of bias assessment was summarized in Figure 2. The quality of all included studies was poor. While all the eight studies reported randomization, none of them described the specific methods applied. Additionally, none of the eight studies mentioned the allocation concealment, blinding of participants and personnel, and blinding of outcome assessment. All of the eight studies addressed the incomplete outcomes as well as selective reporting. No other bias was identified.

3.4. The Therapeutic Effects of the Combination of TGP and LEF versus LEF Alone

To evaluate the therapeutic effects of the combination of TGP and LEF or LEF alone, data were extracted from four trials including 318 patients. A fixed-effect model was employed to pool the data because no significant heterogeneity was identified among the included trials (, ). As shown in Figure 3, a significantly higher effective rate was identified in the LEF group compared with the combination of TGP and LEF group (, 95% CI = 2.02 to 9.16, and ).

3.5. The Effects of the Combination of TGP and LEF or LEF Alone on Serum Levels of ESR, CRP, and RF

Six, three, and four trials reported the effects of the combination of TGP and LEF or LEF alone on serum levels of ESR, CRP, and RF. Significant heterogeneity was found among these studies (all or ). Therefore, a random-effect model was used to analyze the data. The pooled results revealed significant differences in serum levels of ESR (, 95% CI = −9.88 to −3.479, and ), CRP (, 95% CI = −8.66 to −3.05, and ), and RF (, 95% CI = −21.82 to −8.14, and ) between the combination of TGP and LEF group and the LEF alone group (Figure 4).

(a)

(b)

(c)

3.6. Safety Profile and AEs

The safety profile was assessed for all included trials. The main AEs included abnormal liver function that was defined as follows: the serum level of alanine aminotransferase (ALT) or aspartate aminotransferase (AST) was >1.5-fold above the upper limits of the normal value and gastrointestinal discomfort including nausea, emesis, and diarrhea. A fixed-effect model was applied to pool the data because no heterogeneity was observed (all or ). Our results revealed a higher rate of abnormal liver function (, 95% CI = 0.12 to 0.84, and ) in the LEF group compared with the combination of TGP and LEF group. However, no significant difference in gastrointestinal discomfort was identified between these two groups (, 95% CI = 0.81 to 3.09, and ) (Figure 5).

(a)

(b)

4. Discussion

4.1. Summary of Evidence

To the best of our knowledge, this is the first meta-analysis of the efficacy and safety of the combination of TGP and LEF for the treatment of RA. Eight RCTs including 319 patients in the treatment group and 324 individuals in the control group were included in the present meta-analysis. The pooled results suggest better therapeutic effects of the LEF alone compared to TGP plus LEF. The efficacy assessment system based on the improvement of signs and symptoms may lead to the heterogeneity of results. Only one study described the clinical outcomes defined by the American College of Rheumatology (ACR) criteria. The results in this study showed a higher response rate in the combination of TGP and LEF group compared with the LEF alone group [20]. In addition, one trial reported the clinical outcomes evaluated according to the European League Against Rheumatism (EULAR) response criteria [28]. This study also showed better treatment effects in the combination of TGP and LEF group than the LEF alone group [18]. Given the relatively small sampling size, we did not pool these results. Next, we should include internationally recognized standards such as the ACR or EULAR criteria and expand sampling size to further study the effects of the combination of TGP and LEF for the treatment of RA. However, the pooled data showed superior effects of the combination of TGP and LEF on reducing serum levels of ESR, CRP, and RF, compared with the LEF alone.

To evaluate the efficacy and safety of drugs, the AEs should also be fully considered. More RA patients receiving the LEF alone treatment had abnormal liver function compared with RA patients receiving the combination of TGP and LEF. However, no significant difference in gastrointestinal discomfort was identified between these two groups. The AEs mentioned above were relieved by relevant treatments.

4.2. Mechanisms of the Combination of TGP and LEF on RA

The mechanisms of TGP for the treatment of RA have been extensively investigated. A large number of studies have analyzed the function and effects of TGP in animal models and patients. It has been shown that TGP suppressed the proliferation of lymphocytes and neutrophils and induced the apoptosis of lymphocytes in animals with collagen-induce arthritis (CIA) or complete Freund’s adjuvant-induced arthritis (AA) [29–33]. Several researchers suggest that TGP inhibited the production of proinflammatory mediators in synoviocytes [33–35]. Furthermore, both in vitro and in vivo studies suggest that TGP could balance the differentiation and function of Th1 and Th2 cells and inhibited the production of proinflammatory mediators, such as TNF-α, IL-1β, IL-6, and GM-CSF, in synoviocytes, macrophages, and lymphocytes [11, 36, 37]. A study in rabbits with antigen-induced arthritis (AIA) showed that TGP reduced the level of RANKL and improved OPG expression, suggesting that TGP inhibited juxta-articular osteoporosis and subchondral bone destruction [35, 38]. LEF, an isoxazole immunomodulatory agent, was approved by the U.S. Food and Drug Administration (FDA) for the treatment of RA in 1999 [17]. It has been proved that LEF inhibits mitochondrial enzyme dihydroorotate dehydrogenase (DHODH), a key enzyme involved in de novo synthesis of pyrimidine ribonucleotide uridine monophosphate (rUMP) [39, 40], causing cell cycle arrest at the G1 phase and decrease in DNA and RNA syntheses. In addition, LEF can suppress the proliferation of autoimmune T-cell and the production of antibodies by B-cells and increase the synthesis of immunosuppressive cytokines such as transforming growth factor beta (TGF-β) [41]. Furthermore, LEF can inhibit the tyrosine kinase, which is critical for signal transduction and differentiation of activated cells and induction cell growth [42]. Taken together, these studies suggest that the combination of TGP and LEF is an effective therapy for the treatment of RA.

4.3. Limitations and Strengths of the Present Meta-Analysis

Nevertheless, some limitations of this meta-analysis should be discussed. First, the number of RCTs and the number of patients included in retrieved studies were limited. In the assessment of publication bias, the power of this meta-analysis was modest due to the limited number of trials and patients. Second, some included studies were of poor quality. Although all trials had a randomization design, very few studies reported the randomization procedure at length. The allocation concealment and blinding of participants or outcome assessment were not available, resulting in high risk of selection or detection bias. Third, heterogeneity was identified in included trials. We believe that differences in dose, treatment duration, detection methods, and evaluation criterion were the major sources of the heterogeneity. Fourth, all the RCTs included in the present meta-analysis were conducted in China and published in Chinese, causing high risk of selection bias. Therefore, the conclusion of the present meta-analysis should be further analyzed in the future.

5. Conclusion

While the therapeutic effects of the combination of TGP and LEF might not be better than that of LEF alone, the combination of TGP and LEF is superior to the LEF alone in reducing the levels of ESR, CRP, and RF. In addition, the combination of TGP and LEF is safer than the LEF alone regarding the abnormal liver functions caused by the treatment. Given the small sample size and heterogeneity of the included trials, multicenter and larger scale RCTs are needed to verify our conclusion.

Conflict of Interests

The authors have declared that they have no conflict of interests.

Authors’ Contribution

Zhitao Feng and Zhengzhi Wu conceived the study. Zhitao Feng, Guochao He, and Juan Xu performed literature searches and study selection. Lihong Duan and Meiqun Cao performed data extraction and quality assessment. Zhitao Feng and Guochao He conducted analysis of the data. Zhitao Feng and Juan Xu wrote the paper. Liguo Chen and Zhengzhi Wu revised the paper.

Acknowledgments

This project was supported by grants from the National Natural Science Foundation of China (no. 81273665), National High Technology Research and Development Program (no. 2014AA020907), the Key Project of Shenzhen Science and Technology Program (no. JCYJ20130401115547212), the Guangdong Provincial Natural Science Foundation (2015A030310067), and Shenzhen Technology Innovation Foundation (no. JCYJ20150401171352927).

References

H. A. Elshabrawy, Z. Chen, M. V. Volin, S. Ravella, S. Virupannavar, and S. Shahrara, “The pathogenic role of angiogenesis in rheumatoid arthritis,” Angiogenesis, vol. 18, no. 4, pp. 433–448, 2015.
View at: Publisher Site | Google Scholar
Z. Feng, G. He, Z. Chen, Z. Wu, and J. Li, “Lack of association of matrix metalloproteinase-3 gene polymorphism with susceptibility to rheumatoid arthritis: a meta-analysis,” BMC Musculoskeletal Disorders, vol. 15, article 376, 2014.
View at: Publisher Site | Google Scholar
T. K. Kvien, “Epidemiology and burden of illness of rheumatoid arthritis,” PharmacoEconomics, vol. 22, no. 2, supplement 1, pp. 1–12, 2004.
View at: Google Scholar
I. B. McInnes and G. Schett, “The pathogenesis of rheumatoid arthritis,” The New England Journal of Medicine, vol. 365, no. 23, pp. 2205–2219, 2011.
View at: Publisher Site | Google Scholar
B. Svensson, A. Boonen, K. Albertsson, D. van der Heijde, C. Keller, and I. Hafström, “Low-dose prednisolone in addition to the initial disease-modifying antirheumatic drug in patients with early active rheumatoid arthritis reduces joint destruction and increases the remission rate: a two-year randomized trial,” Arthritis & Rheumatism, vol. 52, no. 11, pp. 3360–3370, 2005.
View at: Publisher Site | Google Scholar
M. I. Koenders and W. B. van den Berg, “Novel therapeutic targets in rheumatoid arthritis,” Trends in Pharmacological Sciences, vol. 36, no. 4, pp. 189–195, 2015.
View at: Publisher Site | Google Scholar
J. A. Singh, D. E. Furst, A. Bharat et al., “2012 update of the 2008 American College of Rheumatology recommendations for the use of disease-modifying antirheumatic drugs and biologic agents in the treatment of rheumatoid arthritis,” Arthritis Care & Research, vol. 64, no. 5, pp. 625–639, 2012.
View at: Publisher Site | Google Scholar
J. S. Smolen, R. Landewe, F. C. Breedveld et al., “EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2013 update,” Annals of the Rheumatic Diseases, vol. 73, no. 3, pp. 492–509, 2014.
View at: Google Scholar
C. Grigor, H. Capell, A. Stirling et al., “Effect of a treatment strategy of tight control for rheumatoid arthritis (the TICORA study): a single-blind randomised controlled trial,” The Lancet, vol. 364, no. 9430, pp. 263–269, 2004.
View at: Publisher Site | Google Scholar
V. Rantalaiho, M. Korpela, L. Laasonen et al., “Early combination disease-modifying antirheumatic drug therapy and tight disease control improve long-term radiologic outcome in patients with early rheumatoid arthritis: the 11-year results of the Finnish Rheumatoid Arthritis Combination Therapy trial,” Arthritis Research and Therapy, vol. 12, no. 3, article R122, 2010.
View at: Publisher Site | Google Scholar
W. Cao, W. Zhang, J. Liu et al., “Paeoniflorin improves survival in LPS-challenged mice through the suppression of TNF-α and IL-1β release and augmentation of IL-10 production,” International Immunopharmacology, vol. 11, no. 2, pp. 172–178, 2011.
View at: Publisher Site | Google Scholar
H. Huang, E. J. Chang, Y. Lee, J. S. Kim, S. S. Kang, and H. H. Kim, “A genome-wide microarray analysis reveals anti-inflammatory target genes of paeonol in macrophages,” Inflammation Research, vol. 57, no. 4, pp. 189–198, 2008.
View at: Publisher Site | Google Scholar
L.-L. Zhang, W. Wei, N.-P. Wang et al., “Paeoniflorin suppresses inflammatory mediator production and regulates G protein-coupled signaling in fibroblast—like synoviocytes of collagen induced arthritic rats,” Inflammation Research, vol. 57, no. 8, pp. 388–395, 2008.
View at: Publisher Site | Google Scholar
W. Zhang and S.-M. Dai, “Mechanisms involved in the therapeutic effects of Paeonia lactiflora Pallas in rheumatoid arthritis,” International Immunopharmacology, vol. 14, no. 1, pp. 27–31, 2012.
View at: Publisher Site | Google Scholar
M. Zhao, G.-P. Liang, M.-N. Tang et al., “Total glucosides of paeony induces regulatory CD4⁺CD25⁺ T cells by increasing Foxp3 demethylation in lupus CD4⁺ T cells,” Clinical Immunology, vol. 143, no. 2, pp. 180–187, 2012.
View at: Publisher Site | Google Scholar
D. Golicki, M. Niewada, J. Lis, K. Pol, T. Hermanowski, and M. Tłustochowicz, “Leflunomide in monotherapy of rheumatoid arthritis: meta-analysis of randomized trials,” Polish Archives of Internal Medicine, vol. 122, no. 1-2, pp. 22–32, 2012.
View at: Google Scholar
K. E. Donahue, D. E. Jonas, R. A. Hansen et al., Drug Therapy for Rheumatoid Arthritis in Adults: An Update, Agency for Healthcare Research and Quality, Rockville, Md, USA, 2012.
T. T. Wu, R. He, J. N. Liu, and Y. Li, “The efficacy observation on leflunomide combined with total glucosides of paeony capsules for rheumatoid arthritis,” Proceeding of Clinical Medicine, vol. 24, no. 5, pp. 342–345, 2015.
View at: Google Scholar
M. Li, “The clinical efficacy of leflunomide combined with TGP in the treatment of elderly rheumatoid arthritis and its effect on C-reactive protein and erythrocyte sedimentation rate,” China & Foreign Medical Treatment, no. 33, pp. 45–47, 2014.
View at: Google Scholar
W. H. Dong, “The clinical observation on total glucosides of paeony combined with leflunomide for the treatment of elderly rheumatoid arthritis,” Clinical Journal of Traditional Medicine, vol. 26, no. 5, pp. 490–491, 2014.
View at: Google Scholar
L. Tao, Y. Lian, X. H. Guan, and L. H. Lei, “Treating 52 cases of rheumatoid arthritis with leflunomide and total glucosides of paeony capsules. Guide of China medicine,” Guide of China Medicine, vol. 11, no. 17, pp. 403–404, 2013.
View at: Google Scholar
J. H. Yu and H. Zhang, “The clinical research on total glucosides of paeony combined with leflunomide for the treatment of active rheumatoid arthritis,” Forum on Tradtional Medicine, vol. 25, no. 4, pp. 9–10, 2010.
View at: Google Scholar
H. M. Si, “The clinical observation on leflunomide combined with total glucosides of paeony for the treatment of elderly rheumatoid arthritis,” Guide of China Medicine, vol. 8, no. 31, pp. 108–109, 2010.
View at: Google Scholar
F. Y. Ma, “The efficacy and satety of total glucosides of paeony combined with leflunomide in the treatment of rheumatoid arthritis,” Liaoning Journal of Traditional Chinese Medicine, vol. 36, no. 6, pp. 1509–1510, 2009.
View at: Google Scholar
Y.-X. Zhao and Y. Liu, “Clinical observation on effects of leflunomid and total glucosides of paeony on rheumatoid arthritis,” Zhongguo Zhong Xi Yi Jie He Za Zhi, vol. 26, no. 4, pp. 355–357, 2006.
View at: Google Scholar
J. P. T. Higgins, S. G. Thompson, J. J. Deeks, and D. G. Altman, “Measuring inconsistency in meta-analyses,” The British Medical Journal, vol. 327, no. 7414, pp. 557–560, 2003.
View at: Publisher Site | Google Scholar
R. DerSimonian and N. Laird, “Meta-analysis in clinical trials,” Controlled Clinical Trials, vol. 7, no. 3, pp. 177–188, 1986.
View at: Publisher Site | Google Scholar
A. M. van Gestel, M. L. L. Prevoo, M. A. van't Hof, M. H. van Rijswijk, L. B. A. van de Putte, and P. L. C. M. van Riel, “Development and validation of the European League Against Rheumatism response criteria for rheumatoid arthritis: comparison with the preliminary American College of Rheumatology and the World Health Organization/International League Against Rheumatism Criteria,” Arthritis & Rheumatism, vol. 39, no. 1, pp. 34–40, 1996.
View at: Publisher Site | Google Scholar
Y. Chang, L. Zhang, C. Wang, X.-Y. Jia, and W. Wei, “Paeoniflorin inhibits function of synoviocytes pretreated by rIL-1α and regulates EP4 receptor expression,” Journal of Ethnopharmacology, vol. 137, no. 3, pp. 1275–1282, 2011.
View at: Publisher Site | Google Scholar
D. Jiang, Y. Chen, X. Hou, J. Xu, X. Mu, and W. Chen, “Influence of Paeonia lactiflora roots extract on cAMP-phosphodiesterase activity and related anti-inflammatory action,” Journal of Ethnopharmacology, vol. 137, no. 1, pp. 914–920, 2011.
View at: Publisher Site | Google Scholar
H. Tsuboi, K. Hossain, A. A. Akhand et al., “Paeoniflorin induces apoptosis of lymphocytes through a redox-linked mechanism,” Journal of Cellular Biochemistry, vol. 93, no. 1, pp. 162–172, 2004.
View at: Publisher Site | Google Scholar
H.-M. Xu, W. Wei, X.-Y. Jia, Y. Chang, and L. Zhang, “Effects and mechanisms of total glucosides of paeony on adjuvant arthritis in rats,” Journal of Ethnopharmacology, vol. 109, no. 3, pp. 442–448, 2007.
View at: Publisher Site | Google Scholar
Y.-Q. Zheng and W. Wei, “Total glucosides of paeony suppresses adjuvant arthritis in rats and intervenes cytokine-signaling between different types of synoviocytes,” International Immunopharmacology, vol. 5, no. 10, pp. 1560–1573, 2005.
View at: Publisher Site | Google Scholar
Q.-T. Wang, L.-L. Zhang, H.-X. Wu, and W. Wei, “The expression change of β-arrestins in fibroblast-like synoviocytes from rats with collagen-induced arthritis and the effect of total glucosides of paeony,” Journal of Ethnopharmacology, vol. 133, no. 2, pp. 511–516, 2011.
View at: Publisher Site | Google Scholar
L. Zhu, W. Wei, Y.-Q. Zheng, and X.-Y. Jia, “Effects and mechanisms of total glucosides of paeony on joint damage in rat collagen-induced arthritis,” Inflammation Research, vol. 54, no. 5, pp. 211–220, 2005.
View at: Publisher Site | Google Scholar
W.-L. Jiang, X.-G. Chen, H.-B. Zhu, Y.-B. Gao, J.-W. Tian, and F.-H. Fu, “Paeoniflorin inhibits systemic inflammation and improves survival in experimental sepsis,” Basic and Clinical Pharmacology and Toxicology, vol. 105, no. 1, pp. 64–71, 2009.
View at: Publisher Site | Google Scholar
Y.-Q. Zheng, W. Wei, L. Zhu, and J.-X. Liu, “Effects and mechanisms of Paeoniflorin, a bioactive glucoside from paeony root, on adjuvant arthritis in rats,” Inflammation Research, vol. 56, no. 5, pp. 182–188, 2007.
View at: Publisher Site | Google Scholar
C. C. Wei, F. T. You, L. Y. Mei, S. Jian, and C. Y. Qiang, “Total glucosides of paeony prevents juxta-articular bone loss in experimental arthritis,” BMC Complementary and Alternative Medicine, vol. 13, article 186, 2013.
View at: Publisher Site | Google Scholar
R. I. Fox, M. L. Herrmann, C. G. Frangou et al., “Mechanism of action for leflunomide in rheumatoid arthritis,” Clinical Immunology, vol. 93, no. 3, pp. 198–208, 1999.
View at: Publisher Site | Google Scholar
F. M. Meier, M. Frerix, W. Hermann, and U. Müller-Ladner, “Current immunotherapy in rheumatoid arthritis,” Immunotherapy, vol. 5, no. 9, pp. 955–974, 2013.
View at: Publisher Site | Google Scholar
W. W. Cao, P. N. Kao, Y. Aoki, J. C. Xu, R. A. Shorthouse, and R. E. Morris, “A novel mechanism of action of the immunomodulatory drug, leflunomide: augmentation of the immunosuppressive cytokine, TGF-β1, and suppression of the immunostimulatory cytokine, IL-2,” Transplantation Proceedings, vol. 28, no. 6, pp. 3079–3080, 1996.
View at: Google Scholar
F. Behrens, M. Koehm, and H. Burkhardt, “Update 2011: leflunomide in rheumatoid arthritis—strengths and weaknesses,” Current Opinion in Rheumatology, vol. 23, no. 3, pp. 282–287, 2011.
View at: Publisher Site | Google Scholar

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Copyright © 2016 Zhitao Feng et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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