- Research article
- Open Access
Celastrus aculeatusMerr. suppresses the induction and progression of autoimmune arthritis by modulating immune response to heat-shock protein 65
Arthritis Research & Therapy volume 9, Article number: R70 (2007)
Complementary and alternative medicine products are increasingly being used for the treatment of autoimmune diseases. However, the mechanisms of action of these agents are not fully defined. Using the rat adjuvant arthritis (AA) model of human rheumatoid arthritis, we determined whether the ethanol extract of Celastrus aculeatus Merr. (Celastrus), a Chinese herb, can down-modulate the severity of AA, and also examined the Celastrus-induced changes in immune responses to the disease-related antigen mycobacterial heat-shock protein 65 (Bhsp65). AA was induced in the Lewis (LEW; RT.1l) rat by immunization subcutaneously with heat-killed M. tuberculosis H37Ra (Mtb). Celastrus was fed to LEW rats by gavage daily, beginning either before Mtb challenge (preventive regimen) or after the onset of AA (therapeutic regimen). An additional group of rats was given methotrexate for comparison. All rats were graded regularly for the signs of arthritis. In parallel, the draining lymph node cells of Celastrus-treated rats were tested for proliferative and cytokine responses, whereas their sera were tested for the inflammatory mediator nitric oxide. Celastrus feeding suppressed both the induction as well as the progression of AA, and the latter effect was comparable to that of methotrexate. Celastrus treatment induced relative deviation of the cytokine response to anti-inflammatory type and enhanced the production of anti-Bhsp65 antibodies, which are known to be protective against AA. Celastrus feeding also reduced the levels of nitric oxide. On the basis of our results, we suggest further systematic exploration of Celastrus as an adjunct therapeutic modality for rheumatoid arthritis.
Rheumatoid arthritis (RA) is a chronic debilitating autoimmune disorder that affects about 2.1 million Americans [1–5]. The drugs commonly in use for the treatment of RA include glucocorticoids (for example, cortisone and prednisone), non-steroidal anti-inflammatory drugs (NSAIDS; for example, ibuprofen and naproxen), disease-modifying anti-rheumatic drugs (DMARDs; for example, methotrexate (MTX) and leflunomide), and biological response modifiers (for example, tumor necrosis factor-αblocking agents) [6, 7]. However, besides their high cost, the prolonged use of many of these drugs is associated with severe adverse reactions and toxicity, including some risk of infections in subsets of patients being treated with biological response modifiers [6, 7]. As a result, alternative treatments based on natural plant products and herbal mixtures belonging to the realm of complementary and alternative medicine (CAM) are becoming increasingly popular in the US and other countries [2–5, 8]. However, there is skepticism about CAM products in the minds of both the public as well as the scientific community, mostly because the mechanisms of action of many of these products are poorly defined, or not at all. Thus, there is a need to systematically study and define the mechanisms underlying the activity of CAM products that have been used for the treatment of rheumatic diseases in folk medicine around the world for centuries.
Celastrus aculeatus Merr. (Celastrus) [9–15] is a Chinese medicine that belongs to the family Celastraceae and the genus Celastrus. The roots, stem, and leaves of Celastrus have been used in folk remedies in China for centuries to treat RA, osteoarthritis, lower back pain, and so on. Celastrus and some of its defined constituents possess anti-inflammatory, anti-oxidant, and anti-cancer properties [9–15]. However, the mechanisms underlying the anti-arthritic activity of Celastrus have not been fully examined. Considering that RA is an autoimmune disease resulting from a dysregulated immune system [6, 7, 16, 17], it is imperative to examine the immunological basis of Celastrus or any other new potential anti-arthritic therapeutic agent under consideration.
Animal models of RA have contributed significantly both to our understanding of the pathogenesis of autoimmune arthritis as well as to the testing of new therapeutic agents of natural or synthetic origin [18–21]. As a pre-requisite to unraveling the mechanisms underlying the beneficial effects of Celastrus in RA, we set out to first validate the anti-arthritic activity of Celastrus under controlled experimental conditions using a well established model of RA, adjuvant-induced arthritis (AA), which can be induced in the Lewis (LEW; RT.1l) rat by subcutaneous (s.c.) immunization with heat-killed M. tuberculosis H37Ra (Mtb) [18, 22–26]. Thereafter, we examined in LEW rats with AA the effects of Celastrus on the T cell and antibody responses to the disease-related antigen mycobacterial heat-shock protein 65 (Bhsp65) [18, 22–25], which also is the target of T cell and antibody response in RA patients [27, 28].
Our results show that Celastrus can induce protection against arthritis both in the preventive as well as in the therapeutic setting, and that this beneficial anti-arthritic effect of Celastrus is attributable in part to modulation both of the immune response to the disease-related antigen Bhsp65 [22–25] and one of the mediators of inflammation and tissue damage, nitric oxide (NO) [29, 30].
Materials and methods
Inbred male Lewis (LEW/SsNHsd; LEW; RT.11) rats (5 to 6 weeks old, 130 to 160 g) were procured from Harlan Sprague Dawley (Indianapolis, IN, USA), and then maintained in the vivarium facility of the University of Maryland School of Medicine (UMB). All procedures performed on these animals were in accordance with the guidelines of the institutional animal care and use committee (IACUC).
Mtb was obtained from Difco Laboratories (Detroit, MI, USA). Bhsp65 was prepared from BL21 (DE3) pLysS cells (Novagen, Madison, WI, USA) transformed by the vector pET23b-GroEL2 (Colorado State University, Fort Collins, CO, USA) . Synthetic peptide 177–191 of Bhsp65 (B177) and other Bhsp65 peptides were obtained from Global Peptide Services (Fort Collins, CO, USA). Purified protein derivative was purchased from Mycos Research (Fort Collins, CO, USA), whereas hen egg white lysozyme (HEL) and keyhole limpet hemocyanin (KLH) were obtained from Sigma-Aldrich (St. Louis, MO, USA).
Induction and evaluation of adjuvant arthritis
LEW rats were immunized s.c. at the base of the tail with 200 μl (1 mg/rat) of Mtb in mineral oil, and then observed regularly for clinical signs of arthritis like erythema, swelling and induration [24, 32]. The severity of arthritis in each paw was graded on a scale from 0 to 4. The maximum arthritic score for each paw was 4, and the total arthritis score per rat was 16.
For histological assessment of arthritis, hind paws of rats were harvested, fixed for 3 days in a solution containing 10% formalin, HCl, and H2O (10:2:88, v/v), and then embedded in paraffin. Serial paraffin sections (7 μm; Leica RM2135, Leica Instruments, Germany) were stained with hematoxylin and eosin, and then examined and graded under the microscope for histopathological changes in the joints , including inflammatory cell infiltrate, synovial hyperplasia, cartilage damage and bone erosion [33, 34]. Each of these parameters was graded on a scale from 0 to 3 as follows: 0 = absent; 1 = mild; 2 = moderate; and 3 = severe [33, 34]. For each rat, a histological section of either the left or the right hind paw was examined and the results are presented as median (interquartile range).
Preparation and characterization of the ethanol extract of Celastrus
The roots and stems of Celastrus aculeatus Merr. were collected in the Guangdong province of China, and their identity was confirmed by Dr Ye Hua-gu, a plant taxonomist at South China Institute of Botany, the Chinese Academy of Sciences, Guangzhou. The dried roots and stems were minced with a grinder and then the powder was extracted for 2 h with 75% ethanol. The ethanol extract was collected, and the procedure was repeated twice. The final ethanol extract was condensed with a rotary evaporator, and the concentrated extract was dried. The presence of three of the major groups of components of Celastrus, namely triterpenes (for example, celastrol, celasdin C), flavonoids (for example, epiafzelechin), and sesquiterpenes (for example, orbiculin F) [9–15] was confirmed by HPLC and LC/MS analysis (data not shown). However, to assess the anti-arthritic activity of the natural mixture of the constituents in the ethanol extract, rats were fed with unfractionated crude extract. For this reason, the amount of Celastrus extract fed per rat was relatively high. The LD50 for the Celastrus extract was found to be 55.7 g/kg. After performing pilot experiments on the modulation of AA with different doses of Celastrus ranging from 0.5 to 3 g/kg, the two doses finally selected for use in this study corresponded to the LD50 dose as follows: 1.5 g/kg (1/37 of LD50) and 3 g/kg (1/18.5 of LD50).
Feeding of Celastrus to LEW rats
Naïve LEW rats were fed Celastrus (experimental group; 1.5 or 3 g/kg body weight) or the vehicle (water; control group) using a gavage needle (FNC-16-3, Kant Scientific Corporation, Torrington, CT, USA) once daily for 4 days prior to s.c. immunization with Mtb and then continued uninterrupted for the entire duration of the observation period. Following Mtb challenge, all rats were graded regularly for clinical signs of arthritis [24, 32].
Naïve LEW rats were challenged with Mtb s.c. for the induction of AA. Beginning at the onset of AA, and then continued throughout the course of AA, the experimental group of rats was fed Celastrus (1.5 or 3 g/kg) daily by gavage, whereas the control group received the vehicle (water). A third group of arthritic rats was fed MTX (0.5 mg/kg), an established anti-arthritic compound, as a positive control. All these rats were observed regularly for signs of arthritis throughout the period of feeding with Celastrus/water.
Lymph node cell proliferation assay
LEW rats were immunized s.c. with Mtb (1 mg/rat). The draining lymph nodes (inguinal, para-aortic, and popliteal) of sub-groups of these rats were harvested on day 8, 12 or 24 after injection, and a single cell suspension of lymph node cells (LNCs) was prepared . These LNCs (2.5 × 105 to 5 × 105 cells/well) were tested in a proliferation assay in HL-1 serum-free medium (BioWhittaker, Walkersville, MD, USA) in the presence or absence of antigen . Purified protein derivative was used as a positive control, whereas HEL served as a negative control. The results were expressed either as counts per minute (cpm) or as a stimulation index (the ratio of cpm in the presence of antigen and cpm of cells in medium alone).
Measurement of cytokine levels by ELISA
LNCs of Celastrus-treated or control rats were plated in a 96-well plate as for the LNC proliferation assay described above. After 72 h of culture of cells with specific antigens, the culture supernatant was collected and tested for IFN-γ and IL-10 using ELISA kits (Biosource International, Camarillo, CA, USA) following the manufacturer's instructions . After the last reaction, the color intensity (optical density) was measured at 450 nm with an automated Coulter ELISA Reader (Coulter Electronics, Kendall, FL, USA) and the results were expressed as pg/ml.
ELISA for anti-Bhsp65 antibodies
A flat-bottom 96-well microtiter ELISA plate was coated with 100 ng/well each of purified Bhsp65 (test antigen) or KLH (control antigen) in phosphate-buffered saline (pH 7.2) for 16 h at 4°C . After washing, the wells were blocked for 3 h at room temperature with 10% bovine serum albumin (EIA grade; Sigma-Aldrich) in phosphate-buffered saline. The sera were tested at dilutions ranging from 1:50 to 1:8,100. The plate-bound antibody was detected using goat anti-rat immunoglobulin conjugated to horseradish peroxidase (BD Pharmingen, San Diego, CA, USA). Thereafter, the substrate was added for color development, and after 15 minutes the reaction was stopped with 0.5 M sulfuric acid. The color intensity (optical density) was read at 540 nm using an ELISA reader.
Determination of NO levels in serum and LNC culture supernatant
A cohort of LEW rats was fed Celastrus or water following the above-mentioned 'prevention' regimen and then two types of samples were collected, as follows: for serum, these rats were bled at days 8, 16 and 24 after injection with Mtb and then sera were separated from the clotted blood; and for culture supernatant, the draining LNCs harvested from sub-groups of these rats on day 8, 16 or 24 after Mtb injection were restimulated in vitro for 72 h with Bhsp65 (test antigen) or HEL (control antigen), and the culture supernatant was collected. The levels of NO in these samples were then evaluated by measuring the nitrite (NO2-) and nitrate (NO3-) content by using a colorimetric assay kit (Biovision research products, Mountain View, CA, USA). The results were expressed as μM.
Student t-test and Wilcoxon rank sum test were used to analyze the data obtained from different experiments. The results were considered significant at p < 0.05.
Celastrus suppresses the induction of AA in the LEW rat
To examine the effect of Celastrus on the initiation and progression of AA, naïve LEW rats were fed daily either Celastrus (1.5 or 3 g/kg body weight per day) or the vehicle (water; control group) starting day 4 prior to Mtb immunization, and then continued throughout the course of the disease. In the period following Mtb injection, all rats were observed regularly for signs of arthritis. Celastrus-fed rats showed significantly reduced disease severity compared to that of water-fed control rats (Figure 1a–c). The effect of Celastrus on clinical arthritis was also validated by histological examination of arthritic joints. The results (Table 1) show that synovial infiltration by mononuclear cells and the damage to cartilage and bone were significantly reduced in Celastrus-treated rats compared to that in control water-fed rats. Thus, feeding Celastrus to LEW rats significantly reduced the severity of subsequently induced AA.
To define the mechanisms underlying the anti-arthritic activity of Celastrus, we examined the changes in the immune response to the disease-related antigen Bhsp65 as well as in the production of a mediator of inflammatory arthritis (NO) in Celastrus-treated LEW rats. The results of these investigations are described below.
Celastrus feeding to LEW rats induces preferential secretion of anti-inflammatory cytokines over pro-inflammatory cytokines in response to Bhsp65
To test and compare the T cell proliferative and cytokine response to the disease-related antigen Bhsp65 of Celastrus-treated versus control (water-fed) LEW rats, the draining LNCs of these arthritic rats were tested using the appropriate assays on day 12 after Mtb immunization. The two groups of rats had comparable (p > 0.05) levels of proliferative response to Bhsp65/B177–191 (data not shown).
In regard to the cytokine response to Bhsp65, the levels of IFN-γ (a pro-inflammatory cytokine) of the Celastrus-fed and water-fed rats were comparable (Figure 2a), but the levels of IL-10 (an anti-inflammatory cytokine; Figure 2b) were significantly (p < 0.05) up-regulated in Celastrus-fed rats compared to water-fed rats. The mean ratio of IFN-γ and IL-10 secreted in recall response to Bhsp65 by Celastrus-fed rats (ratio 8.79) was significantly lower than that of the water-fed rats (ratio 20.76), demonstrating that Celastrus preferentially facilitated the secretion of IL-10 and, thereby, induced a relative skewing (immune deviation) of the cytokine response towards a predominantly anti-inflammatory type.
Celastrus-fed LEW rats reveal enhanced antibody response to Bhsp65
LEW rats were immunized s.c. with Mtb (1 mg/rat) after 4 days of daily feeding of either Celastrus or water. Thereafter, these rats continued to receive daily either Celastrus or water. The sera collected from these rats at specific time points before and after Mtb immunization were tested at different dilutions, ranging from 1:50 to 1:8,100, by ELISA for total immunoglobulin against Bhsp65. The results (Figure 3) show that the levels of anti-Bhsp65 antibodies increased gradually from day 0 through day 24. At both 1:100 and 1:200 serum dilutions, the level of antibody response to Bhsp65 in Celastrus-treated rats was significantly (p < 0.01) higher than that of water-fed rats on day 18 and day 24. These anti-Bhsp65 antibodies were composed mostly of IgG (data not shown). However, as expected, the sera from both the test and control group of rats had only minimal reactivity against KLH (control antigen), with no significant difference between the two groups of rats (data not shown). Thus, the increased antibody response to Bhsp65 was associated with the Celastrus-induced protection against AA.
Reduced levels of NO in serum and LNC culture supernatant of Celastrus-treated LEW rats
NO production is increased in patients with RA, and its production correlates with the severity of arthritis [29, 30, 35]. Therefore, we reasoned that Celastrus might down-modulate AA, in part by inhibiting the production of NO, and tested this proposition in Celastrus-fed LEW rats. Our results show that the levels of NO in the culture supernatant of LNCs of Mtb-primed rats restimulated in vitro with Bhsp65 were significantly lower in Celastrus-fed rats than that in water-fed rats on days 16 and 24 (Figure 4a). Similarly, the level of serum NO in Celastrus-fed rats was significantly lower than that in water-fed rats on days 16 and 24 (Figure 4b). However, the NO levels in the sera of both these groups were much higher than that in sera of naïve rats (Figure 4b). Taken together, these results show that arthritic LEW rats produced NO in response to Bhsp65, and that Celastrus feeding reduced the levels of NO. This decrease in NO levels in turn correlates with the reduced severity of arthritis in Celastrus-treated rats compared to control rats.
Celastrus feeding suppresses the severity of ongoing AA in the LEW rat and the level of this effect is comparable to that of MTX
We have described above that feeding of Celastrus to naïve LEW rats beginning prior to the induction of AA by Mtb injection can afford protection against AA (Figure 1). However, from the clinical viewpoint of RA patients, it is critical that a potentially beneficial anti-arthritic product displays not only a preventive effect but also a therapeutic effect by suppressing ongoing (established) arthritis. In this regard, we examined the therapeutic potential of Celastrus in the AA model. Naïve LEW rats were challenged with Mtb s.c. for the induction of AA. Beginning at the onset of AA, and then continuing throughout its course, one of the experimental groups of rats was fed Celastrus (test group) and the control group received the vehicle (water). Another group of experimental rats was fed an established anti-arthritic compound, MTX (positive control). All these rats were observed regularly for signs of arthritis. The results (Figure 5a,b) show that both the Celastrus-fed and the MTX-fed experimental groups had a significantly decreased severity of AA compared to the Water-fed control rats, and both the high (3 g/kg) and the low (1.5 g/kg) doses of Celastrus had comparable beneficial effects against AA (Figure 5b). The severity of the disease in each of these two experimental groups of rats (Celastrus-fed and MTX-fed) was significantly reduced compared to control (water-fed) rats (Figure 5b). Intriguingly, the level of the suppressive effect on arthritis of Celastrus was comparable to that of MTX. Thus, Celastrus showed both preventive as well as therapeutic anti-arthritic activity in the AA model.
Our results show that Celastrus aculeatus Merr. (Celastrus) suppresses the induction of AA when fed to LEW rats prior to Mtb challenge, as well as down-modulates the progression of AA when administered to arthritic rats at the onset of the disease. The significant reduction in the severity of clinical AA following Celastrus feeding was further validated by limited histological changes in the joints. Furthermore, the level of suppression of ongoing AA by Celastrus was comparable to that of MTX, a standard anti-arthritic agent used for the treatment of arthritis. This attribute of Celastrus is an important one because many regimens based on synthetic or natural compounds can successfully prevent the induction of arthritis, but they often fail to control the course of the ongoing disease. In this regard, Celastrus is a promising anti-arthritic agent that could be further explored as a therapeutic modality in controlled pilot clinical trials on RA patients. As this is our first study on the effect of Celastrus on AA, we have used the unfractionated ethanol extract of the roots and stems to preserve as much of the natural proportion of different constituents in the mixture as possible. Accordingly, the dose of Celastrus fed to rats is apparently high. However, in subsequent follow up studies, we plan to use one or more of the purified components of the crude extract. It has been reported by others that various components of Celastrus possess anti-inflammatory and anti-tumor properties, and these include a variety of sesquiterpene esters (for example, celastrol, celaphanol, celasdin, orbiculin, esters with the β-dihydroagarofuran skeleton) and flavonoids (for example, epiafzelechin) [9–15]. Some of the reported pathways inhibited by these components are mediated by nuclear factor kappa-B (NF-κB), inducible nitric oxide synthase (iNOS), and cyclooxygenase (COX) [12–15, 35].
We observed that the suppression of clinical arthritis in Celastrus-fed LEW rats was associated with significant changes in the immune response to Bhsp65. Furthermore, both the cell-mediated and the antibody responses to Bhsp65 were affected. AA is driven by pro-inflammatory cytokines (IFN-γ and tumor necrosis factor-α); in this context, Celastrus treatment facilitated the secretion of the anti-inflammatory cytokine IL-10 over the pro-inflammatory cytokine IFN-γ, resulting in the overall skewing (immune deviation) of the cytokine response to an anti-inflammatory type . This relative deviation of the cytokine response, caused either by decreased Th1-type cytokines and/or by enhanced Th2-type cytokines leading to the regression of an autoimmune disease, is reminiscent of other compounds of synthetic (for example, peptides of antigenic proteins or cytokines) [25, 36, 37] or natural origin [38, 39] that can successfully control disease in animal models of arthritis.
Celastrus feeding to LEW rats immunized with Mtb led to enhanced production of antibodies to Bhsp65 compared to the control water-fed rats. Thus, a decrease in inflammatory arthritis in LEW rats was associated with an increase in the anti-Bhsp65 antibody response. This inverse association is supported by previous work by others  and us  demonstrating that anti-Bhsp65 antibodies produced during the course of AA are disease-protective rather than being pathogenic in nature. Unlike in other animal models of RA in which antibodies are arthritogenic [40, 41], in the AA model certain subsets of anti-Bhsp65 antibodies generated either during the course of AA [25, 31] or following AA-protective tolerization with Bhsp65  contribute to disease regulation. It has been proposed that the protective effect of antibodies in AA is probably mediated by the induction of IL-10 production from mononuclear cells . In this regard, our finding of a Celastrus-induced deviation of the cytokine response of arthritic LEW rats towards IL-10 correlates very well with our observation of enhanced anti-Bhsp65 antibody response in Celastrus-treated rats, and the observed immune deviation towards IL-10 might be attributable, in part, to the increased antibody response to Bhsp65. We further suggest that the anti-Bhsp65 antibodies might also contribute to the protection against AA by modulating antigen processing and presentation  and, thereby, facilitating the induction of the immune response to one or more of the regulatory T cell determinants within Bhsp65 previously identified by others [23, 25, 36] and us . Thus, changes in both the cell-mediated and the antibody responses to Bhsp65 following Celastrus feeding might cooperate to down-regulate the severity of AA in the LEW rat.
In addition to the disease-regulating changes in the immune response to Bhsp65, the beneficial effect of Celastrus in AA was also related to inhibition of the production of a well known mediator of inflammation, namely NO [20, 29, 30, 35]. We observed antigen specificity in the production of NO; Bhsp65-restimulated LNCs of Mtb-immunized water-fed (control) LEW rats produced significantly higher levels of NO than those restimulated by the control antigen, HEL. Furthermore, Celastrus treatment significantly reduced the levels of NO in both LNC culture supernatant and sera of Mtb-immunized rats. Taken together, these results document not only a direct association between the levels of NO and the severity of AA, but also provide insight into the in vivo anti-inflammatory activity of Celastrus. These results of Celastrus-mediated suppression of NO production in vivo are further corroborated by reports by other investigators showing a similar effect of Celastrus in vitro using macrophage cell lines (for example, RAW cells) [12, 15]. Furthermore, it has been reported that oral feeding of B6 mice with the ethyl acetate extract of Tripterygium wilfordii Hook F (TWHF) or its active component, triptolide, led to the inhibition of both NO production and iNOS mRNA expression by macrophages , and this decrease in NO production was implicated in mediating the anti-inflammatory effects of TWHF. One of the mechanisms by which Celastrus leads to decreased NO production might involve NF-κB, which controls the expression of genes encoding inducible enzymes, such as iNOS and COX, which in turn generate some of the critical mediators of the inflammatory response [14, 15, 35]. In fact, some of the active components of Celastrus have been shown to serve as inhibitors of the NF-κB pathway (for example, celastrol and celaphanol A) [12, 15] and the COX pathway (for example, epiafzelechin) . In addition, NF-κB activity is inversely related to that of the heat-shock response as the induction of heat-shock proteins is associated with a decrease in NF-κB activity . Celastrol can lead to the induction of heat-shock protein gene expression by activation of heat-shock factor-1 , and the enhanced response to self hsp65 can, in turn, contribute to protection against AA [23, 32]. Thus, by regulating the activity of NF-κB, Celastrus apparently influences multiple inter-connected pathways that participate in the regulation of autoimmune arthritis.
Our results suggest that the ethanol extract of Celastrus as well as its individual components should be explored further for the treatment of RA through double-blind, placebo-controlled preclinical and clinical trials in RA patients following the strategy employed successfully by other investigators for translational research on TWHF [8, 45]. There is a compelling need to fully examine multiple natural products such as TWHF and Celastrus for their potential as anti-arthritic agents because all RA patients may not respond equally well to any single herbal medicine owing to differences in body constitution and genetics, and each natural plant product may have unique compatibility with the standard mainstream medications when taken together. The availability of several different natural plant products having anti-arthritic activity would enlarge the scope of the use of CAM modalities for the treatment of RA in conjunction with conventionally used drugs.
The ethanol extract of Celastrus aculeatus Merr. (Celastrus) has potent anti-arthritic activity. Feeding Celastrus to LEW rats offered protection against the subsequent induction as well as progression of AA. The therapeutic effect of Celastrus was comparable to that of MTX. Celastrus-induced protection against AA involved significant modulation of both the cytokine and antibody responses to the disease-related antigen Bhsp65. In addition, Celastrus suppressed the production of a known mediator of inflammation, NO. Celastrus should be further tested in clinical trials on patients with RA to explore its utility as a natural CAM product that might be beneficial either alone or in combination with conventionally used drugs, with the objective of complementing the beneficial anti-arthritic effects and reducing the side effects of the latter group of drugs.
= adjuvant arthritis
= mycobacterial hsp65
= complementary and alternative medicine
= enzyme-linked immunosorbent assay
= hen eggwhite lysozyme
= heat-shock protein 65
= inducible nitric oxide synthase
= keyhole limpet hemocyanin
= lymph node cell
= M. tuberculosis H37Ra
= nuclear factor kappa-B
= nitric oxide
= rheumatoid arthritis
= Tripterygium wilfordii Hook F.
Kvien TK: Epidemiology and burden of illness of rheumatoid arthritis. Pharmacoeconomics. 2004, 22: 1-12. 10.2165/00019053-200422001-00002.
Barnes PM, Powell-Griner E, McFann K, Nahin RL: Complementary and alternative medicine use among adults: United States, 2002. Adv Data. 2004, 343: 1-19.
Eisenberg DM, Davis RB, Ettner SL, Appel S, Wilkey S, Van Rompay M, Kessler RC: Trends in alternative medicine use in the United States, 1990–1997: results of a follow-up national survey. JAMA. 1998, 280: 1569-1575. 10.1001/jama.280.18.1569.
Taibi D, Bourguignon C: The role of complementary and alternative therapies in managing rheumatoid arthritis. Fam Community Health. 2003, 26: 41-52.
Zhang GG, Lee W, Bausell B, Lao L, Handwerger B, Berman B: Variability in the traditional Chinese medicine (TCM) diagnoses and herbal prescriptions provided by three TCM practitioners for 40 patients with rheumatoid arthritis. J Altern Complement Med. 2005, 11: 415-421. 10.1089/acm.2005.11.415.
Kremers HM, Nicola P, Crowson CS, O'Fallon WM, Gabriel SE: Therapeutic strategies in rheumatoid arthritis over a 40-year period. J Rheumatol. 2004, 31: 2366-2373.
Olsen NJ, Stein CM: New drugs for rheumatoid arthritis. N Engl J Med. 2004, 350: 2167-2179. 10.1056/NEJMra032906.
Cibere J, Deng Z, Lin Y, Ou R, He Y, Wang Z, Thorne A, Lehman AJ, Tsang IK, Esdaile JM: A randomized double blind, placebo controlled trial of topical Tripterygium wilfordii in rheumatoid arthritis: reanalysis using logistic regression analysis. J Rheumatol. 2003, 30: 465-467.
Spivey AC, Weston M, Woodhead S: Celastraceae sesquiterpenoids: biological activity and synthesis. Chem Soc Rev. 2002, 31: 43-59. 10.1039/b000678p.
Guo YQ, Li X, Xu J, Li N, Meng DL, Wang JH: Sesquiterpene esters from the fruits of Celastrus orbiculatus. Chem Pharm Bull (Tokyo). 2004, 52: 1134-1136. 10.1248/cpb.52.1134.
Kim SE, Kim YH, Lee JJ, Kim YC: A new sesquiterpene ester from Celastrus orbiculatus reversing multidrug resistance in cancer cells. J Nat Prod. 1998, 61: 108-111. 10.1021/np9702392.
Jin HZ, Hwang BY, Kim HS, Lee JH, Kim YH, Lee JJ: Antiinflammatory constituents of Celastrus orbiculatus inhibit the NF-kappaB activation and NO production. J Nat Prod. 2002, 65: 89-91. 10.1021/np010428r.
Min KR, Hwang BY, Lim HS, Kang BS, Oh GJ, Lee J, Kang SH, Lee KS, Ro JS, Kim Y: (-)-Epiafzelechin: cyclooxygenase-1 inhibitor and anti-inflammatory agent from aerial parts of Celastrus orbiculatus. Planta Med. 1999, 65: 460-462. 10.1055/s-1999-14016.
Westerheide SD, Bosman JD, Mbadugha BN, Kawahara TL, Matsumoto G, Kim S, Gu W, Devlin JP, Silverman RB, Morimoto RI: Celastrols as inducers of the heat shock response and cytoprotection. J Biol Chem. 2004, 279: 56053-56060. 10.1074/jbc.M409267200.
Nam NH: Naturally occurring NF-kappaB inhibitors. Mini Rev Med Chem. 2006, 6: 945-951. 10.2174/138955706777934937.
Firestein GS: Immunologic mechanisms in the pathogenesis of rheumatoid arthritis. J Clin Rheumatol. 2005, 11: S39-44. 10.1097/01.rhu.0000166673.34461.33.
Antoniv TT, Ivashkiv LB: Dysregulation of interleukin-10-dependent gene expression in rheumatoid arthritis synovial macrophages. Arthritis Rheum. 2006, 54: 2711-2721. 10.1002/art.22055.
Pearson CM: Development of arthritis, periarthritis and periostitis in rats given adjuvants. Proc Soc Exp Biol Med. 1956, 91: 95-101.
Taneja V, Taneja N, Behrens M, Griffiths MM, Luthra HS, David CS: Requirement for CD28 may not be absolute for collagen-induced arthritis: study with HLA-DQ8 transgenic mice. J Immunol. 2005, 174: 1118-1125.
Brahn E, Banquerigo ML, Firestein GS, Boyle DL, Salzman AL, Szabo C: Collagen induced arthritis: reversal by mercaptoethylguanidine, a novel antiinflammatory agent with a combined mechanism of action. J Rheumatol. 1998, 25: 1785-1793.
Mia MY, Durai M, Kim HR, Moudgil KD: Heat shock protein 65-reactive T cells are involved in the pathogenesis of non-antigenic dimethyl dioctadecyl ammonium bromide-induced arthritis. J Immunol. 2005, 175: 219-227.
van Eden W, Thole JE, van der Zee R, Noordzij A, van Embden JD, Hensen EJ, Cohen IR: Cloning of the mycobacterial epitope recognized by T lymphocytes in adjuvant arthritis. Nature. 1988, 331: 171-173. 10.1038/331171a0.
Quintana FJ, Carmi P, Mor F, Cohen IR: DNA fragments of the human 60-kDa heat shock protein (HSP60) vaccinate against adjuvant arthritis: identification of a regulatory HSP60 peptide. J Immunol. 2003, 171: 3533-3541.
Moudgil KD, Chang TT, Eradat H, Chen AM, Gupta RS, Brahn E, Sercarz EE: Diversification of T cell responses to carboxy-terminal determinants within the 65-kD heat-shock protein is involved in regulation of autoimmune arthritis. J Exp Med. 1997, 185: 1307-1316. 10.1084/jem.185.7.1307.
Ulmansky R, Cohen CJ, Szafer F, Moallem E, Fridlender ZG, Kashi Y, Naparstek Y: Resistance to adjuvant arthritis is due to protective antibodies against heat shock protein surface epitopes and the induction of IL-10 secretion. J Immunol. 2002, 168: 6463-6469.
Prakken BJ, Roord S, Ronaghy A, Wauben M, Albani S, van Eden W: Heat shock protein 60 and adjuvant arthritis: a model for T cell regulation in human arthritis. Springer Semin Immunopathol. 2003, 25: 47-63. 10.1007/s00281-003-0128-7.
Strober S, Holoshitz J: Mechanisms of immune injury in rheumatoid arthritis: evidence for the involvement of T cells and heat-shock protein. Immunol Rev. 1990, 118: 233-255. 10.1111/j.1600-065X.1990.tb00818.x.
Celis L, Vandevyver C, Geusens P, Dequeker J, Raus J, Zhang J: Clonal expansion of mycobacterial heat-shock protein-reactive T lymphocytes in the synovial fluid and blood of rheumatoid arthritis patients. Arthritis Rheum. 1997, 40: 510-519. 10.1002/art.1780400317.
Jang D, Murrell GA: Nitric oxide in arthritis. Free Radic Biol Med. 1998, 24: 1511-1519. 10.1016/S0891-5849(97)00459-0.
Bogdan C: Nitric oxide and the immune response. Nat Immunol. 2001, 2: 907-916. 10.1038/ni1001-907.
Kim HR, Kim EY, Cerny J, Moudgil KD: Antibody responses to mycobacterial and self heat shock protein 65 in autoimmune arthritis: epitope specificity and implication in pathogenesis. J Immunol. 2006, 177: 6634-6641.
Durai M, Gupta RS, Moudgil KD: The T cells specific for the carboxyl-terminal determinants of self (rat) heat-shock protein 65 escape tolerance induction and are involved in regulation of autoimmune arthritis. J Immunol. 2004, 172: 2795-2802.
Hom JT, Estridge T, Cole H, Gliszczynski V, Bendele A: Effects of various anti-T cell receptor antibodies on the development of type II collagen-induced arthritis in mice. Immunol Invest. 1993, 22: 257-265.
Matthys P, Hatse S, Vermeire K, Wuyts A, Bridger G, Henson GW, De Clercq E, Billiau A, Schols D: AMD3100, a potent and specific antagonist of the stromal cell-derived factor-1 chemokine receptor CXCR4, inhibits autoimmune joint inflammation in IFN-gamma receptor-deficient mice. J Immunol. 2001, 167: 4686-4692.
Appleton I, Tomlinson A, Willoughby DA: Induction of cyclo-oxygenase and nitric oxide synthase in inflammation. Adv Pharmacol. 1996, 35: 27-78.
Anderton SM, van der Zee R, Prakken B, Noordzij A, van Eden W: Activation of T cells recognizing self 60-kD heat shock protein can protect against experimental arthritis. J Exp Med. 1995, 181: 943-952. 10.1084/jem.181.3.943.
Woods JM, Amin MA, Katschke KJ, Volin MV, Ruth JH, Connors MA, Woodruff DC, Kurata H, Arai K, Haines GK, et al: Interleukin-13 gene therapy reduces inflammation, vascularization, and bony destruction in rat adjuvant-induced arthritis. Hum Gene Ther. 2002, 13: 381-393. 10.1089/10430340252792512.
Haqqi TM, Anthony DD, Gupta S, Ahmad N, Lee MS, Kumar GK, Mukhtar H: Prevention of collagen-induced arthritis in mice by a polyphenolic fraction from green tea. Proc Natl Acad Sci USA. 1999, 96: 4524-4529. 10.1073/pnas.96.8.4524.
Chevrier MR, Ryan AE, Lee DY, Zhongze M, Wu-Yan Z, Via CS: Boswellia carterii extract inhibits TH1 cytokines and promotes TH2 cytokines in vitro. Clin Diagn Lab Immunol. 2005, 12: 575-580. 10.1128/CDLI.12.5.575-580.2005.
Wooley PH, Luthra HS, Krco CJ, Stuart JM, David CS: Type II collagen-induced arthritis in mice. II. Passive transfer and suppression by intravenous injection of anti-type II collagen antibody or free native type II collagen. Arthritis Rheum. 1984, 27: 1010-1017. 10.1002/art.1780270907.
Kouskoff V, Korganow AS, Duchatelle V, Degott C, Benoist C, Mathis D: Organ-specific disease provoked by systemic autoimmunity. Cell. 1996, 87: 811-822. 10.1016/S0092-8674(00)81989-3.
Satpute SR, Soukhareva N, Scott DW, Moudgil KD: Mycobacterial Hsp65-IgG-expressing tolerogenic B cells confer protection against adjuvant-induced arthritis in Lewis rats. Arthritis Rheum. 2007, 56: 1490-1496. 10.1002/art.22566.
Simitsek PD, Campbell DG, Lanzavecchia A, Fairweather N, Watts C: Modulation of antigen processing by bound antibodies can boost or suppress class II major histocompatibility complex presentation of different T cell determinants. J Exp Med. 1995, 181: 1957-1963. 10.1084/jem.181.6.1957.
Wang B, Ma L, Tao X, Lipsky PE: Triptolide, an active component of the Chinese herbal remedy Tripterygium wilfordii Hook F, inhibits production of nitric oxide by decreasing inducible nitric oxide synthase gene transcription. Arthritis Rheum. 2004, 50: 2995-2303. 10.1002/art.20459.
Tao X, Younger J, Fan FZ, Wang B, Lipsky PE: Benefit of an extract of Tripterygium wilfordii Hook F in patients with rheumatoid arthritis: a double-blind, placebo-controlled study. Arthritis Rheum. 2002, 46: 1735-1743. 10.1002/art.10411.
This work was supported by grants (AI059623 and AT001608) to KDM from the National Institutes of Health (NIH), Bethesda, MD. LT was supported by an International Postdoctoral Fellowship Award (F05 AT002013) from the NCCAM, NIH. We thank Hong R Kim and Minjun Yu for helping with experiments, Dr Xiao Changhong for advice and help in quantification of histological sections, and Dr Brian Berman (Center for Integrative Medicine, UMB) for encouragement in pursuing research in the area of CAM.
The authors declare that they have no competing interests.
LT conducted all the experiments, recorded and analyzed the raw data, prepared graphics, and participated in the interpretation of data as well as writing of the manuscript. KDM participated in the planning of experiments, data analysis, interpretation of results and writing of the manuscript.
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Tong, L., Moudgil, K.D. Celastrus aculeatusMerr. suppresses the induction and progression of autoimmune arthritis by modulating immune response to heat-shock protein 65. Arthritis Res Ther 9, R70 (2007). https://doi.org/10.1186/ar2268
- Nitric Oxide
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