Obesity is increasingly recognised as a public health burden, because it is associated with an increased risk for many diseases, including the metabolic syndrome, i.e. hypertension, insulin resistance or type 2 diabetes mellitus, arteriosclerosis and CHD(Reference Yusuf, Hawken and Ounpuu1). Obesity is associated with increased inflammation, as evidenced by increased levels of C-reactive protein, and decreased anti-inflammatory cytokines, such as IL-10(Reference Visser, Bouter and McQuillan2). Obese individuals exhibit impaired immune responses. Immune and autoimmune responses are controlled by a fine balance between effector T cells (Teffs) and regulatory T cells (Tregs). Tregs are essential negative regulators of immune responses. CD4+CD25+ Treg lymphocytes produce IL-10 and transforming growth factor-β; these are important in controlling inflammatory T cells (both Th1 and Th2)(Reference O'Garra and Vieira3). It is now evident that Tregs are important in immunity and inflammation. Sakaguchi demonstrated that depletion of CD4+CD25+ Tregs results in systemic autoimmune disease in mice(Reference Sakaguchi4). CD4+CD25+ Tregs with a reduced in vitro suppressive function were found in some studies performed on patients with type 1 diabetes mellitus and atherosclerosis, especially those with acute coronary syndromes(Reference Brusko, Wasserfall and Clare-Salzler5–Reference Meier, Meier and Blanc7). Furthermore, recent studies have demonstrated that the forkhead family transcription factor (Foxp3) is predominantly expressed in CD4+CD25+ Tregs and plays a critical role for their development and function. Mutations in the transcription factor Foxp3 are associated with severe autoimmune diseases in man and the mouse(Reference Gambineri, Torgerson and Ochs8–Reference Brunkow, Jeffery and Hjerrild10). Thus, enhancement of CD4+CD25+Foxp3− Treg cell activity may be important in controlling immunity and inflammation.
Histone acetylation–deacetylation is an important epigenetic event that plays an important role in inflammation(Reference Rahman, Marwick and Kirkham11). Acetylation by histone acetyltransferases of specific lysine residues on the N-terminal tail of core histones results in uncoiling of the DNA and increased accessibility to transcription factor binding. In contrast, histone deacetylation by histone deacetylases (HDAC) represses gene transcription by promoting DNA winding, thereby limiting access to transcription factors. Furthermore, inhibiting HDAC resulted in enhanced activation of NF-κB(Reference Rahman, Gilmour and Jimenez12) and increased histone acetylation, culminating in increased pro-inflammatory cytokines. HDAC-2 has been reported to function in a corticosteroid-mediated anti-inflammatory mechanism(Reference Ito, Barnes and Adcock13). HDAC-1 and -2 can interact directly with the p65 subunit of NF-κB to exert its co-repressor function in the nucleus(Reference Ashburner, Westerheide and Baldwin14). There is increasing evidence to suggest that HDAC plays an important role in regulating the pro-inflammatory response.
( − )-Epigallocatechin gallate (EGCG) is one of the major green tea catechins that are suggested to have a role as a preventive agent in cancer, obesity, diabetes and CVD(Reference Wolfram15). Due to the dominant role of CVD and the dramatic rise of obesity and type 2 diabetes mellitus as major and interlinked healthcare problems, green tea and EGCG are increasingly being investigated in these areas(Reference Wolfram15). Additionally, there are numerous in vivo studies demonstrating that EGCG exert cardiovascular and metabolic benefits in these model systems. Therefore, EGCG, a food component, can be regarded as useful for the maintenance of cardiovascular and metabolic health(Reference Wolfram15). However, there is a paucity of data examining the modulation of the number and function of Tregs with nutritional supplements.
The antioxidant and/or anti-inflammatory effects of dietary polyphenols (curcumin and resveratrol) have all been shown to play a role in either controlling NF-κB activation or chromatin remodelling through the modulation of HDAC activity and subsequently inflammatory gene expression(Reference Wolfram15–Reference Rahman, Biswas and Kirkham16). However, there is a paucity of data on EGCG and HDAC activity in relation to inflammation and the function of Tregs. Also, there is a paucity of data on Tregs in obesity. Obesity is associated with increased inflammation and decreased anti-inflammatory cytokines, such as IL-10(Reference Visser, Bouter and McQuillan2). Thus, we hypothesise that EGCG enhances the functionality and number of Tregs through suppressing the NF-κB signalling pathway via inducing epigenetic changes, i.e. enhanced HDAC activity in obese human subjects.
Experimental methods
Materials
Anti-HDAC-2 and anti-HDAC-3 were procured from Active Motif (Carlsbad, CA, USA) and anti-NF-κBp65 antibodies were procured from Cell Signaling Technology (Beverly, MA, USA). A CD4+CD25+ Regulatory T Cell Isolation kit was procured from Miltenyi Biotec (Auburn, CA, USA). CD25-allophycocyanin (APC)-Cy7, CD4-phycoerythrin (PE)-Cy7 and Foxp3-Alexa Fluor antibodies were purchased from BD Biosciences (San Jose, CA, USA). A transcription ELISA kit (TransAM NF-κBp65) and HDAC assay kit (colorimetric) were purchased from Active Motif. A Human IL-10 Quantikine HS ELISA kit was purchased from R&D Systems (Minneapolis, MN, USA). All other chemicals, unless otherwise stated, were obtained from Sigma (St Louis, MO, USA). The present study was conducted according to the guidelines laid down in the Declaration of Helsinki and all procedures involving human subjects were approved by the University of California Davis Institutional Review Board. Written informed consent was obtained from all subjects.
Subject selection and regulatory T cell isolation
Fasting blood (40 ml) was obtained from normal-weight healthy donors (BMI < 25 kg/m2) and obese donors (BMI>30 kg/m2) (twelve donors per group). Blood was obtained in heparinised vacutainers and all complete blood cell counts were normal. Twelve lean and twelve obese donors were age-, sex- and race-matched and recruited. Lean and obese subjects were recruited according to the selection criteria (Table 1).
Table 1 Selection criteria of the study subjects
AST, aspartate transaminase; ALT, alanine transaminase.
* 1 inch = 2·54 cm.
† 200 IU vitamin E = 133·33 mg d-α-tocopherol.
‡ 1 oz = 28·35 g.
Peripheral blood mononuclear cells from lean and obese subjects were isolated by Ficoll-Hypaque gradient (Sigma)(Reference Sun, Li and Langnas17) and then CD4+CD25+ Tregs were purified from isolated peripheral blood mononuclear cells using a CD4+CD25+ Regulatory T Cell Isolation kit according to the manufacturer's protocols (Miltenyi Biotec). Briefly, CD4+T cells were negatively selected from the total peripheral blood mononuclear cells, yielding a population of CD4+ cells with purity of 92–98 %. Positive selection on anti-CD25 magnetic microbeads was then used to separate the negative fraction containing CD4+CD25− T cells from the CD4+CD25+T cell fraction, using the CD4+CD25+ Regulatory T Cell Isolation kit from Miltenyi Biotec. The purities of the sorted CD4+CD25+ populations were always>95 % as confirmed by flow cytometry. Cells were then applied to a second magnetic column, washed, and eluted again. Tregs were stained using three different antibodies such as CD4-PE-Cy7, CD25-APC-Cy7 and Foxp3-Alexa Fluor with a different colour using flow cytometry. CD4 and CD25 antibodies were used for the surface staining of the Tregs. The Foxp3 antibody was used for the intracellular staining of the Tregs.
Regulatory T cell staining in whole blood
Tregs were stained using two different antibodies, i.e. CD4-PE-Cy7 and CD25-APC-Cy7, in whole blood by flow cytometry. CD4 and CD25 were used for the surface staining of the Tregs. To 100 μl of whole blood from both groups, 10 μl of Fcy blocking reagent were added. Blood samples were incubated with 10 μl isotype control and/or 10 μl appropriate antibodies (CD25-APC-Cy7 and CD4-PE-Cy7) for 30 min at 4°C in the dark. After incubation, lysis buffer was added to the whole blood. Cells were centrifuged and washed with PBS and re-suspended in 1 % paraformaldehyde (PFA) buffer. At least 10 000 cells were acquisitioned using flow cytometry (BD Biosciences).
Cell culture and treatment with epigallocatechin gallate
Tregs were isolated from normal-weight and obese subjects. Tregs were cultured in Roswell Park Memorial Institute (RPMI) medium containing 10 % heat-inactivated fetal calf serum, 1 % antibiotics and IL-2 (10 ng/ml) for the maintenance of Tregs at 37°C and 5 % CO2. EGCG (dissolved in RPMI medium) was used for the treatment of cells. Tregs (50–60 % confluent) were cultured in the absence or presence of EGCG (20 μm) for 24 h. After 24 h incubation, the medium was saved for the measurement of IL-10 and cells were washed with PBS and then harvested for further studies.
Surface and intracellular staining of regulatory T cells
Tregs were stained using three different antibodies such as CD4-PE-Cy7, CD25-APC-Cy7 and Foxp3-Alexa Fluor by flow cytometry. For Foxp3 intracellular staining, cells were incubated with CD25-APC-Cy7 and CD4-PE-Cy7 antibodies at first for 30 min at 4°C in the dark. After incubation, these cells were washed and then fixed and stained with the Foxp3-Alexa Fluor antibody according to the manufacturer's instructions (BD Biosciences). Cells were washed three times and re-suspended in 1 % PFA buffer. At least 10 000 cells were assayed by flow cytometry (BD Biosciences).
Measurement of IL-10 production in regulatory T cells
After treatment of cells with EGCG and without EGCG for 24 h, the supernatant fraction was saved and stored at − 80°C. IL-10 levels were assayed in the supernatant fraction of treated cells using the Human IL-10 Quantikine HS ELISA kit according to the manufacturer's protocols (R&D Systems).
Preparation of nuclear lysates
After treatment of cells with and without EGCG, the cells were washed twice in PBS (10 mm; pH 7·4). Nuclear lysates were prepared using NE-PER Nuclear and Cytoplasmic Extraction Reagents (Pierce, Thermo Scientific, Rockford, IL, USA). The lysates were collected and cleared by centrifugation and the supernatant fraction sampled and stored at − 80°C. The protein concentration in the lysates was measured by BCA protein assay (Pierce) according to the manufacturer's protocols.
Western blot analysis
For Western blot analysis, 12 μg protein was resolved over 4–20 % 2-amino-2-(hydroxymethyl)propane-1,3-diol (Tris)–glycine polyacrylamide gels (Invitrogen, Carlsbad, CA, USA), transferred onto nitrocellulose membranes, and subsequently incubated in blocking buffer (5 % non-fat dry milk/1 % Tween 20; in 20 mm-Tris-buffered saline (pH 7·6)) for 2 h. The blots were incubated with appropriate primary antibodies (HDAC-2 and NF-κBp65, 1:1000 dilution), washed, and incubated with the appropriate secondary horseradish peroxidase–conjugated antibody (1:2000 dilution). The blots were detected with chemiluminescence (ECL kit; Amersham Biosciences, Piscataway, NJ, USA) and autoradiography, using XAR-5 film (Eastman Kodak, Rochester, NY, USA). Equal loading of protein was confirmed by stripping the blots and reprobing with lamin (Sigma).
Measurement of histone deacetylase activity using ELISA
Following treatment of cells with and without 20 μm-EGCG for 24 h, cells were harvested and nuclear lysates were prepared. A quantity of 10 μg nuclear lysate protein from each group was taken for determination of HDAC activity. The experiment was done according to the manufacturer's instructions (HDAC assay kit; Active Motif). Absorbance was taken at 405 nm by using an ELISA reader (Multiscan MCC/340; Fisher Scientific, Rockford, IL, USA).
Detection of transcription factor NF-κBp65 using ELISA
The commercially available kit for NF-κBp65 (Active Motif) contains the specific oligos with the specific consensus sequence for NF-κBp65 binding. Nuclear lysate protein (5 mg) from each group was taken for quantification of NF-κB activity. The experiment was done according to the manufacturer's instructions. Absorbance was taken at 450 nm by using the ELISA reader (Multiscan MCC/340; Fisher Scientific).
Immunocytochemical staining of histone deacetylase
After 24 h incubation in the absence or presence of EGCG, cells (1 × 104) were placed on slides, the slides were air dried, fixed with 4 % formaldehyde for 30 min at 4°C, and then stained with HDAC-2 and -3 antibodies (1:1000) for 18 h at 4°C. Slides were washed first in PBS (pH 7·2) with Tween 20 and then in PBS (10 min each). After being air dried, slides were incubated with the appropriate secondary antibody (1:2000) for 60 min. The slides were washed as described above, air dried, mounted with mounting medium, and then examined with a fluorescence microscope at × 400 magnification.
Statistical analysis
All in vitro experiments were conducted at least five times in duplicate. Results were expressed as mean values and standard deviations. Statistical analysis was performed using ANOVA followed by Wilcoxon tests. P < 0·05 was considered significant.
Results
Foxp3-positive regulatory T cell numbers are decreased in obese compared with lean human subjects
As shown in Fig. 1(a), the CD4+CD25+ Tregs in whole blood were 10·2 (sd 6·78) and 17·25 (sd 6·15) % in obese and lean subject groups, respectively (Fig. 1(a)). Thus, CD4+CD25+ Tregs were significantly decreased in obese subjects compared with lean subjects (P < 0·05) (Fig. 1(a)). We then evaluated the expression of Foxp3 in CD4+CD25+ Tregs in obese v. lean subjects using flow cytometry. The purity of positively selected CD4+CD25+ Tregs was>96 % as confirmed by flow cytometry in both groups. At least 10 000 cells were assayed using flow cytometry (BD Bioscience). Half of the purified CD4+CD25+ Tregs were Foxp3-positive. Foxp3-expressing CD4+CD25+ Tregs were significantly decreased in obese subjects compared with lean subjects (P < 0·05) (Fig. 1(b)).
Fig. 1 Decreased number of regulatory T cells (Tregs) in obese compared with normal-weight human subjects. (a) Tregs were stained using two different antibodies (CD4-phycoerythrin (PE)-Cy7 and CD25-allophycocyanin (APC)-Cy7) in whole blood by flow cytometry. (b) Tregs were isolated from fasting blood obtained from normal-weight and obese subjects as described in Experimental methods. Tregs of obese and lean subjects were stained with three different antibodies (CD25-APC-Cy7, CD4-PE-Cy7 and forkhead family transcription factor (Foxp3)-Alexa Fluor) by flow cytometry. Results are mean values (for twelve subjects per group), with standard deviations represented by vertical bars. * Mean value was significantly different from that of the normal-weight subjects (P < 0·05).
In vitro treatment with epigallocatechin gallate significantly induced Foxp3+-expressing regulatory T cells among the CD4+CD25+ population and IL-10 secretion in obese and lean subjects
The role of EGCG in the modulation of Tregs has, however, not been studied. Thus, we studied the effect of EGCG on the number and function of Tregs in vitro. Thus, we selected this dose in further experiments. As shown in Fig. 2, Foxp3+-expressing cells among the CD4+CD25+ population were significantly increased after EGCG treatment (20 μm) in vitro in both groups (lean: untreated 50·4 (sd 1·2) %, treated 58·8 (sd 2) %; obese: untreated 54·2 (sd 3) %, treated 55·9 (sd 0·5) %). IL-10 production was also significantly up-regulated by EGCG (20 μm) treatment (n 5; Fig. 2; P < 0·01) in both groups (lean: untreated 2·37 (sd 0·21) pg/mg, treated 5·14 (sd 0·25) pg/mg; obese: untreated 2·68 (sd 0·08) pg/mg, treated 4·53 (sd 0·03) pg/mg). There was a similar increase in Foxp3+ Tregs and increase in IL-10 in the lean and obese subjects following EGCG treatment. Dose–response studies with EGCG (0·5–20 μm) demonstrated that EGCG (20 μm) was the most effective concentration that consistently up-regulated the number of Tregs and IL-10 production (Supplemental Fig. 1).
Fig. 2 (a) Epigallocatechin gallate (EGCG) treatment significantly induced forkhead family transcription factor (Foxp3)-positive regulatory T cells (Tregs) among the CD4+CD25+ Treg population in obese and lean subject groups. Tregs were isolated from fasting blood obtained from obese and lean human subjects as described in Experimental methods. Tregs were cultured in Roswell Park Memorial Institute (RPMI) medium. The cells (50–60 % confluent) were treated with (■) and without (□) 20 μm-EGCG for 24 h. The cells were analysed for the expression of CD4+, CD25+ and Foxp3+ by flow cytometry. (b) EGCG treatment (■) induces anti-inflammatory cytokine IL-10 in the Tregs of obese and lean subjects. IL-10 levels were detected in supernatant fractions using a Human IL-10 Quantikine HS ELISA kit and normalised to mg protein. (□), Untreated cells. Results are mean values (for five different experiments), with standard deviations represented by vertical bars. * Mean value was significantly different from that of the untreated Tregs (P < 0·05).
Effect of epigallocatechin gallate on activation of NF-κB and histone deacetylase levels in regulatory T cells
Next, we studied specific regulation mechanisms. Acetylation of histone protein is associated with increased binding of the transcription factor NF-κB(Reference Rahman, Gilmour and Jimenez12). We studied the effects of EGCG on deacetylation of histone proteins, HDAC activity, transactivation and translocation of NF-κB in Tregs of both subject groups. Using immunoblot analysis, we observed that EGCG treatment (20 μm) of cells resulted in decreased NF-κBp65 in the nuclear fraction in Tregs of the obese and lean subject groups (Fig. 3(a)). We further confirmed the inhibition of NF-κBp65 transactivation (lean: untreated 0·446 (sd 0·019), EGCG treated 0·329 (sd 0·049) v. obese: untreated 0·54 (sd 0·02), EGCG treated 0·3 (sd 0·05) at 450 nm optical density value) by performing ELISA (Fig. 3(c)). Also, EGCG enhanced total HDAC activity (lean: untreated 34·22 (sd 3·87) μm, EGCG treated 51·78 (sd 2·31) μm v. obese: untreated 22·1 (sd 2·1) μm, EGCG treated 38·08 (sd 1·5) μm) and HDAC-2 levels in the Tregs of obese and lean subject groups (Fig. 3(b) and (d) – immunofluorescence). There was no detectable significant difference for the HDAC-3 in the Tregs of lean subjects (Fig. 3(d)). But EGCG increased HDAC-3 levels in the Tregs of obese subjects (Fig. 3(d)). Thus, EGCG appears to enhance IL-10 production and Treg number through, at least in part, suppressing the NF-κB signalling pathway via inducing HDAC activity in the Tregs of both groups.
Fig. 3 (a–c). Epigallocatechin gallate (EGCG) treatment modulated NF-κBp65 and histone deacetylase (HDAC) levels in regulatory T cells (Tregs). The cells (50–60 % confluent) were treated with (■) and without (□) 20 μm-EGCG for 24 h. Cells were harvested and nuclear lysates were prepared. (a) For the Western blot analysis, protein was subjected to SDS-PAGE and used HDAC-2 and NF-κBp65 antibodies (1:1000 dilution) as detailed in the Experimental methods section. Equal loading of protein was confirmed by stripping the blots and reprobing with lamin (Sigma). The immunoblots shown here for lean and obese subjects are representative of five independent experiments with similar results. (b–c) For activity assay of HDAC and NF-κBp65, 10 μg nuclear lysates were taken for determination of HDAC and NF-κBp65 activity. The experiment was done according to the manufacturer's instructions. Absorbance was taken at 405 nm and 450 nm, respectively, by using an ELISA reader. Results are mean values (for five independent experiments), with standard deviations represented by vertical bars. * Mean value was significantly different from that of the untreated Tregs (P < 0·05). (d) EGCG treatment induced HDAC-2 activation in Tregs by immunofluorescence. The cells (50–60 % confluent) were treated with and without 20 μm-EGCG for 24 h. Cells were fixed with 4 % formaldehyde for 30 min at 4°C and stained overnight at 4°C with HDAC-2 and -3 antibodies as described in Experimental methods. Data from a typical experiment of five are shown; magnification × 400. DAPI, 4′,6-diamidino-2-phenylindole; → increased intracellular expression.
Discussion
Obesity predisposes to increased diabetes and atherosclerosis and related complications, which represent the major cause of morbidity and mortality in the Western world. Obese individuals exhibit impaired immune responses. Immune and autoimmune responses are controlled by a fine balance between effector T cells (Teffs) and Tregs(Reference O'Garra and Vieira3). Tregs constitutively express high levels of the IL-2 receptor α chain (CD25) and specifically express the forkhead/winged helix transcription factor Foxp3 which acts in a regulatory capacity by inhibiting the activation and function of both self-antigen- and foreign-antigen-reactive T cells(Reference Levings, Sangregorio and Roncarolo18, Reference Shevach19). Moreover, Foxp3 plays a critical role for the development and function of Tregs(Reference Gambineri, Torgerson and Ochs8–Reference Brunkow, Jeffery and Hjerrild10). The critical physiological role of CD4+CD25+Foxp3 Tregs is to control autoimmune diseases(Reference Jonuleit, Schmitt and Schuler20, Reference Read and Powrie21). Tregs may suppress by a contact-dependent mechanism or through the secretion of anti-inflammatory cytokines IL-10 and transforming growth factor-β(Reference Yusuf, Hawken and Ounpuu1). These cells are a low-frequency subpopulation of CD4+ cells, representing 1 to 2 % of total lymphocytes. We hypothesised that enhancement of CD4+CD25+ Treg cell activity may protect individuals from impaired immune responses in patients with obesity.
Since ancient times, green tea has been considered a health-promoting beverage. Health-promoting effects of green tea are mainly attributed to its polyphenol content. Green tea is a rich source of polyphenols, especially flavanols and flavonols. Catechins are the predominant flavanols and are mainly comprised of EGCG, epigallocatechin, epicatechin gallate and epicatechin(Reference Wolfram15, Reference Yang and Landau22). Several intervention studies have demonstrated that green tea cathechins containing 200–300 mg EGCG exert beneficial effects on cardiovascular and metabolic health. Also, EGCG supplementation has been shown to be anti-inflammatory as evidenced by decreased cytokine release and NF-κB activity(Reference Calixto, Campos and Otuki23–Reference Hong, Kim and Chang26). However, there are no data examining the effect of EGCG on the number and function of Tregs in the obese.
In the present study, we provide important and novel preliminary data showing (1) decreased number and function of Tregs (decreased IL-10) in obese individuals in vivo compared with matched lean controls (Fig. 1) and (2) in vitro treatment with EGCG enhances the number of Foxp3-positive Tregs in obese and lean subjects (Fig. 2); this is associated with increased IL-10 release (Fig. 2), decreased NF-κB activity and up-regulation of HDAC-2 (Fig. 3) in support of the earlier observations(Reference Calixto, Campos and Otuki23–Reference Hong, Kim and Chang26). NF-κB plays a pivotal role in inflammation, and EGCG has been shown to down-regulate NF-κB in other studies; however, the effect of EGCG on Tregs has not been studied. Similar to other previous reports(Reference Calixto, Campos and Otuki23–Reference Hong, Kim and Chang26), in the present study we show that EGCG promotes the number and function of Tregs (IL-10 release) in both lean and obese subjects in vitro. Furthermore, since Foxp3-expressing Tregs are more effective in affecting the functionality of Tregs, we examined the effect of EGCG treatment in vitro on Foxp3+ Tregs and similar findings were observed, i.e. enhancement of Foxp3+ Tregs and IL-10 release in both lean and obese subjects.
Epigenetics refers to heritable changes in phenotype (appearance) or gene expression caused by mechanisms other than changes in the underlying DNA sequence. Histone acetylation–deacetylation is an important epigenetic event that plays an important role in inflammation(Reference Rahman, Marwick and Kirkham11). Acetylation of histone protein is associated with increased binding of the transcription factor NF-κB(Reference Rahman, Gilmour and Jimenez12). While several other nutritional strategies such as curcumin and resveratrol have been shown to promote epigenetic events resulting in decreased inflammation, the effect of EGCG on chromatin remodelling has not been studied. Furthermore, in monocytes, inflammation and NF-κB appear to be regulated by changes in histone acetylation–deacetylation. Thus, we tested if EGCG up-regulates the number and anti-inflammatory activity of Tregs (by suppressing NF-κB) through chromatin remodelling. Here, we show that EGCG alters HDAC activity and severely suppresses NF-κB, leading to increased IL-10 release in both obese and lean subjects.
In conclusion, EGCG up-regulates the number and anti-inflammatory activity of Tregs through chromatin remodelling by alteration of histone acetylation–deacetylation and suppression of NF-κB, leading to the induction of IL-10 release. However, the molecular mechanism of chromatin remodelling for pro-inflammatory genes in Tregs is not yet understood well and will be the focus of future studies. Furthermore, it will be important to confirm these in vitro findings in a placebo-controlled supplementation study of EGCG in obese human volunteers. Understanding of gene expression and epigenetic modulation of Tregs by EGCG may be, at least in part, a promising strategy to modulate the immune response of the complications of obesity and its associated diseases and future studies will examine the effect of EGCG supplementation in obese human subjects.
Acknowledgements
These studies were supported in part from discretionary research funding available to the corresponding author S. D. and through a mentoring award to the co-investigator I. J. (NIH K24 AT 00596). J.-M. Y. performed the research procedures and wrote the manuscript. S. D. supervised all parts of the project, and assisted with obtaining informed consent from subjects and manuscript preparation. I. J. provided assistance with the discussion.
The authors acknowledge the help of Manpreet Kaur for editorial assistance.
No conflicts of interest are reported from any of the authors.
Supplemental Fig. 1 is available online only at http://journals.cambridge.org/action/displayJournal?jid = bjn
