METHODS AND COMPOSITIONS FOR TREATMENT OF METABOLIC DISORDERS

Abstract

The present invention relates to the discovery that increases in invariant NKT cell (iNKT) number and/or activity can reduce the incidence or severity of metabolic disorders such as obesity and diabetes. The invention accordingly features methods, kits, and compositions for the treatment of such metabolic disorders by administration of a composition capable of increasing iNKT activity.

Claims

1. A method of treating a subject suffering from a metabolic disorder, said method comprising administering to said subject a sufficient amount of a composition that increases invariant NKT (iNKT) cell activity.

2. The method of claim 1, wherein said composition comprises a glycolipid; an antibody or an antigen-binding fragment thereof; or an iNKT.

3. The method of claim 2, wherein said glycolipid is a bacterial glycolipid capable of activating iNKT.

4. The method of claim 2, wherein said glycolipid is ?-galactosylceramide or an analog thereof.

5. The method of claim 2, wherein said antibody or antigen-binding fragment thereof specifically binds to an iNKT and increases activity of said iNKT.

6. The method of claim 5, wherein said antibody or antigen-binding fragment thereof binds to the CDR3 loop or the ?-? junction of said iNKT.

7. The method of claim 2, wherein said iNKT is an autologous iNKT.

8. The method of claim 1, wherein said composition further comprises a pharmaceutically acceptable carrier or wherein said composition is administered intravenously, intramuscularly, orally, by inhalation, parenterally, intraperitoneally, intraarterially, transdermally, sublingually, nasally, transbuccally, liposomally, adiposally, ophthalmically, intraocularly, subcutaneously, intrathecally, topically, or locally.

9. (canceled)

10. A method for treating a subject suffering from a metabolic disorder, said method comprising the steps: (a) obtaining a biological sample from said subject, said sample containing a population of iNKT; (b) contacting said sample with a sufficient amount of an agent capable of selectively expanding said iNKT; and (c) administering said iNKT of step (b) to said subject in an amount sufficient to treat said metabolic disorder.

11. The method of claim 10, wherein said biological sample is a blood sample.

12. The method of claim 10, wherein said agent is a glycolipid or said agent is an antibody or an antigen-binding fragment thereof.

13. The method of claim 12, wherein said glycolipid is a bacterial glycolipid capable of activating iNKT.

14. The method of claim 12, wherein said glycolipid is ?-galactosylceramide or an analog thereof.

15. The method of claim 12, wherein said antibody or antigen-binding fragment thereof specifically binds to an iNKT and increases activity of said iNKT.

16. The method of claim 15, wherein said antibody or antigen-binding fragment thereof binds to the CDR3 loop or the ?-? junction of said iNKT.

17. The method of claim 10, wherein said iNKT is administered intravenously, intramuscularly, orally, by inhalation, parenterally, intraperitoneally, intraarterially, transdermally, sublingually, nasally, transbuccally, liposomally, adiposally, opthalmically, intraocularly, subcutaneously, intrathecally, topically, or locally.

18. The method of claim 1, wherein said metabolic disorder is diabetes, obesity, diabetes as a consequence of obesity, hyperglycemia, dyslipidemia, hypertriglyceridemia, syndrome X, insulin resistance, impaired glucose tolerance (IGT), diabetic dyslipidemia, hyperlipidemia, a cardiovascular disease, or hypertension.

19. The method of claim 18, wherein said diabetes is type I diabetes or type II diabetes.

20. The method of claim 1, wherein said subject is a human.

21. (canceled)

22. A kit comprising: (a) a composition that increases iNKT activity; and p1 (b) a therapeutic for treating a metabolic disorder.

23. A composition comprising: (a) a first agent that increases iNKT activity; and (b) a second agent for treating a metabolic disorder, wherein said agents are together present in an amount sufficient to treat said metabolic disorder.

24. The method of claim 10, wherein said metabolic disorder is diabetes, obesity, diabetes as a consequence of obesity, hyperglycemia, dyslipidemia, hypertriglyceridemia, syndrome X, insulin resistance, impaired glucose tolerance (IGT), diabetic dyslipidemia, hyperlipidemia, a cardiovascular disease, or hypertension.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0027] FIGS. 1A-1D are graphs showing that iNKT and innate-like lymphocytes are abundant in murine adipose. FIG. 1A shows representative matched spleen, liver, and fat from wt mice. iNKT (?GC-loaded CD1d tetramer.sup.+) shown as % of T cells (top), % total lymphocytes (middle), unloaded CD1d control (bottom). FIG. 1B shows iNKT % (n=12). FIG. 1C shows the percentage of other lymphoid cells. Similar levels of classical T cells (CD3.sup.+tetramer.sup.?NK1.1.sup.?) and NK cells (NK1.1.sup.+CD3.sup.?) (n=12) were observed. Proportions of NKT (CD3.sup.+NK1.1.sup.+) were significantly higher in fat compared to spleen (p<0.01), but lower than in liver (p=0.008). No significant difference of CD4, CD8, DP or DN T cell levels in each organ was observed. FIG. 1D shows the phenotype of iNKT (n=8). Expression of iNKT CD4, CD8, DP (CD4.sup.+CD8.sup.+), DN (CD4.sup.?CD8.sup.?), NK1.1 and CD69 is shown. Some adipose iNKT were CD8.sup.+. More iNKT co-expressed CD4 and CD8 (DP) from fat compared to liver (p=0.03) and NK1.1 than those in spleen and fat (p<0.05).

[0028] FIG. 2 is a set of graphs showing that iNKT cells are depleted in obesity, but are restored following weight loss in mice and humans. iNKT cell levels were reduced in the peripheral blood of obese patients before bariatric surgery (pre-op) (BMI>50, n=26), compared to lean age-matched controls (BMI=20-25, n=22) and unmatched patients 18 months after surgery (post-op) (n=18, p=0.0002). After 18 months post-op, BMI had significantly dropped, but patients were still in the obese category (mean BMI=38). Seven further patients were analyzed both pre- and post-bariatric surgery. Each patient had increased peripheral iNKT cells (n=7, p=0.001).

[0029] FIGS. 3A and 3B are graphs showing iNKT cytokine production in vivo and in vitro from adipose. FIG. 3A shows representative iNKT cytokine production in response to ?GC in vivo (from wt mice, n=4). iNKT from spleen and liver produced copious IFN?, less IL-4, and very low levels of IL-10. iNKT from fat did not produce IFN? but produced more IL-10 than those from liver and spleen. FIG. 3B shows in vitro iNKT cytokine production stimulated by ?GC-loaded CD1d.sup.+C1R cells (n=3). Adipose iNKT produced low levels of IFN? compared to spleen and liver (p=0.04) and less IL-4 than those from liver. Fat iNKT produced significantly more IL-10 than iNKT from liver and spleen in vitro (p<0.01) and in vivo (p<0.01).

[0030] FIGS. 4A and 4B are graphs showing the impact of obesity on iNKT levels. FIG. 4A shows representative iNKT levels from normal wild type (wt), diet-induced obese mice (DIO), and genetically obese ob/ob mice. FIG. 4B shows that iNKT were significantly reduced in spleen, liver, and fat of DIO mice compared to wt SFD controls (n=5 in each group, *p<0.05, **p<0.01). Reduction was more pronounced in ob/ob mice (n=5, ***p<0.005).

[0031] FIGS. 5A-5D are graphs showing iNKT number in mice on a HFD or SFD diet. FIG. 5A shows representative dot plots of iNKT cell (?GC-loaded tetramer.sup.+) levels in matched fat, liver, and spleen from mice on a HFD or SFD (representative of 8 experiments). FIG. 5B shows that iNKT cells are depleted in fat, liver, and spleen from mice on HFD for 8 weeks (n=8, p<0.005) or ob/ob mice (n=3, p<0.005) as compared to SFD (n=8). FIG. 5C shows that, based on weekly measurements, iNKT cell levels in mice on HFD in matched fat, liver, and spleen (n=4 per week) are significantly lower in fat from week 2 onwards. FIG. 5D shows that mice, following removal HFD after 6 weeks (n=4) and after 10 weeks (n=4), exhibited no significant change in overall weight after removal from HFD for 1 week, but had fat pads that were dramatically lighter 1 week after removal from HFD at 6 weeks (p=0.0007) or 10 weeks (p=0.001). This coincided with a significant increase in iNKT cells in fat and liver after removal from HFD after 6 weeks (n=4, p<0.05) but not 10 weeks.

[0032] FIGS. 6A and 6B are graphs showing overall weight and weight of epididymal fat of wt mice on HFD. As expected, mice gained significantly more weight on HFD compared to SFD (n=4 per group per week, p<0.0001, ANOVA), as shown in FIG. 6A. Weight of fat pads increased dramatically on HFD (n=4 per group per week, *p=0.017, *p=0.05, **p=0.043, **p=0.001, HFD vs SFD), as shown in FIG. 6B.

[0033] FIGS. 7A-7G are graphs showing that the absence of iNKT promotes high fat diet (HFD) weight gain and glucose intolerance. FIG. 7A shows overall weight gain (g) in wt on standard high fat diet (SFD) or HFD, CD1d KO (which lack iNKT cells), and V?24 transgenic (Tg) (which have excess iNKT relative to wt, due presence of the human iNKT TCR-alpha chain) mice on HFD after six weeks (n=4 per group). WT and CD1d KO mice gained more weight on HFD than SFD (*p<0.05). There was no difference in weight between wt SFD and V?24 Tg mice on HFD. CD1d KO on HFD gained more weight than wt or V?24 Tg mice on HFD (*p<0.05). FIG. 7B shows weight in each group over six weeks. CD1d KO mice gained significantly more weight than wt on HFD (p=0.002). FIG. 7C shows abdominal adipose weight (g) after six weeks. CD1d KO mice had significantly more fat mass than wt. V?24 Tg had significantly less fat mass (p=0.01). FIG. 7D shows fasting blood glucose levels. CD1d KO had higher fasting blood glucose than SFD, wt on HFD, and V?24 Tg on HFD (***p<0.001). There was no difference between wt on SFD and V?24 Tg mice on HFD. FIG. 7E shows results from a glucose tolerance test (at time 0, p=0.0002, 30 min p=0.02. Time 90 min: KO vs wt HFD **p=0.01, wt HFD vs Tg HFD *p<0.05, KO vs Tg ***p=0.001). FIG. 7F shows that fasting insulin was higher in CD1d KO but that this difference did not reach significance. FIG. 7G shows that insulin resistance measured by HOMA-IR was higher in the CD1d KO mice, although this did not reach significance.

[0034] FIGS. 8A-8C are a set of graphs and photomicrographs showing CD1d KO mice have increased weigh gain, fasting glucose, adipocyte size, and macrophage infiltration. FIG. 8A shows weight of 6-week-old wt SFD, WT HFD, and CD1d KO HFD mice each week for 4 weeks. Both wt and CD1d KO HFD were significantly heavier than wt SFD at each timepoint after commencement of diet. CD1d KO mice were heavier (*p=0.02, two-way ANOVA) and gained more overall weight than wt SFD (**p<0.01) or wt on HFD (*p<0.05, ANOVA post-hoc Tukey test). FIG. 8B shows that fasting glucose was higher in CD1d KO mice (**p=0.004), as was fasting insulin and insulin resistance as measured by HOMA-IR (ns). N=4 per one-way ANOVA with post-hoc Tukey. For all data, n=4 per group, repeated twice. Data represent one experiment, and error bars represent SEM. FIG. 8C shows adipoyte size of wt HFD and CD1d KO mice, with ob/ob as comparison.

[0035] FIGS. 9A-9F are a set of images and graphs showing the effect of iNKT cell deficiency on weight gain, glucose tolerance, adipocyte size and number, and fat accumulation in liver. FIG. 9A is a set of representative photographs of wt and J?18 KO mice after 8 weeks on HFD. Photograph and DEXA scan show J?18 KO mice were heavier with more fat accumulation compared to wt on HFD. Liver from J?18 KO mice had more fat accumulation, and fat pads were larger. FIG. 9B shows that J?18 KO mice were significantly larger on commencement of HFD and gained significantly more weight each week over 8 weeks on HFD (n=4 per week). Lean mass did not differ between wt and J?18 KO mice on HFD. Epididymal fat was significantly larger in J?18 KO mice compared to wt mice on HFD (p=0.02), wt mice on SFD are shown for comparison (p=0.002). FIG. 9C shows that adipocyte diameter and number were measured on osmium-fixed adipocytes with a particle counter. Adipocytes from J?18 KO mice were significantly larger (4 samples per mouse, 4 mice per group, p=0.01) and fewer in number (p=0.05) than wt on HFD. FIG. 9D shows histology of adipocytes from epididymal fat. Adipocytes from J?18 KO mice on HFD were larger than wt on HFD. WT mice on SFD and ob/ob mice are also shown for comparison. FIG. 9E shows that J?18 KO mice had more fat infiltration in liver than WT on HFD (representative of 4 individual experiments). FIG. 9F shows fasting glucose and glucose tolerance in wt vs. J?18 KO mice after 6 weeks on HFD (n=4 per group) (fasting glucose: p=0.01, t test, glucose tolerance: glucose tolerance, p=0.0001, 2 way analysis of variance (ANOVA) with Tukey), AUC of all mice tested in GTT, p=0.01. Fasting insulin (ns) and insulin resistance as measured by HOMA-IR (n=4 per group, p=0.03). Serum leptin levels were similarly elevated in wt and J?18 KO mice (p=0.002).

[0036] FIGS. 10A-10E are graphs and images showing the effect of iNKT cell deficiency in female mice on weight gain, glucose tolerance, adipocyte size and number, and fat accumulation in liver. FIG. 10A shows food intake was not different between J?18 KO and wt on HFD in males (left) and females (right). FIG. 10B shows weight of female J?18 KO and wt mice per week on HFD (n=4 per week per group). FIG. 10C shows that fasting blood glucose and GTT were not different between female J?18 KO and wt on HFD for 6 weeks. FIG. 10D shows DEXA scan results of female J?18 KO and wt on HFD and that lean mass did not differ, but that fat mass (*p=0.02) and weight of fat pads (n=4 per group, p=0.05) was increased in J?18 KO mice. Adipocyte diameter and number were measured on osmium-fixed adipocytes with a particle counter. Adipocytes from female J?18 KO mice were significantly larger (4 samples per mouse, 4 mice per group, p=0.0001) and fewer in number (p=0.02) than wt on HFD. FIG. 10E shows hematoxylin staining of liver from wt and J?18 KO on HFD for 6 weeks. There were more fat droplets throughout the liver of J?18 KO mice compared to wt mice (representative of 4 mice per group).

[0037] FIGS. 11A-11D are graphs showing adipose macrophages in wt SFD, HFD, CD1d KO, and V?24 Tg mice. FIG. 11A shows representative adipose tissue macrophage (ATM) percentage. FIG. 11B shows the phenotype (F4/80.sup.+CD11c.sup.+) in wt on SFD or HFD and CD1d KO and V?24 Tg mice on HFD after 6 weeks (n=4 mice per group). FIG. 11C shows total ATM as a percentage of stromovascular cells. There was no significant difference in ATM numbers, although wt and CD1d KO mice tended to have higher levels of ATM. FIG. 11D shows levels of F4/80.sup.+CD11c.sup.+ ATM in mice diet groups. CD1d KO mice had significantly more F4/80.sup.+CD11c.sup.+ ATM than wt HFD *p<0.05 and Tg on HFD **p<0.01).

[0038] FIGS. 12A-12D are graphs and images showing the relationship between iNKT cells and macrophages. Left panel of FIG. 12A shows M1 macrophages (F4/80.sup.+CD11c.sup.+ MMR.sup.+) levels in fat for 10 weeks on HFD. M1 macrophages are significantly increased in fat from week 2 on HFD. Right panel of FIG. 12A shows that there was a strong inverse correlation between iNKT cell levels and macrophage number in fat (Pearson r=?0.9612, p=0.0001). FIG. 12B is a set of dot plots of % F4/80.sup.+ total macrophages per fat pad (top) and (bottom) showing the percent of macrophages that are CD11c+MMR+ (M1, gated on total macrophages). Green population=CD11c.sup.? (M2) macrophages, blue=CD11c.sup.+, MMR.sup.lo.red=CD11c.sup.+MMR.sup.h1 macrophages (representative of 4 mice per group). FIG. 12C shows immunohistochemical staining of F4/80.sup.+ macrophages in fat from wt on SFD, wt on HFD, J?18 KO mice on HFD, and ob/ob mice on SFD (Representative of 4 mice per group). FIG. 12D shows immunohistochemical staining of CD68.sup.+ M1 macrophages in fat from wt on SFT, and wt and J?18 KO on HFD (representative of 4 mice per group).

[0039] FIG. 13 is a aset of dot plots showing macrophage levels. The top panel shows macrophage (F4/80) levels in SVF for each group. The bottom panels shows CD11c.sup.+ and CD11c.sup.? macrophage gated on total macrophages.

[0040] FIGS. 14A-14E are graphs and images showing that iNKT null mice have more pro-inflammatory cytokines and macrophages on a SFD. FIG. 14A shows weight of wt, J?18 KO, and CD1d KO mice fed SFD ad lib until 20 weeks age (n=3 per group, *p=0.04, *p=0.02, one-way analysis of variance with post-hoc Tukey). FIG. 14B shows that adipocyte size was larger in CD1d KO mice on SFD (representative of 3 mice per group). FIG. 14C show macrophage level and phenotype in the three types of mice groups on SFD. Left panels shows total macrophages (top) and macrophage phenotype gated on F4/80.sup.+ cells. Both types of iNKT deficient mice had significantly more total macrophages (*p=0.02, *p=0.05), and fewer M1 macrophages (**p=0.001, p=0.02). J?18 KO, but not CD1d KO, had more CD11c.sup.+ macrophages (p=0.03, all measured by ANOVA). FIG. 14D shows that fasting triglycerides (TGL) were elevated in both NKT null mice compared to wt mice (n=3,*p=0.01, *p=0.03, one-way analysis of variance with post-hoc Tukey). Serum TNFa and IL-6 levels in wt and J?18 KO mice on SFD (n=3, p=0.03, t test), CD1d KO mice not tested. FIG. 14E shows fasting glucose (ns, p=0.06) and glucose tolerance (ns) of 20 week old wt, J?18 KO, and CD1d KO mice on SFD.

[0041] FIGS. 15A-15C are graphs showing that adoptive transfer of iNKT cells protect from weight gain and adipocyte hypertrophy and reverse obesity-associated metabolic disorder. FIG. 15A shows wt iNKT cells (>95% pure) or PBS as a control were injected IP into obese J?18 KO mice and GTT was performed 4 days post-injection. Fasting glucose (p=0.004, t test) and glucose tolerance improved following iNKT transfer (p<0.0001, 2 way ANOVA; Area under the curve, p=0.007). Insulin sensitivity was improved, but not significantly. FIG. 15B shows that, post iNKT transfer, J?18 KO mice did not continue to gain weight in contrast to mice that received PBS control. Epididymal fat trended toward being smaller following iNKT transfer (ns, p=0.06). FIG. 15C shows that J?18 KO mice receiving iNKT cells had more adipocytes (***p=0.0002, n=4 per group, t test) and adipocytes were smaller 4 days post-injection (***p=0.0001, 2 samples per mouse, n=4 mice, t test).

[0042] FIGS. 16A-16H are graphs and images showing that ?GC treatment reverses obesity-associated metabolic disorders. FIGS. 16A and 16B show the effect of ?GC treatment on weight gain and adipocytes. Each experiment was performed twice, with 5 or 3 mice per group. Data represent results from one experiment (n=5 per group). DEXA scan images of obese wt mice 4 days post-injection of aGC or vehicle. J?18 KO mice received ?GC as control. FIG. 16B shows matched weights before and after ?GC or vehicle. Mice lost weight following ?GC treatment compared to PBS control (n=5 per group, ***p=0.0002, paired t test). Lean mass did not differ, but % body fat was decreased following aGC treatment (n=5, p=0.02, t test). Adipocyte number did not differ, but adipocyte size was decreased following ?GC treatment (2 samples per mouse, n=4 mice, p=0.0001, t test). FIG. 16C shows fasting glucose and GTT of wt obese mice 4 days post ?GC injection (n=5, fasting glucose: ***p=0.0022, t test; GTT: **p=0.006 2 way ANOVA with post hoc shown; area under curve ***p=0.0007). ?GC treatment did not affect J?18 KO mice (fasting glucose, PBS vs. ?GC-J?18 KO, ***p=0.0006, n=5, GTT: ns). ?GC did not affect fasting glucose or GTT mice on SFD (n=2). FIG. 16D shows that ?GC treatment caused increased insulin sensitivity (n=5, *p=0.05), decreased circulating TGL (n=5, *p=0.01), and circulating leptin (n=5, **p=0.001, all t tests). FIG. 16E shows that ?GC treatment caused decreased serum IL-6 (n=5, *p=0.03), increased serum TNF-a (n=5, *p=0.02), and a non-significant increase in IL-4 (p=0.07). FIG. 16F show Oil Red O staining in liver samples from wt obese mice 4 days post ?GC injection. Two representative images per treatment (representing 5 mice per group) are shown. FIG. 16G shows that ?GC injection caused down-regulation of the invariant TCR after 6 hours, followed by dramatic expansion of iNKT cells in adipose tissue at 4 days post-injection. iNKT cells remained actively producing cytokines 4 days post-activation in adipose tissue only. FIG. 16H shows that neutralizing IL-4 and IL-10 prior to ?GG treatment prevented improvement in fasting glucose and GTT induced by ?GC (n=4 per group).

DETAILED DESCRIPTION

[0043] We have shown adipose is specifically enriched with invariant NKT cells (iNKT), which are known to be potent regulatory cells. As demonstrated below, iNKT plays a fundamental role in regulation of body weight and abdominal fat mass. Our findings also indicate a role for iNKT in control of type 2 diabetes in diet-induced obesity. We have further shown adipose iNKT represent an entirely different subset of iNKTs in terms of cytokine responses and function, as compared to those from other tissues. These results suggest indicate that anti-inflammatory iNKT in adipose may act through macrophage phenotypic switching described herein and iNKT may therefore directly influence adipose inflammation and insulin resistance through production of IL-10. Based on these discoveries, the present invention features methods for treating metabolic disorders such as obesity and diabetes by administering a composition that increases iNKT activity, as well as combination therapies and related kits and compositions.

[0044] In particular, our findings show that in absence of iNKT, weight gain and abdominal fat depots were increased and glucose sensitivity and handling were severely impaired, demonstrating that iNKT play a protective role in obesity and diabetes. This protective role is further supported by findings that, when iNKT were over-expressed, weight gain and abdominal fat mass were reduced, despite a high caloric diet. Furthermore, development of metabolic disorders was prevented, as SFD wt and HFD V?24 Tg mice were similar, compared to HFD wt mice.

[0045] Due to protective effects of iNKT in obesity (vide infra), iNKT deficiency in obesity may be reversed by NKT immunotherapy, such as via ?GC treatment, anti-iNKT cell antibody treatment, bypassing iNKT deficiency by CD1d antibody treatment, or treatment with iNKTs themselves (e.g., iNKT transfers).

Glycolipids

[0046] Certain glycolipids can be used to stimulate iNKT activity, e.g., ?-Galactosylceramide (?GC), a glycolipid derived from a marine sponge that has been observed to activate iNKT. ?GC and analogs of ?GC may therefore be used in the methods, kits, and compositions of the invention. Exemplary, non-limiting, glycolipids are described herein.

?-Galactosylceramide and Analogs

[0047] In certain embodiments, ?-galactosylceramide or an ?-galactosylceramide analog is used in the methods, kits, or compositions of the invention.

##STR00001##

[0048] Analogs of ?-galactosylceramide are described in U.S. Pat. No. 5,936,076 and have the formula:

##STR00002##

[0049] wherein R represents:

##STR00003##

where R.sub.2 represents H or OH and X denotes an integer of 0-26,

[0050] or R represents (CH.sub.2).sub.7CH?CH(CH.sub.2).sub.7CH.sub.3; and

[0051] R.sub.1 represents CH.sub.2(CH.sub.2).sub.YCH.sub.3; CH(OH)(CH.sub.2).sub.YCH.sub.3; CH(OH)(CH.sub.2).sub.YCH(CH.sub.3).sub.2; CH?CH(CH.sub.2).sub.YCH.sub.3, or CH(OH)(CH.sub.2).sub.YCH(CH.sub.3)CH.sub.2CH.sub.3, where Y denotes an integer of 5-17.

[0052] where R.sub.2 represents H or OH and X denotes an integer of 0-26,

[0053] Analogs of ?-galactosylceramide are also described in U.S. Pat. No. 7,273,852 and have the formula:

##STR00004##

wherein X is O or NH; R.sup.1 is selected from the group consisting of (CH.sub.2).sub.11CH.sub.3, (CH.sub.2).sub.12CH.sub.3, (CH.sub.2).sub.13CH.sub.3, (CH.sub.2).sub.9CH(CH.sub.3).sub.2, (CH.sub.2).sub.10CH(CH.sub.3).sub.2, (CH.sub.2).sub.11CH(CH.sub.3).sub.2, and (CH.sub.2).sub.11CH(CH.sub.3)C.sub.2H.sub.5; R.sup.3 is OH or a monosaccharide and R.sup.4 is H, or R.sup.3 is H and R.sup.4 is OH or a monosaccharide; R.sup.5 is H or a monosaccharide; Q.sup.1 is optionally present and is a C.sub.1-10 straight or branched chain alkylene, alkenylene, or alkynylene; X is optionally present and is O, S, or NR.sup.8; Q.sup.2 is optionally present and is a C.sub.1-10 straight or branched chain alkylene, alkenylene, or alkynylene; X is optionally present and is O, S, or NR.sup.8; Q.sup.3 is a straight or branched chain C.sub.1-10 alkyl, alkenyl, or alkynyl, or is hydrogen; wherein each Q.sup.1, Q.sup.2, or Q.sup.3 is optionally substituted with hydroxyl, halogen, cyano, nitro, SO.sub.2, NHR.sup.8, or C(?O)R.sup.9; and wherein R.sup.8 is H, C.sub.1-5 alkyl, C.sub.1-5 alkoxy, halogen, cyano, nitro, SO.sub.2, or C(?O)R.sup.9; R.sup.9 is H, C.sub.1-5 alkyl, C.sub.1-5 alkoxy or NHR.sup.10; R.sup.10 is hydrogen, C.sub.1-5 alkyl, or C.sub.1-5 alkoxy.

[0054] Additional analogs are described in U.S. Pat. No. 7,645,873 and have the formula:

##STR00005##

where R.sub.1 is (i) H or (ii) SO.sub.2R.sub.10, where R.sub.10 is halo; hydroxyl; OR.sub.11; OR.sub.12; amino; NHR.sub.11; N(R.sub.11).sub.2; NHR.sub.12; N(R.sub.12).sub.2; aralkylamino; or C.sub.1-12 alkyl optionally substituted with halo, hydroxy, oxo, nitro, OR.sub.11, OR.sub.12, acyloxy, amino, NHR.sub.11, N(R.sub.11).sub.2, NHR.sub.12, N(R.sub.12).sub.2, aralkylamino, mercapto, thioalkoxy, S(O)R.sub.11, S(O)R.sub.12, SO.sub.2R.sub.11, SO.sub.2R.sub.12, NHSO.sub.2R.sub.11, NHSO.sub.2R.sub.12, sulfate, phosphate, cyano, carboxyl, C(O)R.sub.11, C(O)R.sub.12, C(O)OR.sub.11, C(O)NH.sub.2, C(O)NHR.sub.11, C(O)N(R.sub.11).sub.2, C.sub.3-10 cycloalkyl containing 0-3 R.sub.13, C.sub.3-10 heterocyclyl containing 0-3 R.sub.13, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.5-10 cycloalkenyl, C.sub.5-10 heterocycloalkenyl, C.sub.6-20 aryl containing 0-3 R.sub.14, or heteroaryl containing 0-3 R.sub.14; or C.sub.3-10 cycloalkyl, C.sub.3-10 heterocyclyl, C.sub.5-10 cycloalkenyl, or C.sub.5-10 heterocycloalkenyl optionally substituted with one or more halo, hydroxy, oxo, OR.sub.11, OR.sub.12, acyloxy, nitro, ammo, NHR.sub.11, N(R.sub.11).sub.2, NHR.sub.12, N(R.sub.12).sub.2, aralkylamino, mercapto, thioalkoxy, S(O)R.sub.11, S(O)R.sub.12, SO.sub.2R.sub.11, SO.sub.2R.sub.12, NHSO.sub.2R.sub.11, NHSO.sub.2R.sub.12, sulfate, phosphate, cyano, carboxyl, C(O)R.sub.11, C(O)R.sub.12, C(O)OR.sub.11, C(O)NH.sub.2, C(O)NHR.sub.11, C(O)N(R.sub.11).sub.2, alkyl, haloalkyl, C.sub.3-10 cycloalkyl containing 0-3 R.sub.13, C.sub.3-10 heterocyclyl containing 0-3 R.sub.13, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.5-10 cycloalkenyl, C.sub.5-10 heterocycloalkenyl, C.sub.6-20 aryl heteroaryl containing 0-3 R.sub.14, or C.sub.6-20 heteroaryl containing 0-3 R.sub.14; or C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, aryl, or heteroaryl optionally substituted with one or more halo, hydroxy, OR.sub.11, OR.sub.12, acyloxy, nitro, amino, NHR.sub.11, N(R.sub.11).sub.2, NHR.sub.12, N(R.sub.12).sub.2, aralkylamino, mercapto, thioalkoxy, S(O)R.sub.11, S(O)R.sub.12, SO.sub.2R.sub.11, SO.sub.2R.sub.12, NHSO.sub.2R.sub.11, NHSO.sub.2R.sub.12, sulfate, phosphate, cyano, carboxyl, C(O)R.sub.11, C(O)R.sub.12, C(O)OR.sub.11, C(O)NH.sub.2, C(O)NHR.sub.11, C(O)N(R.sub.11).sub.2, alkyl, haloalkyl, C.sub.3-10 cycloalkyl containing 0-3 R.sub.13, C.sub.3-10 heterocyclyl containing 0-3 R.sub.13, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.5-10 cycloalkenyl, C.sub.5-10 heterocycloalkenyl, C.sub.6-20 aryl containing 0-3 R.sub.14, or C.sub.6-20 heteroaryl containing 0-3 R.sub.14; or (iii) C(O)R.sub.10, wherein R.sub.10 is defined as above; or (iv) C(R.sub.10).sub.2(R.sub.15), wherein R.sub.10 is defined as above; R.sub.15 is H, R.sub.10, or R.sub.15 and R.sub.2 taken together forms a double bond between the carbon and nitrogen atoms to which they are attached; or (v) R.sub.1 and R.sub.2 taken together forms a heterocyclyl of 3-10 ring atoms optionally substituted with R.sub.10; R.sub.2 is H, or R.sub.2 and R.sub.15 taken together forms a double bond between the carbon and nitrogen atoms to which they are attached, or R.sub.2 and R.sub.1 taken together forms a heterocyclyl of 3-10 ring atoms optionally substituted with R.sub.10; R.sub.3, R.sub.4, R.sub.5, R.sub.6, and R.sub.7 are each independently H, C.sub.1-6 alkyl, C.sub.6-12 aralkyl, or C.sub.1-6 acyl; R.sub.8 is (CH.sub.2).sub.xCH.sub.3; R.sub.9 is a linear or branched C.sub.3-100 alkyl; R.sub.11 is C.sub.1-20 alkyl optionally substituted with halo, hydroxy, alkoxy, amino, alkylamino, dialkylamino, sulfate, or phosphate; R.sub.12 is aryl optionally substituted with halo, haloalkyl, hydroxy, alkoxy, nitro, amino, alkylamino, dialkylamino, sulfate, or phosphate; each R.sub.13 is independently halo, haloalkyl, hydroxy, alkoxy, oxo, amino, alkylamino, dialkylamino, sulfate, or phosphate; each R.sub.14 is independently halo, haloalkyl, hydroxy, alkoxy, nitro, amino, alkylamino, dialkylamino, sulfate, or phosphate; and x is 1-100.

[0055] Other Glycolipids

[0056] Other glycolipids, particularly bacterial glycolipids, can be used to activate iNKT. In one example, glycosylceramides from the cell wall of Sphingomonas and a lysosomal glycosphingolipid, iGb3, have been shown to activate iNKT (Mattner et al., Nature 434:525-9, 2005). Additional glycolipids that can be used in the methods, kits, and compositions of the invention can also be identified using methods known in the art. See, for example: Tefit et al., NKT Cell Responses to Glycolipid Activation, Vaccines Adjuvants: Methods and Protocols, 626:149-167, (2010); Cohen et al., Antigen Presentation by CD1 Lipids, T Cells, and NKT Cells in Microbial Immunity, Adv. Immunol. 102:1-94 (2009); and Tupin et al., Activation of Natural Killer T Cells by Glycolipids, Methods. Enzymol. 417:185-201 (2006), each of which is hereby incorporated by reference.

Antibodies

[0057] The methods, kits, and compositions of the invention may also include the use of an antibody capable of stimulating (e.g., expanding) iNKT. As described in PCT Publication WO 01/98357, which is hereby incorporated by reference, antibodies that bind the CDR3 loop or ?-? junction of iNKT are capable of stimulating cytokine secretion and expanding populations of iNKT both in vivo and in vitro. Particular examples of such antibodies (e.g., 6B11 and 3A6), as well as methods of making such antibodies, are described in PCT Publication WO 01/98357.

[0058] Antibodies include, for example, single monoclonal antibodies, antibody compositions with polyepitopic specificity, single chain antibodies, nanobodies, and fragments of antibodies. Antibodies also include intact immunoglobulin or antibody molecules, polyclonal antibodies, multispecific antibodies (e.g., bispecific antibodies formed from at least two intact antibodies), and immunoglobulin fragments (such as Fab, F(ab).sub.2, or Fv), as well as antibodies with other specific functional elements removed, such as sugar residues, so long as they exhibit any of the desired properties (e.g., antigen binding) described herein.

[0059] Antibody fragments comprise a portion of an intact antibody, generally the antigen binding or variable region of the intact antibody. Examples of antibody fragments include Fab, Fab, F(ab).sub.2, and Fv fragments, diabodies, single chain antibody molecules, and multispecific antibodies formed from antibody fragments.

[0060] Humanized forms of non-human (e.g., murine) antibodies are specific chimeric immunoglobulins, immunoglobulin chains, or fragments thereof (such as Fv, Fab, Fab, F(ab).sub.2 or other antigen-binding subsequences of antibodies) which contain minimal sequence derived from non-human immunoglobulin.

[0061] A human antibody is one that possesses an amino acid sequence which corresponds to that of an antibody produced by a human and/or has been made using any of the techniques for making human antibodies known in the art. A human antibody includes antibodies comprising at least one human antibody heavy chain-related polypeptide or at least one antibody human light chain-related polypeptide.

iNKT

[0062] The methods, kits, and compositions of the invention may also include the use of an iNKT (e.g., an iNKT population). Methods for enriching iNKT are known in the art (see, e.g., PCT Publication WO 01/98357, Exley et al., Eur J Immunol 38:1756-66, 2008; Exley et al., Isolation and functional analysis of human NKT cells. In Current Protocols in Immunology Wiley & Sons. Eds. J. E. Coligan, et al., 2002, 2010; and Watarai et al., Nat Protoc 3:70-8, 2008) and include immunological methods such as fluorescence-activated cell sorting (FACS) and the use of antibodies specific for iNKT (e.g., those described herein) to purify iNKT followed by their expansion as described (see, e.g., PCT Publication WO 01/98357, Exley et al., Eur J Immunol 38:1756-66, 2008; M. Exley et al., Isolation and functional analysis of human NKT cells. In Current Protocols in Immunology Wiley & Sons. Eds. J. E. Coligan, et al., 2002, 2010; and Watarai et al., Nat Protoc 3:70-8, 2008).

[0063] In certain embodiments, a sample containing iNKT are taken from a subject, the iNKT are enriched and/or expanded preferentially as described (see, e.g., PCT Publication WO 01/98357, Exley et al., Eur J Immunol 38:1756-66, 2008; Exley et al., Isolation and functional analysis of human NKT cells. In Current Protocols in Immunology Wiley & Sons. Eds. J. E. Coligan, et al., 2002, 2010; and Watarai et al., Nat Protoc 3:70-8, 2008). The enriched and/or expanded cell population is then returned to the subject in order to treat the metabolic disorder (e.g., diabetes or obesity).

Additional Therapeutics for Use in Combination with iNKT and iNKT Stimulants.

[0064] The methods, kits, and compositions of the invention may also include the use of a second therapeutic agent for treating the metabolic disorder (e.g., obesity or diabetes). Examples of antidiabetic agents suitable for use in combination with compounds of the present invention include insulin and insulin mimetics, sulfonylureas (such as acetohexamide, carbutamide, chlorpropamide, glibenclamide, glibornuride, gliclazide, glimepiride, glipizide, gliquidone, glisoxepide, glyburide, glyclopyramide, tolazamide, tolcyclamide, tolbutamide and the like), insulin secretion enhancers (such as JTT-608, glybuzole and the like), biguanides (such as metformin, buformin, phenformin and the like), sulfonylurea/biguanide combinations (such as glyburide/metformin and the like), meglitinides (such as repaglinide, nateglinide, mitiglinide and the like), thiazolidinediones (such as rosiglitazone, pioglitazone, isaglitazone, netoglitazone, rivoglitazone, balaglitazone, darglitazone, CLX-0921 and the like), thiazolidinedione/biguanide combinations (such as pioglitazone/metformin and the like), oxadiazolidinediones (such as YM440 and the like), peroxisome proliferator-activated receptor (PPAR)-gamma agonists (such as farglitazar, metaglidasen, MBX-2044, GI 262570, GW1929, GW7845 and the like), PPAR-alpha/gamma dual agonists (such as muraglitazar, naveglitazar, tesaglitazar, peliglitazar, JTT-501, GW-409544, GW-501516 and the like), PPAR-alpha/gamma/delta pan agonists (such as PLX204, GlaxoSmithKline 625019, GlaxoSmithKline 677954 and the like), retinoid X receptor agonists (such as ALRT-268, AGN-4204, MX-6054, AGN-194204, LG-100754, bexarotene and the like), alpha-glucosidase inhibitors (such as acarbose, miglitol and the like), stimulants of insulin receptor tyrosine kinase (such as TER-17411, L-783281, KRX-613 and the like), tripeptidyl peptidase II inhibitors (such as UCL-1397 and the like), dipeptidyl peptidase IV inhibitors (such as sitagliptin, vildagliptin, denagliptin, saxagliptin, NVP-DPP728, P93/01, P32/98, FE 99901, TS-021, TSL-225, GRC8200, compounds described in U.S. Pat. Nos. 6,869,947; 6,727,261; 6,710,040; 6,432,969; 6,172,081; 6,011,155 and the like), protein tyrosine phosphatase-1B inhibitors (such as KR61639, IDD-3, PTP-3848, PTP-112, OC-86839, PNU-177496, compounds described in Vats, R. K., et al., Current Science, Vol. 88, No. 2, pp. 241-249, and the like), glycogen phosphorylase inhibitors (such as NN-4201, CP-368296 and the like), glucose-6-phosphatase inhibitors, fructose 1,6-bisphosphatase inhibitors (such as CS-917, MB05032 and the like), pyruvate dehydrogenase inhibitors (such as AZD-7545 and the like), imidazoline derivatives (such as BL11282 and the like), hepatic gluconeogenesis inhibitors (such as FR-225659 and the like), D-chiroinositol, glycogen synthase kinase-3 inhibitors (such as compounds described in Vats, R. K., et al., Current Science, Vol. 88, No. 2, pp. 241-249, and the like), incretin mimetics (such as exenatide and the like), glucagon receptor antagonists (such as BAY-27-9955, NN-2501, NNC-92-1687 and the like), glucagon-like peptide-1 (GLP-1), GLP-1 analogs (such as liraglutide, CJC-1131, AVE-0100 and the like), GLP-1 receptor agonists (such as AZM-134, LY-315902, GlaxoSmithKline 716155 and the like), amylin, amylin analogs and agonists (such as pramlintide and the like), fatty acid binding protein (aP2) inhibitors (such as compounds described in U.S. Pat. Nos. 6,984,645; 6,919,323; 6,670,380; 6,649,622; 6,548,529 and the like), beta-3 adrenergic receptor agonists (such as solabegron, CL-316243, L-771047, FR-149175 and the like), and other insulin sensitivity enhancers (such as reglixane, ONO-5816, MBX-102, CRE-1625, FK-614, CLX-0901, CRE-1633, NN-2344, BM-13125, BM-501050, HQL-975, CLX-0900, MBX-668, MBX-675, S-15261, GW-544, AZ-242, LY-510929, AR-H049020, GW-501516 and the like).

[0065] Examples of agents for treating diabetic complications suitable for use in combination with compounds of the present invention include aldose reductase inhibitors (such as epalrestat, imirestat, tolrestat, minalrestat, ponalrestat, zopolrestat, fidarestat, ascorbyl gamolenate, ADN-138, BAL-ARI8, ZD-5522, ADN-311, GP-1447, IDD-598, risarestat, zenarestat, methosorbinil, AL-1567, M-16209, TAT, AD-5467, AS-3201, NZ-314, SG-210, JTT-811, lindolrestat, sorbinil, and the like), inhibitors of advanced glycation end-products (AGE) formation (such as pyridoxamine, OPB-9195, ALT-946, ALT-711, pimagedine and the like), AGE breakers (such as ALT-711 and the like), sulodexide, 5-hydroxy-1-methylhydantoin, insulin-like growth factor-I, platelet-derived growth factor, platelet-derived growth factor analogs, epidermal growth factor, nerve growth factor, uridine, protein kinase C inhibitors (such as ruboxistaurin, midostaurin, and the like), sodium channel antagonists (such as mexiletine, oxcarbazepine, and the like), nuclear factor-kappaB (NF-kappaB) inhibitors (such as dexlipotam and the like), lipid peroxidase inhibitors (such as tirilazad mesylate and the like), N-acetylated-alpha-linked-acid-dipeptidase inhibitors (such as GPI-5232, GPI-5693, and the like), and carnitine derivatives (such as carnitine, levacecamine, levocarnitine, ST-261, and the like).

[0066] Examples of antihyperuricemic agents suitable for use in combination with compounds of the present invention include uric acid synthesis inhibitors (such as allopurinol, oxypurinol, and the like), uricosuric agents (such as probenecid, sulfinpyrazone, benzbromarone, and the like) and urinary alkalinizers (such as sodium hydrogen carbonate, potassium citrate, sodium citrate, and the like).

[0067] Examples of lipid-lowering/lipid-modulating agents suitable for use in combination with compounds of the present invention include hydroxymethylglutaryl coenzyme A reductase inhibitors (such as acitemate, atorvastatin, bervastatin, carvastatin, cerivastatin, colestolone, crilvastatin, dalvastatin, fluvastatin, glenvastatin, lovastatin, mevastatin, nisvastatin, pitavastatin, pravastatin, ritonavir, rosuvastatin, saquinavir, simvastatin, visastatin, SC-45355, SQ-33600, CP-83101, BB-476, L-669262, S-2468, DMP-565, U-20685, BMS-180431, BMY-21950, compounds described in U.S. Pat. Nos. 5,753,675; 5,691,322; 5,506,219; 4,686,237; 4,647,576; 4,613,610; 4,499,289; and the like), fibric acid derivatives (such as gemfibrozil, fenofibrate, bezafibrate, beclobrate, binifibrate, ciprofibrate, clinofibrate, clofibrate, etofibrate, nicofibrate, pirifibrate, ronifibrate, simfibrate, theofibrate, AHL-157, and the like), PPAR-alpha agonists (such as GlaxoSmithKline 590735 and the like), PPAR-delta agonists (such as GlaxoSmithKline 501516 and the like), acyl-coenzyme A:cholesterol acyltransferase inhibitors (such as avasimibe, eflucimibe, eldacimibe, lecimibide, NTE-122, MCC-147, PD-132301-2, C1-1011, DUP-129, U-73482, U-76807, TS-962, RP-70676, P-06139, CP-113818, RP-73163, FR-129169, FY-038, EAB-309, KY-455, LS-3115, FR-145237, T-2591, J-104127, R-755, FCE-27677, FCE-28654, YIC-C8-434, CI-976, RP-64477, F-1394, CS-505, CL-283546, YM-17E, 447C88, YM-750, E-5324, KW-3033, HL-004, and the like), probucol, thyroid hormone receptor agonists (such as liothyronine, levothyroxine, KB-2611, GC-1, and the like), cholesterol absorption inhibitors (such as ezetimibe, SCH48461, and the like), lipoprotein-associated phospholipase A2 inhibitors (such as rilapladib, darapladib, and the like), microsomal triglyceride transfer protein inhibitors (such as CP-346086, BMS-201038, compounds described in U.S. Pat. Nos. 5,595,872; 5,739,135; 5,712,279; 5,760,246; 5,827,875; 5,885,983; 5,962,440; 6,197,798; 6,617,325; 6,821,967; 6,878,707, and the like), low density lipoprotein receptor activators (such as LY295427, MD-700, and the like), lipoxygenase inhibitors (such as compounds described in WO 97/12615, WO 97/12613, WO 96/38144, and the like), carnitine palmitoyl-transferase inhibitors (such as etomoxir and the like), squalene synthase inhibitors (such as YM-53601, TAK-475, SDZ-268-198, BMS-188494, A-87049, RPR-101821, ZD-9720, RPR-107393, ER-27856, compounds described in U.S. Pat. Nos. 5,712,396; 4,924,024; 4,871,721, and the like), nicotinic acid derivatives (such as acipimox, nicotinic acid, ricotinamide, nicomol, niceritrol, nicorandil, and the like), bile acid sequestrants (such as colestipol, cholestyramine, colestilan, colesevelam, GT-102-279, and the like), sodium/bile acid cotransporter inhibitors (such as 264W94, S-8921, SD-5613, and the like), and cholesterol ester transfer protein inhibitors (such as torcetrapib, JTT-705, PNU-107368E, SC-795, CP-529414, and the like).

[0068] Examples of anti-obesity agents suitable for use in combination with compounds of the present invention include serotonin-norepinephrine reuptake inhibitors (such as sibutramine, milnacipran, mirtazapine, venlafaxine, duloxetine, desvenlafaxine and the like), norepinephrine-dopamine reuptake inhibitors (such as radafaxine, bupropion, amineptine, and the like), selective serotonin reuptake inhibitors (such as citalopram, escitalopram, fluoxetine, fluvoxamine, paroxetine, sertraline, and the like), selective norepinephrine reuptake inhibitors (such as reboxetine, atomoxetine, and the like), norepinephrine releasing stimulants (such as rolipram, YM-992, and the like), anorexiants (such as amphetamine, methamphetamine, dextroamphetamine, phentermine, benzphetamine, phendimetrazine, phenmetrazine, diethylpropion, mazindol, fenfluramine, dexfenfluramine, phenylpropanolamine, and the like), dopamine agonists (such as ER-230, doprexin, bromocriptine mesylate, and the like), H.sub.3-histamine antagonists (such as impentamine, thioperamide, ciproxifan, clobenpropit, GT-2331, GT-2394, A-331440, and the like), 5-HT2c receptor agonists (such as 1-(m-chlorophenyl)piperazine (m-CPP), mirtazapine, APD-356 (lorcaserin), SCA-136 (vabicaserin), ORG-12962, ORG-37684, ORG-36262, ORG-8484, Ro-60-175, Ro-60-0332, VER-3323, VER-5593, VER-5384, VER-8775, LY-448100, WAY-161503, WAY-470, WAY-163909, BVT.933, YM-348, IL-639, IK-264, ATH-88651, ATHX-105, and the like (see, e.g., Nilsson B M, J. Med. Chem. 2006, 49:4023-4034)), ?-3 adrenergic receptor agonists (such as L-796568, CGP 12177, BRL-28410, SR-58611A, ICI-198157, ZD-2079, BMS-194449, BRL-37344, CP-331679, CP-331648, CP-114271, L-750355, BMS-187413, SR-59062A, BMS-210285, LY-377604, SWR-0342SA, AZ-40140, SB-226552, D-7114, BRL-35135, FR-149175, BRL-26830A, CL-316243, AJ-9677, GW-427353, N-5984, GW-2696, and the like), cholecystokinin agonists (such as SR-146131, SSR-125180, BP-3.200, A-71623, FPL-15849, GI-248573, GW-7178, GI-181771, GW-7854, A-71378, and the like), antidepressant/acetylcholinesterase inhibitor combinations (such as venlafaxine/rivastigmine, sertraline/galanthamine, and the like), lipase inhibitors (such as orlistat, ATL-962, and the like), anti-epileptic agents (such as topiramate, zonisamide, and the like), leptin, leptin analogs and leptin receptor agonists (such as LY-355101 and the like), neuropeptide Y (NPY) receptor antagonists and modulators (such as SR-120819-A, PD-160170, NGD-95-1, BIBP-3226, 1229-U-91, CGP-71683, BIBO-3304, CP-671906-01, J-115814, and the like), ciliary neurotrophic factor (such as Axokine and the like), thyroid hormone receptor-beta agonists (such as KB-141, GC-1, GC-24, GB98/284425, and the like), cannabinoid CB1 receptor antagonists (such as rimonabant, SR147778, SLV 319, and the like (see, e.g., Antel J et al., J. Med. Chem. 2006, 49:4008-4016)), melanin-concentrating hormone receptor antagonists (including GlaxoSmithKline 803430X, GlaxoSmithKline 856464, SNAP-7941, T-226296, and the like (see, e.g., Handlon A L and Zhou H, J. Med. Chem. 2006, 49:4017-4022)), melanocortin-4 receptor agonists (including PT-15, Ro27-3225, THIQ, NBI 55886, NBI 56297, NBI 56453, NBI 58702, NBI 58704, MB243, and the like (see, e.g., Nargund R P et al., J. Med. Chem. 2006, 49:4035-4043)), selective muscarinic receptor M.sub.1 antagonists (such as telenzepine, pirenzepine, and the like), opioid receptor antagonists (such as naltrexone, methylnaltrexone, nalmefene, naloxone, alvimopan, norbinaltorphimine, nalorphine, and the like), orexin receptor antagonists (such as almorexant and the like), and combinations thereof.

[0069] Other classes of agents that may be used in the methods, kits, and compositions of the invention include non-sulfonylurea secretagogues, glucagon-like peptides, exendin-4 polypeptides, PPAR agonists, dipeptidyl peptidase IV inhibitors, ?-glucosidase inhibitors, immunomodulators, angiotensin converting enzyme inhibitors, adenosine A1 receptor agonists, adenosine A2 receptor agonists, aldosterone antagonists, ?1 adrenoceptor antagonists, ?2 adrenoceptor agonists, angiotensin receptor antagonists, antioxidants, ATPase inhibitors, atrial peptide agonists, ? adrenoceptor antagonists, calcium channel agonists, calcium channel antagonists, diuretics, dopamine D1 receptor agonists, endopeptidase inhibitors, endothelin receptor antagonists, guanylate cyclase stimulants, phosphodiesterase V inhibitors, protein kinase inhibitors, Cdc2 kinase inhibitors, renin inhibitors, thromboxane synthase inhibitors, vasopeptidase inhibitors, vasopressin 1 antagonists, vasopressin 2 antagonists, angiogenesis inhibitors, advanced glycation end product inhibitors, bile acid binding agents, bile acid transport inhibitors, bone formation stimulants, apolipoprotein A1 agonists, DNA topoisomerase inhibitors, cholesterol absorption inhibitors, cholesterol antagonists, cholesteryl ester transfer protein antagonists, cytokine synthesis inhibitors, DNA polymerase inhibitors, dopamine D2 receptor agonists, endothelin receptor antagonists, growth hormone antagonists, lipase inhibitors, lipid peroxidation inhibitors, lipoprotein A antagonists, microsomal transport protein inhibitors, microsomal triglyceride transfer protein inhibitors, nitric oxide synthase inhibitors, oxidizing agents, phospholipase A2 inhibitors, radical formation agonists, platelet aggregation antagonists, prostaglandin synthase stimulants, reverse cholesterol transport activators, rho kinase inhibitors, selective estrogen receptor modulators, squalene epoxidase inhibitors, squalene synthase inhibitors, thromboxane A2 antagonists, cannabinoid receptor antagonists, cholecystokinin A agonists, corticotropin-releasing factor agonists, dopamine uptake inhibitors, G protein-coupled receptor modulators, glutamate antagonists, melanin-concentrating hormone receptor antagonists, nerve growth factor agonists, neuropeptide Y agonists, neuropeptide Y antagonists, SNRIs, protein tyrosine phosphatase inhibitors, and serotonin 2C receptor agonists.

[0070] The following examples are intended to illustrate, rather than limit, the present invention.

EXAMPLE 1

Adipose Tissue is Enriched for iNKT

[0071] Adipose tissue consists of adipocytes and heterogeneous cell populations in the stromovascular fraction (SVF), including vascular endothelium, mesenchymal stem cells, macrophages and unique lymphocytes. iNKT have not previously been described in murine adipose. ?8% of adipose SVF were lymphocytes. The majority of these were T cells (60-80%). Of total lymphocytes in SVF, ?15% were iNKT, compared to 20% in liver and 1% in spleen (FIGS. 1A and 1B). Of total T cells in SVF, up to 60% were iNKT (mean 40%), compared to 2% of splenic T cells and 35% of hepatic T cells (FIGS. 1A and 1B), thus illustrating enrichment of iNKT among adipose T cells. Previous studies showed that the highest iNKT/T cell ratio was seen in murine liver (Eberl et al., J Immunol. 162:6410-9, 1999; Bendelac et al., Annu Rev Immunol. 25:297-336, 2007). In our current studies, we calculated absolute numbers of T cells and iNKT (Tables 1A and 1B). Each fat depot contains ?8.4?10.sup.6 stromovascular cells; of these cells, approximately 6.7?10.sup.5 were lymphocytes, equating to 2.8?10.sup.5 iNKT per fat pad. There were therefore slightly more iNKT in fat than in liver, but fewer than in spleen (Table 1A). In wt mice on SFD, the average weight of fat pads was 0.6 g, equating to a mean number of 4.6?10.sup.5 iNKT per gram of fat (Table 1B). These data indicate that adipose has the highest iNKT/T cell ratio described in the mouse.

TABLE-US-00001 TABLE 1A Total cell counts of wt spleen, liver, and abdominal fat. Total lymphocytes and absolute number of iNKT per sample. Total cell count Total lymphocytes Total iNKT cells Spleen 42.8 ? 10.sup.6 11.6 ? 10.sup.6 1.6 ? 10.sup.6 Liver 2.2 ? 10.sup.6 1 ? 10.sup.6 2.7 ? 10.sup.5 Fat 8.4 ? 10.sup.6 6.7 ? 10.sup.5 2.8 ? 10.sup.5

TABLE-US-00002 TABLE 1B Average weight (g) of abdominal fat per mouse and total cells, lymphocytes, T cells and iNKT per gram of abdominal fat. Ave weight fat Total Lymphocytes/ T cells/ iNKT pad/mouse (g) cells/g g g cells/g 0.6 14 ? 10.sup.6 1.12 ? 10.sup.6 0.95 ? 10.sup.6 4.6 ? 10.sup.5

[0072] We also characterized other immune subsets in adipose. ?40% of adipose T cells were CD4.sup.+ and 20% were CD8.sup.+, which do not significantly differ from liver or spleen levels. ?10% of lymphocytes in adipose were NK cells, slightly elevated but not significantly different to spleen or liver levels. However, ?15% of adipose T cells were NK receptor (NKR).sup.+ T cells, significantly more than spleen, although less than in liver (FIG. 1C).

[0073] iNKT are a heterogenous subset, with two major distinct subsets: CD4.sup.+CD8.sup.? (CD4) and CD4.sup.?CD8.sup.? (DN), as well as a small subset of Th1-biased cytotoxic CD8.sup.+CD4.sup.? (CD8) T cells in humans (Kim et al., Trends Immunol. 23:516-9, 2002). In murine liver, DN iNKT are potent anti-tumor cells (Crowe et al., J Exp Med. 202:1279-88, 2005). In our current studies, we found that adipose-derived iNKT were mainly CD4.sup.+ (60%), which was slightly lower than in liver and spleen, and approximately 35% were DN, not significantly more than seen in liver (27%) and spleen (28%) (FIG. 1D). We also identified a discrete, minor population (0.6%) of CD8.sup.+CD4.sup.? iNKT in fat that was absent in liver and spleen. A population of CD4.sup.+CD8.sup.+(DP) iNKT was also detected in each organ, with significantly more seen in adipose than liver. iNKT subsets upregulate NK1.1 during late development, either in thymus or as recent thymic emigrants in the periphery (McNab et al., J Immunol. 179:6630-7, 2007). In adipose, significantly more iNKT expressed NK1.1 than in liver or spleen (FIG. 1D). Elevated expression of the activation marker CD69 by adipose iNKT was not statistically significant (FIG. 1D).

EXAMPLE 2

iNKT Cells are Depleted in Fat and Liver During the Development of Obesity

[0074] iNKT cells are reduced in the circulation of obese patients compared to lean healthy age-matched controls (FIG. 2). A cross-sectional analysis of obese patients found that obese patients who had lost weight over 18 months following bariatric surgery, had significantly increased circulating iNKT cells levels compared to patients pre-bariatric surgery, although iNKT cells were still reduced compared to lean controls (FIG. 2). We then followed a small group of patients (n=7) longitudinally pre- and post-bariatric surgery, whose BMI decreased from Grade III obesity (mean BMI>50) to Grade II obesity (mean BMI 35-40) over 18 months post-surgery (FIG. 2). Peripheral iNKT cell levels increased in each patient following weight loss (FIG. 2).

EXAMPLE 3

Cytokine Production by Adipose Tissue iNKT

[0075] Following injection of ?GC, adipose iNKT did not produce IFN? in vivo, unlike iNKT in liver or spleen (FIG. 3A, p=0.01). Adipose-derived iNKT also produced slightly less IL-4. However, adipose iNKT produced significantly more IL-10 (FIG. 3A, p<0.01). To verify the cytokine profile, iNKT were isolated (>90% purity) and stimulated in vitro with ?GC. Adipose-derived iNKT produced significantly less IFN? than splenic or hepatic iNKT in vitro. IL-4 production did not differ per iNKT origin. Further confirming the in vivo experiments, adipose iNKT produced significantly more IL-10 per cell than iNKT from liver or spleen (FIG. 3B).

EXAMPLE 4

iNKT are Depleted in Diet-Induced and Genetic Obesity

[0076] We tested the effect of obesity on adipose-derived iNKT using two models: diet-induced obesity (DIO) and obesity due to leptin deficiency (ob/ob). Previous studies have shown that hepatic iNKT and CD1d expression are reduced in ob/ob and DIO livers (Li et al., Hepatology. 42:880-5, 2005), and that reconstitution of iNKT results in reduction of hepatic steatosis (Elinav et al., J Pathol. 208:74-81, 2006). In our studies, mice fed HFD for 8 weeks had markedly reduced levels of iNKT in adipose, liver, and spleen (FIGS. 4A and 4B). Ob/ob were heavier and had higher fasting blood glucose than DIO mice at 14 weeks of age. The reduction of iNKT was more pronounced in ob/ob mice than DIO mice (FIGS. 4A and 4B, p=0.004 ob/ob vs wt SFD), with iNKT almost absent in adipose and liver.

[0077] As described above, iNKT cells home to and are enriched in murine adipose tissue. In mice, iNKT cells are also enriched among T cells in liver and significant numbers are found in spleen (1-2%). Mice fed a HFD for 8 weeks had markedly reduced levels of iNKT cells in adipose tissue and liver (FIGS. 5A and 5B). iNKT cell depletion was more pronounced in ob/ob.sup.?/? mice (FIG. 5B), which were heavier and had higher fasting blood glucose than DIO mice. We next analyzed iNKT cell levels during the development of obesity. As expected, mice gained significantly more weight each week on HFD, and epididymal fat pads dramatically increased during the development of obesity (FIGS. 6A and 6B). iNKT cells in adipose tissue were significantly reduced as early as week 2 of HFD challenge and steadily declined each week during the course of the HFD challenge (FIG. 5C). iNKT levels also declined in the liver upon HFD challenge, but significant differences were not seen until week 6. Splenic iNKT cell levels fluctuated between mice with an overall, although not statistically significant, depletion at week 10 (FIG. 5C). Mice were next removed mice from HFD after 6 weeks or 10 weeks and returned to SFD, which caused a slight drop in overall weight, but a dramatic reduction in fat pad weight (FIG. 5D). There was a significant increase in iNKT cells in fat and liver within a week of SFD after 6 weeks of HFD and a non-significant increase after removal from 10 weeks of HFD (FIG. 5D). These findings show that murine data parallel human iNKT data in obesity remarkably well.

EXAMPLE 5

Implication of Adipose Tissue iNKT in Metabolic Control

[0078] We studied the relationship between iNKT and obesity and related metabolic syndrome in two models: (1) CD1d knockout (KO) mice, which lack all NKT, but have normal levels of T and other immune cells, and (2) V?24J?18 transgenic (Tg) mice which overexpress functional iNKT with human V?24 TCR (Capone et al., J Immunol. 170:2390-8, 2003). These models, along with wt mice, were fed HFD for 6 weeks from 6 weeks of age. After 6 weeks on HFD, wt mice weighed significantly more (FIGS. 7A and 7B) and had more abdominal fat than SFD wt mice (FIG. 7C). However, CD1d KO mice gained significantly more weight that wt mice on HFD (FIGS. 7A and 7B, p<0.05). They also gained significantly more weight than V?24 Tg mice on HFD. V?24 Tg mice on HFD did not differ in weight from wt mice on SFD (FIG. 7A). CD1d KO mice also had significantly more abdominal fat than wt on HFD and V?24 Tg mice; however, HFD V?24 Tg mice did not differ in abdominal fat mass compared to wt mice on SFD (FIG. 7C). The CD1d KO versus V?24 Tg data illustrate a protective effect of iNKT in obesity.

[0079] CD1d KO mice had severely impaired fasting blood glucose levels, with fasting glucose in the diabetic range, significantly higher than other groups (FIG. 7D, p<0.001). There was no difference between fasting glucose levels in V?24 Tg compared to wt mice on SFD (FIG. 7D). Ninety minutes post-challenge, glucose levels in CD1d KO mice were significantly higher than wt on HFD (p=0.01) and SFD (p=0.001) and HFD V?24 Tg mice (p=0.001) (FIG. 7E). V?24 Tg mice, however, were protected from this metabolic consequence, as their glucose levels were lower than HFD wt (p<0.05) and did not differ from wt on SFD (FIG. 7E). CD1d KO mice on a HFD also showed trends toward higher fasting insulin levels (FIG. 7E) and increased insulin resistance measured by HOMA-IR (FIGS. 7F and 7G). These differences did not reach statistical significance, possibly due to experimental variability in such assays.

[0080] In a second experiment, CD1d KO mice were fed a HFD for 5 weeks from 6 weeks of age and compared to wt mice on the same HFD and on a SFD. CD1d KO mice gained significantly more weight than wt mice on a HFD (FIG. 8A). CD1d KO mice on HFD had strikingly higher fasting blood glucose than wt and elevated fasting insulin levels and insulin resistance, although these were not statistically significant, possibly due to higher variability inherent in these insulin assays (FIG. 8B). CD1d KO mice also had larger adipocytes, as measured by immunohistochemistry (FIG. 8C).

[0081] We also performed experiments on J?18 KO mice, which completely lack iNKT cells but have an otherwise normal immune system. These mice were fed HFD from 6-8 weeks of age for 8 weeks, alongside age-matched wt mice on HFD or SFD. Weight measurements as well as dual energy x-ray absorptiometry (DEXA) scanning showed that J?18 KO mice were slightly but significantly larger before HFD challenge, although they also gained significantly more weight than wt mice on HFD, and had significantly larger fat pads, while lean mass was unchanged (FIGS. 9A and 9B). There was no difference in food intake in J?18 KO and wt mice each week (FIG. 10A). Examination of adipocytes by osmium fixation and particle counting found that adipocytes were larger, but fewer in number in J?18 KO mice than wt on HFD (FIGS. 9C and 9D). Furthermore, J?18 KO mice had more fat deposition in liver than wt on HFD (FIG. 9E). Metabolic parameters were also worse in the absence of iNKT cells; fasting blood glucose levels were elevated and glucose tolerance was significantly impaired in J?18 KO mice (FIG. 9F). Furthermore, insulin resistance was increased in J?18 KO mice (FIG. 9F). Serum leptin levels were similarly elevated in both wt and J?18 KO mice on HFD compared to SFD (FIG. 9F).

[0082] The above experiments were performed on males. As there have been some reported sex difference in severity of certain aspects of obesity, we also investigated if female J?18 KO mice had similar metabolic outcome following HFD compared to wt females (FIGS. 10A-10E) Like males, female J?18 KO mice gained significantly more weight than wt females in the first 4 weeks of HFD challenge. Thereafter weight gain was increased but not significantly compared to wt (FIG. 10B). This correlated with eating behavior. At 4 weeks, female J?18 KO mice had reduced food intake compared to wt females unlike males, which had almost identical food intake patterns in wt and J?18 KO mice (FIG. 10A). Lean mass was similar, but both overall fat mass, as measured by DEXA scanning, and fat pad weight were significantly higher in J?18 KO females, similar to males (FIG. 10D). Adipocytes were also significantly larger and fewer in number in J?18 KO females than wt (FIG. 10D). Furthermore, the degree of fat deposition in liver was greater in J?18 KO females compared to wt on HFD (FIG. 10E). Fasting glucose was unchanged and GTT was not impaired in J?18 KO compared to wt females on HFD (FIG. 10C).

EXAMPLE 6

Macrophages in SFD or HFD wt, CD1d KO, & V?24 Tg Mice

[0083] A major function of iNKT is recruitment and regulation or activation of other immune cells (Bendelac et al., Annu Rev Immunol. 25:297-336, 2007; Cerundolo et al., Nat Rev Immunol. 9:28-38, 2009). Macrophage infiltration into adipose in obesity plays an important role in development of insulin resistance and adipose inflammation, possibly due to characteristic changes in adipose tissue macrophages (ATM) in obesity (Lumeng et al., J Clin Invest. 117:175-84, 2007). F4/80.sup.+CD11c.sup.+ cells, which when activated, clasically display enhanced production of inflammatory cytokines such as IL-6, IL-12, and TNF-? are seen in obese adipose. By contrast, alternatively-activated anti-inflammatory macrophages (F4/80.sup.+CD11c.sup.?) generating high levels of anti-inflammatory cytokines like IL-10 are found in lean adipose but are decreased in obesity (Lumeng et al., supra) and such macrophages can be modified by NKT (Kim et al., Nat Med. 14:633-40, 2008).

[0084] We investigated the influence of adipose iNKT on macrophage infiltration and activation. We did not detect any significant difference in overall macrophage levels (F4/80.sup.+ cells) in adipose in each mouse group, although there was a trend towards higher macrophage levels in CD1d KO compared to wt mice on SFD and V?24 Tg mice (FIG. 11B). However the phenotype of ATM was different between groups (FIGS. 11A and 11C). There were significantly more F4/80.sup.+CD11c.sup.+ ATMs in CD1d KO than in wt mice on HFD and V?24 Tg mice. WT mice on SFD had similarly low levels of F4/80.sup.+ CD11c.sup.+ macrophages as Tg mice. This suggests that adipose iNKT can play a critical role in the phenotypic switch of ATM seen in obesity (Lumeng et al., supra), and therefore may regulate metabolic control through their effects on resident ATM. In the absence of iNKT, there was a significant increase in pro-inflammatory ATM. When iNKT were overexpressed, the macrophage profile was similar to that seen in mice on SFD, with an increase in anti-inflammatory macrophages. Such ATM can regulate insulin resistance through IL-10 mediated reversal of TNF-? induced insulin resistance (Lumeng et al., supra).

[0085] Pro-inflammatory M1 macrophages (F4/80.sup.+CD11c.sup.+) are also increased in adipose tissue during the development of obesity, with significant increases seen as early as 1 week after HFD challenge. Furthermore, after removal of HFD for 1 week, pro-inflammatory macrophages were significantly decreased in fat from mice on HFD for 6 and 10 weeks (FIG. 12A). This coincided with a decrease of iNKT cells in fat each week of the HFD challenge (FIG. 12C). There was a strong inverse correlation between iNKT cell levels in fat and pro-inflammatory macrophages (FIG. 12A).

[0086] To determine whether iNKT cells play a causal role in the infiltration and phenotype of macrophages, we investigated macrophages levels in J?18 KO mouse in obesity (FIG. 12B-12D). In the absence of iNKT cells, there were higher overall macrophage levels in adipose tissue, as measured by flow cytometry (FIG. 12B) and confirmed by immunohistochemical staining of adipose tissue with F4/80 (FIG. 12C) and CD68 (FIG. 12D). Furthermore there adipose tissue macrophages displayed increased M1 phenotype in J?18 KO mice, compared to wt on HFD, as measured by flow cytometry (FIG. 12B). We also looked at macrophage levels and phenotype in CD1d KO mice on HFD. CD1d KO mice had similarly high levels of F4/80 macrophages in adipose tissue compared to wt mice on HFD, but had significantly more M1 macrophages than wt on HFD (FIG. 13).

EXAMPLE 7

Mice Lacking iNKT Cells Show Metabolic Disorder on SFD

[0087] Both J?18 KO mice and CD1d KO mice lacking iNKT cells have overtly normal immune systems and do not display any pathological susceptibilities, unless challenged with certain pathogens or tumor. We observed that both J?18 KO mice and CD1d KO mice generally weighed more as they aged, compared to wt mice. This led us to investigate for any evidence of metabolic syndrome in these mouse models fed ad lib for 4-5 months on SFD (FIGS. 14A-14D). Both J?18 KO mice and CD1d KO mice consistently weighed significantly more than their wt aged matched counterparts (FIG. 14A). Immunohistochemical staining in fat also revealed that J?18 KO mice and CD1d KO mice had larger adipocytes on SFD compared to wt on SFD (FIG. 14B). Surprisingly, they also had greatly increased serum triglycerides and TNF?, and non-significantly elevated IL-6 levels (FIG. 14C). Increased adipocyte size and pro-inflammatory cytokines are usually linked with macrophage infiltration and other inflammtory indices in fat, and we found adipose tissue macrophages in these mice were significantly increased, with less M2 in both iNKT knockouts and and more M1 macrophages in J?18 KO mice on SFD (FIG. 14D). J?18 KO mice and CD1d KO mice on SFD had elevated fasting glucose but not significantly so. GTT was elevated in CD1d KO mice but not significantly impaired (FIG. 14E).

EXAMPLE 8

Adoptive Transfer of iNKT Cells in Obese J?18 KO Mice Dramatically Effects Adipocyte Size and Number and Improves Glucose Handling

[0088] To determine whether iNKT cells play a protective role against the development of obesity-induced metabolic syndrome, we adoptively transfered 5?10.sup.5 iNKT cells from wt liver into obese J?18 KO mice. Following i.p. injection of iNKT cells, J?18 KO mice continued on HFD for 4 days, at which time the mice were measured for metabolic outcomes. Mice that received iNKT cells had lower fasting glucose and improved GTT compared to mice receiving contol PBS. Insulin resistance was improved but not significantly, apparently due to variability in fasting insulin (FIG. 15A). Mice that received iNKT cells also failed to gain weight on the 4 days of HFD following injection, whereas mice receiving PBS continued to gain weight (FIG. 15B). Also, mice that received iNKT cells had decreased fat pad weight, although this was not statistically significant. Adoptive tranfer of iNKT cells into obese J?18 KO mice also had a rapid and dramatic effect on adipocytes, which were increased in number and reduced in size after iNKT transfer (FIG. 15C).

EXAMPLE 9

?GC Treatment Expands and Activates iNKT Cells, Results in IL-10 Production in Adipose Tissue, Protection from Inflammation, Adipocyte Hypertrophy, and Metabolic Disorder

[0089] The prototypical ligand for iNKT cells is the glycolipid, ?GC. We investigated whether ?GC treatment could activate the residual iNKT cells in obesity and improve metabolic outcome (FIGS. 16A-16H). Following one injection of ?GC and continued HFD for 4 days, mice lost a significant amount of overall weight and % body fat, but not lean mass, as measured by DEXA scanning (FIGS. 16A and 16B). This weight loss was not seen in obese J?18 KO mice that have no iNKT cells (FIG. 6A), confirming that ?GC treatment is specific for iNKT cells, as is well documented. ?GC treatment also caused a rapid and dramatic reduction in adipocyte size, but did not affect cell number (FIG. 6B). ?GC treatment resulted in marked reduction of fasting blood glucose compared to PBS control injection. This improvement in fasting glucose was not seen in obese J?18 KO mice, whose fasting glucose was extremely high (FIG. 16C). ?GC treatment also caused improved GTT, returning it to almost normal, which was not seen in obese J?18 KO mice. ?GC treatment did not affect fasting glucose or GTT in normal weight mice on SFD with normal glucose levels and handling (FIG. 16C). WT obese mice that received ?GC also had significantly improved insulin resistance, serum triglycerides, and circulating leptin (FIG. 16D). Serum IL-6 decreased, but surprisingly, serum levels of TNF? were increased (FIG. 16E). ?GC treatment also effected fat deposition in the liver. Fatty infiltration was still seen in obese mice that received ?GC, but the fat droplets were smaller and less frequent, compared to mice that received PBS (FIG. 16F).

[0090] We next looked at the effect of ?GC on iNKT cells in fat, liver, and spleen in obese mice. iNKT cells in liver and spleen produced both IFN? and IL-4 within 4-5 hours. In contrast, adipose tissue iNKT cells produced little IFN?, but more IL-4 and IL-10, than those in spleen and liver (data not shown). We also investigated the effects of ?GC on iNKT cells 4 days post-injection, at the time of metabolic analysis. ?GC caused expansion of iNKT cells by day 4 in spleen and liver but the expansion was greater in fat (FIG. 16G). Furthermore, iNKT cells in adipose tissue were still producing cytokines at day 4 post-injection, unlike those in spleen and liver. iNKT cells in adipose tissue from obese mice produced IL-4, IL-10, and IFN-? at day 4 (FIG. 16G). As adipose tissue iNKT cells are skewed towards IL-4 and IL-10 production, we next investigated whether IL-4 and IL-10 were mediators of this protection seen by ?GC treatment. We neutralized IL-4 and IL-10 prior to ?GC treatment and measured metabolic outcomes after 4 days. Mice that received anti-IL-4 and anti-IL-10 before ?GC injection did not experience any improvement in GTT, wherewas mice that received isotype control mAb and ?GC (FIG. 16H), illustrating ?GC treatment acts specifically on iNKT cells through production of anti-inflammatory cytokines.

Materials and Methods

[0091] The following materials and methods were used in the experiments described herein.

[0092] Mice

[0093] Male (and where indicated, female) wt C57BL/6 and ob/ob.sup.?/? mice were purchased from Jackson Laboratories (Bar Harbor, Me.). J?18 KO mice and C57BL/6J CD1d KO mice have been described (Exley et al., Immunology 110:519-526, 2003). In general, experiments began with six-week-old male mice or J?18 KO and wt female mice. For metabolic studies, the mice received either SFD or HFD (Research Diets, 60 kcal % fat for the HFD), from 6 weeks of age for 6 weeks. Mice were housed under specific pathogen-free conditions. Animal experiments were performed in accordance with protocols approved by Institutional Animal Care and Use Committee.

[0094] Subjects

[0095] Ten milliliters of peripheral blood were obtained from 26 consecutive obese subjects who were referred to our hospital-based weight-management clinic (mean age 47, range 24-60 years; mean BMI 48), and 18 patients attending the weight management clinic 18 months after bariatric surgery (mean age 46, range 36-54 years; mean BMI 38) and 22 lean healthy controls (mean age 39, range 23-54 years; mean BMI 24). All blood samples were obtained with written informed consent. The ethics committee at St. Vincent's University Hospital, Dublin granted approval for this study.

[0096] Reagents

[0097] ?GC analogue PBS-57-loaded or empty CD1d tetramers were provided by the NIH tetramer facility (Emory Vaccine Center, Atlanta, Ga.). ?GC (KRN 7000) was purchased from Avanti, Inc. Immune cells were cultured in RPMI-1640, adipose tissue-derived cells in Dulbecco's Modified Eagle Media (DMEM), supplemented with penicillin, streptomycin (Mediatech, Manassas, Va.), and 5% FBS (Hyclone, Logan, Utah).

[0098] Diet and Metabolic Studies

[0099] Wt, J?18 KO and CD1d KO were weighed weekly and food intake was monitored on HFD. Body fat content was measured by an X-ray emitting DEXA scan, performed after mice were sacrificed. Whole abdominal adipose fat pads were weighed after dissecting out the testes and lymph nodes. After 6 weeks on HFD, fasting blood glucose (OneTouch Ultra) and insulin concentrations (Crystal Chem ELISA) were measured. For glucose tolerance tests, fasted (10 h) mice received 1 g glucose per kg body weight intraperitoneally (i.p); for insulin resistance, the homeostatic model assessment of insulin resistance (HOMA-IR) was used (Matthews et al., Diabetologia 28:412-419, 1985) was used: fasting blood glucose x fasting insulin/22.5. Two samples of 5 mm liver were collected and fixed in formalin overnight, prior to paraffin mounting and preparation of H&E or Oil Red O stained slides for measurement of fatty liver or adipose prior to aGC (or control) treatment. For H&E and Oil Red O staining, biopsies were viewed using the 20? objective. Degree of fatty liver was measured by Oil Red O staining intensity around 5 portal tract areas per slide.

[0100] Adipocyte Size

[0101] Adpocyte size and number were measured by osmium and immunohistochemistry. Two samples of 20-30 mg of adipose tissue per mouse were immediately fixed in osmium tetroxide (3% solution in collidine 0.05 M), minced into 1 mm pieces and incubated in the dark at room temperature for 48 hours. Adipose cell size and number were determined by a Beckman Coulter Multisizer III Counter with a 400 ?m aperture. Adipose tissue was also fixed in formalin overnight, prior to paraffin mounting and preparation of H&E slides. Adipocyte number was counted per field of view, in ten fields per sample and related back to the original weight of each fat pad.

[0102] Spleen, Liver and Adipose Tissue, and Human Blood Preparations

[0103] Isoflurane-anesthetized mice were systemically perfused with PBS. Single cell suspensions from spleens were prepared by standard techniques. Liver MNC were isolated as previously described without collagenase digestion (Nowak et al., Eur J Immunol 40:682-7, 2010). Briefly, livers were perfused with PBS, minced and iNKT cells were enriched by centrifugation in a two-step Percoll gradient. Enriched populations typically contained 20-30% iNKT cells. Adipose tissue was dissected carefully, avoiding lymph nodes, minced with opposing scalpels and digested with collagenase (Sigma, 0.2 mg ml.sup.?1 in DMEM for 45 min at 37? C. on a rotary shaker). The digests were filtered through 40 ?m cell strainers and pelleted to enrich fat-associated lymphocytes in the SVF. Cell yields and viability were measured with trypan blue staining.

[0104] Ten milliliters of venous blood was collected in heparinized tubes for measurement of iNKT cell levels. Peripheral blood mononuclear cells were prepared by standard density gradient centrifugation over Lymphoprep (Nycomed) at 400 g for 25 min. Cells were then washed twice with HBSS supplemented with HEPES buffer solution (Invitrogen Life Technologies) and antibiotics. Cell pellets were re-suspended in 1 ml of RPMI 1640 medium, and cell yields and viability were assessed by ethidium bromide/acridine orange staining. The cell suspension was adjusted to 1?10.sup.6 cells/ml in RPMI for staining (100 ?l/tube).

[0105] Flow Cytometry

[0106] Single cell suspensions of splenocytes, liver mononuclear cells (LMNCs), and adipose SVF were blocked with anti-CD16/32 mAb and stained for 30 min at 4? C. in the dark with PBS-57-loaded or empty CD1d tetramer-PE (NIH tetramer facility) and CD3 (1:150 dilution, eBiosciences). Macrophages were labeled with phycoerythrin-conjugated antibody to F4/80 (1 in 100) and CD11c (1 in 200) and CD206 (1 in 200) to differentiate M1 from M2 macrophages in the SVF as previously described.

[0107] For human peripheral blood, mouse anti-human CD3 combined with the iNKT TCR (6B11) and isotype-matched controls were used (BD Biosciences). iNKT cells were also stained with V?24 and V?11 TCR chains from Coulter Immunotech (Marseilles, France). Cells were washed and fixed in 1% PFA and acquired on an LSR II flow cytometer (BD Bioscience) and with FlowJo and Kaluza software.

[0108] iNKT Cell Isolation and Adoptive Transfer

[0109] Hepatic mononuclear cells were stained with CD1d tetramer-PE and sorted to >95% purity using a FacsAriall (Becton Dickinson, Calif.). Purified iNKT cells (5?10.sup.5) were injected i.p. into J?18 KO mice which had been on HFD for 8 weeks. Metabolic parameters were analyzed after 4 days, mice were sacrificed, adipose tissue was weighed, and adipocytes were measured by osmium and immunohistochemistry.

[0110] In Vivo Stimulation of iNKT Cells and Intracellular Cytokine Staining

[0111] Mice were injected i.p. with 2 ?g of ?GC or vehicle, and mice were sacrificed after 5 hours or 4 days, at the time of metabolic analysis. Single cell suspension of splenocytes, LMNC, and adipose tissue SVF were obtained as before, but with the inclusion of Brefeldin A in all media. Single cell suspensions of splenocytes or liver mononuclear cells (LMC) were stained firstly with cell surface labeling anti-CD3 mAb and ?GC-loaded CD1d tetramer. Cells were then fixed, permeabilized, and intracellular cytokine stained for IL-4, IL-10 and IFN-? using Cytofix/cytoperm (BD Biosciences), according to the manufacturer's instructions.

[0112] Statistical Analyses

[0113] Error bars represent the standard error of the mean. The statistical significance of differences between two groups was determined in human data using Mann-Whitney or Student's t-tests, where appropriate. Differences among mice groups were evaluated using one-way or two-way ANOVA followed by post hoc Tukey tests. Values of p<0.05 were considered significant.

[0114] Other Embodiments

[0115] All patents, patent applications, and publications mentioned in this specification are herein incorporated by reference to the same extent as if each independent patent, patent application, or publication was specifically and individually indicated to be incorporated by reference.