While our understanding of the etiology of ulcerative colitis (UC) has grown over the years, the picture emerging is one of a complex interplay between genetic,1,2 microbial,3 and environmental factors4 as well as intestinal epithelial function5 and the mucosal immune system.6 What is also apparent is that no factor alone appears to be sufficient to trigger the development of the disease and the contribution of each individual component may vary between patients.7 The clinical presentation of UC depends on the extent and severity of the disease; however, predominant features include blood in stool, bowel frequency, passage of mucopus, and abdominal pain and tenesmi.8
Effective clinical management of active UC requires a comprehensive understanding of the disease extent, the severity as well as the potential risks and benefits of the available interventions, with a focus on induction and maintenance of remission. Corticosteroids remain the cornerstone of initial therapy, yet a third of patients will fail to respond9 and further management involves critical and timely decisions on whether to use rescue therapy in the form of immunomodulatory drugs such as cyclosporine A or anti-tumor necrosis factor (TNF) therapies such as infliximab.10 Current data suggest that rescue with cyclosporine A and infliximab are efficacious in the short- to medium-term perspective11,12 but the long-term outcome seems less favorable.13 Furthermore, a significant proportion of UC patients will have recurrent flares or chronic continuous disease despite receiving conventional symptomatic treatment, and within a 10-year period some 20% of these patients will require surgical intervention.14
New understanding of the underlying pathogenesis of UC has spurred the development of new biological therapeutics,15 and continued use of conventional therapies has allowed optimization strategies to be designed and tested under appropriate clinical settings.16
The synthetic DNA-based immunomodulatory sequence 0150 (DIMS0150) is a first in class compound under clinical development for severe, chronic active, treatment-refractory UC. It functions as an immunomodulator and induces the activation of the Toll-like receptor 9 (TLR9) pathway in effector cells such as T and B lymphocytes, dendritic cells, and macrophages.17 These cells reside in abundance on mucosal surfaces.18 TLRs play an essential role in the perception of pathogens and shape the complex host immunological responses that occur during infection.19,20 Prior in vitro and in vivo studies (data not published) designed to elucidate the mode of action of DIMS0150 suggest the compound is capable of restoring a subject's sensitivity to glucocorticoids through activation of the TLR9 receptor. Activation results in the production of specific cytokines such as IL-10 and type I interferons from human peripheral blood mononuclear cells (PBMCs). Theses cytokines have been demonstrated to increase steroid sensitivity in cells derived from steroid-resistant UC patients21 and human monocytes.22 Local colonic administration of DIMS0150 in steroid-refractory UC subjects places the agent in direct contact with an abundance of target cells harboring the TLR9 receptor. Upon activation, these cells produce steroid-sensitizing cytokines which, in addition to inducing a local sensitizing effect, are able to enter the systemic circulation and induce a peripheral steroid-sensitizing effect. This appears to be more likely than a direct systemic response to DIMS0150 which, with a molecular size of around 6000 Da, is not able to enter the general circulation following colonic administration. Indeed, there is little evidence to support systemic exposure following colonic delivery. The lack of systemic exposure may also underlie the favorable safety profile observed in preclinical and clinical studies with DIMS0150 (data not published).
We report here the use of DIMS0150 as add-on therapy for the treatment of chronic active UC patients on concomitant glucocorticoid therapies as presented by an uncontrolled, prospective treatment series comprised of eight patients.
MATERIALS AND METHODS
Over the course of 2½ years eight chronic active UC outpatients were treated with DIMS0150 as an add-on to their current therapies, with one special case subject receiving three doses of DIMS0150 with 4 weeks between dosing occasions. A diagnosis of UC was established based on clinical, endoscopic, and histological features. Written consent was received for all patients and the treatment approved by the relevant local Ethics Committees.
All patients were considered for elective colectomy based on the treating physician and surgeon's assessment. All were judged as being treatment failures with a documented history of not responding adequately to effective dosing regimes of available treatments including high-dose intravenous glucocorticoids. Additionally, all patients had previously received two applications of infliximab at 5 mg/kg with 2 weeks between dosing occasions but completely failed to show any response. As this apparent lack of response occurred at the initiation of infliximab treatment, it was reasoned that it was related to low or missing efficacy rather than due to the induction of antibodies. Due to the persistent severe condition of the disease, further treatment with infliximab was not recommended, as this would have required patients to endure their condition for an additional 4 weeks according to the infliximab induction scheme. As a result, all patients were offered DIMS0150 treatment instead.
All subjects were on a stable and tolerable dose of glucocorticoid medication; baseline characteristics are given in Table 1. Subjects who were deemed likely to require prompt clinical intervention or cases of expected colectomy were not considered.
The suitability of DIMS0150 as a potential rescue therapy to prevent colectomy, on a mid-term basis of 6 months, if colectomy was elected as the preferred treatment option, was evaluated. Other objectives addressed response (a decrease in Clinical Activity Index [CAI] score by ≥5 units from baseline) or remission (CAI score of ≤4 points) and the prevention of colectomy on a long-term basis of more than 6 months.
Endoscopy was assessed according to the Rachmilewitz composed activity index23 scale (0–12) where complete endoscopic remission is represented by 0–3. Histological assessments were made in accordance with the Geboes24 scale (0–5) where likewise complete resolution is indicated by a score of zero. Complete clinical remission was defined as a CAI score of 0 or 1, with a concomitant endoscopic score of 0–3. Clinical assessment of all efficacy parameters were made at weeks 1, 4, and 12 for those subjects receiving a single dose of DIMS0150 and additionally at weeks 8, 26, 28, and 36 for the multidosed subject. Those patients who received additional dose(s) of DIMS-1050 due to a relapse of symptoms were likewise evaluated at weeks 1, 4, and 12. For all visit occasions, adverse events were recorded.
On no occasion were any adverse events recorded in relation to treatment with DIMS0150.
Seven of the eight selected patients received a single intracolonic dose of 30 mg of DIMS0150 diluted in 50 mL of sterile water in addition to their current treatments. Application of the drug was performed during colonoscopy with the aid of a spraying catheter inserted through the colonoscopy's biopsy channel and delivered approximately to the upper portion of the descending colon or to the transverse region. In instances of a relapse (as determined by a deterioration of the disease of ≥4 CAI units) an additional dose(s) of DIMS0150 was offered and the patient subsequently followed.
One special case patient received three doses of DIMS0150 at 4-week intervals and blood samples were obtained prior to each treatment. PBMCs derived from these blood samples were subsequently analyzed for steroid sensitivity. Table 2 outlines patient clinical response parameters at weeks 1, 4, and 12 and time of additional dose(s) in those subjects who experienced a relapse.
Determination of Steroid Sensitivity
Around 30 mL sodium heparinized blood was taken from the patient prior to each DIMS0150 dosing occasion (0 days, week 4, and week 8) and at weeks 12, 26, and 36. For control, blood samples from 10 healthy individuals were taken under prior written consent. PBMCs were separated on Ficoll-Hypaque by gradient centrifugation at 400g for 30 minutes at 20°C. Thereafter, the cells were harvested from the plasma/Ficoll interface and washed 3 times in phosphate-buffered saline (PBS, pH 7.4; Ca2+ and Mg2+ free). The number and viability of the cells were determined by Trypan blue exclusion. The cells were diluted to 107 cells/mL with RPMIc (RPMI 1640 containing 10% heat-inactivated fetal bovine serum [FBS], PeSt [100 U/mL penicillin, 100 μg/mL streptomycin], 2 mM L-glutamine, 5 μg/ mL gentamycin, and 5 mM Hepes). Isolated PBMCs were cultured in 96-well culture plates (Becton Dickinson, San Jose, CA) at a concentration of 0.5 × 106 cells/well. Ficoll-Paque was purchased from Amersham Bioscience (Uppsala, Sweden); PBS, gentamycin, and FBS were purchased from Gibco-Invitrogen (La Jolla, CA), and RPMI, PeSt, glutamine, and Hepes were purchased from Sigma Aldrich (Sweden).
In Vitro Stimulation
Immediately after plating, cells were stimulated with lipopolysaccharide (LPS) (100 pg/mL) (InvivoGen, San Diego, CA) in the presence or absence of Dexamethasone (Sigma Aldrich) (10−6, 10−8, or 10−10 M). RPMIc medium alone served as a negative control. Cells were incubated in a humidified SteriCycle CO2 cell culture incubator (Thermo Forma Steri-Cycle, Marietta, OH) at 5% CO2 in air at 37°C for 48 hours. Cell supernatants were then harvested to measure their cytokine content.
Detection of Secreted Cytokines
Interleukin 6 (IL-6) was measured by cytometric bead array (CBA) (Becton Dickinson Biosciences, Heidelberg, Germany) Flex kit according to the manufacturer's protocol on a FACSArray flow cytometer followed by analysis using FCAP Array software (BD Biosciences). The lower detection limit was 20 pg/mL for IL-6 cytokine.
Ethical approval for the treatment of patients with DIMS0150 was granted by the local ethics authority and performed with written consent by the participating patients. For the one subject receiving three consecutive doses of DIMS0150, blood was taken prior to each dose with written consent from the subject.
Efficacy After a Single Dose
After treatment with DIMS0150, 43% (3/7) of patients demonstrated a clinical response at week 1, with one case of clinical remission. By week 4, 71% (5/7) of patients had a clinical response and 43% (3/7) were in remission. At week 12 clinical response and remission rates were 86% (6/7) and 71% (5/7), respectively, with two cases of complete clinical remission. Figure 1a illustrates the individual CAI scores of the patients up to 12 weeks postdosing and Figure 1b shows the median CAI score in the same period.
Endoscopic evaluation at week 1 showed that 86% (6/7) had a decrease in their endoscopic index of ≥2 units from baseline, with one subject (p4) recording a decrease of five units. At week 4, two patients (p3 and p4) were in endoscopic remission and four of the remaining five patients had a baseline improvement of ≥4 units or more. By week 12, 43% (3/7) of patients were in complete endoscopic remission, with further improvement noted for four of the remaining five patients (Table 3). Figure 2a,b provides individual and median endoscopic scores across the 12-week period, respectively. For histological evaluation, three biopsy specimens representing three colonic regions (ascending, transverse, and descending) were taken from the same area at baseline and after treatment and the scores are given in Table 2. Overall, there was a marked improvement in histological scores at week 12 in over 50% (4/7) of subjects with a decrease of at least ≥2 units from baseline. Improvements were also reflected in the extent of the disease, with three patients experiencing reduced colonic involvement.
Four patients (p1–p4) were given additional doses of DIMS0150 due to a relapse of symptoms at the times indicated (Table 2), the first of these occurring 5 months after the initial dose. All subjects had an improvement in their CAI scores following further treatment with DIMS0150. As a result of responding to DIMS0150, all, with the exception of one patient, have so far avoided the need for colectomy, with the longest period currently being around 27 months (Fig. 3). Despite the initial response to DIMS0150, patient (p1) decided to undergo colectomy following a relapse some 17 months after the first treatment.
All subjects were on a stable and tolerable dose of prednisolone at the time of dosing (baseline) ranging from 10–40 mg/day. Following DIMS0150 treatment the median daily prednisolone dose had been reduced from 20 mg/day to 10 mg/day by week 12, with one subject discontinuing use (Table 4).
Efficacy After Multiple Doses
For the special case patient (p8) we administered three doses of 30 mg DIMS0150 as an add-on to current therapies with 4-week intervals between dosing. In addition to monitoring clinical response, endoscopic, and histological parameters (Table 3), we obtained blood samples immediately prior to each dosing occasion and again at weeks 12, 26, and 36 with the intention of monitoring the patient's steroid sensitivity. Following treatment, the subject was in complete remission at week 8; however, experiencing a slight worsening of symptoms by week 26 (Fig. 4). Our previous work suggests that DIMS0150 functions as a glucocorticoid resensitizer and we wanted to determine whether treatment with DIMS0150 had restored the patient’s glucocorticoid sensitivity. Consequently, the steroid dose was increased from 10 mg to 30 mg per day at week 27 and we noted a marked improvement in the CAI score. By week 36 the patient was in complete clinical and histological remission, suggesting that the subject responded to the glucocorticoid treatment.
Monitoring of Steroid Sensitivity in Response to DIMS0150 Treatment
PBMCs were isolated from the collected blood samples derived from patient (p8) and assayed in vitro for steroid sensitivity. One way to achieve this is to monitor the degree of suppression of LPS-induced IL-6.25,26Figure 5 demonstrates that at the time of receiving the first dose of DIMS0150, PBMCs derived from the subject failed to respond to the applied concentrations of dexamethasone as no suppression of IL-6 was seen, suggesting the subject was steroid resistant.
At week 4, just prior to the second dose of DIMS0150, there was a marked suppression in levels of IL-6 seen with the highest concentration of dexamethasone, indicating a partial response of the subject's PBMCs. By week 8 and just prior to the last dose of DIMS0150, further steroid sensitivity was gained, in that both of the two highest concentrations of dexamethasone could repress IL-6. By week 12, derived PBMCs demonstrated steroid sensitivity levels of normal to better than normal, in that all three concentrations were effective at reducing the levels of induced IL-6, indicating that the subject's steroid response had been further improved. These findings correlated with the marked improvement of clinical symptoms in this subject.
Interestingly, by week 26 the lowest steroid dose was no longer able to repress IL-6, indicating a potentially reduced steroid sensitivity. However, this level of sensitivity was still evidently sufficient for the marked improvement observed in the patient following the increased prednisolone dose. By week 36 the patient's steroid sensitivity had decreased further, as now only the highest dose was able to repress IL-6. Collectively, the in vitro steroid sensitivity of the PBMCs derived from subject (p8) appeared to correlate well with the clinical outcome following DIMS0150 treatment, and supports the findings of Hearing et al,27 who demonstrated that in vitro lymphocyte steroid resistance is correlated with outcome in steroid-treated severe UC.
Total proctocolectomy is typically the procedure of choice for debilitated patients with acute, medically refractory UC.28 While surgical intervention may be curative and provide a better quality of life,29 it is not without considerable risks to the patient30 and the procedure itself presents a significant pre- and postoperative morbidity as well was a substantial economic burden to the healthcare system.31 Consequently, the need for alternative treatments is evident.
The results from the present case series indicate that topical administration of the immunomodulatory agent DIMS0150 may have the potential to induce a clinical response in this particular group of refractory UC patients. For those seven cases that received a single treatment of DIMS0150, 71% (5/7) were in clinical remission, with 43% having complete resolution of endoscopic involvement at week 12. Equally, there was a marked improvement in histological scores, with over 50% of patients demonstrating a reduced score of at least two units from baseline. These findings are important, as achievement of mucosal healing has been associated with better outcome, less surgery, and less hospitalization.32,33 No adverse events were recorded following DIMS0150 treatment, reflecting both our previous clinical experiences of DIMS0150 in over 160 patients and the lack of any significant toxicological findings in both rodent and primate studies.
From the perspective of subjects with intractable UC having chronic, continuous symptoms we observed that treatment with single or multiple doses of DIMS0150 circumvented the need for colectomy in 87% (7/8) of patients, and for some subjects this has meant the return to a more normal quality of life. Induction of sustained remission also has other important implications, as patients with longstanding UC have an increased risk of colorectal cancer.34,35
The subanalysis of patient case (p8) in this report has provided further evidence to support the hypothesis that DIMS0150 functions by imparting a clinical response to glucocorticoids by restoring sensitivity. We have been able to document a shift in the steroid sensitivity status of the patient's PBMCs following three doses of DIMS0150 from one of steroid-resistance to one of steroid-sensitivity by week 12, with the subject being in complete remission. There was a good correlation between clinical response and increased steroid sensitivity to the three concentrations of dexamethasone used. Collectively, the response to dexamethasone indicates a gradual increase in steroid sensitivity in the subjects' PBMCs to the applied steroid concentrations up until week 12. Thereafter there was a progressive decrease in response up to week 36, suggesting a likely return to previous resistant levels. This could be indicative of a potential future relapse despite the subject being in complete remission at the time and that additional treatment of DIMS0150 may be needed to maintain a status of steroid sensitivity.
The observation of improved steroid sensitivity of the subjects derived PBMCs following local DIMS0150 treatment would appear to suggest more than a local action of DIMS0150. Administration of DIMS0150 on colonic mucosa restored steroid sensitivity of peripherally derived PBMCs, indicating a systemic sensitization effect to steroids. This may equally offer an explanation regarding previous clinical observations where the extent of disease appeared not to be an important factor regarding where DIMS0150 was locally administered, as subjects with pan-colitis responded equally well as those with just left-sided involvement. The median daily dose of prednisolone following DIMS0150 treatment decreased to 10 mg/day, with one subject achieving steroid-free remission by week 12. Weaning of prednisolone dosage was initiated at week 4, where most DIMS0150-treated subjects had demonstrated a substantial reduction in their CAI scores and the risk of potentially inducing a relapse could be minimized. Tapering of prednisolone dosage was performed on an individual basis according to the physician's judgment and not to a uniform scheme. The intention was to determine whether it was possible to reduce steroid usage without exacerbating the condition. While a fixed tapering scheme may be appropriate for some patients, a more individual approach was favored. Steroid-free remission is clearly a desirable endpoint and most subjects had reduced daily prednisolone doses at week 12, concomitant with improved CAI scores.
Restoring a patient's sensitivity to glucocorticoids is a valuable option, as they still remain one the most efficacious antiinflammatory agents and are the mainstay therapy for moderate to severe attacks of UC.36 No other class of medication acts as rapidly and with such consistent results to control disease activity, improve patient symptoms and in UC, promote endoscopic and histological improvement.37 Furthermore, the need for other immunomodulatory agents such as cyclosporine,38 where the long-term risks/benefits are not clear,39 could be reduced. Moreover, there are concerns regarding sequential treatment of UC patients with various immunomodulatory bio-logics due to the risk that such patients may progress to complicated and difficult to treat cases of UC where colectomy, in this setting, is inevitable and carries a higher risk of mortality.40 It is possible that the clinical threshold for elective colectomy in subjects with inflammatory bowel disease may be too high41 and the threshold criteria and optimal timing of elective surgery should be carefully evaluated.
In conclusion, the collection of case series presented illustrates the potential usefulness of DIMS0150 to induce clinical remission in cases of steroid-refractory elective colectomy patients with the prospect to reduce the need for colectomy on a long-term basis. While DIMS0150 may offer a much-needed alternative treatment option, its true clinical benefit is currently the focus of an ongoing phase III clinical study.
1. Lees CW. Genetics of ulcerative colitis. Inflamm Bowel Dis. 2011:831–848.
2. Cho JH, Brant SR. Recent insights into the genetics of inflammatory bowel disease. Gastroenterology. 2011;140:1704–1712.
3. Wine E, Ossa JC, Gray-Owen SD, et al.. Adherent-invasive Escherichia coli target the epithelial barrier. Gut Microbes. 2010;1:80–84.
4. Cosnes J. Smoking, physical activity, nutrition and lifestyle: environmental factors and their impact on IBD. Dig Dis. 2010;28:411–417.
5. Schmitz H, Barmeyer C, Fromm M, et al.. Altered tight junction structure contributes to the impaired epithelial barrier function in ulcerative colitis. Gastroenterology. 1999;116:301–309.
6. Heller F, Fuss IJ, Nieuwenhuis EE, et al.. Oxazolone colitis, a Th2 colitis model resembling ulcerative colitis, is mediated by IL-13-producing NK-T cells. Immunity. 2002;17:629–638.
7. Xavier RJ, Podolsky DK. Unravelling the pathogenesis of inflammatory bowel disease. Nature. 2007;448:427–434.
8. Riegler G, Tartaglione MT, Carratú R, et al.. Age-related clinical severity at diagnosis in 1705 patients with ulcerative colitis. Dig Dis Sci. 2000;45:462–465.
9. Faubion WA Jr, Loftus EV Jr, Harmsen WS, et al.. The natural history of corticosteroid therapy for inflammatory bowel disease: a population-based study. Gastroenterology. 2001;121:255–260.
10. Turner D, Walsh CM, Steinhart AH, et al.. Response to corticosteroids in severe ulcerative colitis: a systematic review of the literature and a meta-regression. Clin Gastroenterol Hepatol. 2007;5:103–110.
11. Wilhelm SM, McKenney KA, Rivait KN, et al.. A review of infliximab use in ulcerative colitis. Clin Ther. 2008;30:223–230.
12. Filippi J, Allen PB, Hébuterne X, et al.. Does anti-TNF therapy reduce the requirement for surgery in ulcerative colitis? A systematic review. Curr Drug Targets. 2011;12:1440–1447.
13. Sjöberg M, Walch A, Meshkat M, et al.. Infliximab or cyclosporine as rescue therapy in hospitalized patients with steroid-refractory ulcerative colitis: a retrospective observational study. Inflamm Bowel Dis. 2012;18:212–218.
14. Langholz E, Munkholm P, Davidsen M, et al.. Course of ulcerative colitis: analysis of changes in disease activity over years. Gastroenterology. 1994;107:3–11.
15. Triantafillidis JK, Merikas E, Georgopoulos F. Current and emerging drugs for the treatment of inflammatory bowel disease. Drug Des Devel Ther. 2011;5:185–210.
16. Kamm MA, Lichtenstein GR, Sandborn WJ, et al.. Effect of extended MMX mesalamine therapy for acute, mild-to-moderate ulcerative colitis. Inflamm Bowel Dis. 2009;15:1–8.
17. Abreu MT. Toll-like receptor signalling in the intestinal epithelium: how bacterial recognition shapes intestinal function. Nat Rev Immunol. 2010;10:131–144.
18. Maldonado-Contreras AL, McCormick BA. Intestinal epithelial cells and their role in innate mucosal immunity. Cell Tissue Res. 2011;343:5–12.
19. Lemaitre B, Nicolas E, Michaut L, et al.. The dorsoventral regulatory gene cassette spätzle/Toll/cactus controls the potent antifungal response in Drosophila adults. Cell. 1996;86:973–983.
20. Poltorak A, He X, Smirnova I, Liu MY, et al.. Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations in Tlr4 gene. Science. 1998;282:2085–2088.
21. Creed TJ, Lee RW, Newcomb PV, et al.. The effects of cytokines on suppression of lymphocyte proliferation by dexamethasone. J Immunol. 2009;183:164–171.
22. Franchimont D, Martens H, Hagelstein MT, el al. Tumor necrosis factor alpha decreases, and interleukin-10 increases, the sensitivity of human monocytes to dexamethasone: potential regulation of the glucocorticoid receptor. J Clin Endocrinol Metab. 1999;84:2834–2839.
23. Rachmilewitz D. Coated mesalazine (5-aminosalicylic acid) versus sulphasalazine in the treatment of active ulcerative colitis: a randomised trial. BMJ. 1989;298:82–86.
24. Geboes K, Riddell R, Ost A, et al.. A reproducible grading scale for histological assessment of inflammation in ulcerative colitis (comment). Gut. 2000;47:404–409.
25. Duclos M, Gouarne C, Bonnemaison D. Acute and chronic effects of exercise on tissue sensitivity to glucocorticoids. J Appl Physiol. 2003;94:869–875.
26. DeRijk RH, Petrides J, Deuster P, et al.. Changes in corticosteroid sensitivity of peripheral blood lymphocytes after strenuous exercise in humans. J Clin Endocrinol Metab. 1996;81:228–235.
27. Hearing SD, Norman M, Probert CSJ, et al.. Predicting therapeutic outcome in severe ulcerative colitis by measuring in vitro steroid sensitivity of proliferating peripheral blood lymphocytes. Gut. 1999:45:382–388.
28. Fazio VW, Ziv Y, Church JM, et al.. Ileal pouch-anal anastomoses complications and function in 1005 patients. Ann Surg. 1995;222:120–127.
29. Weinryb RM, Gustavsson JP, Liljeqvist L, et al.. A prospective study of the quality of life after pelvic pouch operation. J Am Coll Surg. 1995;180:589–595.
30. Ferrante M, Declerck S, De Hertogh G, et al.. Outcome after proctoco- lectomy with ileal poucheanal anastomosis for ulcerative colitis. Inflamm Bowel Dis. 2008;14:20–28.
31. Rubin DT, Siegel CA, Kane SV, et al.. Impact of ulcerative colitis from patients' and physicians' perspectives: results from the UC: normal survey. Inflamm Bowel Dis. 2009;15:581–588.
32. Sandborn WJ, Rutgeerts P, Feagan BG, et al.. Colectomy rate comparison after treatment of ulcerative colitis with placebo or infliximab. Gastroenterology. 2009;137:1250–1260.
33. Colombel JF, Rutgeerts P, Reinisch W, et al.. Early mucosal healing with infliximab is associated with improved long-term clinical outcomes in ulcerative colitis. Gastroenterology. 2011;141:1194–1201.
34. Niv Y, Bat L, Ron E, et al.. Change in the extent of colonic involvement in ulcerative colitis: a colonoscopic study. Am J Gastroenterol. 1987;82:1046–1051.
35. Rutter M, Saunders B, Wilkinson K, et al.. Severity of inflammation is a risk factor for colorectal neoplasia in ulcerative colitis. Gastroenterology. 2004;126:451.
36. Hanauer SB, Sandborn W. Management of Crohn's disease in adults. Am J Gastroenterol. 2001;96:635–643.
37. Baumgart DC, Sandborn WJ. Inflammatory bowel disease: clinical aspects and established and evolving therapies. Lancet. 2007;369:1641–1657.
38. Lichtiger S, Present DH, Kornbluth A, et al.. Cyclosporine in severe ulcerative colitis refractory to steroid therapy. N Engl J Med. 1994;330:1841–1845.
39. Sharkey L, Bredin F, Nightingale A, et al. The use of cyclosporin A in acute steroid-refractory ulcerative colitis: long term outcomes. J Crohns Colitis. 2011;5:91–94.
40. Ellis MC, Diggs BS, Vetto JT, et al.. Trends in the surgical treatment of ulcerative colitis over time: increased mortality and centralization of care. World J Surg. 2011;35:671–676.
41. Roberts SE, Williams JG, Yeates D, et al.. Mortality in patients with and without colectomy admitted to hospital for ulcerative colitis and Crohn's disease: record linkage studies. BMJ. 2007;335:1033.
Keywords:© Crohn's & Colitis Foundation of America, Inc.
ulcerative colitis; Toll-like receptor agonist; DIMS0150; steroid resistance; colectomy