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Therapy of Inflammatory Bowel Diseases 2013 Gastroenterology Department Division of Medicine Eran Israeli MD.

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Presentation on theme: "Therapy of Inflammatory Bowel Diseases 2013 Gastroenterology Department Division of Medicine Eran Israeli MD."— Presentation transcript:

1 Therapy of Inflammatory Bowel Diseases 2013 Gastroenterology Department Division of Medicine Eran Israeli MD

2 Cosnes J et al. Inflamm Bowel Dis 2002;8:244-50. 24022821620419218016815614413212010896847260483624120 0 20 40 60 80 100 % Cumulative Probability Patients at risk Months 2002552229 95 37 N = Penetrating Stricturing Inflammatory Long Term Evolution of Disease Behavior in CD

3 Goals of Treatment Remission Maintenance

4 Goals of therapy Induce and maintain remission Ameliorate symptoms Improve pts. quality of life Adequate nutrition Prevent complication of both the disease and medications Mucosal healing

5

6 Therapeutic Pyramid for Active IBD Severe Moderate Aminosalicylates/Antibiotics Corticosteroids Immunomodulators Surgery Infliximab ? (Prednisone) Mild (Budesonide)

7 5-aminosalicylates  The mainstay treatment of mild to moderately active UC and CD (colitis).  5-ASA may act by blocking the production of prostaglandins and leukotrienes, inhibiting bacterial peptide–induced neutrophil chemotaxis and adenosine-induced secretion, scavenging reactive oxygen metabolites

8  Sulphasalazine first agent discovered  Group now includes: Pentasa (mesalazine) Asacol (mesalazine) Rafassal (mesalazine) Salazopyrin-EN (sulphasalazine)  Work locally on the lining of the gut to reduce inflammation 5-aminosalycylates

9  Highly effective for the induction of remission in patients with active disease Short-term response rates (12–16 weeks) range from 70–90%  Not effective in maintenance of remission  Topical corticosteroids can be used as an alternative to 5-ASA in ulcerative proctitis or distal UC. Corticosteroids Enter cells and bind to and activate specific cytoplasmic receptors Steroid-receptor dimers enter cell nucleus activate steroid- responsive elements in DNA Gene repression or induction  anti- inflammatory effects Anti-inflammatory effects take several hours

10  IV -for patients who are sufficiently ill to require hospitalization; the majority will have a response within 7 to 10 days  Budesonide: less side effects, its use is limited to patients with distal ileal and right- sided colonic disease Corticosteroids

11 - Acne -“Moon” face -Hair growth -“Buffalo” hump -Obesity -Purple / red streaks (striae) - Bone thinning - Bruising - Muscle weakness Cataract

12 Immunomodulators  Drugs include: Azathioprine 6-mercaptopurine Methotrexate  Interfere with inflammatory pathway  Effective- up to 75% of patients brought into remission  Slow- optimal effect often not seen until after 12 weeks of treatment  Need close monitoring for toxicity  Safety- Methotrexate not to be used in pregnancy Inhibit ribonucleotide synthesis; Induce T cell apoptosis by modulating cell (Rac1) signalling Metabolised to mercaptopurine

13 Azathioprine 6- Mercaptopurine 6-TGN6-MMPN TPMT Azathioprine Metabolism TPMT = thiopurine methyltransferase 6-TGN = 6-thioguanine nucleotide 6-MMPN = 6-methylmercaptopurine ribonucleotide

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15  TPMT Tested before initiating therapy Low TPMT activity related to high 6-TGN levels, increasing risk of toxicity  6-TGN Used to monitor therapy Levels above 230 associated with better effect Levels above 480 associated with more side effects

16 Biological therapy anti-TNF  Infliximab Neutralisation of soluble TNF  TNF  producing macrophages of activated T cells Neutralisation of transmembrane TNF  van Deventer SJH. Gut 1997: 40; 443–8. Scallon BJ et al. Cytokine 1995: 7; 251–9. Feldmann M et al. Adv Immunol 1997; 64: 283–350.

17 Chimeric monoclonal antibody (75% human IgG 1 isotype) Infliximab IgG 1 Mouse Mouse Human Human PEG, polyethylene glycol. Humanized Fab’ fragment (95% human IgG 1 isotype) Certolizumab Pegol PEG PEG VHVL CH1CH1CH1CH1 No Fc Human recombinant antibody (100% human IgG 1 isotype)Adalimumab IgG 1 Construct of Anti-TNF-α Biologic Agents

18 Anti-TNF  safety  Hypersensitivity Allergic reaction at time of infusion – 5%  Autoimmune syndromes Lupus like illness – rare and recovers on stopping on therapy  Infection Profound immunosuppression occurs Opportunistic infections can occur Tuberculosis high risk Hepatitis B can be reactivated  Cancer Recent data suggests that overall cancer rates may be reduced Hepatosplenic T-cell lymphomas – 1 in 20000 patients

19 Integrins MAdCAM-1 VCAM-1 Gut-homing T-cell Integrin     Integrin    


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