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 Antimetabolite
 Benificial in number of c/c inflammatory d/s
  including crohns d/s, rheumatoid arthritis & in cancer
 Given orally, subcutaneously or I/M
DHFA
 Dihydro folate reductase




                    THFA
  This step is important in production of thymidine and
                             purine
 High doses, used in chemotherapy, inhibits cellular
    proliferation.
   Low dose is used in treatment of IBD(12-25mg/wk).
   Interfere with inflammatory actions of interleukin-1.
   Stimulate increased release of adenosine, an
    endogenous anti-inflammatory autocoid.
   Also stimulate apoptosis & death of activated T-
    lymphocytes
 Induce & maintain remission in patients with crohns
  d/s.
 Efficacy in ulcerative colitis is uncertain.
 To induce remission, 15-25mg given once weekly by
  subcutaneous inj.
 If satisfactory response in 8-12wks, dose is reduced to
  15mg/wk
 At high doses, cause BONE MARROW DEPRESSION,
  MEGAIOBLASTIC ANAEMIA, ALOPACIA &
  MUCOSITIS
 Folate supplimentation reduces risk of events without
  impairing anti inflammatory effect.
 Dysregulation of TH1 response is present in IBD.
 Key proinflammatory cytokine in TH1 response is
 TNF-alpha.
 INFLIXIMAB is a chimeric mouse
 human monoclonal Ab to human TNF-
 alpha
 Given I/v, therapeutic dose 5-10mg/kg & plasma
 t1/2 is 8-10days
 TNF-alpha trimers bind to cell-surface TNF-alpha
  receptors.
 INFLIXIMAB bind to soluble TNF-alpha trimers with
  high affinity, preventing cytokine from binding to
  receptors.
 It also bind to membrane bound TNF- alpha &
  neutralises its activity.
 Also promote compliment activation & Ab-mediated
  apoptosis & cellular cytotoxicity of activated T-
  lymphocytes & macrophages.
 Used in a/c & c/c treatment of patients with moderate
  to severe Crohns d/s & Ulcerative colitis.
 INFLIXIMAB induction therapy – dose 5mg/kg at 0, 2,
  &6wks.
 In patients who respond can be treated with repeat
  infusions every 8wks.
 Other anti-TNF agent approved are ADALIMUMAB &
  CERTOLIZUMAB.
 Infection due to suppresion of TH1 inflammatory
    response.
   Reactivation of latent TB, with dissemination.
   Other infections include pneumonia, sepsis,
    pneumosistosis, histoplasmosis, listeriosis &
    reactivation of hepatits B.
   May cause severe hepatic reactions leading to a/c
    hepatic failure.
   May worsen CHF in cardiac disease.
o INTEGRINS are adhesion molecules on surface of
  leucocytes that interact with another class of adhesion
  molecules on the surface of vascular endothelium
  known as SELECTIN, allowing circulating leucocytes
  to adhere & subsequently move through the vessel wall
  into the tissue.
o Integrins contain two subunits alpha & beta.
o NATALIZUMAB a humanized IgG4 monoclonal Ab
  targeted against alpha-2 subunit.
 Used in patients with moderate to severe Crohns
  disease.
 DOSE-300mg every 4 wks by I/V infusion & patient
  should not be on any immunosuppressive treatment.
 ADVERSE EFFECTS- a/c infusion reactions & small
  risk of oppurtunistic infections.
Anti-inflammatory drug mechanisms and uses in IBD

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Anti-inflammatory drug mechanisms and uses in IBD

  • 1.
  • 2.  Antimetabolite  Benificial in number of c/c inflammatory d/s including crohns d/s, rheumatoid arthritis & in cancer  Given orally, subcutaneously or I/M
  • 3. DHFA  Dihydro folate reductase THFA  This step is important in production of thymidine and purine
  • 4.  High doses, used in chemotherapy, inhibits cellular proliferation.  Low dose is used in treatment of IBD(12-25mg/wk).  Interfere with inflammatory actions of interleukin-1.  Stimulate increased release of adenosine, an endogenous anti-inflammatory autocoid.  Also stimulate apoptosis & death of activated T- lymphocytes
  • 5.  Induce & maintain remission in patients with crohns d/s.  Efficacy in ulcerative colitis is uncertain.  To induce remission, 15-25mg given once weekly by subcutaneous inj.  If satisfactory response in 8-12wks, dose is reduced to 15mg/wk
  • 6.  At high doses, cause BONE MARROW DEPRESSION, MEGAIOBLASTIC ANAEMIA, ALOPACIA & MUCOSITIS  Folate supplimentation reduces risk of events without impairing anti inflammatory effect.
  • 7.  Dysregulation of TH1 response is present in IBD.  Key proinflammatory cytokine in TH1 response is TNF-alpha.  INFLIXIMAB is a chimeric mouse human monoclonal Ab to human TNF- alpha  Given I/v, therapeutic dose 5-10mg/kg & plasma t1/2 is 8-10days
  • 8.  TNF-alpha trimers bind to cell-surface TNF-alpha receptors.  INFLIXIMAB bind to soluble TNF-alpha trimers with high affinity, preventing cytokine from binding to receptors.  It also bind to membrane bound TNF- alpha & neutralises its activity.  Also promote compliment activation & Ab-mediated apoptosis & cellular cytotoxicity of activated T- lymphocytes & macrophages.
  • 9.  Used in a/c & c/c treatment of patients with moderate to severe Crohns d/s & Ulcerative colitis.  INFLIXIMAB induction therapy – dose 5mg/kg at 0, 2, &6wks.  In patients who respond can be treated with repeat infusions every 8wks.  Other anti-TNF agent approved are ADALIMUMAB & CERTOLIZUMAB.
  • 10.  Infection due to suppresion of TH1 inflammatory response.  Reactivation of latent TB, with dissemination.  Other infections include pneumonia, sepsis, pneumosistosis, histoplasmosis, listeriosis & reactivation of hepatits B.  May cause severe hepatic reactions leading to a/c hepatic failure.  May worsen CHF in cardiac disease.
  • 11. o INTEGRINS are adhesion molecules on surface of leucocytes that interact with another class of adhesion molecules on the surface of vascular endothelium known as SELECTIN, allowing circulating leucocytes to adhere & subsequently move through the vessel wall into the tissue. o Integrins contain two subunits alpha & beta. o NATALIZUMAB a humanized IgG4 monoclonal Ab targeted against alpha-2 subunit.
  • 12.  Used in patients with moderate to severe Crohns disease.  DOSE-300mg every 4 wks by I/V infusion & patient should not be on any immunosuppressive treatment.  ADVERSE EFFECTS- a/c infusion reactions & small risk of oppurtunistic infections.