Immunosuppressants drug
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Immunosuppressive drugs classification with the mechanism of action
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Immunosuppressants drug
- 1. Presented by: Manju Jakhar M.Pharm (Pharmacology) 2nd Semester
- 2. Immunosuppressants:= are agents which inhibit immunity. It Inhibit both:= cellular/humoral or both types of immune responses. major use :- 1.organ transplantation= (kidney,heart, liver) Almost everyone who receives an organ transplant has to take immunosuppressant drugs. The body recognizes a transplanted organ as a foreign mass. This triggers a response by the body’s immune system to attack it. 2.autoimmune diseases = Immunosuppressant drugs also are used to treat autoimmune diseases such as lupus. An autoimmune disorder is a disease process in which the body attacks its own tissue. Lupus results from just such a misdirected activity of the body’s own immune system. By suppressing this reaction, immunosuppressant drugs can help control the impact of the disease on the body.
- 3. 1. Calcineurin inhibitors (Specific T-cell inhibitors) :- Cyclosporine (Ciclosporin), Tacrolimus 2. m-TOR inhibitors:- Sirolimus, Everolimus 3. Antiproliferative drugs (Cytotoxic drugs):- Azathioprine, Methotrexate, Cyclophosphamide, Chlorambucil, Mycophenolat mofetil (MMF) 4. Glucocorticoids:- Prednisolone and others 5. Biological agents:- (a) TNFα inhibitors: Etanercept,Infliximab, Adalimumab (b) IL-1 receptor antagonist: Anakinra (c) IL-2 receptor antagonists: Daclizumab, (anti CD-25 antibodies) Basiliximab (d) Anti CD-3 antibody: Muromonab CD3 (e) Polyclonal antibodies: Antithymocyte antibody (ATG), Rho (D) immune globulin.
- 4. a. Cyclosporine:- It is a cyclic polypeptide with 11 amino acids, obtained from a fungus and introduced in 1977 as a highly selective immunosuppressant which has markedly increased the success of organ transplantations. MOA It profoundly and selectively inhibits T lymphocyte proliferation, IL-2 and other cytokine production as well as response of inducer T cells to IL-1, without any effect on suppressor T- cells. Lymphocytes are arrested in G0 or G1 phase.
- 5. Cyclosporine, tacrolimus and sirolimus inhibit antigen stimulated activation and proliferation of helper T cells as well as expression of IL-2 and other cytokines by them. Cyclosporine binds to an intracellular protein ‘Cyclophilin’ and this complex inhibits Ca2+ Calmodulin (Ca2+-CAM) activated phosphatase ‘Calcineurin’. Cyclosporine binds to an intracellular protein ‘Cyclophilin’ and this complex inhibits Ca2+- Calmodulin (Ca2+-CAM) activated phosphatase ‘Calcineurin.
- 6. uses :- Cyclosporine is the most effective drug for prevention and treatment of graft rejection reaction. It is routinely used in renal, hepatic, cardiac, bone marrow and other transplantations. For induction . it is started orally 12 hours before the transplant and continued for as long as needed. When graft rejection has started, it can be given i.v., because oral bioavailability is low, dependent on presence of bile and is highly variable. Blood level monitoring is required for effective therapy. Pharmokinetics :- It is concentrated in WBCs and RBCs, metabolized in liver by CYP3A4 and excrete in bile. The plasma t½ is biphasic 4–6 hr and 12–18 hr. ADR:- Rise in BP, precipitation of diabetes, Hyperkalaemia, Hyperuricaemia etc.
- 7. This immunosuppressant is chemically different from cyclosporine, but has the same mechanism of action, and is ~100 times more potent. It binds to a different cytoplasmic immunophilin protein labelled ‘FK 506 binding protein (FKBP)’, but the subsequent steps are the same, i.e. inhibition of helper T cells via calcineurin. Tacrolimus also inhibits calcineurin, but after binding to a different protein FKBP (FK binding protein). Uses:- Prevention and treatment of graft rejection reaction. Side effects :- Rise in BP, precipitation of diabetes, Anorexia, Lethargy, Hyperkalaemia, Hyperuricaemia, Opportunistic Infections, Hirsutism, Gum hyperplasia, Tremor And seizures. Pharmacokinetics:- Tacrolimus is administered orally as well as by i.v. infusion. Oral absorption is variable and decreased by food. It is metabolized by CYP3A4 and excreted in bile with a t½ of 12 hour. Therapeutic application, clinical efficacy as well as toxicity profile are similar to cyclosporine.
- 8. a). Sirolimus This new and potent immunosuppressant is a macrolide antibiotic (like tacrolimus), which was earlier named Rapamycin. MOA:- It binds to the same immunophillin FKBP as tacrolimus, but the sirolimus-FKBP complex inhibits another kinase called ‘mammalian target of rapamycin’ (mTOR), and does not interact with calcineurin. The mTOR is an important link in the cascade of signalling pathways which lead to proliferation and differentiation of T- cells activated by IL-2 and other cytokines. Sirolimus arrests the immune response at a later stage than cyclosporine. Sirolimus also binds to FKBP, but this complex acts at a later stage. It binds to and inhibits a kinase termed m-TOR (mammalian target of rapamycin) which is a key factor for progression of cell proliferation.
- 9. Pharmokinetics:- Sirolimus is absorbed orally, but fatty meal reduces absorption. It is extensively metabolized, mainly by CYP3A4, so that systemic bioavailability is only 15– 20%. Elimination occurs primarily by the biliary route; the t½ is ~60 hours. Inhibitors and inducers of CYP3A4 significantly alter its blood level, which needs to be monitored. Cyclosporine shares the same isoenzyme and raises the blood level of sirolimus. Uses:- For prophylaxis and therapy of graft rejection reaction, sirolimus can be used alone, but is generally combined with lower dose of cyclosporine/tacrolimus and/or corticosteroids and mycophenolate mofetil. The latter combination avoids use of a calcineurin inhibitor, and is particularly suitable for patients developing renal toxicity with cyclosporine. Sirolimus is effective in some steroid refractory cases, and has been used in stem cell transplant as well. However, it is not recommended for liver transplant. Sirolimus coated stents are being used to reduce the incidence of coronary artery restenosis, by inhibiting endothelial proliferation at the site.
- 10. b).Everolimus:- It is similar to sirolimus in mechanism, clinical efficacy, doses, toxicity and drug interactions, but is better absorbed orally and has more consistent bioavailability. The t½ is shorter (~40 hours) so that steady state levels can be reached earlier. 3.ANTIPROLIFERATIVE DRUGS (Cytotoxic immunosuppressants) a). Azathioprine:- It is a purine antimetabolite which has more marked immunosuppressant than antitumour action. The basis for this difference is not clear, but may be due to its selective uptake into immune cells and intracellular conversion to the active metabolite 6- mercaptopurine, which then undergoes further transformations to inhibit de novo purine synthesis and damage to DNA. It selectively affects differentiation and function of T cells and inhibits cytolytic lymphocytes; CMI is primarily depressed.
- 11. Uses:- The most important application of azathioprine is prevention of renal and other graft rejection, but it is less effective than cyclosporine; generally combined with it or used in patients developing cyclosporine toxicity. Relatively lower doses (1–2 mg/kg/day) are used in progressive rheumatoid arthritis and it is frequently employed for maintening remission in inflammatory bowel disease. It may be an alternative to long-term steroids in some other autoimmune diseases as well. It is not combined with Methotrexate. Dose: 50–150 mg/day; orally. b). Methotrexate :- This folate antagonist is a potent immunosuppressant which markedly depresses cytokine production and cellular immunity, and has antiinflammatory property. It has been used as a first line drug in many autoimmune diseases like rapidly progressing rheumatoid arthritis, severe psoriasis, pemphigus, myasthenia gravis, uveitis, chronic active hepatitis. Low dose Mtx maintenance therapy is relatively well tolerated. c). Mycophenolate mofetil (MMF) :-It is a newer immunosuppressant; prodrug of mycophenolic acid which selectively inhibits inosine monophosphate dehydrogenase, an enzyme essential for denovo synthesis of guanosine nucleotides in the T and B cells.
- 12. Pharmokinetic :- MMF is rapidly absorbed orally and quickly converted to the active metabolite mycophenolic acid. This is then slowly inactivated by glucuronidation with a t½ of ~ 16 hours. The glucuronide is excreted in urine. Uses:-Renal transplantation Renal toxicity With cyclosporine/ta crolimusn Side effects:-Vomiting, Diarrhoea, Leucopenia, G.I. Bleeds. 4.Glucocorticoids Glucocorticoids have potent immunosuppressant and anti-inflammatory action, inhibit several components of the immune response. MOA:-They particularly inhibit MHC expression and activation/proliferation of T lymphocytes. Expression of several IL and other cytokine genes is regulated by corticosteroids and production of adhesion molecules is depressed. Accordingly, they have marked effect on CMI but little effect on humoral immunity.
- 13. Uses:- The corticosteroids are widely employed as companion drug to cyclosporine or other immunosuppressants in various organ transplants. In case graft rejection sets in—large doses of corticoids I.V. are employed for short periods. They are used in practically all cases of severe autoimmune diseases, especially during exacerbation. 5.BIOLOGICAL AGENTS These are biotechnologically produced recombinant proteins or polyclonal/monoclonal antibodies directed to cytokines or lymphocyte surface antigens which play a key role in immune response. a).TNFα inhibitors:- TNFα is secreted by activated macrophages and other immune cells to act on TNF receptors (TNFR1, TNFR2) which are located on the surface of neutrophils, fibroblasts, endothelial cells as well as found in free soluble form in serum and serous fluids. The TNFα inhibitors are mainly used in autoimmune diseases, and are briefly described with disease modifying drugs for rheumatoid arthritis. utoimmune diseases and graft versus host reaction.
- 14. Etanercept:- This fusion protein of human TNF receptor and Fc portion of human IgG1 neutralizes both TNFα and TNFβ. It prevents activation of macrophages and T-cells during immune reaction. It is used mostly in combination with Mtx in rheumatoid arthritis patients who fail to respond adequately to the latter. It is also approved for severe/refractory ankylosing spondylitis, polyarticular idiopathic juvenile arthritis and plaque psoriasis. b).IL-1 receptor antagonist :- Stimulated macrophages and other mononuclear cells elaborate IL-1 which activates helper T-cells and induces production of other ILs, metalloproteinases, etc. An endogenous IL-1 receptor antagonist has been isolated and several of its recombinant variants have been produced for clinical use. c). IL-2 receptor antagonist:- The CD-25 molecule is expressed on the surface of immunologically activated, but not resting T-cells. It acts as a high affinity receptor for IL-2 through which cell proliferation and differentiation are promoted. Some anti CD-25 antibodies have been developed as IL-2 receptor antagonist to specifically arrest the activated T-cells.
- 15. d).Anti-CD3 antibody :- Muromonab CD3 It is a murine monoclonal antibody against the CD3 glycoprotein expressed near to the T cell receptor on helper T cells. Binding of muromonab CD3 to the CD3 antigen obstructs approach of the MHCIIantigen complex to the T-cell receptor. Consequently, antigen recognition is interfered, and participation of T-cells in the immune response is prevented. Muromonab CD3 is the oldest (developed in the 1980s) monoclonal antibody that is still occasionally used clinicallya Uses:- Induction therapy of organ transplantation is infrequent now, since better alternatives are available. It has also been used to deplete T cells from the donor bone marrow before transplantation. Side effects:- Chills, Rigor, High fever, Wheezing, Malaise, etc Occasionally aseptic meningitis, intra-graft thrombosis, life-threatening pulmonary edema, Seizures and a shock-like state
- 16. e).Polyclonal antibodies Antithymocyte globulin (ATG) It is a polyclonal antibody purified from horse or rabbit immunized with human thymic lymphocytes which contains antibodies against many CD antigens as well as HLA antigens. It binds to T lymphocytes and depletes them. It is a potent immunosuppressant and has been used primarily to suppress acute allograft rejection episodes, especially in steroid resistant cases, by combining with other immunosuppressants, including steroids. It can also be used in induction regimens, but this has the potential to produce serum sickness or anaphylaxis.