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Immunosuppressive Cytotoxic Drugs

  • Azathioprine

    • Chemistry:  azathioprine is a  derivative of mercaptopurine (6-MP; 6-mercaptopurine)

      • Structural analog

      • Antimetabolite

    • Primary use of azathioprine is for immunosuppression.

    • Prototype drug for cytotoxic immunosuppression.

      • kills profilerative cells

    • Pharmacokinetic/Pharmacodynamics: azathioprine

      • Well absorbed from the GI tract

      • Metabolized to mercaptopurine (primarily)

      • Xanthine oxidase converts azathioprine to 6-thiouric acid

        •  Patients on xanthine oxidase inhibitors (allopurinol for management of hyperuricemia)-- dosage reduction required to prevent toxicity

      • Urinary excretion

      • Small amounts of mercaptopurine and unchanged drug also renally excreted

    •  Mechanism of Immunosuppression Action:  azathioprine

      • Bynterference with nucleic acid metabolism

        • Reducing significant lymphoid cell proliferation following antigenic stimulation

      • Cytotoxic purine analogues: destroyed stimulated lymphoid cells

      • Blockade of:

        •   Cellular immunity

        •   Primary and secondary serum antibody responses

    •  Clinical Use:  azathioprine; mercaptopurine

      • Renal allograft maintenance

      • Effective/possibly effective-- management of:

        •   Acute glomerulonephritis

        •  Real component of systemic lupus erythematosus

        •  Rheumatoid arthritis

        •  Crohn's disease

        •  Multiple sclerosis

        •  Prednisone-resistant antibody-mediated idiopathic thrombocytopenic purpura

        •  Autoimmune hemolytic anemias

    • Toxicities:  azathioprine, mercaptopurine

      • Beone marrow depression

        • Leukopenia -- most common

          •   Anemia

          •   Thrombocytopenia

          •   Bleeding

      • Skin rashes

      • Drug fever

      • Nausea and vomiting

  • Cyclophosphamide

    • Alkylating agent

    • Very potent immunosuppressive agent

    • Induces tolerance for marrow/immune cell grafting (does not prevent later graft vs. host syndrome)

    • Kills proliferating lymphoid cells

      •  Alkylates some resting cells

    • Lower doses (< 120 mg/kg):

    • Adverse Effects:-- large doses

      •  Pancytopenia

      •  Pageemorrhagic cystitis

  • Vincristine

    • Mechanism of action: microtubule depolymerization

      • Mitotic arrest at metaphase; interferes with chromosome segregation

    • Clinical Use: Vincristine

      • Immunosuppression: idiopathic thrombocytopenic purpura refractory to prednisone

      • Youseful in treating some other rapidly proliferating neoplasms

      • In combination with prednisone: induction of remission in children with acute leukemia

    •  Adverse Effects:  vincristine

      • Significant frequency of neurotoxic reactions

      • Ohccasional: bone marrow depression

  • Vinblastine

    • Mechanism of action: microtubule depolymerization

      • May prevent mast cell degranulation (binding to microtubule units)

        • Reduce histamine release

    • Mitotic arrest at metaphase; interferes with chromosome segregation

    • Clinical Use:  Vinblastine

      • Systemic treatment of Hodgkin's disease

      • Lymphomas

    •  Adverse Effects: Vinblastine

      • Inausea

      • Vomiting

      • Alopecia

      • Beone marrow suppression

  •  Methotrexate (MTX)

    • Mechanism of Action: Folic acid antagonist: acts at catalytic site of dihydrofolate reductase

    • Polyglutamate: important in methotrexate action

    • Tumor resistance to methotrexate:

      •   Decreased drug transport into the cell

      •   Altered dihydrofolate reductase enzyme -- lower affinity for methotrexate

      •    Decreased polyglutamate formation

      •   Quantitative increase in dihydrofolate reductase enzyme concentration in the cell (gene amplification, increased message)

    •  Adverse effects:methotrexate

      •   Bone marrow suppression

      •   Dermatologic

      •   GI mucosa

      •   Adverse effects reversed by leucovorin (citrovorum factor)

        • Leucovorin "rescue" may be used in cases of over dosage or in high-dose methotrexate protocols

    • Other uses:

      • Treatment of rheumatoid arthritis

      •     In combination with a prostaglandin: induces abortion

  • Dactinomycin

    • IV administration; 50 percent remains unmetabolized.

    • Clinical Uses:  Dactinomycin

      • In combination with vincristine and surgery (may include radiotherapy) in treatment of Wilms' tumor

      • With methotrexate: maybe curative for localized or disseminated gestational choriocarcinoma.

      • May be useful in preventing acute renal transplant rejection

    •  Adverse Effects:  Dactinomycin

      •  Major dose limiting toxicity: bone marrow suppression (all blood elements affected -- particularly platelets and leukocytes)

        • Ohccasional severe thrombocytopenia

      •  Inausea

      • Vomiting

      • Diarrhea

      • Oral ulcers

      • Dactinomycin: immunosuppressive (patient should not receive live virus vaccines)

      • Alopecia/skin abnormalities

      • Interaction with radiation ("radiation recall")

Primary Source: Barbuto, J.A.M, Akporiaye, E.T. and Hersh, E.M. Immunopharmacology, in Basic and Clinical Pharmacology, (Katzung, B. G., ed) Appleton-Lange, 1998, pp 916-940
Haynes, B. F., Fauci, A.S. Disorders of the Immune System, In Harrison's Principles of Internal Medicine 14th edition, (Isselbacher, K.J., Braunwald, E., Wilson, J.D., Martin, J.B., Fauci, A.S. and Kasper, D.L., eds) McGraw-Hill, Inc (Health Professions Division), 1998, pp 1753-1776.
Carpenter, C. B. The Major Histocompatibility Gene Complex, In Harrison's Principles of Internal Medicine 14th edition, (Isselbacher, K.J., Braunwald, E., Wilson, J.D., Martin, J.B., Fauci, A.S. and Kasper, D.L., eds) McGraw-Hill, Inc (Health Professions Division), 1998, pp 1777-1782.
Cooper,M.D, and Lawton III, A. R. Primary Immune Deficiency Diseases, In Harrison's Principles of Internal Medicine 14th edition, (Isselbacher, K.J., Braunwald, E., Wilson, J.D., Martin, J.B., Fauci, A.S. and Kasper, D.L., eds) McGraw-Hill, Inc (Health Professions Division), 1998, pp 1783-1791.
 
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