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Transplantation: Mechanisms of Tacrolimus. Sarah Barnett, Jordanne Feldberg, Tamara Robinson PHM 142: October 2, 2013. PHM142 Fall 2013 Instructor: Dr. Jeffrey Henderson. Overview of Transplantation.
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Transplantation: Mechanisms of Tacrolimus Sarah Barnett, Jordanne Feldberg, Tamara Robinson PHM 142: October 2, 2013 PHM142 Fall 2013 Instructor: Dr. Jeffrey Henderson
Overview of Transplantation • Transferring cells, tissues or organs from one person (the donor) to another (the recipient) to replace the recipient’s damaged or malfunctioning one(s). • In Ontario transplanted organs can include: • small bowel, kidney, pancreas, liver, heart & lungs. • Process: • Transplant team will determine suitability for transplant • Suitable candidates who decide to move forward are placed on the waitlist • Waitlisted candidates are entered into matching system
Transplant Matching System • Goal of matching system is to find an organ that will be tolerated by the recipient. • Matching occurs in 3 areas: • Blood Type Matching: ABO blood group • Tissue Type Matching: antigens • Crossmatching: identify presence of preformed antibodies donor-recipient compatibility
Following Transplantation • Immune system may still recognize the transplanted organ as foreign & lead to rejection. • Due to antigens on cell surface • Immune response consists of both cellular (lymphocyte mediated) and humoral (antibody mediated) mechanisms. • T-cells play an essential role in the rejection process • To prevent rejection patients are prescribed an immunosuppressant.
Preventing Transplant Rejection • Medications suppress the immune response & prevent destruction of transplanted organ. • Must take for as long as you have the transplant (lower dose during maintenance phase) • Medications currently available: • Immunophilin-binding agents/Calcineurin inhibitors • Tacrolimus & Cyclosporine • Mammalian target of rapamycin (mTOR) inhibitors • Antiproliferative agents • Antibodies • Corticosteroids
Preventing Transplant Rejection • Medications suppress the immune response & prevent destruction of transplanted organ. • Must take for as long as you have the transplant (lower dose during maintenance phase) • Medications currently available: • Immunophilin-binding agents/Calcineurin inhibitors • Tacrolimus & Cyclosporine • Mammalian target of rapamycin (mTOR) inhibitors • Antiproliferative agents • Antibodies • Corticosteroids
Uses for Tacrolimus • Dermatitis, pruritus and psoriasis • Systemic lupus erythematosus • Organ transplants and allograft • Management of severe autoimmune diseases
Structure of Tacrolimus http://www.drugbank.ca/drugs/DB00864
Drug Classes of Tacrolimus Tacrolimus is derived from the bacteria Streptomyces tsukubaensis Drug class: • Antipsoriatic • Immune suppressant: Calcineurin inhibitor
Metabolism • Metabolized hepatically via cytochrome P450 via CYP3A • Metabolites include: 13-demethyltacrolimus and 31-O-demethyltacrolimus. Both are active • Tacrolimus excreted almost entirely as metabolites (less than 1% unchanged in urine)
Adverse events Major events include: • Nephrotoxicity • GI distress • Diabetes mellitus • CNS effects (headache, tremor, confusion, insomnia) • Malignant tumors Pregnancy: it does cross the placenta; renal function must be especially monitored
Summary • Donor-recipient compatibility is optimized through blood type, tissue type & crossmatching • Transplant antigens may be recognized as foreign, leading to an immune response & possibly rejection • Prevent transplant rejection by prescribing immunosuppressive drugs, such as Tacrolimus • Tacrolimus, through inhibition of Calcineurin, deactivates the immune system’s T-cells • Tacrolimus Inhibitory Mechanism • Tacrolimus (or FK506) suppresses the signal-transduction events in T-cell activation by binding to the FK Binding Protein (FKBP), forming the FK506-FKBP complex • This complex interacts with Calcineurin, preventing the dephosphorylation event of NFATc, thus blocking its entry into the nucleus • As a result, the transcription of the IL-2 gene is inhibited in the T-cells • Tacrolimus is metabolized hepatically by P450 via CYP3A. It produces active metabolites and only 1% is excreted unchanged in the urine • Adverse events including: nephrotoxicity, GI distress, CNS effects & will cross the placenta during pregnancy
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