Lecture 38: Solid Organ Transplant Flashcards

1
Q

What is important about the Human Leukocyte Antigen [HLA] Typing?

A
  • Found on short chromosome 6; distinguishing from self and non self
  • Class I = A, B and Class II = DR
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2
Q

Which organ types are at the Higher Risk of rejection?

A
  • Liver is the Lowest;
  • Then Kidney & Pancreas
  • Then Heart
  • And Bowel and Lungs are the Highest

Higher the risk; the most likely to use Prednisone but probably just use pred in general

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3
Q

What are some of the induction agents for immunosuppression in organ transplant?

A
  • Polyclonal [Tymoglobulin (Rabbit) or ATGAM (Horse)]
  • Monoclonal [Alemtuzumab]
  • IL-2a [Basiliximab]
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4
Q

What is the MOA for Rabbit Antithymocyte Globulin [tymoglobulin]?

A
  • T-Lymphocytes depletion for induction and/or rejection
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5
Q

What is the Dosing and Adverse Effects for Thymoglobulin>?

A
  • 1 - 1.5mg/kg/day IV
  • Leukopenia, Thrombocytopenia, Fever, Chills [Premedicate with APAP or benadryl]
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6
Q

What is the MOA for Alemtuzumab?

A
  • Causes profound t-cell depletion by targeting CD52
  • Off label for SOT induction
  • 1 dose needed
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7
Q

What are some of the Adverse Effects for Alemtuzumab?

A
  • Chills, Rigor, Fever [Pretreat with APAP and Benadryl]
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8
Q

What is the MOA for Basiliximab?

A
  • Inhibit IL-2a activiation; being a CD25 antibody
  • NON-lymphdeleting
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9
Q

What is the way that we choose an induction agent?

A
  • Depleting is more common [especially for those that are high risk]
  • Basiliximab: for those that have Hx of Maglignancy, Infection Risk, Immunocompromised, HIV, HCV, Old
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10
Q

what are maintenance agents that are used in SOT?

A
  • Calcineurin Inhibitors
  • Antimetabolites
  • mTOR Inhibitors
  • Corticosteroids
  • T-Cell Co-stimulation Blockers
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11
Q

What are the Calcineurin Inhibitors that are used and what is there MOA?

A
  • Cyclosporine, Tacrolimus [Cornerstone]
  • MOA: Inhibits signal-1 which inhibits calcineurin within T-cells = NO T-Cell activation
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12
Q

What is important to know about Cyclosporine?

Formulations? Dosing? Monitoring?

A
  • Modified [Neoral & Gengraf] are better than NON-Modified
  • Coversion IV:PO = 3:1
  • Want a 12h trough of 100-400
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13
Q

What is important to know about Tacrolimus?

Formulation? Monitoring?

A
  • Prograf [BID] is IM & Astagraf and Envarsus [QD] is ER [ER has lower drug doses, improved adherence, less peak = less ADE]
  • 50x more potent than Cyclosporine [trough of 5-15]
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14
Q

What is the Metabolism and Elimination of CNIs?

A
  • Cyclo: 3A4 & PGP inhibitor; Half-life is longer [10-40h]
  • Tacro: 3A4 inhibitor; Half-life is okish [12-18h]
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15
Q

What are some of the Adverse effects of Cyclosporine?

A
  • Hypertension
  • Hypercholesterolemia
  • Hypertriglceridemia
  • Gingival Hyperplasia
  • Hirsutism
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16
Q

What are some of the Adverse Effects of Tacrolimus?

A
  • Neurotoxicty [headache]
  • Insomia
  • Tremor
  • Dizziness
  • Hyperglycemia
  • Alopecia
17
Q

What is the MOA of Azathioprine?

A
  • “Purine Analog”
  • AZA –> 6-MP goes into Nucleic acids causing inhibition of RNA/DNA synthesis and stops T-cells before then are made
18
Q

What are some of the Adverse Effects and Drug Interactions of Azathioprine?

A
  • GI: Ab pain, N/V/D, Dyspepsia
  • Bone Marrow Suppression
  • DI: Allopurniol & Febuxostat [reduce dose by 50-75%]

Because of these areas having HIGH turn over rates of cells

19
Q

What is the MOA of Mycophenolix Acid?

A
  • Inhibits de novo synthesis of Purines = stopping the development of T-Cells

Most commonly used

20
Q

What are the Adverse Effects and the Drug Interactions of Mycophenolic Acid?

A
  • GI and Bone Marrow stuff [same as AZA] & Pregnancy Cat D [Terategenic]
  • DI: with other myelosuppressive drugs like Valganciclovir or Sirolimus or AZA
21
Q

What is the MOA of the mTOR Inhibitors?

A
  • Binds to FKBP12 fusing with mTOR inhibiting T-cell formation

Same DI as CNIs with 3A4 and PGP

22
Q

What is important to know about Sirolimus & Everolimus?

T1/2? Dosing? Trough? Aprroved for**

A

Siro: T1/2 = 60h; QD; Trough = 5-10; Approved for Kidney
Evero: T1/2 = 30h; BID; Trough = 3-8; Approved for Kidney & Liver

23
Q

What are some of the Adverse Effects for mTORs?

A
  • Edema
  • Hyperlipidemia
  • Hypertriglycerdemia
  • Impaired Wound Healing
  • Mouth Ulcers
  • Proteinuria

wound healing issues is why its never a 1st line agent

24
Q

What is the MOA of Belatacept?

A
  • Blocks signal 2 and CD28 which Inhibits T-cell proliferation
  • ONLY for Kidneys; NOT FOR LIVER TRANSPLANTS
25
Q

What is important to know about Belatacept?

Administraion? Place in therapy? AEs?

A
  • IV only x30mins once a month
  • Replacement or add-on to CNIs
  • Needs postive EBV??

Can replace Tacro or Cyclo

26
Q

What is the Triple Drug Regimen that is used?

A
  • Tacrolimus + Mycophenolate +/- Prednisone
  • Alt: Siro + Myco or AZA + Steroids; Evero + Tacro + Steroids; Bela + Myco + Steroids