Immunology Flashcards

1
Q

What agents are typically used for induction (such as for a new transplant) and what are their mechanisms?

A
  • Alemtuzumab: an anti-CD52 antibody that depletes lymphocytes (referred to as “liquid AIDS”)
  • Corticosteroids: decrease T cell activation
  • Thymoglobulin: anti-thymocyte antibody that attacks T cell production
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2
Q

What agents are typically used for maintenance of immunosuppression and what are their mechanisms?

A
  • Calcineurin inhibitors that decrease T cell activation: cyclosporine and tacrolimus
  • Mycophenolate mofetil that decrease lymphocyte proliferation
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3
Q

List the types of prophylaxis that organ-transplant patients need.

A
  • CMV if they in a high-risk category (use Valcyte)
  • Pneumocystis if they are on steroids (use Bactrim if not G6PD deficient, use dapsone or inhaled pentamidine if they are G6PD deficient)
  • There is no ppx for EBV but it is good to be aware of their status (e.g., D+/R- or D-/R+) because they can have reactivation.
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4
Q

True or false: all organ-transplant patients require chronic prednisone.

A

False

Typically only those who have had confirmed or suspected rejection require long-term steroids.

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5
Q

The original name for rapamycin was _____________.

A

sirolimus

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6
Q

Review the management of allergic reaction and anaphylaxis.

A
  • Always give an H1 and H2 blocker. These are safe medicines and have essentially no reason not to give them in an allergic reaction.
  • Give epinephrine and steroids for anaphylaxis, which is more than one organ system involvement.
  • Give albuterol if wheezing is present.
  • Observe for at least four hours.
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7
Q

What is the weight cutoff for Epi Pen Jr?

A

< 30 kg

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8
Q

Review all the agents available for anaphylaxis.

A

Epinephrine
Antihistamines (H1 and H2 blockers)
Steroids
Glucagon (this works to increase adrenergic tone through the cAMP pathway, not the receptor-mediated pathway)

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9
Q

Review the mechanism of IgE mediated reaction.

A

Type I reactions happen when IgE binds to an antigen. Mast cells then bind to IgE and degranulate, releasing histamine and other vasoactive mediators.

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10
Q

Immune complex deposition is a type ______ immune reaction.

A

III

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11
Q

DRESS is a type ______ immune hypersensitivity reaction.

A

IV (T-cell mediated)

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12
Q

Which cells are responsible for acute and chronic transplant rejection?

A

Acute is CD8, chronic is CD4

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13
Q

What is the pediatric dose of epinephrine for anaphylaxis?

A

0.01 mg/kg IM up to a max of 0.3 mg

Example: a 12 kg toddler (like June) would need 0.12 mg IM. Her auvi-q is 0.1 mg.

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14
Q

What three classes of medications can induce angioedema?

A

ACEi
NSAIDs
tPA

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15
Q

How is the swelling of angioedema different from anaphylaxis?

A

Angioedema is well demarcated

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16
Q

Unlike urticaria, angioedema is usually __________.

A

non-pruritic

17
Q

Why might you give anaphylaxis medicines to those with angioedema?

A

There are histamine-mediated forms of angioedema as well as angioedema-anaphylaxis overlap syndromes that respond to anaphylaxis treatment.

18
Q

Why might you give FFP to someone having angioedema?

A

Although evidence is poor, FFP has ACE in it so can hypothetically relieve ACEi-induced angioedema. FFP also has bradykinin in it, though, so might worsen bradykinin-induced angioedema.

19
Q

The three pathophysiologies of angioedema are what?

A

Histamine-mediated
Bradykinin-mediated
Idiopathic

20
Q

Those with hereditary angioedema can receive what targeted therapies?

A

Concentrated C1 esterase inhibitor
Icatibant (bradykinin receptor antagonist)
Kallikrein inhibitors such as ecallantide

21
Q

How can the history help you figure out which type of angioedema is present (i.e., histaminergic or bradykinin-mediated)?

A
  • Medication-induced angioedema (such as ACEi, NSAIDs, or tPA) is typically bradykinin-mediated
  • Envenomation is usually histaminergic
  • Pruritis and urticaria are usually seen in histaminergic angioedema
22
Q

What cause of angioedema do you need to consider in those with a first-time case of angioedema who are older than 40?

A

Malignancy (typically lymphoproliferative)

23
Q

True or false: angioedema is usually non-pruritic.

A

True

24
Q

In hereditary angioedema, what protein is missing?

A

C1 esterase inhibitor