SA Immune Diseases Flashcards

1
Q

how common are inherited neutrophil defects?

A

very rare

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2
Q

how common are aquired neutrophil defects?

A

very common

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3
Q

are innate or adaptive immune system deficiencies more common?

A

adaptive

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4
Q

what is the most common inherited adaptive immune deficiency?

A

decreased Ab production due to decreased B cell function or lack of B cells

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5
Q

what are the most common causes of acquired adaptive immune deficiencies?

A

Steroid therapy
Cushings
Diabetes Mellitus

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6
Q

what diagnostics can you do to see initial clues of immune deficiencies?

A

history and CBC

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7
Q

is IMHA usually primary or secondary?

A

primary

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8
Q

classic CBC findings of IMHA

A

regenerative anemia
spherocytes
agglutination

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9
Q

biochem findings of IMHA

A

hyperbilirubinemia

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10
Q

Diagnostics for IMHA?
which is more specific?

A

Coomb’s test - direct anti-globulin test (detects IgG bound to RBC)
flow cytometry for RBC Ab (more specific)

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11
Q

what is PIMA?

A

precursor targeted immune mediated anemia

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12
Q

CBC findings of PIMA

A

non-regenerative anemia
no spherocytes
no agglutination

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13
Q

will the Coombs test be - or + with PIMA?

A

negative

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14
Q

Diagnostics for PIMA?

A

bone marrow aspirate and cytology
steroid trial

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15
Q

diagnostics and treatment for PIMA?

A

bone marrow aspirate + cytology
steroid trial

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16
Q

most common causes of death in dogs with IMHA?

A

anemia
thromboembolism

17
Q

how can you prevent thromboembolisms in patients with IMHA?

A

unfractionated heparin
low molecular weight heparin
clopidogel

18
Q

what are the three differentials for severe thrombocytopenia?

A

immune destruction
consumption
decreased production

19
Q

best diagnostic test for IMTP

A

flow cytometry for anti-platelet antibodies (APA)

20
Q

what is the mechanism of immune mediated neutropenia in dogs?

A

anti-neutrophil cytoplasmic antibodies (ANCA)

21
Q

what would you expect to find in a joint tap with polyarthritis?

A

95% non-degenerate neutrophils
supportive, non-septic inflam

22
Q

diagnostics for immune mediated neutropenia in dogs?

A

bone marrow aspirate and cytology

23
Q

key abnormalities for systemic lupus erythematosus

A

cytopenias
polyarthritis
proteinuria

24
Q

diagnostics for systemic lupud erythematosus?

A

antinuclear Ab (ANA)
joint taps
UPC
CBC

25
Q

is prednisone or dexamethasone more potent? which has a longer half life?

A

dexamethasone

26
Q

Mycophenolate
MOA:
side effects:

A

purine synthesis inhibitor - blocks T cell proliferation
GI - vomiting, diarrhea

27
Q

Azathioprine
MOA:
side effects:

A

purine production & DNA synthesis inhibitor - blocks T cell proliferation
hepatotoxicity (idiopathic hepatic necrosis)

28
Q

Leflunomide
MOA:
side effects:

A

pyrimidine synthesis inhibitor - blocks T cell proliferation
GI toxicity, vasculitis

29
Q

Cyclosporine
MOA:
side effects:

A

blocks cytokine production
GI toxicity in dogs, nephrotoxicity in cats

30
Q

Oclacitinib (Apoquel)
MOA:
indications?
side effects?

A

Jax inhibitor = blocks signaling when cytokines bind to target cells
adjunct therapy in autoimmune disease
GI and bladder infection

31
Q

Intravenous Immune Globulines
toxicity?

A

anaphylactic reactions

32
Q

steroid physiologic/replacement dose

A

0.05-0.1 mg/kg/day

33
Q

steroid anti-inflam dose

A

0.25 - 0.5 mg/kg/day

34
Q

steroid immunosuppressive dose

A

1-2 mg/kg/day

35
Q

how should you initially treat an immune disease?

A

high dose steroids (2mg/kg/day)
+ T cell targeted drug (cyclosporine, mycophenolate)
after clinical remission, taper steroids first (50% dose reduction)

36
Q

how should you treat refractory immune disease cases?

A

rescue therapies
- high dose methylprednisolone (10-30 mg/kg/day)
- addition of oclacitinib (apoquel)
- splenectomy

37
Q

when should you begin to taper steroids? by how much?

A

full clinical remission
50% dose reduction of steroids
later taper T cell drugs