Immunology Review Flashcards

1
Q

AE of cisplatin

A

Nephrotoxicity and acoustic nerve damage

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2
Q

AE of bleomycin/ busulfan

A

Pulmonary fibrosis

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3
Q

AE of vincristine

A

Peripheral neuropathy

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4
Q

AE of doxorubicin

A

Cardiotoxicity

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5
Q

AE of cyclophosphamide

A

hemorrhagic cystitis

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6
Q

AE of trastuzumab

A

CHF

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7
Q

Mechanism of trastuzumab

A

monocolnal antibody against HER-2

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8
Q

Disease that rituximab is used for

A

B cell neoplasms (NHL)

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9
Q

Mech of rituximab

A

antibody against CD-20

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10
Q

Mechanism of bevacizumab

A

Ab against VEGF

inhibits angiogenesis

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11
Q

Mechanism of Omalizumab

A

Anti-IGE

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12
Q

When is Omalizumab used

A

severe asthma

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13
Q

Mechanism of Infliximab

A

Anti-TNF alpha

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14
Q

When is inflixumab used

A

Chron’s, RA

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15
Q

When is abciximab used

A

some acute coronary syndromes

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16
Q

Mechanism of abciximab

A

Anti-glycoprotein IIB/IIIA

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17
Q

Type I Hypersensitivity

A
preformed antibody
IgE mediated
immediate symptoms:
-allergy
-atopy
-anaphylaxis
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18
Q

Type II Hypersensitivity

A

cytotoxic reactions of antibody against cells or tissues:
Hemolytic anemia
Goodpastures

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19
Q

Type III Hypersensitivity

A
antigen-antibody complex deposition in tissue:
Vasculitis
serum sickness
post-strep GN
Arthus reaction
20
Q

What is an Arthrus reaction

A

edema and skin necrosis caused by activation on complement

21
Q

Type IV Hypersensitivity

A
T cell mediated
Delayed presentation:
- TB skin test
-contact dermatitis
-Graft v Host disease
22
Q

Antibody found in scleroderma

A

Anti-ScL-70, anti-topoisomerase 1

23
Q

Antibody in drug induced lupus

A

Anti-histone

24
Q

Antibody in Autoimmune hepatitis

A

Anti-smooth muscle

25
Antibody in primary biliary cirrhosis
Anti-mitochondrial
26
Antibody in Celiac's
Anti-tissue transglutaminase
27
Mechanism of hereditary angioedema
decreased C1 esterase inhibitor
28
Infant boy (4-6 months) encapsulated organism sepsis absent B cells
X-linked (Bruton's) agammaglobulinemia
29
``` Young adult recurrent sinusitis, pneumonia, bonchiectasis splenomegaly malignancies GI malacpsorbption ```
Common variable immunodeficiency (B and T cell deficiency)
30
CHD (truncus arteriosis) hypoparathyroid facial abnormalities low T cells
congenital thymic aplasia | DiGerorge
31
Recurrent Nisseria infections
Terminal complement deficiency (C5-C9)
32
Boy chronic catalase + infections + nitroblue tetrazolium
Chronic Granulomatous Disease
33
Eczema, thrombocytopenia x linked combined B and T cell deficiency
Wiskott Aldrich
34
Agammaglobulinemia lymphopenia infant
SCID | By either adenosine deaminase deficiency or defective IL2 receptors
35
``` Infant recurrent bacterial infections persistent neutrophilia absent pus delayed separation of the umbilical cord ```
Leukocyte adhesion deficiency
36
Mechanism by which steroids cause low WBC?
glucocorticoid induced demargination and storage poor release of neutrophils
37
What drugs can induce neutropenia?
Sulfa drugs | PTU
38
Which antibodies are produced in delayed transfusion reactions?
anti-Kell and Duffy
39
``` Post transfusion uticaria puritis wheezing fever ```
Allergic reaction | Type 1 hypersensitivity against plasma proteins in transfused blood
40
``` Post transfusion Dyspnea bronchospasm hypotension resspiratory arrest ```
Anaphylactic reaction | IgA deficient patients after receiving blood
41
Post transfusion fever, chilld within 12 hours no hemolysis
Febrile non hemolytic transfusion reaction | Type II- host antibodies against donor antigens and WBCs
42
``` Post transfusion immediate fever hypotension flank pain brown urine immediate ```
Acute hemolytic transfusion reaction | ABO mismatch
43
Post transfusion (1-2 weeks) jaundice slow hmeolysis
Delayed hemolytic transfusion reaction
44
Shortness of air during transfusion | lung crackles
Volume overload
45
``` Post transfusion fever dyspnea noncardiogenic pulmonary edema esp after FFP ```
transfusion associated acute lung injury (TRALI)