18th Page Flashcards

1
Q

What is the Type I hypersensitivity skin test?

A

Skin test / Prick test

A. Cutaneous B. Intradermal - more sensitive

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2
Q

What indicates a positive reaction in a Type I hypersensitivity skin test?

A

Formation of a wheal that is 3 mm greater in diameter than the negative control.

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3
Q

What is the Radio Immunosorbent Test (RIST)?

A

A competitive RIA test for Total IgE.

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4
Q

What is the Radioallergosorbent Test (RAST)?

A

A non-competitive RIA test for Specific IgE.

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5
Q

Skin and Prick test

A

Cutaneous and Intradermal (more sensitive)

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6
Q

What is the Direct Antiglobulin Test (Coomb’s test) used for?

A

Test for Hemolytic Disease of the Newborn (HDN)

Hemolytic Transfusion Reactions (HTR), and

Autoimmune Hemolytic Anemia (AIHA).

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7
Q

What is the purpose of Direct Fluorescence examination?

A

To examine renal tissue biopsy for Goodpasture’s syndrome.

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8
Q

What does Indirect fluorescence immunoassay detect In Type II?

A

Autoantibodies.

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9
Q

What tests are used for autoantibodies in autoimmune disorders in Type III?

LIF

A

Latex agglutination
Immunoassays
Fluorescent staining.

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10
Q

What is the gold standard test for contact dermatitis (Type IV)?

A

Patch test.

This test must be done when the patient is free of symptoms or at least has a clear test site.

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11
Q

What indicates a positive patch test?

A

Redness with papule or tiny blister.

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12
Q

What is the Mantoux Method/Tuberculin Test/PPD?

A

A test using 0.1 mL of 5 tuberculin units (TU) of PPD injected intradermally into the forearm.

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13
Q

When is an induration considered positive in the Mantoux test?

A

An induration of 15 mm or more in individuals with no risk factors.

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14
Q

What is a positive Mantoux test result in high-risk groups?

Recent immigrants of high prevalence countries
intravenous drug users
employees of heath care
persons with clinical condition
children younger than 5 yrs old

A

A reaction of 10 mm or greater

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15
Q

What indicates a positive result for individuals with HIV or immunosuppression?

or chest x-ray with tuberculosis
recent contact with TB

A

An induration reaction of 5 mm or more.

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16
Q

What does a positive Mantoux test indicate?

A

Previous exposure to M. tuberculosis or a related organism, but not necessarily an active infection.

17
Q

positive test results in Mantoux method can also occur in:

A

Persons who have previous BCG (Bacillus Calmette Guerin) vaccine for tuberculosis.

18
Q

It uses M. tuberculosis Ag extract prepared from PPD (purified protein derivative )

A

Mantoux/tuberculin/PPD test

19
Q

What is Humoral Immunity?

A

B-cell deficiency.

20
Q

What is Cellular Immunity?

A

T-cell deficiency.

21
Q

What is a defect of phagocytic function?

A

It is characterized by the inability of a phagocyte to kill ingested microorganisms due to enzyme deficiency in NADPH oxidase or impaired oxidative/respiratory burst.

22
Q

Humoral Immunity examples

TSCX

A

Transient hypogammaglobulinemia of infancy
Selective IgA deficiency
Common variable immunodeficiency
X-linked agammaglobulinemia/Bruton’s agammaglobulinemia

23
Q

What is Selective IgA deficiency?

A

It is the most common immunodeficiency.

24
Q

What is X-linked agammaglobulinemia?

A

Patients lack circulating mature CD19 positive B cells and exhibit a deficiency of immunoglobulins of all classes.

The underlying genetic mechanism is a deficiency of an enzyme called Bruton’s tyrosine kinase in B-cell progenitor cells.

25
Q

What is DiGeorge syndrome?

A

It is a developmental abnormality of the third and fourth pharyngeal pouches that affects thymic development.

26
Q

What is Purine Nucleoside Phosphorylase (PNP) Deficiency?

A

affects an enzyme involved in the metabolism of purines, leading to decreased T cell numbers due to toxic metabolite accumulation called Deoxyguanosine triphosphate

27
Q

Examples

Severe combined immunodeficiency (SCID)
Wiskott-Aldrich Syndrome
What is Ataxia-telangiectasia

A

Combined deficiency of T and B cells

28
Q

What is Wiskott-Aldrich Syndrome?

A

It is characterized by a triad of eczema, thrombocytopenia, and immunodeficiency.

29
Q

What is Chronic Granulomatous Disease (CGD)?

A

Both sex-linked/autosomal recessive are normal but function abnormally

It is characterized by a phagocyte’s inability to kill ingested microorganisms due to enzyme deficiency (NADPH oxidase)

Macrophage-rich granulomas ae in liver, spleen, etc

Macrophage-rich granulomas can be found in the liver, spleen, and other organs.

30
Q

What is the Nitroblue Tetrazolium Reduction Test?

A

It tests the ability of white blood cells to reduce yellow water-soluble tetrazolium to a BLUE insoluble formazan.

Normal WBC: able to reduce; CGD: remains yellow, colorless.

31
Q

What is the Flow Cytometry Test?

A

It uses Dihydrorhodamine to assess the fluorescence of white blood cells when it is reduced

Normal WBC: fluorescence when reduced; CGD: no fluorescence.

32
Q

Bruton Tyrosine Kinase (BTK)

A

enzyme deficiency in B cell progenitor cells Bruton’s agammaglobulinemia (X-linked)

33
Q

CGD IN Nitroblue Tetrazolium Reduction

Chronic Granulomatous Disease ??

A

Yellow/Colorless

34
Q

CGD in flow Cytometry

Chronic Granulomatous Disease ??

A

No fluorescence