Allergy/Immunology Flashcards

0
Q

Antibody mediated allergic response

A

Type II Allergic Reaction

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1
Q

IgE mediated (anaphylactic) allergic reaction

A

Type I Allergic Response

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2
Q

Immune Complex Deposition

A

Type III Allergic Reaction

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3
Q

Delayed Hypersensitivity (Poison Ivy) Reaction

A

Type IV Allergic Reaction

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4
Q

Recurrent pyogenic infections

A

B cell (Ab) dysfunction

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5
Q

Chronic or recurrent candida infection (nails, scalp, or mouth)

A

T cell dysfunction

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6
Q
  • Eczema and petichiae (thrombocytopenia)
  • X-linked
  • low IgM
  • humoral and cellular immunodeficiency
  • autoimmune disease and malignancy
  • Tx: manage bleeding and infx, BMT
A

Wiskott Aldrich Syndrome

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7
Q
  • absence of lymphoid tissue
  • defect in B and T cell function
  • dermatitis, diarrhea, FTT, thrush, otitis, LTI
  • low normal WBC
  • Dx: analysis of T, B, and NK cell subsets
  • Tx: BMT
  • also adenosine deaminase deficincy
A

SCID

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8
Q
-absence of thymic shadow
Cardiac defects
Abnl face (low set ears)
Thymic hypoplasia
Cleft palate
Hypocalcemia (tetany)
22- long arm of Xsome 22
A

DiGeorge Syndrome

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9
Q
  • “ataxia” w/ discoloration of the conjunctiva

- frequent sinus infx

A

Ataxia Telangectasia

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10
Q
  • No B cells
  • decr lymphoid tissue
  • recurrent infx with encapsulated pyogenic bacteria (pseudomonas, S. pneumo, H. flu)- pna, otitis
  • X-linked
  • low IgGAMEs–>B&T cell subsets
  • require IVIG
A

Bruton’s X-linked agammaglobulinemia

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11
Q
  • defective Ab response
  • B lymphocytes don’t differentiate
  • deficiency of Ig sub-types
  • may have T cell defects too
  • recurrent URTI, LRTI, herpes zoster
  • associated with autoimmune disease, lymphoma and EBV
  • require IVIG
A

CVID

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12
Q
  • recurrent overwhelming meningococcal disease

- most are autosomal recessive

A

Complement deficiency

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13
Q
  • T cell abnl prevents IgM–>IgG
  • absence of CD 40 ligand
  • disruption of B cell differentiation
  • frequent otitis, sinopulmonary infx, diarrhea, and opportunistic infx
  • low IgG, A, E, incr IgM
  • X linked (males)
  • Tx: IVIG
A

Hyper IgM

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14
Q
  • MC immunodeficiency

- recurrent sinopulmonary infx

A

IgA deficiency

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15
Q
  • eosinophilia, eczema, incr IgE
  • recurrent sinus infx, thrush, fractures, skeletal abnl, sinopulmonary infx
  • Tx: Abx, steroids
A

Job Syndrome (Hyper IgE)

16
Q
  • decr T-helper function–>decr IgG, IgA
  • manifests by 6 months
  • outgrow by 3-6 years
  • no intrinsic B cell deficiency
A

Transient Hypogammaglobulinemia of Infancy

17
Q
  • disorder of phagocyte function
  • cannot kill bacteria ad fungi
  • 2/3 X-linked, 1/3 AR
  • present by age 5
  • skin, GI, lung, liver, lymph node, and spleen infx
  • granulomas of skin, GI, GU
  • Dx: NTB test
  • Tx: Abx & interferon gamma
A

Chronic Granulomatous Disease

18
Q
  • defect in chemotaxis
  • high WBC
  • perirectal abscess, skin infx, omphalitis
  • no pus and minimal inflammation
  • delayed wound healing (umbilical cord separation)
  • Tx: BMT
A

Leukocyte Adhesion Deficiency

19
Q
  • fevers, wt loss, night sweats, malaise
  • decr CD4 count
  • incr Ig in 1st year
  • must receive PCP PPx
  • Tx: 2 nucleosidase analogs and a protease inhibitor
A

HIV

20
Q

-nucleosidase analog

A

Zidovudine

21
Q

-reverse transcriptase inhibitor

A

Nevirapine

22
Q

-Protease inhibitor

A

Indinavir

23
Q

-tests neutrophil activity (not number)

A

NBT (Nitroblue Tetrazdium)

24
Q

-tests the complement system

A

CH50

25
Q

-tests for cell mediated immunity associated with T cell defects

A

TB/Candida skin test

26
Q

-tests the humoral system

A

IgGAMEs

27
Q

-tests the ability of the cells to migrate in LAD

A

Rebuck Skin Window