5/3- Immuno heavy Flashcards

1
Q

Type of immune cells that attack in various transplant reactions, and time, and type of hypersensitivity reaction: hyperacute, acute, chronic, graft-v-host

A

Hyperacute (minutes): Recipient pre-existing antibodies (type II) against donor

Acute (weeks-mo): Recipient CD8 against donor (type IV)

Chronic (mo-years): Recipient CD4 against donor peptides brought in by APCs (type II and IV)

Graft-vs-Host (varies): Donor T cells against recipient (type IV)

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2
Q

IL-4 function

A

growth and differentiation of B cells

B cell isotype switching- esp. to IgE after allergen

differentiation to Th2

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3
Q

IL-5 function

A

growth and differentiation of B cells

IgA production

Eosinophils

Parasitic activity

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4
Q

Poison ivy is what type of hypersensitivity reaction

A

type IV- CD8

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5
Q

where does isotype switching occur?

A

germinal center of lymph node

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6
Q

which CD does isotype switching need and which cytokines stimulate it?

A

CD40

Il-2,4,5,6, IFNgamma

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7
Q

candidal antigen skin test

A

assesses T cell activity via type IV hypersensitivity test

uses CD4, CD8, and macrophages

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8
Q

Chediak-Higashi syndrome

A

Aut rec

defect in lysosomal trafficking regulator gene (LYST) and microtubule function in phag-lys fusion–> defective neutrophils

recurrent pyogenic infections (staph, strep), albinism, neuropathy, neurodegeneration)

giant granules, panctyopenia

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9
Q

Wiskott-Aldrich syndrome

A

WAS mutation- x linked rec- cant reorganize actin skeleton

Thrombocytopenia, Eczema, recurrent infections

high IgE, IgA

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10
Q

Chronic granulomatous disease

A

defect of NADPH oxidase– no resp burst in PMNs

x linked rec

susceptible to catalase positive organisms

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11
Q

Leukocyte adhesion deficiency

A

Aut rec- defect in LFA-1-integrin on phagocytes- no CD18

impaired neutrophil migration to inflamm sites

recurrent bacterial skin and mucosal inf, impaired wound healing, delayed separation of umbilical cord

leukocytosis

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12
Q

Hyper IgM syndrome

A

defective CD 40 L on TH cells– cant class switch

x linked rec

severe pyogenic infections- Pneumocystis, Crypto, CMV

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13
Q

Ataxia- telengtasia

A

defect in ATm- cant repair DNA ds breaks

ataxia and telengiectasia

IgA deficiency, high AFP

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14
Q

SCID

A

defective IL-2R gamma chain (x-linked)

or adensoine deaminase deficiency (aut rec)

diarrhea, thrush, recurrent infections, absent thymic shadow

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15
Q

IL-12 function and deficiency

A

TH1 differentiation

deficiency: mycobacterial infections. treat with IFNgamma

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16
Q

x-linked (bruton) agammaglobulinemia

A

defect in BTK, tyrosine kinase gene- x-linked rec

no B cell maturation- no CD19,20

recurrent bacterial and enteroviral/parasite infections (giradia)

17
Q

steps of leukocyte path to site of inflammation and cells involved

A
  1. Margination- microvasculature leak- wall shear stress
  2. Rolling- selectings
  3. Activation - signal cascade
  4. Tight adhesion- integrins (Mac-1 and LFA) and ICAM-1
  5. Transmigration- PECAM-1
18
Q

which cytokines help with the formation and maintenance of granulomas?

A

IL-12 –> Th1 –> IFNgamma –> macrophages–> TNF alpha

19
Q

Common variable immunodeficiency

A

defect in B cell differentiation

risk of autoimmune, bronchiectasis, lymphoma

20
Q

IL-12 receptor deficiency

A

Aut rec- decreased Th1 response–> decrease IFNgamma

mycobacterial and fungal infections

21
Q

autosomal dominant hyper-IgE syndrome

Job Syndrome

A

Deficiency of Th17 - STAT3 mutation

cant recruit PMNs

coarse facies, staph abscesses, eczema

high IgE

22
Q

chronic mucocutaneous candidiasis

A

T cell dysfunction

candida infection

23
Q

marker of infectivity in Hep B graph serotypes

A

HbeAg

24
Q

what does rheumatoid factor bind?

A

Fc component of IgG and anti-citrullinated protein antibodies (ACPAs)

25
Q

where are T cells in lymph node

A

paracortex