immunology review Flashcards

1
Q

3 things immune cells do when active?

A
  1. Proliferate 2. Cytokine production 3. Adhesion molecules and trafficking
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2
Q

Cytokines do what

A

Make TF that enters nucleus affect gene transcription profile of cell

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3
Q

4 compartments of immune system

A
  1. Complement - land mines
  2. Phagocytes- the marines (neutrophils and macrophages)
  3. B cells - Air Force make deploy missile
  4. T cells - the generals, assasians, the psychologists
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4
Q

Complement immune system 3 pathways

A
  1. Classical (immune)
  2. lectin (pathogen)
  3. alternative (pathogen)
  • All Activate c3 and form membrane attack complex (MAC)
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5
Q

Encapsulated organism infections, or lupus or lupus like glomerulonephritis

A

Classical pathway early defect

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6
Q

Invasive infections with neisserial species

A

Late complement pathway defect

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7
Q

How test complement pathway of immune system, how treat?

A
  • Measure number by serum c3 and c4
  • measure function ch50 test (defect - absent response)
  • treatment- fresh frozen plasma, Eculizumab (HUS, hemolytic uremic syndrome)
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8
Q

C1q absent leads to?

A
  • lupus 90% time
  • early complement defect
  • made in bone marrow, so bone marrow transplant cure
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9
Q

Delayed separation umbilical cord

A

Leukocyte adhesion deficiency

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10
Q

Phagocyte deficiency-chronic granulomatus disease commonly present with?

A
  • Catalase + organism infections
  • Staph aureus, serratia marcesans, aspergillus
  • lack oxidative burst
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11
Q

Absent CD18 means

A

Leukocyte adhesion deficiency

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12
Q

Neutrophil oxidative burst absent means what

A

Patient has chronic granulomatous disease (phagocyte deficiency)

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13
Q

Treatment that target neutrophils

A
  • Colchicine- target microtubule formation
  • treat gout and rheumatism
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14
Q
  • Infection with no pus (clear weepy fluid)
  • very high circulating neutrophils (trapped can’t get out)
A

Leukocyte adhesion deficiency

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15
Q

Patient has recurrent bacterial sinopulmonary infection (ear and sinus infection, bronchitis)

A

B cell pathology

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16
Q
  • 5 year old boy history of ear infections and diffuse bronchiectasis (scarring)
  • labs: normal T cells, low B cells, low IgG, low IgM, low IgA
A
  • X Linked Agammaglobulinemia
  • BTK gene mutation, block B cell development
17
Q

8 year old boy with chronic cough and bronchoscopy show pneumocystis jirovecii

labs: normal T and Bcell count, low IgG, high IgM, low IgA

A

X linked hyper IgM syndrome (CD40 ligand deficiency)

18
Q
  • 17 year old female with recurrent sinusitis 2-3 sinus infections per year for 3 years, 2 bacterial pneumonias last 3 years. Has chronic cough and exercise intolerance. Feels tired all the time.
  • CXR show ground glass appearance in R lower lobe. Enlarged lymph nodes mediastinum
  • normal T cell count, low B cell, low IgG, normal IgM, low IgA, low vaccine response
A

Common variable immunodeficiency

19
Q
  • 7 month old boy episodic Otis media since 2 months, failure to thrive, now worsening respiratory status
  • CXR patchy infiltrates
  • Lab:lymphopneia, low T cell, normal B cell, low NK, Iow IgG, normal IgM, low IgG
A

Severe Combined Immune Deficiency (SCID)

20
Q
  • 5 month old boy with petechiae since 3 months, has thrombocytopenia (low platelets) 14000-32000, prolonged bleeding for 24 hours after circumcision, wheezing, recurrent Otis media
  • Mild eczema face
  • Labs: normal IgG, IgM and IgA
A

Wiskott-Aldrich Syndrome

21
Q

Inflammatory cytokines

A

TNF-alpha, IL-1, IL-6

22
Q

Cytokine growth factors

A
  • T cell: IL-2 and IL-7
  • B cell: IL-4 and IL-5
  • NK cells: IL-15
  • Neutrophils: G-CSF
  • Macrophages: GM-CSF
  • erythocytes
23
Q

What immune system defect can cause virus infections?

A

Tydpe 1 interferons (IFN-alpha, beta), and type II interferon (IFN-gamma), they generate in response to viral infection

24
Q

What defect in immune system would cause myobacteria infections?

A

IL-12, and interferon gamma

25
Q

Recurrent candida infections on skin caused by defect in what immune cytokines?

A

IL-17, Th17, and IL -23

26
Q
A