Lecture 19 Flashcards

(30 cards)

1
Q

Innate immunity

A
  • cellular: neutrophils, NK cells
  • humoral: complement, antibodies
  • cancer therapies and immunosuppressive drugs reduce function
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2
Q

Adaptive immunity

A
  • cellular: T cells
  • humoral/spleen: B cells
  • monoclonal antibodies targeting B cells impair antibody production
  • no spleen/function heighten risk
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3
Q

Mucosal barriers

A
  • mucoliliary clearance in lungs
  • acidic environment in stomach
  • gut microbiota provides colonization resistance
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4
Q

barrier injury

A
  • skin disrupted by needles/catheter
  • chemotherapy/cytotoxic treatment causes mucosal damage, facilitates bacterial infections
  • malnutrition impairs neutrophils and T-cells
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5
Q

Comorbidities

A
  • psychological stress, diabetes, smoking
  • treatment for malignancies can harm surrounding tissue
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6
Q

Immunodeficiency disorders

A

one or more components of the adaptive or innate immune response is impaired
- inability to effectively resolve infections

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7
Q

Primary immunodeficiency

A

inherited immune disorders resulting from genetic mutations
- usually present at birth, childhood
- single gene mutations or unknown genetic susceptibility

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8
Q

Secondary immunodeficiency

A
  • acquired from other condition: HIV, malnutrition, medical treatment
  • managed by treating the primary condition
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9
Q

Burden of disease

A
  • 70-90% are undiagnosed
  • SID more common than PID
  • complications have significant cost-burden
  • diagnosis before 3.5 months could reduce costs
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10
Q

Age associations

A
  • most people diagnosed as a child: most severe cases
  • some diagnosed as adults: less serious but many infections
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11
Q

Young children diagnosis

A
  • recurrent infections within 1 year
  • failure to thrive
  • family history of PID
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12
Q

B cell immunodeficiencies

A
  • adaptive
  • loss of antibody production
  • risk of severe recurrent bacterial infections
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13
Q

T cell immunodeficiencies

A
  • adaptive and both
  • combined immunodeficiencies (defective T and B cell function)
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14
Q

Severe combined immune deficiencies (SCID)

A
  • immune and adaptive
  • lack T cells and reduced B cells
  • usually diagnosed in the first year
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15
Q

Phagocyte (WBC)

A
  • innate
  • phagocytes can’t destroy pathogens
  • infections cause severe disease
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16
Q

Complement defects

A
  • innate
  • lack complement proteins
  • highly susceptible to meningitidis
17
Q

Asplenia

A
  • lack of spleen function
  • innate, adaptive, and both
18
Q

Prevention

A
  • bone marrow transplant before 3 months
  • screen for disorders at birth
19
Q

Treatment

A

supportive therapy:
- preventative antibiotics and antifungals
- antibody replacement therapy
key vaccines recommended but live vaccines avoided
- herd immunity

20
Q

SID causes

A
  • protein calorie malnutrition
  • immunosuppressive drugs for transplants
  • chronic infections: HIV/AIDS
21
Q

Asplenia types

A
  • congenital asplenia
  • surgical splenectomy: trauma, immune disorders
  • sickle cell dz: progressive asplenic infarction
22
Q

post-splenectomy infection bacteria

A
  • encapsulated bacteria: s pneumoniae, h influenzae type B (Hib), n meningitidis
  • unusual gram negatives: capnocytophaga canimorsus (dog bites/scratches)
23
Q

post-splenectomy infection protozoa

A
  • babesia microti (ticks, blood transfusion)
  • plasmodium falciparum
  • severe parasitemia and complications
24
Q

Prevention for post-splenectomy infections

A
  • daily antibiotic prophylaxis
25
Infections in cancer
- rates of infection vary based on type/intensity of chemotherapy, disease status - highest rates occur in acute myeloid leukemia during high intensity treatment phase
26
Cancer treatment impacts
- mucositis and microbiota alterations contribute to increased risk - chemo/radiation reduce beneficial bacteria - central venous catheters increase risk - surgical site infections
27
Neutropenic fever
development of fever when low neutrophils - deeper and longer the neutropenia, higher risk of fever - risk increases after 7 days - mortality rates up to 70%
28
Neutropenic fever causes
- microbiologically defined infection - clinically defined infection - fever of unclear origin
29
neutropenic pathogens
80% of microorganisms arose from endogenous microbial flora - caused by all types of pathogens, many causes - gram negative dominant (p aeruginosa) in 60s-70s, gram positive (staph, s aureus) dominant after 80s
30
Cancer patient infection prevention
- prophylaxis recommended for all - influenza vaccine - little impact but no real alternative