3.1.11 Immune Failures Flashcards

1
Q

What is evasion of immune response?

A
  • Caused by antigenic variation and stereotypes
  • Same microorganism can express different antigens on its surface
    -Antibody in first immune response is useless when it interacts w/ different antigen
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2
Q

___ is important in influenza viral infections

A

Genetic recombination

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3
Q

Is there genetic recombination in covid?

A

No

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4
Q

Antigenic shift can lead to ___. Why?

A

Pandemic

Results in new virus that humans don’t have antibodies for and the entire population is vulnerable

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5
Q

Describe latency

A
  • Once you’re infected (w/ certain illnesses) you have it for your whole life
  • Certain viruses become latent and hidden from immune response
  • When activated, they cause recurrent infection
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6
Q

Herpes virus is an example of

A

Latency

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7
Q

Superantigens are produced by ___ bacteria. They stimulate a ___ response. What do they bind to and what do they connect?

A

Gram +
Ineffective and nonspecific response
Binds to MHC and connect MHC to T cell receptor

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8
Q

Superantigens have a big response of

A

IL-2
Gamma IF
TNF alpha

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9
Q

Can primary/ secondary immunodeficiency diseases be genetic or developmental?

A

Primary
NOT secondary

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10
Q

When does primary and secondary immunodeficiency diseases occur?

A

Primary at birth
Secondary after birth

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11
Q

Cause and treatment of Bruton’s agammaglobulinemia. What phase of B cycle is it stuck in? What’s a major problem with this disease?

A

Loss of tyrosine kinase results in lack of antibodies ( B cell defect)

IV-IG monthly

early B cell phase, WONT go to immature B cell phase

recurrent urinary tract infections

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12
Q

Cause of X-linked hyper-IgM syndrome

A

Lack of receptor for CD40 ligand or CD154 which is expressed by CD4+ T cells

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13
Q

What antibody is produced in X-linked hyper-IgM syndrome? Will macrophages be activated? why/why not?

A

IgM

No, b/c CD4 normally interacts w/ macrophage and releases gamma IF to activate macrophage to destroy, but since there’s no CD40 ligand, CD4 can’t be activated to interact

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14
Q

Symptom: patients become neutropenic and can develop sores/blisters in mouth
is for what syndrome?

A

X-linked hyper-IgM syndrome

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15
Q

What is the most common primary immunodeficiency? Describe it. What antibody is found in saliva?

A

Selective IgA deficiency

IgA is foreign

IgM found in saliva

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16
Q

Digeorge’s syndrome is also called

A

thymic hypoplasia

17
Q

Describe Digeorge’s syndrome

What’s an example?

A

Lack of thymus (T cell defect)

Patients have problems w/ viral infections, fungal infections, intracellular bacterial infections (ex: tuberculosis), parasitic infections…

nude mouse (hairless mouse)

18
Q

Result of Digeorge’s syndrome

A

antibody levels are lower than normal b/c lack of CD4+ TfH+ T cells

19
Q

___ disease lacks cell mediated immunity and humoral immunity

What’s an example?

A

severe combined immunodeficiency disease

Scid mice

20
Q

XSCID, RAG deficiency, ADA deficiency are examples of. what are each of their gene defects?

A

severe combined immunodeficiency disease

XSCID = IL-2 receptor gamma chain
RAG deficiency = RAG1 & RAG2
ADA deficiency = ADA

21
Q

Chronic granulomatous disease is a defect in ___. What can’t they produce? What does this affect?

A

patients phagocytic cells

O2 radicals and hydrogen peroxide

affects neutrophils and macrophages

22
Q

Leukocyte adhesion deficiency has 2 types. What are they?

A

Type I: lack of a specific integrin on PMNs (LFA-1)
- most common

Type II: lack of selectin receptor on PMNs (neutrophil)

23
Q

What is the common theme in leukocyte adhesion deficiency?

A

Patients can develop widespread pyogenic bacterial infections, diapedesis won’t occur (neutrophils can’t respond and kill microorganism)

24
Q

IL-8 is a ___ which is also a ___

A

Chemokine
Cytokine

25
Q

Within complement deficiencies, there is a lack of what 4 things?

A

Early C components (C1, 2, 4)
C3
membrane attack complexes (C5-9)
C1-esterase inhibitor

26
Q

In complement deficiencies, a lack of early C components (C1, 2, 4) is associated w/

A

immune-complex diseases, often autoimmune disease

27
Q

In complement deficiencies, a lack of C3 leads to

A

pyogenic bacterial infections
- deficiency in susceptibility to capsulated bacteria

28
Q

In complement deficiencies, a lack of membrane attack complex (C5-9) leads to

A

infection w/ neisseria SPP

29
Q

In complement deficiencies, a lack of C1-esterase inhibitor leads to

A

hereditary angioneurotic edema (HANE)

30
Q

complement deficiencies can affect ___ components/leads to defects in taking up of ___

A

early complement

immune complexes

31
Q

3 causes of secondary response

A

Malnutrition
Malignancy
Infections

32
Q

AIDS is caused by ___ , which infects ___

A

HIV

HIV infects CD4+ T cells all CD4+ subsets

33
Q

How can primary immune diseases be cured from patient? What are the steps?

A

Through BM transplant

Steps:
- Irradiation and chemotherapy (destroys bone marrow)
- Bone marrow infusion (Take donor blood w/ activated stem cells)
- Healthy patient

34
Q

Immunosuppressive therapy is used in treating patients w/

A

autoimmune diseases & in transplant setting

35
Q

Opportunistic infections are caused by

A

microbes held in check by immune system but in the immunocompromised host the infection may be life threatening

36
Q

Infections may be caused by

A

parasites, bacteria, fungi and viruses