Midterm Part 5 Flashcards

1
Q

What are the three main types of secreted antibodies?

A

IgM, IgG, IgA

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2
Q

How does IgG kill pathogens? Where is it located?

A
  • Neutralization, opsonization, complement activation

- bodily secretions

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3
Q

Which antibody contributes to passive immunity from mother’s immune system across the placenta?

A

IgG

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4
Q

What is the purpose of IgA? Where is it found?

A

bodily secretions (tears, saliva, mucus, mother’s milk, etc.). Its purpose is to bind to and neutralize pathogens

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5
Q

Where is IgE found? What does it do?

A

In serum, it binds to mast cells and triggers histamine response, also gets rid of worms/parasites
- located in tissues

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6
Q

How does IgM kill pathogens? Where is it located?

A
  1. Neutralization
  2. Complement activation
    (Opsonization happens through complement activation)
    - blood
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7
Q

If the T helper cell produces IFNy, what will the antibody class switch to?

A

IgG

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8
Q

What is the most appropriate response for an intracellular bacterial infection? (Cell-mediated response)

A
  1. Local innate responses to contain pathogen Spread
  2. Activation of adaptive immunity
    • CD4+ T helper cells
    • Effector function: cytokines to help MP activation
    (B cells are less important)
3. Ag-specific CD4+ Th cell activation
• Cytokine mediated activation of Mϕ function
• Mϕ activation
• Enhanced phagocytosis
• Destroy pathogen
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9
Q

How does the dendritic cell uptake the viral peptide and display it through cross presentation?

A

DC—Phagocytosis of the viral pathogen, and displays on both MHC I and II

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10
Q

What is the appropriate response for a viral pathogen?

A
Cell-mediated immunity:
- TH cells to coordinate CTLs and B cells
- CTLs to kill infected cells
Humoral immunity:
- Antibodies to neutralize and prevent 
entry
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11
Q

True or False: The TCR of a thymocyte must be able to interact with an MHC protein in order for the thymocyte to escape apoptosis.

A

True

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12
Q

True or false: Healthy cells present MHC without a peptide on the cell surface

A

False

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13
Q

True or False: A vaccine that contains “live” virus particles will generate a CTL response and an antibody response.

A

True

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14
Q

True or false: A vaccine that contains a protein isolated from a virus particle will generate a CTL response and an antibody response.

A

False

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15
Q

What are the steps of an extracellular bacterial response?

A
  1. Tissue damage is a danger signal to activate mast cell degranulation
  2. Leads to the characteristic signs of inflammation
  3. Macrophages activate by PRR recognition (phagocytic and TLRs) of bac PAMP
  4. Alternative activation of complement cascade
  5. Macrophages release IL-1, IL-6 and TNFa and CXCL8
  6. DC phagocytosis bacteria and migrates to the lymph node to present the peptide to the T cell (could also travel through the lymph node on its own)
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16
Q

What kinds of lymphocytes generate long lived memory cells?

A

B cells, T helper cells, and cytotoxic T cells

17
Q

Why is the secondary response better, faster, and bigger?

A
  1. More antigen specific cells - BIGGER
  2. Memory cells are easier to activate than naïve cells - FASTER
  3. Memory cells have improved their ability to function (especially for
    B cells) - BETTER
18
Q

Why are effector functions increased and improved in secondary response?

A
Increased: Ab production, Th cytokines, and CTL killer function
Improved: already class switched
19
Q

Where do long lived plasma cells live?

A

In the bone marrow

20
Q

Where do long lived memory B cells live?

A

Secondary lymphoid organs

21
Q

What is active immunity?

A

The immune system is doing the work of making antibodies
•B cells and T cells are becoming activated, proliferating and differentiating
•Memory responses develop
Example: influenza infection or vaccine

22
Q

What is passive immunity?

A
  • you are getting antibodies made by someone (or something) else
  • your immune system has done zero work in making these antibodies
  • you will not develop memory responses
  • temporary - the antibodies are degraded over time
23
Q

What kind of antibody does mother’s milk have?

A

IgA

24
Q

What are polyclonal antibodies and how are they prepared?

A
  • Multiple targets

* Prepared by immunising an animal (rabbit, goat) and collecting blood

25
Q

What are monoclonal antibodies and how are they prepared? What are they useful for?

A
  • One target
  • Prepared by fusing B cells with a cancer cell to form a hybrid cell called a “hybridoma”

Useful for:

  1. Testing if someone has been exposed to an infectious agent or had a vaccine for one
  2. Measuring soluble proteins (cytokines or hormones)
  3. Visualizing cells and proteins they produce within tissues
  4. Identifying the presence, quantity, and phenotype of different cell types
  5. Treating disease
26
Q

How is ELIZA used to test if someone has antibodies against a particular agent?

A
  1. Bind a known target (antigen) to the plastic
  2. Add primary antibody (from hybridoma) specific for the target, incubate, then wash away
  3. Add Secondary Ab, specific for the primary Ab, eg. anti-human IgG, bound to an enzyme, incubate and then wash
  4. Add Substrate for the enzyme, that produces a colour
27
Q

How is ELIZA used to measure the concentration of a soluble protein in a sample?

A
  1. Add known primary antibody
  2. Add diluted patient serum (and a known concentration of protein as a control), incubate and wash
  3. Add enzyme-linked secondary antibody, incubate and wash
  4. Add coloured substrate for enzyme
28
Q

How do you used fluorescence microscopy?

A
  1. Take a throat swab from a patient and rub it onto a microscope slide.
  2. Fix the bacteria to the slide.
  3. Soak the slide in a solution of fluorescent antibodies that recognises the bacteria.
  4. Wash away unbound antibodies.
  5. Place the slide on a fluorescence microscope. The microscope has a light source that emits light of the proper wavelength in order to excite the fluorescent molecule. It also has filters that allow you to see only the light emitted by the fluorescent molecules.
  6. If bacteria are present, bacteria on the slide will be lit up and visible through the microscope.
29
Q

What is graft rejection? What are the two types?

A

when the recipient’s T cells mount an attack against the donor organ

  1. INDIRECT ALLORECOGNITION: antigen presenting cells (APCs) from the recipient take up and process MHC proteins from the transplanted organ/tissue. The recipient T cells then recognize the presented peptide as foreign and mount a response
  2. DIRECT ALLORECOGNITION: donor-derived antigen-presenting cells are able to move out of the transplanted organ and interact with the recipient’s T cells. The recipient T cells recognize the MHC proteins on these donor-derived APCs as foreign and react very strongly (independent of the peptide presented)
30
Q

What is tissue typing?

A

the process that determines the specific HLA alleles that an individual has.

31
Q

What is graft vs host disease?

A

If hematopoietic stem cells are transplanted into a recipient’s body with the allograft, the transplanted immune cells might recognize the host’s MHC as foreign and mount an immune response against the host’s cells, tissues and organs