Lecture 19 Immunology and Pathogenicity and Infection Flashcards

1
Q

What is the major mechanism that involves the rearrangement of antibody gene segments

A

VDJ Recombination

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2
Q

Describe VDJ Recombination

A
  • Recombination Activating Gene (RAG) enzymes
  • Activated in B cells
  • Randomly cut and paste gene segments.
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3
Q

When does Random Rearrangement of antibody gene segments occur?

A
  • As B cells develop in the bone marrow

- Early in embryonic life, before infection

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4
Q

What is tolerance?

A

Removal of self-reactive B cells

Largely occurs in bone marrow

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5
Q

What happens to the B cell upon infection?

A
  • antigen “selects” B cell with antibody that matches it.

- B cell proliferates, forming clone of identical cells, each with antibody for the antigen.

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6
Q

Secondary Response to antigen.

A

Activation of memory B cell strong response

- Basis of Immunization

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7
Q

Humoral

A

B cell and production of antibodies

- extracellular pathogens

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8
Q

Cell - Mediated

A
  • intracellular pathogens

- T cell

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9
Q

T cells

A
  • Originate in bone marrow, mature in thymus

- Activated when their receptors bind antigens presented by other cells

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10
Q

Helper T cells

A

-Make cytokines, activate B cells, macrophages, or other T cells

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11
Q

Cytotoxic T cells

A
  • kill cells expressing foreign antigens using

Perforins and Granzymes (enzymes)

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12
Q

What are the enzymes that Cytotoxic T cells use and what is there function?

A

Perforins - form pores

Granzymes - induce apoptosis

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13
Q

Describe Cluster of Differentiation (CD) molecules and the common examples.

A
  • membrane proteins on immune cells
  • Call also be used to determine cell’s identity
  • Helper T cells - CD4
  • Cytotoxic T cells - CD8
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14
Q

T - Cell Receptors (TCRs)

A
  • Receptors bind antigens (usually peptides) presented to the, by other cells
  • Only when presented with a MHC molecule
  • TCRs are expressed from gene segments rearranged in thymus.
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15
Q

Human Leukocyte Antigen (HLA)

A
  • Humans have 2 sets of MHC genes
  • One from each parent both are expressed

-Closer 2 people related, more similar their HLAs, important in donor selection for tissue, bone marrow and organ transplant- HLA Typing.

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16
Q

Class 1 MHC

A
  • on all nucleated cells
  • present peptides that originate in cytoplasm from intracellular pathogens
  • Present peptides to CD8+ Cytotoxic T cells
17
Q

Class 2 MHC

A
  • only on antigen-presenting cells (dendritic cells, macrophages, B cells)
  • Present peptides from extracellular pathogens, taken up by phagocytosis
  • Present peptides to CD4+ Helper T Cells
18
Q

What is a Pathogen

A
  • Organism that produces disease
19
Q

Opportunistic Pathogen

A

-Infects host with weakened immune system

20
Q

Carrier

A

-Infected individual potential source of infection (no observable symptoms)

21
Q

Zoonoses

A

-diseases transmitted to humans from animals

22
Q

Vector

A

-Organisms (usually insects) that transmit disease to humans - mosquitoes, ticks, fleas

23
Q

Pathogenicity

A

ability to produce disease

24
Q

Virulence

A

degree of pathogenicity

25
Q

Latency

A

Pathogen stops reproducing, dormant, can become active again

26
Q

How do we measure virulence?

A
  • Lethal Dose 50 (LD50)
  • # to kill 50% of hosts
  • Infectious Dose 50 (ID50)
  • # of pathogens required to cause clinical disease in 50% of inoculated hosts
27
Q

How do we study pathogens, Virulence and Pathogenicity.?

A

Model Systems - animal models, cell culture

Human Studies - Clinical Trials, Case studies

Epidemiology - Examine incidence, distribution, control of disease