Midterm Part 1 Flashcards

1
Q

Which cells stem from the MCP?

A

monocytes (that mature into macrophages),
mast cells, and
granulocytes (neutrophils, basophils, and eosinophils).

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2
Q

Which cells stem from the CLP?

A

cytotoxic T cells (CTLs),
T helper (Th) cells,
T regulatory (Treg) cells,
B cells.

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3
Q

What are cytokines?

A
  • Soluble, secreted proteins of the immune system (interleukins)
  • Chemical messengers produced by immune and non-immune
    cells to regulate immune cell development and function
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4
Q

Where are DC’s derived from?

A

Some types are derived from the CMP, some from the CLP

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5
Q

What are the primary lymphoid organs, and what is their function

A

The place where developing lymphocytes mature:

the bone marrow (the center part of the long bones), and
the thymus (a flat, bi-lobed organ that is situated above your heart).
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6
Q

What is the function of secondary lymphoid organs are what are they?

A
  • place where mature lymphocytes encounter pathogens or foreign molecules and where adaptive immune responses begin
  • The spleen and the lymph nodes
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7
Q

What is lymph?

A

It is like blood, but no RBCs or platelets

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8
Q

What is an example of a physical and a chemical barrier that acts as a first layer of defence?

A

Physical: skin (dry and high salt environment)
Chemical: HCL in stomach, lysozyme in sweat and tears, lactic acid in vagina

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9
Q

After a pathogen breaks through the first layer of defence, what innate immune responses happen within MINUTES?

A
  • compliment activation

- macrophages phagocytose the pathogen

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10
Q

After a pathogen breaks through the first layer of defence, what innate immune responses happen within HOURS?

A
  • increased vasodilation, increased vascularity, recruitment of opsonins (leaky and sticky blood vessels)
  • Recruitment of more phagocytic cells (neutrophils and monocytes) to
    engulf and kill the pathogen. The changes in the blood vessel allow
    these cells to leave the blood and enter the tissue
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11
Q

Where do B cells mature?

A

In the bone marrow

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12
Q

?Where do T cells develop/mature? Where do they migrate after that?

A

In the thymus, in the secondary lymphoid organs

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13
Q

What happens if your spleen is removed?

A
  • When the spleen is surgically removed, some of its
    functions are taken over by the bone marrow and liver;
    other functions are simply absent, and the body manages
    without them
  • People without spleens are prone to systemic bacterial
    infections
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14
Q

What circulates through the lymph? (Options: erythrocytes, platelets, leukocytes)

A

Leukocytes (WBC)

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15
Q

Does lymph enter the spleen?

A

No

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16
Q

How are immune responses to tissue-borne infections initiated?

A

When naïve cells and lymph meet in lymph nodes,

pathogens can be detected

17
Q

What are the five types of Pathogen Associated Molecular Patterns?

A
  1. are not produced by the multi-cellular host organism,
  2. are shared by large groups of pathogens,
  3. do not undergo frequent mutation,
  4. are often essential for pathogen’s survival, and
  5. are recognised by PRRs in the innate response.
18
Q

What are the two main groups of Pathogen Recognition Receptors?

A
  1. phagocytosis receptors (that are used to bring the particle inside the phagocyte) and
  2. Toll-like Receptors (TLRs, to allow the phagocyte to determine if the particle is dangerous, i.e., a pathogen).
19
Q

What is the structure of TLR?

A
  • an extracellular leucine-rich domain that recognises the PAMP,
  • a transmembrane domain,
  • cytoplasmic domain that is homologous to the IL-1 receptor (a receptor that binds the cytokine, interleukin-1 (IL-1)
20
Q

What is the classical pathway? (Complement)

A

complement proteins are activated when antibodies made during a previous adaptive immune response bind to the pathogen surface

21
Q

What is the alternate pathway?

A
  • complement proteins bind directly to the bacteria and initiate the complement activation cascade directly (does not need antibodies)
  • There is alot of c3 in blood, so the reaction can happen spontaneously
22
Q

Explain how the complement cascade goes

A

The C3 convertase cleaves additional C3 into C3a and C3b; after binding, C3b recruits additional proteins to form the enzyme complex C5 convertase that cleaves C5 into C5a and C5b

23
Q

What is the function of C3 convertase and C5 convertase?

A
  • C3 convertase breaks down the protein C3 into C3a and C3b

- C5 convertase breaks down the protein C5 into C5a and C5b

24
Q

What is the function of C3a and C5a?

A
  • increases permeability of the blood vessels and induces the expression of adhesion molecules that allow leukocytes such as neutrophils and monocytes to attach to the blood vessels (leaky and sticky)
  • bind to receptors on the resident mast cells and resident macrophages to release additional histamine (C5a) and TNF-α (C3a)
  • C5a: chemoattractant of neutrophils and monocytes
25
Q

What is the function of C3b?

A

Opsonization (sticks to pathogen and gets macrophage to eat it)

26
Q

What is opsonization?

A
  • alteration of the pathogen surface or particle surface so that phagocytic cells can engulf it more efficiently (fork helps you eat your food more easily)
27
Q

What is the function of C5b?

A

Sticks to the cell and initiates forming the MAC (punches hole through the cell)

28
Q

What is the function of TLR? Where are they found?

A
  • Toll-like receptors (TLRs) are a type of PRR that allow innate cells of the immune system to identify something as dangerous to the host.
  • the plasma membrane of cells as well as endosomal membranes.