Immunology 3- complement system and connection to acquired responses Flashcards

1
Q

Are there normally low or high levels of inactive complement system proteins in the extracellular fluid?

A

Low.

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2
Q

How can the complement system become activated?

A

With hydrostatic pressure some of these proteins can leak out from the capillary beds into extracellular fluids. If a pathogen is present , the complement system can be activated which causes a cascade of chemical reactions.

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3
Q

What do the chemical reactions caused by the activated complement system prompt?

A
  • Opsonization of pathogens
  • Direct pathogen killing
  • Acute inflammation
  • Leukocyte recruitment
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4
Q

What is C3, what happens to it, and what does it do?

A

It is a protein of the complement system.

C3 (inactive form) ——> C3b + C3b (active) by cleaving.

Causes down stream pathways.

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5
Q

What are the three ways in which C3 can be cleaved?

A
  • Classical pathway
  • Mannose-binding lectin pathway
  • Alternative pathway
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6
Q

What do C5b and C3b do?

A

Are a good opsonins which means they enhance phagocytosis

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7
Q

What do C5a and C3a do?

A

Are involved in acute inflammation create a positive feedback loop, changing the vasculature etc. Also have an effect on mast cells.

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8
Q

What are dendritic cells?

A

Phagocytic cells which create a link between the innate and the acquired immune systems. They are activated by the acute inflammatory signals and play an important role in activating T cells. Present antigens on their cell surfaces (professional antigen presenting cell)

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9
Q

Describe the alternative pathway.

A

C3b is unstable. If there is a pathogen present, it can bind to the molecules on the pathogen’s surface and become stable. It can feed back into the alternative pathway with chemical signals from C3b) which generates an enzyme complex called C3 convertase which can then make more C3.

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10
Q

Why in a non infectious environment is the complementary system inactive?

A

Cells have inhibitory molecules on them that make sure C3b doesn’t activate and cause down stream pathways without the presence of a pathogen.

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11
Q

Describe the Mannose-binding lectin pathway.

A

Mannose binding lectin (MBL) Binds to certain sugars including mannose found specifically on types of bacteria. Mannose is not shown on human cells. Binding of Mannose-binding lectin to mannose it will activate C3 convertase and cause a cascade of down stream events which will lead to the formation of an enzyme which will cleave C3 to C3b and C3a.

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12
Q

Describe the downstream complement pathway.

A

C3b binds to pathogen and interacts with other inactive molecules which will generate an enzyme complex to form C5a and C5b. C5b activates MAC (membrane attack complex) which forms pores and can directly kill pathogens.

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13
Q

What are the two types of lymphocytes?

A

B cells and T cells.

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14
Q

What do B cells do (general)?

A

They are responsible for humoral (through fluids) immune responses. They play a key role in attacking extraceullar pathogens and they produce antibodies that attack pathogens circulating in the blood and lymph.

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15
Q

What do T cells do (general)?

A

They are responsible for cellular immune responses. They play a key role in defence against intracellular pathogens.

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16
Q

What are the two types of T cells?

A

CD4+ T cells and CD8+ T cells

17
Q

Antigen receptors can only bind to one specific antigenic epitope. True or false?

A

True.

18
Q

What is the B cell receptor (BCR)?

A

A membrane bound antibody.

19
Q

Describe the structure of an antibody.

A
  • It has a unique variable region (antigen binding site)
  • it has 2 identical light polypeptide chains and 2 identical heavy polypeptide chains.
  • a protein
20
Q

What is the only type of antigen that a T cell can recognise?

A

peptide antigens (presented by MHC molecules)

21
Q

Describe a T cell receptor (TCR).

A
  • unique to one peptide antigen

- tips of the alpha and beta TCR chains form the hyper-variable binding site.

22
Q

What are MHC molecules?

A
  • Major histocompatibility complex

- display peptide antigens to T cells

23
Q

What are the two classes of MHC molecules?

A

MHC class I and MHC class II

24
Q

Which type of T cell recognises MHC I molecules?

A

CD8+ T cells

25
Q

Which type of T cell recognises MHC II molecules?

A

CD4 + T cells

26
Q

Describe MHC I.

A

They are expressed on ALL nucleated cells

27
Q

Describe MHC II.

A

They are expressed ONLY on professional antigen presenting cells (APCs) e.g. dendritic cells and macrophages etc.

28
Q

Where are B cells made?

A

Bone marrow.

29
Q

Where are T cells made?

A

Thymus.

30
Q

What are primary lymphoid tissues?

A

Bone marrow and Thymus.

31
Q

What are secondary lymphoid tissues?

A

Spleen and lymph nodes.

32
Q

Where are T and B cells activated by antigens?

A

Secondary lymphoid tissues.

33
Q

What vessels do T and B cells enter and exit the lymph nodes from?

A

Afferent lymphatics (entry) and Efferent lymphatics (exit)

34
Q

How do B cells encounter antigens?

A

After a pathogen has been phagocytosed and the debris (antigens) has been released, the opsonised antigens travel to the B cell zones in lymph nodes where a B cell can detect the antigen.

35
Q

How do T cells encounter pathogens?

A

Dendritic cells phagocytose pathogen-derived particles and antigens. TNFa then stimulates immature tissue-resident Dendritic cells to increase expression of co-stimulatory molecules. Dendritic Cells digest ingested proteins and display small peptides derived from these on their cell surface in complex with MHC proteins. Dendritic cells with the digested proteins then goes into a lymph node.