Immunology Flashcards

1
Q

What are the key features of the Immune System?

A
  • Able to specifically identify non-self and danger signals.
  • Able to modify the response to deal with different pathogens.
  • Able to actively promote tissue repair and healing.
  • Able to remember any pathogen it encounters. (Immunological Memory)
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2
Q

Name some constitutive barriers to infection?

A
  • Skin.
  • Mucous.
  • Commensal Bacteria.
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3
Q

Describe the skin barrier.

A
  • Physical barrier: multi-layered, renewal and replacement.
  • Physiological factors: low pH 5.5, low O2 tension.
  • Sebaceous glands: secrete hydrophobic oils, lysozyme, ammonia, antimicrobial peptides.
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4
Q

Describe the mucous barrier.

A
  • Mucous membranes: Secrete mucous where cavities come into contact with the environment.
  • Physical barrier: traps invading barriers.
  • Secretory IgA: prevents Bac and Virus attaching and penetrating epithelial cells.
  • Contains enzymes: lysozymes, defensins and antimicrobial peptides directly kill. Lactoferrin starve bacteria of iron.
  • Cillia trap and physically remove pathogens.
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5
Q

Describe the commensal bacteria.

A
  • 100 trillion (10^14) normally reside at epithelial surfaces.
  • Produce Bactercidins influencing other bacteria.
  • Reduction in pH of large bowel.
  • Competition for essential nutrients,
  • Production of anti-microbial short-chain fatty acids.
  • Synthesis of vitamins K and B12.
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6
Q

How important are commensal bacteria?

A
  • Eradication of normal flora with broad-spectrum antibiotics commonly result in infection.
  • Organisms rapidly colonize an undefended ecological niche.
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7
Q

How are constitutive barriers breached during health care?

A
  • Insertion of intravenous lines, catheters, nasogastric tubes.
  • Antibiotics.
  • Anti-acids, nasal decongestants, anti-bacterial wipes.
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8
Q

Name the Major Components of the immune system.

A
  • Cells: Leukocytes, White blood cells.

- Soluble factors: Humoral factors.

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9
Q

Name Phagocytes.

A
  • Neutrophils.
  • Monocytes and macrophages.
  • Dendritic cells.
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10
Q

Name Lymphocytes.

A
  • T cells.
  • B cells.
  • Natural killer cells.
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11
Q

Name other cells.

A

Mast cells, Eosinophils and Basophils.

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12
Q

Name Humoral factors.

A
  • Antibodies.
  • Complement system proteins.
  • Cytokines.
  • Acute phase proteins.
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13
Q

Cytokines.

A
  • Diverse collection of small proteins and peptides produced in response to infection, inflammation and damage.
  • Modulate behaviour of cells so play a key role in coordinating the immune system.
  • Multiples overlapping functions.
  • Short half-life.
  • Local or systemic.
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14
Q

Antibodies.

A
  • Protein produced in response to specific antigen.
  • Produced by antigen-activated B Cells.
  • Defend against pathogens, viruses and toxins.
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15
Q

T cells and B cells.

A
  • Mature cells circulate through the blood, lymph, and secondary lymphoid tissues.
  • Inactive until meet pathogen/antigen.
  • Some are very long lived. (memory T and B).
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16
Q

B Lymphocytes.

A
  • Responsible for production and secretion of antibodies to defend against pathogens.
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17
Q

T Lymphocytes.

A
  • Helper T cells: Key regulators of immune system.

- Cytotoxic T cells: Kill virally infected body cells.

18
Q

Natural Killer cells.

A
  • Large granular lymphocytes.
  • Can detect and kill tumour cells and virally infected cells.
  • Can kill antibody-bound cells/pathogens.
19
Q

Mast cells.

A
  • Reside in tissues and protect mucosal surfaces.
20
Q

Basophils, Eosinophils.

A
  • Circulate in blood.

- Recruited to sites of infection by inflammatory signals.

21
Q

Mast, Basophils and Eosinophils.

A
  • Highly granular.
  • Release Histamine, Heparin, and pro-inflammatory cytokines.
  • Defense against pathogens that cannot be phagocytosed. (worms)
  • Key role in mediating allergic responses.
22
Q

Complement system.

A
  • Approx. 30 proteins.
  • Produced in Liver.
  • Circulate in blood as inactive precursors.
  • Enter infected/inflamed tissues.
  • Enzymatically cleave and activate more in biological cascade.
23
Q

Monocytes, Macrophages, and Neutrophils.

A
  • Phagocytes.
  • Ingest and clear debris from body.
  • Important source of Cytokines.
24
Q

Monocytes.

A
  • Circulate in the blood.

- Migrate to peripheral tissues and differentiate into macrophages.

25
Q

Macrophages.

A
  • Long-lived tissue resident in phagocytes.
  • Kupffer = Liver.
  • Alveolar = Lung.
  • Mesangial = Kidney.
  • Microglial = Nervous.
  • Limit inflammation, tissue repair, antigen presentation.
26
Q

Neutrophils.

A
  • Phagocytic cells that circulate in the blood.

Rapidly recruited into inflamed, damaged, and infected tissues.

27
Q

Dendritic cells.

A
  • Present in peripheral tissues in an immature state.
  • Phagocytose antigens.
  • Mature and migrate into secondary lymphoid tissues where they play a key role in antigen presentation.
28
Q

Comparing dendritic, macrophage, and neutrophils.

A
  • Neutrophils: Complete destruction of proteins are seen.
  • Dendritic: Partially degraded for antigen presentation and stimulation of adaptive response.
  • Macrophages: Neutral = Clearance of dead host cells.
    Activated = phagocytosis of pathogens.
    Repair = reduced activity, produce pro-inflammatory cytokines.
29
Q

Primary Lymphoid Tissues.

A
  • Sites of Leukocyte development.
30
Q

Where do Lymphocytes mature and circulate?

A
  • Mature: bone marrow or thymus.

- Circulate: between blood, secondary peripheral lymphoid tissues and lymph.

31
Q

What are the immunological precursors found in bone marrow?

A
  • Hematopoietic stem cells.
32
Q

Secondary Lymphoid Tissues.

A
  • Sites where T cells and B cells become activated by antigen. (initiates adaptive immunity).
33
Q

Name secondary lymphoid tissues.

A
  • Lymph Nodes: imp stations for monitoring tissues infections.
  • Spleen: imp in monitoring blood-borne infections.
  • Mucosal: associated lymphoid tissues.
34
Q

Lymphatic system.

A
  • System of vessels draining lymph fluid from body tissues.
35
Q

Lymph.

A
  • Derived from blood plasma in tissues.

- Drains back to blood via lymphatic vessels and the right subclavian vein.

36
Q

Lymph Nodes.

A
  • Positioned along lymph vessels to monitor the lymph for signs of infection.
37
Q

Lymphoedema.

A
  • Lymphatic obstruction.
  • Inherited, cancer treatment and parasitic infections.
  • At increased risk of infection.
38
Q

Immune system compromised of two arms.

A
  • Innate Immune.

- Adaptive Immune.

39
Q

Innate Immune system.

A
  • Acute inflammation.
  • Macrophages.
  • Mast cells.
  • NK cells.
  • Neutrophils.
  • Complement.
  • Leads to Dendritic cells.
40
Q

Adaptive Immune system.

A
  • B cells, Antibodies.
  • T cells.
  • D cells and macrophages present antigens.
  • Activates T cells.
  • T cells produce cytokines that help phagocytes.
  • B cells produce antibodies that coat bacteria and help phagocytes.
41
Q

Innate system response.

A
  • Rapid response (mins-hrs).

- Generic biological response is produced in response to many pathogens.

42
Q

Adaptive system response.

A
  • Slow response (days).
  • A unique response for every pathogen.
  • Mediated by T and B cells.
  • Responsible for immunological memory.