Immunology Flashcards

1
Q

What is the role of the thymus?

A

Site of T lymphocyte maturation (leave as either CD4+ helper cells of CD8+ killer cell) and selects and deletes auto-reactive cells to prevent autoimmunity. A primary lymphoid organ.

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2
Q

What are lymph nodes?

A

Nodular aggregates, located along the lymphatic system when the immune response is initiated and where antigen is concentrated having arrived via the lymph.

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3
Q

What is a type I hypersensitivity reaction?

A

Type I reactions (ie, immediate hypersensitivity reactions) involve immunoglobulin E (IgE)–mediated release of histamine and other mediators from mast cells and basophils. Examples include anaphylaxis and allergic rhinoconjunctivitis.

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4
Q

What are the hypersensitivity reactions?

A
4 types:
Type I- Immediate hypersensitivity
Type II-Antibody-mediated
Type III-Immune complex mediated
Type IV-T cell mediated
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5
Q

What is an organ-specific autoimmune disease?

A

Autoimmune attack versus self antigens of a given organ. This leads to damage of the organs structure and function. Examples: Type 1 diabetes mellitus, Goodpasture’s syndrome, MS, Graves Disease, Myasthenia Gravis.

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6
Q

What is a non-organ specific (systemic) autoimmune disease?

A

Widespread self-antigens are targets for autoimmune attacks. Damage effects structure such as blood vessel and cell nuclei etc. Examples: Rheumatoid arthritis, scleroderma.

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7
Q

What causes Graves disease?

A

Autoantibodies against the thyroid stimulating hormone receptor leading to hyperthyroidism- overproduction of thyroid hormones.

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8
Q

What is primary immunodeficiency?

A

The deficiency is the primary cause of the disease. Primary immunodeficiencies are usually congenital, resulting from genetic defects in component of the immune system. Most common class of primary immunodeficiency is in B lymphocytes/antibodies, 50% of cases.

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9
Q

What is secondary immunodeficiency?

A

Deficiency as acquired as a result of other diseases or conditions eh. HIV, malnutrition, immunosuppression.

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10
Q

What happens in transplant rejection?

A

T cells are activated against donor transplantation antigens, stimulated in peripheral lymphoid tissues, Both CD4 and CD8 cells.

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11
Q

What is the autoantibody target in Myasthenia Gravis?

A

Acetylcholine receptor.

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12
Q

What is the autoantibody target in Guillain-Barre syndrome?

A

Gangliosides (peripheral nerves). Triggered by infections including Campylobacter jejuni. Common cause of acute paralysis.

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13
Q

What are the 3 pathways to activate complement?

A
  • Classical pathway.
  • Lectin pathway.
  • Alternative pathway.
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14
Q

How does the classical pathway to complement work?

A

Classical pathway- antibody binds to specific antigen on pathogen surface.

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15
Q

How does the lectin pathway to complement work?

A

Lectin pathway-Mannose binding lectin binds to pathogen surface.

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16
Q

How does the alternative pathway to complement work?

A

Alternative pathway-pathogen surface creates local environment conducive to complement activation.

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17
Q

Where are MHC class I proteins found and what cells do they present to?

A

MHC1 found on all nucleated cells and present to CD8+ T cells.

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18
Q

Where are MHC class II proteins found and what cells do they present to?

A

Restricted to DC, macrophages, B cells etc. (antigen presenting cells). Presents to CD4+ T cells.

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19
Q

What is an antigen?

A

Any molecule that can bind to an antibody or generate peptide fragments that are recognised by T-cell receptors.

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20
Q

What does the bone marrow do?

A

Produces red blood cells and lymphocytes. Site of haematopoietic stem cells- can give rise to all of the different mature blood cel types and tissues.

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21
Q

What happens in bone marrow failure?

A

The liver, thymus and spleen may resume their haemtopoeitic function. This is called extramedullary hematopoiesis. It may cause organs to increase in size substantially.

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22
Q

In the developing embryo where does blood formation take place?

A

Occurs in in the yolk sac then as the organs develop the spleen, liver and lymph nodes take over this task until finally bone marrow develops and makes the majority of blood cells.

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23
Q

What shape is an IgM molecule?

A

A pentamer.

24
Q

What is the principal class of antibody in secretions including salvia, tears, milk etc.?

A

IgA, principal class of Ab in the gut and many secretions. IgA is a dimer.

25
Q

What is Crohn’s disease?

A

An inflammatory condition of the gut-can affect anywhere from the mouth to the anus.

26
Q

What is psoriasis?

A

A common (10% of the population) skin condition which is also associated with arthritis in some people.

27
Q

What is sarcoidosis?

A

A rare multisystem autoinflammatory disorder affecting skin, joints, neurology and causing lymphadenopathy.

28
Q

What is uveitis?

A

Inflammation in the uveal treat (eye).

29
Q

What is ankylosing spondylitis?

A

One of the types of inflammatory arthritis that affects the spine.

30
Q

What is juvenile idiopathic arthritis?

A

A group of childhood onset arthritis.

31
Q

What is the meaning of ‘rubor’ and how does it occur?

A

Red, local vasodilation.

32
Q

What is the meaning of ‘dolor’ and how does it occur?

A

Pain, stimulating nerve endings by cytokines.

33
Q

What is the meaning of ‘calor’ and how does it occur?

A

Heat, local vasodilation.

34
Q

What is the meaning of ‘tumor’ and how does it occur?

A

Swelling, vasodilation accompanied by increased permeability of vessels and increased interstitial fluid (taking important immune responses and cells with it).

35
Q

What is the meaning of ‘functiolaesa’ and how does it occur?

A

Loss of function due to the other signs of inflammation: redness, heat, swelling and pain.

36
Q

What are the 4 basic components of complement?

A

1) Opsonisation-enhancing phagocytosis of antigens.
2) Chemotaxis-attracting macrophage and neutrophils.
3) Cell lysis-rupturing membranes of foreign cells.
4) Clumping- clumping of antigen-bearing agents.

37
Q

What is the thoracic duct?

A

Largest lymphatic vessel in the body. It connects the lymphatic vessels of the legs, abdomen, left arm and left side of head, neck and thorax to the brachiocephalic vein.

38
Q

What are Peyer’s Patches?

A

Small masses of lymphatic tissue found throughout the ileum region of the small intestine. Also known as aggregated lymphoid nodules, they form an important part of the immune system by monitoring intestinal bacteria populations and preventing the growth of pathogenic bacteria in the intestines.

39
Q

How many tonsils are there in the body?

A
  1. 2 lingual, 2 palatine and 1 pharyngeal.
40
Q

What is chyle?

A

A white milky substance in the lymphatic system due to transportation of the fatty acids from the digestive system into the circulation.

41
Q

What is elephantiaisis?

A

An infection of parasitic worms int he lymphatic system which causes the limb to swell to elephant-like proportions.

42
Q

What is ‘oxidative burst’?

A

Rapid release of reactive oxygen species (superoxide radical and hydrogen peroxide) from different types of cells, including neutrophil in response to bacteria.

43
Q

What does granulocyte colony stimulating factors do?

A

Stimulates neutrophils to proliferate, but is not chemoattractive.

44
Q

What are proinflammatory cytokines?

A

Small messenger proteins released by immune cells in response to infection which interact to mediate the acute inflammatory response.

45
Q

What is humoral immunity?

A

The term for a specific adaptive immune response activated by TH2 cells, which leads to the production of B cells and antibodies.
This immune response is designed to fight extracellular infections, including most bacteria and fungi, protozoans such as Giardia, and parasitic worms such as Schistosoma.

46
Q

What is cell-mediated immunity?

A

The term for a specific adaptive immune response activated by TH1 cells, which leads to activation of antigen presenting cells and a cytotoxic T cell response.
This immune response is designed to fight intracellular infections, including viruses, some bacteria and fungi, and protozoans such as Plasmodium and Toxoplasma.

47
Q

What is autoimmunity?

A

Loss of immunological tolerance to self. Various mechanisms:

  • Dysfunction in tolerance.
  • Presentation of self-antigens.
  • Molecular mimicry.
  • Loss of regulatory mechanisms.
48
Q

What is tolerance?

A

Controlled unresponsiveness to self. Maintained by numerous control mechanisms.

49
Q

What is rheumatoid arthritis?

A

A chronic, systemic symmetrical polyarthropathy characterised by joint pain, stiffness, swelling and destruction. Severity measured using disease activity score (DAS). Anything about 5.1 is high disease activity. Alteration of the disease course is the treatment goal.

50
Q

What is a DMARD?

A

Disease modifying anti-rheumatic drugs. The main ones are methotrexate, sulfasalazine and antimarial drugs ie. hydroxychloroquinine.

51
Q

What is methotrexate?

A

A dihydrofolatereductase inhibitor. Cannot synthesise DNA.

52
Q

What is sulphsalazine?

A

2 parts: Sulfapyridine- antibiotic and 5-aminosalicylic acid-a non steroidal.

53
Q

How does hydroxychloroquinine work?

A

It accumulates in lysosomes and stabilises them by inhibiting acid proteases. Inhibits TLR9.

54
Q

What is Rituximab and how does it work?

A

A monoclonal antibody against CD20 on B cells- causes their depletion and so helps reduce inflammation. A biologic therapy- very expensive!

55
Q

What is Abatacept and how does it work?

A

A CTLA-4 fusion protein. CTLA-4 is unregulated in activated T cells and can bind to CD80/86 (protein B7). Therefore, blockade of this prevents signal II and T cell activation. In short, it blocks the 2nd signal in T cell activation.