How the body responds to infection Flashcards

1
Q

Where do lymphocytes develop from?

A

Pluripotent stem cells in the primary lymphoid organs
B lymphocytes- fully mature in bone marrow
T lymphocytes- Leave bone marrow in bloodstream to mature in the thymus

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2
Q

When lymphocytes are released from primary lymphoid organs what happens?

A

Circulate in body to secondary lymph tissue- here the lymphocytes accumulate
E.g. Lymph nodes found throughout body , spleen and mucosa- associated lymph tissues: lining of respiratory tract, GI, urinary tract, tonsils and adenoids

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3
Q

Explain lymphocyte recirculation

A
  • Can cross walls into secondary lymphoid tissue e.g. spleen/ lymph node for 1/2 days then circulate around in the bloodstream
  • Leave lymph nodes via efferent lymphatic at major point between blood circulation and lymphatic system- thoracic duct
  • Some lymphocytes will enter peripheral tissues- drain out of tissues into tissue fliud and enter afferent lymphatics going back to the lymph node
  • Majority lymphocytes come straight from blood into lymph node, yet some does still come from peripheral tissue
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4
Q

Different types of infectious organisms? Is bodies response to these the same/ different and what may be a consequence of 1 part of the immune response being impaired?

A
  • Viruses
  • Bacteria
  • Fungi
  • Protozoa
  • Worms/ Helmets
  • 1st 4 all simple unicellular but worms multicellular
  • Effective immune system must defend against all these infectious agents
  • Hence some individuals mat be able to deal with some infectious agents and not others
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5
Q

Outline briefly ways of classifying immune cells

A
  • Leukocytes/ WBC- immune cells all produced from haematopoietic stem cells in the bone marrow
  • Include neutrophils, basophils, eosinophils, monocytes and leukocytes
  • Derived from myeloid (bone marrow) lymphoid tissue
  • Myeloid and lymphoid lineages both are involved in dendritic cell formation. Myeloid cells include monocytes, macrophages, neutrophils, basophils, eosinophils, erythrocytes, and megakaryocytes to platelets. Lymphoid cells include T cells, B cells, and natural killer cells.
  • Granulocytes- susceptible to dying revealing their granules- neutrophils, eosinophils, basophils
  • Others Agranulocytes
  • Polymorphonucleocytes- lobulated nuclei same as above but especially neutrophils due to lobed appearance
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6
Q

Define recognition and defence

A

Recognition- interaction with microbes and their components

Defence- elimination of microbes and their produces

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7
Q

Explain the innate immune response

A

Innate immune response- same quick response to infection hence moderate efficiency

  • General recognition occurs of PAMPS (pathogen associated molecular patterns)
  • Recognised by PRR- pattern recognition receptors
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8
Q

Explain features of adaptive immune response

A
  • slowly activated
  • High efficiency fully able to fight infection due to recognition of microbes down to sub-species level due to antigen receptors specific to the antigen
  • Lymphocytes will have specific antigen receptors which are clonally expressed (all in same clone have same receptor)
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9
Q

Define an antigen

A

anything specifically recognised by a lymphocyte of the body (functionality defined)

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10
Q

Primary immune response

A

1) Skin contains epithelial barrier consisting of a hard keratinised surface- if this is cut microbe can get into the soft underlying dermal tissues (warm nutritious environment ideal for replication
2) Immediate (innate) local response- macrophages activated by binding to the PAMP of the bacteria, complement proteins interact with the surface of the microbe making holes in cell wall
3) Early induced response (innate/ inflammatory)- inflammatory mediators form activated macrophages and mast cells, complement proteins also act as mediator
- Activates walls of nearby blood vessels, making leaky- causing fluid to enter infected tissues causing inflammation
4) Later adaptive immune response- dendritic cells carry processed antigen to the lymph node or soluble antigens carried in lymph
- Activation of specific T and B cells occur which can bind to specific antigen (clonal secretion)
- Clonal expansion occurs
- Recirculate to site of infection
- Some lymphocytes form memory cells

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11
Q

Different categories of infections

A
  • Extra-cellular pathogen- don’t penetrate cells- susceptible to anything that gains access to surface- complement proteins, phagocytes or antibodies
  • Intracellular cytosolic pathogen- viruses (not free living parasites that need cells machinery to replicate)- interferons proteins interfere with virus replication, natural killer cells, cytotoxic T cells
  • Intra-cellular vesicular pathogen- survive within the vesicles of the macrophage- have to by hyper-stimulated by helper T cells to help degrade ingested pathogen
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12
Q

What is immunopathology and outline different types

A

Diseases involving defects in, or inappropriate activity of, the immune system
- Immunodeficiency, allergy, autoimmunity, transplant rejection and lymphoproliferative diseases

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13
Q

Outline immunodeficiency

A

Immune system does not function properly- partial/ full impairment of the immune system so patient unable to effectively resolve infections and disease

  • Primary immunodeficiencies- due to genetic defects
  • Secondary immunodeficiencies- caused by environmental factors- HIV/AIDS/ malnutrition
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14
Q

Outline allergy

A
  • Inappropriate triggering of the immune system caused by external stimuli e.g. allergens
  • Pollen granules act as antigens which activate lymphocytes causing inflammation in airways and deeper in lungs in asthma
  • Food allergies- leading to anaphylaxis
  • Contact dermatitis e.g. nickel allergy
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15
Q

Outline autoimmunity

A

Autoimmunity= immune system triggered by auto-antigens activating auto-reactive lymphocytes causing autoimmune disease
e.g. in rheumatoid arthritis (attack on synovial joints- damage and degradation

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16
Q

Transplant rejection

A

Antigens on transplant tissue recognised as foreign and attacked by body
- Only transplant guaranteed to work= identical twin

17
Q

Lymphoproliferative diseases

A

Cancers of immune system e.g. Myelomas (plasma cells), leukaemia (myeloid), lymphomas (lymphoid)