06-10-21 - Chronic Inflammation Flashcards

1
Q

What are the usual sequelae of acute information?

What can cause it to take difference routes?

A
  • Acute inflammation typically ends in resolution
  • If there is excess exudate, this can lead to suppuration, which can cause the discharge of pus, and eventually leads to repair and resolution
  • If there is excessive necrosis (dead tissue), this can lead to repair and organisation, which can cause fibrosis (thickening or scarring of the tissue)
  • If the causal agent Is persistent, this can cause chronic inflammation, which can lead to fibrosis)
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2
Q

What are the 4 factors that favour resolution from acute inflammation?

A
  • Minimal cell death and tissue damage
  • Occurrence in an organ or tissue with regenerative capability, such as the liver
  • Rapid destruction of the causal agent
  • Rapid removal of fluid and debris by good local vascular drainage
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3
Q

What is organisation?

What is fibrous tissue made from?

What are the 3 factors that favour organisation?

What are indications of organisation on a diagram?

A
  • Organisation is the replacement of destroyed tissue by granulation tissue, which leads to fibrosis (thickening/scarring) (fibrous tissue is composed of parallel bundles of collagen)
  • Factors that favour organisation:
  • Large amounts of fibrin (protein involved in wound healing)
  • Substantial necrosis
  • Exudate and debris can not be removed or discharged
  • Indications of organisation on a diagram:
  • Formation of sprouting capillaries
  • Infiltration of inflammatory cells e.g macrophages
  • Proliferation of fibroblasts – fibroblasts are the most common cell type in connective tissue.
  • Fibroblasts secret collagen which is used to maintain a structural framework in tissues. They are also involved in healing in wounds.
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4
Q

What happens during healing of a severe burn?

What does granulation appear like in a severe burn?

What is the inflammatory exudate replaced by during organisation?

A
  • In a severe burn, much of the skin is destroyed, and the underlying tissue will be undergoing repair.
  • The damaged area is being replaced by vascular granulation tissue
  • The burn is red and has a moist, bumpy appearance due to the new sprouting capillary beds in the granulation tissue.
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5
Q

Why is inflammatory exudate replaced during organisation?

What is it replaced by?

What are the growth factors that regulate this process?

A
  • When inflammatory exudate cannot be cleared away properly, it is replaced by granulation tissue containing:
  • Capillaries
  • Macrophages
  • Fibroblasts
  • Collagen
  • This is regulated by growth factors: EGF, FGF, TNF
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6
Q

What are the 3 ways in which chronic inflammation develops?

A
  • Primary Chronic Inflammation – occurs without previous episode
  • Progression from acute inflammation
  • Recurrent episodes of acute inflammation
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7
Q

What are 6 ways Primary Chronic inflammation develops?

What are example diseases of each?

A
  • Resistance of infectious agent to phagocytosis and intracellular killing e.g tuberculosis, leprosy, brucellosis, viral infections
  • Foreign body reactions to endogenous materials (from inside of the body) ) (might be acute or chronic) e.g gout which is caused by accumulation of urate crystals in the joint
  • Foreign body reactions to exogenous materials (from outside of the body) e.g asbestos
  • Some autoimmune disease e.g rheumatoid arthritis, which is the body’s immune system destroying cartilage in the joints
  • Specific diseases of unknown aetiology (cause) e.g ulcerative colitis
  • Primary granulomatous diseases e.g TB and sarcoidosis, which is the accumulation of inflammatory like cells which form granulomas
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8
Q

What are 3 factors that favour the progression from acute inflammation to chronic inflammation?

What are examples of this?

A

• Persistence of substances that can cause acute inflammation at the start, then long term chronic inflammation e.g indigestible substances like glass, suture material

  • Deep seated suppurative inflammation where abscess draining is delayed or inadequate
  • This can be due to:
  • Thick abscess wall
  • Fibrous/granulation tissue
  • Pus in access becomes organised
  • Formation of fibrous tissue
  • An example of this is osteomyelitis, which is a chronic abscess in the bone that is extremely difficult to eradicate
  • Recurrent episodes of acute inflammation and healing may result in chronic inflammation
  • An example of this is chronic cholecystitis, which is the replacement of the wall in the gallbladder with fibrous tissue.
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9
Q

What are 5 examples of what Chronic Inflammation can look like?

A
  • Chronic ulcer
  • This is a breach in the mucosal surface (GI or respiratory tract)
  • The breach of chronic ulcers is lined by granulation tissue
  • Chronic ulcers can form fibrous tissue throughout muscle layers, which is what is seen in peptic ulcers.
  • Chronic abscess cavity e.g osteomyelitis, empyema thoracis (collection of pus in pleural space)
  • Thickening of the wall of a hollow viscus
  • Granulomatous inflammation - chronic inflammation in which a compact collection of immune cells (chiefly macrophages and cells derived from them) are present e.g TB and Sarcoidosis
  • Fibrosis
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10
Q

What are the primary cells associated with chronic inflammation?

What is this usually accompanied by?

A

• Chronic inflammation is an inflammatory process in which lymphocytes, plasma cells (activated differenciated B-lymphocyte WBCs) and macrophages predominate.
• Macrophages can also fuse to produce mutli-nucleate giant cells, which are very characteristic of some immune responses.
• This is usually accompanied by the formation of granulation tissue, resulting in fibrosis.
Macrophages are the major cells associated with chronic inflammation.

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11
Q

What are indications of chronic inflammation on a diagram?

A
  • Plasma cells, which consist of differentiated B-lymphocytes
  • Lymphocytes around the vessel
  • Multinucleate cell formed by the fusion of macrophages
  • Macrophages
  • Fibroblasts (secrete collagen and used in structure of tissues and wound healing)
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12
Q

How are macrophages related to chronic inflammatory response?

What are their capabilities?

How big are they?

What do they produce?

How are they activated and deactivated?

What can be a potential issue with macrophages?

A
  • Macrophages are the most common cell associated with chronic inflammatory response.
  • They have considerable phagocytic capabilities, and can ingest a wide range of materials
  • They are relatively larger cells (larger than lymphocytes)
  • They produce a range of important cytokines, which activated and inhibit other cells.
  • The are activated on migration to an area of inflammation by macrophage activation factor (MAF)
  • They are inhibited by migration inhibition factor (MIF)
  • A problem with macrophages, is they can harbour viable organisms’ resistance to lysosomal enzymes, which gives them protection from immune responses. e.g mycobacterium TB
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13
Q

What are the macrophages derived from?

What is the name for macrophages in the blood?

Why do macrophages get new names?

A
  • Macrophages are derived from haematopoietic stem cells
  • Monocytes are macrophages in the blood
  • Macrophages then slightly differentiate depending what tissue/organ they end up in, so they are all referred to by a different name, despite being very similar.
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14
Q

What is a granuloma?

Where might granulomas be found?

What does a granuloma look like?

A
  • A granuloma is an aggregate of epithelioid histiocytes (macrophages in connective tissue) into giant cells that have very little phagocytic activity, but maintain their secretory function
  • Granulomas can be found in sarcoidosis of the liver (accumulation of inflammatory cells) and TB
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15
Q

What are 5 causes of Granulomatous disease?

How do many causative agents get in the body?

A
  • Specific infections
  • Foreign bodies reactions (endogenous/exogenous)
  • Specific chemicals
  • Drugs
  • Unknown.
  • Many caustaive agents are ingestible (foreign bodies and speicifc infections)
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16
Q

What are the 2 forms of histiocytic giant cells?

A
  • Langerhans giant cell

* Foreign body giant cell

17
Q

How are chronic and acute inflammation distinguished?

A
  • Chronic inflammation is typically much longer lasting than acute inflammation
  • The primary cells associate with acute inflammation are neutrophils
  • The primary cells associated with chronic inflammation are macrophages
18
Q

What are the differences between exudate and transudate?

A
  • Exudate – occurs in circumstances of acute inflammation, high protein content, increased vascular permeability
  • Transudate – occurs in normal circumstances, low protein content, normal vascular permeability.
19
Q

What is the difference between granuloma and granulation?

A
  • Granuloma – aggregation of macrophage like cells (typically histiocytes)
  • Granulation – important healing process with new capillaries sprouting and connective tissue.
20
Q

What is the difference between fibrin and fibrous?

A
  • Fibrin is deposited from fibrinogen during acute inflammation to from a mesh that impedes blood flow
  • Fibrous – typical scar tissue that is formed with collagen