Chronic inflammation Flashcards

1
Q

What is chronic inflammation?

A

can follow on from an unresolved acute inflammation, or be chronic from the outset
composed of cellular infiltration and proliferation of local connective tissue
the principal cells involved are
1. lymphocytes,
2. plasma cells,
3. macrophages,
4. fibroblasts, and
5. vascular endothelium

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2
Q

Lymphocytes in chronic inflammation?

A

formed in bone marrow, spleen, thymus, lymph nodes and the mucosal surface associated lymphoid follicles e.g. Peyer’s patches in the intestine and the tonsils of the oropharynx

circulate between the blood, tissues and lymphatic system

life span up to 200 days

round cells with a densely staining nucleus and a thin, often indistinct, rim of cytoplasm

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3
Q

Plasma cells in inflammation?

A

Derived from B-lymphocytes at the area of tissue damage and/or arrive in efferent lymph from sites of differentiation in lymph nodes
Presence of plasma cells in a tissue indicates the body is producing an antibody response against an antigen
Round to oval shaped cells with an eccentric round nucleus and abundant plum/purple cytoplasm

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4
Q

Macrophages in inflammation?

A

large round cells with central to eccentric round nucleus and abundant clear, often vacuolated (foamy) cytoplasm

normally present in tissues as fixed histiocytes e.g. sentinel macrophages in the lung

in inflammation most are derived from circulating monocytes, which leave blood vessels and enter tissue

functions: phagocytosis, antigen presentation, stimulation of fibroplasia and fibrosis

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5
Q

Macrophage accumulation in tissues

A

inability to lyse irritants (foreign material)
antigen-antibody complexes forming around infectious agents forming ‘tissue grains’
survival of infectious agents within macrophages (e.g. acid-fast bacilli)

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6
Q

Macrophage subtypes

A

A. Epithelioid cells - look like squamous epithelial cells with a pink cytoplasm and indistinct borders, may be binucleate
- primarily secretory rather than phagocytic
B. Giant cells - multinucleated cells formed by the fusion of macrophages or epithelioid cells
Seen in tissues in association with stable foreign material or intracellular bacteria

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7
Q

What is granulomatous inflammation?

A

An important type of chronic inflammation usually caused by organisms of low virulence but great persistence in the tissues or by implanted foreign bodies. The macrophage is the main effector cell.

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8
Q

Microscopic structure of a granuloma

A

a. central core containing agent or irritant
b. surrounding chronic inflammatory cells
macrophages (often as ‘epithelioid’ cells), lymphocytes and plasma cells
eosinophils in parasitic granulomas
necrosis in mycobacterial and fungal granulomas
calcification in mycobacterial granulomas in some species
c. outer fibrous capsule

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9
Q

Process of tissue repair

A
  1. Removal of necrotic debris
  2. Ingrowth of immature blood vessels (granulation tissue)
  3. Production of immature scar tissue
  4. Production of mature scar tissue (fibrosis)
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10
Q

Fibroblasts and endothelial cells

A

Fibroblasts - derived from local connective tissue cells and involved in the organisation of damaged tissue (fibroplasia)
Endothelial cells - in conjunction with fibroplasia there is a proliferation of the vascular endothelium into the organising tissue (granulation tissue).

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11
Q

Granulation tissue formation

A

vascular connective tissue
capillary loops
fibroblasts - collagen production
leukocytes - granulocytes & macrophages
extremely resistant to infection
supports migration of epithelium
its contraction reduces the amount of tissue to be replaced

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12
Q

What is fibrosis?

A

Granulation tissue is replaced by immature then mature fibrous tissue
The formation of immature fibrous tissue is fibroplasia
The formation of mature scar tissue is fibrosis
The mature fibrous scar is as strong or stronger than the original tissue

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13
Q

Factors affecting healing

A
  1. the species affected
  2. age
  3. the nature of the tissue damaged
    highly specialised tissue rarely repairs successfully unless the injury was mild e.g. fibrocartilaginous embolism in the spinal cord of dogs
  4. the extent of tissue damage
    If there is substantial fibrosis in the tissue, progressive destruction of the tissue continues due to further injury to adjacent normal tissue from the fibrous tissue as it matures and contracts, e.g. the liver in cirrhosis and the kidney in chronic renal disease
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14
Q

Regeneration vs repair

A

Repair is the process of replacement of damaged tissue by fibrous scar tissue (fibrosis), does not retain the same characteristics

Regeneration is the process of replacement of damaged tissue by normal tissue of the same type, the functional status of the tissue is restored

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15
Q

Regeneration vs repair tissue types

A
  1. labile - constantly replenishes its tissue cells throughout life
    - skin and mucous membranes which normally desquamate their outer layer of cells during life
    - bone marrow and fat are other examples
  2. stable – able to regenerate in response to damage: e.g. liver, some endocrine glands and renal tubular epithelium
    or able to respond to an increased demand on function: e.g. skeletal and smooth muscle
  3. permanent - poor or no regenerative capacity: highly specialised tissues whose cells generally have only one function
    neuronal cell bodies in the central nervous system, the retina of the eye, and the cells responsible for hearing in the ear
    axons in the peripheral nervous system, when severed, can regenerate to a limited extent
    -cardiac muscle myofibres have very poor regenerative capacity, and undergo repair by fibrosis or fat replacement
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16
Q

Stages in skin wound healing - haemostasis

A

blood escapes from damaged blood vessels and fills the defect
platelet degranulation > mediator release
fibrin clot loosely binds the edges and dries to form a surface scab

17
Q

Stages in skin wound healing - inflammation

A

acute inflammation develops and within 24hrs adds exudate to the site
inflammatory cells produce enzymes which begin to degrade the clot and act as scavengers to remove debris
macrophage products promote repair
fibrin & fibronectin network provides stability and framework for cell migration

18
Q

Stages in skin wound healing - repair

A

epithelial cells start to regenerate and bridge the gap within 48hrs
blood vessels re-grow and may form a small amount of granulation tissue

Consolidation/Reconstruction
final scar is small and inconspicuous
sufficient tensile strength for suture removal 7-10d