Chronic Lymphocytic Leukemia ARTICLE SF3B1-mutated chronic ...
Thomas V Widiyatno - s1.fkh.unair.ac.ids1.fkh.unair.ac.id/images/PPT/CHRONIC INFLAMMATION.pdf ·...
Transcript of Thomas V Widiyatno - s1.fkh.unair.ac.ids1.fkh.unair.ac.id/images/PPT/CHRONIC INFLAMMATION.pdf ·...
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Thomas V Widiyatno
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CHRONIC INFLAMMATION Chronic inflammation is inflammation of prolonged
duration (weeks to months to years) in which acute inflammation , tissue destruction and tissue repair occur simultaneously
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Chronic inflammation arises :
(1) when the acute inflammatory response fails to eliminate the inciting stimulus
(2) after repeated episodes of acute inflammation, or
(3) in response to unique biochemical characteristics and/or virulence factors in the inciting stimulus or microbe
such as :
*those caused by Mycobacterium spp
*Fungi : Aspergillus
*SLE, Rheumatoid Arthritis
*retained suture etc.
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As the chronic inflammation develops, cytokines, chemokines and other inflammatory mediators are released and incited :
(1) active inflammation (chronic to granulomatous
with lymphocytes, macrophages, plasma cells, and
multinucleated giant cells /MGCs)
(2) tissue destruction (necrosis)
(3) proliferation of fibroblasts and deposition of
collagen (desmoplasia / fibroplasia)
(4) angiogenesis and neovascularization (granulation
tissue formation
(5) initiation of wound healing (reepithelialization and
tissue repair)
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Beneficial aspects of Chronic Inflammation
the body attempts to overcome the inciting stimulus via macrophages and the adaptive immune response
If the responses fail, the stimulus is then “walled off” with collagen produced by fibroblasts, encapsulating the stimulus and functionally placing it “outside” of the body, and in time can lead to a return to normal activity
Small granulomas or abscesses in the lung, liver, or even in areas of skin, with time, eventually go unnoticed by the innate and adaptive immune systems an do not stimulate pain or interference to function
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Harmful effects of Chronic Inflammation
The mononuclear leukocyte infiltrates (macrophages, lymphocytes, NK cells) within areas of CI take up space, often displace, replace and sometimes obliterate the structure of the original tissue.
If the lesion expands, the inflammatory response can affect function of adjacent tissues, for example, chronic inflammatory response in the skin can result in ulcerations and obliterate adjacent hair follicles
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Progression of AIR to CI , Fibrosis and Abscess formation
AIR can either fully resolve, or repair by healing.
If the conditions do not allow for complete resolution of the AIR, three outcomes can result :
(1) Progression to chronic/granulomatous inflammation
(2) Healing by fibrosis, or
(3) Abscess formation
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fibrosis
The Outcome of tissue injury and unresolved acute inflammation
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1. Progression to Chronic Inflammation
Failure of AIR is characterized by :
a. The inciting stimulus persisting for a long period of time (weeks to months)
b. Extensive tissue injury and necrosis (third-degree burn)
c. A shift of the cellular elements : from neutrophils to lymphocytes, macrophages and sometimes MGCs
d. Extensive connective tissue reorganization followed by fibrosis
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2. Healing by fibrosis
Tissue injury due to AIR neutralized by tissue destruction (necrosis)
Dead tissue and the acute inflammatory exudate are removed by macrophages, and the space filled with fibrovascular tissue (granulation tissue) commonly seen in healing process.
Granulation tissue is eventually replaced by immature fibrous connective tissue that is poorly collagenized and then by mature connective tissue that is well collagenized, healing the wound and forming a scar (cicatrix)
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3. Abscess formation
Abscess formation occurs when the AIR fails to rapidly eliminate the inciting stimulus, and the enzymes and inflammatory mediators from neutrophils in the exudate liquefy the affected tissue and neutrophils to form “pus”
Abscesses can have a septic or sterile origin :
Septic abscess most commonly from bacterial infections (such as Streptococcus and Staphylococcusspp.) whereas sterile abscess arise from incompletely degraded foreign materials or from the failure of injected medications to be completely absorbed.
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A. Abscess, lung. Cow. B. The exudate in fig A consists of cell debris and a large number of neutrophils admixed with lesser numbers of degenerating macrophages and lymphocytes and bacteria (the latter not visible with H&E stain)
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GRANULOMATOUS INFLAMMATION
Is a distinct type of chronic inflammation in which cells of monocyte-macrophage system are predominant and take the form of Macrophage, epitheloidmacrophage and MGCs
Development of granulomatous inflammation requires multiple factors :
(1) An inciting agent, usually with indigestible, poorly degradable and persistent antigens(e.g Mycobacteriaspp.)
(2) A host immune response, usually an intense T cell-mediated response
(3) The interplay of various cytokines produced by cells within the chronic inflammation lesion.
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Classification of granulomatous inflammation :
1. Diffuse (lepromatous) granuloma
2. Nodular (tuberculoid) granuloma
3. Eosinophilic granuloma
@ 1. Diffuse (lepromatous) granuloma
The lesion can be poorly delineated (poorly defined border) and have a widespread distribution, a heavy bacterial burden, relatively few lymphocytes and variable fibrosis
e.g : Johne’s disease (Mycobacterium avium-intracellulare paratuberculosis)
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Diffuse lepromatous granuloma, Johne’s disease. ileum, cow.
A. Thickened mucosa because of a dense infiltrate of granulomatousinflammatory cells in the lamina propria
B. The lamina propriacontains macrophages arranged in sheets. Inset : Higher magnification
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Mycobacterium avium-intercellulare bacilli.Diffuse (lepromatous) granuloma, with numerous
macrophages and MGCs that contain abundant bacilli stained red. Acid fast stain
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@2. Nodular (tuberculoid) granuloma
Three distinctive morphologic areas :
The innermost area is often a centrally located region of cellular necrosis surrounded by middle area containing macrophages, epitheloid and MGCs, and the outermost : consists of B and T cell, plasma cells, macrophages and fibrous capsule
Examples :
Granulomatous inflammation caused by
M. tuberculosis
M. bovis
Coccidioidomycosis
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Nodular (tuberculoid) granuloma, coccidioidomycosisGranulomas are round to oval with a central core of numerous
macrophages surrounded by lymphocytes, plasma cells, macrophages, and a peripheral zone of fibroblasts, which produce
fibrous capsule. The granuloma on the left contains a single central fungal element (inset). H&E stain
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@ 3 . Eosinophilic Granuloma
Grossly, eosinophilic granuloma appears as papule, nodule or plaque and ulcer in the skin
Microscopically, the inflammatory response consists of eosinophils, macrophages and areas of dense eosinophilia around collagen
Examples :
- Develop in response to migrating parasites , such as larval migrans of T.canis
- Eosinophilic granuloma of cat
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Eosinophilic granuloma, oral mucosa, cat.
The mixture of eosinophils, macrophages and lymphocytes in the
superficial dermis accompanied by collagenolysis
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Effector Cells of the Chronic Inflammatory Response :
- fibroblasts
- Monocyte/macrophage
- Epitheloid macrophage
- MGCs
- Dendritic cells
- Lymphocytes
- NKcells
- Mast cell
- Endothelial cells
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Macrophage attacking E.coli
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NK cell destroying cancer cell
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Dendritic cell with a lymphocyte
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Mast cell with granules and filopodial processes
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Platelet, red blood cell and white blood cell (lymphocyte)
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