pathophysiology immune response and inflammation
TRANSCRIPT
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Pathophysiology
Immune Response
and Inflammation
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Inflammation-definitionReaction of vascularized living tissue to
local injury
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Acute inflammation
Chronic inflammation
RepairResolution
Abscess
Injury
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Definition
• -Reaction of tissues to injury, characterized clinically by heat, swelling, redness, pain, and loss of function; pathologically by vasoconstriction followed by vasodilatation, stasis, hyperemia, accumulation of leukocytes, exudation of fluid, and deposition of fibrin; and according to some authorities, the processes of repair, the production of new capillaries and fibroblasts, organization, and cicatrization.
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-itis
Appendicitis
Cellulitis
Meningitis
Pneumonitis
Nephritis
Myocarditis
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Etiologies• Microbial infections--pneumonia, skin
infections, etc.• Physical agents: burns, trauma--like
cuts, radiation• Chemicals: toxins and caustic
substances like battery acid• Others: immunologic reactions--
rheumatoid arthritis
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Inflammation• Time course
– Acute inflammation: Less than 48 hours– Chronic inflammation: Greater than 48
hours (weeks, months, years)• Cell type
– Acute inflammation: Polymorphonuclear leukocyte (PMN)
– Chronic inflammation: Mononuclear cells (Macrophages, Lymphocytes, Plasma cells)
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Acute inflammation
Chronic inflammation
RepairResolution
Abscess
Injury
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Acute inflammation:
• Changes which take place usually within the first few minutes to several hours to days after an injury
• Most commonly involves PMN’s as mediators
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Key physiologic events:
• Changes in vascular flow and caliber (hemodynamic changes)
• Changes in vascular permeability (vascular leakage)
• Leukocyte exudation
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Vascularized Connective Tissue
Blood Hydrostatic Pressure The fluid pressure of blood confined within vessels High near the arterial end of the capillary Fluid is forced out of the vessel to form tissue fluid
Tissue Osmotic Pressure Solute molecules in the interstitial spaces Assists in outward flow of fluid from the blood
Blood Osmotic Pressure Loss of fluid from the tissue spaces concentrates the
plasma proteins Tissue Hydrostatic Pressure
Fluids in the interstitium confined within its spaces
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HyperemiaBlood flow changes at the scene of an
injury almost immediatelyCapillary sphincters dilate
Reduces vascular resistance Blood flow to the area increases
Hyperemia
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Changes in vascular flow and caliber (hemodynamic changes)
Slowing of the circulation outpouring of albumin rich fluid into the
extravascular tissues results in the concentration of RBCs in small vessels and increased viscosity of blood.
Leukocyte margination PMNs become oriented at the periphery of
vessels and start to stick
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Cellular FactorsMargination
Flow rate decreases in inflamed tissue Leukocytes are forced to the periphery of
the vessel Loss of plasma fluid to the tissues causes
erythrocytes to aggregate and assume a central position in the vessel
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Time scale:
Variableminor damage--15-30 minutessevere damage--a few minutes
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Changes in vascular permeability (vascular leakage)
In normal tissue from arteriole to venule:
Intravascular hydrostatic pressure
@Colloidosmotic pressure
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Changes in vascular permeability (vascular leakage)
In inflammation from arteriole to venule:
Intravascular hydrostatic pressure
Colloidosmotic pressure
+ = Edema
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Lymphatics in inflammation:
Lymphatics are responsible for draining edema.
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Related definitions:
Edema: An excess of fluid in the interstitial tissue or
serous cavities--either a transudate or an exudate
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Related definitions:
Transudate: Increased blood hydrostatic pressure
occursForces blood out of vessel and into
the tissues low protein content ( mostly albumin)
specific gravity less than 1.012
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Related definitions:
Exudate:A filtrate of blood plasma mixed with
inflammatory and cellular debris. permeability of endothelium is usually
alteredhigh protein content
pecificgravity greater than 1.020
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Related definitions:
Pus:A purulent exudate--an inflammatory
exudate rich in leukocytes (mostly neutrophils) and parenchymal cell debris.
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Phagocytosis
• 3 distinct steps –Recognition and attachment–Engulfment–Killing or degradation
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Killing or degradation
• 2 mechanisms–Oxygen dependent
• Myeloperoxidase dependent (the most important!)
• Myeloperoxidase independent–Oxygen independent
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Oxygen-Independent Killing Involves the release of preformed
substances that damage bacterial cell walls, disrupt bacterial replication and produce a low pH For example, lysozyme, major basic
protein, lactoferrin (also in tears and saliva)
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Oxygen-Dependent KillingMore important than oxygen-independent
killingRelease of oxygen free radicals
Hydrogen peroxide Superoxide
Neutrophils produce an enzyme (Myeloperoxide) that causes hydrogen peroxide and a halide (Cl-, I-, Br-) to produce hypochlorous acid (swimming pool acid)
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Another view of chemical mediators
• Fever– --IL-1, IL-6, TNF– --Prostaglandins
• Pain– --Prostaglandins– --Bradykinin
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Acute Brain Swelling
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Acute inflammation has one of four outcomes:
• Abscess formation• Progression to chronic
inflammation• Resolution--tissue goes back to
normal• Repair--healing by scarring or
fibrosis
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Acute inflammation
Chronic inflammation
RepairResolution
Abscess
Injury
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Abscess formation:
• Stedman's dictionary: "A circumscribed collection of pus appearing in an acute or chronic localized infection, and associated with tissue destruction, and frequently, swelling."-- It is usually the result of a pyogenic organism.
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Abscess formation:
• “A hole filled with goo.”
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Acute inflammation
Chronic inflammation
RepairResolution
Abscess
Injury
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Chronic Inflammation
• Time course: – Greater than 48 hours (weeks, months,
years)• Cell type
– Mononuclear cells (Primarily Macrophages, Lymphocytes, Plasma cells)
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Chronic inflammation
• Chronic inflammation arises in various organs in 1 of 3 ways. – Following acute inflammation– After repeated bouts of acute inflammation
(pneumonia)– Without prior acute inflammation (Tb,
viruses, silica, asbestos, rheumatoid arthritis)
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Cells and mediators
• Histologically chronic inflammation includes:– Lymphocytes, plasma cells, and
macrophages– Proliferation of fibroblasts and small blood
vessels– Increased connective tissue– Tissue destruction
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Mononuclear phagocytes (Macrophages/MOs/histiocytes)
• The PMN is central to acute inflammation.
• The macrophage is central to chronic inflammation– Synonyms:
• Macrophages (MOs)• Histiocytes• Kuppfer cells (etc.)
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Macrophage origin:
• MOs come from the same cell line but differ depending on their microenvironment. They belong to the mononuclear phagocyte system (RES). The RES system consists of the bone marrow, peripheral blood, and tissue.
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MO's share in common:
• Mobility --although slower than PMNs• Phago- and pinocytosis• Ability to become activated--especially by
lymphokines, T cells, and anything that disturbs the cell membrane—and this allows more aggressive behavior in inflammation.
• Ability to secrete large quantities of chemical mediators
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MO functions
• Produce toxic, biologically active substances such as oxygen metabolites
• Cause influx of other cells such as other macrophages and lymphocytes
• Cause fibroblast proliferation and collagen deposition
• Phagocytosis
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MO time scale:
• MO’s begin emigration during acute inflammation and are the predominate cell type at 48 hours
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3 ways in which MOs accumulate:
• Continued recruitment from the circulation--secondary to chemotactic factors
• Division• Prolonged survival
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Acute inflammation
Chronic inflammation
RepairResolution
Abscess
Injury
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Chronic Granulomatous Inflammation (GI)
• Definition:--a type or pattern of chronic inflammation defined by the presence of granulomas• Small, 0.5 to 2 mm collections of modified
"epithelioid " histiocytes/macrophages and (Langhan's) giant cells (coalesced histiocytes), usually surrounded by a rim of lymphocytes.
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Chronic Granulomatous Inflammation (GI)
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Granulomas occur in response to various diseases:
• Foreign body• Tuberculosis (tb) • Fungal infections • Sarcoidosis• Schitosomiasis• Leprosy
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2 factors necessary for granuloma formation:
• Presence of indigestible organisms or particles (Tb, mineral oil, etc)
• Cell mediated immunity (T cells)
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Outcome of chronic inflammation:
• Resolution/regeneration/restitution of normal structure
• Repair/organization/healing by connective tissue/fibrosis/scarring
• It can continue indefinitely--some disease processes are capable of continuing indefinitely such as rheumatoid arthritis..
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Acute inflammation
Chronic inflammation
RepairResolution
Abscess
Injury
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Resolution
• Definition: Resolution is the return of tissue to its normal state.
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Factors necessary for resolution:
• Removal of the offending agent• Regenerative ability if cells have been
destroyed• Intact stromal framework
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Acute inflammation
Chronic inflammation
RepairResolution
Abscess
Injury
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Repair
• aka organization/healing by connective tissue/fibrosis/scarring
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Granulation tissue
• The early specialized vascular and fibrous tissue formed is termed granulation tissue. Grossly it looks pink and granular. Histologically one sees vessels and fibroblasts.
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Components necessary for repair
• Angiogenesis or neovascularization of new blood vessels
• Migration and proliferation of fibroblasts • Deposition of extracellular matrix (ECM) • Remodeling or maturation and
organization of the fibrous tissue
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Angiogenesis
• BM degradation of parent vessel• Migration of endothelial cells toward an
angiogenic stimulus• Proliferation of endothelial cells behind
the leading front of migrating cells.• Maturation of endothelial cells and
organization into capillary tubes
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Primary Healing (Healing by First IntentionHealing of an incision or severing
wound of the skin Damage is minimal
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In Second Intention Healing (compared to first):
• There is a big hole that needs to be filled in• The hole is filled in with abundant
granulation tissue• With time the wound contracts more than a
wound which healed by first intention. This occurs with the passage of time and is secondary to myofibroblasts.
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Pathologic aspects of inflammation and wound repair
• Systemic and local host factors influence the adequacy of the inflammatory-reparative response. – Protein deficiency– Vitamin deficiency (esp Vit C)– Steroids– Infection is the single most important
cause of delay in healing– Rupture (wound dehiscence)
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Pathologic aspects of inflammation and wound repair
• Aberrations in growth:– Excessive amounts of collagen: Keloid– Excessive amounts of granulation tissue:
Proud Flesh– Uncontrolled proliferation of fibroblasts:
Fibromatoses
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Types of InflammationSerous
In response to mild injury Only fluid escapes to the interstices Fibrinogen may be secreted into the
tissues = Fibrin Gelled Exudate may form such as in
pneumonia
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Additional definitions:
• Fibrinous inflammation: • Serous fluid plus plasma proteins like
fibrinogen. Seen commonly in infections of the pleural cavity and pericardial sac.
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Types of InflammationPurulent or Suppurative
Exudate contains large numbers of leukocytes called neutrophils
Pus = neutrophils + necrotic debris + fluid exudate
Abscess = localized accumulation of pus Injury can’t be immediately neutralized
Cellulitis = Diffuse suppurative inflammationCyst = fluid-filled sac after inflammation is
neutralized
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Additional definitions:
• Ulcer: • A local defect, or excavation of the
surface of an organ or tissue, which is produced by the sloughing (shedding) of inflammatory necrotic tissue. Ulceration is defined by the presence of necrotic tissue on or near a surface.
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QUESTION 1
XY presents to your clinic. He explains that last night he broke up with his girlfriend, the name of whom he had tattooed on his thumb. In the throws of his drunken misery, he burned the tattoo off with his Bic lighter. Clinical signs and symptoms of the lesion on his thumb include which of the following:
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QUESTION 1
a. Rubor (redness)b. Tumor (swelling)c. Calor (heat)d. Dolor (pain)e. All of the above
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QUESTION 1
a. Rubor (redness)b. Tumor (swelling)c. Calor (heat)d. Dolor (pain)e. All of the above
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QUESTION 2 A week later XY again presents to your clinic.
Apparently he received a lot of grief from his co-workers at the gas station about the Power Ranger’s Band-Aids you used to cover his thumb lesion, and so took them off. The wound looks worse in that it is much more erythematous and more painful to touch. Upon culture, numerous pathogenic Staphylococcus aureus organisms grow. The most important system for the killing of bacteria processed by XY’s PMNs (assuming they are normal) is which of the following:
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QUESTION 2
a. Oxygen dependent, myeloperoxidase independent systemb. Oxygen dependent, myeloperoxidase
dependent systemc. Oxygen independent,
myeloperoxidase independent systemd. Oxygen independent, myeloperoxidase
dependent systeme. AK-47 system
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QUESTION 2
a. Oxygen dependent, myeloperoxidase independent systemb. Oxygen dependent, myeloperoxidase
dependent systemc. Oxygen independent,
myeloperoxidase independent systemd. Oxygen independent, myeloperoxidase
dependent systeme. AK-47 system
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QUESTION 3
Several days later XY shows up again. This time the lesion is bulging and quite warm to touch. You suspect an abscess has formed, especially because when you lance it, foul-smelling purulent debris is exuded. You take some of the debris, smear it out on a slide, and stain it. You expect to see mostly which of the following:
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QUESTION 3
a. Lymphocytes, plasma cells, and macrophages
b. Proliferation of fibroblasts and small blood vessels
c. PMNs and necrotic debrisd. Collections of histiocytes and giant cellse. All of the above
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QUESTION 3
a. Lymphocytes, plasma cells, and macrophages
b. Proliferation of fibroblasts and small blood vessels
c. PMNs and necrotic debrisd. Collections of histiocytes and giant cellse. All of the above
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QUESTION 4 Upon lancing the abscess, you accidentally
created an incision to large to be closed with Band-Aids and anyway, XY does not want anymore Band-Aids. Sutures are needed. You know that suturing the wound will allow it to heal by primary intention. Even if you did not suture the wound and left it open, it would heal by secondary intention. Features shared by both primary and secondary intention healing include which of the following:
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QUESTION 4
a. Angiogenesis or neovascularization of new blood vessels
b. Migration and proliferation of fibroblastsc. Deposition of extracellular matrix (ECM)d. Remodeling or maturation and
organization of the fibrous tissuee. All of the above
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QUESTION 4
a. Angiogenesis or neovascularization of new blood vessels
b. Migration and proliferation of fibroblastsc. Deposition of extracellular matrix (ECM)d. Remodeling or maturation and
organization of the fibrous tissuee. All of the above
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QUESTION 5
While you suture up his wound, XY tells you that he is back together with his girlfriend. He wants to know if his skin will eventually be strong enough to allow for the re-tattooing of her name. You tell him the following except:
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QUESTION 5a. Keep the wound clean because infection
is the number one cause of delayed healingb. Eat well and take your vitamins in order not
to delay healing.c. At the end of one week wound strength is
about 10% of the strength of the unwounded skin.
d. Wound strength rapidly increases over 4-5 weeks following damage.
e. Because scars are made of collagen, the wound will regain the original if not more tensile strength.
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QUESTION 5
a. Keep the wound clean because infection is the number one cause of delayed healing.
b. Eat well and take your vitamins in order not to delay healing.
c. At the end of one week wound strength about 10% of the strength of unwounded skin.
d. Wound strength rapidly increases over 4-5 weeks following damage
e. Because scars are made of collagen, the wound will regain the original if not more tensile strength.
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QUESTION 6
If XY had used an eraser to rub out his girlfriend’s name tattooed on his thumb, and rubbed so hard that flecks of rubber from the eraser penetrated and became embedded into the underlying dermis, you would expect to see a granulomatous-type inflammatory reaction. True statements regarding granulomatous inflammation include all of the following except:
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QUESTION 6
a. It is dependent on humoral mediated immunity
b. It is considered a chronic inflammator process
c. It is characterized histologically by aggregates of histiocytes and giant cells
d. It most often occurs in response to indigestible organisms or particles
e. It progresses to repair if there is damage to stromal framework
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QUESTION 6
a. It is dependent on humoral mediated immunity.
b. It is considered a chronic inflammatory process
c. It is characterized histologically by aggregates of histiocytes and giant cells.
d. It most often occurs in response to indigestible organisms or particles
e. It progresses to repair if there is damage to stromal framework
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Non-Specific Immune Response
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Cell Mediated Immune Response
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Antibody Mediated Immune Response
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