Inflammation Flashcards

1
Q

Tuberculosis is a disease that produces foci of chronic inflammation in the
lung. If a biopsy of tissue from such a focus were examined, immune cells of
which of the following types would you expect?

A

Macrophages, monocytes and lymphocytes are expected in chronic granuloma inflammation.

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2
Q

What are some things that can trigger a mast cell as an inflammatory mediator?

A
  1. IgE release
  2. C3a/ C5a
  3. allergens
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3
Q

What 3 events occur as mast cells are being activated by IgE?

A

Crosslinking of IgE to mast cell receptors stimulates:

  1. Degranulation of histamine
  2. Cytokines
  3. Eicosanoids (prostaglandings, leukotrienes)
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4
Q

Histamine causes the leakage of what type of circulatory vessels?

A

Leakage is confined to post-capillary venules.

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5
Q

Define histamine’s biggest change on the blood vessel wall.

A

Opening of inter-endothelial junctions to allow leakage as contents of blood are exposed to the basement membrane.

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6
Q

During local inflammation, describe what occurs in the process of stasis.

A

Blood viscosity increases with local hematocrit to slow down local blood flow just before WBCs migrate to site.

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7
Q

What are the 2 cell adhesion molecules that interact with WBCs during leukocyte migration?

A
  1. ICAM-1 interacts with CD11/CD18 of WBC

2. VCAM interacts with VLA-4 on WBC

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8
Q

When a bacteria is engulfed, what metabolic pathway increases in rate?

A

HMP Pathway increases NADPH and NADH needed for phagocytosis. This increases overall metabolic function of the phagocyte.

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9
Q

What is NADPH needed to make to help phagocytes kill engulfed pathogens? What is the significance of this?

A

NADPH helps make O2 radicals and H2O2 for bacterial killing, in a process known as oxidative burst. The reactive H2O2 is broken down by catalase, but lack of it in a phagocyte accounts for the short lifetime.

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10
Q

Describe Chronic Granulomatous Disease (inheritance pattern, leukocyte defect, symptoms).

A

CGD is an autosomal recessive disease that usually affects males. A lack of NADH/NADPH activity (from decreased oxidative burst) has affected children suffer with recurrent infections of the skin, lymph nodes, lung and bone. Common findings include granulomas or lipid-filled abscesses.

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11
Q

Describe what occurs in Chediak-Higashi Syndrome (inheritance pattern, leukocyte defect, symptoms).

A

CH is an autosomal recessive disorder in which leukocytes don’t function as well since mutations affect proteins for lysosomal membrane trafficking. Symptoms include hypo-pigmentation, recurrent lung and viral infections and increased azurophilic granules in neutrophils.

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12
Q

What complements serve as chemotactic agents for leukocyte activation and migration?

A

Complements C3a and C5a are chemotactic.

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13
Q

How does chronic inflammation differ from that of acute?

A

Irreversible changes occur in the tissue in which new blood vessels are formed and CT appears as scars from granulation by fibroblasts.

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14
Q

Angiogenesis can be stimulated by _____ and _____. Describe the significance of one of these stimulants.

A

Inflammatory chemokines and hypoxia. Chemokines act indirectly by attracting leukocytes that secrete pro-angiogenic factors such as VEGF.

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15
Q

What role does the cytokine TGF-beta have in inflammation?

A

In chronic inflammation, TGF-beta is important for fibrosis (avascular scar-formation).

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16
Q

What are some features in Interstitial pulmonary fibrosis?

A
  • Honey-combed appearance of the lung from loss of alveoli

- enormous increase in fibrous tissue (pulmonary fibrosis) and air space

17
Q

Define what an abscess is in context of inflammation.

A

Abscess is a pus-filled granuloma that’s avascular in the interior. This destroys surrounding tissue.

18
Q

Define empyema.

A

Build up of pus in an “existing” body cavity such as the pericardial sac of pleural space.

19
Q

What is the key feature of Granulomatous inflammation?

A

Appearance of multinucleated giant cells and lesions that form because the many macrophages are unable to clear the offending agent. This is the last mode of protection.

20
Q

Describe the key features of Tuberculosis.

A
  • Ghon complex in which calcified granuloma are present in lung tissue (looks like cottage cheese = “Caseation”)
  • secondary TB features disseminated lung granulomas
  • mycobacterium stained pink with acid fast stain
21
Q

What does a peripheral smear with band cells indicate?

A

Immature neutrophils (band cells) in a peripheral blood smear indicates an acute infection.

22
Q

Silicon breast augmentation after a mastectomy puts a patient at risk for developing what type of inflammatory response?

A

Chronic granulomatous inflammation: in which silicon that’s seen as foreign material can result in dense fibrosis from TGF-beta cytokines.

23
Q

List the 5 steps that occurs for neutrophil infiltration into a tissue during inflammation.

A
  1. Margination
  2. Rolling via selectins
  3. Adhesion via integrins
  4. Migration across the vessel wall
  5. Migration through tissues.
24
Q

Describe 3 features that may appear in a patient with Acute Pyelonephritis.

A
  1. Renal scarring showing protein in the urine
  2. Sepsis as indicated by bacteria (i.e. E. coli) in the urine
  3. loci of acute inflammation (necrosis and hemorrhage) with indicated PMNs in a renal biopsy.
25
Q

What type of inflammation is a blister from a skin burn?

A

Serous inflammation that may develop pus underneath.