Autoimmune Diseases part 2 Flashcards

1
Q

Breakdown in normal communication
between nerves and skeletal muscles

A

Myasthenia Gravis causes

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2
Q

Risk factors:
 Recent viral infections
 Cancer or leukemia
 Family history

Symptoms:
 Eyes: ptosis, diplopia
 Face/throat: dysarthria, dysphagia, decreased facial expressions
 Neck/limb weakness

Treatment:
 Cholinesterase inhibitors
 Corticosteroids
 Immunosuppressants
 Plasmapheresis
 Intravenous immunoglobulins
 Surgery to remove thymus

A

Myasthenia Gra vis risk factors, symptoms, treatment

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3
Q

Hyperacute Rejection occurs when

A

blood vessels, (thrombosis)
- mismatch of ABO
- within minutes

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4
Q

Acute rejection

A

n begins as early as one week after transplant, the risk
being highest in the first three months, though it can occur months to
years later.

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5
Q

Type 1 Hypersensitivity: Immediate hypersensitivity

A

 IgE mediated via mast cell
inflammation
 E.g., anaphylactic shock, allergic
rhinitis (“hayfever”), bronchial
asthma

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6
Q

Type II: Antibody-mediated
hypersensitivity

A

 IgG and IgM antibodies formed against cellsurface antigens predispose cells to
phagocytosis/lysis

 E.g., drug interactions, hemolytic disease of newborn, mismatched blood transfusions

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7
Q

IgG, IgM, IgA antibodies form antigen-antibody complexes leading to vessel or
tissue injury via complement system’s
inflammatory response
 E.g., autoimmune diseases (lupus, RA

A

Type III: Immune complex mediated
hypersensitivity

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8
Q

 Sensitized cytotoxic and/or helper T cells cause
cell and tissue injury directly
 E.g., contact dermatitis, transplant rejection, TB,
hepatitis

A

Type IV: Cell-mediated hypersensitivity

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9
Q

 Rare disorder in which skin and mucous
membranes become significantly
inflamed, presenting like burns.

 Represents a “milder”form of toxic
epidermal necrolysis

 Example of a Type 4 Hypersensitivity
Rejection

A

Stevens-Johnson syndrome

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10
Q

 Causes: allergic reactions to medications, viral infections, radiation treatment, UV light

 Risk factors: viral infections, immune-compromising diseases,
chronic inflammatory disease, carrying HLA-B12 gene

 Example CBZ (Tegertol)

A

Stevens-Johnson Syndrome: Causes, risk factors, Example

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11
Q

What are Immunodeficiency disorders

A

-prevent your body from fighting
infections and diseases.

 This type of disorder makes it easier for you to catch viruses and
bacterial infections.

 Immunodeficiency disorders are either congenital or acquired.

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12
Q

Primary Immunodeficiency Disorders: B cell deficiency

A

decrease antibody production—>
susceptible to infections in body fluid or respiratory/GI tract

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13
Q

impaired ability to organize immune
response
susceptible to fungal, protozoan, viral and intracellular bacteria
infections (e.g., DiGeorge Syndrom]

A

Primary Immunodeficiency Disorders: T-cell deficiency:

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14
Q

Primary Immunodeficiency Disorders Combined B and T-cell
deficiency

A

overall immune response impaired —->
requires bone marrow transplant for surviva

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