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NR 507 Midterm Exam Questions and Answers

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NR 507 Midterm Exam Questions and Answers

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NR 507 Midterm Exam




Hypersensitivity Type 1 - Answer-Type 1: Allergic Reaction

Mediated by IgE

Inflammation due to mast cell degranulation

local symptoms: Itching, rash

Systemic symptoms: wheezing

Most dangerous form: anaphylactic reaction-systemic hypotension, severe bronchoconstriction

Main treatment: epinephrine



Hypersensitivity Type 2 - Answer-Type 2: Cytotoxic, tissue-specific (thyroid tissue)

Primary effector cells: Macrophages

Can cause tissue damage or alter the function

Example: Graves disease (alters thyroid function but does not alter tissue)

Example: Incompatible blood type (cell/tissue damage)- Severe transfusion reaction occurs and the
transfused erythrocytes are destroyed by agglutination or complement-mediated lysis



Hypersensitivity Type 2 and 3 difference - Answer-Type 2: Organ-specific, the antibody binds to an
antigen on the cell surface

, Type 3: Not organ-specific, the antibody binds to soluble antigen outside the cell surface that was
released into the blood or body fluids and then the complex is distributed into tissues



Hypersensitivity Type 3 Examples - Answer-Rheumatoid Arthritis: antigen/antibodies are deposited in
the joints

Systemic Lupus Erythematosus (SLE)- very closely related to autoimmunity-antigen/antibodies deposit in
organs that cause tissue damage



Scope of damage of SLE- Type 3 Hypersensitivity- autoimmune response - Answer-rash confined to
cheeks (malar rash)

discoid rash (raised, patchy, scaly)

photosensitivity

oral/nasopharyngeal ulcers

hematologic disorders

immunologic disorders

non-erosive arthritis

serositis

renal disorder (proteinuria)

neurologic disorders (seizures)

antinuclear antibody (ANA)



Autoimmunity - Answer-Familial

Affected family members may not have same dz, but several members may have other disorders
characterized by a variety of hypersensitivity reactions that include autoimmune or allergic reactions

Associations with particular autoimmune diseases have been identified for a variety of major
histocompatibility complex (MHC) alleles or non-MHC genes

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