Disorders of immunity Flashcards
B-lymphocytes deficiency
increased chance of Bacterial infection
T-lymphocyte deficiency
fungal & viral infections
primary deficiency disease =
1) Burton’s diease (male, B-cell system)
2) Thymic aplasia (diGeorge’s syndrome)
- -defective T-cell system
3) Combo immunodeficiency
secondary deficiencies =
1) stress = more glucocorticoids
2) latrogenic = result of treatment (too much advil)
3) senescent = age relates loss of immune
cross reaction =
when multiple antigens act with an antibody
hypersensitivities
type 1 = anaphylactic
type 2 = antibody depend hypersensitivity
type 3 = immune complex injury
type 4 = delayed hypersensitive
type 2 (antibody depend hypersensitivity)
1) complement mediated mech
2) antibody dependent cytotoxicity
- -low antibody
3) antireceptor antibodies
- -block cell membrane r/c (ex-graves mimic TSI)
type 3 (immune complex injury)
antigens & antibodies
- -serum sickness
- -acute glomerulonephritis
- -systemic lupus erythematosus (SLE) *
- -arthus reactions
type 4 (delayed hypersensitivity)
cell mediated = skin rashes, contact dermatitis, tuberculosis
HLA (human leukocyte antigens)
these are the “flags” that molecules use to signal
MHC = surface protein = major histocompatability antigens
–located on chromosome 6
MHC 1 = on nucleated cells & platelets
MCH 2 = antigen presenting cells (dendritic cells, macrophages, B-cells, active T-cells
MHC 3 = complement system NOT a HLA
HLA disease & associations
- -ankylosing spondylitis = HLA-B27
- -B8 = autoimmune disease
- -D2/D3 = lupus
- -D4 = rheumatoid arthritis
major autoimmune diseases
1) single cell disorders
- -graves, hashimotos, myasthenia
2) multisystemic disorders
- -systemic lupus erythematosus, rheumatoid arthritis, enthesopathies, scleroderma, sjogrens syndrome
systemic lupus erythematosus (SLE)
- -chronic inflammation **SKIN, kidney, serosal membrane, joints, heart, CNS
- -young women 90% are 15-35yrs
- -Genetic = no actual “lupus” gene tho. & intrinsic factor
- -proliferation of B cells = inactivated suppressor cells
- -numerous antibodies (well duh if B cells are increased)
–antibuclear antibodies (ANA) =double-strand DNA & the “SMITH antigen” 1/3 pts have this*
environmental factors for lupus (SLE)
1) UV light
2) Drugs
3) psoralens = tanning, cosmetics (P for plastics)
4) Estrogen
5) viruses (which (+) B cell production)
6) parasites = hypersensitivity
7) stress
classic triad associated with lupus (SLE)
butterfly rash
joint pain
fever
causes of death due to SLE
1) immune deficiency
2) glomerular disease
3) CNS disturbances
SCLERODERMA
excessive fibrosis!
–elevated Von Willebrand facter
CREST syndrome
organ / tissue response of scleroderma
- -skin = raynaud’s phenomenon
- -aligmentary trac= rubbery hose
- -muscles = more kinase = weak
- -kidneys = onion skinning
- -lungs = restrictive lung disease
CREST =
Calcinosis Raynaud's phenomenon Esophageal dysfunction Sclerodactyly Telangiectasias (dilated vessels in skin)
Mixed connective tissue disease =
combo of lupus, plymyositis, scleroderma
fibromyalgia syndrome
morning stiffness, trigger points. often disabling
–young woman who dislike alcohol. LOL
polymyositis
inflammatory disease that damages skeletal muscle
- -butterfly rash,, heliotrope eyelids, purple bumps on knuckles
- -affects proximal muscles of extremities (hips, shoulders, neck flexors)
- *spares extra-ocular muscles