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77 Cards in this Set

  • Front
  • Back
HLA A3
hemochromatosis
HLA B27
PAIR
psoriasis, ankylosing spondylitis, inflammatory bowel disease, reiter's syndrome
HLA B8
Grave's dse
HLA DR2
MS, hay fever, SLE, Goodpastures
HLA DR4
RA, DM type 1
also see DR3 with DM type 1
HLA DR5
Pernicious anemia- B12 def
Hashimoto's thyroiditis
HLA DR7
steroid-responsive nephrotic syndrome
IL-12
forms Th1 cell
cell mediated response
makes IL-2, ifn gamma, and activate macrophages and cd8+ t cells
IL-4
forms Th2 cells- humoral response
make il 4, il 5, and help b cells make ab (ige>igg)
APCs
Macrophage, Dendritic cell, B cell
Macrophage-lymphocyte interaction
activated lymphocytes release ifn gamma
activated macrophages release IL-1, tnf alpha
stimulate one another
Th1 cell
regulate cell med response
secretes il 2, ifn gamma
activates macrophages and cd8+ t cells
inhibited by il 10
Th2 cell
regulates humoral response
secretes il 4, il 5, il 10
helps b cells make antibody
inhibited by ifn gamma
Regulatory T cells
help maintain specific immune tolerance by suppressing cd4 and cd8 t cell effector functions
express CD3, CD4, CD25
produce anti inflamm cytokines like IL-10 and tgf beta
Antibody structure
variable part recognizes antigens
Fc portion of igm and igg fixes complement
Mature B lymphocytes express what Ig isotypes
IgM and IgD on their surfaces
may differentiate by isotype switching into plasma cells that secrete IgA, IgE, IgG
Ig with lowest concentration in serum
IgE
Thymus independent ag
ag lack peptide component ex lps from cell envelope of gram neg bacteria, cant be presented by MHC to t cells, stimulate release of IgM ab only, no immunologic memory
Thymus dependent ag
ag containing protein component ex conjugated H flu vax, class switching and memory occur as result of direct contact of B cells with Th2 cells and release of il 4,5,6
MAC
membrane attack complex of complement, defends against gram neg bacteria, cytolysis
C5b-9
C1-4
viral neutralization
C3b and IgG
opsonization
C3a and C5a
anaphylaxis
C5a also does neutrophil chemotaxis
Inhibitors of complement activation on self cells, ex RBCs
Decay accelerating factor (DAF) and C1 esterase inhibitor
Classic complement activation pathway
IgG or IgM mediated
alternative pathway- activated by microbe surface molecules
C1 esterase inhibitor def
hereditary angioedema
ACE inhibitors contraindicated
C3 def
severe recurrent pyogenic sinus and resp tract infxns, inc susceptibility to type III hs rxns
C5-8 def
recurrent Neisseria bacteremia
DAF- GPI anchored enzyme- def
complement mediated lysis of RBCs and PNH- paroxysmal nocturnal hemoglobinuria
Cytokine functions
Hot T Bone stEAk
IL-1- fever Hot
IL-2- stimulates T cells
IL-3- stimulates Bone marrow
IL-4- stimulates igE prod
IL-5- stimulates igA prod
Neutrophils recruited by what cytokine
IL-8
Clean up on aisle 8
recruited by IL-8 to clear infxns
IL 3
supports growth and differentiation of bm stem cells
functions like GM CSF
IL 5
promotes diff of B cells, enhances class switching to IgA, stim growth and diff of eosinophils
IL 10
anti inflammatory
inhib th1 and activated t cel
activates th2
sec by regulatory T cells
TGF beta
anti inflammatory
sec by regulatory T cells
Interferons
interfere with viruses
alpha and beta inhibit viral protein synthesis by producing ribonuclease that degrades viral mRNA
gamma inc MHC I and II expression and ag presentation in all cells
activates NK cells
IL 12
induces diff of T cells into Th1 cells
activates NK cells, also secreted by B cells
Cell surface protein receptor for EBV
CD 21 on B cells
you can drink Beer at the Barr when you're 21
B cells, Epstein Barr virus, CD 21
Cell surface proteins on macrophages
CD 14, 40
MHC II, B7
Fc and C3b receptors- enhance phagocytosis
Unique marker for NK cells
CD56
also have CD16- binds Fc of IgG
Superantigens
GBS and staph aurus
stim ifn gamma release from Th1 cells, subsequent release of il 1, 6, and tnf alpha from macrophages
Endotoxins/LPS
from gram neg bacteria, directly stim macrophages by binding endotoxin receptor CD14, Th cells not involved
When is a patient give passive immunity
after exposure to Tetanus toxin, Botulinum toxin, Hbv, or Rabies virus, pts given preformed antibodies To Be Healed Rapidly
Live attenuated vax induces
cellular response
Inactivated or killed vax induces
humoral immunity
Serum sickness
immune complex dse- type III hs rxn- ab to foreign proteins produced- takes 5 days, immune complexes form, deposit in membranes, fix complement, leads to tissue damage
sx fever urticaria arthralgias proteinuria lymphadenopathy
more common than arthus rxn
Arthus rxn
local subacute ab med type ii hs rxn, intradermal injection of ag induces ab, form ag ab complexes in skin
sx edema necrosis activation of complement
Types of HS rxns
ACID
Anaphylactic and Atopic I
Cytotoxic (ab med) II
Immune complex III
Delayed (cell med) IV
4 T's of type iv hs
T lymphocytes (t cell mediated), Transplant rejections, TB skin test, Touching (contact dermatitis)
delayed type!
not transferable by serum!
Febrile non hemolytic transfusion rxn
type II hs, host ab against donor HLA ag and leukocytes
sx fever ha chills flushing
Acute hemolytic transfusion rxn
type ii hs, intravasc hemolysis (ABO blood group incompatibility) or extravasc hemolysis (host ab rxn against foreign ag on donor RBCs)
sx fever hypotension tachypnea tachycardia flank pain
hemoglobinemia in intravasc
jaundice in extravasc
Anti ds DNA
SLE glomerulonephritis
Anti histone
drug induced lupus
anticentromere
limited scleroderma
CREST
Anti SCl 70 (anti DNA topoisomerase I)
diffuse scleroderma
Antimitochondrial
primary biliary cirrhosis
Anti basement membrane
Goodpastures
Anti gliadin, antiendomysial
celiac
Anti desmoglein
Pemphigus vulgaris
Antimicrosomal, anithyroglobulin
Hashimoto's thyroiditis
Anti Jo 1
polymyositis, dermatomyositis
Ati U1 RNP (ribonucleoprotein)
Mixed connective tissue disease
Anti smooth muscle
Autoimmune hepatitis
Anti glutamate decarboxylase
DM type 1
c ANCA
Wegener's granulomatosis
C my Wedgie!
p ANCA
other vasculitides
ex Churg Strass, microscopic polyangiitis
Thymic aplasia
DiGeorge syndrome- 22q11 deletion, failure to develop 3rd and 4th pharngeal pouches
sx tetany- hypocalcemia, recurrent viral/fungal infxns- t cell def, congenital heart and great vessel defects
Brutons agammaglobuminemia
X linked recessive, higher in Boys, defect in BTK a tyrosine kinase gene, blocks pro B conversion to pre B
recurrent bacterial infxns after 6 mo- when maternal igG dec, due to opsonization defect
Hyper IgM syndrome
defective cd40L in Th2 cells, inability to class switch, severe pyogenic infxns in early life
IL 12 receptor def
dec Th1 response, disseminated mycobacterial infxns, dec ifn gamma
Hyper IgE syndrome (Job's syndrome)
Th1 cells fail to produce ifn gamma, neutrophils cant respond to chemotactic stimuli
FATED- course Facies, staph Abscesses, retained primary Teeth, inc igE, Derm problems ex eczema
SCID
defective IL 2 receptor most common, x linked
ADA def, failure to synMHC II ag
b and t cell def, recurrent infxns, tx with bone marrow transplant
Ataxia telangiectasia
defects in ATM gene which codes for DNA repair enzymes
sx cerebellar defects, spider angiomas, IgA def
Wiskott Aldrich syndrome
X linked recessive, progressive deletion of b and t cells
sx TIE- Thrombocytopenic pupura, Infections, Eczema
inc ige,iga; dec igm
Leukocyte adhesion deficiency type 1
defect in LFA 1 integrin (CD 18) protein on phagocytes, recurrent bacterial infxns, absent pus formation, delayed sep of umbilicus
Chediak Higashi syndrome
AR, defect in lysosomal regulator trafficking gene, microtubule dysfunction in phago-lyso funsion, recurrent pyogenic infxns with staph and strep, partial albinism, peripheral neuropathy
GVHD
type iv hs rxn, grafted immunocompetent t cells prolif in irradiated immunocomp dise host and reject cells with "foreign" proteins, elading to sever organ dysfunction
ras, jaundice, HSM, diarrhea