Immuno/Micro Flashcards
Anti-nuclear Abs
SLE, nonspecific
Anti-dsDNA
SLE
Anti-Smith
SLE
Antihistone
Drug-induced lupus
Anti-IgG (Rheumatoid factor)
RA
Anticentrosome
Scleroderma (CREST)
Anti-Scl70 (anti-DNA topoisomerase I)
Scleroderma (diffuse)
Anti-mitochondrial
Primary biliary cirrhosis
Antigliadin
Celiac
Antiendomysial
Celiac
Anti-basement membrane
Goodpasture’s
Anti-desmoglein
Pemphigus vulgaris
Antimicrosomal
Hashimoto’s
Antithyroglobulin
Hashimoto’s
Anti-Jo-1
Polymyostitis, dermatomyostitis
Anti-SS-A (anti-Ro)
Sjogren’s
Anti-SS-B (Anti-La)
Sjogrens’s
Anti-U1 RNP
Mixed CT disease
Anti-smooth muscle
Autoimmune hepatitis
Anti-glutamate decarboxylase
Type 1 DM
c-ANCA
Wegener’s
p-ANCA
Churg-Strauss (asthma)
Polyangitis
Ulcerative colitis
Recurrent infections with Staph, Kleb, serratia, cacdida, PA and aspergillus.
CGD
NADPH oxidase deficiency
Catalase + bacteria infections
NBT test yellow (-)
IgA in small vessel walls
Henoch-Schonlein purpura
Recurrent infections, omphalitis, gum inflammation, CD18-
Leukocyte adhesion deficiency
No integrins = no leukocyte migration
Failure to form pus
Partial albinism, recurrent bacterial infections, CD56-
Chediak-Higashi
Recurrent infections with Candida, no anti-CD3, no concanavalin or phytohemagglutinin
DiGeorge syndrome
No T-cells
Failure of 3rd and 4th pouches
Facial abnormalities, cardiac
No live vaccines
MHC class I deficiency
Failure of TAP1
NO CD8
CD4 normal
Normal DTH, Ab
MHC class II deficiency
SCID
No CD4
Recurrent meningitis or gonoccoal infections
C5-9 (MAC) deficiency
Tx = ceftriaxone
C1-inhibitor deficiency
Hereditary angioedema
C1-4
Viral Neutralization
C3b
Opsonization (also IgG)
C3a, C5a
Anaphylatoxins
Binds mast cells directly
C5a
Neutrophil Chemotaxis
C5b-9
MAC
Pneumonia for 6mo. Recurrent infections w/ encapsulated bacteria and viral infections, CD19-
Bruton’s
Tyrosine Kinase
No B-cells
CD19-
Recurrent bacterial infections and severe diarrhea, high serum IgM
Hyper IgM
Deficiency of CD40L
Most common immune deficiency
IgA deficiency
Repeated sinopulmonary & GI infections
Deficiency of gamma chain IL-2
X-linked SCID
Adenosine deaminase deficiency
SCID
Recombinase deficiency
SCID
Rag1 or 2 nonsense mutations
No B or T cells
Thrombocytopenic purpura, eczema, low Ig
Wiskott-Aldrich syndrome
Classic triad