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201 Cards in this Set
- Front
- Back
lymph nodes
b cells are in _ t cells are in _ |
follicle
paracortex |
|
high endothelial venules are in...
fxn? |
paracortex of lymph node
high endothelial venules, through which T and B cells enter from blood |
|
a viral infection in the body, may affect structure of _ part of a lymph node
|
enlargement of paracortex
|
|
_ of lymph node is not well developed in _ pts
|
DiGeorge syndrome
|
|
lymph node has 3 major parts
|
follicle
medulla paracortex |
|
lymph node medulla has what parts, containing what cells?
|
cords
--lymphocytes --plasma cells sinuses --reticular cells --macrophages |
|
_ of lymph node communicates with efferent lymphatics
|
medullary sinuses
|
|
lymph drainage
axillary drains |
upper limb
lateral breast |
|
lymph drainage
stomach --> duodenum, jejunum --> |
celiac
superior mesenteric |
|
sigmoid colon
rectum anal canal drains to _ lymph node |
colic --> inferior mesenteric
internal iliac superficial inguinal |
|
superficial inguinal lymph nodes receive drainage from...
|
anal canal
scrotum thigh (superficial) |
|
testes drain to
|
superficial and deep plexuses
--> para-aortic |
|
_ lymph nodes in leg surprisingly receive drainage from...
|
popliteal
lateral dorsum of foot |
|
R lymphatic duct receives drainage from
|
R arm
R side of head |
|
sinusoids of spleen are in what part of spleen
describe two histological features |
red pulp
fenestrated "barrel hoop" basement membrane macrophages found nearby |
|
T cells are found where in spleen
|
--PALS
--white pulp |
|
B cells are found where in spleen?
|
follicle within white pulp
|
|
RBCs are found where in spleen?
|
red pulp
(presumably w/in the sinusoids) |
|
5 cell types listed by FA as being w/in the spleen
what part of the spleen are they in? |
RBCs (red pulp)
T cells (PALS; white pulp) B cells (follicles w/in white pulp) macrophages (nearby sinusoids) APCs (marginal zone) |
|
macrophages in spleen serve what immune function?
|
remove encapsulated bacteria
|
|
splenic dysfunction -->
|
v IgM -->
v complement activation --> v C3b opsonization --> ^ susceptibility to encapsulated organisms: S SHiN Salmonella Strep pneumo Haemophilus influenzae Neisseria meningitidis |
|
postsplenectomy (3)
|
Howell-Jolly bodies
Target cells Thrombocytosis |
|
thymus develops from _
|
epithelium of 3rd branchial pouches
|
|
lymphocytes are of _ (tissue) origin
|
mesenchymal
|
|
thymus histology / cell types
cortex: medulla: |
cortex: immature T cells
Medulla: "HEM" --Mature T cells --epithelial reticular cells --Hassall's corpuscles |
|
MHC I binds...
|
TCR
CD8 |
|
MHC I =
MHC II = |
HLA-A, B, C
HLA-DR, DP, DQ |
|
MHC I vs. MHC II
expressed on... |
~ all cells except RBCs
only APCs |
|
MHC I mediates _ immunity
|
viral
|
|
antigen is loaded for MHC I where?
what antigen? |
RER
mostly intracellular peptides |
|
one of the MHCs pairs with ___
why? |
beta-2 microglobulin
aids in transport to cell surface |
|
antigen is loaded onto MHC II following ______
|
release of invariant chain in an acidified endosome
|
|
HLA-A3
|
hemochromatosis
|
|
hemochromatosis HLA
|
HLA-A3
|
|
HLA-B27
|
PAIR
psoriasis ankylosing spondylitis inflammatory bowel disease reiter's syndrome |
|
HLA-B8
|
"your grave will B 8 feet under"
Graves' disease |
|
HLA-DR2
|
"you think there are Multiple Good Systems for mowing Hay, but DeR are only 2."
MS Goodpasture's SLE Hay fever |
|
diabetes type 1 HLA
|
HLA-DR3, DR4
|
|
HLA-DR4
|
rheumatoid arthritis, diabetes type 1
|
|
HLA-DR5
|
pernicious anemia
hashimoto's thyroiditis |
|
HLA-DR7
|
steroid-responsive nephrotic syndrome
|
|
natural killer cells use _ _ to accomplish _ _
|
perforin
granzymes induce apoptosis of virally-infected and tumor cells |
|
NK cells' activity is enhanced by
|
IL-12, IFN-beta, IFN-alpha
"I'Ll Interfere with bacteria in 12 ways, in my Alpha and Beta brain waves, w/o even thinking about it, b/c I'm a Natural Killer" |
|
IL-12 a couple effects
|
+ NK cells activity
Helper T --> Th1 cell |
|
NK cells are induced to kill when _____ is found on target cell
|
nonspecific activation signal
absence of class I MHC |
|
which Ig neutralizes viruses
|
Ig
|
|
CD4+ T cells functions
|
help B cells make antibody
make gamma-interferon --> activates macrophages |
|
helper T cell differentiates into _ where?
|
IL-12 --> Th1 (cell-mediated)
IL-4 --> Th2 (humoral) in lymph node |
|
+ selection
- selection of T lymphocytes occurs where? |
+ selection: cortex
- selection: medulla |
|
which Ig mediates type II = ____
type III = ______ hypersensitivity? |
IgG
cytotoxic immune-complex |
|
APCs =
|
Macrophage
Dendritic cell B cell |
|
APC cell stimulates CD4+ T cell by MHC II
but also talks to the CD4+ T cell's _ by APC's _ |
CD28
B7 |
|
virus infected cell talks to CD8+ T cell by MHC I
but the Th1 cell talks to the CD8+ T cell's _ by Th1's _ |
IL-2R
IL-2 |
|
Th2 cell talks to B cell by ____
|
Th2 cytokines: IL-4, IL-5, IL-6
Th2's CD40L --> B cell's CD40 |
|
Th1 cell secretes _ cytokines
|
IL-2
IFN-gamma |
|
Th1 cell helps what?
|
macrophage
CD8+ T cell |
|
Th1 cell is inhibited by ...
|
IL-10 (from Th2)
|
|
Th2 cell secretes _ cytokines
|
IL-4, IL-5, IL-10
|
|
Th2 cell helps...
|
helps antibody production
(IgE > IgG) |
|
Th2 cell is inhibited by
|
IFN-gamma (from Th1)
|
|
macrophage-lymphocyte interaction
|
lymphocytes (secrete IFN-gamma)
macrophages (secrete IL-1, TNF-alpha) stimulate one another |
|
cytotoxic T cells kill by... _
|
inducing apoptosis
|
|
cytotoxic T cells mechanism
|
release cytotoxic granules containing
--perforin --granzyme (serine protease; + apoptosis) --granulysin (antimicrobial; + apoptosis) |
|
complement binding part of heavy chain is...
|
CH2
|
|
complement enhances...
|
opsonization
lysis |
|
antibody diversity is generated by (4)
|
1. random "recombination" of VJ (light) or V(D)J (heavy)
2. random combination of heavy & light 3. somatic hypermutation (following antigen stimulation) 4. addition of nucleotides during (1) by terminal deoxynucleotidyl transferase |
|
Ig _ ... take on different forms...
|
IgA--monomer in circulation;
dimer when secreted IgM--monomer on B cell; pentamer |
|
IgA crosses epithelial cells by _ and something else re: epithelial cells
|
transcytosis
picks up secretory component from them before secretion |
|
which Ig is found in breast milk?
|
IgA
|
|
lowest [ ] Ig in serum
|
IgE
|
|
MAC defends against _ bacteria
|
G -
|
|
the two opsonins
|
C3b
IgG |
|
_ aids in the clearance of immune complexes
|
C3b
|
|
_ help prevent complement activation on self-cells
|
DAF (decay accelerating factor)
C1 esterase inhibitor |
|
complement _ --> viral neutralization
|
C1, C2, C3, C4
|
|
complement _ --> anaphylaxis
|
C3a
C5a |
|
deficiencies of complement
|
C1 esterase inhibitor
--> hereditary angioedema C3 --pyogenic sinus & respiratory infections -- ^ type III hypersensitivity C5-C8 --> Neisseria bacteremia DAF --> complement-mediated lysis of RBCs and paroxysmal nocturnal hemoglobinuria |
|
C1 esterase inhibitor deficiency
|
hereditary angioedema
|
|
decay-accelerating factor deficiency -->
|
complement-mediated lysis of RBCs and paroxysmal nocturnal hemoglobinuria
|
|
C3 deficiency -->
|
--pyogenic sinus & respiratory infections
-- ^ type III hypersensitivity |
|
C5-C8 deficiency -->
|
Neisseria bacteremia
|
|
pyrogens
|
IL-1
IL-6 |
|
IL-1 -->
|
--fever
--acute inflammation --endothelium expression of adhesion molecules --chemokine secretion to recruit leukocytes |
|
IL-6
|
--fever
--acute-phase proteins |
|
IL-6 is secreted by...
|
macrophages
Th cells |
|
macrophages secrete
|
IL-1, 6, 8, 12, TNF-alpha
|
|
IL-8
|
chemotactic for neutrophils
|
|
IL-12 is secreted by...
|
macrophages
B cells |
|
IL-12
|
differentiation into Th1 cells
activation of NK cells |
|
TNF-alpha
|
septic shock
leukocyte recruitment vascular leak |
|
T cells secrete
|
IL-3
|
|
IL-3
|
+ bone marrow stem cells
fxns like GM-CSF |
|
Th1 cells make...
|
IL-2
interferon-gamma |
|
IL-2
|
+ T cells
|
|
interferon-gamma
|
activates:
--macrophages --Th1 suppresses Th2 antiviral antitumor |
|
Th2 cells make...
|
IL-4
IL-5 IL-10 |
|
IL-4
|
--differentiation into Th2 cells
--growth of B cells --class switching to IgE and IgG |
|
IL-5
|
differentiation of B cells
class switching to IgA growth/differentiation of eosinophils |
|
IL-10
|
modulates inflammatory response
- actions of activated T cells and Th1. activates Th2 |
|
IL-10 is secreted by...
|
Th2
regulatory T cells |
|
interferons place .... cells in an...
|
uninfected cells
antiviral state |
|
interferons induce production of
|
a ribonuclease that degrades viral mRNA
|
|
interferons alpha, beta, gamma interfere with viruses by...
|
alpha & beta
--inhibit viral protein synthesis gamma -- ^ MHC I and II expression and antigen presentation on all cells interferons --activate NK cells (to kill virus-infected cells) |
|
_ is associated with TCR
|
CD3
|
|
6 T cell surface proteins
|
TCR; CD3
CD28 (binds B8 on APC) Th: CD4, CD40L CD8 |
|
6 B cell surface proteins
|
CD 19, 20, 21 (21--receptor for EBV)
CD40 MHC II B7 (binds CD28 on T cell) |
|
6 cell surface receptors on macrophages
|
MHC II, B7
CD40, CD14 receptors for Fc and C3b |
|
3 cell surface receptors on NK cells
|
receptors for MHC I
CD16 (binds Fc of IgG) CD56 (unique to NK) |
|
which becomes more anergic?
|
T cells
|
|
anergy in T cells
|
self-reactive T cells
become nonreactive w/o costimulation |
|
superantigens are found in _ bacteria
|
S pyogenes
S aureus |
|
superantigens mechanism
|
cross-link beta-region of TCR
with MHC class II on APCs --> IFN-gamma from Th1 --> IL-1, IL-6, TNF-alpha from macrophages |
|
endotoxins from G - bacteria MOA
|
stimulate macrophages by
endotoxin receptor CD14 |
|
antigen variation examples (5)
|
salmonella (2 flagellar variants)
borrelia (relapsing fever) N. gonorrhoeae (pilus) influenza (major shifts; minor drifts) trypanosomes (programmed rearrangement) |
|
influenza shift MOA
|
RNA segment reassortment
|
|
half-life of IgA in breast milk and other antibodies that are passively administered
|
3 weeks
|
|
preformed antibodies are given in (4) cases
|
To Be Healed Rapidly
Tetanus Botulinum HBV Rabies |
|
Type I hypersensitivity includes
|
anaphylactic
atopic |
|
vasoactive amines in Type I hypersensitivity act @
|
postcapillary venules
|
|
test for type I hypersensitivity
|
scratch test
radioimmunosorbent assay |
|
Type I is mediated by Ig_
Type II is mediated by Ig_ Type III is mediated by Ig_ |
E
G, M G |
|
mechanisms of Type II
|
antibodies...
1. complement, phagocytosis 2. recruit neutrophils or macrophages 3. bind cellular receptors & interfere |
|
test for Type II
|
Coombs (direct or indirect)
|
|
immune complex mechanism
|
IgG complexes
--> activate complement --> attracts neutrophils --> release lysosomal enzymes |
|
types of type III
|
immune complex
serum sickness arthus reaction |
|
serum sickness mechanism
|
antibodies are deposited in membranes where they fix complement
|
|
arthus reaction is...
|
local subacute antibody-mediated hypersensitivity
e.g. @ skin |
|
arthus reaction is characterized by (3)
|
edema
necrosis activation of complement |
|
arthus reaction test
|
immunofluorescent staining
|
|
serum sickness sxs
|
PAUL has a Fever
Proteinuria Arthralgias Urticaria Lymphadenopathy Fever |
|
type IV mechanism
|
sensitized lymphocytes encounter antigen
release lymphokines --> macrophage activation |
|
type _ hypersensitivity is not transferable by serum
|
IV
|
|
type IV causes (3) clinical
|
Transplant rejection
TB skin test Contact dermatitis |
|
5 allergic/atopic disorders caused by Type I
|
rhinitis
hay fever eczema hives asthma |
|
Type II --> 11 disorders
|
wouldn't let that Pimp with his Bull near My Grave even for a Roomful of Good Wreaths. He's just Acute Perv, and an Idiot
--pemphigus vulgaris --bullus pemphigoid Myasthenia gravis Graves' --rheumatic fever --goodpasture's --erythroblastosis fetalis hemolytic anemia acute hemloytic transfusn rxn pernicious anemia --idiopathic thrombocytopenic purpura |
|
type II vs. type III general idea
|
II--specific to tissue or site of antigen
III-- vasculitis, systemic manifestations |
|
Graves vs. Hashimoto's which type of hypersensitivity?
|
Graves: type II
Hashimoto's: type IV |
|
rheumatic fever vs. rheumatoid arthritis, which type of hypersensitivity?
|
type II
type III |
|
type III disorders (7)
|
SLE
Rheumatoid arthritis Polyarteritis nodosum --poststreptococcal glomerulonephritis --serum sickness --arthus reaction hypersensitivity pneumonitis (e.g. farmer's lung) |
|
an example of arthus rxn
|
swelling & inflammation
2^ tetanus vaccine |
|
type IV hypersensitivity (7) pathologies
|
Type I DM
MS Guillain-Barre Hashimoto's Graft-vs-host disease PPD Contact dermatitis (e.g. poison ivy, nickel) |
|
autoantibodies
nonspecific for SLE specific for SLE |
ANA
dsDNA, Smith |
|
autoantibodies:
antihistone |
drug-induced lupus
|
|
drug-induced lupus, what autoantibodies?
|
antihistone
|
|
rrheumatoid factor is anti...
|
anti-IgG
|
|
scleroderma autoantibodies
|
CREST: antiCentromere
diffuse: Scl-70 (DNA topoisomerase I) |
|
antimitochondrial autoantibodies indicates...
|
1^ biliary cirrhosis
|
|
celiac disease has _ autoantibodies besides gliadin
|
endomysial
|
|
pemphigus vulgaris antibodies
|
desmoglein ("a pimp in a glen")
|
|
hashimoto's autoantibodies
|
microsomal
thyroglobulin |
|
antibodies for polymyositis, dermatomyositis
|
anti-Jo-1
|
|
antibodies for Sjogren's
|
SS-A (anti-Ro)
SS-B (anti-La) |
|
mixed connective tissue disease autoantibodies
|
U1 RNP (ribonucleoprotein)
|
|
autoimmune hepatitis autoantibodies
|
smooth muscle
|
|
type 1 diabetes autoantibodies
|
anti-glutamate decarboxylase
|
|
B-cell immune deficiencies
|
i Have a B Cell Syndrome
Bruton's agammaglobulinemia Hyper-IgM syndrome Selective Ig deficiency CVID (common variable immunodeficiency) |
|
T-cell disorders
|
i Have T Cell Issues
Thymic aplasia (DiGeorge) IL-12 receptor deficiency Hyper-IgE syndrome (Job's) Chronic mucocutaneous candidiasis |
|
DiGeorge: genetics
|
22q11 deletion
|
|
DiGeeorge presentation
|
tetany (hypocalcemia)
recurrent viral/fungal infections congenital heart and great vessel defects |
|
DiGeorge labs etc.
|
v T cells
v PTH v Ca++ absent thymic shadow on cxr |
|
IL-12 receptor deficiency
defect, presentation, labs |
v Th1 response
disseminated mycobacterial infections v IFN-gamma |
|
hyper-IgE syndrome
defect |
Th1 cells fail to produce IFN-gamma
--> inability of neutrophils to respond to chemotactic stimuli |
|
hyper-IgE syndrome presentation
|
FATED
--coarse Facies --cold (noninflamed) staphylococcal Abscesses --retained primary Teeth --^ IgE --Dermatologic problems (eczema) |
|
chronic mucocutaneous candidiasis defect
|
T-cell dysfunction
|
|
chronic mucocutaneous candidiasis presentation
|
Candida albicans
infections of skin & mucus membranes |
|
Bruton's agammaglobulinemia defect
|
X-linked recessive ("Boys")
BTK defect (a tyrosine kinase) --> blocks B-cell differentiation |
|
bruton's agammaglobulinemia presentation
|
recurrent bacterial infections
(after 6 months b/c v maternal IgG) due to opsonization defect |
|
Bruton's agammaglobulinemia labs
|
normal pro-B
v maturation v number of B cells v Ig (all classes) |
|
hyper-IgM defect
|
defective CD40L on helper T cells
--> inability to class switch |
|
hyper-IgM syndrome presentation
|
severe pyogenic infections early in life
|
|
selective Ig deficiency presentation
|
sinus and lung infections
milk allergies and diarrhea Anaphylaxis on exposure to blood products with IgA |
|
the most common selective Ig deficiency
its mechanism |
IgA
failure to mature into plasma cells |
|
CVID defect
|
B-cell maturation
|
|
CVID presentation
|
acquired in 20s-30s
autoimmune disease lymphoma sinopulmonary infections |
|
CVID labs
|
normal number of B cells
v plasma cells v immunoglobulin |
|
B and T cell disorders
|
SAW
SCID Ataxia-telangiectasia Wiskott-Aldrich |
|
Phagocyte dysfunction disorders
|
Leukocyte adhesion deficiency type 1
Chediak-Higashi Chronic granulomatous disease |
|
SCID types
|
IL-2 receptor defect (most common, X-linked)
adenosine deaminase deficiency failure to synthesize MHC II antigens |
|
SCID presentation
|
all types of infections
|
|
SCID rx
|
bone marrow transplant (no allograft rejection)
|
|
SCID labs
|
v IL-2R --> v T-cell activation
or... ^ adenine |
|
ataxia-telangiectasia defect
|
DNA repair enzymes
|
|
ataxia-telangiectasia triad
|
cerebellar defects (ataxia)
spider angiomas (telangiectasia) IgA deficiency |
|
labs in ataxia-telangiectasia
|
IgA deficiency
|
|
Wiskott-Aldrich syndrome basic defect
|
X-linked recessive
progressive delection of B and T cells |
|
wiskott-aldrich triad
|
TIE
thrombocytopenic purpurra infections eczema |
|
wiskott-aldrich labs
|
^ IgE, IgA
v IgM |
|
leukocyte adhesion deficiency type 1 defect
|
defect in LFA-1 integrin (CD18) protein on phagocytes
|
|
leukocyte adhesion deficiency type 1 presentation
|
bacterial infections
absent pus delayed separation of umbilicus |
|
leukocyte adhesion deficiency type 1 labs
|
neutrophilia
|
|
chediak-higashi syndrome
|
recessive
v polymerization of microtubules v phagocytosis pyogenic infections (staph & strep) partial albinism peripheral neuropathy |
|
chronic granulomatous disease defect
|
lack of NADPH oxidase
v reactive oxygen species absent respiratory burst in neutrophils |
|
CGD presentation
|
^ susceptibility to catalase-positive organisms -- SEA:
S. aureus E. coli Aspergillus |
|
CGD labs
|
negative nitroblue tetrazolium dye reduction test
|
|
a transplant from an identical twin is called a...
|
syngeneic graft
|
|
which transplant rejection is mediated by antibodies?
which type of hypersensitivity is it? |
hyperacute
type II |
|
hyperacute rejection
|
type II
preformed antibodies within minutes occludes graft vessels --> ischemia, necrosis |
|
acute rejection is reversible by...
|
cyclosporine
OKT3 |
|
acute rejection = (3)
|
cytotoxic T's against foreign MHCs
weeks vasculitis @ graft--interstitial lymphocytic infiltrate |
|
chronic rejection =
|
T-cell and antibody
obliterative vascular fibrosis months to years irreversible fibrosis of graft tissue and blood vessels |
|
symptoms of graft-vs-host disease
|
maculopapular rash
jaundice hepatosplenomegaly diarrhea |