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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