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55 Cards in this Set

  • Front
  • Back
Macrophage marker:
CD 14
****B-Cell Marker:
CD 19, 20, 21
T Cell Marker:
CD3
NK lymphocyte marker:
CD 16+CD 56
What are the Ag receptor for naive B cells (mature B-cells)?
IgM & IgD
What are the latin designation for LC?
Kappa
or
Lamda
Idiotype VS Isotype
3D shape formed by AA in variable region (N-terminus)

Class (C-terminus)
BCR will bind _____, TCR only bind ____.
Unprocessed Ag; Peptide
What is the structure of TCR?
Alpha/Beta chain anchored by Cytoplasmic C-terminus

Rigid b/c no hinge
What are the signalling complex of BCR?
Ig-alpha, Ig-beta, Cd 19&21
What is the signalling complex of TCR?
CD3
**5 MOA of Diversity (4 works w/ TCR too)
1.V/D/J segments
2. V/D/J recombinations
3. N-nucleotide addition (B=HC only, T=both chain)
4. Combinatorial Association of LC (or Beta) & HC (or Alpha) (eg: multiply the combinations of both)
5. Somatic Hypermutation (BCR only, after Ag stimulation)
**Production of HC is just like production of __ chain in T-cell;
Production of LC is just like production of __ chain in T-cell.
Beta

Alpha
****CV: Showing diagram of the Lymphocyte Ag receptor genes:
1. How to differentiate between HC & LC?

2. How do u know if a gene can be expressed?
HC and D

VDJ if separated by intron--> Not rearranged --> CAN'T be expressed (germ-line DNA cannot be expressed w/o recombination)
What are the steps in HC (or B-chain) production?
1. D-J joining (gene rearr)
2. V-D/J joining (gene rearr)
3. Tc
4. RNA Splice joining V/D/J-C

D=For recombo
C=Idiotype
What are the steps in LC (or Alpha-chain) production?
1. V-J joining (gene rearr)
2. Tc
3. RNA splicing joining V/J-C

(K/lamda constant domain are added at the end to complete LC)
**What is the function of Tdt (terminal deoxyribonucleotidyl transferase)?
Randomly insert bases at jct of V/J/D creating more variability
**What is Tdt a marker for?
ALL (acute b/c starting to make T & B cells)
What is allelic exclusion?
Once rearrangement achieves a viable product, the cell shuts of rearrangement AND expression of the other allele on the homologous chromosome (the reason homologous chromosome is there is that if rearrangement screws up the first chromosome, the homologous chromosome provide 2nd chance for a viable rearranged product)
What are the first two constant domain on HC and thus are made first?
IgM & IgD

(Proximity allow co-expression on same B-Cell)
What are the only LC constant domains?
Kappa

Lamda
****What is RAG?
Recombination Activation Gene--> Cause recombination --> Gene expression
Omenn Syndrome/SCID:
Omenn: RAG have only partial activity --> Decrease B/T cell

SCID: NO RAG--> No B/T cell
What does Il-3 do?
Stimulate Myeloid SC development
What does Il-7 do?
Stimulate Lymphoid SC development
What is the difference between primary and secondary lymphoid organs?
Site of development VS site of Ag exposure
What are the steps of B-Cell maturation?
BM: Lymphoid SC -->Progenitor -->Pre-B -->Immature B

Periphery: Immature B --> Mature B (IgM+/D+) --> Ag --> Blast B (aka Activated) --> Plasma/Memory
How is tolerance in B-Cells cultivated?
Clonal Deletion (BM)= Overactivates apoptosis if binding to cells in BM

Clonal Anergy (Periphery)= Stay immature B Cells
What are the two primary lymphoid organs?
BM

Thymus
**How is tolerance in T-Cell cultivated?
In thymus, MHC I & II loaded w/ self-peptide interact w/ T cells:

1. Positive selection: Low affinity for MHC
2. Negative selection: High affinity for MHC
3. No positive selection: No affinity for MHC (no cross talk--> no growth signal)
Difference between MHC1 & 2:

Name=
Distribution=
Structure=
A/B/C (1 letter) VS DP/DQ/DR (2 letters)

All (except RBC) VS APC only

Tong VS Hot-dog bun
What are the general steps in the synthesis of a T cell?
1. CD3 expression(signal transduction)
2. CD4 & 8 simultaneously (co-receptor that enhance binding so TCR can see closer)
3. TCR expression
When does CD4 & 8 stop being co-expressed?
Until T-cell reach portal-medullary junction
What is CD2's function in T-cell?
Adhesion
What are the general structures of MHC I & II?
I: alpha chain + B2-microglobulin (help MHC I get to membrane)

II: Alpha + B chain
AChEI OD S/S & Tx:
DUMBBELSS=PANS + Sweating + Sk. mm. contraction

Atropine + 2-PAM (pralidoxime)=regenerate AChE or else permanent depolarization of diaphragm
Atropine (M-blocker) OD S/S & Tx:
SANS + Block sweating

Ctrl hyperthermia + Physostigmine (tert. amine --> cross BBB)
CO OD MOA & Tx
Shift O2 dissociation curve L (N/V/Vertigo)

Hyperbaric chamber
What is the main difference between atropine and amphetamine, since both make you hot?
Atropine: Hot + DRY

Amphetamine: Hot + MOIST
CNS stimulant OD (eg: amphetamine) S/S & Tx:
Warm and sweaty, psychosis

Ctrl CV/Hyperthermia/seizure+ BZD/Antipsychotics
OD opioids S/S & tx:
Respiratory depression/Miosis

Naloxone
ASA OD S/S & tx:
Tinnitis

Urinary alkalinization
Sedative-hypnotics/EtOH OD S/S & tx:
Disinhibition (initial), lethargy

Flumazenil (BZD only)
SSRI OD S/S & tx:
Serotonine syndrome

Ctrl hyperthermia & seizure
TCA OD S/S & tx:
Block M (like atropine) & Alpha1

Ctrl seizure and hyperthermia
What is the environmental source of As?
H2O

Coal burning
S/S of As poisoning:
Acute: Gastroenteritic, garlic breath

Chronic: Stocking glove neuropathy
**Fe OD S/S:
Blood out both ends
(Necrotizing gastroenteritis + hematemesis)
**Tx of Fe OD:
Deferoxamine
**Pb OD S/S:
Acute: Lead colic, encephalopathy, tinnitis

Chronic: Lead palsy (Wrist drop)
**Tx of Pb poisoning:
Succimer PO (mild)

Dimercaprol (severe)
**CV: Kid w/ microcytic sideroblastic anemia, what does lab show?
Decrease heme synthesis --> Increase delta-ALA in plasma
What is the biochemical defect in sideroblastic anemia?
Enough Fe, but can't be incorporated in heme -->accumulate Fe in mito around nucleus
What are the differentials for Sideroblastic anemia?
Decrease B6 (INH, Chronic alcholism)

Pb poisoning
What is Hg's route of entry?
Acute: Vapor/Inorganic salt ingestion

Chronic: Organic Hg ingestion