• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/76

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

76 Cards in this Set

  • Front
  • Back
Complement Receptor Type I
Found on phagocytes, neutrophils, B cells, Eosinophils, RBC

Serve to phagocytize and clear immune complexes

cleaves c3b and c4b as a regulatory control - make sure their isnt over production of complement
Complement Receptor Type II
Found on B cells, Dendritic Cells

B cells - helps to activate

dendritic cells - helps to trap antigens in the germinal center

Serves as a receptor for EBV -HIJACKER
Complement Receptor Type III
Found on Mononuclear phagocytes, neutrophils, and NK Cells

Serves to phagocytize

Helps the WBC adhere to the endothelium via ICAM
Complement Receptor Type IV
Found on mononuclear phagocytes, neutrophils, and NK Cells

Serves to phagocytize

Helps the WBC adhere to the endothelium
Purpose of Complement (3)
1. to opsonize the macrophage for phagocytosis (c3b or c4b)

2. stimulate immune response (c3a and c5a)

3. cell lysis via mac - c3b

4. B Cell Activation - C3d (cleavage product of C3b) binds to C receptors on B cells; initiates immune responses
Complement Deficiencies of the Classical Pathway
C2 & C4 - autoimmune dieases (SLE)

C3 - leads to gram + bacterial infections
Complement Deficiencies of the Alternative Pathway
Properdin & Factor D - leads to gram + bacterial infections
Complement Deficiencies of the MAC
CD5-9 leads to Neisseria bacterial infections
Receptors on T helper lymphocytes, T cytotoxic cells, B lymphocytes, and NK Cells
T helper cells: CD 3+. CD 4+

T cytolytic cells: CD 3+, CD 8+

B lymphocytes: Fc Receptors; Class II MHC, CD 19 & CD 21

NK Cells: Fc receptor for IgG
Name all 5 Immunoglobulins and their subclasses

What are elevated Ig indicative of?
IgG - gamma 1-5

IgM - none

IgA - alpha 1 and alpha 2

IgE - none

IgD

-ANy Ig elevations are indicative of cancer
IgG

IgG3
- principal mediator of secondary immunity

- can cross the placenta and provide passive protection to the fetus

IgG3 - most effective at binding complement bc it has a large hinge region, however the large hinge is susceptible to proteases
Elevated IgG levels are indicative of:
infections, liver diseases, autoimmune diseases, cystic fibrosis, sarcoidisis

severe: myeloma, monoclonal gammopathy
IgM
-prinicipal mediator of primary immune response

- pentamer with s-s bond to a j chain

- increases antigen agglutination visibility
Elevated IgM levels are indicative of:
IgM monoclonal gammopathy, infection,PARASITIC INFECTION, liver diseases, autoimmune diseases, nephrotic syndrome, polycythemia vera, HEROIN ADDICTION, Waldenstrom's macroglubulinemia
IgA1 & IgA2
IgA1 - monomer present in the circulation

IgA2 - dimer is the predominant antibody in mucosal secretions
Elevated IgA levels are indicative of:
IgA monoclonal gammopathy, infections, liver diseases, cystic fibrosis, CELIACS, Berger's disease, sarcoidosis,

memory jog: A = Angel Hair Pasta can't be eaten in Celiacs
IgD
rare; found on surface of B cells
IgE
-binds to very high affinity Fc receptor on mast cells & basophils, lymphocytes

- mediator of hypersensitivity, allergies, asthma

- primary antiparasitic antibody, sensitizes worms and other parasites for destruction by eosinophils

- sends signals to mast cells saying "fire"
Elevated IgE levels are indicative of:
allergic disorders, hypersensitivity disorders, parasitic infections, immunologic disorders, infectious mononucleosis, IgE myeloma
Toll like receptors
-found on phagocytes

TLR 1, 2, 4, 5 9 - bacteria sensitive
- TLR 2 - bacterial comp
- TLR 4 - for LPS
- TLR 9 - for bacterial and
viral DNA sequences

TLR 3, 7, 8 are viral sensitive and found on the endosome - not the plasma membrane
- TLR 3 - recognizes ds RNA
Chromosome location of heavy chain gene
chromosome 14
Chromosome location of light chain kappa
chromosome 2
chromosome location of light chain gamma
chromosome 22
Origin of Acute Lymphocitic Leukemia
Pro B Cell
Origin of Chronic Lymphocytic Leukemia
Mature B Cell with overexpression of kappa or lambda light chains
Origin of Myeloma
Mature Plasma Cell leading to Bence Jones Proteinuria - light chains in the urine
Burkitt's Lymphoma
translocation of chromosomes 14 and 8 . So the heavy chains on chromosome 14 are affected.

C-myc gene is placed in front of the heavy chain promoter which leads to gross overproduction of heavy chains
Isotype Switching Methods
1. IL - 4 induces IgE isotype switching
2. TGF - B increases IgA production
3. IFN- Gamma enhances IgG2a
An increased sedimentation rate for erythrocytes is associated with:
Induction of fibrinogen by IL-6
Which neurotransmitter associated with the induction of fever?
Prostaglandin E
Role of IL 1/ TNF
Leukocyte migration to site of injury
Role of EGF
epithelial and fibroblast growth
Role of TGF Beta
inhibits the division of the cell
Role of TGF alpha
promotes the division of the cell
Immunodeficiency Disease Types
- B & T Cell Maturation deficits
- B & T cell activation deficits
- signaling deficits
- multi - system deficiencies
-phagocyte disorders
- complement system deficiencies
SCIDS - signs
-failure to thrive
- candidiasis
- chronic diarrhea
SCIDS - causes
-IL 2 gamma receptor deficits - 2, 7, 9, and 4 - especially 7
-JAK
-ADA - adenosine deaminase
- RAG 1/RAG2 deficits - so no TCR or Ig
DiGeorge's Syndrome - signs
-Deficient T cells - so susceptible to intracellular microbes and viruses
-absent parathyroids = Tetany due to Ca2+ deposits
- facial deformities
-
X-Linked agammaglobulinemia - causes
-B Cell tyrosine kinase gene deficiency leading to lack of maturation past Pre-B stage
Di Georges - Causes
failure of development of the third and the fourth pouch
X linked Agammaglobulinemia - signs
-reduced plasma cells
- no germinal centers
- normal t cells
- autoimmune diseases
Bare lymphocyte Syndrome - types and differences
-MHC Class II deficit - affects both MHC I and MHC II

- MHC Class I deficit - TAP deficiency and shows up as NK Cells and gamma-delta T cells
Bare Lymphocyte Syndrome - symptoms
-Frequent URIs
- chronic lung infections
-skin lesions
Signaling Defects
-Zap 70 defects
-CD3 error
- X-Linked Hyper IgM
Ataxia Telangiectasia - cause
mutation @ ATM gene on chromosome 11 leading to neurologic deficits and hematopoietic cancer
Wiskott ALdrich Syndrome
No platelets leads to Eczema .

- due to mutation in WAS protein
- results in low IgM levels

hint: Baby with Ezcema
Chronic Grabulomatous Disease
deficit in cytochrome b558 results in inability to produce peroxide

- results in inflammatory reactions and non malignant granulomas

hint: Michael Jackson nose
Leukocyte Adhesion Deficiency - LAD 1
deficiency of CD 18 Beta 2 on WBC prevents it from migrating to inflammatory site
Leukocyte Adhesion Deficiency - LAD2
No fucose - so Leukocyte can not interact with E and P selectins
Heriditary Angioneurotic Edema
failure of C1 inhibitor to stop complement cascade resulting in edema
Location of B cells in the Lymph node and spleen
B cells are found primarily in the marginal zone of the spleen and in the follicles of the lymph nodes
Location of T helper & T cytolytic cells in the Lymph nodes and spleen
T helper cells localize in the periarteriolar lymphoid sheath (PALS) in the spleen ad the paracortex of lymph nodes.
Purpose of Pcam
diapedesis of WBC
Purpose of Il 1 and TNF alpha
stimulation of inflammatory response
LFA Icam
involved in wbc adhesion
Positive Selection
Process by which T cells which express a low avidity to MHC are selected to survive
Negative Selection
process by which T cells which express a high avidity to MHC are eliminated
Medullary areas of the Lymph node are inhabited by:
activated T cells and plasma B cells
Where are idiotypic determinants found on on Antibodies
In the variable region
What does TdT regulate?
Increased diversity in both the TCR and Ig molecules.
What cells are capable of antigen presentation?
B cells, macrophages, activated T cells and others
what bonds are responsible for the formation of antibody/antigen interactions?
All non covalent bonds

1. hydrogen bonds,
2. electrostatic interactions,
3. Van Der Waals interactions [induced dipoles],
4. hydrophobic interactions [exclusion of water]).
true or false: Before Th Cells differentiate into Th1 and Th2 they are doubly positive
false: T helper cells are not shown to be doubly positive at any point
How are Th1 cells stimulated from Th Cells? What do they produce?
-Th 1 cells are stimulated by IL 12 and make :
-IFN gamma which is involved in macrophage activation and isotype switching
- LT and TNF activate and recruit WBC to the site of inflammation

* think : CMI responses to viruses/intracellular pathogens.

How are Th 2 cells stimulated from Th Cells and what do they produce?
-Th2 cells are stimulated by IL-4 and make :
-IL 4 - stimulates IgE production
-IL - 5 - stimulates Eosinophil recruitment
- IL 10 which inhibits the activation of macrophages
What can happen if you mount the wrong Th (1 v 2) response to a bacterial infection?
If a person is infected w/ M. Leprae, two responses can occur:
-Th1 = tuberculoid leprosy
- Th2 = Lepramatous Leprosy --> FAR HIGHER BACTERIAL COUNT!!
During development, which of the following is the first protein product synthesized by a B cell?
Mu heavy chain
define epitope and paratope
-epitope - part of antigen that binds directly to the antigen
- paratope - region of the antibody that binds directly to the antigen
what components of CTL are important for killing?
Perforin and granzyme B stored in granules

-also contains IFN gamma, but it is not stored in granules
What cells are associated with a granulomatous reaction?
epithelioid macrophage
What is the characteristic inflammatory cell associated with an allergic response?
Eosinophil
A patient with severe asthma gets no relief from antihistamines. The symptoms are MOST likely caused by:
Leukotrienes
Where is IgD most often seen?
IgD is primarily seen on the surface of B cells and is used as a marker of B cell development
Poison Ivy
A T cell response to a specific antigen
Where in the Antibody does somatic hypermutation occur?
Occurs in the hypervariable region
What immunoglobulins to peripheral or circulating immunoglobulins express?
IgM and IgD, after undergoing rearrangement of heavy and light chain genes