Exam 3 (Lect. 22-26) Flashcards
Which of the following is associated with antigen presentation by phagocytes, but not by epithelial
cells?
A. MHC1 picks up an external antigen circulating in the blood serum.
B. MHC2 picks up an antigen from the phagocyte’s cytoplasm.
C. MHC1 picks up an antigen from the phagolysosome.
D. MHC2 picks up an external antigen circulating in the blood serum.
E. MHC2 picks up an antigen from the phagolysosome.
MHC2 picks up an antigen from the phagolysosome.
Which of the following is NOT common to all three complement activation pathways?
A. The inflammatory response is triggered by C3a and C5a.
B. The adaptive immune response is needed for activation of the pathway.
C. Complement protein C3b is needed as part of the C5 convertase.
D. A molecule from your blood serum must bind the surface of a pathogen.
E. The MAC is formed from C5b and C6 - C9.
The adaptive immune response is needed for activation of the pathway.
Bacteria respond to phagocytosis by . . .
A. forming granulomas
B. releasing their capsule antigens
C. producing leukocidins
D. enhancing motility to swim out of the phagocyte
E. producing an oxidative burst to kill the phagocyte
producing leukocidins
MHC Class II receptors . . .
A. Are found only on phagocytes and B-cells
B. Pick up antigen from the infected cell’s cytoplasm
C. Serve as binding receptors for TC cells
D. bind to the CD8 receptor on T cells
E. are found on T cells and used as transporters for cytokine secretion
Are found only on phagocytes and B-cells
How does interferon fight a viral infection in an infected host?
A. It is a viricidal protein.
B. It induces antiviral proteins (AVP) in virus-infected cells.
C. It boosts the production of B cells in a virus-infected host.
D. It activates inactive AVPs in virus-infected cells.
E. It is produced in virus-infected cells and induces AVP in neighboring cells.
It is produced in virus-infected cells and induces AVP in neighboring cells.
Which of the following is required for granuloma formation?
A. B cells must continually secrete antibodies
B. TC cells must continually secrete cytotoxins
C. NK cells must continually secrete perforins
D. Macrophages must continually secrete chemokines
E. APC cells must continually secrete antigens
Macrophages must continually secrete chemokines
Which of the following is correct regarding the body’s interferon defense system?
A. It can be activated when antibodies bind to an organism.
B. Cells that produce interferon apoptose when infected by a virus.
C. Interferon induces the production of antiviral proteins in adjacent cells.
D. Interferon is only produced by antigen presenting cells (APCs).
E. Interferon is produced in the phagolysosome of macrophages with activated TLRs.
Interferon induces the production of antiviral proteins in adjacent cells.
The three complement activation systems share many common features, but there are also
differences. Which of the following is NOT common to all three complement pathways?
A. Diapedesis is induced by peptide C3a
B. Properdin is required to stabilize the C5 convertase
C. C3b opsonizes foreign cells for phagocytosis
D. A pore complex is assembled and inserted into a foreign cell to lyse it
E. PMNs are recruited to the site of complement activation by peptide C5a
Properdin is required to stabilize the C5 convertase
Why does a bacterium produce antioxidants?
A. To help your body fight off infections from other bacteria.
B. To signal phagocytes to engulf it.
C. To survive the harsh environment inside the phagolysosome.
D. The bacterium is producing its own chemoattractants.
E. To kill the phagocyte that is trying to engulf it.
To survive the harsh environment inside the phagolysosome.
Some bacteria live and divide inside the phagolysosome. What will be a symptom associated with
a chronic infection of a patient with such a bacterium?
A. Clumps of infected macrophages and TH cells will be seen in the patient’s tissues.
B. There will be a lower-than-normal number of phagocytes in the patient’s body.
C. The patient will suffer from constant high fever.
D. The patient will not produce antibodies against the bacterium.
E. The patient will suffer hypovolemia and DIC.
Clumps of infected macrophages and TH cells will be seen in the patient’s tissues.
Which of the following is associated with antigen presentation by dendritic cells, but not by
epithelial cells?
A. MHC1 picks up an external antigen circulating in the blood serum.
B. MHC2 picks up an antigen from the phagocyte’s cytoplasm.
C. MHC1 picks up an antigen from the phagolysosome.
D. MHC2 picks up an external antigen circulating in the blood serum.
E. MHC2 picks up an antigen from the phagolysosome.
MHC2 picks up an antigen from the phagolysosome.
Which of the following is NOT a consequence of activating the complement cascade on the surface
of a bacterium?
A. Peptide C3b attaches to the bacterium, making it easier to phagocytize.
B. Peptide C5b recruits a pore complex to kill the bacterium.
C. Convertases are assembled that proteolyze other complement proteins.
D. Peptide C3a induces B cells to produce antibodies that attach to the bacterium.
E. Peptide C5a recruits PMNs to the site of the infection, where they engulf bacteria.
Peptide C3a induces B cells to produce antibodies that attach to the bacterium.
One of the complement activation pathways is called the “alternate” pathway. What is different
between this pathway and the “classical” pathway?
A. It kills bacteria in a different manner than the classical pathway.
B. It requires a bacterial surface to be coated with lectins.
C. It only kills infected “self” cells, rather than pathogenic bacteria.
D. It can be activated even before the humoral immune response is active.
E. It alternates between inducing inflammation and keeping fever from getting too high.
It can be activated even before the humoral immune response is active.
Which of the following is required for granuloma formation?
A. production of antibodies against a bacterium
B. epithelial cell damage
C. persistent antigen presence inside macrophages
D. binding of the B7 on APCs to CD28 on TC cells
E. high titer of a pathogen circulating in the blood
persistent antigen presence inside macrophages
Which of the following could be considered to be a phagocyte?
A. TC cell
B. TH cell
C. lymphocyte
D. antigen presenting cell
E. mast cell
antigen presenting cell
We said that MHC2 is mainly for presentation of exogenous antigens, whereas MHC1 is mainly
for presentation of endogenous antigens. Why is this so?
A. MHC2 is on the outside of cells, MHC1 is on the inside.
B. MHC2 binds to bacteria to allow macrophages to engulf the bacteria.
C. MHC1 is found in the nucleus of infected cells, MHC2 in the cell membrane.
D. MHC1 is involved in elimination of antibodies that recognize self antigens.
E. MHC2 passes through the endocytic vesicle on its way to the cell surface.
MHC2 passes through the endocytic vesicle on its way to the cell surface.
What is the purpose for our immune system to opsonize bacterial cells?
A. It makes the bacteria easier for the oxidative burst and hydrolases to digest.
B. It causes phagocytes to produce more lysosomes.
C. It makes the surface of the bacteria more slippery so that we can excrete them better.
D. It adds surface features to the bacterium that makes it easier for our cells to recognize.
E. It is a way to neutralize bacteria so that they do not attach to our cells and infect us.
It adds surface features to the bacterium that makes it easier for our cells to recognize.
Granuloma formation involves all of the following EXCEPT . . .
A. antibodies
B. cytokines
C. macrophages
D. bacteria
E. T cells
antibodies
Which of the following statements is true of MHC-II, but not of MHC-I?
A. It must be matched in transplanted tissues or the transplant will be rejected.
B. It mainly displays antigens from the phagolysosome.
C. It typically displays self antigens as well as foreign antigens.
D. It is more important for fighting viral infections than bacterial infections.
E. It recruits TC cells and attaches specifically to them so the infected APC will be killed.
It mainly displays antigens from the phagolysosome.
How is interferon produced during an infection?
A. It is produced by induction of viral genes in the phagolysosome.
B. Bacteria produce it in response to the phagocyte oxidative burst.
C. A second-messenger pathway induces it when viral RNA binds to an RLR receptor.
D. It is produced when MHC-I phosphorylates a response regulator in infected cells.
E. TH cells produce it when they bind to MHC-II that is displaying viral antigens.
A second-messenger pathway induces it when viral RNA binds to an RLR receptor.
Which of the following is true of infections that are characterized by granuloma formation?
A. Bacteria that cause these infections lack PAMPs on their surface.
B. APCs associated with these infections fail to engulf bacterial pathogens.
C. Bacteria that cause these infections produce many leukocidins and oxidants.
D. Bacteria prevent lysosomes in infected macrophages from fusing with phagosomes.
E. Infected macrophages fail to produce MHC-II, and so are not recognized by IgG.
Bacteria prevent lysosomes in infected macrophages from fusing with phagosomes.
What is the function of a Toll-like receptor?
A. It allows macrophages and dendritic cells to bind specifically to pathogens.
B. It allows TH cells to bind specifically to B cells.
C. It allows pathogens to bind specifically to epithelial cells.
D. It allows bacteria to bind the FC part of antibodies.
E. It allows the immune system to recognize when a viral infection has occurred.
It allows macrophages and dendritic cells to bind specifically to pathogens.
What molecule is typically recognized by the immune system to signal that a cell has been infected
by a virus?
A. Complement protein C3b
B. Viral capsomeres
C. Viral envelope lipids
D. Viral spike proteins
E. Double stranded RNA
Double stranded RNA
How does interferon (IFN) function during a viral infection?
A. Cells that produce IFN apoptose when infected by a virus.
B. IFN is an oxidant that kills the virus by oxidizing viral capsid proteins.
C. IFN is an inducer that turns on genes for antiviral proteins in neighboring cells.
D. IFN is a cytotoxin that kills neighboring cells to prevent them from getting infected.
E. IFN is a chemokine signal that induces antibody production by TC cells.
IFN is an inducer that turns on genes for antiviral proteins in neighboring cells.