Biol 430 Question Bank MHC and Antigen Presentation
Biol 430 Question Bank MHC and Antigen Presentation
Biol 430 Question Bank MHC and Antigen Presentation
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The diagram to the right shows a cross-section of the MHC-I binding cleft. Add to the
diagram a 15 amino acid peptide of around
showing how it would be positioned. Label
the position of the anchor amino acids.
2. Complete this table to show the arrangement of MHC-I, MHC-II and MHC-III regions and genes
on the chromosome.
MHC class:
Locus:
N/A
A.
Although there are the same number of MHC-I and MHC-II loci, a greater number of MHCII peptides can be created. Why?
B.
MHC-II loci include pseudogenes; what are these and do they contribute to the range of
peptides presented by MHC proteins?
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A. DR and DR :
B. DRA and DRB :
C. DRB1, DRB2, DRB3, etc :
D. DRB1*01, DRB1*02, DRB1*03, etc :
E. DRB1*0101, DRB1*0102, DRB1*0103, etc :
F. DR1, DR2, DR3, etc
A. A, B,
A
B
C
DR
A1 B7 Cw3 DR2
A2 B8 Cw2 DR3
A3 B44 Cw4 DR4
A11 B35 Cw1 DR7
A3 B44 Cw4 DR7
DQ
DQ1
DQ2
DQ2
DQ3
DQ3
DP
DP1
DP2
DP3
DP4
DP5
F
G
H
E
R
different ___________________.
B. A1, B8, Cw3, DR2, etc., represent different ___________________
C. F, G, H, E, and R designate different _____________________.
D. If a HLAG/H man marries a HLAH/E woman, what are the potential haplotypes among their
children. (Hint: predicting haplotypes among offpring can be treated like a monohybrid
cross.)
E. In theory, would a person who is HLAF/F or a person who is HLAF/G be better able to raise an
immune response against the greatest number of pathogens? Explain.
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6. Consider a hypothetical allelic combination HLA-B4 and HLA-C6 that presents a relative risk of
150 for a particular autoimmune disease.
A. Will all people that have the disease carry these two alleles?
B. Will everyone with these two alleles get the disease?
C. What other factors might influence incidence of the disease?
7. You cross a homogenous C57Bl/6 (H-2b) mouse and homogenous CBA (H-2k) mouse, and
examine the H-2 protein expression among the offspring. This diagram shows the arrangement of
MHC genes in the mouse MHC complex.
MHC class:
Locus:
I
K
II
A
III
E
I
D
A. What H-2 haplotype(s) will be carried by the F1 offspring? Will the offspring be syngeneic?
B. Which types of MHC will be expressed on the liver cells of the offspring? Which will be
expressed on dendritic cells?
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8. As a student in an immunology laboratory class, you have been given spleen cells from a mouse
immunized with the LCM virus. You determine the antigen-specific functional activity of these cells
with two different assays: in assay 1, the spleen cells are incubated with macrophages that have
been briefly exposed to the LCM virus; the production of interleukin 2 (IL-2) is a positive response;
in assay 2, the spleen cells are incubated with LCM -infected target cells; lysis of the target cells
represents a positive response in this assay. The results of the assays using macrophages and target
cells of different haplotypes are presented in the table below.
MHC Haplotype of macrophages
and virus-infected target cells
Mouse strain used as
source of macrophages
& target cells
C3H
BALB/c
BALB/c x B10.A
A.Tl
B10.A (3R)
B10.B (3R)
MHC-I
K
k
d
d/k
s
b
k
MHC-II
A
E
k
k
d
d
d/k
d/k
k
k
b
b
k
--
MHC-I
D
k
d
d/d
d
d
b
9. For each of the following cell types, indicate if it will express MHC I, II, both (B), or neither (N).
___ B-cells
___ Dendritic cell
___ Liver cell
___ Red blood cell
___ T-cell
___ Macrophage
___ Skin cell
10. In order to function as effective APCs, DCs muct undergo a series of activation steps. What
change to a DC occurs during each one of these steps:
A. What are several ways in which DCs receive a danger signal and capture an antigen? What
are some of the changes that occur to a DC cell upon sensing a danger signal?
B. What changes occur to a DC cell after engaging a T-cell?
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C.
16. Morrison and Braciale performed experiments that demonstrated the presence of two antigen
processing pathways. They used two Tc cell clones
Activation of Tc cells
DC
that recognize antigens on:
that recognized influenza hemagglutin (HA, one of the
treatment
MHC-I
MHC-II
immunogenic surface proteins of the flu virus)
presented either on MHC-I or MHC-II. DCs were
Infectious virus
+
+
incubated with either infectious or inactivated forms
of the virus. The inactivated form retained its antigenic
Inactivated virus
+
properties but was unable to infect host cells.
Furthermore, the treatments included chloroquine (the
Infectious virus
+
+ emetine
most common treatment for malaria) which blocks
Infectious virus
endocytosis, or emetine, which inhibits viral
+
+ chloroquine
replication. After each treatment, the DCs were tested
for their ability to activate the Tc cells and the results are shown in the table.
A. Why are both cell types activated by DCs treated with infectious virus.
B. Which antigen processing pathway would you expect to not function in cells:
a. exposed to inactivated virus? _________________________
b. treated with emetine? ________________________
c. treated with chloroquine? _______________________
C. Do the results concur with these predictions? Explain.
D. Explain how these results demonstrate the operation of two separate pathways of antigen
processing.
E. Does cross-presentation appear to be occurring in these DC cells? Explain.
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14. Ziegler and Unanue performed some of the key experiments that demonstrated antigen
processing in DC cells. As part of the experiments, the DCs were treated with paraformaldehyde to
cause fixation, such as in a
histology procedure, which blocks
all enzymatic activity and locks the
cells proteins in place. The ability
of the DCs to activate TH cells that
recognize egg-white albumin
(ovalbumin, OVA) was tested by
measuring release of IL-2 after
several alternative treatments:
(a) DCs were fixed and then
exposed to the OVA.
(b) DCs were incubated with
OVA for an hour and then fixed.
(c) DCs were fixed and then
incubated with OVA peptide
fragments.
In the diagram, OVA peptides in
MHC are colored red, other peptides
are colored blue. The results are
shown in the right-hand column. (Figure is adapted from Goldsby, et al. 2003. Immunology. 5th ed. Figure 8.3)
A. Why are peptides present in the MHC proteins even before exposure to OVA?
B. Does fixation appear to alter the ability of MHC proteins to interact with T-cell receptors?
Explain.
C.
D.
What does experiment C show about the ability of mature MHC proteins to exchange
peptides? Do you think this process is likely to occur in vivo?
E. Explain how this experiment demonstrates the need for antigen processing.
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