|
Immunology Review Corner
Immunology Review Corner: chapter 4 review of the 5th edition
of Cellular and Molecular Immunology, edited by Abul K. Abbas
and Andrew H.
Lichtman.
By Nathanael Horne, M.D.
Fellow-In-Training, Allergy and Immunology
Nassau University Medical Center
1. MHC Class I Genes include:
a. HLA A
b. HLA B
c. HLA C
d. HLA DR
e. a,b,and c
2. MCH Class II molecules are generally recognized by which
cells:
a. CD8+ Tcells
b. CD4+ Tcells
c. Erythrocytes
d. Neutrophils
3. The non-polymorphic portion of MCH molecule contain:
a. polymorphic regions for binding presented peptide sequences
b. binding sites for CD4+, CD8+ T-cells
c. the invariant chain
d. TAP
4. The location of the polymorphic residues on the MHC Class II
molecule
a. alpha-2 and beta-2 domains
b. alpha-1 and alpha-2 domains
c. alpha-1 and beta-1 domains
d. alpha-1 and beta-1 domains
e. beta-2 microglobulin
5. MHC Class I molecules accommodate peptide residues:
a. 8-11 resides
b. 10-30 residues
c. 60-80 residues
d. 3-4 residues
6. When full assembled the MHC class I molecules is composed of
what chains?
a. alpha and beta chains
b. delta and gamma chains with peptide
c. alpha and beta-2 microglobulin chains
d. alpha and beta-2 microglobulin chains with bound antigenic peptide
e. beta-pleated sheet supported by two parallel strands of alpha-helix
7. What is the binding site on the MHC molecule for the T cell
coreceptor CD8?
a. alpha-3 region
b. beta-2 region
c. alpha-1 and alpha-2 domains
d. beta-3 domain
e. alpha-1 and beta-1 domains
8. What is the binding site on the MHC molecule for the T cell
coreceptor CD4?
a. alpha-3 region
b. beta-2 region
c. alpha-1 and alpha-2 domains
d. beta-3 domain
e. alpha1 and beta-1 domains
9. When full assembled the MHC class II molecules is composed
of what chains?
a. alpha and beta chains
b. delta and gamma chains with peptide
c. alpha and beta-2 microglobulin chains
d. alpha and beta-2 microglobulin chains with bound antigenic peptide
e. beta-pleated sheet supported by two parallel strands of alpha-helix
10. MHC Class II molecules accommodate peptide residues:
a. 8-11 resides
b. 10-30 residues
c. 60-80 residues
d. 3-4 residues
11. What is the function of anchor residues?
a. Bind firmly to CD8 or CD4 coreceptors to increase TCR affinity.
b. Bind to either alpha or beta chains to maintain the overall
structure of the MHC molecule
c. They form the conserved regions that the TCR binds to upon antigen
presentation
d. Antigen peptide residues that bind to the alpha-helices and
beta-strands on the MHC securing the antigen peptide in the binding
groove
e. Serve as signal transducers upon antigen presentation and t cell
activation
12. With regards to T cell antigen recognition which of the
following is a true statement?
a. Amino acids from both the antigenic peptide and the MHC molecules
contribute to T cell antigen recognition
b. The MHC molecule is responsible for the fine specificity of antigen
recognition as well as MHC restriction of the T cells
c. Only the amino acids from the antigenic peptides are responsible
for T cell antigen recognition
d. The interaction of CD4 with the MHC class II molecule is
responsible for the fine specificity of antigen recognition
e. The fine specificity of antigen recognition is due to anchor
residues unique to MHC class II molecules
13. In humans, what chromosome are the MHC genes located on?
a. Short arm of chromosome 2
b. Short arm of chromosome 6
c. Chromosome 15
d. Chromosome 4
e. Chromosome 7
14. There are genes between the class I and class II clusters
that code for several proteins important to the immune system. These
genes are referred to as?
a. MHC-like genes
b. Immune response genes
c. MHC class III genes
d. Leukocyte trafficking genes
e. The cluster of differentiation
15. Several transcription factors that bind class II promoter
regions can increase the expression of MHC molecules. Mutations in
these transcription factors result in immunodeficiency disease
associated with defective expression of MHC molecules. Which syndrome
listed is the best studied of these disorders?
a. Wiskott-Aldrich Syndrome
b. Ommen’s Syndrome
c. Bare lymphocyte Syndrome
d. common gamma chain deficiency
e. ZAP-70 deficiency
ANSWERS
1. e, pg. 69
2. a, pg. 69
3. b, pg. 69
4. c, pg. 70
5. a, pg. 70
6. d, pg. 71
7. a, pg. 70, table 4-1
8. b, pg. 70, table 4-1
9. a, pg. 72
10. b, pg. 72 and 74
11. d, pg. 75
12. a, pg. 75
13. b, pg. 76
14. c, pg. 76
15. c, pg. 79
|
|