Chapter 5 quiz Flashcards
T cells recognize antigen when the antigen ___________________.
a. forms a complex with membrane-bound MHC molecules on another host-derived cell.
b. is internalized by T cells via phagocytosis and subsequently binds to T-cell receptors in the endoplasmic reticulum
c. is presented on the surface of a B cell on membrane-bound immunoglobulins
d. forms a complex with membrane-bound MHC molecules on the T cell
e. bears epitopes derived from proteins, carbohydrates, and lipids
a. forms a complex with membrane-bound MHC molecules on another host-derived cell.
If viewing the three-dimensional structure of
a T-cell receptor from the side, with the T-cell membrane at the bottom and the receptor pointing upwards, which of the following is inconsistent with experimental data?
a. The highly variable CDR loops are located across the top surface.
b. The membrane-proximal domains consist of Cα and Cβ.
c. The portion that makes physical contact with the ligand comprises Vβ and Cβ, the domains farthest
from the T-cell membrane.
d. The transmembrane regions span the plasma membrane of the T cell.
e. The cytoplasmic tails of the T-cell receptor α and β chains are very short
c. The portion that makes physical contact with the ligand comprises Vβ and Cβ, the domains farthest
from the T-cell membrane.
Unlike B cells, T cells do not engage in any of the following processes except _______________.
a. alternative splicing to produce a secreted form of the T-cell receptor
b. alternative splicing to produce different isoforms of the T-cell receptor
c. isotype switching
d. somatic hypermutation
e. somatic recombination
e. somatic recombination
Unlike the C regions of immunoglobulin heavy-chain loci, the C regions of the T-cell receptor β-chain loci ______.
a. are functionally similar
b. do not contain D segments
c. are more numerous
d. are encoded on a different chromosome from the variable β-chain gene segments of the T-cell
receptor
e. do not encode a transmembrane region
f. possess non-templated P and N nucleotides
a. are functionally similar
Which of the following statements regarding Omenn syndrome is incorrect?
a. A bright red, scaly rash is due to a chronic inflammatory condition.
b. Affected individuals are susceptible to infections with opportunistic pathogens.
c. It is invariably fatal unless the immune system is rendered competent through a bone marrow
transplant.
d. It is the consequence of complete loss of RAG function.
e. There is a deficiency of functional B and T cells.
f. It is associated with missense mutations of RAG genes.
d. It is the consequence of complete loss of RAG function.
All of the following statements regarding γ:δ T cells are correct except ___________.
a. they are more abundant in tissue than in the circulation
b. the δ chain is the counterpart to the β chain in α:β T-cell receptors because it contains V, D, and J segments in the variable region
c. they share some properties with NK cells
d. activation is not always dependent on recognition of a peptide:MHC molecule complex
e. expression on the cell surface is not dependent on the CD3 complex
e. expression on the cell surface is not dependent on the CD3 complex
During T-cell receptor _____-gene rearrangement, two D segments may be used in the final rearranged gene sequence, thereby increasing overall variability of this chain.
a. α
b. β
c. γ
d. δ
e. ε.
d. δ
The degradation of pathogen proteins into smaller fragments called peptides is a process commonly referred to as
a. endocytosis
b. promiscuous processing
c. antigen processing
d. antigen presentation
e. peptide loading
c. antigen processing
The primary reason for transplant rejections is due to differences in _____ between donor and recipient.
a. CD3
b. MHC molecules
c. T-cell receptor α chains
d. γ:δ T cells
e. β2-microblobulin
b. MHC molecules
When describing the various components of the vesicular system, which of the following is not included?
a. Nucleus
b. Golgi apparatus
c. endoplasmic reticulum
d. exocytic vesicles
e. lysosomes
a. Nucleus
Which of the following is not a characteristic of immunoproteasomes?
a. They make up about 1% of cellular protein.
b. They consist of four rings of seven polypeptide subunits that exist in alternative forms.
c. They are produced in response to IFN-γ produced during innate immune responses.
d. They produce a higher proportion of peptides containing acidic amino acids at the carboxy terminus
compared with constitutive proteasomes.
e. They contain 20S proteasome-activation complexes on the caps.
d. They produce a higher proportion of peptides containing acidic amino acids at the carboxy terminus
compared with constitutive proteasomes.
Identify which of the following statements is true regarding the transporter associated with antigen processing (TAP).
a. TAP is a homodimer composed of two identical subunits.
b. TAP transports proteasome-derived peptides from the cytosol directly to the lumen of the Golgi
apparatus.
c. TAP is an ATP-dependent, membrane-bound transporter.
d. Peptides transported by TAP bind preferentially to MHC class II molecules.
e. TAP deficiency causes a type of bare lymphocytes syndrome resulting in severely depleted levels of
MHC class II molecules on the surface of antigen-presenting cells.
c. TAP is an ATP-dependent, membrane-bound transporter.
All of the following are included in the peptide-loading complex except _____________.
a. tapasin
b. calnexin
c. calreticulin
d. ERp57
e. β2-microglobulin
b. calnexin
Which of the following best describes the function of tapasin?
a. Tapasin is an antagonist of HLA-DM and causes more significant increases in MHC class I than MHC class II on the cell surface. b. Tapasin is a lectin that binds to sugar residues on MHC class I molecules, T-cell receptors, and immunoglobulins and retains them in the ER until their subunits have adopted the correct conformation. c. Tapasin is a thiol-reductase that protects the disulfide bonds of MHC class I molecules. d. Tapasin participates in peptide editing by trimming the amino terminus of peptides to ensure that the fit between peptide and MHC class II molecules is appropriate. e. Tapasin is a bridging protein that binds to both TAP and MHC class I molecules and facilitates the selection of peptides that bind tightly to MHC class I molecules.
e. Tapasin is a bridging protein that binds to both TAP and MHC class I molecules and facilitates the selection of peptides that bind tightly to MHC class I molecules.
Which of the following characteristics is common to both T-cell receptors and immunoglobulins?
a. Somatic recombination of V, D, and J segments is responsible for the diversity of antigen-binding sites.
b. Somatic hypermutation changes the affinity of antigen-binding sites and contributes to further diversification.
c. Class switching enables a change in effector function.
d. The antigen receptor is composed of two identical heavy chains and two identical light chains.
e. Carbohydrate, lipid, and protein antigens are recognized and stimulate a response.
a. Somatic recombination of V, D, and J segments is responsible for the diversity of antigen-binding sites.
The antigen-recognition site of T-cell receptors is formed by the association of which of the following domains?
a. Vα and Cα
b. VβandCβ
c. CαandCβ
d. VαandCβ
e. Vα and Vβ
e. Vα and Vβ
How many complementarity-determining regions contribute to the antigen-binding site in an intact T-cell receptor?
a. 2
b. 3
c. 4
d. 6
e. 12
d. 6
IgG possesses _______ binding sites for antigen, and the T-cell receptor possesses _______ binding sites for antigen:
a. 1;1
b. 2; 1
c. 1;2
d. 2;2
e. 2;4.
b. 2; 1
In B cells, transport of immunoglobulin to the membrane is dependent on association with two invariant proteins, Igα and Igβ. Which of the following invariant proteins provide this function for the T-cell receptor in T cells?
a. CD3γ
b. CD3δ
c. CD3ε
d. ζ
e. All of the above
e. All of the above
Which of the following is not a characteristic of native antigen recognized by T cells?
a. peptides ranging between 8 and 25 amino acids in length
b. not requiring degradation for recognition
c. amino acid sequences not found in host proteins
d. primary, and not secondary, structure of protein
e. binding to major histocompatibility complex molecules on the surface of antigen-presenting cells.
b. not requiring degradation for recognition