Module B Quiz Questions Flashcards
The major function of a T-cell receptor is to
present a specific peptide to the MHC complex.
recognize antigen, process the antigen, and present the peptide to other immune cells.
recognize a specific MHC-peptide complex in order to destroy the target cell.
recognize a virus before it integrates into a host cell.
recognize a specific MHC-peptide complex.
recognize a specific MHC-peptide complex.
MHC diversity is generated by
somatic recombination of the MHC locus.
somatic hypermutation during an immune response.
gene families and genetic polymorphisms.
affinity maturation during an immune response.
clonal selection and expansion during an immune response.
gene families and genetic polymorphisms.
Which of the following is paired correctly?
CD8 T cell and MHC class II
CD4 T cell and MHC class I
MHC class I and extracellular pathogens
CD4 T cell and MHC class II
MHC class II and intracellular pathogens
CD4 T cell and MHC class II
All nucleated cells in the body express MHC class I because they
have the propensity to become infected with a virus.
must have a way to interact with helper T cells in the body.
have the ability to capture an extracellular pathogen and present it to helper T cells.
have the propensity to become infected with an extracellular pathogen.
express both MHC class I and MHC class II in the body.
have the propensity to become infected with a virus.
All the alleles of every MHC class I and class II gene in an individual make up that person’s _, which provides the overall MHC diversity.
isotype
haplotype
gene family
phenotype
allotype
haplotype
T cells that recognize antigen presented on MHC class I typically are
also able to recognize antigen presented on MHC class II.
part of the innate immune response to a pathogen.
activated to fight off extracellular pathogens.
not activated during a viral infection.
activated to fight off intracellular pathogens.
activated to fight off intracellular pathogens.
Which cells play an important role in pathogen clearance by activating other cells during an adaptive immune response?
B cells
Plasma cells
Neutrophils
T cells
NK cells
T cells
Phagocytic cells that have taken up intracellular pathogens through phagocytosis present phagocytosed material via MHC class I molecules because cross-presentation activates
the CD4 T cells responsible for combating the intracellular infection.
both B cells and helper T cells.
the CD4 T cells responsible for combating the extracellular infection.
both innate and adaptive responses.
the CD8 T cells responsible for combating the intracellular infection.
the CD8 T cells responsible for combating the intracellular infection.
Which protein provides a necessary costimulatory activation signal to naïve T cells?
CD28
CD3
CD45
CD4 and/or CD8
CTLA-4
CD28
A T cell that has CD4 as a coreceptor is a(n) _ cell.
plasma
cytotoxic T
helper T
dendritic T
NK-T
helper T
During T cell rolling adhesion, the T-cell surface molecule _ binds to adhesion molecules on the endothelial cell surface, including CD34 and _.
L-selectin; GlyCAM-1
ICAM-1; GlyCAM-1
ICAM-1; LFA-1
GlyCAM-1; LFA-1
GlyCAM-1; L-selectin
L-selectin; GlyCAM-1
_ are effector B cells that secrete soluble immunoglobulins.
Helper B cells
Dendrocytes
Plasma cells
Thymocytes
Centrocytes
Plasma cells
The most important type of cells in T-cell activation are
NK cells.
B cells.
macrophages.
dendritic cells.
neutrophils.
dendritic cells.
Interaction between the T-cell receptor and an MHC-peptide complex, coupled with the proper costimulatory signaling, promotes the formation of a(n)
immunological synapse between the T cell and an NK cell.
secondary focus in the lymph node.
immunological synapse between the T cell and an APC.
germinal center in the lymph node.
primary focus between a T cell and a corresponding NK cell.
immunological synapse between the T cell and an APC.
The three cell types that present antigen to T cells in secondary lymphoid tissues are dendritic cells, macrophages, and
neutrophils.
thymocytes.
B cells.
eosinophils.
NK cells.
B cells.
Macrophages mainly specialize in phagocytosis and
are not involved in T-cell activation.
do not interact with T cells.
present antigen to dendritic cells in the peripheral tissues.
remain in the peripheral tissues and do not perform T-cell activation.
travel to secondary lymphoid tissue to activate naïve T cells.
are not involved in T-cell activation.
Phagocytes of the innate immune system engulf pathogens at the site of infection and transport them to _, where antigen presentation occurs.
the liver
Langerhans cells
primary lymphoid tissue
the bloodstream
secondary lymphoid tissue
secondary lymphoid tissue
B cells can act like antigen-presenting cells (APCs), but this activity is limited to
the one type of antigen recognized by the immunoglobulin.
antigens phagocytosed by macrophages.
antigens previously tagged by the Toll-like receptors.
antibody-antigen complexes formed by a variety of immunoglobulins.
B cell-dependent antigens.
the one type of antigen recognized by the immunoglobulin.
Which statement about B cells is true?
They are activated by CD8 cytotoxic T cells.
They are localized in the T-cell zone of a secondary lymphoid tissue and can activate naïve T cells if they recognize the same antigen.
They present multiple antigens simultaneously, leading to widespread T-cell activation.
They degrade antigen in a lysosome before displaying antigen peptides on the surface via the MHC class I pathway.
They play a major role in T-cell activation.
They are localized in the T-cell zone of a secondary lymphoid tissue and can activate naive T cells if they recognize the same antigen.
T-cell activation requires an interaction between the T-cell receptor and MHC-peptide complex on an APC and a costimulatory signal from
a different APC.
another T cell.
the same APC.
LFA-1.
IL-16.
the same APC.
_ migrate from the bone marrow to the spleen.
Pre-B cells
Early pro-B cells
Transitional B cells
Mature B cells
Late pro-B cells
Transitional B cells
The first step in the development of B lymphocytes from a lymphoid progenitor cell is
V segment recombining with DJ segment of the heavy chain loci.
VJ recombination of the light chain loci.
DJ recombination of the heavy chain loci.
positive selection.
receptor editing.
DJ recombination of the heavy chain loci.
Rearrangement of the heavy chain loci is tested through the use of a surrogate light chain during the
immature B cell stage
early pre-B cell stage
pro-B cell stage
lymphoid progenitor stage
late pre-B cell stage
pro-B cell stage
Hematopoietic stem cells (HSCs) first appear in the human fetus in the
placenta
fetal bone marrow.
fetal yolk sac
aorta-gonad-mesonephros (AGM) region.
fetal liver.
fetal yolk sac