Chapter 11 Flashcards
Which of the following statements is incorrect regarding memory B cells?
a. Memory B cells are maintained for life.
b. In secondary responses, the number of pathogen-specific B cells is about 10–100-fold that seen in primary responses.
c. The sensitivity of memory B cells is improved compared with naive B bells because affinity maturation has occurred.
d. Memory B cells express lower levels of MHC class II and B7 than do naive B cells.
e. Memory B cells differentiate into plasma cells more rapidly than do naive B cells.
Memory B cells express lower levels of MHC class II and B7 than do naive B cells.
Which of the following characterizes immunological memory? (Select all that apply.)
a. The host retains the capacity to mount a secondary immune response.
b. The host retains the ability to respond to pathogen many years after primary exposure.
c. Naive T cells are activated more quickly when exposed to pathogen.
d. Memory B cells produce higher-affinity antibody than naive B cells.
e. Memory T cells undergo somatic hypermutation.
f. Memory T cells express CD45RA.
a. The host retains the capacity to mount a secondary immune response.
b. The host retains the ability to respond to pathogen many years after primary exposure.
d. Memory B cells produce higher-affinity antibody than naive B cells.
What would be the outcome if a naive B cell were to bind to pathogen coated with specific antibody made by an effector B cell in a primary immune response using FcγRIIB1, and simultaneously bind to the same pathogen using its B-cell receptor?
a. a positive signal leading to the production of low-affinity IgM antibodies
b. a positive signal leading to isotype switching and the production of IgG, IgA, or IgE antibodies
c. a positive signal leading to somatic hypermutation and the production of high-affinity IgM antibodies
d. a negative signal leading to inhibition of the production of low-affinity IgM antibodies
e. a negative signal leading to apoptosis
a negative signal leading to inhibition of the production of low-affinity IgM antibodies
Which of the following explains why the first baby born to a RhD– mother and a RhD+ father does not develop hemolytic disease of the newborn?
a. Fetal erythrocytes do not cross the placenta and therefore do not stimulate an antibody response.
b. The antibodies made by the RhD– mother during the first pregnancy are predominantly IgM and have low affinity for the Rhesus antigen.
c. Maternal macrophages in the placenta bind to anti-Rhesus antibodies and prevent their transfer to the fetus.
d. Hemolytic disease of the newborn is a T-cell-mediated disease and maternal T cells do not cross the placenta during pregnancy.
e. The Rhesus antigen is not immunogenic and does not stimulate an antibody response.
The antibodies made by the RhD– mother during the first pregnancy are predominantly IgM and have low affinity for the Rhesus antigen.
By which process are fetal erythrocytes destroyed in hemolytic anemia of the newborn?
a. lysis of erythrocytes by cytotoxic T cells
b. lysis of erythrocytes by complement activation
c. clearance of antibody-coated erythrocytes by macrophages in the fetal spleen
d. lysis of erythrocytes by NK cells via antibody-dependent cell-mediated cytotoxicity
e. cytotoxicity caused by major basic protein released from eosinophils
clearance of antibody-coated erythrocytes by macrophages in the fetal spleen
When a naive B cell binds to an IgG:antigen complex on its cell surface using FcγRIIB1, while simultaneously binding to the same antigen using membrane-bound IgM, _____.
a. the IgG:antigen complex is endocytosed
b. the B cell becomes anergic
c. the B cell will switch isotype to IgG
d. the B cell undergoes affinity maturation
e. the B cell secretes large amounts of IgM before becoming a memory B cell
the B cell becomes anergic
“Original antigenic sin” is best described as a phenomenon in which _____.
a. a highly mutable virus gradually escapes from immunological memory and interferes with compensatory immune responses.
b. latent viruses periodically activate effector T cells specific for the original antigen recognized in the primary immune response.
c. the persistence of antigen is necessary to sustain maintenance of immunological memory.
d. memory T cells no longer express the same profile of adhesion molecules and cytokine receptors compared with the original profile of the naive precursor T cell.
a highly mutable virus gradually escapes from immunological memory and interferes with compensatory immune responses.
Imagine a situation in which an individual who has a latent cytomegalovirus (CMV) infection receives a hematopoietic stem-cell transplant. Which of the following is likely to occur?
a. The memory T cells present at the time of transplantation would inhibit activation of newly generated naive T cells.
b. The CMV viral load would increase exponentially, overcoming the host and causing death.
c. The transplant-derived naive T cells would be activated and give rise to memory T cells that would persist and control viral load.
d. There would be a rapid increase in CMV viral load and expansion of T cells bearing CD45RA.
The transplant-derived naive T cells would be activated and give rise to memory T cells that would persist and control viral load.
Which of the following are not a component of immunological memory?
a. effector B cells
b. memory T cells
c. memory B cells
d. long-lived plasma cells
effector B cells
The efficiency and specificity of adaptive immune defenses and immunological memory improve each time a particular pathogen is encountered because _____.
a. of protective immunity
b. effector memory T cells outnumber central memory T cells
c. the half-life of antibodies made in secondary and tertiary immune responses exceeds that of antibodies made in primary immune responses.
d. of affinity maturation
of affinity maturation
Unlike naive lymphocytes, memory lymphocytes _____.
a. do not recirculate between the blood and secondary lymphoid organs
b. do not require the receipt of survival signals through their antigen receptors in order to persist
c. are immortal and continue to divide throughout the lifetime of an individual
d. secrete antibody continuously, although at a much lower rate than plasma cells
e. do not express CD27
do not require the receipt of survival signals through their antigen receptors in order to persist
All of the following are ways in which plasma cells differ from memory cells except _____.
a. plasma cells lack surface immunoglobulin
b. cellular morphology
c. plasma cells are CD27-negative
d. plasma cells have undergone isotype switching
e. plasma cells are short-lived
plasma cells have undergone isotype switching
During a secondary immune response, high-affinity IgG antibodies are produced. Which of the following best explains why low-affinity IgM antibodies are not made?
a. Naive pathogen-specific B cells are suppressed by negative signaling through FcγRIIB1.
b. Naive pathogen-specific B cells isotype switch and hypermutate much more quickly during secondary immune responses.
c. Memory B cells outnumber naive B cells.
d. Low-affinity IgM antibodies are made only when antigen concentration is exceedingly high.
Naive pathogen-specific B cells are suppressed by negative signaling through FcγRIIB1.
Which of the following molecules is not elevated on the surface of memory B cells compared with naive B cells?
a. MHC class II molecules
b. CD45RA
c. antigen receptor
d. CD27
e. co-stimulatory molecules
CD45RA
_____ accounts for the production of different isoforms of the CD45 protein observed in naive, effector, and memory T cells.
a. Isotype switching
b. Affinity maturation
c. Alternative splicing
d. Somatic hypermutation
e. Recirculation to peripheral tissues
Alternative splicing
Memory B cells differ from memory T cells in the following ways. (Select all that apply.)
a. They suppress naive antigen-specific lymphocytes during secondary immune responses.
b. They recirculate only through secondary lymphoid organs.
c. They secrete their antigen receptors throughout their life-span.
d. They generate long-lived clones of memory cells during the primary immune response.
a. They suppress naive antigen-specific lymphocytes during secondary immune responses.
b. They recirculate only through secondary lymphoid organs.
RhoGAM is administered to pregnant RhD– women so as to _____. (Select all that apply.)
a. stimulate only anti-RhD IgM antibody
b. cause selective removal of anti-RhD memory B cells from the maternal circulation
c. inhibit a primary immune response to RhD antigen
d. block transcytosis of IgG to fetal circulation by interfering with FcRn function
e. prevent hemolytic anemia of the newborn
c. inhibit a primary immune response to RhD antigen
e. prevent hemolytic anemia of the newborn
Identify the mismatched pair. (Select all that apply.)
a. variolation: smallpox
b. Salk vaccine: killed poliovirus
c. vaccinia virus: cowpox
d. rotavirus: segmented DNA virus
e. Sabin vaccine: TVOP
f. rabies vaccine: live attenuated vaccine
d. rotavirus: segmented DNA virus
f. rabies vaccine: live attenuated vaccine
Recombinant DNA technology has been especially useful for the production of _____ that are used in subunit vaccines.
a. viral proteins
b. viral nucleic acids
c. mutated viruses
d. viral polysaccharides
e. infectious particles
viral proteins