a. Memory B cells are maintained for life.
b. In secondary responses, the number of pathogen-specific B cells is about 10Ð100-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.
d. Memory B cells express lower levels of MHC class II and B7 than do naive B cells.
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
d. a negative signal leading to inhibition of the production of low-affinity IgM antibodies
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.
b. The antibodies made by the RhD(-) mother during the first pregnancy are predominantly IgM and have low affinity for the Rhesus antigen.
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
c. clearance of antibody-coated erythrocytes by macrophages in the fetal spleen
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
b. the B cell becomes anergic
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. a highly mutable virus gradually escapes from immunological memory and interferes with compensatory immune responses.
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.
c. The transplant-derived naive T cells would be activated and give rise to memory T cells that would persist and control viral load.
a. effector B cells
b. memory T cells
c. memory B cells
d. long-lived plasma cells
a. effector B cells
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
d. of affinity maturation
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
b. do not require the receipt of survival signals through their antigen receptors in order to persist
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
d. plasma cells have undergone isotype switching
a. Naive pathogen-specific B cells are suppressed by negative signaling through FcgammaRIIB1.
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.
a.Naive pathogen-specific B cells are suppressed by negative signaling through FcgammaRIIB1.
a. MHC class II molecules
b. CD45RA
c. antigen receptor
d. CD27
e. co-stimulatory molecules
b. CD45RA
a. Isotype switching
b. Affinity maturation
c. Alternative splicing
d. Somatic hypermutation
e. Recirculation to peripheral tissues
c. Alternative splicing
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 and prevent hemolytic anemia of the newborn
d. block transcytosis of IgG to fetal circulation by interfering with FcRn function
c. inhibit a primary immune response to RhD antigen and prevent hemolytic anemia of the newborn
a. variolation: smallpox
b. Salk vaccine: killed poliovirus
c. vaccinia virus: cowpox
d. rotavirus: segmented DNA virus
e. Sabin vaccine: TVOP
d. rotavirus: segmented DNA virus
a. viral proteins
b. viral nucleic acids
c. mutated viruses
d. viral polysaccharides
e. infectious particles
a. viral proteins
a. It is an attenuated vaccine derived from a human rotavirus, and it is nonpathogenic in humans unless a genetic reversion occurs.
b. It has been genetically engineered to express a variety of human VP4 and VP7 glycoproteins.
c. It is a mixture of five cattle rotaviruses.
d. Standard tissue culture methods are used for its production.
e. It took decades of research to develop this vaccine to an adequate standard.
a.It is an attenuated vaccine derived from a human rotavirus, and it is nonpathogenic in humans unless a genetic reversion occurs.
a. hepatitis B vaccine and Bexsero
b. Bacille Calmette-Guerin (BCG) vaccine
c. trivalent oral polio vaccine
d. influenza vaccine
a. hepatitis B vaccine and Bexsero
a. alum
b. MF59
c. inactivated Bordetella pertussis
d. virosomes
e. RhoGAM
e. RhoGAM
a. interfering with the alternative pathway of complement activation
b. binding to host-derived heparin
c. increasing the adhesiveness of the bacterium
d. inhibiting phagocytosis
e. inducing inflammation
a. interfering with the alternative pathway of complement activation
a. Conjugation
b. Attenuation
c. Reverse vaccinology
d. Herd immunity
e. Neutralization
c. Reverse vaccinology
a. the antigens that stimulate protection against influenza virus are inside the virion and not on the surface
b. influenza is an RNA virus with a higher mutation rate
c. influenza stimulates T-independent responses that fail to generate memory cells
d. the polysaccharide antigens of influenza stimulate poor immune responses.
b. influenza is an RNA virus with a higher mutation rate
a. reverse vaccinology
b. subunit vaccination
c. partial immunization
d. combined immunity
e. herd immunity
e. herd immunity