1. Which of the following correctly describes the
primary immune response?
A. Rapid response with
mainly IgG antibodies
B. Slow response, mainly IgM antibodies
first
C. Requires memory cells from a previous exposure
D.
Occurs faster due to affinity-matured B cells
B. Slow response, mainly IgM antibodies first
2. During the secondary immune response, the
predominant antibody type is:
A. IgM
B. IgA
C.
IgG
D. IgD
C. IgG
3. Which statement best explains why the secondary
immune response is faster?
A. Naïve cells divide faster
B.
Memory cells already exist and have higher affinity receptors
C.
New somatic mutations occur immediately
D. Antigens are smaller
and easier to detect
B. Memory cells already exist and have higher affinity receptors
4. Memory B cells differ from long-lived plasma cells
in that memory B cells:
A. Continuously secrete antibodies
B. Are terminally differentiated
C. Circulate and can re-enter
germinal centers upon re-exposure
D. Are only found in bone marrow
C. Circulate and can re-enter germinal centers upon re-exposure
5. The FcγR2B(1) receptor on B cells functions
to:
A. Activate B cells and increase antibody secretion
B.
Inhibit B cell activation to prevent overreaction
C. Promote
antibody isotype switching
D. Stimulate plasma cell differentiation
B. Inhibit B cell activation to prevent overreaction
6. Hemolytic disease of the newborn occurs
when:
A. Rh+ mother has an Rh− baby
B. Rh− mother has an
Rh+ baby and develops antibodies against fetal RBCs
C. Rh−
mother has an Rh− baby
D. Rh+ father and Rh+ mother produce Rh− baby
B. Rh− mother has an Rh+ baby and develops antibodies against fetal RBCs
7. Rhogam prevents erythroblastosis fetalis by:
A. Stimulating antibody production in the mother
B. Blocking
fetal Rh receptors
C. Destroying fetal Rh+ cells before the
mother’s immune system can react
D. Neutralizing maternal
anti-Rh antibodies
C. Destroying fetal Rh+ cells before the mother’s immune system can react
8. Which of the following distinguishes naïve from
memory T cells?
A. Naïve T cells express CD45RO
B. Memory
T cells express CD45RA
C. Naïve T cells express CD45RA; memory T
cells express CD45RO
D. Both express the same CD45 isoform
C. Naïve T cells express CD45RA; memory T cells express CD45RO
9. Which memory T cell type primarily remains in
tissues such as skin, gut, and lungs?
A. Effector memory
(Tem)
B. Central memory (Tcm)
C. Tissue-resident memory
(Trm)
D. Naïve T cells
C. Tissue-resident memory (Trm)
10. Which model of memory cell differentiation is
currently considered most accurate?
A. Only effector cells can
become memory cells
B. Only early progenitors form memory
cells
C. A combination of both early and effector-derived memory
cells
D. Memory cells arise from plasma cells only
C. A combination of both early and effector-derived memory cells
11. The concept of original antigenic sin
explains that:
A. The immune system always produces new
antibodies for each new strain
B. The immune system reuses old
memory responses even to mutated viruses
C. The immune system
forgets previous infections
D. Antibodies mutate faster than viruses
B. The immune system reuses old memory responses even to mutated viruses
12. Why is influenza a good example of original
antigenic sin?
A. It never mutates
B. Its antibodies are
very stable
C. It has a high mutation rate, leading to
mismatched immune memory
D. It only infects once
C. It has a high mutation rate, leading to mismatched immune memory
13. Cross-reactivity leads to:
A. Immune
response against completely unrelated antigens
B. Antibodies
recognizing structurally similar antigens
C. No immune response
to related pathogens
D. Complete protection from all viruses
B. Antibodies recognizing structurally similar antigens
14. Cross-protection provides:
A. Temporary
protection against related pathogens
B. Immediate full
immunity
C. No benefit across infections
D. Autoimmune disease
A. Temporary protection against related pathogens
15. Which statement best describes the key timeline difference between primary and secondary immune responses?
A. Primary is faster and produces IgG; secondary is slower and
produces IgM
B. Primary is slow (7–10 days, mainly IgM);
secondary is fast (1–3 days, mainly IgG)
C. Both occur at the
same speed but differ in antibody type
D. Secondary responses
occur only after vaccination
B. Primary is slow (7–10 days, mainly IgM); secondary is fast (1–3 days, mainly IgG)
16. How do DNA-level changes differ between primary and secondary immune responses?
A. Secondary responses require new class-switch recombination
B. Primary responses use pre-mutated DNA from memory cells
C.
Primary responses perform SHM and class switching for the first time;
secondary responses use pre-mutated, high-affinity DNA
D. DNA
changes do not differ between the two
C. Primary responses perform SHM and class switching for the first time; secondary responses use pre-mutated, high-affinity DNA.
17. Which of the following lists the major cell types involved in immunological memory?
A. Mast cells, NK cells, neutrophils
B. Memory B cells,
long-lived plasma cells, memory T cells
C. Macrophages,
dendritic cells, eosinophils
D. Th17 cells only
B. Memory B cells, long-lived plasma cells, memory T cells
18. Which statement correctly compares long-lived plasma cells and memory B cells?
A. Plasma cells circulate; memory B cells stay in bone marrow
B. Plasma cells divide frequently; memory B cells never divide
C. Plasma cells secrete antibodies continuously; memory B cells wait
for reactivation
D. Memory B cells secrete antibodies constitutively
C. Plasma cells secrete antibodies continuously; memory B cells wait for reactivation
19. What is the role of FcγR2B(1) on B cells?
A. Enhances B-cell activation
B. Functions as an inhibitory
receptor to prevent overactivation
C. Triggers complement
activation
D. Activates macrophages
B. Functions as an inhibitory receptor to prevent overactivation
20. What causes erythroblastosis fetalis (hemolytic disease of the newborn)?
A. ABO incompatibility between mother and fetus
B. Rh− mother
makes anti-Rh antibodies that attack a later Rh+ fetus
C. Excess
maternal IgA crosses the placenta
D. Fetal T cells attack
maternal RBCs
B. Rh− mother makes anti-Rh antibodies that attack a later Rh+ fetus
21. How does Rhogam prevent hemolytic disease of the newborn?
A. By blocking maternal IgG from crossing the placenta
B. By
suppressing fetal antigen expression
C. By destroying fetal Rh+
RBCs before the mother can recognize them
D. By increasing
maternal T-cell tolerance
C. By destroying fetal Rh+ RBCs before the mother can recognize them
22. What is the difference between CD45RA and CD45RO?
A. CD45RO is on naïve T cells; CD45RA on memory T cells
B.
CD45RA on naïve T cells; CD45RO on memory T cells, allowing faster
responses
C. CD45RA is a B-cell marker; CD45RO is a macrophage
marker
D. They are identical splice variants
B. CD45RA on naïve T cells; CD45RO on memory T cells, allowing faster responses
23. Which of the following correctly describes the migration patterns of the three types of memory T cells?
A. Tcm in blood; Tem in lymph nodes; Trm in bone marrow
B. Tcm
in tissues; Tem only in lymph nodes; Trm circulate widely
C. Tcm
in lymph nodes; Tem circulate in blood and tissues; Trm reside
permanently in tissues
D. All memory T cells circulate freely everywhere
- C. Tcm in lymph nodes; Tem circulate in blood and tissues; Trm reside permanently in tissues
24. What is original antigenic sin?
A. When a pathogen mutates to evade T cells
B. When the immune
system responds only with innate immunity
C. Preferential use of
old antibodies from a prior strain, even if the new strain is
different
D. Failure to produce antibodies after vaccination
C. Preferential use of old antibodies from a prior strain, even if the new strain is different
Why is cross-reactivity important?
A. It causes autoimmunity
B. It allows antibodies to recognize
similar pathogens and provide partial protection
C. It prevents
memory B-cell formation
D. It blocks antibody production
B. It allows antibodies to recognize similar pathogens and provide partial protection
1. A child receives their second MMR vaccine dose and
produces antibodies faster than after the first dose. What explains
this?
A. The child’s immune system has more naïve B cells.
B. The second vaccine causes stronger inflammation.
C. Memory B
and T cells respond rapidly with high-affinity receptors.
D. The
vaccine is more concentrated.
C. Memory B and T cells respond rapidly with high-affinity receptors.
2. A pregnant Rh− woman who never received Rhogam
after her first Rh+ pregnancy is now carrying another Rh+ baby. What
is likely to occur?
A. The baby will produce anti-Rh
antibodies.
B. Maternal memory B cells will attack fetal red
blood cells.
C. The baby’s immune system will reject maternal
antibodies.
D. The mother will be protected by Rhogam
B. Maternal memory B cells will attack fetal red blood cells.
3. A nurse who had chickenpox as a child is exposed
to shingles but does not become ill. What best explains her
protection?
A. Naïve B cells immediately produce IgM.
B.
Long-lived plasma and memory T cells provide rapid immunity.
C.
She has innate resistance to herpesviruses.
D. The exposure dose
was too low to infect her.
B. Long-lived plasma and memory T cells provide rapid immunity.
4. A patient has a genetic defect in the FcγR2B(1)
receptor. Which immune issue might they experience?
A. Impaired
antibody production
B. Reduced T cell activation
C.
Increased risk of autoimmune reactions
D. Weakened complement activation
C. Increased risk of autoimmune reactions
5. After receiving a flu vaccine, a patient becomes
infected with a slightly different strain but has only mild symptoms.
Which concepts explain this?
A. Antigenic drift and original
antigenic sin
B. Cross-reactivity and cross-protection
C.
Autoimmunity and tolerance
D. Antigenic variation and suppression
B. Cross-reactivity and cross-protection
6. Two mice are studied: one exposed to a virus for
the first time, and one exposed twice. Which statement is true?
A. Both mice produce mostly IgM in equal amounts.
B. The first
exposure causes a faster response.
C. The second exposure
produces mainly IgG antibodies more quickly.
D. The second
exposure produces fewer antibodies overall.
C. The second exposure produces mainly IgG antibodies more quickly.
7. During a viral infection, a memory T cell in the
skin releases cytokines immediately without returning to lymph nodes.
What type of memory T cell is this?
A. Central memory
(Tcm)
B. Effector memory (Tem)
C. Tissue-resident memory
(Trm)
D. Naïve T cell
C. Tissue-resident memory (Trm)
8. Researchers find that people exposed to an old flu
strain respond poorly to a new, mutated strain. What does this
illustrate?
A. Cross-protection
B. Original antigenic
sin
C. Antigenic drift
D. Clonal deletion
B. Original antigenic sin
9. Two patients develop memory cells differently: one
forms them early, and the other from surviving effector cells. What
conclusion is correct?
A. Only early formation is
possible.
B. Only effector survival can produce memory.
C.
Both models occur, depending on the immune environment.
D.
Neither model is accurate.
C. Both models occur, depending on the immune environment.
10. A researcher studies two T cell groups. Group A
expresses CD45RA, while Group B expresses CD45RO. Which statement is
correct?
A. Group A are memory T cells; Group B are naïve.
B. Group B are memory T cells that respond faster due to altered CD45
signaling.
C. Both groups are naïve but differ in cytokine
production.
D. Group A cells are effector memory cells.
B. Group B are memory T cells that respond faster due to altered CD45 signaling.