Type the term that completes each statement, using the word bank. Pull it from memory first.
Word bank
Active artificialNegative selectionTargetBorn in bone marrowCD4+ helper T (Tʈ)Plasma cellMHC IIIgAOpsonizationT-dependent activationPrecipitationMemory T cellsVaccinationPrimary responseIgE
migrate to thymus to mature
must not react too strongly to self-peptide
recognizes antigen on MHC II (APCs); orchestrates response
persist after infection; fast response on re-exposure
on antigen-presenting cells; presents exogenous (engulfed) antigen to CD4+
mucosal & secretions (tears, saliva, breast milk); dimer
allergy & parasites; binds mast cells
tags pathogen for phagocytes
soluble antigens clumped out of solution
first exposure; latency 5-10 days; IgM dominant; modest titer
safely creates a primary response so the next exposure is the easier secondary
vaccination
Define it: high-yield vocabulary
Write a clear definition in your own words for each term.
Antigen
Helper T cell (CD4+)
Cytotoxic T cell (CD8+)
B cell
Plasma cell
Memory cell
Antibody
MHC class I
MHC class II
Clonal expansion
Primary vs secondary response
Active immunity
Passive immunity
Part 2 of 4 · Anatomy lab
Draw and label
Box A. B cell vs T cell action
Directions
Left half: a B cell encountering a free-floating antigen (e.g., a bacterial toxin). Draw the antigen binding the B cell receptor on the surface. Show the B cell differentiating into a plasma cell (label, with rough ER for antibody synthesis) and a memory B cell. Draw antibodies leaving the plasma cell into the surroundings.
Right half: a cytotoxic T cell (CD8) encountering an infected host cell. The infected cell presents a viral antigen on its surface bound to MHC class I (draw both). The T cell's T-cell receptor (TCR) binds the MHC-I + antigen complex. The T cell releases perforin and granzymes, punching the infected cell and triggering apoptosis. Draw the infected cell dying.
Label B cell, plasma cell, memory B cell, antibody on the left. Label cytotoxic T cell, TCR, MHC I, perforin/granzyme, apoptosis on the right.
ColorSizeTool
Box B. Antibody structure
Directions
Draw a single antibody molecule as a Y shape.
Show four protein chains: two heavy chains (long) forming the stem and inner arms of the Y, two light chains (short) on the outer arms. Label.
Draw disulfide bonds (small dashes) connecting the chains.
Color or shade the TOPS of the two arms differently from the rest: these are the variable regions where antigen binding happens. Label antigen-binding site (two per antibody).
The rest of the molecule is the constant region. Label.
Below the antibody, draw a small antigen with surface features (epitopes) that fit the antigen-binding sites. Show the antibody-antigen binding.
ColorSizeTool
Structures to label
Label each on your drawing.
B cell
Plasma cell
Memory B cell
B cell receptor
Antibody
Cytotoxic T cell (CD8)
Helper T cell (CD4)
T cell receptor (TCR)
MHC class I
MHC class II
Perforin
Granzyme
Apoptosis
Heavy chain
Light chain
Variable region
Constant region
Antigen-binding site
Antigen (epitope)
Part 3 of 4 · Physiology lab
Reason it through
A. Primary vs secondary immune response
Explain the main structure-function relationship for this topic.
B. Synthesis
1. Explain how a vaccine works using the primary vs secondary response. Why does a vaccine produce immunity even though no real infection ever occurred?
2. HIV preferentially infects and destroys helper T cells (CD4). Predict the consequences for both the B cell response and the cytotoxic T cell response, and explain why HIV patients eventually develop opportunistic infections (AIDS).
3. Autoimmune disease occurs when adaptive immunity targets self tissues. Pick one autoimmune disease (e.g., Type 1 diabetes, rheumatoid arthritis, lupus, multiple sclerosis). Identify which self tissue is targeted and predict the consequences when adaptive immunity attacks that tissue.
Submit
Save as PDF, then upload to Canvas.
The exported PDF stamps your name and paste-attempt count. Drawn-here or hand-drawn diagrams only; typed or AI-generated diagrams are not accepted.