Every problem in the chapter beside the book’s answer, a chapter at a time as you scroll.
Chapter 18: Adaptive Specific Host Defenses
36 problems · 0 figures18-1 §18.MC source ↗
- a.plasma cells
- b.T cells
- c.bone marrow
- d.Macrophages
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18-2 §18.MC source ↗
- a.B cells
- b.T cells
- c.bone marrow
- d.neutrophils
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18-3 §18.MC source ↗
- a.T-cell receptors
- b.B-cell receptors
- c.MHC II
- d.epitopes
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18-4 §18.MC source ↗
- a.polysaccharides
- b.lipids
- c.proteins
- d.carbohydrates
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18-5 §18.MC source ↗
- a.processed self-antigens from proteasomes.
- b.processed foreign antigens from phagolysosome.
- c.antibodies.
- d.T cell antigens.
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18-6 §18.MC source ↗
- a.processed self-antigens from proteasomes.
- b.processed foreign antigens from phagolysosomes.
- c.antibodies.
- d.T cell receptors.
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18-7 §18.MC source ↗
- a.MHC II
- b.MHC I
- c.antibodies
- d.B-cell receptors
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18-8 §18.MC source ↗
- a.MHC I
- b.MHC II
- c.T-cell receptors
- d.B-cell receptors
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18-9 §18.MC source ↗
- a.a protein that is highly efficient at stimulating a single type of productive and specific T cell response
- b.a protein produced by antigen-presenting cells to enhance their presentation capabilities
- c.a protein produced by T cells as a way of increasing the antigen activation they receive from antigen-presenting cells
- d.a protein that activates T cells in a nonspecific and uncontrolled manner
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18-10 §18.MC source ↗
- a.antigens presented with MHC I molecules
- b.antigens presented with MHC II molecules
- c.free antigen in a soluble form
- d.haptens only
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18-11 §18.MC source ↗
- a.antigens presented with MHC I molecules
- b.antigens presented with MHC II molecules
- c.free antigen in a soluble form
- d.haptens only
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18-12 §18.MC source ↗
- a.T-cell receptor
- b.B-cell receptor
- c.MHC I
- d.cluster of differentiation
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18-13 §18.MC source ↗
- a.TH1
- b.TH2
- c.TH17
- d.CTL
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18-14 §18.MC source ↗
- a.lipopolysaccharide
- b.glycolipid
- c.protein
- d.carbohydrate
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18-15 §18.MC source ↗
- a.CD4
- b.MHC II
- c.MHC I
- d.IgD
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18-16 §18.MC source ↗
- a.activation of helper T cells
- b.class switching to IgG
- c.presentation of antigen with MHC II
- d.binding of antigen to BCRs
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18-17 §18.MC source ↗
- a.Natural active immunity
- b.Artificial active immunity
- c.Natural passive immunity
- d.Artificial passive immunity
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18-18 §18.MC source ↗
- a.Natural active immunity
- b.Artificial active immunity
- c.Natural passive immunity
- d.Artificial passive immunity
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18-19 §18.M source ↗
Match the antibody class with its description.
| ___IgA | A. This class of antibody is the only one that can cross the placenta. |
| ___IgD | B. This class of antibody is the first to appear after activation of B cells. |
| ___IgE | C. This class of antibody is involved in the defense against parasitic infections and involved in allergic responses. |
| ___IgG | D. This class of antibody is found in very large amounts in mucus secretions. |
| ___IgM | E. This class of antibody is not secreted by B cells but is expressed on the surface of naïve B cells. |
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18-20 §18.M source ↗
Match each type of vaccine with the corresponding example.
| ___inactivated vaccine | A. Weakened influenza virions that can only replicate in the slightly lower temperatures of the nasal passages are sprayed into the nose. They do not cause serious flu symptoms, but still produce an active infection that induces a protective adaptive immune response. |
| ___live attenuated vaccine | B. Tetanus toxin molecules are harvested and chemically treated to render them harmless. They are then injected into a patient’s arm. |
| ___toxoid vaccine | C. Influenza virus particles grown in chicken eggs are harvested and chemically treated to render them noninfectious. These immunogenic particles are then purified and packaged and administered as an injection. |
| ___subunit vaccine | D. The gene for hepatitis B virus surface antigen is inserted into a yeast genome. The modified yeast is grown and the virus protein is produced, harvested, purified, and used in a vaccine. |
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Problems and answers are adapted from Microbiology by Nina Parker, Mark Schneegurt, Anh-Hue Thi Tu, Philip Lister and Brian M. Forster, OpenStax, and are used under the CC BY-NC-SA 4.0 licence. Access for free at https://openstax.org/books/microbiology/pages/1-introduction. Illustrations: Copyright Rice University, OpenStax, under CC BY-NC-SA 4.0 license. This adaptation is released under the same licence, is non-commercial, and is neither affiliated with nor endorsed by OpenStax or Rice University.