CHAPTER 2. Cells of the immune system
1. Be able to describe the origin of the leukocytes, lymphocytes,
and
RBCs found in the blood.
2. What is the HSC? What progenitors are produced from this cells? What are
stromal cells? What
is the role of stromal cells during T and B cell development?
3. Describe apoptosis, genes promoting or preventing apoptosis, and the
difference
between
apoptosis and necrosis.
Why is apoptosis important in hematopoiesis?
4. Among the lymphoid cells, be able to describe unique surface markers (CD molecules) for B, T
and NK cells.
5. How can NK cells achieve ADCC? What are the NK1-T cells?
6. Be able to describe the process of phagocytosis and the mediators
of antimicrobial and cytotoxic
activity (oxygen-independent and oxygen-dependent).
7. Be able to provide example of fixed and wandering macrophages.
8. Provide the function(s) of macrophages. (We saw 3 in class)
9. Be able to identify granulocytes and provide their main biological
function.
10. Be able to provide the role of dendritic cells as well as their types (4).
11. Be able to provide the main differences between primary and
secondary
lymphoid organs.
12. Be able to identify the location of immune cells in the spleen
and lymph nodes.
13. Know about the lymphatic system. Why is it important? How the lymphatic
system and lymph
nodes come together?
14. What is the main role played by the spleen?
15. Provide one example of a MALT. What type of cell is involved in
antigen uptake in the
intestines?
CHAPTER 3. Antigens.
1. What are the definitions of: antigens, epitopes, immunogens and
antibodies.
2. What are the differences between immunogenicity
and antigenicity? How can you explain that
haptens in order to induce an immune
response need to be linked to a carrier protein.
3. Be prepared to explain for example, why one would expect
that the humoral immune response to
the GP120 HIV virus receptor would be expected to
elicit
antibodies with many different
specificities (for different antigenic
determinants). In this
respect, know what is meant by a
polyclonal antibody response.
4. Why antigens need to be greater than 5,000 molecular weight in
order to efficiently stimulate an
immune response. Think about why that might be so.
Overall, you need to know the factors that
contribute to the immunogenicity of an antigen.
5. What are adjuvants? What are the most commonly used adjuvants? How
they work?
6. For what sorts of antigens do we mount the strongest and the weakest
immune responses?
7. You need to be familiar with how antigens are seen by T and B cells?
(Table 3.4)
8. What do we mean by sequential or conformational epitopes? (Table 3.5)
9. What are Pattern-recognition receptors? Be able to provide examples
as well as their ligands.
CHAPTER 4. Immunoglobulins: Structure and Function.
1. Be able to describe and draw the basic structure of an antibody
molecule indicating: antigen
binding sites, biological activity site, constant domains,
variable domains, hinge regions, intra- and
extra-chain disulfide bonds, complement binding
site, carboxy and amino ends, etc.
2. What are complementary-determining regions (CDRs)?
3. Be familiar with the roles of the different parts of the antibody
molecule (ex. antigen binding)
4. Be able to describe experiments used to demonstrate antibody
structure:
pepsin, papain, papain
and mercaptoethanol. What are the end
products?
5. Be able to know the types of light and heavy chains?
6. You need to know what is an imunoglobulin fold. How many
domains are present in each class
of antibody? What is the difference between IgG and
IgE?
7. Be able to know what makes a molecule part of the immunoglobulin
superfamily. Provide
examples.
7. Be able to identify within the variable regions the CDRs. How many?
Why are they important?
8. What are the roles of the CH1 and the CL domains?
9. Be able to describe the antibody-mediated effector functions
(opsonization, etc).
10. This is a must: the biological activities of immunoglobulin classes
(opsonization, etc).
11. Know the main 2-3 properties of each antibody type (fixes
complement,
crosses placenta, etc.)
12. How IgA acquires its secretory component?
13. Know the difference between isotype and allotype.
14. Be able to describe the structure and properties of the “B cell
receptor”.
15. Be able to outline the process of generating monoclonal antibodies.
What are the critical steps?
What are the selection strategies?