Exam 2 Flashcards

(26 cards)

1
Q

A high affinity antibody associated with long-term immunity:

A

IgG

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2
Q

Low affinity antibody with ten antigen binding sites:

A

IgM

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3
Q

The main type of antibody found in gastrointestinal mucus secretions:

A

IgA

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4
Q

If a cell surface molecule is labeled as Fc mew R, this tells you that it
a. binds to the Fc end of any antibody molecule
b. is an IgM receptor
c. serves as a paratope for the Fc epitope
d. has affinity for the Fab region of antibodies

A

b. is an IgM receptor

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5
Q

What is the role of the proteasome?
a. It is used by phagocytes to kill bacteria inside a phagolysosome
b. it is the molecule that binds to a TCR
c. it is used by infected cells to degrade antigens in the cytoplasm
d. it is the molecule used by cytotoxic T cells to recognize infected cells

A

c. it is used by infected cells to degrade antigen in the cytoplasm

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6
Q

Which of the following does not apply to T cell receptors?
a. secreted
b. 2 chains
c. antigen specific
d. MHC restricted

A

a. secreted

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7
Q

An Ig isotype switch from IgM to IgG involves
a. RNA splicing
b. hypermutations
c. VDJ recombinations
d. DNA deletion
e. all of the above

A

d. DNA deletion

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8
Q

MHC Class II molecules are found on
a. CD4 T cells
b. macrophages
c. infected cells
d. CD8 T cells
e. none of the above

A

b. macrophages

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9
Q

To prevent grafted tissues to be rejected, donors and recipients must be matched for
a. VJ genes
b. VDJ genes
c. red blood cell types
d. specific HLA genes
e. all of the above

A

d. specific HLA genes

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10
Q

The CD8 molecule
a. is a co-receptor
b. is a molecule that protects the TCR
c. is a type of T cell receptor
d. presents antigens to cytotoxic T cells

A

a. is a co-receptor

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11
Q

Affinity maturation of B cells takes place in
a. the bone marrow
b. germinal centers
c. the bloodstream
d. the T cell area of lymph nodes

A

b. germinal centers

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12
Q

Negative selection of B cells takes place in the
a. germinal centers
b. spleen
c. thymus
d. bone marrow

A

d. bone marrow

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13
Q

Which of the following is associated with allergies?
a. IgD
b. IgM
c. IgE
d. IgG

A

c. IgE

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14
Q

Which of the following cells can be activated (induced) by a CD4 T cell?
a. b cells
b. mast cells
c. red blood cells
d. plasma cells

A

a. B cells

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15
Q

Define Affinity

A

The strength of the interaction between the antigen-binding site (paratope) on an antibody and the epitope on an antigen

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16
Q

Define Avidity

A

The overall strength of binding between an antibody and a multivalent antigen, considering all binding sites

17
Q

Define Epitope

A

the specific part of an antigen that is recognized and bound by an antibody or a T cell receptor

18
Q

Define paratope

A

the specific region on an antibody or T cell receptor that binds to an epitope on an antigen

19
Q

Define tolerance

A

the immune system’s ability to recognize and avoid attacking the body’s own cells and tissues

20
Q

Define MHC restriction

A

The requirement that T cells recognize antigens only when they are presented on host cells by Major Histocompatibility Complex (MHC) molecules. CD8 T cells are restricted to MHC class I, while CD4 T cells are restricted to MHC class II molecules

21
Q

Differentiate between MHC I and MHC II molecules. What are their respective roles in immunity? On what cells are they found and what do they do?

A

> MHC I: Found on All nucleated cells, presents intracellular antigens, recognized by CD8+ T cells, function is to activate cytotoxic T cells to destroy infected or abnormal cells

> MHC II: Found on APCs (dendritic cells, macrophages, B cells), presents extracellular antigens, recognized by CD4+ T cells, function is to activate helper T cells to coordinate immune responses

22
Q

What happens to B cells that bind to self-antigens on bone marrow stromal cells?

A

They undergo negative selection
> Receptor editing: The B cell modifies its B cell receptor (BCR) to create a new, non-self-reactive receptor
> apoptosis: the self-reactive B cells is eliminated through programmed cell death

23
Q

What are the differences in the type of antigens recognized by antibodies and T cell receptors?

A

> Antibodies: recognize intact, extracellular antigens. Can be proteins, polysaccharides, lipids, or nucleic acids, and antibodies bind directly to the surface of these antigens in their native form
T cell receptors: recognize process antigens that are presented as small peptide fragments bound to MHC molecules. These antigens must be presented by an antigen-presenting cell (APC) on MHC class I or II molecules

24
Q

In response to a given antigen, B cells differentiate; some cells secrete IgM whereas other cells secrete IgG. How is this possible? How can two different Ig molecules be produced against the same antigen?

A

> It is possible because B cells can go through a process called class switch recombination (CSR) which allows them to make antibodies of a different isotype.
B cells start producing IgM when exposed to an antigen.
As the immune response progresses, B cells receive additional signals from helper T cells and cytokines, and undergo CSR. This happens in the constant region of Ig gene (not the variable region).
B cell now produces IgG antibodies while maintaining the same antigen specificity. The signals that induce CSR are usually provided by T cells through cytokines like IL-4 or IFN-gamma
allows them to use antibodies with the different effector functions for same pathogen

25
What are the differences (and possible similarities) between DNA recombination of gene segments and RNA splicing of exons? How does this relate to our understanding of the immune response as it applies to B cells and immunoglobulins?
Differences: >DNA recombo happens at DNA level in B cells during their development. It rearranges VDJ gene segments to create diverse Ag-binding regions in Ab (permanent DNA change) >RNA splicing occurs after transcription at the RNA level in all cells. It removes introns and joins exons to produce mature mRNA. In B cells it helps determine whether an Ab is membrane-bound or secreted, or which isotype is expressed. Similarities: >Both processes create diversity, DNA recombo creates Ag binding variety, while RNA splicing allows diff forms of the same Ab >Both involve precise cutting and joining of genetic material Ig relevance: >DNA recombo generates diverse Ag specificities >RNA splicing controls Ab form and isotype, influcing B cell response to Ag
26
What mechanisms are responsible for generating antibody diversity?
V(D)J Recombo: >During B cell development VDJ are randomly recombined >heavy chains (VDJ), light chains (VJ), produces unique variable regions, determining Ag specificity of the Ab Junctional Diversity: >During VDJ recombo, nucleotides are randomly added or removed at the junction between V,D, and J segments by enzymes such as TdT >Increases diversity by altering the sequence of the Ag binding region Somatic Hypermutation: >After B cell encounters an Ag, the variable region of the Ab gene undergoes SH in the germinal centers >This introduces point mutations at a high rate in the DNA coding for the VR, resulting in slight changes in the Ab's affinity for its Ag Class Switch Recombo: >B cells switch Ig produced by changing the constant region, no change in variable >enables different effector functions without changing antigen specificity