B Cells Flashcards

1
Q

Membrane bound antibody or surface immunoglobulin

A

B Cell Receptor

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2
Q

Each B cell expresses only one

A

BCR

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3
Q

Many bacteria that cause infections in humans replicate in the

A

Extracellular spaces of the body

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4
Q

Causes the destruction of extracellular pathogens and prevent the spread of intracellular infections

A

Humoral immune response

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5
Q

The humoral immune response functions by the production of antibodies by

A

B cells

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6
Q

Antibodies destroy pathogens and prevent the spread of intracellular infections in which 4 main ways?

A
  1. ) Neutralization
  2. ) Opsonization
  3. ) ADCC (antibody dependent cytotoxicity)
  4. ) Complement activation
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7
Q

Neutralize these agents, opsonize them for phagocytosis, sensitize them for antibody-dependent cellular cytotoxicity, and activate the complement system

A

Antibodies

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8
Q

Blocks binding of microbe and infection of cell

A

Antibody

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9
Q

Antibodies block the infection of the

A

Adjacent cell

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10
Q

Antibodies block the binding of toxin to its

A

Cellular receptor

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11
Q

Opsinization of the microbe by IgG leads to binding of the opsinized microbes to

A

Phagocyte Fc receptors

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12
Q

The Fc receptors activate the

-leads to ingestion and death of microbe

A

Phagocyte

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13
Q

The overall goal of B-cell development is to generate a B cell with

A

BCR on the surface

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14
Q

Bone marrow stromal cells provide signals that are critical for developing

A

B cells

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15
Q

Ig (or V(D)J) recombination provides diversity by generating many different

A

BCRs

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16
Q

However, this is “dangerous” as it often results in unsuccessful

A

Rearrangements

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17
Q

Tonic signaling via the correctly assembled BCR keeps B cells alive and indicates

A

Productive rearrangement

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18
Q

The first checkpoint occurs in the

A

preBCR

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19
Q

The second checkpoint is checking for proper

A

L chain rearrangement

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20
Q

Must be purged from the repertoire

A

Autoreactive B cells

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21
Q

Immature BCR repertoire selected by random recombination. Thus, much of the BCR repertoire is potentially

A

Self-reactive (leading to autoimmunity)

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22
Q

The autoreactive B cells must be

A

Eliminated or inactivated

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23
Q

This is called central tolerance because it occurs in a central lymphoid organ known as the

A

Bone marrow

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24
Q

Auto-reactive B cells that escape this process in the bone marrow are eliminated in the periphery by a process called

A

Peripheral tolerance

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25
What percentage of B cells actually make it and survive?
5%
26
During B cell production, if the B cell is self-reactive, we see receptor editing. What happens if the new receptor is 1. ) Still self-reactive? 2. ) No longer self-reactive?
1. ) Apoptosis | 2. ) B cell matures
27
Mature B cells that recognize high affinity self Ag in peripheral tissues in the absence of specific helper T cells may be rendered -also may die by apoptosis
Functionally unresponsive (anergy)
28
Occurs when helper T cells that are specific for self Ag which then allows self reactive B cells to escape these mechanisms
Autoimmunity
29
Humoral immune response is initiated when B cells bind
Cognate antigen
30
There are two types of antigenic B cell responses. What are they?
1. ) B cell responses to Protein antigens | 2. ) B cell responses to Microbial constitutes
31
B cell responses to protein antigens requires
T cell help
32
These antigens are unable to induce antibody responses in humans or mice that lack
T cells
33
Thus, these antigens are known as
Thymus dependent (or T-dependent) antigens
34
B cell responses to MICROBIOAL CONSTITUTES (like bacterial polysaccharides) antigens do not require
T cell help
35
The antigens are known as
T-independent
36
B cell activation (T-dependent or T-independent) requires
Two signals
37
The first signal is cross-linking of the
BCR
38
Activation requires BCR cross-linking. When we have a polyvalent antigen (contains more than one copy of the specific antigenic epitope) this can happen
Directly
39
In case of monovalent antigen, antigen is “presented” to B cell by an
APC
40
Can help mediate B cell activation
Complement
41
Causes increased survival and proliferation of B cells
B cell activation
42
B cell activation results in increased expression of
B7-1 and B7-2
43
B cell activation results in increased expression of
Cytokine receptors
44
B cell activation also results in the increased expression of CCR7 and migration from follicle to
T cell areas
45
B cell activation (T-dependent or T-independent) requires two signals (just like T cells). What is signal 2 in 1. ) T-dependent? 2. ) T-independent?
1. ) CD40 (B cell) and CD40L (T cell) | 2. ) TLR activation
46
In signal 2, interaction between B cell and T cell is mediated by
MHC class II antigen presentation
47
This provides specificity to the
Immune response
48
Thus, we only get B cell activation when you have T cell specific for the same
Antigen
49
Immature B cells mature in the
Periphery (spleen)
50
Make IgM that normally circulates in the blood called natural antibodies
B1 B-cells
51
These antibodies are highly cross reactive and bind with low affinity to
Microbial antigens
52
Produce most of antibodies that mediate adaptive immune responses
Follicular B cells
53
Reside in the marginal sinus of the white pulp in the spleen
Marginal zone B cells
54
Data suggests a role in defense against bacteria that penetrate the blood stream
Marginal Zone B cells
55
Have restricted BCR diversity that might recognize common bacterial antigens and contribute to the very early phase of the adaptive immune response
Marginal Zone B cells
56
T-dependent and T-independent immune responses are mediated by different subtypes of
B cells
57
Recirculating cells that receive T cell help when they respond to protein antigens and thus initiate T-dependent antibody responses
Follicular B cells
58
These responses can lead to the formation of germinal centers, where class switching and somatic mutation of antibody gene occur, resulting in specialized high-affinity
Antibody responses
59
T-independent responses to multivalent antigens such as lipids, polysaccharides, and nucleic acids are mediated mainly by
Marginal zone B cells in the spleen and B-1 cells in mucosal sites
60
The activation of B cells is initiated by specific recognition of antigens by the surface Ig receptors of the
Cells
61
Antigen and other stimuli, including helper T cells, stimulate the proliferation and differentiation of the specific
B cell clones
62
Progeny of the clone may produce IgM or other Ig isotypes (e.g., IgG), may undergo affinity maturation, or may persist as
Memory Cells
63
Second phase of immune response occurs when activated B cells traffic into lymphoid follicles and form
Germinal Centers
64
Immune responses are initiated by the recognition of antigens by
B cells and Helper T cells
65
The activated lymphocytes migrate toward one another and interact, resulting in B cell
Proliferation and differentiation
66
Restimulationof B cells by helper T cells in extrafollicular sites leads to early isotype
Switching
67
The late events occur in germinal centers and include somatic mutation and the selection of high-affinity cells. This is called
Affinity maturation
68
B cells and T cells recognize the same
Antigen
69
Provides important check point for the initiation of
Germinal center response
70
Activated helper T cells that migrate toward the B cell zone express
CD40L
71
Their T cell receptors recognize peptide-class II MHC complexes on B cells that have been triggered by antigen and have in turn migrated to the interface between
T and B cell zones
72
CD40L on the activated T helper cell then binds to
CD40 on B cell
73
This initiates B cell
Proliferation and differentiation
74
Bind to cytokine receptors on the B cells and also stimulate B cell responses
Cytokines
75
What are the two main outcomes of the germinal center response (T-dependent antigens)
1. ) Affinity maturation | 2. ) Isotope switching
76
B cells that have been activated by T helper cells at the edge of a primary follicle migrate into the follicle and proliferate, forming the dark zone of the
Germinal center
77
Germinal center B cells undergo extensive
Isotope switching
78
Somatic hypermutation of Ig V genes occur in these
B cells
79
These B cells then migrate into the light zone, where they encounter follicular dendritic cells displaying antigen and
TFH cells
80
B cells with the highest affinity Ig receptors are selected to survive, and they differentiate into
Antibody secreting or memory B cells
81
The antibody-secreting cells leave and reside in the bone marrow as long-lived
Plasma Cells
82
Early in the immune response, low-affinity antibodies are produced. During the germinal center reaction, somatic mutation of Ig V genes and selection of mutated B cells with high-affinity antigen receptors result in the production of antibodies with
High antigen affinity
83
Antigen is limiting in GC, thus only B cells with high affinity BCR specific for antigen will be able to
Survive and function
84
Only B cells with high affinity BCR specific for antigen will be able to take up sufficient
Antigen from follicular DC
85
Binding of the B cells to antigen displayed on follicular dendritic cells is necessary to rescue the B cells from
Programmed Cell Death
86
Isotope switching requires
AID (Activation Induced Deaminase) and CD40 ligation on B-cell
87
B cells activated by helper T cell signals (CD40L, cytokines) undergo switching to different
Ig isotopes
88
The activation of B cells is initiated by specific recognition of
Antigens
89
Naive B cells are stimulated by antigen, become activated, and differentiate into antibody-secreting cells that produce antibodies specific for the eliciting antigen in a
Primary immune response
90
Antigen is limiting in GC, thus only B cells with high affinity BCR specific for antigen will be able to process and present the antigen in the context of
MHC II
91
Only B cells with high affinity BCR specific for antigen will be able to efficiently interact with
T follicular helper cells
92
Only B cells with high affinity BCR specific for antigen will be able to receive signals from T cells that allow high affinity
B cell survival