B Lymphocytes Flashcards

1
Q

What are the general features of humoral immunity?

A
  1. Major arm of “adaptive immune response”
  2. Defend against extracellular microbes
  3. Neutralize & eliminate extracellular microbes & microbial toxins
  4. Mediated by Abs that are produced by activated B cells
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2
Q

Where is humoral immunity initiated?

A

Initiated in peripheral (2) lymphoid organs
1. Spleen - for blood borne Ag
2. Lymph nodes - for Ag entering via skin & other epithelial lining
3. Mucosal lymphoid tissues - for some inhaled & ingested Ag

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3
Q

What are the two types of antigens? State their differences.

A
  1. Protein Ag
    - Require both B & T cells
    - Generate Abs of different isotypes (distinct effector function) & high affinity
    - Affinity maturation - repeated exposure to protein Ag results in the production of Abs with increasing affinity for the Ag
  2. Non protein Ag (polysaccharides, lipids)
    - Require little or no Ag specific T helper cells
    - Abs produced show little heavy chain isotype switching & affinity maturation
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4
Q

What are the Ab responses in humoral immunity? Compare and contrast the responses.

A
  1. Primary response (1st exposure to Ag)
    - 5-10 days
    - Amount Abs produced are smaller*
  2. Secondary response (subsequent exposure)
    - 1-3 days
    - Amount Abs produced are larger*
    - With protein Ag, the responses also show increased heavy chain isotype switching (IgG & possibly IgA or IgE) & affinity maturation
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5
Q

*What are the different phases of B cell activation?

A
  1. Recognition of foreign Ag
  2. Activation of B-lymphocytes (Th stimulate B cells to produce Abs)
  3. Proliferation - giving rise to clonal expansion
  4. Differentiation
    - some activated B cells undergo heavy chain isotype switching ex. IgM/IgD into IgG
    - affinity maturation: some become long-lived memory B cells
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6
Q

What signals are required for B cell activation?*

A
  1. Signal 1 - B cell receptors recognize the Ag
  2. Signal 2
    - Produced during innate immune reactions to microbes (ex. complement proteins C3d binds to complement receptor on B cells CR2)
    - Derived from cell-cell interaction with T helper cells: CD40 (on B cells) interacts with CD40L (on Th cells)
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7
Q

Describe the B cell receptor complex.

A

BCR attached to Ig-alpha & Ig-beta

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8
Q

Describe the Ag receptor-mediated signal transduction in B cells.

A
  1. When 2 or more Ag receptors clustered, tyrosine in ITAMs get phosphorylated
  2. Net result of receptor-induced signalling in B cells = activation of transcription factors that turn on genes whose protein products are involved in B cell proliferation & differentiation
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9
Q

What are the components of B cell co-receptors?

A

Co-receptor complex = CR2, CD19 & CD81 on mature B cell surface

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10
Q

What is the significance of B cell co-receptors in B cell activation?

A
  1. Microbial Ag + bound C3d can simultaneously engage both membrane IgM and CR2
  2. Initiate signalling cascade from both BCR complex and CR2 complex
  3. Response is greatly enhanced when compared with the response to Ag alone
  4. Complement proteins provide 2nd signal for B cell activation, functioning in concert with Ag (signal 1) to initiate B cell proliferation & differentiation
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11
Q

Can T cells of different Ag specialties bind to the same B cell?

A

Yes

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12
Q

Describe the Ag presentation by B cells to T helper cells

A
  1. Ag bound to receptors, endocytosed & processed in the endosomal vesicles & displayed by MHC class II for recognition by CD4+ T helper cells
  2. B and Th cells are specific for the same Ag, however, B cells recognize a conformational epitope of a protein Ag and Th cells recognize peptide fragments of the same Ag
    - *** Recognize different epitopes of the same protein Ag
  3. Activated B cells express costimulators B7-1/B7-2 that interact with CD28 on Th cells
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13
Q

How do Th cells and B cells interact in lymphoid tissues?

A
  1. CD4+ Th cells recognize processed protein Ag & become activated (proliferate and differentiate)
  2. Effector T cells migrate toward lymphoid follicles
  3. T-B cell interactions at the edge of follicle
  4. Naive B cells recognize Ag and are activated, migrate out of follicle
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14
Q

Describe the mechanisms of Th cell activation of B lymphocytes.

A
  1. Th cells recognize Ag presented by B-cells and co-stimulators (ex. B7) on B cells
  2. Th cells are activated to express CD40L and secrete cytokines, both of which bind to their receptors on the same B cell and activate the B cell
  3. CD40L-CD40 interaction is very important - isotype switching, affinity maturation and memory B cell generation in response to protein Ag

Th function cannot be replaced by cytokines, need direct Tcell-Bcell contact

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15
Q

What are the outcomes of B cell activation?

A
  1. T cell - independent: production of IgM Abs
  2. T cell - dependent
    - Production of IgG or IgA Abs
    - Provide cytokines needed for both class switching and somatic hypermutation
    - Both processes require ligation of CD40 on B cells by CD40L on T cells
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16
Q

Outline the terminating process of the humoral immune response.

A
  1. Ab binds to Ag that is still available in the blood and tissues to form immune complexes (IC)
  2. B cells specific for the Ag bind to the Ag part of the IG with their Ig receptors while the Fc tail of the attached Ab is recognized by a special type of Fc receptor on B cells
  3. This delivers inhibitory signals which terminates B cell responses

This process (Ab bound to Ag inhibits further Ab production) is called ANTIBODY FEEDBACK ***

17
Q

What are the factors the affect the immune response?

A
  1. Chemical nature - proteins, lipids, etc.
  2. Chemical complexity - more complex, better
  3. Molecular size - Good > 10000d
  4. Conformation - folding vs denatured
  5. Foreignness - more foreign, better
  6. Mode of administration - route (IV, IM), dose
  7. Genetic constitution of the recipient - MHC
  8. Condition of recipient - age, health status
  9. Adjuvant - important in enhancing the immune response