Chapter 7
1 / 38

Chapter 7 - PowerPoint PPT Presentation

  • Uploaded on

Chapter 7. Humoral Immune Response Activation of B Lymphocytes and Production of Antibodies. Antibodies. Part of the adaptive immune response functions to neutralize and eliminate extracellular microbes and microbial toxins

I am the owner, or an agent authorized to act on behalf of the owner, of the copyrighted work described.
Download Presentation

PowerPoint Slideshow about ' Chapter 7' - philip-herring

An Image/Link below is provided (as is) to download presentation

Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author.While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server.

- - - - - - - - - - - - - - - - - - - - - - - - - - E N D - - - - - - - - - - - - - - - - - - - - - - - - - -
Presentation Transcript
Chapter 7

Chapter 7

Humoral Immune Response

Activation of B Lymphocytes and Production of Antibodies


  • Part of the adaptive immune response functions to neutralize and eliminate extracellular microbes and microbial toxins

  • More useful against polysaccharide and lipids and these types of toxins – B cells respond to many Ag types

  • Naïve B cells recognize Ag but can’t make Ab until activation allows differentiation to Ab secreting plasma cells

Phases and types of hir
Phases and Types of HIR

  • Naïve B-cells have 2 classes of membrane bound Ab – IgM and IgD

    • act as receptor for Ag

  • Activation of Ag specific cells leads to clonal expansion

    • Go from 1 to 4000 Ab secreting cells

  • Differentiation into effector cells called plasma cells

    • secreted Ab is same specificity of as naïve membrane bound receptor but during differentiation can cause Ab with different heavy chain and effector function – heavy chain class (isotype) switching

    • can handle different types of microbes

  • Repeated exposure to causes Ab with increasing affinity to Ag – affinity maturation

    • improved capacity to bind and neutralize Ag

T cell dependence
T-Cell Dependence??

  • Ab response to different Ag may depend on the requirement of T-cell help or not

  • B-cells recognize many Ags – protein, polysaccharide, lipid and small chemicals

  • Protein Ag makes poor or no Ab response when T-cells are absent = T-dependent Ab response

    • T-helper cells play role in activation and powerful inducer of isotype switching

  • Polysaccharidde, lipid and non-protein Ag stimulate Ab production without T helper cells = T independent Ab response

    • little to no heavy chain switching or affinity maturation

B cell subsets respond differently
B-Cell Subsets Respond Differently

  • Protein and non-protein Ag result in different responses

  • Majority are follicular B-cells (follicles of lymph organs) make the majority of T-dependent, class-switched ans high-affinity Ab to protein Ag

    • also long-lived plasma cells

  • Marginal zone B-cells (marginal zone of spleen white pulp) respond to blood bourne-polysaccharide Ag

  • B-1 B-cells respond to non-protein Ag in mucosa and peritoneum

  • Marginal zone and B-1 B-cells have Ag receptors of limited diversity and mainly IgM response


  • Ab responses differ qualitatively and quantitatively

  • 1 response is the first time exposed

    • small amounts of Ab produced

  • 2 response is the subsequent exposure

    • more Ab produced

    • if to a protein, see isotype switching and affinity maturation

    • increase in TH cells with repeated stimulation

  • Ag recognition ACTIVATES B-lymphocytes

Stimulation of b cells by ag
Stimulation of B-Cells by Ag

  • Initiated when Ag-specific B-cells in lymphoid follicles of the spleen, LN and mucosal lymphoid tissues recognize Ag

  • Ag of microbes in tissues or blood are transported and concentrated in B-cell rich follicles by possible method of:

    • macrophages in subcapsular sinus may capture Ag and display to B-cells in adjacent follicles

    • use BCR to recognize Ag in native conformation – triggers pathway for signal transduction

    • require additional signals from innate system

  • Ag without processing – NATIVE CONFORMATION

Ag induced signaling in b cells
Ag-Induced Signaling in B-Cells

  • Membrane Ig receptors cluster (bind and move together) and trigger biochemical signals that are transduced by receptor-associated signal molecules

    • similar to T-cells activation

    • must cross-link 2 or more receptors for signal transduction – 2 or more Ag in an aggregate or repeating epitopes of one Ag molecule – binds adjacent Ig molecules

  • Polysaccharide, lipid and other non-protein Ag have multiple identical epitopes in each molecule (bind numerous Ig receptors on B-cell)

    • transduced by receptor-associated proteins


  • Receptor IgM and IgD – highly variable with short cytoplasmic domains

    • recognize Ag but do not transduce signals

  • IgM and IgD are non-covalently linked to Ig and Ig to make the B-cell receptor (BCR) complex

    • Ig and Ig contain conserved immunoreceptor tyrosine-based activation motifs (ITAM) – seen in other activation receptors

    • 2 or more Ag receptors cluster, Tyr in ITAM of Ig and Ig are phosphorylated by kinase associated with BCR complex

    • Tyr-PO4 is the docking sites for adaptor protein which gets phosphorylated and recruits a number of signal molecules

  • Signal cascade not as well understood as T-cells but essentially similar – activates trnscription factor that turn on genes whose proteins involved in B-cell proliferation and differentiation

B cell activation
B-Cell Activation

  • Syk is similar to ZAP-70

Complement and b cell activation
Complement and B-Cell Activation

  • B-cells express receptor for a complement protein which provides signals to activate B-cells when bound to ligand

  • Complement is activated by microbes and Ab attached to microbes – functions as effector mechanism of host defense (Chapter 8)

Complement activation of b cells
Complement Activation of B-Cells

  • Microbe has C3d (cleavage product of C3) coating the surface

  • B-cells has type 2 complement receptor (CR2 or CD21) and it binds to C3d

  • B-cells recognize microbe Ag by the Ig receptor and also recognizes C3d on CR2 receptors

    • C3d acts as the 2nd signal for B-cell activation

    • CR2 enhances Ag-dependent activation of B-cells

    • Ag recognition is 1st step and C3d-CR2 binding is the 2nd signal


  • Microbes themselves or innate immune response to microbes provide signals in addition to Ag recognition to activate lymphocytes or microbial products attaching to TLR on B-cell

  • C3d is similar to co-stimulators in T-cell activation

Consequences of ag mediated b cell activation
Consequences of Ag-Mediated B-Cell Activation

  • Initiate B-cell proliferated and differentiation and prepare B cells to interact with TH cells if protein Ag

  • B-cell enters cell cycle and proliferates – clonal expansion

  • Produces more IgM and secrete IgM – early phase immune response induced

Early phase is greatest
Early Phase is Greatest

  • Response is greatest for polysaccharide and T-independent Ag

    • multivalent

    • cross-links many Ag-receptors

    • activates C’ strongly

  • Proteins can’t do the 1st 2 so make weak response without TH response

    • lack multiple, identical epitopes

Additional steps
Additional Steps

  • At least 3 other changes to the B-cell to enhance ability to interact with TH cells – acting as APC

    • increase the expression of B7 costimulator molecule (2nd signal for T-cells), may amplify helper T-cell response and expression of cytokine receptors – cytokine mediators of TH cell functions

    • decrease the expression of chemokine receptors – chemokines keep B-cell in follicles, without chemokines they can migrate out of follicle to where TH cells are concentrated

Function of t helper cells
Function of T-Helper Cells

  • Required for strong response to protein Ag

  • B-cell and T-cell must recognize protein Ag and come together to stimulate B-cell proliferation and differentiation in the lymphoid tissue

    • takes 3-7 days for Ab response

Activation and migration
Activation and Migration

  • Activated helper T-cells (effector cells) interact with Ag-stimulated B-cells at edge of follicles in lymphoid tissue

T h and b cell interaction
TH and B-Cell Interaction

  • Naïve CD4+ T-cell is stimulated to proliferate and differentiate into cytokine secreting effector cell

    • Ag recognition and co-stimulation

      • microbial Ag and protein Ag with adjuvants that cause expression of co-stimulators on APC

    • extracellular microbes and vesicular microbes on MHC II in T-cell rich zones in LN

      • depending on Ag – become TH1, TH2 or TH17 subset

      • portion of cells move out of LN to look for Ag

    • T-cells move out of LN to circulation – remove microbes CMI

    • some T-cells migrate to the edge of lymphoid follicles while B-cells are moving outward; dependent on changes in chemokine receptors on activated lymphocytes and the chemokines are also expressed to bind receptors

Ag presentation by b cells
Ag Presentation by B-Cells

  • B-cells bind protein Ag (extracellular) by specific receptors and endocytose them – process in endosome vesicles and display on MHC II for recognition by helper T-cells

  • Membrane bound Ig can bind Ag with high affinity (low Ag concentration); very efficiently endocytosed and processed to be peptide on MHC II = act as APC

    • specific recognition of Ag by Ig on the surface

  • B-cells have ability to display multiple Ag for T-cell recognition – B and T cells can recognize different epitopes of same Ag

    • interactions remains Ag specific

  • Ag-activated B-cells also express co-stimulators such as B7 to stimulate T-cells that recognize Ag on B-cells

    • cannot activate naïve T-cells

T h cell mediated activation
TH-Cell Mediated Activation

  • TH-cell recognize Ag on APC B-cell and activate it by expressing CD40L and secreting cytokines – similar to T-cell activation of macrophages in CMI

  • CD40L binds CD40 on B-cell – sends signals for B-cell expansion and for synthesis and secretion of Ab

    • Cytokines made in the T-cell bind to the B-cell and enhance proliferation and Ig production

    • CD40L:CD40 interaction insures that B-cells are activated only when they come in contact with T-cell

  • Helper T- cell signals trigger heavy chain switching and affinity maturation – as seen in T-dependent protein Ag recognition

Isotype switching
Isotype Switching

  • Heavy class chain is switched to a different isotype to broaden functional capabilities

  • Helper T-cell help with the switch from IgM/IgD to another isotype

    • allows humoral immune response to adapt in order to combat microbe optimally

      • IgG is used to opsonize microbes and extracellular viruses – phagocytosed by neutrophils and macrophages; usually IgG1 and IgG3 classes

        • bind the Fc receptor on the phagocyte with high affinity and specificity for  heavy chain

      • IgE is used to fight helminths by recruiting eosinophils which recognize the  heavy chain by way of Fc receptor

Effector functions of ab
Effector Functions of Ab

  • Know cytokines and which Ab

Reasons for switching
Reasons for Switching

  • Need to make a response that can remove various microbes – needs to be more than IgM and IgD

  • Class switching is mediated by CD40L:CD40 mediated signals – different cytokines involved

    • cytokines influences which heavy chain class an individual B-cell and progeny will switch to

  • No CD40L or CD40 – B-cells secrete only IgM

X linked hyper igm syndrome
X-Linked Hyper IgM Syndrome

  • Inactivating mutations in CD40L gene on the X-chromosome – no functioning forms of CD40L

  • Mostly IgM Ab produced due to the defective heavy chain switching

  • Also defective CMI because of the effect on T-cell activation (use of CD40L)

Class switching switch recombination
Class Switching (Switch Recombination)

  • Process is well understood

  • In IgM B-cells the VDJ region of variable portion is adjacent to C gene splice mRNA of VDJ RNA to CRNA = make  heavy chain

  • Cytokines and CD40 signals stimulate transcription thru a C gene segment to make something other than IgM – 5’ end intron has conserved sequence that is the switch region

    • activation causes 3’ switch region of C to link to 5’ switch region of downstream constant region and delete entire intron, removing the  gene RNA

      • switch region is not present for C gene

    • enzyme Activation-Induced Deaminase (AID) plays a role in switch recombination


  • VDJ region in contact with C regions downstream – Ab may have new heavy chain but the specificity in the variable region is the same as IgM

    • VDJ region stays the same (where Ab specificity resides)

Cytokine impact
Cytokine Impact

  • INF complements both B-cells and phagocytes

    • INF makes opsonizing Ab (from TH1 cells)

      • promotes phagocytosis – also INF is phagocyte activating

    • bacteria and viruses stimulate the formation of TH1 cells (secretes INF)

  • IgE class switching is ruled by IL-4 (TH2 cytokine) and eosinophil activation by IL-5 (also from TH2 cells)

  • Nature of helper cell activity guides the Ab response

    • optimized for the microbe

    • helper T-cells may act as “master controller” of the immune response

  • Also influenced by site of immune response

    • mucosal epithelium has IgA – B cells and unknown cytokine to switch to IgA

Affinity maturation
Affinity Maturation

  • Affinity of Ab produced to protein Ag increases with prolonged or repeated exposures to that Ag

    • Ab binding to microbe or Ag increases if infection is persistent or recurrent

    • due to point mutations in the V region – Ag binding hypervariable region

      • happens only in T-dependent protein Ag

      • mutation rate 1:1000 nucleotides – somatic hypermutation

Helper cells are critical
Helper Cells Are Critical

  • Affinity maturation occurs in germinal center of lymphoid follicles – Somatic Hypermutation of Ig genes in dividing B-cells – followed by selection of high affinity B-cells by Ag displayed by follicular dendritic cells

  • As response goes on, increase in the level of Ab and decrease in the Ag so B-cells with high affinity Ab receptors will bind Ag on the FDC and therefore survive apoptosis

    • B cells are selected to survive must bind Ag at lower and lower Ag concentration

    • germinal center B-cells die unless rescued by Ag-recognition

    • Ag:Ab complex can activate complement


  • Occurs in different parts of lymphoid tissue

  • Mature naïve B-cell recognize Ag and move to peripheral edge of the follicle where it encounters the T helper cell and start to secrete Ab

  • Plasma cells move away from B-cell rich regions continue to secrete Ab even when Ag is gone

  • Fraction of cells after heavy class switching (occurs outside of follicle) will become memory cells and wander until contact the Ag again

T independent ab response
T-Independent Ab Response

  • Know the bottom part of this table

  • Needs no T-cell help

  • Polysaccharides, lipids and non-protein molecules

    • no T-cell recognition / no MHC

    • response happens because these Ag are multi-valent (have multiple identical epitopes) and can activate B-cell

  • Two types of Ab differ

Ab feedback
Ab Feedback

  • Most B-cells will die by apoptosis except for memory and small number of plasma cells

  • Removal comes from the B-cell having a Fc receptor, FcRII that will bind Fc part of Ab and receptor mediated signaling

    • terminates the humoral immune response when sufficient IgG present