time course of the primary immune response
DESCRIPTION
Time Course of the Primary Immune Response. Innate immunity. Acquired immunity. Ig Maturation. Journey of a B Cell. Contact Between the TCR and MHC/peptide: Not All Peptides are Created Equal. The Two-Signal Theory of T-cell Activation. 2. 1. 1. 2. No response or Anergy. Activation. - PowerPoint PPT PresentationTRANSCRIPT
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Time Course of thePrimary Immune Response
Innate immunity
Acquired immunity
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Ig Maturation
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Journey of a B Cell
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Contact Between the TCR and MHC/peptide:
Not All Peptides are Created Equal
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The Two-Signal Theory of T-cell Activation
APC = Antigen-presenting cellsTCR = T-cell receptor for antigenDC = Dendritic cellCD80 = Co-stimulatory receptor
2 1 1 2
No responseNo response
or AnergyActivation
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V
C C
V
peptide
CD3
TCRCD4
MHC II
V
C C
V
CD3
TCR
MHC I
CD8
(1) Interacts with MHC class II expressing cells (APCs)
(2) Helps B cells to synthesize antibody(3) Induces and activates macrophages(4) Secretes cytokines
(1) Interacts with MHC class I-expressing cells (all nucleated cells)
(2) Kill MHC class I-expressing target cells(3) Secretes cytokines
CD4+ T cell CD8+ T cell
peptide
Two Major Functional T Cell Subsets
LckLck
APC APC
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CD4+ T Cells Activate Macrophages and B cells
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ImmunityImmunity Tolerance ToleranceActivation Suppression
Regulation of the Immune Response:
a Conceptual View
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ImmunityImmunity Tolerance Tolerance
Activation Suppression
Regulation of the Immune Response:
a Conceptual View
AutoimmunityAutoimmunity ImmunodeficiencyImmunodeficiency
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ImmunityImmunity Tolerance ToleranceActivation
Suppression
Regulation of the Immune Response:
a Conceptual View
AutoimmunityAutoimmunity ImmunodeficiencyImmunodeficiency
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Antibodies: Secreted or Transmembrane
TCR: Transmembrane
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Figure 4-2DNA Rearrangement RemovesSequences Between V, D and J Segments
RNA Splicing Removes Sequences Between J and C Segments
DNA
RNA
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Antigen-Independent B-Cell Development
1. DNA rearrangements establish theprimary repertoire, creating diversity
2. Allelic exclusion ensures that each clone expresses a single antibody on the surface, establishing specificity
3. Deletion of self-reactive clones establishes tolerance
Bone Marrow
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THE B CELL RECEPTOR
1. Bound antigen is inter- nalized and presented to T cells.
2. Bound antigen gives signals to the B cell to proliferate and differentiate.
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Signalling from the BCR
Lack of Btk causes Bruton’s X-linkedagammaglobulinemia
(blocked at pre-B stage)
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Antigen-Dependent B Cell Development
In Periphery (spleen and LN)
Antigen and TH cells give B cells two signals: 1) proliferate 2) differentiate
T-cell dependent responses are refined two ways: 1) higher affinity antibodies
2) IgG/A/E (“switched”) isotypes
Two products of B cell development:1) plasma cells secrete Ig (final effector)
2) memory cells respond to IIo antigen
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T Cell-B Cell Communication
1. Cell-cell signals from CD40L/CD40 andother surface molecules.
2. Secreted cytokines
(B cells signal T cells by presenting Ag inassociation with MHC II)
T cells provide 2 kinds of help to B cells:
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The Germinal Center
1. Affinity maturationa. Somatic hypermutationb. Selection for high affinity clones
2. Isotype switch recombination
4. Final maturation to memory or plasma cell.
3. Peripheral tolerance
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Proliferation
Ag(FDC) + T cell help
(Iterative cycles)
SURVIVAL
butT help and no Ag(eliminates low affinity clones)
orAg and no T help(eliminates self-reactive clones, giving tolerance)
DEATH
+ Somatic Hypermutation
AFFINITY MATURATION IN THE GC
Darkzone
Lightzone
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1. Memory B cells
Surface Ig, usually IgGHigh affinity for antigenLong-lived, even in the absence of antigenRespond rapidly to secondary stimulation
2. Plasma Cells
Secrete copious amounts of Ig, no surface IgNon-dividingSome are short-lived, some become long-lived in the bone marrow
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Secreted AntibodiesFunction in Various WaysTo EliminateForeign Invaders
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Notion of immunological “SELF”Skin graft transplantation compatibility
• Graft compatibility genetically determined
Extremely polymorphic trait -many alleles
Governed by genes of major histocompatibility complex (MHC) that encode MHC molecules, the principal targets of rejection
• Rejection by adaptive immune system T cell response
Differences in MHC molecules between individuals are central to determining “SELF”
How T cells recognize antigen
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The selection process (Thymic “education”) has two stages
• First stage selects clones capable of recognizing self peptide in an individual’s own MHC molecules - positive selection
• Second stage eliminates overtly self reactive clones with high affinity for self peptide:MHC- negative selection
(Self-peptides are used as a surrogate for foreign peptides since there are few non-self peptides)
***
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• The specificity of self/non-self peptide binding to MHC molecules determined by pockets that only bind certain amino acid side chains
• MHC genes are extremely polymorphic and alleles encode pockets with specificities for different amino acid side chains
The TCR is specific for both peptide and MHC- A complex ligand Polymorphic
residues of MHC
The TCR repertoire differs from individual to individual
The definition of immunologic self is made by selecting the clonal T cell repertoire on self-peptides bound to the individual’s particular allelic forms of MHC molecules
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Cytosolic Virusor Pathogen
Ingested Bacteria or Endocytic Pathogen
Extracellular Pathogenor Toxin
Peptide degraded in:
Peptides bind to:
Presented to:
Effect on presenting cell of T cell recognition:
Cytosol
MHC class I
CD8 T cells
Death of cell presenting the viral antigen
Endocytic vesicles
MHC class II
CD4 T cells
Provision of help to B cell for production of antibodies
Endocytic vesicles
MHC class II (or I)
CD4 T cells (or CD8)
Activation of cell to enhance pathogen killing
Challenge:
Any cell Macrophage/DC B cell
The immune system makes this distinction by loading and recognizing peptides in either class I or class II MHC
Presenting cell:
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Structure of peptide-binding class I MHC domain
N
1
2
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Codominant expression of MHC alleles
a/b c/d
a/d b/c a/c b/d
a=paternal haplotype
b=paternal haplotype
c=maternal haplotype
d=maternal haplotype
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Polymorphic amino acids that distinguish alleles of MHC class I molecules are found primarily in pockets that determine peptide binding or on the surface that interacts with the TCR
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Because the TCR recognizes both peptide and MHC molecule, T cell recognition of MHC-peptide is both MHC restricted and specific for the immunizing peptide
Peptide from virus X
T cell
APC
HLA-B7
Peptide from virus X
APC
HLA-B27
T cell
Peptide from virus Y
T cell
APC
HLA-B7
Target killed:Yes No No
In each of the 3 experiments the T cell is from a HLA-B7 person who recovered from infection by virus “X”. The APC target cell is either infected with virus X or Y and is from an individual who is either HLA-B7 or HLA-B27
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CD4 Staining
CD
8 S
tain
ing
CD4-CD8-
CD4+CD8-
CD4+CD8+
CD4-CD8+
3%
5% 80%
12%
TCR repertoire selection and thymocyte differentiation into CD4+ or CD8+ T cells
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• Individuals with different MHCs have different TCR repertoires
• T cells mature into CD4 or CD8 single-positive cells as a result of positive selection.
Implications of Positive/Negative Selection
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MHC class II/autopeptide
TCR
CD3
CD80
CD40
MHC class II
CD40CD40
CD40L
CD28 CD80
Activated T cell
(1) induction of cytokines/chemokines (IL-8, IL-12, TNF-, MIP-1)
(2) stimulation of CD80 and CD86 expression and co-stimulatory function with activation of T cell growth
(3) augmentation of antigen-presenting function
Key molecular interactions between T cells and APCs
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Naïve CD4+ T cells differentiate into Th1 and Th2 subsets
Resting CD4+ cell
“pTh”
Activated CD4+ cell
IL-2 IL-2 IFN- TNF
IL-4 IL-5 IL-6 IL-10
IFN-, IL-12
IL-4, IL-13
IL-4 IL-10(–)
IFN-(–)
Th1 Cells
Th2 Cells
Antigen + APC
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IL-2 IFN- TNF
IL-4 IL-5 IL-6 IL-10
IL-4 IL-10(–)
IFN-(–)
Th1 Cells
Th2 Cells
Functions of Th1 subsets• Activate macrophages/dendritic cells
augment antigen presentation• induce delayed type hypersensitivity
(DTH) responses important in eradicating intracellular pathogens (TB, leprosy, listeria
• mediate Th1 diseases (ie; rheumatoid arthritis, multiple sclerosis and type I diabetes
• Help B cells and induce humoral immunity
• mediate allergic and immediate hypersensitivity responses
• involved in antibody mediated immune diseases like SLE and ITP
Functions of Th2 subsets
Functions of T helper subsets
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MHC Class llANTIGEN
Internalization of antigen/Ig
Antigenic peptidesbind to MHC class IImolecules
B cell
BCR(SmIg)
Peptide
Antigen binds specifically to BCR (surface membrane Ig), is internalized into vesicles and cleaved into peptides which displace and bind to MHC class II molecules. The peptide/MHC complex is then transported to the surface membrane.
Antigen Processing and Presentation by B cells
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CD3TCR
CD4
Fc receptor
IL-12 IL-1IL-6IL-12TNFTGF-
MHC class II
IFN-cytotoxic granules
IL-2Receptor
IL-2
MHC II
Macrophage
Activated MacrophageActivated Th1 Cell
T Cell- Macrophage Interactions
CD4 Th1 CellCD28 B7 (CD80)
CD40L
CD28
TCR
CD4
CD80
CD80
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Maximum number of different types of HLA molecules expressed on the cell surface
Class I (HLA-A)Class I (HLA-B)Class I (HLA-C)Class II (HLA-DR)Class II (HLA-DQ)Class II (HLA-DP)
Total
222000
6
Nucleated cells
Antigen presenting cells
222244
16
Each of these MHC molecules selects its own T cell repertoire that only recognizes peptides presented by that particular type of MHC molecule
(actually more)
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V. Cytokines you need to know
IL-2 (big family e.g. IL-7 & IL-15)IL-4 (small family inc. IL-13)IL-6 (large family inc. G-CSF)IL-10 (growing family)IL-12 (small family inc. IL-23)IFN- IFN- (large family)
IL-1IL-18
LT-TNF-CD40LFasL
TGF- (very large family)
Chemokines (see Fig. 11.6)InflammatoryNon-inflammatory
See Figs. 11.1 (p244), 11.2 (p245), 11.3 (p248) Tables 11-3 (p249), 11.4 (p264) in Abbas
Innate Adaptive
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√ √√
√√√
√√√√
√√
√√ √√
√√ √√
√√ √√
Type I & IICytokine Receptors
(Hematopoietin R.)
Toll (TLR) /IL-1Receptors
TNF RelatedReceptors
TGF-Receptors
ChemokineReceptors
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V. Cytokines you need to know
IL-2 (big family e.g. IL-7 & IL-15)IL-4 (small family inc. IL-13)IL-6 (large family inc. G-CSF)IL-10 (growing family)IL-12 (small family inc. IL-23)IFN- IFN- (large family)
IL-1IL-18
LT-TNF-CD40LFasL
TGF- (very large family)
Chemokines (see Fig. 11.6)InflammatoryNon-inflammatory
See Figs. 11.1 (p244), 11.2 (p245), 11.3 (p248) Tables 11-3 (p249), 11.4 (p264) in Abbas
Innate Adaptive
√√
√√
√√ √
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Type I & IICytokine Receptors
(Hematopoietin R.)
Toll (TLR) /IL-1Receptors
TNF RelatedReceptors
TGF-Receptors
ChemokineReceptors
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QuickTime™ and aGIF decompressor
are needed to see this picture.
IL-2 activates T-cells in an autocrine manner
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QuickTime™ and aGIF decompressor
are needed to see this picture.
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VIII. Chemokines
• Important chemoattractantsImportant chemoattractants
• Regulate steady state and inflammatory Regulate steady state and inflammatory leukocyte trafficleukocyte traffic
• Signal through G-protein coupled receptorsSignal through G-protein coupled receptors
• Therefore good drug targets for big PharmaTherefore good drug targets for big Pharma
• Two chemokine receptors serve as co-recpetors Two chemokine receptors serve as co-recpetors for HIV infection (CXCR4 and CCR5)for HIV infection (CXCR4 and CCR5)
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Question:
How do viruses that don’t infect “professional APCs” such as dendriticcells elicit a primary immune response?After all, virally-infected cells don’t normally traffic to 2˚ lymphoid organs
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PVR expressed onnon-hematopoietic
cells.
Infection withPoliovirus
Endocytosis ofvirus, nuclear entry,
synthesis of viralproteins in cytosol.
Presentation ofviral peptides on
MHC Class I to CD8+cytotoxic T-cells
Proliferation ofcytotoxic T-cells
(CTLs)
Perforin/granzyme-mediated cell death
“Classic” view of CTL responseagainst virus-infected cells
Cross-priming of exogenousantigens by dendritic cells
PVR expressed onnon-hematopoietic
cells.
Infection withPoliovirus
Cytopathicchanges; recognition
and phagocytosisby dendritic cell
Phagosome-to-cytosolprotein export;
ubiquitin-mediatedproteolysis of viral proteins;Presentation of peptide via
MHC Class I
•Perforin/granzyme-mediated cell deathof DC; proliferation
of CD8+ CTL;Killing of virus-infectedepithelial cells by CTL
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Why do NK Cells Fail to
Recognize Healthy Cells?
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1. For cytotoxic CD8 T-cells, ligation of the TCR by MHC I/peptide + co-stimulation results in release of granzymes and perforin and/or FasL, leading to apoptosisof the target cells.
2. Viruses evade host defense, in part, by down-regulating MHC Class I. Uninfected dendritic cells circumvent this by “cross-priming”: phagocytosis of virus-infected cell and presentation of “exogenous” viral antigens on MHC Class I.
3. The innate immune system has a rapid onset and recognizes molecular patterns in a non-clonal fashion.
4. NK cells lack TCRs, but instead express both activating and inhibitory (e.g., KIRs) receptors at their surfaces. The relative expression and ligation of these receptors determines the outcome (i.e., killing or not) of the NK effector response.
5. Innate immune B-cells (e.g., B-1 cells and marginal zone B cells) recognizecarbohydrate antigens, secrete IgM, and are not long-lived.
6. Innate immune T-cells ( T-cells, and NK T cells) recognize non-peptide antigens innon-classical MHC-like molecules. They mediate cytotoxicity & rapid cytokine secretion.
Summary