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Innate Immunity

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Regulate Migration of Leukocytes Into Sites of Inflammation and of Pathogens Out ... non-adaptive immunity, i.e. production of anti-fungal and anti-bacterial peptides ... – PowerPoint PPT presentation

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Title: Innate Immunity


1
Innate Immunity
  • William H. Chambers, PhD
  • University of Pittsburgh Cancer Institute and
  • Department of Immunology
  • University of Pittsburgh School of Medicine
  • G.17e Hillman Cancer Center
  • 412-623-3218
  • chamberswh_at_msx.upmc.edu

2
Phagocytic Cell Function Macrophages and
Neutrophils
3
Macrophages in Tissues Regulate Migration of
Leukocytes Into Sites of Inflammation and of
Pathogens Out of Sites of Inflammation
Macrophages are in normal tissues, neutrophils
are not!
4
Bactericidal Agents in Phagocytic Cells
5
Recognition of Infectious Agents by Receptors in
the Non-adaptive Immune System
  • Non-adaptive effectors recognize microbes via
    pattern recognition receptors
  • Pattern recognition receptors bind components of
    microbes that are fundamentally different from
    those on host cells, e.g. LPS, peptidoglycan
  • Oligosaccharide ligands have been identified for
    pattern recognition receptors
  • Ligands are often called pathogen associated
    molecular patterns (PAMPs)

6
Examples of Pattern Recognition Molecules
  • fMLP receptor N-formylated peptides produced
    by bacteria, serves as a chemoattractant for
    neutrophils
  • Macrophage Mannose Receptor/CD206 collectin
    family proteins that bind mannose residues on
    bacteria and viruses, e.g. HIV
  • Macrophage Scavenger Receptors 1-6/CD204 MSR1
    bind anionic polymers and acetylated LDLs, and
    some structures which have lost normal expression
    of terminal sialic acid capping residues on
    oligosaccharides
  • Mannose Binding Lectins serum collectins
    which recognize a particular orientation of sugar
    residues and their spacing

7
Toll-like Receptors
  • Toll was defined as a signaling molecule in
    Drosophila sp. Responsible for dorso-ventral
    morphogenesis via induction of apoptosis
  • Toll shares homology with IL1r cytoplasmic domain
    which raised the question of whether TLRs are
    important in immune responses
  • Toll was found to be important in activating
    Drosophila sp. non-adaptive immunity, i.e.
    production of anti-fungal and anti-bacterial
    peptides
  • At least 10 TLRs in man some can dimerize and
    form homo- or heterodimers
  • Data suggest a role for TLR in non-adaptive
    responses, i.e. TLR activation results in NFkB
    translocation and production of IFN, TNF and ROI
  • Activation via Toll/TLRs induces production of
    IL12 and expression of co-stimulatory molecules
    by DCs

8
Toll-Like Receptors
  • TLRs 1, 2, 4, 5 and 6 seem to specialize in the
    recognition of mainly bacterial products that are
    unique to bacteria and not made by the host.
    Their detection therefore affords a
    straightforward self-non-self discrimination.
  • TLRs 3, 7, 8 and 9, in contrast, specialize in
    viral detection and recognize nucleic acids,
    which are not unique to the microbial world. In
    this case, self-non-self discrimination is
    mediated not so much by the molecular nature of
    the ligands as by their accessibility to the
    TLRs. These TLRs are localized to intracellular
    compartments and detect viral nucleic acids in
    late endosomes-lysosomes.

9
TLR Expression
  • Receptor Cell types
  • TLR1 dimer mf, MDCs, iDCs, mDCs/-
  • TLR2 dimer mf, MDCs, iDCs, mDCs /-, mast
    cells, renal epithelial cells
  • TLR3 mDCs
  • TLR4 mf, MDCs, iDCs, mDCs/-, mast cells,
    intestinal epithelial cells low, renal
    epithelial cells, pulmonary epithelial cells,
    corneal epithelial cells, dermal endothelial
    cells
  • TLR5 mf, MDCs, iDCs, mDCs/-, intestinal
    epithelial cells
  • TLR6 dimer mf, mast cells
  • TLR7 mf, PDCs
  • TLR8 mf, MDCs, mast cells
  • TLR9 mf, pDCs, B cells

10
Toll-like Receptors and Their Ligands
  • TLR family Ligands (origin)
  • TLR1 Tri-acyl lipopeptides (bacteria,
    mycobacteria), Soluble factors (Neisseria
    meningitides)
  • TLR2 Lipoprotein/lipopeptides (a variety of
    pathogens), Peptidoglycan (Gram-positive
    bacteria),
  • Lipoteichoic acid (Gram-positive bacteria),
    Lipoarabinomannan (mycobacteria), A
    phenol- soluble modulin (Staphylococcus
    epidermidis), Glycoinositolphospholipids
    (Trypanosoma cruzi), Glycolipids (Treponema
    maltophilum), Porins (Neisseria), Zymosan
    (fungi), Atypical LPS (Leptospira interrogans),
    Atypical LPS (Porphyromonas gingivalis), HSP70
    (host)
  • TLR3 Double-stranded RNA (virus)
  • TLR4 LPS (Gram-negative bacteria), Taxol
    (plant), Fusion protein (RSV), Envelope proteins
    (MMTV), HSP60 (Chlamydia pneumoniae), HSP60
    (host), HSP70 (host), Type III repeat extra
    domain A of fibronectin (host), Oligosaccharides
    of hyaluronic acid (host), Polysaccharide
    fragments of heparan sulfate (host), Fibrinogen
    (host)
  • TLR5 Flagellin (bacteria)
  • TLR6 Di-acyl lipopeptides (mycoplasma)
  • TLR7 Imidazoquinoline (synthetic compounds),
    Loxoribine (synthetic compounds), Bropirimine
    (synthetic compounds)
  • TLR8 ?

11
LPS Binds TLR-4/MD-2/RP105 Complex Following CD14
Association
12
TLR Signal Transduction Pathway
Toll-like receptor (TLR) signaling pathway. TLRs
recognize specific patterns of microbial
components. MyD88 is an essential adaptor for all
TLRs and is critical to the inflammatory
response. Lipopolysaccharide (LPS)-induced
activation of signaling molecules such as IRF-3,
PKR, MAP kinase, and NF-kB has been reported,
indicating the presence of the MyD88-independent
pathway. TIRAP/Mal was identified as a component
specifically involved in TLR4-mediated
signaling.
13
Nod-like Receptors NLRs
  • A new family of intracellular receptors including
    at least 5 types of molecules NOD1-5, NALP1-14,
    CIITA, IPAF and NAIP have recently been defined
  • These molecules contain an leucine rich repeat
    domain LRR, a domain for oligomerization
    NACHT, one or more of three signaling domains
    PYD-NALPs CARD-NODs/CIITA/IPAF BIRs-NAIP
  • Stimulate cytokine release IL1b/IL18 or
    caspases apoptosis

14
Macrophages are key players in inflammation
15
Macrophage-derived Cytokines
16
Local effects of TNF-a
17
Macrophage derived cytokines also act systemically
18
The Acute Phase Response
19
Too much of a good thing Systemic effects of
TNF-a can be lethal
20
Cytokines with chemoattractant properties induce
directed cell migration and are called chemokines
21
Properties of Chemokines
22
Properties of Chemokines
23
Non-adaptive, cellular mechanisms include
cytolytic cells
24
Natural Killer (NK) Cells
  • Lymphoid cells with an LGL morphology
  • No evidence for clonality in recognition of
    targets
  • Innate function i.e. no clonal expansion, no
    memory
  • Cytolytic function vs virus infected cells and
    some tumor cells

25
III. NK Cell Recognition Receptors
  • Missing Self Hypothesis
  • Activation and Inhibition via Receptors
  • Recognition of Self
  • Recognition of Tumor Cells
  • Recognition of Virus-infected Cells

26
Missing Self Hypothesis
  • NK cells do not require expression of MHC Class I
    determinants for recognition of target cells.
  • There is, in fact, an inverse relationship
    between expression of MHC Class I and
    susceptibility to lysis by NK cells, i.e. less
    Class I equals more lysis.
  • Led to the hypothesis that NK cells surveyed the
    surface of target cells for self. If it was
    present, the cell was presumed to be normal and
    not lysed. If self was absent, as is often the
    case in tumor cells and virus-infected cells, NK
    cells could be activated to lyse the abnormal
    cell.
  • Ljunggren, H.G. and K. Karre, 1990.
    Immunology Today 11237-244.

27
Recognition NK cells
  • There is no evidence supporting clonally
    restricted recognition molecules expressed by NK
    cells, nor for recombinatorial events being
    important for development of an NK cell
    repertoire
  • NK cells recognize MHC determinants, but these
    structures, nor peptides expressed by MHC, are
    target antigens for activation of NK lytic
    function
  • Some NK cells express CD8 homodimers, but it is
    unclear whether binding to MHC Class I affects
    activation
  • NK cell recognition of targets involves a balance
    between inhibitory signals and activation signals
  • Receptorligand pairs providing inhibitory
    signals are fairly well defined
  • Receptorligand pairs providing activation
    signals are rapidly being defined

28
NK Cell Gene Complex (NKC)
  • The NKC is a genomic region, first described on
    NK cells, encoding structurally related receptors
  • NKC maps to Chromosome 12p13, 6 and 4 in man,
    mouse and rat, respectively
  • Type II integral membrane proteins with external
    domain similar to C-type (Ca-dependent)
    lectins. However, they lack amino acid residues
    that coordinate binding of Ca, and do not bind
    carbohydrates in the same manner as conventional
    C-type lectins. Can be expressed homo- or
    heterodimers.
  • Highly conserved evolutionarily found in sea
    squirt and several poxviruses
  • Activating and inhibitory receptors for immune
    cells can be either primary or co-stimulatory
    receptors.

29
NK Cell Gene Complex (NKC)
- Contains genes encoding C type lectin related
receptors - Disease resistance elements mapped to
this locus, e.g. Cmv1 - Conserved across species
Human Chromosome 12 Mouse
Chromosome 6 Rat Chromosome 4
30
Leukocyte Receptor Cluster (LRC)
LRC is a 1 mb region located on chromosome
19q13.42
31
NK Cell Inhibitory Receptors CLRR and KIR
  • Name Alternative Names Cellular
    Ligand Viral Ligand
  • p58.1 KIR2DL1 HLA-Cw2,4,5,6
  • p58.2 KIR2DL2 HLA-Cw1,3,7,8
  • p70 KIR3DL1 HLA-Bw4
  • p140 KIR3DL3 HLA-A3, -A11
  • p49 KIR2DL4 HLA-G
  • LIR1 ILT2/LILRB1 HLA-G HCMV-UL18
  • LIR2 ILT4/LILRB2 HLA-F
  • CD94 KLRD1 HLA-E
  • NKG2A KLRC1/CD159A HLA-E
  • NKR-P1B, D CD161B, D Clrb
  • p40 LAIR1 ?
  • IRC1 IRp60/CMRF35H ?
  • p75AIRM1 Siglec-7 Sialylated sugars
  • CD94 forms heterodimers with NKG2A, -C and E
  • CD94/CD159A heterodimer is specific for HLA-E

32
ITIM
  • Immunoreceptor tyrosine-based inhibitory motif
  • Based upon the amino acid motif I/VxYxxL
  • Commonly expressed in signaling receptors in
    lymphocytes
  • Recruits SHP-1/SHP-2 phosphatases
  • Linked to inhibition of function in lymphocytes

33
NK Cell Activating Receptors
  • Name Alternative Names Cellular Ligand
    Viral Ligand
  • NKp46 Ly94/NCR1 ? SV-HA, IV-HA
  • NKp30 IC7/NCR3 ?
  • NKp44 Ly95/NCR2 ? SV-HA, IV-HA
  • 2B4 CD244 CD48
  • NTB-A KALI ?
  • NKp80 KLRF1 ?
  • CD16 FcgRIII IgG
  • CD2 LFA-2 CD58, LFA-3
  • DNAM-1 CD226 PVR/CD155, Nectin-2/CD112
  • NKG2D D12S2489E/CD159D MICA, MICB, MULT1
    ULBP1-4
  • NKR-P1A CD161A IC-21
  • NKR-P1C CD161C ?
  • NKR-P1F CD161F Clrg
  • P40 LAIR1 ?
  • IRC1 IRp60/CMRF35H ?
  • p75AIRM1 Siglec-7 Sialylated sugars

34
ITAM
  • Immunoreceptor tyrosine-based activating motif
  • Based upon the amino acid motif
    YxxL/Ix6-8YxxL/I
  • Serves as a signaling partner to transmembrane
    receptors with a charged residue in the
    transmembrane region which allows docking of
    signal transducers such as DAP12, CD3z-CD3z
    homodimers, CD3z-Fcer1g heterodimers
  • Activation of cells either via PI3 kinase, or
    ZAP70 or Syk tyrosine kinases

35
NKG2D
  • Single gene
  • Distantly related to other NKG2 family members
  • Alternatively spliced isoforms (short and long)
    in mice
  • NKG2D-s and NKG2D-l, short from binds both DAP10
    and DAP12
  • Expressed in NK cells, CD8 cells and macrophages

36
Ligands for NK Cell Activating Receptors
  • MICA, MICB Stress-inducible molecules encoded
    within the human MHC, also can be induced by some
    infections. Normally expressed by
    gastrointestinal epithelium, but also by some
    epithelial, lung, breast, kidney, ovary, prostate
    and colon tumors, and by some melanomas.
    Transmembrane with a1, a2, and a3 domains but do
    not associate with b2m and do not bind peptides.
  • ULBP1-4 1-3 are GPI-linked, cell surface
    molecules which bind human cytomegalovirus UL-16
    4 is a cell surface molecule with transmembrane
    and cytoplasmic domains. ULBPs have a1 and a2
    MHC Class I-like domains.
  • Rae1b Retinoic acid inducible protein, in mice,
    that shares sequence homology with ULBPs.
    Expressed in early embryogenesis and in some
    tumors, but generally absent in normal tissues.
  • H60 Minor histocompatibility antigen expressed
    by Balb/c mice, target for alloreactivity
    responses by C57Bl/6 mice.
  • DCs Known that NKp30 is required for
    recognition of immature DCs by activated NK
    cells.
  • IC-21 Known that rat CD161A is required for
    recognition of IC-21 tumor cells to mediate their
    lysis.

37
Recognition of Infected Cells by NK Cells
38
Pre-adaptive immune mechanisms or innate-like
lymphocytes
39
gd-T cells
  • Clonal receptor expression
  • Two major subsets
  • -Diversity in repertoire in gd-T cells in
    lymphoid tissues
  • -Limited repertoire in IEL gd-T cells
  • Do not need to recognize antigen in the context
    of MHC
  • Recognize antigens directly, e.g. HSP or MHC
    Class IB
  • May have important regulatory effects
  • Localized at internal epithelial surfaces
  • No memory

40
NK/T Cells
  • Potent producers of cytokines
  • Ligands are glycolipids bound to the Class I-like
    CD1d molecule
  • Highly skewed in TCR gene utilization one alpha
    chain vs three beta chains
  • No boost/memory
  • Important as anti-tumor effectors for liver
    metastases

41
B-1 CD5 Cells
  • Limited Clonal receptor expression
  • Produce IgM antibody, often to oligos
  • No memory
  • Primarily found in the peritoneal cavity

42
B-1 Cell Function
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