L15 - Cell mediated immune reactions Flashcards
Which immune cells are involved in cell-mediated immunity?
T cells: Th and CTLs
Phagocytes (e.g. macrophages, neutrophils)
List the 3 main effector mechanisms of Cell-mediated immunity?
– Cell-mediated cytotoxicity (CLT, NK)
– Chemotaxis & phagocytosis (MQ)
– Cytokine-mediated direct target cell killing (TH1)
Classify cell-mediated immunity?
T cell dependency:
– T-dependent (specific): CLT, TH
– T-independent (early phase/ non-specific): NK, MQ
What are the 3 subtypes of cell-mediated cytotoxicity?
- Cytotoxic T Lymphocyte (CTL)-mediated Killing
- Antibody-dependent Cell-mediated Cytotoxicity (ADCC)
- Natural Killer (NK) Cell-mediated Killing
Which cells are targeted by CTL-mediated killing??
- Altered self cells (virus infected or tumour cells)
- Intracellular bacteria and parasites
What antagonizes CTL-mediated killing?
antibody-binding blocks CTL recognition
Ab bind to peptide antigen directly on MHC-I of APCs
Describe the 5 steps of CTL mediated killing?
1) Attachment – CD8+ CTL’s TCR binds to antigen presented by MHC-I on target cells
2) 2 signals:
a) TCR + MHC + CD8
b) ) Co-activators: CD80/CD86 on CTL bind CD28 on APC
3) IL-2 from T helper cells cause degranulation of CTL»_space; release Perforins, Lymphotoxins and Granzymes to target cell
4) IFN-γ activates macrophages
5) Recycle CTLs for additional attacks, target cell dies when CTL detaches
Describe the MoA of perforins?
–Released from cytoplasmic granules of CTLs
–Forms pores in the target cell membrane
–Allows granzymes, water to enter target cell
–May cause osmotic lysis
Which cytotoxic factors induce apoptosis of target cells?
Lymphotoxin
Granzymes
Describe the MoA of granzymes?
activate caspase pathway, endonuclease»_space; apoptosis
- toxic to actual intracellular pathogens
Which cytokine is critical for CTL killing ?
IL-2 from Th
Describe the process of ADCC?
Antibody-dependent Cell-mediated Cytotoxicity:
- Fc Receptor on Large granular lymphocytes/ cytotoxic cells bind to Ab on target cells/ pathogens not using TCR
> > Release cytotoxic factors to directly kill
What provides the specificity in ADCC?
Ab binding to target cell and Fc recognized by Large Granular Lymphocytes (LGL)
Ab gives Ag specificity
Which type of cell-mediated toxicity is not specific?
Natural Killer (NK) Cell-mediated Killing
no antigen specificity
Compare the 2 signals in NK cell mediated killing?
Signal 1 = Killer activatory receptor (KAR / lectin) on NK cell + Carbohydrate on target cell
Signal 2 = Killer inhibitory receptor (KIR / Ly49) + Self MHC-I presenting own antigen
Describe how NK cells target abnormal cells but not own cells?
- Normal cell = equal activation of Killer activatory receptor (KAR / lectin) and Killer inhibitory receptor (KIR / Ly49)
» no killing - Abnormal cell with no MHC-I or abnormal antigen»_space; only activate KAR
» activate NK cell cytotoxicity
Define which cells can activate NK cell killing?
Cells with altered MHC-I or presenting abnormal/ non-self Ag
- Tumor cells (no MHC-I)
- Grafts (non-self MHC-1)
- Virus-infected cells (foreign Ag)
What is the action of Fas ligand in cell-mediated killing?
Fas ligand binds to Fas on target cell»_space; activate caspase, endonuclease»_space; apoptosis
List all phagocytes
– Neutrophils
– Monocytes
– Macrophages
Describe the action of chemotatic factors in T-Independent Macrophage Activation?
Ab- Ag complex activate complement system
> > concentration gradient of chemotactic components / fragments
> > attract phagocytes to target cells (e.g. infected) / invading pathogenic microorganisms
List 3 chemotactic molecules for T-Independent Macrophage Activation?
Bacterial components (e.g. fMLP = polysaccharide from bacterial cell wall)
Complement products (e.g. C5a)
Locally released chemokines and cytokines
Define the 5 steps of T-Independent Macrophage Activation?
- Chemotaxis
- Attachment/ adherence
- Uptake by phagocytosis
- Destruction
- Release degradation products
- T-independent chemotaxis activation of other macrophages (release TNFa and IL-12) granulocytes
Define 3 ways for phagocytes to recognize and attach to target cells/pathogens?
1) Fc receptor on phagocyte bind to Ab on pathogen
2) Complement receptor on macrophage bind to opsonized pathogen
3) Mannose receptor bind to mannose-, fucose-containing oligosaccharides on pathogen (e.g. bacteria)
List 3 complement receptors on phagocytes?
C3b, C3bi or C1q
Describe effector mechanisms of phagocytes to kill engulfed pathogens?
Inside phagolysozymes:
1) Reactive oxygen intermediates (ROIs) e.g. superoxide anion
2) Reactive nitrogen intermediates (RNIs), e.g. nitric oxide
3) Others: e.g. complements, defensins, lysozyme, cytokines, proteases
Define the 2 reactive oxygen intermediate pathways in phagocytes?
Peroxidase-independent: generate H2O2 and anions from O2 for direct effect
Peroxidase-dependent: Phagosome fuses
with lysosome to generate toxic oxidants for killing
Describe the signalling event that generates Reactive nitrogen intermediates in phagocytes?
1) IFNγ»_space; nitric oxide synthetase (NOS)»_space; NOS with tetrahydrobiopterin»_space; NO
2) TNF»_space; NOS with tetrahydrobiopterin»_space; NO
Describe the processing of degradation products in phagocytes?
Release degradation products (with free radicals)
> > antigens associate with MHC-II molecule
> > present MHC-Ag complex to activate naïve T helper cells
> > produce cytokines for other processes
Describe how activated macrophages signal other cells?
Type 1 cytokines (e.g. TNFα) = further recruit and activate other macrophages/ granulocytes
IL-12, TNFα to NK
» NK releases IFNγ to activate MORE macrophages/ granulocytes
Describe the process of TH1-dependent macrophage activation?
1) TCR binds to MHC-II on primed macrophage with inactivated pathogens / exogenous peptide
2) CD40L (CD154) binds to CD40 on macrophage
3) Cytokine release:
i) IL-2 to self-stimulate Th clonal proliferation
ii) IFN-γ to activate macrophage to completely kill inactivate pathogens
3) Macrophage increase MHC, IL-12 expression to attract more Th
4) Macrophage increase lysosome formation, Phago-lysosomal fusion, Inducible NO synthase
Which process precedes Th1- dependent macrophage activation?
T cell independent activation»_space; unable to kill pathogen completely»_space; need Th1 for more enhancement of killing
List examples of cytokines with autocrine and endocrine function?
Autocrine = IL-2
Endocrine = IL-8
Define the difference between lymphokines and monokines?
Lymphokines: cytokines produced by lymphocytes
•Monokines: cytokines produced by monocytes/phagocytes
List examples of interleukins and chemokines?
Interleukins: interleukin 1 -39 (IL-1– IL-39) interferons (IFN), TNF etc
Chemokines: CXC (IL-8), CC (MDC), CX3C (Fractalkine)
Cytokines can activate over-lapping receptors. T or F?
False
Unique receptor for each cytokine
One regulatory effect can be regulated by one cytokine only. T or F
False
Pleiotropic & redundant (have multiple, overlapping cell regulatory actions)
List the source and function of IL-1?
Macrophages
- Activate T, B cell 2. Mobilize PMNs 3. Induce acute phase proteins
List the source and function of IL-2?
T cells (Th1 self prolif.) Proliferation of T, NK cells
List the source and function of IL-4?
Mast cells»_space; IgE response
Th2 to suppress Th1»_space; Th2 dominant response»_space; Activate B cells
List the source and function of IL-8?
Macrophages T cells Fibroblasts Keratinocytes
Chemotaxis of PMNs
List the source and function of IL-10?
Th2 cells =Activate B cell, suppress Th1
Macrophages = Suppress macrophages
List the source and function of IL-12?
B cells = Stimulate TH1
Macrophages
= Inhibit TH2
List the source and function of TGFβ ?
T cells
Inhibits other cytokines
List the source and function of TNFα?
Macrophages
Inflammation
Define the Th cell type for intra and extracellular pathogen?
Intracellular pathogens (e.g. virus, mycobacteria, some protozoa) = Th1 >> Cell-mediated immunity
Extracellular pathogens (e.g. bacteria, parasitic worms) = Th2»_space; Ab production/ Humoral response
Which cytokines direct Th0 cells to differentiate into Th1?
IL-12(MQ, DC)
IL-18 (MQ, DC, Kupffer cell)
IFN-γ (T cells, NK, DC) ***
Which cytokines direct Th0 cells to differentiate into Th2?
IL-4 (mast cell, NK-T, DC)
IL-6 (T, MQ)
IL-10 (T, MQ, DC)
Th1 and Th2 differentation can occur simultaneously. T or F?
False
Reciprocal control: Th1 and Th2 mutaully inhibit each other:
Define the cytokines involved in the reciprocal activation of Th1 and Th2?
Th1»_space; IFN-γ»_space; inhibit TH2 proliferation
Th2»_space; IL-4, IL-10»_space; inhibit Th1 proliferation
Which Th cell is vital for activation of cell-mediated immunity?
Th1»_space; because IFN-γ has widespread effect on many effector cells
What is the role of B cells in cell-mediated immunity?
Produce antibodies»_space; mediate ADCC
Define the 4 phases of delayed type hypersensitivity reaction?
1) Induction phase: sensitized Th1 release cytokines after 2nd contact with same Ag
2) Inflammatory phase
3) Effector phase: activated MQ kill intracellular pathogen
4) Chronic DTH reaction: can’t kill persistent pathogen (e.g. MTB), granuloatous inflammation ensues
Define the cytokines and reactions involved in the inflammatory phase of DTH?
IFN-γ activates local macrophages
Chemokines attract / recruit more macrophages, TH1 cells
What causes chronic DTH reactions?
Persistent source of Ag (e.g. mycobacteria TB)
Define the type of inflammation that occurs in DTH?
Granulomatous inflammation»_space; Granuloma formation to contain persistent pathogen
Describe the composition of granulomas?
large mass of macrophages, TH1 cells
+ Multinucleated giant cell (Langhans type) + Epitheloid cell + Fibroblasts (producing fibrous tissue) + Peripheral lymphocytes
Compare the type of immune response mediated by Th1 and Th2?
Th1 = CMI Th2 = Humoral response
Define the 4 key characteristics of cytokines?
– Local & systemic effects
– Unique receptor for each cytokine
– Pleiotropic, synergistic & autocrine
– Complex network
Which type of immunity defends against tumours and cause transplant rejection?
Both cell-mediated immunity
• Immunity against tumors (CTLs, NKs)
• Transplantation graft rejection (CTLs, NKs) – Delayed hypersensitivity reactions (DTH) – Cell-mediated cytotoxicity