Host Defense Flashcards
Innate vs. Adaptive Immunity
Innate vs. Adaptive Immunity
Innate immunity
- fast response
- not as selective
- always working
- no memory
Adaptive immunity
- slower response
- very specific
- needs to be activates
- memory
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Innate immunity: overview of features
Innate immunity: overview of features
- constitutional factors
- natural barriers and flora
- cytocines/interferons
- phagocytosis
- complement
Innate immunity: constitutional factors
Innate immunity: constitutional factors
factors that make one species succeptable and another resistant to certain infections.
- genetics- species differences
- age
- metabolic factors
- neuroendocrine factors
- environment- resource availability, population dynamics
Innate immunity: natural barriers & flora
Innate immunity: natural barriers & flora
Natural barriers= literally just shit thats there naturally that prevents shit.
- mechanical barrier: physical structure/aspect that prevents disease
- ex. epidermis/dermis of skin
- chemical barrier: chemical interactions that prevent disease
- ex. high salt, organic acids, and defensins present in skin
Normal flora= some microbiota prevent colonization by others
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Innate immunity: cytokines/interferons
Innate immunity: cytokines/interferons
Cytokines- glycoproteins that are released to tell body to initiate immune response
Interferons- special cytokines related to viral infections
- Type I interferons- role in viral immune defense
- IFN System- crucial for viral defense… discussed how mice with different aspects of IFN inhibited showed reduced immune ability
Innate immunity: phagocytosis
Innate immunity: phagocytosis
phagocytosis= engulfment & digestion of infectious agents
- two cell types
- macrophage
- neutrophil
- eosinophils (rare)
- see steps below…
- ingested bacterium= phagosome
- fused with lysosome= phagolysosome
- lysosome= enzymes digest captured bacteria
- know what cells to digest using pattern recognition receptors (PRR)
- PRRs recognize pathogen-associated molecular patterns (PAMP) on pathogens
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Neutrophils and macrophages ?
Phagocytic cells in innate immune response
Macrophage:
- several receptors specific for bacterial constituents (PRR)
- when bacteria bind receptor and PAMP is recognized, macrophage engulfs and digests it.
Neutrophils: primarily target extracellular bacteria and fungi
- express receptors for many bacteria and fingi (PRR)
- when bound by pathogen (PAMP), engulf and destroy with toxic constituents of neutrophil granules
- *** note, encapsulated bacteria connot be bound by neutrophils. antibodies bind to these bacteria, permitting binding to neutrophil and facilitating engulfment
Natural Killer Cells
Innate immunity: Natural Killer Cells
NK Cells-
- Structure: large granular lymphocytes
- no antigen-specific receptors
- Increse rapidly after viral infection
- Recognize “self-altered” cells (INF)
- has two receptor binding technique
- one receptor activates nk if cell is infected
- one receptor blocks nk if cell is not
- has two receptor binding technique
- kills cells by releasing perforins and granzymes (cytokines)
- perforate membranes and trigger caspase
- MHC I
Innate immunity: complement
Innate Immunity: compliment pathways
- classical pathway
- alternative pathway
- lectin
- all end in terminal pathway, but activation factors are different
See video from lecture for clarification (host II)
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classical pathway
Innate immunity: classical pathway
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Activatior: C1 binds to reactive protein or binding of antibody to antigen
Initial complement: activates the classical pathway, in which it breaks c4 into multiple parts (c4a=small c4b= big).
C3 convertase- C4bC2b
C5 convertase- C4bC2bC3b
lectin pathway
Innate immunity: lectin pathway
activator- mannan binding lectin (MBL), MBL-associated serine protease-2 (MASP-2)
Initial complement component- C4, C2
C3 convertase- C4bC2b
C5 convertase- C4bC2bC3b
Alternative pathway
Innate immunity: alternative pathway
activator- contact of microbial cell wall with C3
Initial complement component- C3, Factor B, Factor D, & properdin
C3 convertase- C3bBb
C5 convertase- C3bBbC3b
Results of compliment activation
Results of compliment activation
- clearance of immune complexes
- cell lysis
- bioactive substances
- removal of particulate antigens
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Adaptive immunity: Humoral immunity
Adaptive immunity: Humoral immunity
= mediated by antibodies secreted by antigen-activated B cells and their progeny plasma cells
- Primary
- Secondary
Adaptive immunity: primary and secondary
Adaptive immunity: Humoral immunity
Primary vs. Secondary immune response
- primary response
- more time
- weaker response
- utilizes IgM
- secondary response
- shorter lag phase
- greater magnitude
- class-switched IgG (IG=immunoglobin)
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Adaptive immunity: Cell Mediated Response
Adaptive immunity: Cell Mediated Response
- mediated by antigen-activated T-cells
- CD8 T cells function as cytotoxic T cells (CTL)
- CD4 T cells and activated Macrophages function in DTH responses (delayed type hypersensitivity) Helper T cells
MHC
MHC= Major histocompatibility complex
part of adaptive immunity
2 classes of proteins- T-cells require MHC presentation
- MHC class I- destroy extracellular pathogens
- Location: nucleated cells
- function: present Ag to cytotoxic t cells
- result: t-cell mediated toxicity
- MHC class II-destroy intracellular pathogens
- location: b cells, macrophage and dendritic cells
- function: present Ag to T helper cells
- result: t-cell mediated help
Note: mhc restriction restricts immune response!
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APCs
APCs= Antigen presenting cells
- macrophages, dendritic cells and be cells
- must be MHC-II positive
- … SOOOO MUCH STUFF MISSED IN PPT 3. FIGURE IT OUT LOSER!!!
ADCC
Antibody Dependent Cell-mediated Cytotoxicity
=cell-mediated immune defense
- effector cell lyses target cells with membrane surface antigens that can be bound by specific antibodies.
- ex. NK cells, Macrophages, Neutrophils, eosinophils
NEED : NK cell, antibodies, and antigen
Neutrophils
Neutrophils
- Function: phagocytosis
- super effective in extracellular bacterial infections
- involved in acute inflammation
- live only 24 hours
- Stored in bonemarrow
Eosinophils
Super effective in parsite infections (helminths)
PRR and PAMP
Pathogens have PAMPs- “pathogen associated molecular patterns”
Immune cells have PRRs- “pathogen recognition receptors”
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