Innate Immunity. Mechanisms that do not depend on prior exposure to the pathogen Have evolved over...
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![Page 1: Innate Immunity. Mechanisms that do not depend on prior exposure to the pathogen Have evolved over time to protect against groups of organisms that.](https://reader036.fdocuments.net/reader036/viewer/2022082518/56649ebc5503460f94bc5d51/html5/thumbnails/1.jpg)
Innate Immunity
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Innate Immunity Mechanisms that do not depend on prior
exposure to the pathogen
Have evolved over time to protect against groups of organisms that have distinctive molecular features
Some elements have also been co-opted for use in the specific acquired immune response
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Elements of Innate Immunity
External Barriers Phagocytic cells Complement Humoral mechanisms Extracellular Killing
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External Barriers Skin
Very effective barrier to infection – cuts, burns etc, infection is major complication
Mucus and mucosal surfaces Mucus can trap and move foreign things along Some secretions have bacteriocidal components
Normal bacterial flora can play a protective fole Environment (e.g: vaginal pH) Colicins
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Phagocytic Cells
Polymorphonuclear Leukocytes (a.k.a PMNs or “Polys”
Macrophages (lit: “big eater” Gr.)
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Phagocytic Cells Polymorphonuclear neutrophils: PMNs
White cells (leukocytes), multi-lobed nuclei (look like many nuclei in section)
Neutrophil: does not take up the major dyes Short-lived; lots of glycogen (energy from
glycolysis even if O2 is not available)
Macrophages Mononuclear cells Long lived, significant RER Do not circulate, but hang out in lymph nodes and
other interesting places
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Recognition by Phagocytic cells Phagocytes have evolved a system of receptors that can
recognize molecular patterns on the surface of pathogen that are Conserved
Shared by many infections agents
Different from “self”-patterns
Examples: The lipopolysaccharide of certain bactreia
Yeast cell wall mannans
Mycobacterial glycolipids
But not glactose and sialic acid group that are typical the ends of mammalian surface polysaccharides
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Phagocytosis Engagement of receptors generates internal
signal to start phagocytosis An actin—myosin contractile sytsem for putting
pseudopods around the particle
Lysosomes discharge their contents into the phagosome
Several biochemical pathways ensue to degrade content
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Complement A system of 20 or so different proteins that are “set
off” in a cascade of events.
Cascade: one molecule, when activated, catalyzes a change in the next, makes it active, so that it catalyzes a change in the next etc. Such protein cascades allow a profound response to a trigger.
Complement proteins modify each other, and the fragments may have other effects as well
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Complement has 2 pathways: the classical and the “alternative”
The classical pathway was figured out first, but may be more recent in evolution, because it depends acquired immune response (antibodies) So we will talk about that later!
The “alternative” pathway is activated by microbial polysaccharides, and is part of innate immunity
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Complement: Act I, Scene 1 Complement activation by bacterial cell walls
C3 is routinely cleaved at slow rates to C3b
Factor B is cleaved by a plasma enzyme, Factor D to Bb
C3b and Bb bind together to form an enzyme, C3bBb, or C3 convertase.
This convertase very actively cleaves C3 to C3a and C3b
C3b is the central molecule – sets off complement-mediated killing ….. so how is this prevented from running amok in the uninfected state?
A protein H binds to C3bBb, and then another protein I binds to the C3bBbH complex, inhibiting it.
However ….
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Complement: Act I, Scene 2
If certain bacteria are present, the cascade is not inhibited.
Some mico-organisms can stabilize the convertase C3bBb, so that it does not bind Factor H
If the convertase does not bind H, it also does not bind I, so it is not inhibited, so….
The reaction does get amplified, and much more
C3b is made
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Complement: Act II
The C3b can for a short time, react covalently with local hydroxyl or amino groups at the microbial cell surface C3b bound to the surface makes the cell “tasty to
macrophages” – the surface is “opsonized”
In the presence of extra C3b, the C3bBb changes its enzymatic specificity such that it now cleave C5 into C5a and C5b
C5b stays bound to C3b at the surface of the invading cell.
Seeing C5b bound, C6, C7, C8 and C9 bind, and form a membrane pore (called the Membrane Attack Complex)
The cell lyses
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Complement: Act III
The smaller fragments C3a and C5a stimulate Phagocytosis
Mast cell degranulation Histamine (causes vasodialation, capillary permeability,
bronchioconstriction) Proteases and other degradative enzymes Chemotactic factors (recruit phagocytes) Interleukins further activation of macrophage activity ,
and other things
= basic inflammatory response
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Overview --complement alternative pathway
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Humoral Mechanisms provide a second defensive strategy
The term “humoral” means soluble in serum of other fluids; non involving cells
Antibodies are humoral defenses (but specific acquired immunity, so discussed later)
Among the innate humoral immune defenses: Complement
Clotting Factors (cascade, fibrin and fibinogen)
Lysozyme (in many secretions, attacks bacterial cell wall)
Acute phase proteins
Intereferons
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Complement
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Clotting Cascade
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Acute Phase Proteins Concentration increases in response to alarm proteins,
such as IL-1 IL-1 is released by macrophages when they are activated
(by bacterial endotoxins, foreign molecular patterns, complement etc)
Increase in C-Reactive protein, and mannan binding proteins (as much as 1000-fold). These bind to bacteria, and activate the classical pathway of
complement (take the place of the C1 proteins that are normally activated by Ab)
C3b opsonizes the foreign cells
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Extracellular Killing
NK (Natural Killer) cells kill virally- infected cells using perforin
Induce apoptosis Apoptosis = Programmed cell death
A series of reactions, cascade of proteolytic enzymes (capases); the end result is rapid degradation of the nucleus, and cutting DNA in to nucleosome size pieces