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Chapter 2 Innate Immunity
Three Defense Categories ,[object Object],[object Object],[object Object],[object Object],[object Object]
Physical Barriers  Innate immunity ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],-  Completely determined by genes inherited and ready at all times physical barrier = “fixed defenses” + innate immunity
Are the defenses of the innate immune response easy to assess?  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Let’s look at the benefits of innate and adaptive immunity ,[object Object],[object Object],[object Object]
Infectious diseases are caused by pathogens of diverse types that live and replicate in the human body ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Pathogens damage tissue in different ways ,[object Object],[object Object],[object Object]
Different components of the immune system contribute to immunity against different types of microbes in different locations ,[object Object],[object Object],[object Object],[object Object]
Extracellular vs. intracellular  infections can be further subdivided ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Most pathogens infect only  a few related host species ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
The Pathways ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Complement Fixation
 
Complement activation  by the alternative pathway tags microorganisms for destruction ,[object Object],[object Object],[object Object],[object Object]
The Thioester Bond
1 st  Step in the alternative pathway involves spontaneous hydrolysis and activation of complement component C3 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Thioester bond
 
C3 convertase of the alternative pathway ,[object Object],[object Object],[object Object],[object Object]
 
C3b Tags Pathogens for Phagocytosis ,[object Object],[object Object],[object Object]
How is the sequence of complement-activating reactions continued?  ,[object Object],[object Object],[object Object],[object Object],[object Object]
 
 
What about protecting the host cell? Regulatory Proteins ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
What about protecting the host cell? Regulatory Proteins ,[object Object],[object Object]
 
Complement activation limits bacterial infections…but some bacteria mimic human cells to evade the actions of complement  ,[object Object],[object Object],[object Object]
Inflammation ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Several classes of plasma protein limit the spread of infection ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Serpins and   -macroglobulin inhibit potentially damaging proteases
Antimicrobial Peptides - Defensins ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Phagocytosis by macrophages provides a first line of cellular defense against invading microorganisms ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Enhance phagocytosis    more efficient using macrophage surface receptors ,[object Object],[object Object],[object Object],[object Object]
Phagocytosis by macrophages is aided by receptors of innate immunity that bind directly to microbial surface components Phagocytic Receptors ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Macrophages have several types of  surface receptor  that bind to constituents of microbial surfaces and promote  phagocytosis
Binding of Microbe to Phagocytic Receptors Initiates the Phagocytosis ,[object Object],[object Object],[object Object],[object Object]
Receptors that detect microbial products signal macrophage activation and  cytokine secretion ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Some TLR’s need to be on the outside and some on the inside.
[object Object],[object Object],[object Object],[object Object],[object Object]
TLR-4 Can also Signal Interferon alpha and Beta Synthesis and Secretion ,[object Object]
Activation of resident macrophages induces inflammation at sites of infection ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Chemokines    CXCL8 = IL-8 And IL-12 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
TNF-   released by macrophages induces protection at the local level ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
TNF-   can lead to catastrophe when released systemically ,[object Object],[object Object],[object Object],[object Object]
Fixed Defenses ,[object Object],[object Object],[object Object]
Innate Immunity ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Distinct but complementary properties of Macrophages and Neutrophils  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Neutrophils are dedicated phagocytes that are summoned to sites of infection ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Neutrophils are excluded  from healthy tissue ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Inflammatory Response ,[object Object],[object Object],[object Object],[object Object],[object Object]
Leukocyte adhesion molecules ,[object Object],[object Object],[object Object],[object Object],[object Object]
Leukocyte adhesion molecules
The homing of neutrophils  to infected tissues is induced by inflammatory mediators ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
The  homing  of neutrophils  to infected tissues is induced by inflammatory mediators ,[object Object],[object Object],[object Object],[object Object]
Step 1    cytokines/inflammatory mediators induce selectin expression on vascular endothelium to bind neutrophils Transient interaction between neutrophil (sialyl-Lewis X) and selectin on the endothelium
Step 2    Rolling adhesion    tight binding    migration to infection site  Interactions between LFA-1 to ICAM-1 Strong interaction is induced by CXCL8 held on ECM proteoglycans   chemokine attraction    neutrophil squeezes between endothelial cells
Terms to know ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Neutrophils are potent pathogen killers but are themselves programmed to die ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Two types of Granules for Killing
Bacterial agents produced or released by phagocytic cells on the ingestion of microorganisms  (macrophage & neutrophil) Are toxins or bind  to essential nutrients 
Respiratory Burst ,[object Object],[object Object],[object Object],[object Object],[object Object]
Respiratory Burst    Kill pathogens
Toxic Oxygen species  produced during the respiratory burst  can diffuse out  and damage host cells ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Neutrophils    apoptosis    phagocytosed by macrophage
Macrophages produce cytokines: TNF-  , IL-1 and IL-6 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
What’s the role of fever? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Inflammatory cytokines raise body temperature and activate hepatocytes to make the acute-phase response
Acute phase proteins ,[object Object],[object Object],[object Object],[object Object]
C-reactive protein ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Mannose-binding lectin (MBL) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Acute-phase response increases the supply of the recognition molecules of innate immunity
MBL activates a proteolytic enzyme complex: MBL-associated serine protease = MASP ,[object Object],[object Object],[object Object],[object Object],[object Object]
C-reactive protein and MBL are present at low levels in plasma ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
Initiation of the Classical Pathway
Close structural relationships between components of the alternative,  lectin-mediated & classical pathways  of complement activation Major divergence
Intracellular Infection: Type I interferons inhibit viral replication and activate host defenses ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Type I interferons inhibit viral replication and activate host defenses ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Virus-infected cells are stimulated to produce type 1 interferons ,[object Object],[object Object],[object Object],[object Object]
Virus-infected cells are stimulated to produce type 1 interferons ,[object Object],[object Object],[object Object],[object Object],4 3 2 1
In addition to interfering with viral replication… ,[object Object],[object Object],[object Object],[object Object],[object Object]
Major functions of type I interferons
Almost all human cells  can secrete type I interferon ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
NK cells provide an early defense  against intracellular infections ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
NK cells provide an  early response to virus infection ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
NK cells provide an  early response to virus infection    effector T cells take over to finish the job ,[object Object],[object Object]
NK cells provide an early response to virus infection ,[object Object],[object Object],[object Object],[object Object],[object Object]
NK-cell receptors differ in the ligands they bind and the signals they generate ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
NK cells express diverse inhibitory and activating receptors
NK-cell Killing: A Balancing Act ,[object Object],[object Object],[object Object],[object Object]
 
Three genetic complexes contribute to NK-cell recognition of ‘missing-self” ,[object Object],[object Object],[object Object]

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