Induced innate immune response and lymphoid tissue Flashcards
Increase in vascular permeability has what affect on BP?
Decrease BP - in severe cases (coupled with vasodilation) can cause ischemic tissue injury
TLR3, TLR4, and NOD activavtion
Diagram
Signaling PRRs
Can be external (to detect extracellular PAMPs) or internal (to detect intracellular PAMPs)
TLR4
The prototype extracellular TLR that detects bacterial LPS
LPS binding protein (LBP) in serum facilitates TLR4 activation by binding to and transporting LPS to the TLR4 receptor complex
LPS/TLR4 binding activates the transcription factor NF-κβ
TLR3
Intracellular TLR and binds to dsRNA (viral PAMP) and utilizes a signalling pathway leading to production of type I interferons (IFN-α or IFN-β)
PAMP induction of inflammation
NOD-like receptors
NODR or nucleotide oligomerization domain-like receptors
Family of intracellular signaling PRRs that detect PPG subunits inside of cell
NF-κβ
Upregulates many host cell genes (like pro-inflammatory cytokines) that ultimately activate induced innate and adaptive immune functions
Including NADPH oxidase and iNOS
Activation of inflammatory cytokines
- Signaling PRRs activate NF-κβ which increases cytokine gene transcription
- Inflammasome activation - contains proteases that cleave cytokine pro-forms (like pro-IL1β) into mature active cytokines (like IL-1β)
Inflammasome activation also induces cell death by pyroptosis which is very pro-inflammatory due to DAMP release
Tumor necrosis
factor alpha
(TNF-α) and
Interleukin-1β
(IL-1β):
Increase vasodilation, vascular permability, and vascular endothelial adhesion molecule expression (E-selectin and VCAM-1) by binding their receptors on the endothelium and vascular smooth muscle - particularly TNF-alpha
Increase body temperature (these cytokine are endogenous pyrogens that act directly on the hypothalamus) - particularly IL-1beta
Increase tissue factor (TF) release from macrophages and endothelial cells this promotes local clotting by the extrinsic clotting pathway - or if systemic promotes disseminated intravascular coagulation (DIC) - particaularly IL-1beta
Both act on mucosal goblet cells and increase mucus secretion
TNF-alpha is the major mediator of vascular effects in SIRs and sepsis
IL-6
Increases liver release of actue phase proteins (like CRP, MBL, and fibrinogen)
Because IL-6 increases clotting factor production, it also involved in pathophysiology of DIC
Increases body temp (major endogenous pyrogen acting directly on hypothalamus)
IL-12
Activates NK cells to better kill target cell and produce the cytokine IFN-gamma
IL-8
Chemokine that increases recruitment of neutrophils to the site of infection or injury - bacterial PAMPs and DAMPs are strong inducers of IL-8 production and induce a strong neutrophil response
Binding of IL-8 to neutrophil receptors activates “inside out” signaling that increases the affinity of neutrophil LFA-1 for ICAM-1 on the enothelium
iNOS
Inducible nitric oxide synthase enzyme
Potent vasodilator
Pro-inflammatory cytokines
Tumor necrosis factor alpha (TNF-α) and Interleukin-1β (IL-1β) and IL-6
Produced in infected/damgaged peripheral tissues can enter circulation, CNS, and act on specific regions of the brain
Allows peripheral inflammatory responses to evoke sickness behaviors - appetite loss, fatigue, and sleepiness, increased pain sensitivity, social withdrawal, and anhedonia
TLR3
Binds viral dsRNA initiates IFN-α or IFN-β secretion
Type I IFN binding to IFN receptors on uninfected host cells
Activates transcription of genese that encode the enzymes ribonuclease L (RNase L) and protein kinase R (PKR)
These enyzmes are inactive unless host cell is subsequently virus infected
RNase L
Degrades viral and cellular mRNA - inhibiting translation of viral and host proteins
PKR
Inactivates a host ribosomal sub-unit (protein synthesis initiation factor elF-2) -turning off host cell ribosomes and preventing translation of viral and host mRNAs
IFN-α/β Therapy
Increases NK cell killing activity
Antiviral effects of type I IFNs are short lived and reversible:
Used in HPV and Hep C infections
What happens when an iDC binds a PAMP to its PRR?
This stimulates the iDC carrying pathogen antigen to migrate to nearby secondary lymphoid tissues and mature
Increase B7 co-stimulatory molecule
Local vs. systemic inflammatory responses
Molecular basis of sepsis-induced organ failure
Compensatory anti-inflammatory response syndrome
Neuroinflammatory signals inhibit pro-inflammtory cytokine production, immune cells undergo apoptosis, anti-inflammatory immune cell populations (reg T cells and myeloid suppressor cells) expand and anti-inflammatory cytokines are produced
Can lead to lasting immunosuppression
SIRS
Sepsis
The presence of SIRS in response to a suspected or culture confirmed infection
Two most common types of infection associated w/ sepsis
Pneumonia and UTIs
Septic shock
BP<90 mmHG or a reduction >40 mmHg from baseline in the absence of other causes for hypotension
MODS
Multiple organ dysfunction syndrome
i.e. adult respiratory distress syndrome (ARDS), central nervous system dysfunction, CV, renal, and liver failure
Electron micrograph of plasma cells
“clock face” nucleus and golgi halo (asterisk)
IgA secretion in the mammory gland
- Plasma cells produce IgA dimers
- Membrane-bound Fc receptors on the basal surface of mammary epithelial cells recognize these IgA dimers
- IgA is internalized via receptor-mediated endocytosis
- IgA is transported in membrane-bound vesicles to the apical epithelial surface
- IgA is released into the mammary secretions
Areas of the body that lack lymphatics
CNS - immunoligically priviledged site
Cartilage (lymph and blood vessels)
Bone/teeth despite high metabolic activity
Placenta
Thymic parenchyma (functional tissue of thymus)
Lymphatic capillaries
Originate as blind-ended vessels
Single layer of endothelial cells - are not associated with pericytes (pericytes provied structural support and regulate endothelial permeability in blood capillaries)
Not fenestrated - lack small pores
No tight junctions between cells
Lacteals
Lymphatic capillaries that transport chylomicrons (lipids) to the liver
Chylomicrons are synthesized by intestinal epithelial cells and are exocytosed into lacteals
Smaller image - plica circularis
Lymphoreticular organs
- Thymus
- Lymph nodes
- Spleen
Characterized by internal structure consisting of network of retigular or stromal cells that surround and support parenchymal cells