NORMAL MICROBIOTA & NONSPECIFIC HOST DEFENSES
I. Normal Microbiota of the Human Body
A.
Skin
B.
Respiratory tract
C.
Digestive tract
D.
Genitourinary tract
II. Introduction to Host Defenses
A. Severity of disease
B. Human body's defense system has two parts
III. Factors Affecting Resistance to Infection
A.
Nutrition
B.
Age
C.
Genetic factors
IV. First-Line of Defense
A. Physical (Anatomical) Barriers
1. skin
2. mucous membranes
3. nasal passage
4. lavage (washing)
5. eye lids
B. Chemical Resistance
1. skin secretions
2. stomach acidity
3. lysozyme
4. iron binding proteins
C. Competition with normal flora
V. Second Line of Defense
A. Inflammation
1. Events of inflammation
a) tissue injury
chemotaxins
bradykinins
histamine
prostoglandins
arachidonic acid
b)
activated endothelial cells
c)
neutrophils slowed down
d)
neutrophils adhere to endothelial adhesion molecules
e)
extravasation
f)
other WBCs may follow
g)
fibrin clot formation
2. Signs of Inflammation
a)
swelling (edema)
b)
heat
c)
redness
d)
pain
e)
loss of function
3. Summary
control/limit infections
can get out-of-hand
chronic
inflammation
B. Phagocytosis
1. Phagocytic cells
a) granulocytes:
eosinophils: (~3% circulating WBCs)
basophils: (~0.5%)
neutrophils: (50-70%)
leukocytosis
band forms
b) mononuclear phagocytes
1. monocytes: (5-10% total WBC in circulation)
2. fixed macrophage
Kupffer, microglial, alveolar, and dendritic cells 2. Mechanism of phagocytosis
a)
phagocyte migration b)
contact
interaction between pathogen & phagocyte
opsonins
surface phagocytosis c)
ingestion d)
killing
phagosome fuses with lysosome
O2 independant: hydrolyases
O2 dependant: toxic forms of Oxygen
reactive nitrogen intermediates
defensins 3. Summary
PMNs arrive
first
phagocytic
dysfunction
nonprofessional
phagocytic cells VI. Complement System
A. Introduction
precise sequence of enzymatic activation (cascade)
cascade has an amplification affect
B. Mechanisms of Activation
Two main pathways of activation
1. classical
2. alternative
properidin system
3. consequences
a) inflammation
b) opsonins
c) cell lysis