Lymphatic System: Overview • Lymph – interstitial fluid once in lymphatic vessels • Consists of 2 semi-independent parts: – A network of lymphatic vessels – Lymphoid.

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Transcript Lymphatic System: Overview • Lymph – interstitial fluid once in lymphatic vessels • Consists of 2 semi-independent parts: – A network of lymphatic vessels – Lymphoid.

Lymphatic System: Overview
• Lymph – interstitial fluid once in
lymphatic vessels
• Consists of 2 semi-independent
parts:
– A network of lymphatic vessels
– Lymphoid tissues and organs
scattered throughout body
• Returns interstitial fluid and
leaked
plasma proteins back to blood
• One-way system: lymph
flows toward the heart
• Lymph vessels include:
– Microscopic, permeable
lymphatic capillaries
– Lymphatic collecting
vessels
– Lymphatic trunks and
ducts
Lymphatic Capillaries
• Similar to blood capillaries,
with modifications:
– More permeable
– Loosely joined minivalves
– Withstand interstitial
pressure and remain open
• Minivalves function as one-way gates that:
– Allow interstitial fluid to enter, but not escape lymph
capillaries
• During inflammation, lymph capillaries absorb cell debris,
pathogens, cancer cells
• Lacteals – specialized lymph capillaries present in
intestinal mucosa - absorb digested fat and deliver chyle
to the blood
Lymphatic Vessels & Transport
• Have 3 tunics (as veins)
• Have thinner walls, with more internal
valves
• Collecting vessels in the skin travel along
superficial veins
• Deep vessels travel along arteries
• Nutrients are supplied from branching
vasa vasorum (network of small
arterioles, capillaries, and venules that
supply the outer tissue of large blood
vessels)

The lymphatic system lacks a pumping organ

Vessels are low-pressure conduits

Uses the same methods as veins to propel
lymph:
 Pulsations of nearby arteries
 Contractions of smooth muscle in the walls
of lymphatics
Lymphatics & the
Breast
Lymphatic Trunks
• Lymphatic trunks are formed by
union of largest collecting ducts
• Major trunks include:
– Paired lumbar,
bronchomediastinal,
subclavian, and jugular trunks
– A single intestinal trunk
• Lymph is delivered into 1 of 2
large trunks
– Right lymphatic duct – drains
right
upper arm and the right side of
head and thorax
– Thoracic duct – arises from
cisterna chyli and drains rest
of body
Lymphoid Cells
• Lymphocytes are THE main cells
involved in immune response
• 2 main kinds: T cells and B cells,
they protect body against antigens
• Antigen – anything the body
perceives as foreign: bacteria,
viruses, mismatched RBCs or cancer
cells
• T cells: manage immune response;
attack foreign cells
• B cells: produce plasma cells, which
secrete antibodies => Antibodies
immobilize antigens
Other lymphoid cells:
• Macrophages – phagocytize foreign
substances and activate T cells
• Dendritic cells – spiny-looking cells,
functions similar to macrophages
• Reticular cells – supports other cell
types in lymphoid organs
Lymphoid Tissue

Scattered reticular tissue elements in every
body organ
Lymph Nodes
• Principal lymphoid organs of the
body
• Within connective tissue and along
lymphatic vessels
• Aggregations of nodes occur near
body surface in inguinal, axillary,
and cervical regions of the body
• 2 basic functions:
– Filtration – macrophages destroy
microorganisms and debris
– Immune system activation –
monitor and attack antigens
Structure of a Lymph Node
• Nodes are bean-shaped and surrounded by a capsule
• Trabeculae extends inward from capsule and divide node into
compartments
• Nodes have 2 histologically distinct regions: a cortex and a medulla
• Cortex contains follicles with dividing B cells
• Cortex houses T cells
Lymph nodes
2 Regions:
• Cortex
– B cells
– T cells
• Medulla
– Lymph Sinuses &
macrophages
Lymph Nodes Animation
Lymphoid Organs
•
•
•
•
•
•
Lymph Nodes
Spleen
Thymus
Tonsils
Peyer’s patches
MALT
Spleen
• White pulp
– B and T cells carry
out immune function.
• Red pulp
– Removes aged and
defective RBCs
– Stores breakdown
products of RBCs
• Erythrocyte
production in fetus
• Stores blood
platelets
• Has regenerative
properties
Thymus
• Secretes
thymopoietin,
thmosins to make
T-cells
immunocompetent
• Bilobed organ
• Trabeculae divide
lobe into lobules.
• Thymic corpuscles
Tonsils & Adenoids
• Trap bacteria
which work
their way into
the follicles
where they
are
destroyed
• This helps
develop
memory
Appendix
• Possibly works
with the Peyer's
patches to help
defend against
invaders from the
digestive system
Aggregates of Lymphoid Follicles
• Peyer’s patches – isolated clusters,
similar to tonsils
– In the wall of the distal portion
of the small intestine
– Similar structures are found in
the appendix
• Peyer’s patches and the appendix:
– Destroy bacteria
– Generate “memory” lymphocytes
for long-term immunity
MALT
• Mucosa-associated lymphatic tissue
– Peyer’s patches, tonsils, and appendix (digestive
tract)
– Lymphoid nodules in the walls of the bronchi
(respiratory tract)
• MALT protects the digestive and respiratory systems
from foreign matter
Causes of Edema
• Edema Accumulation of
interstitial fluid
• Blockage of lymphatic system
• Increased pressure in veins
• Lack of albumin
– Decreases fluid returning to blood
capillaries by osmosis
• Inflammation
Homeoimbalances of the
Lymphatic System
–
–
–
–
–
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Autoimmune Lymphoproliferative Syndrome (ALPS)
Lymphatic Filariasis
Mesenteric Lymphadenitis
Swollen Lymph Nodes
Castleman Disease
Adenoids
Splenomegaly
Hodgkin's disease
Kawasaki disease
Immunity: 2 Defense Systems
• Innate (nonspecific) system
responds quickly and consists of:
– First line of defense – skin and
mucosae prevent entry of
microorganisms
– Second line of defense –
antimicrobial proteins, phagocytes
• Inhibit spread of invaders
throughout the body
• Inflammation is its most
important mechanism
• Adaptive (specific) defense system
– Third line of defense – mounts
attack against foreign substances
• Has memory, antigen-specific,
and antigen-mediated immunity
• Works in conjunction with the
innate system
• Recognizes specific foreign
substances
– Immobilizes, neutralizes,
or destroys foreign
substances
First line of defense: Surface membrane
barriers
• Skin and mucous membrane
– Layered epidermis and shedding of epithelial
cells
– Sebum inhibits growth of bacteria and fungi
– Mucous traps microbes, dust and pollutants.
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•
•
•
Lacrimal apparatus
Saliva
Vaginal secretions
Flow of urine
Defecation and vomiting
Gastric juices destroy bacteria and
their toxins
First line of defense: Surface membrane
barriers
• Skin and mucous membrane
– Layered epidermis and shedding of epithelial
cells
– Sebum inhibits growth of bacteria and fungi
– Mucous traps microbes, dust and pollutants.
•
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Lacrimal apparatus
Saliva
Vaginal secretions
Flow of urine
Defecation and vomiting
Gastric juices destroy bacteria and
their toxins
Second line of defense:
chemical and cellular defenses
• Antimicrobial proteins
– Interferon
– Complement
– Transferrins
• Natural killer cells
• Phagocytes
– Neutrophils
– Dendritic cells
– Macrophages
• Wandering
• Fixed
– Eosinophils
Interferons
• Produced by
lymphocytes,
macrophages and
fibroblasts.
• Interfere with
translation of viral
proteins
• Degrade viral RNA
• Activate macrophages
and NK cells
• Interferon Animation
Complement
Complement Cascade Animation
Phagocytes
• Macrophages are the chief phagocytic cells
– Free macrophages wander in search of cellular debris
•
•
•
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Kupffer cells (liver) and microglia (brain) are “fixed” macrophages
Neutrophils become phagocytic when encountering infectious material
Eosinophils are weakly phagocytic against parasitic worms
Mast cells bind and ingest a wide range of bacteria
Mechanism
• Pseudopods engulf the antigen into a phagosome
• Invaders are digested by proteolytic enzymes
• Indigestible and residual material is
removed by exocytosis
Figure 21.2a
Phagocytosis
Phagocyte Mobilization
Fever
• Abnormally high body temperature in response to invading
microorganisms
• Body’s thermostat is reset upwards in response to pyrogens,
chemicals secreted by leukocytes and macrophages exposed
to bacteria and other foreign substances
• High fevers are dangerous because they can denature
enzymes
• Moderate fever can be beneficial, as it causes:
– Liver and spleen to sequester iron and zinc
– Increases metabolic rate, which speeds up tissue repair
Inflammatory response
Stages
Inflammation Animation
• Release of Chemical Alarms
• Vasodilatation & Permeability of BV
• Emigration of phagocytes: Dispose cellular debris &
pathogens
• Sets the stage for repair
• Prevent spread of damaging chemicals & pathogens
Signs of inflammation
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Redness
Heat
Swelling
Pain
Impairment of function
Comparison of Immune Cells
Adaptive Resistance
• Specificity—recognition of
particular antigens
• Memory—remembers previously
encountered antigens
• Systemic—immunity is not
restricted to the initial
infection site
• Immune responses
– Antibody-mediated or
humoral immune responses
(late 1800s)
– Cell-mediated immune
responses (mid 1900s)
Antigens and antigen receptors
• Antigens can be entire microbes, parts of
microbes or chemical components of
pollen, egg white, blood cells,…….
Antibodies “immunoglobulins”
• Four looping polypeptide
chains linked together
through disulfide bonds.
• Heavy chains are identical
and have a hinge
• Light chains are half as
long.
• Variable region is the
antigen binding site
• Constant region forms the
stem of the antibody and
determines its class
• Do not destroy antigen;
inactivate and tag it for
destruction
• form an antigen-antibody
(immune) complex
Antibody Action
• Defensive mechanisms used by antibodies:
– Complement fixation – antibodies bound to cells change shape
and expose complement binding sites
– Complement activation – uses a positive feedback cycle to
promote phagocytosis
– Neutralization – antibodies block binding sites on viruses
– Precipitation – soluble molecules are cross-linked into large
insoluble complexes
Immunoglobulin classes
• IgD is attached to B-cell plasma
membrane
• IgM is released during primary
response. Indicates current
infection.
• IgG is the most aboundant. Can
cross placenta & blood vessel
walls.
• IgA found in body secretions
prevents attachment to body
surfaces.
• IgE causes release of histamine
(allergies) by attaching to mast
cells & basophils.
Immunological memory
• Primary immune
response
• Secondary
immune response
Lymphocytes
• Immature lymphocytes released from bone marrow are
essentially identical
• Whether a lymphocyte matures into a B cell or a T cell
depends on where in the body it becomes immunocompetent
– B cells mature in the bone marrow
– T cells mature in the thymus
Key:
Red bone
marrow
Immature
lymphocytes
Circulation
in blood
1
Thymus
2
Immunocompetent,
but still naive,
lymphocyte migrates
via blood
3
Activated
Immunocompetent
B and T cells
recirculate in
blood and lymph
1
Bone marrow
= Site of lymphocyte origin
= Site of development of
immunocompetence as
B or T cells; primary
lymphoid organs
= Site of antigen challenge,
activation, and final
diff erentiation of B and
T cells
1 Lymphocytes destined
to become T cells
migrate to the thymus
and develop
immunocompetence
there. B cells develop
immunocompetence
in red bone marrow.
2
2 After leaving the thymus
or bone marrow as naïve
immunocompetent cells,
lymphocytes “seed” the
lymph nodes, spleen, and
other lymphoid tissues
where the antigen
challenge occurs.
Lymph nodes,
spleen, and other
lymphoid tissues
3
3 Antigen-activated
immunocompetent
lymphocytes circulate
continuously in the
bloodstream and lymph
and throughout the
lymphoid organs of
the body.
Figure 20.8
T Lymphocytes
• CD4 T cell - also
known as a T Helper
(Th) cell
• CD8 T cell - also
known as a
Cytotoxic T (Tc) cell
B Lymphocytes
Clonal Selection
•Production of clones
initiated by antigen
binding
•Plasma cells
secrete antibodies
•Memory cells are
long lived
Humoral & Cell-Mediated Immunity
• Humoral = antibody
mediated immunity
– Involves B cells
– Antibodies circulate
through “humors”
inactive and mark
invaders for destruction
• Cell-mediated = cellular
immunity
– Involves T cells
– Attack targets directly
or release chemical
mediators to enhance
inflammation/ activate
other WBCs
Homeostatic imbalances :
Immunodeficiencies
• Abnormally behaving immune cells
• Severe combined immunodeficiency (SCID)
syndromes
– Congenital conditions
• Acquired immune deficiency syndromes
– Hodgkin’s Disease
– HIV
– AIDS
Homeostatic imbalances :
Autoimmune disease
– Tend to be more prevalent in women
• Type I diabetes—destroys pancreatic beta
cells
• Multiple sclerosis—destroys myelin sheaths
• Myasthenia gravis—impairs communication
between nerve and muscle
• Lupus erythematosus—systemic disease of
skin, kidneys, heart, and lungs
• Rheumatoid arthritis—destruction of joints
Organ transplants
• Autografts—grafts from the same
person to another body site
• Isografts—grafts between genetically
identical individuals
• Allografts—grafts among the same
species
• Xenografts—grafts taken from another
animal species
Hypersensitivities
Hypersensitivity Reactions in the Skin
Hypersensitivities
Delayed
complex
Acute
Subacute
Subacute
Immediate
cytotoxic
Immune
Type I Hypersensitivity
Type I Hypersensitivity Animation
Type II Hypersensitivity
Type III Hypersensitivity
Type III Hypersensitivity
Animations
• Flash animation of a NK cell interacting with
a normal body cell.
• Flash animation of a NK cell interacting with
a virus-infected cell or tumor cell not
expressing MHC-I molecules.
• Flash animation of apoptosis by NK cells.
• HIV Replication