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WEEK 1 - Chapter 16 - Lymphatic System and Immunity
WEEK 1 - Chapter 16 - Lymphatic System and Immunity
AND IMMUNITY
OBJECTIVES
1. Describe the functions of the lymphatic vessels
2. Identify and describe the parts of the major lymphatic pathways
3. Distinguish between the thoracic duct and the right lymphatic duct
INTRODUCTION
Lymphatic system:
A vast collection of cells and biochemical that travel in lymphatic vessels
Contains a network of vessels that assist in circulating fluids
Closely associated with the cardiovascular system
The term “immune system” refers to the fact that many cells of the lymphatic system
provide both defense against disease and permanent immunity against future
infections
LYMPHATIC PATHWAYS
Lymphatic capillaries lymphatic vessels
lymph nodes larger lymphatic vessels
lymphatic trunks lymphatic collecting ducts
subclavian veins in thorax
Lymphatic system carries excess fluid from
interstitial spaces back to bloodstream
Lacteals are lymphatic capillaries that absorb
fats, and transport them to the blood
LYMPHATIC
CAPILLARIES
Microscopic, closed-ended tubes.
Networks parallel blood capillaries
throughout the body.
Thin-walled.
Walls formed from simple
squamous epithelium.
Tissue (interstitial) fluid enters
lymphatic capillaries; fluid is now
called lymph.
Merge into lymphatic vessels.
LYMPHATIC VESSELS
Walls are similar to veins, but thinner.
Contain one-way valves.
Larger vessels lead to lymph nodes and
then to larger lymphatic trunks.
LYMPHATIC TRUNKS AND
COLLECTING DUCTS
Lymphatic trunks:
Drain lymph from lymphatic vessels.
Lymphatic organs:
Consists of encapsulated lymphatic tissue
Lymph nodes, thymus, spleen
LYMPH
NODES
Lymph nodes are usually bean-
shaped, <2.5 cm long
Located along lymphatic vessels;
filter pathogens from lymph
Contain lymphocytes to attack
viruses, bacteria, and parasitic cells
Contain macrophages to engulf
and destroy foreign substances,
damaged cells, and cellular debris
LYMPH NODES
LOCATIONS OF LYMPH NODES
Lymph nodes are found in groups or chains
along the paths of the larger lymphatic
vessels throughout the body.
Not found in central nervous system.
Major locations of lymph nodes:
Cervical region
Axillary region
Supratrochlear region
Inguinal region
Pelvic cavity
Abdominal cavity
Thoracic cavity
FUNCTIONS OF LYMPH NODES
2 primary functions of lymph nodes:
Filter potentially harmful particles from the lymph
Immune surveillance: monitor body fluids via macrophages and lymphocytes
Along with the red bone marrow, the lymph nodes are centers for lymphocyte
production
Lymphocytes attack various pathogens in lymph nodes
Macrophages engulf and digest foreign substances, damaged cells, debris
THYMUS
Soft, bilobed gland in mediastinum.
Most cells are inactive; called
thymocytes.
Some cells mature into functional T cells
Lymph nodes In groups or chains along the paths Filter foreign particles and debris from lymph; house
of larger lymphatic vessels lymphocytes that destroy foreign particles in lymph;
house macrophages that engulf and destroy foreign
particles and cellular debris carried in lymph
Thymus In the mediastinum posterior to the Houses lymphocytes; differentiates thymocytes into T
upper portion of the body of the lymphocytes
sternum
Spleen In the upper left portion of the Houses macrophages that remove foreign particles,
abdominal cavity, inferior to the damaged red blood cells, and cellular debris from the
diaphragm and posterior and lateral blood; contains lymphocytes
to the stomach
1. Distinguish between innate (nonspecific) defenses
and adaptive (specific) defenses
2. List seven innate body defense mechanisms, and
describe the action of each mechanism
Chemical Distinct type of lymphocyte that secretes perforins that lyse virus-infected cells and cancer
barriers cells.
Natural killer A tissue response to injury that helps prevent the spread of infectious agents into nearby
cells tissues.
Phagocytosis Neutrophils, monocytes, and macrophages engulf and destroy foreign particles and cells.
Fever Elevated body temperature indirectly inhibits microbial growth and increases phagocytic
activity
INNATE DEFENSES: SPECIES
RESISTANCE
Refers to fact that certain species are resistant to diseases that affect other species
Certain species do not have the appropriate temperature or chemical environment for
a particular pathogen to survive and proliferate
INNATE DEFENSE:
MECHANICAL BARRIERS
Skin and mucous membranes form mechanical barriers
Prevent entrance of pathogens
Considered the first line of defense (all other non-specific defenses are part of the
second line of defense)
Examples:
As epidermis sloughs off, removes superficial bacteria
Ciliated epithelium in respiratory tract traps and sweeps away pathogens
Hair traps pathogens
Tears, saliva and urine wash away microorganisms
INNATE DEFENSES:
CHEMICAL BARRIERS
Enzymes
Examples: Pepsin in gastric juice and lysozyme in tears destroy microorganisms
Interferons
Blocks viral replication, act against growth of tumors, stimulate phagocytosis
Defensins
Peptides produced by neutrophils and other granulocytes
Penetrate microbial cell membranes or walls and cause lysis
Collectins
Proteins that protect against many bacteria, yeast and some viruses
Complement
Group of proteins in plasma and other body fluids that stimulates inflammation, attracts phagocytes and enhances
phagocytosis.
INNATE DEFENSES: NATURAL
KILLER (NK) CELLS
NK cells are a small population of lymphocytes
Very different from B-cells and T-cells that provide adaptive defenses.
Defend against viruses and cancer cells by secreting cytolytic substances called
perforins, that lyse cell membrane
NK cells also enhance inflammation
MAJOR ACTIONS OF AN
INFLAMMATION RESPONSE
Inflammation produces local redness,
swelling, heat, and pain
A process that walls off infection site,
and inhibits spread of infection
INNATE DEFENSE:
PHAGOCYTOSIS
Removes foreign particles from the lymph
Phagocytes in the blood vessels and the tissues of the spleen, liver or bone marrow
remove particles from blood
The most active phagocytic cells are neutrophils and monocytes
Positive chemotaxis
Chemicals from damaged tissue attract these phagocytic cells to the injury
Monocytes that leave the blood become macrophages, which can be free or fixed in
tissues
INNATE DEFENSES: FEVER
A fever begins when a viral or bacterial infection stimulates lymphocytes to
proliferate, producing cells that secrete a substance called interleukin-1 (IL-1) which
raises thermoregulatory set point
IL-1 is also called endogenous pyrogen (fire maker from within)
Elevated body temperature indirectly inhibits microbial growth; causes liver and
spleen to take up iron, making it unavailable for bacteria and fungi to use in their
normal metabolism
High body temperature also increases phagocytic activity
ADAPTIVE (SPECIFIC)
DEFENSES
Third line of defense is resistance to particular pathogens or to their toxins or
metabolic by-products
Based on the ability to distinguish between “self” and “non-self” antigens
Tumor necrosis factor Stops tumor growth, releases growth factors, causes fever
that accompanies bacterial infection, stimulates
lymphocyte differentiation
B CELLS AND THE HUMORAL
IMMUNE RESPONSE
B cells can be activated when an antigen fits the shape of their receptors, and binds
to them
Further B cell activation requires cytokines from T cells
Once proper cytokines are released from helper T cells, B cells respond by
proliferating, enlarging clone of identical cells
Some new B cells become memory B cells, which provide future immunity
Other new B cells differentiate into plasma cells, which produce and secrete large globular proteins
called antibodies or immunoglobulins
Since antibodies are carried by the blood (a body fluid) to the infection site, this type
of response is called the humoral immune response, or the antibody-mediated
immune response
T CELL AND B CELL
ACTIVATION
B cells and T cells both require proper
activation. Helper T cells secrete
cytokines to activate B cells to
proliferate.
B CELL
PROLIFERATION
B cell proliferation produces both
dormant memory B cells and
antibody-secreting plasma cells
STEPS IN ANTIBODY
PRODUCTION
B Cell Activities
1. Antigen-bearing agents enter tissues.
2. B cell encounters an antigen that fits its antigen receptors.
3. Either alone or more often in conjunction with helper T cells, the B cell is activated. The B cell
proliferates, enlarging its clone.
4. Some of the newly formed B cells differentiate further to become plasma cells.
5. Plasma cells synthesize and secrete antibodies whose molecular structure is similar to the
activated B cell’s antigen receptors
T Cell Activities
1. Antigen-bearing agents enter tissues
2. An accessory cell, such as a macrophage, phagocytizes the antigen-bearing agent, and the macrophage’s
lysosomes digest the agent.
3. Antigens from the digested antigen-bearing agents are displayed on the membrane of the accessory cell.
4. Helper T cell becomes activated when it encounters a displayed antigen that fits its antigen receptors.
5. Activated helper T cell releases cytokines when it encounters a B cell that has previously combined with an
identical antigen-bearing agent.
6. Cytokines stimulate the B cell to proliferate, enlarging its clone.
7. Some of the newly formed B cells give rise to cells that differentiate into antibody-secreting plasma cells.
ANTIBODY MOLECULES
Globular proteins.
Make up the gamma globulin fraction of
plasma proteins.
Also called immunoglobulins.
Y-shaped proteins, composed of 4 amino
acid chains: 2 heavy and 2 light chains.
Each type of antibody has unique amino
acid sequence and conformation,
making it specific for its antigen.
CHARACTERISTICS OF MAJOR
IMMUNOGLOBULINS
There are 5 major types of antibodies or
immunoglobulins (Ig):
IgG: 80% of antibodies
IgA: 13% of antibodies
IgM: 6% of antibodies
IgD: <1% of antibodies
IgE: <1% of antibodies
ACTIONS OF ANTIBODIES
Antibodies react to antigens in 3 ways:
Direct attack on antigens
Activation of complement
Stimulation of local change, inflammation, to
help prevent spread of infection
IMMUNE RESPONSE
Primary immune response Secondary immune response
Produced by first encounter with antigen Subsequent exposure to antigen produces high
First antibodies appear in 5-10 days, and concentration of antibodies in 1-2 days
remain for several weeks Antibodies remain for months or years
Memory B cells are also produced Memory B cells live for many years
PRACTICAL CLASSIFICATION
OF IMMUNITY
Naturally acquired Passive immunity
Obtained by a natural process Temporary immunity obtained via antibodies
Getting and recovering from the disease No antigen exposure
Given from mother to fetus or infant
No immune response is evoked by person’s
immune system
Artificially acquired
Obtained by an injected, instead of a natural Active immunity
process Permanent immunity obtained via antigen
contact
Immune response is evoked
Memory B cells are produced
PRACTICAL CLASSIFICATION
OF IMMUNITY
Type Mechanism Result
Naturally acquired active Exposure to live pathogens Stimulation of an immune
immunity response with symptoms of a
disease
Artificially acquired Exposure to a vaccine containing Stimulation of an immune
active immunity weakened or dead pathogens or their response without symptoms of a
components disease
Naturally acquired Antibodies passed to fetus from Short-term immunity for
passive immunity pregnant woman with active immunity newborn without stimulating an
or to newborn through colostrum or immune response
breast milk from a woman with active
immunity
Artificially acquired Injection of antiserum containing Short-term immunity without
passive immunity specific antibodies or antitoxin stimulating an immune response
AUTOIMMUNITY
An attack by the immune system against own tissues
The immune system fails to distinguish “self” from “non-self”, and the body
produces antibodies called autoantibodies
Also, cytotoxic T cells attack the body’s tissues and organs
Various autoimmune disorders affect different types of cells
There are several theories concerning the cause(s) of autoimmune disorders, but no
single cause has been established
AUTOIMMUNE
Disorder Symptoms
DISORDERS
Antibodies Against
Glomerulonephritis Lower back pain Kidney cell antigens that resemble streptococcal
bacteria antigens
Graves disease Restlessness, weight loss, irritability, Thyroid gland antigens near thyroid-stimulating
increased heart rate and blood pressure hormone receptor, causing overactivity
Type I diabetes mellitus Thirst, hunger, weakness, emaciation Pancreatic beta cells
Hemolytic anemia Fatigue and weakness Red blood cells
Multiple sclerosis Weakness, incoordination, speech Myelin in peripheral nerves and in the white matter
disturbances, visual complaints of the central nervous system
Myasthenia gravis Muscle weakness Receptors for neurotransmitters on skeletal muscle
Pernicious anemia Fatigue and weakness Binding site for vitamin B on cells lining stomach
Rheumatic fever Weakness, shortness of breath Heart valve cell antigens that resemble
streptococcal bacteria antigens
Rheumatoid arthritis Joint pain and deformity Cells lining joints
Systemic lupus Red rash on face, prolonged fever, Connective tissue
erythematosus weakness, kidney damage, joint pain
Ulcerative colitis Lower abdominal pain Colon cells
LIFE-SPAN CHANGES
Immune system function declines early in life, as the thymus gland shrinks (only 25% as
powerful as it once was)
There is a higher risk of infection and cancer
T cell numbers decrease very slightly, and B cell numbers do not change, but activity
level declines in both types of lymphocytes
Antibody response to antigens becomes slower
IgA and IgG antibodies increase
IgM and IgE antibodies decrease
Elderly may not be candidates for certain medical treatments that suppresses immunity,
such as chemotherapy
IMMUNITY BREAKDOWN:
HIV/AIDS
HIV (Human Immunodeficiency Virus):
A virus that breaks down immune system function
May stay silent for years, and then progress to AIDS (acquired immune deficiency syndrome); then
opportunistic infections begin
HIV attacks macrophages and then Helper T cells
When Helper T cell numbers decline, B cells cannot produce antibodies, due to lack of cytokine
activation
Later, HIV variants affect Cytotoxic T cells too
Person dies from loss of immune response against pathogens, cancers
Modes of transmission: sexual contact, contaminated needles, birth or milk from infected mother,
receiving infected blood or tissues from donor
QUESTIONS?