The Lymphatic System and Body Defenses: Elaine N. Marieb

Essentials of Human Anatomy & Physiology

Seventh Edition
Elaine N. Marieb

Chapter 12
The Lymphatic System
and Body Defenses

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Lymph Nodes
Figure 12.3
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

The Lymphatic System
 Two parts
 Lymphatic vessels
 Lymphoid tissues and organs
 Lymphatic system functions
 Transport fluids back to the blood
 Play essential roles in body defense and
resistance to disease
 Absorb digested fat at the intestinal villi Slide 12.1
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings
Lymphatic Characteristics
 Lymph – excess tissue fluid carried by
lymphatic vessels
 Properties of lymphatic vessels
 One way system toward the heart
 No pump
 Lymph moves toward the heart
 Milking action of skeletal muscle
 Rhythmic contraction of smooth muscle
in vessel walls
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide 12.2
Lymphatic Vessels
Figure 12.1

Lymphatic Vessels
 Lymphatic
collecting vessels
 Collects lymph
from lymph
capillaries
 Carries lymph to
and away from
lymph nodes
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.2 Slide
Lymphatic Vessels
 Lymphatic
collecting vessels
(continued)
 Returns fluid to
circulatory veins
near the heart
 Right lymphatic
duct
 Thoracic duct
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.2 Slide
Lymph
 Materials returned to the blood

 Water
 Blood cells
 Proteins

Lymph
 Harmful materials that enter lymph

vessels
 Bacteria
 Viruses
 Cancer cells
 Cell debris

Lymph Nodes
 Filter lymph before it is returned to the

blood
 Defense cells within lymph nodes
 Macrophages – engulf and destroy foreign
substances
 Lymphocytes – provide immune response to
antigens

Lymph Nodes
Figure 12.3

Lymph Node Structure
Figure 12.4

Other Lymphoid Organs
 Several other
organs contribute
to lymphatic
function
 Spleen
 Thymus
 Tonsils
 Peyer’s patches
Figure 12.5
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide 12.9
The Spleen
 Located on the left side of the abdomen

 Filters blood
 Destroys worn out blood cells
 Forms blood cells in the fetus
 Acts as a blood reservoir

The Thymus
 Located low in the throat, overlying the

heart
 Functions at peak levels only during
childhood
 Produces hormones (like thymosin) to
program lymphocytes

Tonsils
 Small masses of lymphoid tissue around

the pharynx
 Trap and remove bacteria and other
foreign materials
 Tonsillitis is caused by congestion with
bacteria

Peyer’s Patches
 Found in the wall of the small intestine

 Resemble tonsils in structure
 Capture and destroy bacteria in the
intestine

Mucosa-Associated Lymphatic
Tissue (MALT)
 Includes:
 Peyer’s patches
 Tonsils
 Other small accumulations of lymphoid
tissue
 Acts as a guard to protect respiratory
and digestive tracts
OBJECTIVES:
(i) To differentiate the non-specific defense system from
specific defense system.
(ii) To identify the structures and functions the non-

specific defense system and the specific defense system.
(iii) To identify four major types of grafts.
(iv) To name selected disorders of immunity.

Body Defenses
 The body is constantly in contact with
bacteria, fungi, and viruses (pathogens)
 The body has two defense systems for
foreign materials
 Nonspecific defense system
 Mechanisms protect against a variety of
invaders
 Responds immediately to protect body
from foreign materials
Body Defenses
Specific defense system

 Specific defense is required for each type
of invader
 Also known as the immune system

Nonspecific Body Defenses
 Body surface coverings

 Intact skin
 Mucous membranes
 Specialized human cells
 Chemicals produced by the body

Surface Membrane Barriers –
First Line of Defense
 The skin
 Physical barrier to foreign materials
 pH of the skin is acidic to inhibit bacterial
growth
 Sebum is toxic to bacteria
 Vaginal secretions are very acidic

Surface Membrane Barriers –
First Line of Defense
 Stomach mucosa
 Secretes hydrochloric acid
 Has protein-digesting enzymes
 Saliva and lacrimal fluid contain
lysozyme
 Mucus traps microogranisms in
digestive and respiratory pathways
Defensive Cells
 Phagocytes
(neutrophils and
macrophages)
 Engulfs foreign
material into a
vacuole
 Enzymes from
lysosomes digest
the material
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.6b Slide
Macrophage attacking e-coli.
•

Defensive Cells
 Natural killer cells

 Can lyse and kill
cancer cells
 Can destroy virus-
infected cells
Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.6b Slide
Inflammatory Response -
Second Line of Defense
 Triggered when body tissues are injured
 Produces four cardinal signs
 Redness
 Heat
 Swelling
 Pain
 Results in a chain of events leading to
protection and healing
Functions of the Inflammatory
Response
 Prevents spread of damaging agents

 Disposes of cell debris and pathogens
 Sets the stage for repair

Steps in the Inflammatory Response
Figure 12.7
Antimicrobial Chemicals
 Complement
 A group of at
least 20
plasma
proteins
 Activated when
they encounter
and attach to
cells
(complement
fixation) Figure 12.8

 Complement
(continued)
 Damage
foreign cell
surfaces
 Will rupture or
lyse the foreign
cell membrane
Figure 12.8

 Interferon
 Secreted proteins of virus-infected cells
 Bind to healthy cell surfaces to inhibit viruses
binding

Interferons are a family species-specific proteins synthesized by
eukaryotic cells in response to viruses and a variety of natural and
synthetic stimuli. There are several different interferons commonly
used as therapeutics, termed alpha, beta, and gamma. These peptides
are used to treat hairy cell leukemia, AIDS-related Kaposi's sarcoma,
laryngeal papillomatosis, genital warts, and chronic granulomatous
disease. Side effects include black tarry stools, blood in the urine,
confusion, and loss of balance.
Fever
 Abnormally high body temperature
 Hypothalmus heat regulation can be
reset by pyrogens (secreted by white
blood cells)
 High temperatures inhibit the release of
iron and zinc from liver and spleen
needed by bacteria
 Fever also increases the speed of tissue
repair
Specific Defense: The Immune
System – Third Line of Defense
 Antigen specific – recognizes and acts

against particular foreign substances
 Systemic – not restricted to the initial
infection site
 Has memory – recognizes and mounts
a stronger attack on previously
encountered pathogens
Types of Immunity
 Humoral immunity
 Antibody-mediated immunity
 Cells produce chemicals for defense
 Cellular immunity
 Cell-mediated immunity
 Cells target virus infected cells

Antigens (Nonself)
 Any substance capable of exciting the
immune system and provoking an immune
response
 Examples of common antigens
 Foreign proteins
 Nucleic acids
 Large carbohydrates
 Some lipids
 Pollen grains
 Microorganisms
Self-Antigens
 Human cells have many surface

proteins
 Our immune cells do not attack our own
proteins
 Our cells in another person’s body can
trigger an immune response because
they are foreign
 Restricts donors for transplants
Allergies
 Many small molecules (called haptens
or incomplete antigens) are not
antigenic, but link up with our own
proteins
 The immune system may recognize and
respond to a protein-hapten
combination
 The immune response is harmful rather
than protective because it attacks our
own cells
Cells of the Immune System
 Lymphocytes
 Originate from hemocytoblasts in the red bone
marrow
 B lymphocytes become immunocompetent in
the bone marrow
 T lymphocytes become immunocompetent in
the thymus
 Macrophages
 Arise from monocytes
 Become widely distributed in lymphoid organs
Activation of Lymphocytes
Figure 12.9
Humoral (Antibody-Mediated)
Immune Response
 B lymphocytes with specific receptors

bind to a specific antigen
 The binding event activates the
lymphocyte to undergo clonal selection
 A large number of clones are produced
(primary humoral response)

Humoral (Antibody Mediated)
Immune Response
 Most B cells become plasma cells

 Produce antibodies to destroy antigens
 Activity lasts for four or five days
 Some B cells become long-lived memory
cells (secondary humoral response)

Humoral Immune Response
Figure 12.10
Active Immunity
 Your B cells
encounter
antigens and
produce
antibodies
 Active immunity
can be naturally
or artificially
acquired
Figure 12.12

Passive Immunity
 Antibodies are obtained from someone
else
 Conferred naturally from a mother to her
fetus
 Conferred artificially from immune serum or
gamma globulin
 Immunological memory does not occur
 Protection provided by “borrowed
antibodies”
Antibodies (Immunoglobulins) (Igs)
 Soluble proteins secreted by B cells

(plasma cells)
 Carried in blood plasma
 Capable of binding specifically to an
antigen

Antibody Classes
 Antibodies of each class have slightly
different roles
 Five major immunoglobulin classes –
(Do Not Need to know!)
 IgM – can fix complement
 IgA – found mainly in mucus
 IgD – important in activation of B cell
 IgG – can cross the placental barrier
 IgE – involved in allergies
Cellular (Cell-Mediated) Immune
Response
 Antigens must be presented by
macrophages to an immunocompetent
T cell (antigen presentation)
 T cells must recognize nonself and self
(double recognition)
 After antigen binding, clones form as
with B cells, but different classes of cells
are produced
Cellular (Cell-Mediated) Immune
Response
Figure 12.15

T Cell Clones
 Cytotoxic T cells
 Specialize in killing infected cells
 Insert a toxic chemical (perforin)
 Helper T cells
 Recruit other cells to fight the invaders
 Interact directly with B cells

T Cell Clones
 Suppressor T cells
 Release chemicals to suppress the activity
of T and B cells
 Stop the immune response to prevent
uncontrolled activity
 A few members of each clone are
memory cells

Summary of the Immune Response
Figure 12.16
Organ Transplants and Rejection
 Major types of grafts
 Autografts – tissue transplanted from one
site to another on the same person
 Isografts – tissue grafts from an identical
person (identical twin)
 Allografts – tissue taken from an unrelated
person
 Xenografts – tissue taken from a different
animal species
Organ Transplants and Rejection
 Autografts and isografts are ideal

donors
 Xenografts are never successful
 Allografts are more successful with a
closer tissue match

Disorders of Immunity:
Immunodeficiencies
 Production or function of immune cells

or complement is abnormal
 May be congenital or acquired
 Includes AIDS – Acquired Immune
Deficiency Syndrome

Autoimmune Diseases
 The immune system does not

distinguish between self and nonself
 The body produces antibodies and
sensitized T lymphocytes that attack its
own tissues

Autoimmune Diseases
 Examples of autoimmune diseases
 Multiple sclerosis – white matter of brain
and spinal cord are destroyed

Autoimmune Diseases
 Examples of
autoimmune
diseases
 Myasthenia gravis
– impairs
communication
between nerves
and skeletal
muscles

Autoimmune Diseases
 Examples of
autoimmune
diseases
 Juvenile
diabetes –
destroys
pancreatic beta
cells that
produce insulin

Autoimmune Diseases
 Examples of
autoimmune
diseases
(continued)
 Systemic lupus
erythematosus
(SLE) – affects
kidney, heart, lung
and skin
Autoimmune Diseases
 Examples of
autoimmune
diseases
(continued)
 Glomerulonephritis –
impairment of renal
function
Immune Deficiency: AIDS
• HIV targets cells

• Retrovirus attaches to CD4 receptors of
T helper cells
– Transmission: Body fluids, i.e., blood, semen,
breast milk, vaginal secretions
The Structure of HIV
Figure 9.19
Time Course of the Progression of
AIDS after HIV Infection
Figure 9.21
•AIDS progression:
–Phase I: few weeks to a few years; flu like symptoms, swollen
lymph nodes, chills, fever, fatigue, body aches. Virus is
multiplying, antibodies are made but ineffective for complete
virus removal
–Phase II: within six months to 10 years; opportunistic
infections present, Helper T cells affected, 5% may not
progress to next phase
–Phase III: Helper T cells fall below 200 per cubic millimeter
of blood AND the person has an opportunistic infection or type
of cancer. Person is now termed as having “AIDS” May
include pneumonia, meningitis, tuberculosis, encephalitis,
Kaposi’s sarcoma, and non-Hodgkin’s lumphoma….
AIDS Pandemic
• More than 36 million infected with HIV

worldwide
• Most infections in sub-Sahara of Africa
• Increasing spread in Asia and India
• Most often spread by heterosexual contact
outside U.S.

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What are the two parts of the lymphatic system?

What are the two parts of the lymphatic system?

What are the functions of the lymphatic system?

What are the functions of the lymphatic system?

Essentials of Human Anatomy & Physiology

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Materials returned to the blood

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Harmful materials that enter lymph

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Filter lymph before it is returned to the

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Located on the left side of the abdomen

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Located low in the throat, overlying the

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Small masses of lymphoid tissue around

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Found in the wall of the small intestine

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

(ii) To identify the structures and functions the non-

(iii) To identify four major types of grafts.

(iv) To name selected disorders of immunity.

Specific defense system

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Body surface coverings

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Natural killer cells

 Prevents spread of damaging agents

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Antigen specific – recognizes and acts

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Human cells have many surface

 B lymphocytes with specific receptors

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Most B cells become plasma cells

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Soluble proteins secreted by B cells

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Autografts and isografts are ideal

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 Production or function of immune cells

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

 The immune system does not

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide

Copyright © 2003 Pearson Education, Inc. publishing as Benjamin Cummings Slide