Title: Anatomy and Physiology
1Anatomy and Physiology
- Chapter 14
- Lymphatic System and Immunity
2Introduction to the Lymphatic System
- Network of vessels that transports fluids
- Consists of a collection of cells and
biochemicals that travel in lymphatic vessels and
the organs and glands that produce them - Carries away excess fluid from interstitial
spaces in most tissues and returns it to
bloodstream
3Link to unlabeled diagram
Schematic representation of lymphatic vessels
transporting fluid from interstitial spaces to
the bloodstream
4- Lacteals special lymphatic capillaries located
in the lining of the small intestine that absorb
digested fats and transports them to venous
circulation. - Cells and biochemicals of the lymphatic system
launch both generalized and targeted attacks
against foreign particles enabling the body to
destroy infectious microorganisms and viruses - Also attacks toxins and cancer cells
- When abnormal, can cause allergies or cancer,
autoimmune disorders in which the body attacks
itself
5Lymphatic Pathways
- Begin as lymphatic capillaries which merge to
form larger and larger vessels that unite with
veins in the thorax - Lymphatic capillaries are microscopic
closed-ended tubes that extend into interstitial
spaces forming complex networks that parallel
those of blood capillaries
6Lymphatic capillaries are microscopic,
closed-ended tubes that begin in the interstitial
spaces of most tissues.
7- Walls of capillaries (like those of blood
capillaries) are formed from a single layer of
squamous epithelial cells. - Thin layer makes it possible for tissue fluid to
enter lymphatic capillaries - Lymph fluid inside lymphatic capillaries
- Lymphatic Vessels
- Walls similar to those of veins but thinner
- Have flaplike valves that help prevent backflow
(similar to veins) - Lead to lymph nodes then merge to larger vessels
called lymphatic trunks
Light micrograph of the flaplike valve (arrow)
within a lymphatic vessel
8Lymph enters and leaves a lymph node through
lymphatic vessels.
9- Lymphatic trunks
- Drain lymph
- Named for the regions they serve
- Join one of 2 collecting ducts thoracic duct
and right lymphatic duct
10- Thoracic Duct
- Larger and longer
- Receives lymph from the lower limbs and abdominal
regions, left upper limb and left side of thorax,
head and neck - Empties into the left subclavian vein near the
left jugular vein.
11- Right Lymphatic Duct
- Receive lymph from the right side of the head and
neck, right upper limb and right thorax - Empties into the right subclavian vein near the
right jugular vein.
12Lymphatic Pathways. The right lymphatic duct
drains lymph from the upper right side of the
body, whereas the thoracic duct drains lymph from
the rest of the body.
13- After leaving collecting ducts, lymph enters the
venous system to become part of plasma just
before blood returns to the right atrium. - The skin has many lymphatic capillaries. If skin
is broken or something is injected (venom from
insect sting), foreign substances rapidly enter
the lymphatic system.
14Lymphatic Pathway
- Lymphatic capillary
- Vessel
- Node
- Vessel
- Trunk
- Collecting duct
- Subclavian vein
15Tissue Fluid and Lymph
- Lymph is tissue fluid that has entered a
lymphatic capillary, thus lymph formation depends
upon tissue fluid formation. - Tissue fluid originates from blood plasma
- Composed of water and dissolved substances that
leave blood capillaries - Capillary blood pressure causes filtration of
water and small molecules from the plasma
16- Resulting fluid has much the same composition as
blood plasma (nutrients, gases, hormones) except
plasma proteins, which are too large to pass
through capillary walls. - Osmotic effect of the plasma proteins helps draw
fluid back into the capillaries by osmosis
(plasma colloid osmotic pressure)
17Lymph Formation and Function
- Filtration from plasma normally exceeds
reabsorption leading to net formation of tissue
fluid (interstitial fluid) - This increases interstitial fluid hydrostatic
pressure favoring movement of tissue fluid into
lymphatic capillaries forming lymph. - Lymph returns most of the small proteins to the
blood stream and transports foreign particles
(bacteria, virus) to the lymph nodes.
Step through of net movement of fluids
18Lymph Movement
- Hydrostatic pressure of tissue fluid drives the
entry of lymph into lymphatic capillaries
(pressure is low, similar to venous blood) - Other forces that influence the movement of
lymph - Contraction of skeletal muscles that compress
lymphatic vessels - Contraction of smooth muscles in walls of larger
lymphatic trunks - Pressure changes associated with breathing
19- Valves prevent backflow
- Continuous movement of fluid stabilizes the
volume of fluid in these spaces.
20Edema
- Swelling that results from interference of lymph
movement causing tissue fluids to accumulate
within interstitial spaces - May occur when surgery removes lymphatic tissue,
obstructing vessels. - Ex. Breast cancer surgery often includes removal
of nearby lymph nodes to prevent associated
vessels from transporting cancer cells to other
sites. This can interfere with drainage from
upper limb.
21Lymph drainage of the right breast illustrates a
localized function of the lymphatic system.
Surgery to remove a cancerous breast can disrupt
this drainage, causing painful swelling.
22Lymph Nodes
- Located along lymphatic pathways throughout the
body, but absent in CNS - Contain large numbers of lymphocytes and
macrophages that fight invading microorganisms
23Structure of a Lymph Node
- Vary in size and shape. Usually less than 2.5 cm
long and bean-shaped. - Hilum indented region where blood vessels and
nerves join a lymph node - Afferent vessels (leading to a node) enter at
various points on its concave surface - Efferent vessels (leaving node) exit from the
hilum - Capsule of connective tissue encloses each lymph
node and subdivides it into compartments called
lymph nodules
24A section of a lymph node.
25Major locations of lymph nodes.
26Lymph Nodules
- The structural units of a lymph node
- Occur singly or in groups associated with mucous
membranes of the respiratory and digestive
tracts. - Contain dense masses of lymphocytes and
macrophages - Tonsils partially encapsulated lymph nodules
- Peyers patches aggregations of nodules.
Scattered throughout the mucosal lining of the
ileum of the small intestine
27Lymph Sinuses
- Spaces within a node
- Provide complex network of chambers and channels
through which lymph circulates - Macrophages most highly concentrated
28Functions of Lymph Nodes
- Filtering potentially harmful particles from
lymph before returning it to the bloodstream - Immune surveillance
- Provided by lymphocytes and macrophages.
- Nodes are centers for lymphocyte production.
- Lymphocytes attack invading viruses, bacteria,
and other parasitic cells - Macrophages engulf and destroy foreign
substances, damaged cells and cellular debris
29Lymphangitis
- Superficial lymphatic vessels inflamed by
bacterial infection. - Appear as red streaks beneath the skin
30Lymphadenitis
- Inflammation of lymph nodes
- Nodes enlarge and may be quite painful
- Often follows lymphangitis
31Thymus
- Soft, bi-lobed structure enclosed in a connective
tissue capsule - Located anterior to the aorta and posterior to
the upper part of the sternum. - Relatively large during infancy and early
childhood but shrinks after puberty. - Small in adult
- In elderly, replaced by adipose and connective
tissue - By age 70, the thymus is 1/10th the size it was
at age 10. The immune system is only 25 as
powerful
32Thymus and Spleen. The thymus gland is bilobed
and located between the lungs and superior to the
heart. The spleen is located inferior to the
diaphragm and posterior and lateral to the
stomach.
33- Lobules
- Sub-divisions of the thymus
- Contain lymphocytes called thrombocytes that are
inactive, but some mature into T cells (T
lymphocytes) - T cells leave the thymus and provide immunity
- Epithelial cells in the thymus secrete hormones
called thymosins, which stimulate maturation of T
cells after they leave the thymus and migrate to
other lymphatic tissues
A cross section of the thymus. Note how the gland
is subdivided into lobules.
34Spleen
- Largest lymphatic organ
- Located in the upper left portion of the
abdominal cavity, just inferior to the diaphragm
and posterior and lateral to the stomach. - Resembles a large lymph node
- Sub-divided into lobules
- Venous sinuses of spleen contain blood instead of
lymph (unlike sinuses of lymph node) - 2 types of tissues White pulp and Red pulp
35The spleen resembles a large lymph node.
36White Pulp
- Distributed throughout the spleen in tiny
islands. - Composed of splenic nodules similar to those in
lymph nodes - Contains many lymphocytes
Light micrograph of the spleen
37Red Pulp
- fills the remaining spaces of the lobules.
Surrounds the venous sinuses. - Contains numerous RBCs which give it color, plus
many lymphocytes and macrophages - Blood capillaries within red pulp are permeable
RBCs can squeeze through pores in capillary
walls and enter venous sinuses. - Older RBCs may rupture as they pass through
pores. Cellular debris removed by phagocytic
macrophages within splenic sinuses. - Macrophages also engulf and destroy foreign
particles in the blood
38Body Defenses Against Infection
- Infection the presence and multiplication of a
disease-causing agent or pathogen (virus,
bacteria, fungi, protozoan) - Non-specific and Specific defenses work together
to protect the body
39Non-specific Defense
- Also called Innate Immunity (inborn protection)
- General mechanisms that protect against many
types of pathogens - Response is rapid.
- Mechanisms include
- Species resistance
- Mechanical barriers
- Chemical barriers (enzyme action and interferon)
- Fever
- Inflammation
- Phagocytosis
40Specific Defense / Immunity
- Also called Acquired or Adaptive Immunity
(stimulated by environmental factors) - Precise defense mechanisms that target certain
pathogens. - Specialized lymphocytes recognize foreign
molecules (non-self antigens) and respond to
execute specific defense. - Slower response
41Nonspecific Defenses
42Species Resistance
- Refers to the fact that a given kind of organisms
(species) develops a set of diseases that is
unique to it. - Species may be resistant to diseases that affect
other species. - Tissues fail to provide the temperature or
chemical environment that a particular pathogen
requires.
43Mechanical Barriers
- First line of defense that prevents entry of
some infectious agents. Must remain intact. (All
other nonspecific defenses are the 2nd line of
defense) - Hair of the skin
- Skin
- Mucous membranes lining passageways of the
respiratory, digestive, urinary, and reproductive
systems. - Fluids (sweat and mucous) rinse away
microorganisms
44Chemical Barriers
- Enzymes in body fluids
- Gastric juice contains the protein-splitting
enzyme pepsin. Has a low pH due to HCl lethal to
many pathogens that enter the stomach. - Tears contain enzyme lysozyme which has
antibacterial action against certain pathogens
that get onto the eye surface - Salt from perspiration kills certain bacteria on
the skin
45- Interferons
- Hormone-like peptides produced by lymphocytes and
fibroblasts in response to viruses or tumor cells - Once released from virus-infected cell,
interferon binds to receptors on uninfected cells
stimulating them to synthesize anti-viral
proteins that block replication of a variety of
viruses - Interferon also stimulates phagocytosis and
enhances activity of other cells that help the
body resist infections and growth of tumors.
46Fever
- Elevated body temperature
- Causes liver and spleen to sequester iron,
reducing levels in blood - Bacteria and Fungi require more iron as
temperature rises. Their growth and reproduction
in fever-ridden body slows or ceases - Phagocytic cells attack more vigorously when
temperature rises.
47Inflammation
- Tissue response to injury or infection producing
localized redness, swelling, heat and pain. - Redness results from blood vessels dilation and
increased blood volume within affected tissues.
More phagocytes to remove microorganisms - Swelling is due to increased permeability of
nearby capillaries causing edema - Heat comes from blood from deeper body parts.
Speeds phagocytic activity - Pain results from stimulation of nearby pain
receptors
48- Infected cells release chemicals that attract
WBCs to inflammation sites to phagocytize
pathogens. - Pus thick fluid formed of WBCs, bacterial
cells, and damaged tissue from an infection - Body fluids containing fibrinogen and other
clotting factors collect inflamed tissue - Clotting forms a network of fibrin threads within
the affected region. - Fibroblasts arrive and secrete fibers until area
is enclosed in a sac of connective tissue with
many fibers which inhibits the spread of
pathogens and toxic substances.
49Phagocytosis
- Bloods most active phagocytic cells are
neutrophils and monocytes - Can leave bloodstream by squeezing between the
cells of blood vessel walls (diapedesis) - Chemicals released from injured tissues attract
these cells (chemotaxis) - Neutrophils engulf and digest smaller particles
monocytes phagocytize larger ones - Monocytes give rise to macrophages (histocytes)
which become fixed in various tissues and attach
to the inner walls of blood and lymphatic vessels - Found in lymph nodes, spleen, liver, and lungs.
Makes up the Mononuclear Phagocytic System
(Reticuloendothelial System) - Phagocytosis removes foreign particles from the
lymph as it moves from interstitial spaces to the
blood stream.
50Specific Defenses / Immunity
Scanning electron micrograph of a human
circulating lymphocyte.
51Specific Defenses
- Third line of defense
- Resistance to particular pathogens or to their
toxins or metabolic byproducts - Includes lymphocytes and macrophages that
recognize and remember specific foreign molecules
and carry out immune responses
52Antigens
- May be proteins, polysaccharides, glycoproteins,
or glycolipids located on a cells surface. - Before birth, body cells inventory the proteins
and other large molecules in the body learning
to recognize them as self - Receptors on the lymphocytes surface recognize
and respond to nonself or foreign antigens.
(normally no response to self)
53- Antigens most effective in eliciting an immune
response are large and complex with few repeating
parts. - Hapten smaller molecule that combines with
larger ones to be able to elicit an immune
response. - Found in certain drugs (penicillin), household
and industrial chemicals, dust particles, and
dander.
54Lymphocyte Origins
- During fetal development, red bone marrow
releases undifferentiated lymphocytes into
circulation - Half reach thymus and specialize into T-cells and
become 70-80 of the circulating lymphocytes - Others reside in lymphatic organs (especially
lymphnodes, thoracic duct, and spleen) - Other lymphocytes remain in red bone marrow until
they differentiate into B cells (B lymphocytes) - Blood distributes B cells (20-30 of circulating
lymphocytes) - Settle in lymphatic organs along with T cells.
Abundant in lymph nodes, spleen, bone marrow, and
intestinal linings
Link to step through of bone marrow releasing
lymphocytes
55Bone marrow releases undifferentiated
lymphocytes, which after processing become T
cells (T lymphocytes) or B cells (B lymphocytes).
Note that in the fetus, the medullary cavity
contains red marrow.
56Lymphatic Functions
- Each person has millions of varieties of T and B
cells - The members of each variety have a particular
type of antigen receptor on their cell membranes
that can respond only to a specific antigen. - Clone identical cells originating from the
division of a single cell. - T and B cells respond to antigens in different
ways. - T Cells and the Cellular Immune Response
- B Cells and the Humoral Immune Response
57Cellular Immune Response
- T cells attach to foreign, antigen-bearing cells
(bacteria) and interact directly by cell-to-cell
contact. - Also called Cell-mediated Immunity
- T cells and some macrophages also synthesize and
secrete polypeptides called cytokines
(specifically, lymphokines) that enhance certain
cellular responses to antigens. - Stimulate other T cells to synthesize cytokines
- Help activate T cells
- Cause T cells to proliferate
- Stimulate leukocyte production in red bone marrow
causing B cells to grow and mature and activate
macrophages - T cells may also secrete toxins that kill their
antigen-bearing target cells. - Growth-inhibiting factors that prevent
target-cell growth - Interferon that inhibits the proliferation of
viruses and tumor cells
58T Cell Activation
- A lymphocyte must be activated before it can
respond to an antigen. - T cell activation requires the presence of
processed fragments attached to the surface of an
accessory cell (antigen-presenting cell) such as
a macrophage or a B cell - T cell activation begins when a macrophage
phagocytizes a bacterium, digesting it in its
lysosomes
59- Some bacterial antigens exit lysosomes and move
to the macrophages surface. - Antigens are displayed on the cell membrane near
certain protein molecules called the major
histocompatibility complex (MHC) - Helper T cell becomes activated if it contacts,
fits and combines with a displayed foreign
antigen. - Activated helper T cell stimulates B cell to
produce antibodies specific for the displayed
antigen.
60Link to antigen processing animation
Link to step through of this diagram
T cell and B cell activation. 1.) After digesting
antigen-bearing agents, a macrophage displays
antigens on its surface. 2.) Helper T cells
become activated when they contact displayed
antigens that fit their antigen receptors. 3.) An
activated helper T cell interacts with a B cell
that has combined with an identical antigewn and
causes the B cell to proliferate.
61Cytotoxic T Cell
- Recognizes nonself antigens that cancerous cells
or virally infected cells display on their
surfaces near MHC proteins. - Becomes activated when it combines with an
antigen that fits its receptors. - T cell proliferates, enlarging its clone of cells.
62- Cytotoxic T cells then bind to the surfaces of
antigen-bearing cells and release a protein that
cuts porelike openings, destroying these cells. - Continually monitor body cells, recognizing and
eliminating tumor cells and cells infected with
virus. - Some do not respond to antigen on first exposure
but remain as memory cells which can immediately
differentiate into cytotoxic T cells upon
subsequent exposure to same antigen.
63Humoral Immune Response
- B cells attack foreign antigens in a different
way. - Differentiate into plasma cells which produce and
secrete larger globular proteins called
antibodies or immunoglobins - Body fluids carry antibodies which then react in
various ways to destroy specific antigens or
antigen-bearing particles. (humoral fluid) - Also called Antibody-mediated Immune Response
64B Cell Activation
- B cell becomes activated when it encounters an
antigen whose molecular shape fits the shape of
its receptors. - B cell divides repeatedly expanding its clone.
- Most require T cell help to become activated.
- When activated, helper T encounters B cell that
has already combined with identical foreign
antigen. - Helper T releases cytokines which stimulate B
cell to proliferate and enlarge clone of
antibody-producing cells. - Cytokines also attract macrophages and leukocytes
into inflamed tissues and help keep them there.
65- Some activated B cells clone differentiate
further into memory cells. Memory B cells respond
rapidly to subsequent exposure to a specific
antigen. - Others differentiate into Plasma Cells which
secrete antibodies - Antibodies are similar in structure to the
antigen receptor molecules on the original B
cells surface. - Antibodies can combine with the antigen-bearing
agent that has invaded and react against it. - An individuals B cells can produce an estimated
10mil -1bil different varieties of antibodies.
Each reacting against a specific antigen
(pathogen) - Secrete 2000 identical antibodies/second during
its lifespan - Antibodies are soluble, globular proteins that
constitute the gamma globulin fraction of plasma
proteins.
66Link to step through of this diagram
An activated B cell proliferates after
stimulation by cytokines released by helper T
cells. The B cells clone enlarges. Some cells of
the clone give rise to anti-body-secreting plasma
cells and others to dormant memory cells.
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69Types of Antibodies (immunoglobins)
- Immunoglobulin G (IgG) In plasma and tissue
fluids. Effective against bacteria, viruses, and
toxins. Activates complement - Immunoglobulin A (IgA) Commonly found in
exocrine gland secretions in breast milk,
tears, nasal fluid, gastric juice, intestinal
juice, bile, and urine - Immunoglobulin M (IgM) Develops in blood plasma
in response to contact with antigens in foods or
bacteria. Anti A and Anti B are examples. Also
activates complement
70- Immunoglobulin D (IgD) Found on surfaces of most
B cells, especially infants. Important in
activating B cells. - Immunogloulin E (IgE) Appears in exocrine
secretions along with IgA. Associated with
allergic reactions.
71- Newborn does not yet have its own antibodies.
- Retains IgG passed through placenta from mother.
Protects against some illnesses to which the
mother is immune. - Receive IgA from colostrum, which protects
against certain digestive and respiratory
infections.
72Antibody Actions
- Directly attack antigens
- Activate complement to attack antigens
- Stimulate changes in local areas that help
prevent the spread of antigens
73Direct Attack
- Antibodies combine with antigens and cause them
to clump together (agglutinate) or to form
insoluble substances (precipitate) - Make it easier for phagocytic cells to engulf the
antigen-bearing agents and eliminate them. - Antibodies cover the toxic portions of antigen
molecules and neutralize their effects.
74Complement
- More important than direct attack
- A group of proteins in plasma and other body
fluids - IgG or IgM combine with antigens and expose
reactive sites on antibody molecules, triggering
a series of reactions leading to activation of
complement proteins.
75- Effects of Complement Proteins include
- Coating the antigen-antibody complexes
(opsonization) making them more susceptible to
phagocytosis - Attracting macrophages and neutrophils into
region (chemotaxis) - Clumping antigen-bearing agents
- Rupturing membranes of foreign cells (lysis)
- Altering molecular structure of viruses rendering
them harmless - Promote inflammation which helps prevent the
spread of infectious agents
76Actions of the Complement System
77Immune Responses
- Primary Immune Response
- Secondary Immune Response
78Primary Immune Response
- When B and T cells become activated after first
encountering their matching antigen - Plasma cells release antibodies (IgM, then IgG)
into lymph - Antibodies enter the blood and distribute
throughout body where they help destroy
antigen-bearing agents. - As a result of primary immune response,
detectable concentrations of antibodies usually
appear in the body fluids within 5-10 days
following an exposure to antigens - Continues for several weeks.
79A primary immune response produces a lesser
concentration of antibodies than does a secondary
immune response
80Secondary Immune Response
- Circulating memory B and memory T cells enlarge
clone and respond rapidly with IgG if they come
into contact with the antigen to which they were
previously sensitized. - Body may produce additional antibodies within a
day or two. - Secondary response is faster and produces a
higher antibody concentration - Newly formed antibodies may persist in the body
for a few months or years. Memory cells live much
longer.
81Superantigens
- Foreign antigens that elicit unusually vigorous
lymphocyte responses - Staphylococcus aureus 2 types
- 1 type causes food poisoning until digestive
enzymes destroy it - 2nd type causes toxic shock syndrome. Plummeting
blood pressure, confusion, high fever, diarrhea,
vomiting, potentially fatal
82Practical Classification of Immunity
83Vaccines
- Stimulate active immunity against a variety of
diseases - Consists of
- Bacteria or viruses that have been killed or
weakened so that they cannot cause a serious
infection - A toxoid, which is a toxin from an infectious
organism that has been chemically altered to
destroy its toxic effects - Includes the antigens that stimulate a primary
immune response but does not produce the severe
symptoms of disease.
84- Vaccine distribution is not equitable worldwide.
Some of these disease still pose a serious
threat. - Typhoid fever Cholera Whooping cough
- Diphtheria Mumps Influenza
- Hepatitis B Bacterial pneumonia Smallpox
- Tetanus Polio Chicken pox
- Measles (rubeola) German measles (rubella)
85Allergic Reactions
- An immune attack against a non-harmful substance
- Similar to normal immune response because
lymphocytes are sensitized and antibodies may
bind to antigens. - Unlike normal response because allergic reactions
can damage tissues. - Allergen antigens that trigger allergic
responses.
86Delayed-Reaction Allergy
- Result from repeated exposure of the skin to
certain chemicals commonly household or
industrial chemicals or some cosmetics. - Presence of foreign substance activates T cells
(many of which collect in the skin) - T cells and macrophages they attract release
chemical factors which in turn cause eruptions
and inflammations of the skin (dermatitis) - Delayed takes 48 hours
87Immediate-Reaction Allergy
- Occurs within minutes after allergen contact
- Inherited tendency to overproduce IgE antibodies
in response to certain antigens. (IgE normally
comprises a minute fraction of plasma proteins.) - During initial exposure
- B cells become sensitized
- IgE attaches to the membranes of widely
distributed mast cells and basophils.
88- Subsequent exposures to allergen trigger allergic
reactions and release allergy mediators
histamine, prostaglandin D2, and leukotrienes. - Allergy mediators cause severe inflammation
reaction - Dilation of blood vessels
- Increased vascular permeability that swells
tissues (hives, eczema) - Contraction of bronchial and intestinal smooth
muscles (asthma, gastric disturbances) - Increased mucus production (hay fever)
89Anaphylactic Shock
- Severe form of Immediate-Reaction Allergy
- Mast cells release allergy mediators throughout
the body - Person may feel inexplicable apprehension, then
itchy, red hives, vomiting or diarrhea - Face, tongue, and larynx swell causing breathing
difficulty. Loss of consciousness and death
within 5 minutes. - Treatment injection of epinephrine (adrenalin)
and sometimes tracheotomy (an incision into the
windpipe to restore breathing). - Most often from allergy to penicillin or insect
stings. - Fewer than 100 deaths/year due to prompt medical
attention and avoidance to known allergens.
Link to Video on Allergies
90Transplantation and Tissue Rejection
- Transplantation of tissues or organ can replace a
nonfunctional, damaged, or lost body part. - Ex. Skin, kidney, heart, liver
- Donated organs need to be transplanted quickly
- Heart can last outside body for 3-5 hours.
- Liver can last 10 hours
- Kidney can last 24-48 hours
91Tissue Rejection Reaction
- The danger the immune system poses to
transplanted tissue is that the recipients cell
may recognize the donors tissues as foreign and
attempt to destroy the transplanted tissue. - Rejection resembles the cellular immune response
against a nonself antigen. - The more antigenic difference between recipient
and donor tissues, the more rapid and severe the
rejection reaction. - Matching donor and recipient tissues can minimize
rejection reaction (similar to blood typing
before a transfusion)
92Immunosuppresive Drugs
- Used to reduce rejection of transplanted tissues
- Interfere with recipients immune response by
suppressing formation of antibodies or production
of T cells. Reduces humoral and cellular immune
responses. - Can leave recipient unprotected against
infections. - Not uncommon for patient to survive transplant
but die of infection due to weakened immune
system.
93Autoimmunity
- Attack against self when immune system fails to
distinguish self from nonself. - Producing autoantibodies and cytotoxic T cells
that attack and damage tissues and organs. - Example of autoimmune disorders
- Juvenile diabetes
- Rheumatoid arthritis
- Systemic lupis erythematosis
94Possible Causes of Autoimmunity
- Virus borrows proteins from the host cells
surface while replicating within human cell and
incorporates them onto its own surface. - When immune system learns surface of virus in
order to destroy it, it also learns to attack
human cells that normally bear that protein. - T cells never learned to distinguish self from
nonself. - Nonself antigen coincidentally resembles a self
antigen such as infection by streptococcus
bacteria that triggers inflammation of heart
valves.
95Topics of Interest Immunity Breakdown AIDS
p.382-383
- Infection by the human immunodeficiency virus
(HIV) which causes Acquired Immune Deficiency
Syndrome (AIDS) - Virus attacks lymphocytes by attaching to
receptors on helper T cells and sending in its
RNA - An enzyme called reverse transcriptase
manufactures viral DNA from the RNA which then
directs cell activities to make new viral parts. - Dying T cell can no longer release cytokines or
stimulate B cells. Eventually bursts releasing
new HIV particles - New HIV replicate and overwhelm the immune system.
96- Common AIDS-related conditions include
- Persistent lymphadenopathy (swollen lymph glands)
- Constant low-grade fever
- Nausea and vomiting
- Fatigue
- Night sweats
- Headaches
- Wasting syndrome (persistent diarrhea, severe
weight loss, weakness, fever) - Dementia (confusion apathy, inability to
concentrate, memory loss, insomnia,
disorientation, sudden strong emotions) - Cancers (Kaposi sarcoma, cervical cancer,
lymphoma, others) - Opportunistic infections (pneumonia, brain
infection, diarrhea, spinal meningitis,
tuberculosis, fungal infections, many others)
97- Three Stages of HIV infection
- Initial symptoms
- Acute stage
- Weakness, recurrent fever, night sweats, swollen
neck glands, weight loss - Varies in duration and severity
- Latency period
- Last 5 10 years
- Person feels well although the immune system is
struggling to contain the growing HIV population
in the lymph nodes and then in the blood stream - AIDS
- Opportunistic infections that appear when the
immune system is compromised.
98- Modes of Transmission
- Requires contact with a body fluid containing
abundant HIV such as blood or semen. - Virus has been detected in sweat, tears, and
saliva but levels are so low that transmission is
unlikely. - Whether or not a person becomes infected depends
on - Amount of infected fluid contacted
- Site of exposure in the body
- Individuals health
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100- Progress
- Three groups of people are providing the clues
that may lead to conquering HIV infection - Infected individuals who never develop symptoms
(long-term nonprogressors). Have a weakened
strain of HIV that lacks a gene HIV normally uses
to replicate. Enough of the virus remains to
alert the immune system to protect against other
strains. A vaccine might be based on this
weakened strain. - People exposed repeatedly who never become
infected. 1 of population has gene variant that
protects them from becoming infected by HIV.
Cells of individuals lack either of two receptor
molecules that HIV requires to enter cells. - Infected individuals who apparently become
uninfected. Several infants infected at birth
have lost the virus as their immune system
matured.
101- Research study these groups and use knowledge to
develop prevention and treatment strategies.
102- Treatment
- Drugs target HIV infection at various stages.
- Block viral replication AZT, ddI, ddC, and 3TC
- Protease inhibitors prevent HIV from processing
its proteins to a functional size, crippling the
virus. - Fusion inhibitors block the binding of HIV to T
cell surfaces - Combining drugs can keep viral load low and delay
symptom onset and progression - Viral variants emerge that resist the drugs
- Goal is to enable infected people to live normal
life spans in relatively good health. - More than 200 drugs available to treat
AIDS-associated opportunistic infections and
cancers.
103Also see
- Clinical Connection Scleroderma p 386
- Genetics Connection Conquering Inherited
Immunodeficiency p.384-385
104Clinical Terms Related to the Lymphatic System
and Immunity
105Allograft
Which tissue can be donated and how is it used?
- Transplantation of tissue from an individual of
one species to another individual of that species.
Skin Thin top dermis recovered from the donor's
back, causing no disfigurement and allowing for
open casket viewing Implanted on adults and
children suffering from severe burns, bed sores,
diabetic ulcers and corrective surgical
procedures Skin implantation decreases pain
significantly, provides a barrier against
infection, regulates the body temperature,
prevents body fluid loss and helps clean the
wound.
Corneal Transplant
106Orthopedic Meniscus / Humerus / Hemi-Pelvis /
Femur / Tibia / Patellar Tendon / Tibialis Tendon
/ Quadriceps Tendon / Femoral Condoyle / Achilles
Tendon all recovered with prosthetics
replacements and surgical stitching, causing no
disfigurement and allowing for open casket
viewing Implanted in adults and children for
reconstruction related to trauma, tumors,
degenerative diseases and fractures including
total hip revisions, cervical spinal fusion,
repairs of congenital and traumatic facial
deformity, rotator cuff repair, replacement of
Achilles' tendon and repair of bladder
suspension.
Heart Valves Aortic Valve / Pulmonary Valve /
Mitral Valve / Non-valved Conduit / Pericardial
Patch Material Implanted in adults and
children to replace damaged heart valves
primarily due to congenital heart defects and
infective endocarditis
107Peripheral Nerve Peripheral nerves along the
arms and legs when orthopedic and vascular
tissues are recovered with no disfigurement
allowing for open casket viewing Implanted in
adults and children due to injuries from
collisions, motor vehicle accidents, gun wounds,
fractures, dislocations, lacerations, or some
other form of penetrating trauma including
surgery resulting in major source of disability,
impairing the ability to move muscles or to feel
normal sensations. Repairs and regenerate
peripheral nerves, beginning with relief and
restoring functionality to patients who suffer
PNS injuries due to trauma or surgery.
Vascular Saphenous Vein / Femoral Vein / Artery
/ Superficial Femoral / Vein Valve / Aortoiliac
Graft recovered from inner leg area with surgical
stitching which causes no disfigurement allowing
for open casket viewing Implanted to adults
and children to restore circulation in the heart
and extremities as well as for use for dialysis
access.
108Asplenia
Asplenia refers to the absence ('a-') of normal
spleen function and is associated with some
risks. Asplenia may be congenital (congenital
asplenia), or acquired through surgery
(splenectomy) or through processes that destroy
the spleen, generally through its function to
filter the blood and therefore referred to as
autosplenectomy (eg spherocytosis and sickle-cell
disease). Asplenia increases the risk of
septicaemia from encapsulated bacteria, and can
result in a syndrome known as overwhelming post
splenectomy infection (OPSI) which can kill
within a few hours. In particular patients are at
risk from Pneumococcus, but also Haemophilus
influenzae Meningococcus. To minimise these
risks, antibiotic vaccination protocols have
been established,but are often poorly adhered to
by doctors and patients. The risk to asplenic
patients has been expressed as equivalent for a
child to die in home accident, and for adults
dying in a road traffic accident - so sensible
precautions are needed, but no panic.
109Autograft
- Transplantation of tissue from one part of the
body to another part of the same body.
Skin Graft following Rattlesnake bite (Click to
read whole story)
110Immunocompetence
- Ability to produce an immune response to the
presence of antigens
111Immunodeficiency
- Inability to produce an immune response
112Lymphadenectomy
- Surgical removal of lymph nodes
113Lymphadenopathy
- Enlargement of lymph nodes
114Lymphadenotomy
115Lymphocytopenia
- Too few lymphocytes in blood
116Lymphocytosis
- Too many lymphocytes in blood
117Lymphoma
- Tumor composed of lymphatic tissue
118Lymphosarcoma
- Cancer within the lymphatic tissue
119Splenectomy
- Surgical removal of the spleen
120Splenitis
- Inflammation of the spleen
121Splenomegaly
- Abnormal enlargement of the spleen
122Splenotomy
123Thymectomy
- Surgical removal of the thymus
124Thymitis
- Inflammation of the thymus