an animal must defend itself against...
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• An animal must defend itself against unwelcome
intruders - the many potentially dangerous viruses,
bacteria, and other pathogens it encounters in the
air, in food, and in water.
• 3:00 – How pathogens got everywhere. NPR
• It must also deal with abnormal body cells, which, in
some cases, may develop into cancer, often due to
carcinogens in the environment.
• What is cancer, again?
• How do you think carcinogens cause cancer?
Introduction
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SC.912.L.14.52 Explain the basic functions of the human
immune system, including specific and nonspecific
immune response, vaccines, and antibiotics.
Explain the significance of genetic factors,
environmental factors, and pathogenic agents to health from
the perspectives of both individual and public health.
HE.912.C.1.4 Analyze how heredity and family history can
impact personal health.
HE.912.C.1.8 Analyze strategies for prevention, detection,
and treatment of communicable and chronic diseases.
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Benchmark Clarifications
Students will identify and/or explain the basic functions of the
human immune system, including specific and nonspecific
immune responses.
Students will describe how the human immune system
responds to vaccines and/or antibiotics.
Content Limits Items assessing the significance of genetic
factors, environmental factors, and pathogenic agents to
health are limited to a conceptual understanding.
Stimulus Attribute Scenarios are limited to those commonly
included in a biology course.
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• Three cooperative lines of defense have evolved to
counter these threats.
• Two of these are nonspecific - that is, they do not
distinguish one infectious agent from another.
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Fig. 43.1
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• Intact skin is a barrier that cannot normally be
penetrated by bacteria or viruses, although even
minute abrasions may allow their passage.
• Likewise, the “inside skin” - mucous membranes that
line the digestive, respiratory, and genitourinary
tracts - bar the entry of potentially harmful microbes.
1. The skin and mucous membrane provide
first-line barriers to infection
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• Beyond their role as a physical barrier, the skin
and mucous membranes counter pathogens with
chemical defenses.
• In humans, for example, secretions from sebaceous and
sweat glands give the skin a pH ranging from 3 to 5,
which is acidic enough to prevent colonization by many
microbes.
• Microbial colonization is also inhibited by the washing
action of saliva, tears, and mucous secretions that bathe
the exposed epithelium.
• All these secretions contain antimicrobial proteins.
• One of these, the enzyme lysozyme, digests the cell
walls of many bacteria, destroying them.
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• Mucus, the viscous fluid secreted by
cells of mucous membranes, also traps
microbes and other particles that
contact it.
• In the trachea, ciliated epithelial
cells sweep out mucus with its
trapped microbes, preventing them
from entering the lungs.
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• Microbes present in food or water, or
those in swallowed mucus, must contend
with the highly acidic environment of the
stomach.
• The acid destroys many microbes before
they can enter the intestinal tract.
• One exception, the hepatitis A virus, can
survive gastric acidity and gains access
to the body via the digestive tract.
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• Microbes that penetrate the first line of defense face
the second line of defense, which depends mainly on
phagocytosis, the ingestion of invading organisms
by certain types of white cells.
• Phagocyte function is coupled with an effective
inflammatory response and also with certain
antimicrobial proteins.
2. What if the intruders get past the gates?
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• After a few hours in the blood, some white cells migrate
into tissues and develop into macrophages: large, long-
lived phagocytes.
• These cells extend long
pseudopodia that can attach
to polysaccharides on a
microbe’s surface, engulfing
the microbe by phagocytosis,
and fusing the resulting
vacuole with a lysosome.
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Fig. 43.3
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Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings
Fig. 43.4a
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• Damage to tissue by a physical injury or by the
entry of microorganisms triggers a localized
inflammatory response.
• Damaged cells or bacteria release chemicals
that cause nearby capillaries to dilate and
become more permeable, leading to clot
formation at the injury.
• Increased local blood supply leads to the
characteristic swelling, redness, and heat of
inflammation.
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Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings
Fig. 43.5
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• One of the chemical signals of the
inflammatory response is histamine.
• Histamine triggers both dilation and
increased permeability of nearby capillaries.
• Leukocytes and damaged tissue cells also
discharge prostaglandins and other
substances that promote blood flow to the
site of injury.
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• Enhanced blood flow and vessel permeability have
several effects.
• First, they aid in delivering clotting elements to the
injured area.
• Clotting marks the beginning of the repair process
and helps block the spread of microbes elsewhere.
• Second, this also enhances the migration of phagocytic
cells from the blood into the injured tissues.
• Phagocyte migration usually begins within an hour
after injury.
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• The pus that accumulates at the site of some infections
consists mostly of dead phagocytic cells and the fluid
and proteins that leaked from capillaries during the
inflammatory response.
• This pus is usually absorbed by the body within a few
days. Mmmmm……
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• Fever, another systemic response to infection, can be
triggered by toxins from pathogens or by pyrogens
released by certain leukocytes.
• This resets the body’s thermostat and the higher
temperature helps by inhibiting growth of some
bacteria, facilitating phagocytosis, and speeding up
repair of tissues.
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• Too much of a good thing….
• Certain bacterial infections like MRSA can induce
an overwhelming systemic inflammatory response
leading to a condition known as septic shock.
• Characterized by high fever and low blood pressure,
septic shock is the most common cause of death in U.S.
critical care units.
• Clearly, while local inflammation is an essential step
toward healing, widespread inflammation can be
devastating.
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• While pathogens are under assault by phagocytic
cells, the inflammatory response, and antimicrobial
proteins, they inevitably encounter lymphocytes, the
key cells of the immune system - the body’s third
line of defense.
• Lymphocytes are WBC’s that generate efficient and
selective immune responses that work throughout the
body to eliminate particular invaders.
• This includes pathogens, transplanted cells, and even
cancer cells, which they detect as foreign.
Introduction: specific defense
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• The vertebrate body is populated by two main
types of lymphocytes: B lymphocytes (B cells)
and T lymphocytes (T cells).
• Both types of lymphocytes circulate throughout
the blood and lymph and are concentrated in
the spleen, lymph nodes, and other lymphatic
tissue.
1. Lymphocytes provide the specificity and
diversity of the immune system
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• Because lymphocytes recognize and respond to
particular microbes and foreign molecules, they
are said to display specificity.
• A foreign molecule that elicits a specific
response by lymphocytes is called an
antigen.
• Antigens include molecules belonging to
viruses, bacteria, fungi, protozoa, parasitic
worms, and nonpathogens like pollen and
transplanted tissue.
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• One way that an antigen elicits an immune
response is by activating B cells to secrete proteins
called antibodies.
• Each antigen has a particular molecular shape and
stimulates certain B cells to secrete antibodies that
interact specifically with it.
• Antibodies attach to antigens.
• Now, where do antibiotics fit in to this topic?
• Very confusing in the EOC benchmarks!
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• B and T cells recognize specific antigens through
their plasma membrane-bound antigen receptors.
• A single T or B lymphocyte bears about 100,000
receptors for antigen, all with exactly the same
specificity.
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Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings
Fig. 43.6
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• In this process of clonal selection, each
antigen, by binding to specific receptors
selectively, activates a tiny fraction of
cells from the body’s diverse pool of
lymphocytes.
• This relatively small number of selected
cells gives rise to clones of thousands of
cells, all specific for and dedicated to
eliminating only that antigen.
• Let’s look at animation 43.1.3
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• The selective proliferation and differentiation of
lymphocytes that occur the first time the body is
exposed to an antigen is the primary immune
response.
• Let’s look at it in graph form.
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Fig. 43.7
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• Lymphocytes, like all blood cells,
originate from pluripotent stem cells in
the bone marrow or liver of a
developing fetus.
3. Lymphocyte development gives rise to an
immune system that distinguishes self from
nonself
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• Early lymphocytes are all alike,
but they later develop into T cells
or B cells, depending on where
they continue their maturation.
• Lymphocytes that migrate
from the bone marrow to the
thymus develop into T cells.
• Lymphocytes that remain
in the bone marrow and
continue their maturation
there become B cells.
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Fig. 43.8
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• There are two main types of T cells
• Cytotoxic T cells (TC) have antigen receptors that bind
to protein antigen fragments displayed by infected body
cells.
• Helper T cells (TH) have receptors that bind to antigens
displayed by macrophages that have engulfed a
pathogen and digested it and brought them to their
surface.
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Fig. 43.9
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Copyright © 2002 Pearson Education, Inc., publishing as Benjamin CummingsFig. 43.10
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• Both types of immune responses are initiated by
interactions between antigen-presenting cells (APCs)
and helper T cells.
• The APCs, including macrophages and some B cells, tell
the immune system, via helper T cells, that a foreign
antigen is in the body.
• See animation 43.1.1 por favor.
1. Helper T lymphocytes function in both
humoral and cell-mediated immunity:
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Fig. 43.11
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• Antigen-activated cytotoxic T lymphocytes kill
cancer cells and cells infected by viruses and other
intracellular pathogens.
2. In the cell-mediated response, cytotoxic T
cells counter intracellular pathogens: a
closer look
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• If the cell contains a replicating virus, class I MHC
molecules expose foreign proteins that are
synthesized in infected or abnormal cells to
cytotoxic T cells.
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Fig. 43.12a
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• The death of the infected cell not only
deprives the pathogen of a place to
reproduce, but it also exposes it to
circulating antibodies, which mark it for
disposal.
• Once activated, the TC cells kills other
cells infected with the same pathogen.
Animation 43.1.2
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• In the same way, TC cells defend against malignant
cancerous tumors.
• Because tumor cells carry distinctive molecules not
found on normal cells, they are identified as foreign by
the immune system.
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• B cells and the antibodies they make are the basis
of what is called the humoral response.
• See animation 43.1.4
• Review:
• Antibodies are molecules, not cells. They are made
by B cells, which are lymphocyte type white blood
cells.
• Antigens are molecules, not cells. They stick out of
the surface of pathogens like viruses, and cancer
cells.
• Antibiotics are molecules, not cells, and they aren’t
part of your defense system. They kill only bacteria
cells, unless resistance has evolved. Remember?Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings
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• Immunity conferred by recovering from an infectious disease
such as chicken pox is called active immunity because it
depends on the response of the infected person’s own
immune system.
• Active immunity can be acquired naturally, as above, or
artificially by immunization, also known as vaccination.
Watch the story of the first one.
• Vaccines must include the antigen molecules of the bad
guy so that your immune system is stimulated, but not the
whole bad guy.
1. Immunity can be achieved naturally or artificially
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• Routine immunization of infants and children has dramatically reduced the incidence of infectious diseases such as measles and whooping cough, and has led to the eradication of smallpox, a viral disease.
• Unfortunately, not all infectious agents are easily managed by vaccination, and there are dangers such as the risk of being infected by the vaccine as well as side effects such as were suspected with vaccines causing autism.
• This however, has been shown by many studies with thousands of subjects to NOT BE TRUE!!!!
• See what happens when you don’t understand science? Measles in California, 2015. 15 min.
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• Antibodies can be transferred from one individual
to another, providing passive immunity.
• This occurs naturally when antibodies of a pregnant
woman cross the placenta to her fetus.
• In addition, antibodies are passed from mother to
nursing infant in breast milk.
• Passive immunity persists as long as these antibodies
last, a few weeks to a few months.
• This protects the infant from infections until the
baby’s own immune system has matured.
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• Passive immunity can be transferred artificially by
injecting antibodies from an animal that is already
immune to a disease into another animal.
• This confers short-term, but immediate protection against
that disease.
• For example, a person bitten by a rabid animal may be
injected with antibodies against rabies virus because
rabies may progress rapidly, and the response to an active
immunization could take too long to save the life of the
victim.
• Actually, most people infected with rabies virus are given
both passive immunizations (the immediate fight) and
active immunizations (longer term defense).
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• In addition to attacking pathogens, the immune
system will also attack cells from other individuals.
• For example, a skin graft from one person to a
nonidentical individual will look healthy for a day or two,
but it will then be destroyed by immune responses.
• We all have different molecules on the surfaces of our
cells. Another person’s will be recognized as a foreign
pathogen by your immune system.
2. The immune system’s capacity to distinguish
self from nonself limits blood transfusion and
tissue transplantation
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• In ABO blood groups, a person with type A blood has
A antigens on the surface of red blood cells.
• This is not recognized as an antigen by the “owner,”
but it can be identified as foreign if placed in the
body of another individual.
• B antigens are found on type B red blood cells.
• Both A and B antigens are found on type AB red blood
cells (an example of codominance, remember).
• Neither antigen is found on type O red blood cells.
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• A person with type A blood already has antibodies
to the B antigen, even if the person has never been
exposed to type B blood.
• These antibodies arise in response to bacteria that have antigens very similar to blood group antigens.
• Thus, an individual with type A blood does not make antibodies to A-like bacterial antigens - these are considered self - but that person does make antibodies to B-like bacterial antigens.
• If a person with type A blood receives a transfusion of type B blood, the preexisting anti-B antibodies will induce an immediate and devastating transfusion reaction.
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• Allergies are when a non-dangerous substance like
pollen triggers the inflammatory response.
• High levels of histamines cause dilation and
increased permeability of small blood vessels.
• These inflammatory events lead to typical allergy
symptoms: sneezing, runny nose, tearing eyes, and
smooth muscle contractions that can result in breathing
difficulty.
• Antihistamines diminish allergy symptoms by blocking
receptors for histamine.
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• Sometimes the immune system loses tolerance for self and
turns against certain molecules of the body, causing one of
many autoimmune diseases; your immune system attacks
your own cells.
• Rheumatoid arthritis leads to damage and painful
inflammation of the cartilage and bone of joints.
• In insulin-dependent diabetes mellitus, the insulin-
producing beta cells of the pancreas are the targets of
autoimmune cell-mediated responses.
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• Multiple sclerosis (MS) is the most
common chronic neurological disease in
developed countries,
• In MS, T cells reactive against myelin,
a kind of fatty covering of some nerve
cells, infiltrate the central nervous
system and destroy the myelin of
neurons.
• People with MS experience a number
of serious neurological abnormalities.
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• In 1981, increased rates of two rare diseases, Kaposi’s sarcoma, a cancer of the skin and blood vessels, and pneumonia caused by the protozoan Pneumocystis carinii, were the first signals to the medical community of a new threat to humans, later known as acquired immunodeficiency syndrome, or AIDS.
• Both conditions were previously known to occur mainly
in severely immunosuppressed individuals.
• People with AIDS are susceptible to opportunistic
diseases.
4. AIDS is an immunodeficiency disease
caused by a virus
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• In 1983, a retrovirus, now called human
immunodeficiency virus (HIV), had been identified as the
causative agent of AIDS. Here’s how it works
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Fig. 43.19
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• With the AIDS mortality close to 100%,
HIV is the most lethal pathogen ever
encountered.
• Molecular studies reveal that the virus
probably evolved from another HIV-like
virus in chimpanzees in central Africa
and appeared in humans sometimes
between 1915 and 1940.
• These first rare cases of infection and
AIDS went unrecognized.
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Fig. 43.20
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• After an initial peak, virus levels in the blood fall
as anti-HIV antibodies, produced 1 to 12 months
after infection, rise.
• A person who is HIV-positive is infected, having tested
positive for the presence of antibodies to the virus, but it
is not very active yet. This lasts for an average of 10
years.
• When they become active, the HIV start killing helper T
cells, and effectively destroy the immune system.
• Death comes not from HIV directly, but from some
other pathogen that you can’t fight off anymore.
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• At this time, HIV infection cannot be cured, and the progression
to AIDS cannot be prevented.
• New, expensive drug therapies can slow this progression.
• These drugs slow viral replication by inhibiting DNA
synthesis, reverse transcriptase, and protease.
• Protease inhibitors prevents a key step in the synthesis of
HIV proteins.
• Combinations of these drugs decrease viral load and
therefore allow the number of helper T cells to rise.
• Other drugs treat the myriad of opportunistic diseases as
they develop. Good time for a video clip, eh?
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• Transmission of HIV requires the transfer of body
fluids containing infected cells, such as semen or
blood, from person to person, because HIV dries out
and “dies” when in the open air. Luckily.
• Unprotected sex is the main way HIV is transmitted. Just what is “protected” sex?
• In Africa and Asia, transmission has been primarily by heterosexual sex, especially where there is a high incidence of genital sores from other diseases.
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• HIV is not transmitted by casual contact.
• Transmission of HIV from mother to child can occur
during fetal development or during nursing.
• HIV screening has virtually eliminated blood
transfusions as a route of transmission in developed
countries, but shared needles among drug users is still a
cause of transmission.
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Herd immunity occurs when a high enough percentage of a
population becomes protected against a disease so that the
disease cannot spread in that population. Which of the
following is the best example of herd immunity?
A. A school reduces the number of colds in children by encouraging frequent hand-washing
B. Polio is unknown in the Americas today because most children receive polio vaccines
C. Employees at a company are encouraged to get flu shots to avoid becoming sick and missing work
D. A county sprays trees to kill mosquitoes in order to prevent people from becoming sick after being bitten
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Many diseases have been nearly eliminated because of
widespread vaccination. How do vaccines help the body to
resist disease?
A. They alter the shapes of antigens
B. They stimulate the production of antibodies
C. They kill bacteria or prevent them from
reproducing
D. They transfer antibodies from one organism to
another
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Antibiotics can be used to treat some infectious
diseases. Which pathogens cause these diseases?
A. Bacteria
B. Viruses
C. Toxins
D. Fungi
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By which process can a person acquire
active immunity to a disease?
A. Healthy eating
B. Treatment with antibiotics
C. Vaccination
D. Following hygienic procedures