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Chapter 7: Cellular response in defence.

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Title: Chapter 7: Cellular response in defence.


1
Chapter 7 Cellular response in defence.
  • Higher Human

Unit 1 Cell Function and Inheritance
2
Learning Intentions
  • You should be able to describe self and non-self
    antigens as in ABO blood group system.
  • You should be able to explain the production of
    antibodies and the role of blood cells.
  • Describe phagocytosis and the function of
    lysosomes.
  • Know the differences between innate, acquired,
    active and passive immunity.
  • Describe what is meant by auto immunity and what
    causes allergy in the body.

3
Previous knowledge
  • Every body cell has a membrane
  • There are proteins in and on this membrane
    (phospholipid bi-layer)
  • What are the 6 functions of these proteins?
  • What is an immune system?

4
THE IMMUNE SYSTEM
  • We all get sick sometimes...but then we get
    better.
  • What happens when we get sick?
  • Why do we get better?

5
Cellular Defence
  • We are constantly surrounded by an almost
    infinite number of micro-organisms on surfaces,
    airborne, inside us, on our skin, in food,
    clothing. Everywhere.

VIRUSES
FUNGI
BACTERIA
6
Random facts about bacteria
  • There are typically 40 million bacterial cells in
    a gram of soil and a million bacterial cells in a
    millilitre of fresh water in all, there are
    approximately five nonillion (51030) bacteria on
    Earth, forming much of the world's biomass
  • You can fit thousands upon thousands of bacteria
    on a pinhead.
  • There are approximately ten times as many
    bacterial cells in the human flora of bacteria as
    there are human cells in the body, with large
    numbers of bacteria on the skin and as gut flora.

7
Random facts cont
  • One survey found 20,000 species of bacteria in a
    litre of seawater.
  • The number of scientifically recognized species
    of animals is about 1,250,000 (most are insects).
    There are almost 300,000 recognized species of
    plants. There are an estimated 10-100 million
    different species of bacteria.

8
back to Cellular Defence.
  • Most micro-organisms are actually harmless, but a
    few species can cause disease if they enter our
    bodies and grow to sufficient numbers.
  • We call these microbes pathogens.
  • Of all the species of bacteria, only about 30
    are pathogenic. And only a small percentage of
    that 30 can cause harm to human hosts.

9
So what is an immune system?
  • Immunity is the ability of the body to resist
    infection by a disease causing organism
    (pathogen) o to overcome the organism if it
    succeeds in invading and infecting the body.
  • Immunity can be
  • INNATE (non-specific) or
  • ACQUIRED (specific)

10
IMMUNITY
INNATE (nonspecific)
ACQUIRED (Specific)
Skin, HCl, cilia, mucus etc.
ACTIVE
PASSIVE
ARTIFICIAL
NATURAL
ARTIFICIAL
NATURAL
Antibodies self made after vaccination. E.g.
polio, measles.
Antibodies pre-made by mother breastmilk,
across placenta. Various antibodies.
Antibodies self made after infection. E.g.
Chickenpox, flu
Antibodies pre-made by other organism such as a
horse. E.g. tetanus
11
INNATE IMMUNITY Nonspecific
When you were born, you brought with you several
mechanisms to prevent illness. This type of
immunity is also called nonspecific immunity.
  • Innate immunity consists of
  • Outer barriers
  • Cellular response
  • phagocytosis
  • inflammatory reaction
  • NK (natural killer) and mast cells
  • Soluble factors

12
INNATE IMMUNITY INBORN and UNCHANGING
  • Nonspecific - the same response works against
    many pathogens.
  • This type of response is the same no matter how
    often it is triggered.
  • The types of cells involved are
    macrophages/neutrophils, natural killer cells,
    and mast cells.

13
INNATE IMMUNITY The barriers
  • Physical
  • skin
  • hair
  • mucous
  • Chemical
  • sweat
  • tears
  • saliva
  • stomach acid
  • urine

14
Inflammatory response
INNATE IMMUNITY Cellular response
  • chemical and cell response to injury or
    localized infection
  • eliminates the source of infection
  • promotes wound healing

Step 1. Circulation to the site increases ?
tissue warm, red and swollen Step 2. WBCs leak
into tissues ? phagocytes engulf and destroy
bacteria
15
Inflammatory response (contd)
INNATE IMMUNITY Cellular response
Fevers have both positive and negative effects on
infection and bodily functions
  • POSITIVE
  • indicate a reaction to infection
  • stimulate phagocytosis
  • slow bacterial growth
  • increases body temperature beyond the tolerance
    of some bacteria
  • decreases blood iron levels
  • NEGATIVE
  • extreme heat ? enzyme denaturation and
    interruption of normal biochemical reactions
  • gt 39 C (103F) is dangerous
  • gt 41C (105F) could be fatal and requires
    medical attention

16
Phagocytosis Cell Eating
  • When foreign cells such as bacteria and viruses
    invade the human body the body will respond by
    attacking them.
  • This is done by white blood cells.
  • Types of phagocytic white blood cells are
  • Monocytes
  • Macrophages engulf pathogens and dead cell
    remains.
  • Neutrophils release chemicals that kill nearby
    bacteria.

17
The reason for PUS
During an infection hundreds of white cells
migrate to the infected area and engulf the
infected bacteria by phagocytosis. Phagocytes and
and dead pathogens accumulate causing PUS
18
Phagocyte migration
CELLS alive!
Neutrophils and macrophages recognise chemicals
produced by bacteria in a cut or scratch and
migrate "toward the smell". Here, neutrophils
were placed in a gradient of a chemical that is
produced by some bacteria. The cells charge out
like a "posse" after the bad guys.
19
Macrophages
  • WBCs that ingest bacteria, viruses, dead cells,
    dust.
  • Most circulate in the blood, lymph and
    extracellular fluid.
  • They are attracted to the site of infection by
    chemicals given off by dying cells.
  • After ingesting a foreign invader, they wear
    pieces of it called antigens on their cell
    membrane receptors this tells other types of
    immune system cells what to look for.

20
Macrophage and E. coli
21
Macrophage ingesting yeast
CELLS alive!
This human macrophage, like the neutrophil, is a
professional "phagocyte" or eating cell (phago
"eating", cyte "cell"). Here, it envelops
cells of a yeast, Candida albicans
22
Neutrophils
  • WBCs are phagocytic, like macrophages
  • neutrophils also release toxic chemicals that
    destroy everything in the area, including the
    neutrophils themselves

23
Neutrophil phagocytosing S. pyogenes, the cause
of strep throat
Human neutrophils are WBCs that arrive quickly at
the site of a bacterial infection and whose
primary function is to eat and kill bacteria.
This neutrophil is ingesting Streptococcus
pyogenes.
24
Neutrophil killing yeast
NEUTROPHIL
?
YEAST ?
One way that neutrophils kill is by producing an
anti-bacterial compound called superoxide
anion, a process called oxidative burst. Here,
a neutrophil senses, moves toward and ingests a
yeast. In the next two panels, oxidation can be
seen by using a dye.
25
Phagocytosis summary
  • A phagocyte detects chemicals released by the
    bacterium and moves along a concentration
    gradient (low to high).
  • The phagocyte attaches to the bacterium and
    engulfs it in a vacuole formed by an infolding
    cell membrane.
  • The phagocyte has organelles called LYSOSOMES
    which contains digestive enzymes.

26
Surround and attack!
  • What happens when the bacteria is under attack?
  • White blood cells senses bacteria.
  • White blood cell moves towards bacteria.
  • White blood cell begins to surround bacteria.
  • White blood cell surrounds bacteria.
  • White blood cell kills bacteria.

27
The stages of attack.
28
IMMUNITY
INNATE (nonspecific)
ACQUIRED (Specific)
Skin, HCl, cilia, mucus etc.
ACTIVE
PASSIVE
ARTIFICIAL
NATURAL
ARTIFICIAL
NATURAL
Antibodies self made after vaccination. E.g.
polio, measles.
Antibodies pre-made by mother breastmilk,
across placenta. Various antibodies.
Antibodies self made after infection. E.g.
Chickenpox, flu
Antibodies pre-made by other organism such as a
horse. E.g. tetanus
29
Remember immunity can be
  • Immunity can be
  • INNATE (non-specific) we have just done this so,
    ........... On to
  • ACQUIRED (specific) IMMUNITY

30
  • Your moms antibodies were effective for just a
    short time at birth, but your innate immune
    system can be activated quickly. It is always
    your first line of defense during an infection,
    but it cant always eliminate the germ.
  • When this happens, your body initiates a focused
    attack against the specific pathogen that is
    causing the infection. This attack may lead to
    long-term protection against that pathogen.
  • This type of immunity is called acquired
    immunity, the customized second line of defense.

31
Acquired immunity Depends on the action of
antibodies to combat antigens
  • Acquired immunity can be split into a further 2
    groups
  • PASSIVE (antibodies made by another organisms
    i.e. mother, horse)
  • ACTIVE (self production of antibodies)
  • Each with a natural and an artificial aspect to
    them.

32
Antigens
  • An antigen is a complex molecule such as protein
    or polysaccharide which is recognised as alien by
    LYMPHOCYTES (type of wbc).
  • The presence of an antigen stimulates WBCs to
    produce special protein molecules called
    antibodies

33
Antibodies
  • An antibody is a Y-shaped molecule.
  • Each of its arms bears a receptor binding site
    which is specific to a particular antigen.
  • The body has 1000s of different types of
    lymphocytes each capable of responding to one
    specific antigen and producing the appropriate
    antibody.

34
IMMUNITY
INNATE (nonspecific)
ACQUIRED (Specific)
Skin, HCl, cilia, mucus etc.
ACTIVE
PASSIVE
ARTIFICIAL
NATURAL
ARTIFICIAL
NATURAL
Antibodies self made after vaccination. E.g.
polio, measles.
Antibodies pre-made by mother breastmilk,
across placenta. Various antibodies.
Antibodies self made after infection. E.g.
Chickenpox, flu
Antibodies pre-made by other organism such as a
horse. E.g. tetanus
35
Natural acquired immunity
  • Acquired active natural.
  • Acquired passive natural.
  • Both of these types of immunity require
    antibodies which are produced by LYMPHOCYTES.
    These are made in bone marrow.
  • There are two types of lymphocyte.
  • T-lymphocyte (T-cells) from the thymus
  • B-lymphocytes (B-cells) from other places.

36
Acquired immunity Natural - B lymphocytes
  • The antibodies are made by B-lymphocytes.
  • In the presence of antigens, the B-cells will
    multiply to produce many antibodies.
  • After the infection some of these B-cells will
    remain to serve as memory cells ready to
    respond more quickly if body is exposed to same
    antigens.

37
  • The production of extra-cellular molecules
    (antibodies) that deal with specific foreign
    material is called a HUMORAL RESPONSE.
  • B-lymphocytes are matured in the bone marrow.
  • Leukaemia.

38
T-Lymphocytes Helper T cells
  • These do not kill pathogens directly.
  • These cells patrol the body, and on recognising
    foreign antigens, the activate killer T cells, B
    cells and macrophages.

Helper T-cell  the judge that identifies germs
and orders their destruction
39
Acquired immunity Natural - T lymphocytes
  • The second type of Lymphocytes are T-Lymphocytes
  • AKA killer T cells.

40
T-Lymphocytes Killer T cells
  • A killer T cell will attack and destroy body
    cells (self antigen markers) that signal (by
    foreign antigens) that they have been invaded by
    a pathogen.

Killer T-cell  Kills germs.
  • The T cell releases a chemical to destroy the
    cell and the pathogen in it.
  • This is called a CELL MEDIATED RESPONSE

41
Immunological memoryPrimary and secondary esponse
  • Primary response after seeing a pathogen for
    the first time it takes a while before enough
    antibodies are found in the bloodstream. The
    infected person usually still gets sick.
  • Secondary response happens when there is
    another exposure to the same antigen. Antibody
    production is rapid, and a higher concentration
    is reached and maintained for a longer time. Here
    disease is usually prevented.

42
Immunological memory -memory cells
  • Following the first exposure to the antigen, some
    B- and T-lymphocytes specific to the antigen
    remain in the body as memory cells.
  • If exposed to the pathogen again memory cells
    quickly produce clones of antibody forming
    B-cells and Killer T-cells
  • HERE THE PERSON HAS AQUIRED IMMUNITY IN A NATURAL
    WAY!

43
Immunological memory -memory cells
44
Essay Question 2002
  • Give an account of immunity under the following
    headings.
  • B-lymphocytes and T-Lymphocytes (7)
  • Macrophages (3)

45
IMMUNITY
INNATE (nonspecific)
ACQUIRED (Specific)
Skin, HCl, cilia, mucus etc.
ACTIVE
PASSIVE
ARTIFICIAL
NATURAL
ARTIFICIAL
NATURAL
Antibodies self made after vaccination. E.g.
polio, measles.
Antibodies pre-made by mother breastmilk,
across placenta. Various antibodies.
Antibodies self made after infection. E.g.
Chickenpox, flu
Antibodies pre-made by other organism such as a
horse. E.g. tetanus
46
NATURAL PASSIVE IMMUNITY
Natural Antibodies from mother passes into
babys blood via breast milk or across the
placenta. This is temporary until babys own
immune system develops.

While your immune system was developing, you were
protected antibodies. These antibodies traveled
across the placenta from the maternal blood to
the fetal blood.
  • Antibodies (Y) are also found in breast milk.
    The antibodies received through passive immunity
    last only several weeks.

47
Essay Question 2009
  • 2. A. Describe how immunity is naturally
    acquired. (10).

48
IMMUNITY
INNATE (nonspecific)
ACQUIRED (Specific)
Skin, HCl, cilia, mucus etc.
ACTIVE
PASSIVE
ARTIFICIAL
NATURAL
ARTIFICIAL
NATURAL
Antibodies self made after vaccination. E.g.
polio, measles.
Antibodies pre-made by mother breastmilk,
across placenta. Various antibodies.
Antibodies self made after infection. E.g.
Chickenpox, flu
Antibodies pre-made by other organism such as a
horse. E.g. tetanus
49
Artificial Aquired immunity.....Active
  • Artificial Vaccinations. Forced exposure to a
    dead pathogen. This exposure introduces the
    white blood cells to the antigens so they can
    produce antibodies. Memory cells remain,
    allowing a secondary response in needed.
  • Small pox vaccine is a harmless form of the
    pathogen
  • Polio vaccine is a weakened form of the vaccine.
  • Cholera vaccine is a dead microbe whose antigens
    are unaltered.

50
Vaccines cont
  • No matter how the vaccine is made or what it
    contains, its job is to promote production of B
    and T cells and the formation of antibodies.....
    Then some will persist as memory cells.
  • HERE A PERSON ACQUIRED IMMUNITY BY ARTIFICIAL
    MEANS!

51
IMMUNITY
INNATE (nonspecific)
ACQUIRED (Specific)
Skin, HCl, cilia, mucus etc.
ACTIVE
PASSIVE
ARTIFICIAL
NATURAL
ARTIFICIAL
NATURAL
Antibodies self made after vaccination. E.g.
polio, measles.
Antibodies pre-made by mother breastmilk,
across placenta. Various antibodies.
Antibodies self made after infection. E.g.
Chickenpox, flu
Antibodies pre-made by other organism such as a
horse. E.g. tetanus
52
Acquired immunity -Passive
  • Artificial antibodies made by a non related
    organism, usually a different species such as a
    horse, are injected into bloodstream. This only
    lasts a few years. E.g. tetanus.

53
Essay Question 2001
  • Give an account of immunisation under the
    following headings.
  • Artificial active immunity. (6)
  • Artificial passive immunity (2)
  • The impact of vaccination on childhood diseases.
    (2)

54
TASK Testing you knowledge!
  • Complete Torrance Pg 56 Questions 1-3

55
CO-OPERATIVE TASK
  • Social goal Equal participation
  • Academic goal Describe what is meant by active
    immunity and passive immunity and give natural
    and artificial examples.

56
TASK Essay question
  • Give an account of specific immunity (10)

57
TASK Essay question, on Scholar
  • Give an account of the role of lymphocytes in the
    immune system.(10)

58
Expected Answer
  • B-lymphocytes (4 marks)
  • B-lymphocytes mature in the bone marrow
  • They produce specific antibodies
  • to foreign (or non-self) antigens
  • The response of B-lymphocytes is called the
    humoral response (because the antibodies have
    their effects away from the B-lymphocytes)
  • (After the initial response) memory cells remain
    in the body
  • The memory cells cause a faster/stronger
    secondary immune response (on subsequent exposure
    to the pathogen)
  • T-lymphocytes (4 marks)
  • T-lymphocytes mature in the thymus
  • The antigens on infected cells are changed and
    recognised as foreign antigens by T-lymphocytes
  • The T-lymphocytes destroy the infected cells
    directly
  • This is known as the cell-mediated response
  • (After the initial response) memory cells remain
    in the body
  • The memory cells cause a faster/stronger
    secondary immune response (on subsequent exposure
    to the pathogen)
  • Coherence (1 mark)
  • One mark is given if sub-headings are used, or
    points placed correctly in two groups.
  • Relevance (1 mark)
  • One mark is deducted if macrophages are
    discussed.
  • Marks for points 5. and 6. of T-lymphocytes
    cannot be given if they have already been given
    for points 5. and 6. in B-lymphocytes.

59
What makes us sick?
  • Enemies in the environment in the form of
    microbes and chemicals are constantly attacking
    our bodies, disrupting homeostasis
  • Smetimes immune system homeostasis is disrupted
    on its own

?
?
it may over-react to antigens such as with
allergies
it may react to self proteins as with autoimmune
disease
?
it may under-react as with human
immunodeficiency virus infection (HIV)
60
Allergies
  • Allergies are basically an overreaction by the
    immune system to a harmless foreign material.
  • There are several types of allergic reactions
    sneezing, wheezing, watering, running nose,
    itching, coughing, swelling, anaphylaxis

61
  • There are many substances that cause to these
    over reactions pollen, dust, dust mites, foods,
    feather fibres, antibiotics, insect bites
  • Hayfever is an allergy. The allergen (pollen)
    causes the B cells to release antibodies which
    attach to tissues leading to the release of a
    chemical called histamine.
  • Histamine is responsible for nasal congestion,
    running nose, constriction of airways etc.

62
Self and Non-self
  • Membranes have a unique combination of surface
    proteins that are specific to an individual
    (except identical twins).

These proteins are called antigens. The immune
system recognises this antigenic signature and
so knows that these cells belong to self.
63
Non-self
  • Cells that do not have this unique combination of
    antigens are recognised as foreign or non-self
    and will then be attacked by the immune system.

64
ABO Blood Grouping
  • Blood is made from
  • PLASMA (liquid part, clear)
  • RBCs (carry oxygen, makes blood red, have no
    nucleus but do have a membrane)
  • WBCs (far fewer in number, part of immune
    system)
  • Human blood is not as simple as just that.
  • There are different types and these variations
    cannot be overlooked.

65
Blood grouping
  • RBC membranes, like all other cells, have a
    protein signature (antigens).
  • There are 4 main blood groups

66
Blood transfusions save many lives.
  • However, the blood of the donor has to be
    compatible with that of the patients.
  • For e.g. If a patient who has blood group A
    receives blood from a donor with blood group B
    then

.
Antibodies in the plasma will attack the RBCs
(as they have B antigens).
The patients anti-B
67
The patient recognises the donors B antigens as
non-self.
  • Antibodies in the plasma will attack the RBCs
    (as they have B antigens).
  • This results in the blood clumping/thickening
    (agglutination) therefore clogging up blood
    vessels.
  • AGGLUTINATON
  • of the blood

68
So when are groups compatible
35
11
3
51
69
Tissue Rejection
70
Tissue Rejection cont
  • When living organs/tissues are transplanted from
    one organism to another, they are recognised as
    foreign by the receiver.
  • As a result their immune system will target these
    cells and destroy the new organ.
  • This attempt to destroy the foreign tissue is
    called tissue rejection.

71
Tissue Rejection can be prevented with
IMMUNOSUPPRESORS
  • Transplants can be successful if the donor is
    genetically very similar to the recipient.
  • IMMUNOSPPRESSOR drugs are then administered.
    This will inhibit/weaken the patients immune
    system so it is less able to destroy the new
    tissue.
  • This, however, puts the patient at a much higher
    risk of contracting diseases/infections such as
    pneumonia.

72
Autoimmunity
AUTOIMMUNITY Why does the immune system attack
the body that its supposed to protect?
  • Autoimmunity is a malfunction of the immune
    system where it starts to attack cells with self
    antigens. In other words the body attacks its
    own cells.
  • Examples of autoimmune diseases
  • Rheumatoid Arthritis
  • IS attacks cartilage tissue between joints. It
    is eventually replaced, but by fibrous tissue,
    making the joint immovable.
  • Multiple Sclerosis
  • Nerve cells are attacked leading to poor
    transmission of nerve impulses therefore various
    disabilities.

73
TASK Testing you knowledge!
  • Complete Torrance Pg 59 Questions 1-4

74
WHAT CAN YOU DO TO HELP YOUR IMMUNE SYTSEM?
Exercise and stress
  • Exercise has been shown to boost the immune
    response
  • moderate exercise increases the immune response
    in all age groups
  • intensive exercise can stress the immune system
  • Lack of sleep and exhaustion decrease immune
    function
  • Psychological stress has also been found to
    decrease immune function

75
Diet
  • A well-balanced diet is essential for good immune
    system health
  • fats are very important in the production of
    WBCs, cytokines and natural killer cells
  • selenium, zinc, and copper are required in small
    amounts, which you get if you eat a balanced diet
  • vitamin E has been shown to boost antibody
    production in the elderly
  • vitamin B6 aids in antibody synthesis
  • But mega-dosing can be harmful, too!

76
Environment
Exposure to certain things in their environment
may activate the immune systems of some people
  • Chemicals
  • dioxin
  • pesticides
  • solvents
  • Sunlight
  • Medication
  • Viruses
  • Bacteria
  • Food

77
Acquired immunodeficiency syndrome (AIDS)
  • First identified in 1981 - Caused by the human
    immunodeficiency virus (HIV) and is spread by
    contact with body fluids.
  • Infects CD4 (helper) T cells, which decrease in
    number.
  • Decreased numbers of CD4 T cells lead to
    increased susceptibility to opportunistic
    infections.
  • Treatments include drugs that inhibit the
    activity of HIV proteins, thereby preventing
    production of the virus

Worldwide HIV infection, 1999
HIV virus particle
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