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Lymphatic System
•
    lymphatic organs: red bone marrow, thymus gland,
    tonsils, spleen, lymph vessels, and lymph nodes
•
    lymphatic capillaries take up and return excess fluid to
    the bloodstream
•
    lacteals receive lipoproteins and transport them to the
    bloodstream
•
    helps defend body against disease
Lymphatic System
Lymphatic System
Spleen
 •
    Found in all vertebrates
 •
     Mechanical filtration of red blood cells to remove old red
     blood cells
 •
     Active immune response through humoral and cell-
     mediated pathways
Lymphatic System
Thymus
 •
   Also an organ of the immune system
 •
      Active immune response through humoral and cell-
      mediated pathways
  •
      Develops T-lymphocytes from hematopoietic
      progenitor cells
 •
      Thymus begins to atrophy during early teens as its
      stroma begins to get filled with adipose tissues
Lymphatic System
Appendix
 •
   Blind-ended tube connecting to the caecum
 •
      Vestigial organ in humans
  •
      Shrunken remnant of the part of the caecum
Lymphatic System
Appendix
 •
     found in the digestive tracts of many extant
     herbivores
 •
     house mutualistic bacteria which help animals
     digest the cellulose molecules that are found in
     plants
Lymphatic System
Appendix
 •
   may harbour and protect bacteria that are beneficial in
   the function of the human colon
 •
     Appendicitis – inflammation of the appendix
Villi of small intestine, showing blood vessels and lymphatic vessels
Immune System
Recall: BLOOD

Formed elements (45 %) – produced by bone marrow
First Line of Defense
–
    in humans, 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

–
    these secretions contain antimicrobial proteins.
    •   Lysozyme - digests the cell walls of many bacteria
Second Line of Defense
•
     microbes that penetrate the first line of defense face
     the second line of defense, which depends mainly on
     phagocytosis

•
     phagocytic cells called neutrophils constitute about
     60%-70% of all white blood cells

•
     monocytes, about 5% of leukocytes, provide an even
     more effective phagocytic defense



    Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings
Second Line of Defense
macrophage – develop from monocytes (5% of white blood cells)
   – attack foreign microbes by phagocytosis
    – major component of the vertebrate lymphatic system
Second Line of Defense

•
    eosinophils (1.5% of all leukocytes) - for defense
    against large parasitic invaders, such as the blood
    fluke, Schistosoma mansoni
    –
        position themselves against the external wall of a
        parasite and discharge destructive enzymes from
        cytoplasmic granules
Schistosoma mansoni
Second Line of Defense
•
    Natural killer (NK) cells do not attack
    microorganisms directly but destroy virus-infected
    body cells
    –
        also attack abnormal body cells that could become
        cancerous
    –
        mount an attack on the cell’s membrane, causing the
        cell to lyse
Second Line of Defense
•
    some microbes have evolved mechanisms for
    evading phagocytic destruction
    –
        outer capsules
    –
        Mycobacterium tuberculosis are readily engulfed but are
        resistant to lysosomal destruction and can even
        reproduce inside a macrophage
Second Line of Defense
•
    damage to tissue by physical injury or entry of
    microorganisms triggers a localized inflammatory
    response
Second Line of Defense
–
    histamine is released by basophils and mast cells in
    connective tissue


–
    leukocytes and damaged tissue cells also discharge
    prostaglandins and other substances that promote
    blood flow to the site of injury
Second Line of Defense
•
    chemokines secreted by blood vessel endothelial
    cells and monocytes, attract phagocytes to the area

    –
        a group of about 50 different proteins

    –
        bind to receptors on many types of leukocytes

    –
        induce the production of toxic forms of oxygen in
        phagocyte lysosomes and the release of histamine from
        basophils
Second Line of Defense
–
    fever, another systemic response to infection, can be
    triggered by toxins from pathogens or by pyrogens
    released by certain leukocytes


–
    resets the body’s thermostat


–
    higher temperature contributes to defense by inhibiting
    growth of some microbes, facilitating phagocytosis, and
    speeding up repair of tissues
Second Line of Defense
–
    other antimicrobial agents include about 20 serum
    proteins, known collectively as the complement system.
    •   carry out a cascade of steps that lead to lysis of
        microbes
    •   some complement components work with
        chemokines to attract phagocytic cells to sites of
        infection
Second Line of Defense

•
    interferons, - proteins secreted by virus-infected
    cells
    –
        diffuse to neighboring cells and induce them to produce
        other chemicals that inhibit viral reproduction
    –
        limits cell-to-cell spread of viruses
Third Line of Defense
•
    Lymphocytes are the key cells of
    the immune system

•
    two main types of lymphocytes: B
    lymphocytes (B cells) and T
    lymphocytes (T cells)
Third Line of Defense

•
    a foreign molecule that elicits a specific response by
    lymphocytes is called an antigen

•
    Antigens react to specific antibodies that are either
    attached to lymphocytes or are secreted
•
    Antibodies constitute a group of globular serum
    proteins called immunoglobins (Igs)
    –
        a typical antibody molecule has two identical antigen-
        binding sites specific for the epitope that provokes its
        production
–
    an antibody interacts with a small, accessible portion of the
    antigen called an epitope or antigenic determinant
•
    antigen receptors on a B cell are transmembrane
    versions of antibodies and are often referred to as
    membrane antibodies (or membrane immunoglobins)

•
    antigen receptors on a T cell, called T cell receptors,
    are structurally related to membrane antibodies but
    are never produced in a secreted form
•
    there is an enormous variety of B and T cells in the
    body, each bearing antigen receptors of particular
    specificity

•
    this allows the immune system to respond to millions
    of antigens, and thus millions of potential pathogens
•
    although a microorganism encounters a large
    repertoire of B cells and T cells, it interacts only with
    lymphocytes bearing receptors specific for its various
    antigenic molecules
•
    the “selection” of a lymphocyte by one of the
    microbe’s antigens activates the lymphocyte
•
    stimulated to divide and differentiate
•
    produce two clones of cells
        –
            effector cells
        –
            memory cells
•
    clonal selection
•
    the selective proliferation and differentiation of
    lymphocytes that occur the first time the body is
    exposed to an antigen is the primary immune
    response
    –
        selected B cells and T cells generate antibody-producing
        effector B cells, called plasma cells, and effector T cells,
        respectively
•
      a second exposure to the same antigen at some
      later time elicits the secondary immune response
        –
            faster (only 2 to 7 days), of greater magnitude, and more
            prolonged
        –
            antibodies produced tend to have greater affinity for the
            antigen than those secreted in the primary response




    Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings
•
    While B cells and T cells are maturing in the bone
    marrow and thymus, their antigen receptors are
    tested for potential self-reactivity
    –
        capacity to distinguish self from nonself continues to
        develop as the cells migrate to lymphatic organs
    –
        autoimmune diseases
         •   Caused when the immune system mistakes its own cells as
             pathogens and attack them
•
    T cells interact with one important group of native
    molecules

    –
        collections of cell surface glycoproteins encoded
        by a family of genes called the major
        histocompatibility complex (MHC)
–
    Two main classes of MHC molecules mark body
    cells as self:

    •   Class I MHC molecules, found on almost all
        nucleated cells

    •   Class II MHC molecules, restricted to
        macrophages, B cells, activated T cells, and
        those inside the thymus
•
    two main types of T cells, each responds to one
    class of MHC molecule:

    –
        Cytotoxic T cells (TC) have antigen receptors that bind to
        protein fragments displayed by the body’s class I MHC
        molecules


    –
        Helper T cells (TH) have receptors that bind to peptides
        displayed by the body’s class II MHC molecules
(APC)




– Cytotoxic T cells respond by killing the infected cells
– helper T cells send out chemical signals that incite other
-
  cell types to fight the pathogen
Helper T-cell Signal Pathway
•
    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
    –
        this interaction is greatly enhanced by a T surface
        protein CD8 which helps keep the cells together while
        the TC cell is activated
Complement System
Five Classes of Immunoglobulins

            • first to be produced after
              initial exposure to antigen

            • promotes neutralization and
              cross-linking of antigens


            • very effective in complement
              system
Five Classes of Immunoglobulins

            • most abundant Ig in blood

            • present in tissue fluids

            • promotes opsonization,
              neutralization and cross-
              linking of antigens

            • only Ig that crosses placenta
Five Classes of Immunoglobulins

            • present in tears, saliva,
              mucus, and breast milk

            • provides localized defense of
              mucous membranes by
              neutralization and cross-
              linking of antigens
Five Classes of Immunoglobulins

            • present on surface of B cells
              that have not been exposed
              to antigens

            • acts as antigen receptor in the
              antigen-stimulated
              proliferation and
              differentiation of B cells
Five Classes of Immunoglobulins

            • present in blood at low
              concentrations

            • triggers release from mast
              cells and basophils of
              histamine and other
              chemicals that cause allergic
              reactions
52
     Blood Transfusions
Hemolytic Disease of the Newborn
   (Erythroblastosis fetalis)
Summary of Immune Response

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Lecture 6 transport circulation_part 2

  • 1. Lymphatic System • lymphatic organs: red bone marrow, thymus gland, tonsils, spleen, lymph vessels, and lymph nodes • lymphatic capillaries take up and return excess fluid to the bloodstream • lacteals receive lipoproteins and transport them to the bloodstream • helps defend body against disease
  • 3. Lymphatic System Spleen • Found in all vertebrates • Mechanical filtration of red blood cells to remove old red blood cells • Active immune response through humoral and cell- mediated pathways
  • 4. Lymphatic System Thymus • Also an organ of the immune system • Active immune response through humoral and cell- mediated pathways • Develops T-lymphocytes from hematopoietic progenitor cells • Thymus begins to atrophy during early teens as its stroma begins to get filled with adipose tissues
  • 5. Lymphatic System Appendix • Blind-ended tube connecting to the caecum • Vestigial organ in humans • Shrunken remnant of the part of the caecum
  • 6. Lymphatic System Appendix • found in the digestive tracts of many extant herbivores • house mutualistic bacteria which help animals digest the cellulose molecules that are found in plants
  • 7. Lymphatic System Appendix • may harbour and protect bacteria that are beneficial in the function of the human colon • Appendicitis – inflammation of the appendix
  • 8. Villi of small intestine, showing blood vessels and lymphatic vessels
  • 10. Recall: BLOOD Formed elements (45 %) – produced by bone marrow
  • 11.
  • 12. First Line of Defense – in humans, 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 – these secretions contain antimicrobial proteins. • Lysozyme - digests the cell walls of many bacteria
  • 13. Second Line of Defense • microbes that penetrate the first line of defense face the second line of defense, which depends mainly on phagocytosis • phagocytic cells called neutrophils constitute about 60%-70% of all white blood cells • monocytes, about 5% of leukocytes, provide an even more effective phagocytic defense Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings
  • 14. Second Line of Defense macrophage – develop from monocytes (5% of white blood cells) – attack foreign microbes by phagocytosis – major component of the vertebrate lymphatic system
  • 15. Second Line of Defense • eosinophils (1.5% of all leukocytes) - for defense against large parasitic invaders, such as the blood fluke, Schistosoma mansoni – position themselves against the external wall of a parasite and discharge destructive enzymes from cytoplasmic granules
  • 17. Second Line of Defense • Natural killer (NK) cells do not attack microorganisms directly but destroy virus-infected body cells – also attack abnormal body cells that could become cancerous – mount an attack on the cell’s membrane, causing the cell to lyse
  • 18. Second Line of Defense • some microbes have evolved mechanisms for evading phagocytic destruction – outer capsules – Mycobacterium tuberculosis are readily engulfed but are resistant to lysosomal destruction and can even reproduce inside a macrophage
  • 19. Second Line of Defense • damage to tissue by physical injury or entry of microorganisms triggers a localized inflammatory response
  • 20. Second Line of Defense – histamine is released by basophils and mast cells in connective tissue – leukocytes and damaged tissue cells also discharge prostaglandins and other substances that promote blood flow to the site of injury
  • 21. Second Line of Defense • chemokines secreted by blood vessel endothelial cells and monocytes, attract phagocytes to the area – a group of about 50 different proteins – bind to receptors on many types of leukocytes – induce the production of toxic forms of oxygen in phagocyte lysosomes and the release of histamine from basophils
  • 22. Second Line of Defense – fever, another systemic response to infection, can be triggered by toxins from pathogens or by pyrogens released by certain leukocytes – resets the body’s thermostat – higher temperature contributes to defense by inhibiting growth of some microbes, facilitating phagocytosis, and speeding up repair of tissues
  • 23. Second Line of Defense – other antimicrobial agents include about 20 serum proteins, known collectively as the complement system. • carry out a cascade of steps that lead to lysis of microbes • some complement components work with chemokines to attract phagocytic cells to sites of infection
  • 24. Second Line of Defense • interferons, - proteins secreted by virus-infected cells – diffuse to neighboring cells and induce them to produce other chemicals that inhibit viral reproduction – limits cell-to-cell spread of viruses
  • 25. Third Line of Defense • Lymphocytes are the key cells of the immune system • two main types of lymphocytes: B lymphocytes (B cells) and T lymphocytes (T cells)
  • 26. Third Line of Defense • a foreign molecule that elicits a specific response by lymphocytes is called an antigen • Antigens react to specific antibodies that are either attached to lymphocytes or are secreted
  • 27. Antibodies constitute a group of globular serum proteins called immunoglobins (Igs) – a typical antibody molecule has two identical antigen- binding sites specific for the epitope that provokes its production
  • 28. an antibody interacts with a small, accessible portion of the antigen called an epitope or antigenic determinant
  • 29. antigen receptors on a B cell are transmembrane versions of antibodies and are often referred to as membrane antibodies (or membrane immunoglobins) • antigen receptors on a T cell, called T cell receptors, are structurally related to membrane antibodies but are never produced in a secreted form
  • 30.
  • 31. there is an enormous variety of B and T cells in the body, each bearing antigen receptors of particular specificity • this allows the immune system to respond to millions of antigens, and thus millions of potential pathogens
  • 32. although a microorganism encounters a large repertoire of B cells and T cells, it interacts only with lymphocytes bearing receptors specific for its various antigenic molecules
  • 33. the “selection” of a lymphocyte by one of the microbe’s antigens activates the lymphocyte • stimulated to divide and differentiate • produce two clones of cells – effector cells – memory cells • clonal selection
  • 34.
  • 35.
  • 36. the selective proliferation and differentiation of lymphocytes that occur the first time the body is exposed to an antigen is the primary immune response – selected B cells and T cells generate antibody-producing effector B cells, called plasma cells, and effector T cells, respectively
  • 37. a second exposure to the same antigen at some later time elicits the secondary immune response – faster (only 2 to 7 days), of greater magnitude, and more prolonged – antibodies produced tend to have greater affinity for the antigen than those secreted in the primary response Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings
  • 38.
  • 39. While B cells and T cells are maturing in the bone marrow and thymus, their antigen receptors are tested for potential self-reactivity – capacity to distinguish self from nonself continues to develop as the cells migrate to lymphatic organs – autoimmune diseases • Caused when the immune system mistakes its own cells as pathogens and attack them
  • 40. T cells interact with one important group of native molecules – collections of cell surface glycoproteins encoded by a family of genes called the major histocompatibility complex (MHC)
  • 41. Two main classes of MHC molecules mark body cells as self: • Class I MHC molecules, found on almost all nucleated cells • Class II MHC molecules, restricted to macrophages, B cells, activated T cells, and those inside the thymus
  • 42. two main types of T cells, each responds to one class of MHC molecule: – Cytotoxic T cells (TC) have antigen receptors that bind to protein fragments displayed by the body’s class I MHC molecules – Helper T cells (TH) have receptors that bind to peptides displayed by the body’s class II MHC molecules
  • 43. (APC) – Cytotoxic T cells respond by killing the infected cells – helper T cells send out chemical signals that incite other - cell types to fight the pathogen
  • 45. 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 – this interaction is greatly enhanced by a T surface protein CD8 which helps keep the cells together while the TC cell is activated
  • 47. Five Classes of Immunoglobulins • first to be produced after initial exposure to antigen • promotes neutralization and cross-linking of antigens • very effective in complement system
  • 48. Five Classes of Immunoglobulins • most abundant Ig in blood • present in tissue fluids • promotes opsonization, neutralization and cross- linking of antigens • only Ig that crosses placenta
  • 49. Five Classes of Immunoglobulins • present in tears, saliva, mucus, and breast milk • provides localized defense of mucous membranes by neutralization and cross- linking of antigens
  • 50. Five Classes of Immunoglobulins • present on surface of B cells that have not been exposed to antigens • acts as antigen receptor in the antigen-stimulated proliferation and differentiation of B cells
  • 51. Five Classes of Immunoglobulins • present in blood at low concentrations • triggers release from mast cells and basophils of histamine and other chemicals that cause allergic reactions
  • 52. 52 Blood Transfusions
  • 53.
  • 54. Hemolytic Disease of the Newborn (Erythroblastosis fetalis)
  • 55. Summary of Immune Response