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Animals: Immunity Defenses Against Disease Outline 1. Key concepts 2. Physical barriers: Skin, Mucus and HCL in stomach 3. Non-specific 4. Specific responses – Immune System a. Components of Immune system b. Immune responses 5. Defenses Enhanced (Vaccines and allergies) 6. AIDS (acquired immune deficiency syndrome) 7. Conclusions Key Concepts: 1. Vertebrates have physical, chemical, and cellular defenses against pathogenic organisms, tumors, and other agents 2. In the early stages of invasion and damage, white blood cells escape from capillaries and execute a counter attack 3. Some white blood cells make immune responses

Defenses Against DiseaseNonspecific Defenses – First Line Nonspecific internal Defenses 1.Phagocytic cells a. Neutrophils and macrophages (developed from monocytes) engulf and digest

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  • Animals: Immunity

    Defenses Against Disease

    Outline1. Key concepts2. Physical barriers: Skin, Mucus and HCL in

    stomach3. Non-specific4. Specific responses – Immune System

    a. Components of Immune systemb. Immune responses

    5. Defenses Enhanced (Vaccines and allergies)6. AIDS (acquired immune deficiency

    syndrome)7. Conclusions

    Key Concepts:1. Vertebrates have physical, chemical, and

    cellular defenses against pathogenic organisms, tumors, and other agents

    2. In the early stages of invasion and damage, white blood cells escape from capillaries and execute a counter attack

    3. Some white blood cells make immune responses

  • Key Concepts:

    4. The antigen triggers an immune response5. One type of immune response involves the

    production of antibodies6. Another type of immune response involves

    whole cell responses

    Three Lines of DefensePathogens

    Viruses, bacteria, fungi, protozoa, parasitic worms

    1.Surface barriersSkin, Mucus and HCL in stomach

    2.Nonspecific responses3.Immune responses

    Three Lines of Defense

  • Nonspecific Defenses – First Line1. Skin: a. cells – Prevent entry of pathogens

    b. glands (oil and sweat pH 3-5, discourages microbial growth)

    c. earwax – trap microorganisms2. Mucous membranes - trap pathogens3. Hair & hair-like structures (cilia)

    filter air (nasal hairs)transport mucus

    4. Acid: a. stomach b. vagina (limits growth of fungi and bacteria)

    5. Saliva, tears with lysozyme (enzyme attacks the cell walls of many bacteria)

    6. “harmless bacteria” - suppress pathogenic bacterial growth

    Nonspecific Defenses – First Line

    Nonspecific internal Defenses

    1.Phagocytic cellsa. Neutrophils and macrophages (developed from monocytes) engulf and digest foreign cells. Eosinophils bombard large parasites

    2. Natural killer cells – another white blood cells that attack the body’s own cells that have been invaded.

  • Nonspecific internal Defenses3. Inflammation – literally means “to set a fire”

    Redness

    VasodilationWarmth

    Increase blood flowSwelling

    Increase capillary permeabilityAttracts phagocytotic white blood cells

    Blood clots isolate the injury site

    Nonspecific internal Defenses4. Fever-an attempt to inhibit

    bacterial growthWhite blood cells release pyrogens (hormone)

    1) Raise body temperature set point

    2) Increase the body's temperature

    3) Decrease iron and zinc concentration in the bloodstream (to slow down bacterial reproduction)

    The Roles of Phagocytes

    Macrophages - Engulf and digest all foreign objects

  • The Roles of Killer Cells

    Specific responses – Immune System

    1. Components of Immune systema. Lymph nodes and spleen: WBCs maturation

    sitesb. Thymus glands: T-cell lymphocytes

    maturationc. Bone marrow: stem cells produce blood cells;

    B-cell lymphocytes maturation sited. Blood cells – WBCs

    Phagocytes (macrophage), B-cells and T-cellse. Antibodies

    2. Immune responses

    Specific responses – Immune System

  • White Blood Cells1. Phagocytes (Macrophages) – big eater.

    WBCs that both destroy invading microbes and help alert other immune cells (+Dendritic Cell)

    2. B cells – Lymphocytes that produce antibodies; when stimulated, certain of their daughter cells (plasma cells) secrete large quantities of antibodies into the bloodstream.Memory B cells – long-lived, provide future immunity.Plasma cells – secrete antibodies – circulate (3,000 – 30,000 AB/cell/second); 5-day delay.

    White Blood Cells3. T cells – A set of lymphocytes that regulate

    the immune response or kill certain types of cells.Cytotoxic T cells – destroy foreign cells, infected own body cells, or cancerous body cells.Helper T cells – stimulate immune responses by both B cells and killer T cells.Suppressor T cells – turn off immune response.Memory T cells – long – lived, provide future immunity.

    White Blood Cells

  • White Blood Cells

    White Blood Cells

    AntibodiesY-shaped protein; 4 polypeptides and each has constant region and variable region.; genetic rearrangements during B cell maturation; bind to antigen (neutralization, promotion of phagocytosis).

  • Antibodies (rearrangement)

    Light and heavy chain diversity together yield about

    21 billion possibilities.

    Formation of Antigen-Specific Receptors

    Antigen-binding sites

    Antigen fits into grooves

  • Antibodies

    Antibodies bind to a hormone secreted by newly pregnant woman

    Memory

    First and secondary response to the same antigen

    Memory cells

    The Immune Response1. Recognition

    a. B cells and T cells

    b. Antibody specificity and diversity

    c. Recognition of foreign antigens, not "self" antigens

    2. Attack

    3. Memory

    a. B and T memory cells survive many years

    b. Memory cells activate a quicker second defense against the same invader

  • The Immune Response2. Attack

    a. Humoral immunity

    1) Protection against invading organisms

    2) B cells with antibodies circulate in the bloodstream

    3) Plasma cells mass-produce the required antibody

    4) Antibody bind to antigen: a) Neutralization

    b)Promotion of phagocytosis

    b. Cell-mediated defense

    The Immune Response2. Attack: b. Cell-mediated defense

    1) Protection against infected or cancerous cells

    2) Cytotoxic T cells

    a) Bind to antigens on the surface of infected cells

    b) Release proteins that disrupt the infected cell's plasma membrane

    3) Helper T cells

    a) Promote formation of B cells and cytotoxic T cells

    b) Create long-term memory cells

    4) Suppressor T cells: Turn off immune response

    The Immune Response

  • Defenses Enhanced(Vaccines and allergies)

    ImmunizationsVaccines – like

    antigens but not pathogenic

    Vaccination – injection of weakened or killed

    microbes stimulate development of memory cells

    AllergensPollen, foods, dust,

    sporesAllergies – inappropriate

    immune response (to some generally harmless substance)

    Hepatitis BHepatitis B boosterHepatitis B boosterHepatitis B assessmentDTP (Diphtheria; Tetanus; and

    Pertussin, or whooping cough)DTP boosterDTP boosterDTHiB (Hemophilus influenzae)HiB boosterPolioPolio boosterPolio boosterMMR (Measles, Mumps, Rubella)MMR boosterMMR assessmentVaricellaVaricella assessment

    Birth–2 months1–4 months6–18 months11–12 years

    2, 4, and 6 months 15–18 months4–6 years11–16 years4 and 6 months12–15 months2 and 4 months6–18 months4–6 years12–15 months4–6 years11–12 years12–18 months11–12 years

    RECOMMENDED VACCINES

    RECOMMENDEDAGES

    AIDS: Acquired Immune Deficiency Syndrome

    SymptomsFlu-likeWeight loss, fever, night

    sweatsEnlarged lymph nodes

    1. Caused by RNA viruses2. Destroy helper-T cells3. Helper T cells make more

    viruses4. Infect more helper T cells5. Immune system quit work

  • AIDS: Acquired Immune Deficiency Syndrome(1997)

    AIDS: Acquired Immune Deficiency

    Syndrome

    AIDS posters

  • In Conclusion1. Skin and mucous membranes lining body

    surfaces are physical barriers to infection2. Immune responses shows specificity,

    memory, and normally doesn’t fight one’s own self-marker proteins

    3. After recognition of antigen, repeated cell division form clones of B and T cells

    In Conclusion

    4. T cells arise in bone marrow but continue to develop in the thymus and B cells arise and mature in bone marrow

    5. Antibodies are protein molecules with binding sites for one kind of antigen

    6. Allergic reactions are immune responses to some generally harmless substance