Inmuno 1


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Inmuno 1

  1. 1. inmunohematología Jul 20, 2012
  2. 2. The Immune System - includes all parts of the body that help in the recognition and destruction of foreign materials. White blood cells, phagocytes and lymphocytes, bone marrow, lymph nodes, tonsils, thymus, and your spleen are all part of the immune system.
  3. 3. • First-Line Defenses /Innate Immune System- The bodys first line of defense against pathogens uses mostly physical and chemical barriers such as• Skin – acts as a barrier to invasion• Sweat – has chemicals which can kill different pathogens.• Tears - have lysozyme which has powerful digestive abilities that render antigens harmless.• Saliva – also has lysozyme.• Mucus - can trap pathogens, which are then sneezed, coughed, washed away, or destroyed by chemicals.• Stomach Acid – destroys pathogens
  4. 4. • Second-Line Defenses - If a pathogen is able to get past the bodys first line of defense, and an infection starts, the body can rely on its second line of defense. This will result in what is called an……….
  5. 5. • Inflammatory response causes• Redness - due to capillary dilation resulting in increased blood flow• Heat - due to capillary dilation resulting in increased blood flow• Swelling – due to passage of plasma from the blood stream into the damaged tissue• Pain – due mainly to tissue destruction and, to a lesser extent, swelling.
  6. 6. • Third-Line Defenses - Sometimes the second line of defense is still not enough and the pathogen is then heading for the bodys last line of defense, the immune system.• The immune system recognizes, attacks, destroys, and remembers each pathogen that enters the body. It does this by making specialized cells and antibodies that render the pathogens harmless.• Unlike the first line and second line defense the immune system differentiates among pathogens.• For each type of pathogen, the immune system produces cells that are specific for that particular pathogen.
  7. 7. • An antibody is a protein produced in response to an antigen.• Antigens are macromolecules that elicit an immune response in the body. The most common antigens are proteins and polysaccharides.
  8. 8. • Antigens can enter the body from the environment. These include• inhaled macromolecules (e.g., proteins on cat hairs that can trigger an attack of asthma in susceptible people)• ingested macromolecules (e.g., shellfish proteins that trigger an allergic response in susceptible people)• molecules that are introduced beneath the skin (e.g., on a splinter or in an injected vaccine)
  9. 9. • antigens can be generated within the cells of the body. These include• proteins encoded by the genes of viruses that have infected a cell• aberrant proteins that are encoded by mutant genes; such as mutated genes in cancer cells
  10. 10. • Lymph is a milky body fluid that contains a type of white blood cells, called lymphocytes, along with proteins and fats.• Lymph seeps outside the blood vessels in spaces of body tissues and is stored in the lymphatic system to flow back into the bloodstream.
  11. 11. • Through the flow of blood in and out of arteries, and into the veins, and through the lymph nodes and into the lymph, the body is able to eliminate the products of cellular breakdown and bacterial invasion.
  12. 12. • There are more than 100 tiny, oval structures called lymph nodes. These are mainly in the neck, groin and armpits, but are scattered all along the lymph vessels.• They act as barriers to infection by filtering out and destroying toxins and germs. The largest body of lymphoid tissue in the human body is the spleen.
  13. 13. • As the lymph flows through lymph vessels, it passes through lymph nodes.• White blood cells called macrophages trap and engulf cell debris and pathogens. Other white blood cells, called• Lymphocytes - are a type of white blood cell capable of producing a specific immune response to unique antigens. They produce antibodies which are chemicals that mark pathogens for destruction.
  14. 14. The scanning electron micrograph above, shows a humanmacrophage (gray) approaching a chain of Streptococcuspyogenes (yellow). Riding atop the macrophage is a sphericallymphocyte. Both macrophages and lymphocytes can befound near an infection, and the interaction between thesecells is important in eliminating infection.
  15. 15. • Once a white cell has left the blood vessel and migrated to the enemy, the next job is to EAT the microbe.• The macrophage is a large phagocyte. A phagocyte is an eating cell (phago = "eating", cyte = "cell") which engulfs invaders.
  16. 16. • Immunity is the result of the action of two types lymphocytes, the B lymphocytes and the T lymphocytes.• B cells produce antibodies that are secreted into the blood and lymph.• T cells attack the cells that have antigens that they recognize.
  17. 17.  Killer T Cells (lymphocytes) recognize surfacemarkers on other cells labeled for destruction. They,Killer T Cells, help to keep virus-infected or malignantcells in check. Here, a smaller Killer T Cell (arrow) is attacking andkilling a much larger flu virus-infected target. Thesequence represents 30 minutes elapsed time.
  18. 18. • It has been estimated that during our lifetime, we will encounter a million foreign antigens capable of causing disease, and our bodies need the same amount of lymphocytes to defend against them.• There will always be a different type of lymphocyte for each possible antigen.
  19. 19. •Active Immunity occurs when whenone makes his/her own antibodies. Thistype of immunity is long term.•Getting the disease : If you get aninfectious disease (like ChickenPox), often times, that stimulates theproduction of MEMORY cells whichare then stored to prevent theinfection in the future.
  20. 20. Vaccination: A vaccination is an injectionof a weakened form of the actual antigenthat causes the disease. The injection istoo weak to make you sick, but your Blymphocytes will recognize the antigenand react as if it were the "real thing".Thus, you produce MEMORY cells forlong term immunity.
  21. 21. Passive Immunity occurs when theantibodies come from some other source.This type of immunity is short term.Breastmilk : Milkfrom a mothersbreast containsantibodies. Thebaby is acquiringpassiveimmunity. Theseantibodies willonly last severalweeks.
  22. 22. Gamma Globulin: A Gamma Globulin shot is purely an injection of antibodies to provide temporary immunity. You might receive an Gamma Globulin shot if you travel outside of the country.
  23. 23. Types of Acquired ImmunityI. Naturally Acquired Immunity: Obtained in the course of daily life. A. Naturally Acquired Active Immunity: – Antigens or pathogens enter body naturally. – Body generates an immune response to antigens. – Immunity may be lifelong (chickenpox or mumps) or temporary (influenza or intestinal infections). B. Naturally Acquired Passive Immunity: – Antibodies pass from mother to fetus via placenta or breast feeding (colostrum). – No immune response to antigens. – Immunity is usually short-lived (weeks to months). – Protection until child’s immune system develops.
  24. 24. Types of Acquired Immunity (Continued)II. Artificially Acquired Immunity: Obtained by receiving a vaccine or immune serum. 1. Artificially Acquired Active Immunity: – Antigens are introduced in vaccines (immunization). – Body generates an immune response to antigens. – Immunity can be lifelong (oral polio vaccine) or temporary (tetanus toxoid). 2. Artificially Acquired Passive Immunity: – Preformed antibodies (antiserum) are introduced into body by injection. • Snake antivenom injection from horses or rabbits. – Immunity is short lived (half life three weeks). – Host immune system does not respond to antigens.
  25. 25. Duality of Immune SystemI. Humoral (Antibody-Mediated) Immunity – Involves production of antibodies against foreign antigens. – Antibodies are produced by a subset of lymphocytes called B cells. – B cells that are stimulated will actively secrete antibodies and are called plasma cells. – Antibodies are found in extracellular fluids (blood plasma, lymph, mucus, etc.) and the surface of B cells. – Defense against bacteria, bacterial toxins, and viruses that circulate freely in body fluids, before they enter cells. – Also cause certain reactions against transplanted tissue.
  26. 26. Antibodies are Produced by B Lymphocytes
  27. 27. Antibodies are Proteins that Recognize Specific Antigens
  28. 28. Duality of Immune System (Continued)II. Cell Mediated Immunity – Involves specialized set of lymphocytes called T cells that recognize foreign antigens on the surface of cells, organisms, or tissues: • Helper T cells • Cytotoxic T cells – T cells regulate proliferation and activity of other cells of the immune system: B cells, macrophages, neutrophils, etc. – Defense against: • Bacteria and viruses that are inside host cells and are inaccessible to antibodies. • Fungi, protozoa, and helminths • Cancer cells • Transplanted tissue
  29. 29. Cell Mediated Immunity is Carried Out by T Lymphocytes
  30. 30. AntigensMost are proteins or large polysaccharidesfrom a foreign organism.– Microbes: Capsules, cell walls, toxins, viral capsids, flagella, etc.– Nonmicrobes: Pollen, egg white , red blood cell surface molecules, serum proteins, and surface molecules from transplanted tissue.Lipids and nucleic acids are only antigenicwhen combined with proteins orpolysaccharides.Molecular weight of 10,000 or higher.– Hapten: Small foreign molecule that is not antigenic. Must be coupled to a carrier molecule to be antigenic. Once antibodies are formed they will recognize hapten.
  31. 31. AntigensEpitope: Small part of an antigen that interacts with an antibody. Any given antigen may have several epitopes. Each epitope is recognized by a different antibody.
  32. 32. Epitopes: Antigen Regions that Interact with Antibodies
  33. 33. AntibodiesProteins that recognize and bind to aparticular antigen with very highspecificity.Made in response to exposure to theantigen.One virus or microbe may have severalantigenic determinant sites, to whichdifferent antibodies may bind.Each antibody has at least two identicalsites that bind antigen: Antigen bindingsites.Valence of an antibody: Number of antigenbinding sites. Most are bivalent.
  34. 34. Antibody StructureMonomer: A flexible Y-shaped moleculewith four protein chains:– 2 identical light chains– 2 identical heavy chainsVariable Regions: Two sections at the endof Y’s arms. Contain the antigen bindingsites (Fab). Identical on the same antibody,but vary from one antibody to another.Constant Regions: Stem of monomer andlower parts of Y arms.Fc region: Stem of monomer only.Important because they can bind tocomplement or cells.
  35. 35. Antibody Structure
  36. 36. Immunoglobulin ClassesI. IgG Structure: Monomer Percentage serum antibodies: 80% Location: Blood, lymph, intestine Half-life in serum: 23 days Complement Fixation: Yes Placental Transfer: Yes Known Functions: Enhances phagocytosis, neutralizes toxins and viruses, protects fetus and newborn.
  37. 37. Immunoglobulin ClassesII. IgM Structure: Pentamer Percentage serum antibodies: 5-10% Location: Blood, lymph, B cell surface (monomer) Half-life in serum: 5 days Complement Fixation: Yes Placental Transfer: No Known Functions: First antibodies produced during an infection. Effective against microbes and agglutinating antigens.
  38. 38. Immunoglobulin ClassesIII. IgA Structure: Dimer Percentage serum antibodies: 10-15% Location: Secretions (tears, saliva, intestine, milk), blood and lymph. Half-life in serum: 6 days Complement Fixation: No Placental Transfer: No Known Functions: Localized protection of mucosal surfaces. Provides immunity to infant digestive tract.
  39. 39. Immunoglobulin ClassesIV. IgD Structure: Monomer Percentage serum antibodies: 0.2% Location: B-cell surface, blood, and lymph Half-life in serum: 3 days Complement Fixation: No Placental Transfer: No Known Functions: In serum function is unknown. On B cell surface, initiate immune response.
  40. 40. Immunoglobulin ClassesV. IgE Structure: Monomer Percentage serum antibodies: 0.002% Location: Bound to mast cells and basophils throughout body. Blood. Half-life in serum: 2 days Complement Fixation: No Placental Transfer: No Known Functions: Allergic reactions. Possibly lysis of worms.
  41. 41. How Do B Cells Produce Antibodies?– B cells develop from stem cells in the bone marrow of adults (liver of fetuses).– After maturation B cells migrate to lymphoid organs (lymph node or spleen).– Clonal Selection: When a B cell encounters an antigen it recognizes, it is stimulated and divides into many clones called plasma cells, which actively secrete antibodies.– Each B cell produces antibodies that will recognize only one antigenic determinant.
  42. 42. Clonal Selection of B Cells isCaused by Antigenic Stimulation
  43. 43. Humoral Immunity (Continued)Apoptosis– Programmed cell death (“Falling away”).– Human body makes 100 million lymphocytes every day. If an equivalent number doesn’t die, will develop leukemia.– B cells that do not encounter stimulating antigen will self-destruct and send signals to phagocytes to dispose of their remains.– Many virus infected cells will undergo apoptosis, to help prevent spread of the infection.
  44. 44. Humoral Immunity (Continued)Clonal Selection– Clonal Selection: B cells (and T cells) that encounter stimulating antigen will proliferate into a large group of cells.– Why don’t we produce antibodies against our own antigens? We have developed tolerance to them.– Clonal Deletion: B and T cells that react against self antigens appear to be destroyed during fetal development. Process is poorly understood.
  45. 45. Consequences of Antigen-AntibodyBindingAntigen-Antibody Complex: Formed when an antibody binds to an antigen it recognizes.Affinity: A measure of binding strength.1. Agglutination: Antibodies cause antigens (microbes) to clump together. • IgM (decavalent) is more effective that IgG (bivalent). • Hemagglutination: Agglutination of red blood cells. Used to determine ABO blood types and to detect influenza and measles viruses.2. Opsonization: Antigen (microbe) is covered with antibodies that enhances its ingestion and lysis by phagocytic cells.
  46. 46. Consequences of Antibody Binding
  47. 47. Humoral Immunity (Continued)3. Neutralization: IgG inactivates viruses by binding to their surface and neutralize toxins by blocking their active sites.4. Antibody-dependent cell-mediated cytotoxicity: Used to destroy large organisms (e.g.: worms). Target organism is coated with antibodies and bombarded with chemicals from nonspecific immune cells.5. Complement Activation: Both IgG and IgM trigger the complement system which results in cell lysis and inflammation.
  48. 48. Consequences of Antibody Binding
  49. 49. Immunological MemoryAntibody Titer: The amount of antibody in the serum.Pattern of Antibody Levels During InfectionPrimary Response:– After initial exposure to antigen, no antibodies are found in serum for several days.– A gradual increase in titer, first of IgM and then of IgG is observed.– Most B cells become plasma cells, but some B cells become long living memory cells.– Gradual decline of antibodies follows.
  50. 50. Immunological Memory (Continued)Secondary Response:– Subsequent exposure to the same antigen displays a faster and more intense antibody response.– Increased antibody response is due to the existence of memory cells, which rapidly produce plasma cells upon antigen stimulation.
  51. 51. Antibody Response After Exposure to Antigen
  52. 52. T Cells and Cell Mediated ImmunityAntigens that stimulate this response are mainly intracellular.Requires constant presence of antigen to remain effective.Unlike humoral immunity, cell mediated immunity is not transferred to the fetus.Cytokines: Chemical messengers of immune cells.– Over 100 have been identified.– Stimulate and/or regulate immune responses. • Interleukins: Communication between WBCs. • Interferons: Protect against viral infections.
  53. 53. T Cells and Cell Mediated ImmunityCellular Components of Immunity:– T cells are key cellular component of immunity.– T cells have an antigen receptor that recognizes and reacts to a specific antigen (T cell receptor).– T cell receptor only recognize antigens combined with major histocompatability (MHC) proteins on the surface of cells. • MHC Class I: Found on all cells. • MHC Class II: Found on phagocytes.– Clonal selection increases number of T cells.
  54. 54. T Cells Only Recognize AntigenAssociated with MHC Molecules on Cell Surfaces
  55. 55. T Cells and Cell Mediated ImmunityTypes of T cells1. T Helper (TH) Cells: Central role in immune response. • Most are CD4+ • Recognize antigen on the surface of antigen presenting cells (e.g.: macrophage). • Activate macrophages • Induce formation of cytotoxic T cells • Stimulate B cells to produce antibodies.
  56. 56. Central Role of Helper T Cells
  57. 57. Types of T cells (Continued)2. Cytotoxic T (Tc) Cells: Destroy target cells. • Most are CD4 negative (CD4 -). • Recognize antigens on the surface of all cells: – Kill host cells that are infected with viruses or bacteria. – Recognize and kill cancer cells. – Recognize and destroy transplanted tissue. • Release protein called perforin which forms a pore in target cell, causing lysis of infected cells. • Undergo apoptosis when stimulating antigen is gone.
  58. 58. Cytotoxic T Cells Lyse Infected Cells
  59. 59. Types of T cells (Continued)3. Delayed Hypersensitivity T (TD) Cells: Mostly T helper and a few cytotoxic T cells that are involved in some allergic reactions (poison ivy) and rejection of transplanted tissue.4. T Suppressor (Ts) Cells: May shut down immune response.
  60. 60. Nonspecific CellularComponents1. Activated Macrophages: Stimulated phagocytes. • Stimulated by ingestion of antigen • Larger and more effective phagocytes. • Enhanced ability to eliminate intracellular bacteria, virus-infected and cancerous cells.2. Natural Killer (NK) Cells: • Lymphocytes that destroy virus infected and tumor cells. • Not specific. Don’t require antigen stimulation. • Not phagocytic, but must contact cell in order to lyse it.
  61. 61. Relationship Between Cell-Mediated and Humoral Immunity1. Antibody ProductionT-Dependent Antigens: – Antibody production requires assistance from T helper cells. – A macrophage cells ingest antigen and presents it to TH cell. – TH cell stimulates B cells specific for antigen to become plasma cells. – Antigens are mainly proteins on viruses, bacteria, foreign red blood cells, and hapten-carrier molecules.T-Independent Antigens: – Antibody production does not require assistance from T
  62. 62. Humoral Response to T Dependent Antigens
  63. 63. Humoral Response to T Dependent Antigens
  64. 64. Relationship Between Cell-Mediated and Humoral Immunity2. Antibody Dependent Cell Mediated Cytotoxicity – Target cell is covered with antibodies, leaving Fc portion sticking outwards. – Natural killer and other nonspecific cells that have receptors for Fc region are stimulated to kill targeted cells. – Target organism is lysed by substances secreted by attacking cells. – Used to destroy large organisms that cannot be
  65. 65. Destruction of Large Parasites by ADCC
  66. 66. Overview of the Immune Response