Immunology Lecture day 1 ADDU section D

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Lecture on Immunology Day1 section D ateneo de davao university colloege of nursing

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Immunology Lecture day 1 ADDU section D

  1. 1. DAY 1 IMMUNOLOGY LECTURE<br />BACHELOR OF SCIENCE IN NURSING <br />Ateneo de davao University<br />
  2. 2. OBJECTIVES<br />Review the inflammatory process<br />Review the anatomy and physiology of the immune system<br />Understand the different types of immune response<br />Enumerate the different stages of immune response<br />Learn about the different types of primary immunodeficiencies<br />
  3. 3. IMMUNOLOGY<br />
  4. 4. Inflammation<br />the complex biological response of vascular tissues to harmful stimuli, such as pathogens, damaged cells, or irritants.<br />It is a protective attempt by the organism to remove the injurious stimuli as well as initiate the healing process for the tissue<br />
  5. 5.
  6. 6. As soon as the tissue is ruptured, the damaged cells release chemicals such as histamine, which serve as alarm signals.<br />The chemicals released activate numerous defense mechanisms in the body. Histamine forces nearby blood vessels to dilate and to allow more diffusion by becoming leakier. Due to this, blood flow to the affected area increases, and the plasma of the blood seeps into the interstitial fluid of the damaged tissues.<br />
  7. 7. Other chemicals that are released attract phagocytes and other leukocytes to the affected area. These leukocytes squeeze out of the blood vessels into the interstitial fluid and tissue spaces. This increase in blood flow, blood plasma, and white blood cells causes the redness, heat, and swelling that are normally found in inflammation.<br />The leukocytes that have been attracted to the area engulf the bacteria, and any dead body cells damaged by the pathogens or by the injury. This may result in the death of the leukocytes, as well, and their remains are also digested. Pus found at the site of infection consists mainly of white blood cells and blood plasma<br />
  8. 8.
  9. 9. The Immune System<br />
  10. 10. Bone marrow<br />Production site of white blood cells.<br />Which type of bone marrow?<br />
  11. 11. RED<br />
  12. 12. WHITE BLOOD CELLS<br />Also called LEUKOCYTES<br />are cells of the immune system defending the body against both infectious disease and foreign materials<br />Generally divided into 2 types:<br />Granulocytes and agranulocytes<br />
  13. 13.
  14. 14.
  15. 15. a.Basophils- capable of engulfing invaders and secreting histamine<br />b. Eosinophils- dispose of cellular debris and involved in allergic and parasitic reactions.<br />c.Neutrophils- involved in inflammatory process and phagocytosis<br />
  16. 16. d. Monocytes- migrate to tissues to become macrophages, and serves as antigen presenting cell<br />e.Lymphocytes- may become B and T lymphocytes to defend against invaders <br />
  17. 17. Lymphoid Tissues<br />1.Spleen, which is composed of red and white pulp that acts like a filter where red blood cells are destroyed <br />It synthesizes antibodies in its white pulp and removes, from blood and lymph node circulation, antibody-coated bacteria along with antibody-coated blood cells<br />It also contains in its reserve, half of the body&apos;s monocytes<br />
  18. 18.
  19. 19. Lymph nodes, which are connected to lymph channels & capillaries remove foreign material from the lymph before it enters the blood stream.<br />
  20. 20. 3. Tonsils & adenoids, contain immune cells that defend the body’s mucosal surfaces.<br />
  21. 21. Immunity<br />the body’s specific protective response to an invading agent.<br />Has 2 general types:<br />1. Natural<br />2. Acquired<br />
  22. 22. 1.Natural immunity<br />nonspecific immunity- present at birth<br />“self versus non-self”<br />Ex. physical and chemical barriers and white blood cell action<br />
  23. 23. 2. Acquired immunity<br />develops after birth, usually after prior exposure to an antigen<br />has 2 types:<br />1.Active acquired-defenses are developed by the own person’s body<br />2.Passive acquired- temporary immunity transmitted from another source. <br />
  24. 24. Active or Passive?<br />Immunity to tetanus<br />Answer: active<br />Immunity on the first 6 months of life<br />Answer: passive<br />
  25. 25. IMMUNE RESPONSES<br />Antigen- part of an invading organism that stimulate antibody production<br />
  26. 26.
  27. 27. Antibodies<br />Are also called immunoglobulins<br />They arise from a plasma cell which arose also from B-lymphocytes<br />Some actions of antibodies include:<br />Agglutination<br />Opsonization<br />Release of vasoactive substances<br />Phagocytosis<br />
  28. 28. Types of Immunoglobulins<br />1.IgG- 75% <br /><ul><li>In serum and insterstial tissues
  29. 29. Crosses the placenta</li></ul>2.IgA- 15% <br /><ul><li>In body fluids
  30. 30. Passes to neonate through breastmilk</li></ul>3.IgM- 10%<br /><ul><li>In intravascular serum
  31. 31. First produced in bacterial and viral infection</li></ul>4.IgD-0.2%<br /><ul><li>Influences B-lymphocyte differentiation</li></ul>5. IgE-0.004%<br /><ul><li>Takes part in allergic/hypersensitivity reaction
  32. 32. Combats parasitic infection</li></li></ul><li>
  33. 33. IMMUNE RESPONSE TYPES<br />
  34. 34. 1.Phagocytic Immune Responseinvolves granulocytes and macrophages<br />
  35. 35. What are macrophages?<br />These are matured monocytes capable of engulfing invading organisms<br />
  36. 36. Which granulocytes are capable of engulfing?<br />Basophils and neutrophils<br />
  37. 37. 2. Humoral Responsealso called antibody response,begins with B lymphocytes becoming plasma cells that produce antibodies which combine to disable the invader<br />
  38. 38.
  39. 39. 3. Cellular Response<br />Involves T lymphocytes that turn into special cytotoxic cells that attack pathogens.<br />T cells arise from stem cells that migrated to the thymus gland <br />
  40. 40. What is a thymus gland?<br /><ul><li>located in the upper anterior portion of the chest cavity just behind the sternum
  41. 41. main function is to provide an area for T cell maturation, and is vital in protecting against autoimmunity.</li></li></ul><li>Types of T cells are1. Helper T cells- also called CD4 cells, are activated upon recognition of antigens and release different cytokines to stimulate the immune system2. Cytotoxic/ killer T cells or effector T or CD 8 cells, attack the antigen directly by altering its cell membrane causing cell lysis.<br />
  42. 42. 3. Supressor T cells- decrease B-cell production4. memory T cells- are responsible for recognizing antigens from previous exposure <br />
  43. 43.
  44. 44. Stages of Immune Response<br />
  45. 45. A. Recognition Stagethe body recognizes the invaders as foreign by using lymph nodes and lymphocytes as surveillance <br />
  46. 46. B. Proliferation Stagethe circulating lymphocyte returns to the nearest lymph node with the antigenic message and the lymph node in turn stimulates its resident B and T lymphocytes to enlarge and divide.<br />
  47. 47. c. response stageinitiation of humoral and cellular response forming the t cells.d.effector stageresults to the total destruction of the microbes or neutralization of toxins. <br />
  48. 48. WHITE BLOOD CELL COUNT<br />Normal WBC count : 5000-10,000 cells/mm3<br />Leukocytosis<br />Leukopenia<br />
  49. 49.  <br />Bone marrow biopsy-the removal of soft tissue from inside bone for study- commonly taken from the hip bone, check for bleeding problems- patient may feel sharp pain<br />
  50. 50. PRIMARY IMMUNODEFICIENCIESare disorders due to deficient components with genetic origins seen in infants and children. <br />
  51. 51. Phagocytic Dysfunction<br />1.Hyperimmunoglobinemia E /Job’s Syndrome<br />Hyper IgE syndrome (HIES)<br />no known cause<br />Sx: recurrent staphylococcal infections,<br />unusual eczema-like skin rashes, <br />severe lung infections <br />very high concentrations of the serum antibody IgE<br />skeletal abnormalities such as fractures<br />scoliosis and dental problems such as retention of deciduous teeth<br />
  52. 52. no existing cure, only symptomatic<br />IV gamma globulin<br />Source: www.jobsyndrome.com<br />
  53. 53. Chronic Granulomatous Disease<br />pt. has no inflammatory response. <br />Sx: increased incidence of bacterial, fungal & viral infectioncold abscess, mouth ulcers, stomatitis8 or more ear infections in a year<br />Management: Early Diagnosis is essentialGranulocyte transfusionAntibiotic therapy<br />
  54. 54. B-cell deficiencies<br />Aggamaglobulinemia/Bruton’s Disease<br />Sex-linked<br />Males are mostly affected<br />Results from lack of differentiation form B-cell precursors into mature B-cells<br />No plasma cells are formed leading to complete lack of antibody production<br />
  55. 55. Symptoms:Pyogenic infection starting 5-6 months of age<br />frequent ear and sinus infections, pneumonia, and gastroenteritis. Certain viruses, such as hepatitis and polio viruses, can also pose a threat. <br />Children with XLA grow slowly, have small tonsils and lymph nodes, and may develop chronic skin infections<br />
  56. 56. Hypogammaglobulinemia<br />Results from lack of differentiation of some B <br /> cells into plasma cellsalso called common variable immunodeficiency, etiology is unknown.<br />Symptoms:pernicious anemia high susceptibility to infection<br />Management:Intravenous immunoglobulinAntibioticsVitamin B12 injection<br />
  57. 57. T-cell deficiencies<br />DiGeorge syndrome/thymichypoplasia<br />Velo-Cardio-Facial syndrome, DiGeorge Syndrome, Shprintzen syndrome, conotruncal anomaly face syndrome, Congenital ThymicAplasia, Strong Syndrome, Thymichypoplasia, and DiGeorge anomaly<br />Congenital in origin, thymus fails to develop normally due to deletion of chromosome 22<br />Sx: hypoparathyroidism, which results in hypocalcemia<br />hypoplastic thymus or absent thymus, which results in problems in the immune system<br />
  58. 58. heart defects (e.g., tetralogy of Fallot, interrupted aortic arch, ventricular septal defects, vascular rings)<br />cleft lip and/or palate<br />Cardiac Abnormality Abnormal faciesThymicaplasiaCleft palateHypocalcemia<br />
  59. 59. Management:<br />There is no cure, the key is to identify each of the associated features and manage each using the best available treatments<br />Management of hypocalcemia<br />Antibiotics<br />Thymus transplantation, cardiac surgery<br />
  60. 60. COMBINED T-CELL & B-CELL DEFICIENCIES<br />Ataxia-Telangectasia<br />Also called Boder-Sedgwick syndrome or Louis–Bar syndrome<br /> a rare, neurodegenerative, inherited disease that affects many parts of the body and causes severe disability. Ataxia refers to poor coordination and telangiectasia to small dilated blood vessels, both of which are hallmarks of the disease.<br />It affects the cerebellum and also weakens the immune system in about 70% of the cases, leading to respiratory disorders<br />
  61. 61. about half the people with A-T have immune problems. These usually take the form of repeated colds and runny noses <br />Treatment is symptomatic and supportive. Physical and occupational therapy may help maintain flexibility. <br />Gamma-globulin injections may be given to help supplement a weakened immune system. High-dose vitamin regimens may also be used.<br /> Antibiotics are used to treat infections,low doses of chemotherapy to reduce the risk of cancer but this is controversial. <br />
  62. 62. SECONDARY IMMUNODEFICIENCIES<br />
  63. 63. Human ImmunodeficieNCy Syndrome<br />
  64. 64. AIDS is pandemic<br />In 2007, it was estimated that 33.2 million people lived with the disease worldwide, and that AIDS killed an estimated 2.1 million people, including 330,000 children.<br />
  65. 65. History<br />Scientists identified a type of chimpanzee in West Africa as the source of HIV infection in humans. The virus most likely jumped to humans when humans hunted these chimpanzees for meat and came into contact with their infected blood. Over several years, the virus slowly spread across Africa and later into other parts of the world<br />
  66. 66. AIDS was first reported June 5, 1981, when the U.S. Centers for Disease Control (CDC) recorded a cluster of Pneumocystiscarinii in five homosexual men in Los Angeles<br />
  67. 67. AIDS<br />Acquired immune deficiency syndrome or acquired immunodeficiency syndrome (AIDS) is a disease of the human immune system caused by the human immunodeficiency virus or HIV<br />
  68. 68. HIV<br />HIV is a retrovirus that primarily infects vital organs of the human immune system such as CD4+ T cells , macrophages<br />HIV belongs to the group retroviruses that carry their genetic material in RNA<br />
  69. 69. WHAT IS A RETROVIRUS?<br />A retrovirus is an RNA virus that is replicated in a host cell via the enzyme reverse transcriptase to produce DNA from its RNA genome<br />The DNA is then incorporated into the host&apos;s genome by an integrase enzyme. The virus thereafter replicates as part of the host cell&apos;s DNA. <br />
  70. 70.
  71. 71. Transmission<br />involve anal, vaginal or oral sex, <br />blood transfusion, contaminated hypodermic needles, <br />exchange between mother and baby during pregnancy, childbirth, <br />breastfeeding or other exposure to one of the above bodily fluids.<br />
  72. 72. STAGES OF HIV DISEASE<br />1.Primary Infection/Acute HIV Syndrome, Stage I<br />From period of infection to development of antibodies and intense viral replication<br />Sx: none to severe flu-like symptoms<br />
  73. 73. Criteria for Stage I<br />During the first stage of HIV, an individual generally has flu like symptoms which last for a week or two. WHO provides the following criteria for placing a patient in this stage:<br />Asymptomatic<br />Persistent generalized lymphadenopathy<br />
  74. 74. 2. HIV asymptomatic/Category A/stage II<br />More than 500 CD4 cells<br />In stage II, many people are completely asymptomatic, but others demonstrate a number of physical symptoms that healthcare providers can use to stage the patient. WHO criteria for this stage include the following:<br />Moderate unexplained weight loss<br />Recurring respiratory tract infections<br />Herpes Zoster (shingles)<br />Angular cheilitis (lesions at the corner of the mouth)<br />Recurring oral ulceration<br />Papularpruritic eruptions (skin rash possibly related to insect bites)<br />Seborrhoeic dermatitis (a skin disorder that causes scaly, itchy, flaky skin)<br />Fungal nail infections.<br />
  75. 75. HIV symptomatic/ Category B/stage iii<br />Consists of symptomatic conditions not listed in category C<br />Criteria for Stage III<br />In stage III, HIV patients begin to exhibit more serious symptoms. This is also when opportunistic infections begin to take advantage of the weakened immune system. WHO criteria for placing a patient in this stage include the following:<br />
  76. 76. Unexplained severe weight loss<br />Unexplained chronic diarrhea lasting for longer than one month<br />Unexplained persistent fever, either intermittent or constant<br />Persistant oral candidiasis (yeast infection of the mouth)<br />Oral hairy leukoplakia (a white patch on the side of the tongue with a hairy appearance)<br />Pulmonary tuberculosis<br />
  77. 77. Severe bacterial infections (for example, pneumonia, meningitis, and empyema)<br />Acute necrotizing ulcerative stomatitis (inflammation of the stomach mucous lining), gingivitis (inflammation of the gums), or periodontitis (inflammation of the tissue that supports the teeth)<br />Unexplained anemia), neutropenia, and/or chronic thrombocytopenia<br />
  78. 78. AIDS category C/stage IV<br />Less than 200 CD4 cells<br />Criteria for Stage IV (AIDS)<br />In stage IV, a patient is considered to have progressed from HIV to AIDS. This stage is characterized by more severe symptoms and an even greater number of opportunistic infections. WHO criteria for this stage include the following:<br />
  79. 79. HIV wasting syndrome<br />Pneumocystis pneumonia (pneumonia caused by a yeast-like fungus)<br />Recurrent severe bacterial pneumonia<br />Chronic herpes simplex infection<br />Esophageal candidiasis (yeast-like infection of the esophagus)<br />Extrapulmonary tuberculosis<br />Kaposi sarcoma (a tumor caused by human herpesvirus 8)<br />Cytomegalovirus infection (an infection caused by human herpesvirus 5)<br />Central nervous system toxoplasmosis (a parasite affecting the central nervous system, including brain)<br />HIV encephalopathy (a brain disorder)<br />Extrapulmonarycryptococcosis including meningitis <br />
  80. 80. Disseminated non-tuberculousmycrobacteria infection<br />Progressive multifocal leukoencephalopathy (the reactivation of a common virus in the central nervous system)<br />Chronic cryptosporidiosis (a parasitic disease)<br />Chronic isosporiasis (a parasitic intestinal disease)<br />Disseminated mycosis (a fungus that causes infection)<br />Recurrent septicemia (also known as blood poisoning)<br />Lymphoma (cerebral or B cell non-Hodgkin)<br />Invasive cervical carcinoma<br />Atypical disseminated leishmaniasis (a parasite transmitted by the sand fly)<br />Symptomatic HIV-associated nephropathy or HIV-associated cardiomyopathy.<br />
  81. 81. DIAGNOSIS<br />HIV antibody test<br />Once infected the body usually responds by producing antibodies 3 to 12 weeks / “window period”<br />EIA or Enzyme Immunoassay or ELISA<br />Identifies antibodies directed against HIV<br />
  82. 82. Western Blot<br />Confirms seropositivity when the EIA is also positive<br />

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