1 / 22

Chapter 18

Chapter 18. Practical Applications of Immunology. Vaccine History. Variolation: Inoculation of smallpox into skin (18 th century) Vaccination: Inoculation of cowpox into skin Herd immunity results when most of a population is immune to a disease. Jenner.

swann
Download Presentation

Chapter 18

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Chapter 18 Practical Applications of Immunology

  2. Vaccine History • Variolation: Inoculation of smallpox into skin (18th century) • Vaccination: Inoculation of cowpox into skin • Herd immunity results when most of a population is immune to a disease.

  3. Jenner • On 14th May 1796, Edward Jennerused cowpox-infected material obtained from the hand of Sarah Nemes, a milkmaid from his home village of Berkley in Gloucestershire to successfully vaccinate 8 year old James Phipps. On 1st July 1796, Jenner challenged the boy by deliberately inoculating him with material from a real case of smallpox.He did not become infected!

  4. How Vaccines work • Trigger your own immune response • Artificially acquired active immunity • Virus, Bacterial or Toxins • Attenuated - no longer virulent • Inactivated or Killed - formalin, phenol or heat destroyed

  5. Types of Vaccines • Attenuated whole agent vaccines: • Live, attenuated (weakened) microbes - virus or bacteria • Long term immunity • May back mutate to virulent strain (rare) • Inactivated (killed) vaccines: • Killed by formalin, phenol or heat • Toxoids • Not as long lasting • Safe • Subunit vaccine: • Uses fragments from virus or bacteria • Produced by recombinant methods Recombinvac • Safe • Clean • Conjugated vaccines: • Bind to larger particle or protein to enhance antigenicity

  6. Principal Vaccines Used in the United States to Prevent Bacterial Diseases in Humans • DTaP - Trivalent (three in one) • Diphtheria: Purified diphtheria toxoid • Pertussis: Acellular fragments of B. pertussis • Tetanus: Purified tetanus toxoid • Meningococcal meningitis: Purified polysaccharide from N. meningitidis • Haemophilus influenzae type b meningitis: Polysaccharides conjugated with protein • Pneumococcal conjugate vaccine: S. pneumoniae antigens conjugated with protein

  7. Vaccine Schedule

  8. Principal Vaccines Used in the United States to Prevent Viral Diseases in Humans • Smallpox: Live vaccinia virus • Poliomyelitis: Inactivated virus • Rabies: Inactivated virus • Hepatitis A: Inactivated virus • Influenza: Inactivated or attenuated virus • Measles: Attenuated virus • Mumps: Attenuated virus • Rubella: Attenuated virus • Chickenpox: Attenuated virus • Hepatitis B: Antigenic fragments (recombinant vaccine)

  9. Other Diagnostic applications: Serological Tests Diagnostic Immunological tests: • Direct tests detect antigens (from patient sample) • Indirect tests detect antibodies (in patient's serum)

  10. Diagnostic Immunology: Precipitation Reactions Precipitation Reactions: • Involve soluble antigens with antibodies • Precipitin Ring test Figure 18.3

  11. Agglutination Reactions • Involve particulate antigens and antibodies • Antigens may be: • On a cell (direct agglutination) • Attached to latex spheres (indirect or passive agglutination) Figure 18.4

  12. Hemagglutination • Hemagglutination involves agglutination of RBCs. Figure 18.7

  13. Neutralization Reactions • Antibodies help eliminate the harmful effect of a virus or exotoxin • Viral hemagglutination inhibition tests for the presence of antibodies in a patients serum by the antibodies' ability to prevent viruses from agglutinating RBCs. Figure 18.8b

  14. Antibody Titer • Is the concentration of antibodies against a particular antigen Figure 18.5

  15. Complement Fixation Figure 18.9.1

  16. Complement Fixation Figure 18.9.2

  17. Fluorescent Antibody Techniques (Direct) Figure 18.10a

  18. Fluorescent Antibody Techniques (Indirect) Figure 18.10b

  19. Enzyme-Linked Immunosorbent Assay(Direct ELISA) Figure 18.12a

  20. Enzyme-Linked Immunosorbent Assay (Indirect ELISA) Figure 18.12b

  21. Serological Tests Figure 18.13

  22. Serological Tests: Summary • Precipitation: Soluble antigens • Agglutination: Particulate antigens • Hemagglutination: Agglutination of RBCs • Neutralization (inhibition): Inactivates toxin or virus • Fluorescent-antibody technique: Antibodies linked to fluorescent dye • Complement fixation: RBCs are indicator • ELISA: Enzyme linked to antibody amplifies results for easier visibility and more sensitivity.

More Related