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Vaccination Dr. Mitova
The  immune system  is a complex network of specialized organs and cells protects the body from destruction by foreign agents and microbial pathogens , degrades and removes damaged or dead cells, and exerts a surveillance function to prevent the development and growth of malignant cells. The immune system is composed of immune cells and central and peripheral lymphoid structures. The immune cells move throughout the body, searching for and destroying foreign substances but avoiding cells regarded as self.  
Natural immunity: It is not produced by the immune response. This type of immunity is present at birth and appears to be present in all members of a species.   Acquired immunity:   It develops after birth as a result of exposure to an antigen, thereby activating the immune response. Acquired immunity can be either active or passive, depending on whether the immune response took place in the host or a donor.
Differences of immune system of children and adult The normal human no fully active immune system at birth because of immaturity. It relies instead on passively transferred antibodies from the mother. This maternal antibody slowly decreases in concentration and for all practical purposes, has waned by 1 year. The infant own production of antibody begins to be meaningful at 7 or 8 months of age when the total of maternal and infant antibody is low. One has waned and the other is not up to full strength. This is  age when many of the infectious disease processes of infancy begin /e.g. otitis media, pneumonia.
Vaccination ,[object Object],[object Object],[object Object],[object Object]
Early History of Vaccination ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Era of Vaccination ,[object Object],[object Object],[object Object],[object Object]
Era of Vacinnation ,[object Object],[object Object],[object Object],[object Object]
Early History of Vaccination   ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Vaccination Today ,[object Object],[object Object]
Human Vaccines against pathogens Immunological Bioinformatics, The MIT press.
 
 
 
Type of Vaccination
Type of Vaccination Live Vaccines ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Subunit Vaccines ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Subunit Vaccines: Polysaccharides ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Subunit Vaccines: Toxoids ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Subunit Vaccines: Recombinant   ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],For more information se:  http://www.nci.nih.gov/ncicancerbulletin/NCI_Cancer_Bulletin_041205/page5
Genetic Vaccines ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Type of Vaccination ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Passive Immunity ,[object Object],[object Object],[object Object]
Sources of Passive Immunity ,[object Object],[object Object],[object Object],[object Object]
IMMUNOGLOBULIN PREPARETION  Normal human Ig. Normal human Ig is an antibody-rich fraction, obtained from a pool of at least 1000 donors. The preparation should contain at least 90% intact IgG; it should be as free as possible from IgG aggregates; all IgG sub-classes should be present; there should be a low IgA concentration; the level of antibody against at least two bacterial species and two viruses should be ascertained  Normal human Ig used to prevent measles in highly susceptible individuals and to provide temporary protection /up to 12 weeks/ against hepatitis A infection. Live vaccines should not normally be given for 12 weeks after an injection of normal human Ig.
           Specific human Ig. These preparations are made from the plasma of patient who have recently recovered from an infection or are obtained from individuals who have been immunized against a specific infection. The advantages of Ig-s are: 1.      freedom from hepatitis B 2.      concentration of the antibodies into a small volume for intramuscular use. 3.      stable antibody content, if properly stored.
Route of Administration
Route of Adminstration DPT, DT Tetanus, HepatitisA, HepatitisB,  Pneumococcal , Rabies, Hib,  Influenza Intramuscular Measles, Mumps, Rubella, MMR, IPV,  Pneumoccocal, Influenza Subcutaneous BCG, Rabies Intradermal OPV Oral
Site of Administration Anterolateral aspect of the thigh in infants and deltoid muscle in older children or adult. Intramuscular Anterolateral aspect of the thigh or the upper arm Subcutaneous Over the insertion of left deltoid muscle Intradermal
Who should not be vaccinated? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Allergy ,[object Object],[object Object],[object Object]
Allergy ,[object Object],[object Object],[object Object],[object Object]
Allergy ,[object Object],[object Object]
Fever ,[object Object],[object Object]
Vaccination in Pregnancy ,[object Object],[object Object],[object Object]
Vaccination in Pregnancy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
HIV Infection ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Immunosupression ,[object Object],[object Object]
Neurological disorder ,[object Object],[object Object],[object Object]
Reactions ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Reactions ,[object Object],[object Object]
Reactions ,[object Object],[object Object]
VACCINE REACTIONS ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
RARE, MORE SERIOUS REACTIONS BCG Hib HepB Measles/ MMR/MR ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Reaction Incidence
RARE, MORE SERIOUS REACTIONS (2) Tetanus Pertussis  ( DTP-  whole cell)  Reaction Incidence Polio (OPV) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Simutaneous administration of Vaccine ,[object Object],[object Object]
V accine  C old  C hain ,[object Object],[object Object],[object Object]
Recommended Storage Temperatures
Recommended Schedule for Immunization of Healthy Infants and Children/BULGARIA/   24 h  HB vax  0.5 ml  i.m. 48h    BCG  0.1 ml  i.d. 1mo  HB vax  0.5ml  i.m. 2mo  Pentaxim(DTaP,  I PV,Hemophilus infl B).0.5ml i.m. ;vaccineS.pneumoniae-0,5i.m. 3mo  Pentaxim(DTaP, IPV,Hemophilus infl B).0.5ml i.m. vaccineS.pneumoniae-0,5i.m 4mo  Pentaxim(DTaP, IPV,Hemophilus infl B).0.5ml i.m. vaccineS.pneumoniae-0,5i.m 6mo  HB vax 1 2 mo  vaccine against S.pneumoniae-0,5i.m. (booster) 13mo  MMR  0.5ml  i.m. 16-24mo  Pentaxim(DTaP, IPV,Hemophilus infl B).0.5ml   6у   Tetraxim( IPV ,  DTaP)-0.5ml i.m.   7y  Mantoux  0.1i.d .(negative<5mm-BCG)   1 1 y  Mantoux  .(negative<5mm-BCG)   12y  MMR , Td 17y  Td,Mantoux  .(negative<5mm-BCG)   25,35,45…y  Td  0.5ml i.m.
 

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Vaccination

  • 2. The immune system is a complex network of specialized organs and cells protects the body from destruction by foreign agents and microbial pathogens , degrades and removes damaged or dead cells, and exerts a surveillance function to prevent the development and growth of malignant cells. The immune system is composed of immune cells and central and peripheral lymphoid structures. The immune cells move throughout the body, searching for and destroying foreign substances but avoiding cells regarded as self.  
  • 3. Natural immunity: It is not produced by the immune response. This type of immunity is present at birth and appears to be present in all members of a species.   Acquired immunity: It develops after birth as a result of exposure to an antigen, thereby activating the immune response. Acquired immunity can be either active or passive, depending on whether the immune response took place in the host or a donor.
  • 4. Differences of immune system of children and adult The normal human no fully active immune system at birth because of immaturity. It relies instead on passively transferred antibodies from the mother. This maternal antibody slowly decreases in concentration and for all practical purposes, has waned by 1 year. The infant own production of antibody begins to be meaningful at 7 or 8 months of age when the total of maternal and infant antibody is low. One has waned and the other is not up to full strength. This is age when many of the infectious disease processes of infancy begin /e.g. otitis media, pneumonia.
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  • 12. Human Vaccines against pathogens Immunological Bioinformatics, The MIT press.
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  • 26. IMMUNOGLOBULIN PREPARETION  Normal human Ig. Normal human Ig is an antibody-rich fraction, obtained from a pool of at least 1000 donors. The preparation should contain at least 90% intact IgG; it should be as free as possible from IgG aggregates; all IgG sub-classes should be present; there should be a low IgA concentration; the level of antibody against at least two bacterial species and two viruses should be ascertained Normal human Ig used to prevent measles in highly susceptible individuals and to provide temporary protection /up to 12 weeks/ against hepatitis A infection. Live vaccines should not normally be given for 12 weeks after an injection of normal human Ig.
  • 27.           Specific human Ig. These preparations are made from the plasma of patient who have recently recovered from an infection or are obtained from individuals who have been immunized against a specific infection. The advantages of Ig-s are: 1.      freedom from hepatitis B 2.      concentration of the antibodies into a small volume for intramuscular use. 3.      stable antibody content, if properly stored.
  • 29. Route of Adminstration DPT, DT Tetanus, HepatitisA, HepatitisB, Pneumococcal , Rabies, Hib, Influenza Intramuscular Measles, Mumps, Rubella, MMR, IPV, Pneumoccocal, Influenza Subcutaneous BCG, Rabies Intradermal OPV Oral
  • 30. Site of Administration Anterolateral aspect of the thigh in infants and deltoid muscle in older children or adult. Intramuscular Anterolateral aspect of the thigh or the upper arm Subcutaneous Over the insertion of left deltoid muscle Intradermal
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  • 50. Recommended Schedule for Immunization of Healthy Infants and Children/BULGARIA/   24 h HB vax 0.5 ml i.m. 48h BCG 0.1 ml i.d. 1mo HB vax 0.5ml i.m. 2mo Pentaxim(DTaP, I PV,Hemophilus infl B).0.5ml i.m. ;vaccineS.pneumoniae-0,5i.m. 3mo Pentaxim(DTaP, IPV,Hemophilus infl B).0.5ml i.m. vaccineS.pneumoniae-0,5i.m 4mo Pentaxim(DTaP, IPV,Hemophilus infl B).0.5ml i.m. vaccineS.pneumoniae-0,5i.m 6mo HB vax 1 2 mo vaccine against S.pneumoniae-0,5i.m. (booster) 13mo MMR 0.5ml i.m. 16-24mo Pentaxim(DTaP, IPV,Hemophilus infl B).0.5ml 6у Tetraxim( IPV , DTaP)-0.5ml i.m. 7y Mantoux 0.1i.d .(negative<5mm-BCG) 1 1 y Mantoux .(negative<5mm-BCG) 12y MMR , Td 17y Td,Mantoux .(negative<5mm-BCG) 25,35,45…y Td 0.5ml i.m.
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