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VACCINES
Dr. Rajeev K Sookun
M.D
Dept. of Community Medicine
Definitions
 VACCINE-suspension of attenuated live or
killed microorganisms administered to
induce immunity
 TOXOID-modified bacterial toxin,now non-
toxic,which stimulates formation of
antitoxins
 IMMUNITY-resistance of a body to the effects
of a deleterious agent, such as pathogenic
microorganism
Types Of Vaccines
 Live Attenuated Vaccines
 Inactivated Vaccines
 Toxoids
 Sub-Unit Vaccines
 Conjugate Vaccines
 DNA Vaccines
BCG Vaccine
 Calmette and Guerin, two French scientists
began attenuating avirulent strain of M.Bovis
on 1906.
 After 230 subcultures over a period of 13
years, they were able to evolve a strain
known as bacilli Calmette Guerin or BCG.
 The WHO has recommended the ‘Danish
1331’ strain for the production of BCG
vaccine.
AIM
 The aim of BCG vaccination is to induce a
benign, artificial primary infection which will
stimulate an acquired resistance to possible
subsequent infection with virulent tubercle
bacilli.
Types of Vaccine
 There are 2 types of BCG vaccine.
 1) The liquid (fresh) vaccine
 2) The freeze-dried vaccine
 The freeze-dried vaccine is more stable
preparation than liquid vaccine.
 Present day vaccines are distributed in the
freeze-dried form
Dosage
 For vaccination,the usual strength is 0.1 mg
in 0.1 ml volume.
 The dose for newborn aged below 4 weeks is
0.05ml.
( This is because the skin of the newborn is
rather thin and intradermal injection with full
dose 0.1ml might penetrate into deeper tissue
and give rise to local abscess formation and
enlarged regional lymph nodes.
Administration
 The vaccine is injected intradermally using a
‘Tuberculin’ syringe
 The site of injection should be just
above the insertion of the deltoid
muscle
 A satisfactory injection should produce a
wheal of 5mm in diameter.
Age
 BCG should be administered very early in
infancy either at birth ( for institutional
deliveries) or at 6 weeks of age.
 BCG administration early in life provides a
high level of protection,particularly against
the severe forms of childhood tuberculosis
and tuberculous meningitis.
Complications
 Prolong severe ulceration at site of
vaccination.
 Suppurative lymphadenitis.
 Osteomyelitis.
 Disseminated BCG infection.
 Death
Protective Value
 The duration of protection is from 15 to 20
years.
 Studies have shown that the range of
protection offered by BCG varied from 0 to
80 % in different parts of the world.
Contraindications
Should not be given to people suffering from
 1) Generalised eczema
 2) Infective dermatitis
 3) Hypogammaglobulinaemia
 4) Deficient Immunity
 5) Leukemia
 6) Lymphoma
 7) General malignant diseases
 8) In pregnancy.
Oral Polio Vaccine
 Oral polio vaccine was described by Sabin in
1957.
 It contains live attenuated virus types 1, 2 and
3 grown in primary monkey kidney or human
diploid cell cultures.
 For administrative convenience the Trivalent
(TOPV) vaccine is given.
Dosage
• The dose is 2 drops.
 WHO recommends that vaccinators use
dropper supplied with the vial of oral polio
vaccine as this is the most direct and effective
way to deliver the correct drop size.
Administration
 The back of the child is tilted and gently squeeze
the cheek or pinch the nose to make the mouth
open.
 The drop is allowed to fall on
the child’s tongue from the
dropper.
 The OPV induces both local and systemic
immunity.
Advantages of OPV
 Does not require the use of highly trained
personnel.
 Induces both humoral and intestinal immunity.
 Antibody is quickly produced in a large
proportion of vaccines.
 The vaccinee excretes the virus and so infects
others who are also immunised
thereby
 (i) Useful in controlling epidemics
 (ii) relatively inexpensive.
Complications
 OPV vaccine associated with paralytic polio.
Contraindications
 Live vaccine is not usually given to
immunocompromised individuals.
 Leukemia
 Malignancy
 On corticosteroids therapy
Storage
 Sterilised vaccine should be kept at +4oc for a
year and at +25oc for a month
 Non-sterilised vaccine should be kept at -20oc
in deep freeze.
DPT Vaccine
 It gives protection against 3 diseases
 1) Diphtheria
 2)Pertusis
 3)Tetanus
 The vaccine is a toxoid preparation of 2 types
 1)Plain
 2) Absorbed
 Has a protective efficacy of 85%
Dosage and Administration
 0.5ml is available
 Administrated in deep intramuscular
injection in upper and outer aspect of thigh.
Schedule
 3 doses at 3, 10, 14 weeks.
 Booster dose at 18 months.
Adverse Reaction
 Fever
 Mild local reactions
 Pain
 Swelling
 Induration at site of injection
 Neurological complications (encephalitis)
 Encephalopathy
 Convulsion
 Reye’s syndrome
Contraindications
Severe reaction to previous dose like:
 Collapse
 Shock
 Persistent screaming
 Convulsions
 Other neurological and anaphylactic
reactions
Measles Vaccine
 Only live attenuated vaccines are
recommended for use.
 Presented as a freeze-dried product.
 Before use, the vaccines is reconstituted with
sterile diluent.
Dosage
 0.5ml single dose given subcutaneously at 9
months old.
 Suspected contacts are
immunised with vaccine
within 3 days of exposure
Storage
 Kept at 20-80C in dark, refrigerated in freeze
compartment.
 The vaccine in sensitive to sunlight, hence it
is kept in coloured vials.
Immune response
 It induces both humoral and cellular
immunity
Reactions
 When injected, the attenuated virus
multiplies and induces a mild ‘measles’
illness (fever and rash) 5-10 days after
immunization
 Fever may last for 1-2 days and rash 1-3 days.
Immunity
 It develops within 11-12 days after vaccination
and usually persists for life
Contraindications
 Pregnancy
 HIV infection
 Immunodeficiency
 Malignancy
 Steroid therapy
 Radiation therapy
Adverse Reaction
 Toxic shock syndrome
Hepatitis B Vaccine
 The recombinant hepatitis B vaccine was
introduced in 1986.
 The active substance in recombinant
hepatitis B vaccine is HBsAg.
Dosage
 Adult dose is 10-20 mcg initially (depending
on formulation) and again at 1 and 6 months.
 Children under 1o yrs of age should be given
half of the adult dose at the same time
intervals.
Administration
 For greatest reliability of absorption, the
deltoid muscle is preferred for injection as
gluteal injection often results in deposition of
vaccine in fat rather than muscle.
Advantages
 All children and adolescent aged less than 18 yrs and
not previously vaccinated should receive the vaccine.
 Indicated for certain groups at high risk of
contracting HBV infection. E.g.
 High risk sexual behaviour
 Partner
 Household contacts of HBsAg positive persons
 Injecting drug users
 Person who frequently required blood transfusions
 Recipient of solid organ transplantation
 Health care workers dealing with HBV patients
 International travellers to endemic countries
Contraindications
 History of allergic reactions
Storage
 The vaccine should be stored at 2 – 8oc .
 Freezing must be avoided.
Tetanus Toxoid
 2 types
 1) Plain
 2) Fluid (purified)
 Fluid tetanus toxoid stimulates higher and
longer immunity response than plain toxoid
Dosage and Schedule
 A primary course of immunisation consists of
2 doses given at interval of 1-2 months.
 1st booster at 1 yr after the initial 2 doses.
 2nd booster given 5 yrs after 3rd dose.
 In pregnancy, 2 doses are given:
 1st at 16-2o weeks
 2nd at 20-24 weeks
Administration
 Intramuscular in upper arm into deltoid
muscle.
Complications
 Allergy
Storage
 Tetanus Toxoid is stored at 4-10oc.
 It is not allowed to freeze.
Rabies Vaccine
 Against the rabies virus.
 Prevention by
 1) post exposure prophylaxis
2) pre exposure prophylaxis
 3) Post exposure treatment of persons who
have been vaccinated previously.
Dosage
 Adult 0.5 ml or 1ml depending on type of
vaccine
Administration
 Rabies vaccine is given intramuscular or
intradermal
Complications
 Minor and transient erythema, pain and
swelling at site of injection.
 Fever, headache, dizziness, gastro intestinal
symptoms.
YO, IT’S
OVER

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Immunizing Agents by Dr. Sookun Rajeev Kumar

  • 1. VACCINES Dr. Rajeev K Sookun M.D Dept. of Community Medicine
  • 2. Definitions  VACCINE-suspension of attenuated live or killed microorganisms administered to induce immunity  TOXOID-modified bacterial toxin,now non- toxic,which stimulates formation of antitoxins  IMMUNITY-resistance of a body to the effects of a deleterious agent, such as pathogenic microorganism
  • 3. Types Of Vaccines  Live Attenuated Vaccines  Inactivated Vaccines  Toxoids  Sub-Unit Vaccines  Conjugate Vaccines  DNA Vaccines
  • 4. BCG Vaccine  Calmette and Guerin, two French scientists began attenuating avirulent strain of M.Bovis on 1906.  After 230 subcultures over a period of 13 years, they were able to evolve a strain known as bacilli Calmette Guerin or BCG.  The WHO has recommended the ‘Danish 1331’ strain for the production of BCG vaccine.
  • 5. AIM  The aim of BCG vaccination is to induce a benign, artificial primary infection which will stimulate an acquired resistance to possible subsequent infection with virulent tubercle bacilli.
  • 6. Types of Vaccine  There are 2 types of BCG vaccine.  1) The liquid (fresh) vaccine  2) The freeze-dried vaccine  The freeze-dried vaccine is more stable preparation than liquid vaccine.  Present day vaccines are distributed in the freeze-dried form
  • 7. Dosage  For vaccination,the usual strength is 0.1 mg in 0.1 ml volume.  The dose for newborn aged below 4 weeks is 0.05ml. ( This is because the skin of the newborn is rather thin and intradermal injection with full dose 0.1ml might penetrate into deeper tissue and give rise to local abscess formation and enlarged regional lymph nodes.
  • 8. Administration  The vaccine is injected intradermally using a ‘Tuberculin’ syringe  The site of injection should be just above the insertion of the deltoid muscle  A satisfactory injection should produce a wheal of 5mm in diameter.
  • 9. Age  BCG should be administered very early in infancy either at birth ( for institutional deliveries) or at 6 weeks of age.  BCG administration early in life provides a high level of protection,particularly against the severe forms of childhood tuberculosis and tuberculous meningitis.
  • 10. Complications  Prolong severe ulceration at site of vaccination.  Suppurative lymphadenitis.  Osteomyelitis.  Disseminated BCG infection.  Death
  • 11. Protective Value  The duration of protection is from 15 to 20 years.  Studies have shown that the range of protection offered by BCG varied from 0 to 80 % in different parts of the world.
  • 12. Contraindications Should not be given to people suffering from  1) Generalised eczema  2) Infective dermatitis  3) Hypogammaglobulinaemia  4) Deficient Immunity  5) Leukemia  6) Lymphoma  7) General malignant diseases  8) In pregnancy.
  • 13. Oral Polio Vaccine  Oral polio vaccine was described by Sabin in 1957.  It contains live attenuated virus types 1, 2 and 3 grown in primary monkey kidney or human diploid cell cultures.  For administrative convenience the Trivalent (TOPV) vaccine is given.
  • 14. Dosage • The dose is 2 drops.  WHO recommends that vaccinators use dropper supplied with the vial of oral polio vaccine as this is the most direct and effective way to deliver the correct drop size.
  • 15. Administration  The back of the child is tilted and gently squeeze the cheek or pinch the nose to make the mouth open.  The drop is allowed to fall on the child’s tongue from the dropper.  The OPV induces both local and systemic immunity.
  • 16. Advantages of OPV  Does not require the use of highly trained personnel.  Induces both humoral and intestinal immunity.  Antibody is quickly produced in a large proportion of vaccines.  The vaccinee excretes the virus and so infects others who are also immunised thereby  (i) Useful in controlling epidemics  (ii) relatively inexpensive.
  • 17. Complications  OPV vaccine associated with paralytic polio.
  • 18. Contraindications  Live vaccine is not usually given to immunocompromised individuals.  Leukemia  Malignancy  On corticosteroids therapy
  • 19. Storage  Sterilised vaccine should be kept at +4oc for a year and at +25oc for a month  Non-sterilised vaccine should be kept at -20oc in deep freeze.
  • 20. DPT Vaccine  It gives protection against 3 diseases  1) Diphtheria  2)Pertusis  3)Tetanus  The vaccine is a toxoid preparation of 2 types  1)Plain  2) Absorbed  Has a protective efficacy of 85%
  • 21. Dosage and Administration  0.5ml is available  Administrated in deep intramuscular injection in upper and outer aspect of thigh.
  • 22. Schedule  3 doses at 3, 10, 14 weeks.  Booster dose at 18 months.
  • 23. Adverse Reaction  Fever  Mild local reactions  Pain  Swelling  Induration at site of injection  Neurological complications (encephalitis)  Encephalopathy  Convulsion  Reye’s syndrome
  • 24. Contraindications Severe reaction to previous dose like:  Collapse  Shock  Persistent screaming  Convulsions  Other neurological and anaphylactic reactions
  • 25. Measles Vaccine  Only live attenuated vaccines are recommended for use.  Presented as a freeze-dried product.  Before use, the vaccines is reconstituted with sterile diluent.
  • 26. Dosage  0.5ml single dose given subcutaneously at 9 months old.  Suspected contacts are immunised with vaccine within 3 days of exposure
  • 27. Storage  Kept at 20-80C in dark, refrigerated in freeze compartment.  The vaccine in sensitive to sunlight, hence it is kept in coloured vials.
  • 28. Immune response  It induces both humoral and cellular immunity
  • 29. Reactions  When injected, the attenuated virus multiplies and induces a mild ‘measles’ illness (fever and rash) 5-10 days after immunization  Fever may last for 1-2 days and rash 1-3 days.
  • 30. Immunity  It develops within 11-12 days after vaccination and usually persists for life
  • 31. Contraindications  Pregnancy  HIV infection  Immunodeficiency  Malignancy  Steroid therapy  Radiation therapy
  • 32. Adverse Reaction  Toxic shock syndrome
  • 33. Hepatitis B Vaccine  The recombinant hepatitis B vaccine was introduced in 1986.  The active substance in recombinant hepatitis B vaccine is HBsAg.
  • 34. Dosage  Adult dose is 10-20 mcg initially (depending on formulation) and again at 1 and 6 months.  Children under 1o yrs of age should be given half of the adult dose at the same time intervals.
  • 35. Administration  For greatest reliability of absorption, the deltoid muscle is preferred for injection as gluteal injection often results in deposition of vaccine in fat rather than muscle.
  • 36. Advantages  All children and adolescent aged less than 18 yrs and not previously vaccinated should receive the vaccine.  Indicated for certain groups at high risk of contracting HBV infection. E.g.  High risk sexual behaviour  Partner  Household contacts of HBsAg positive persons  Injecting drug users  Person who frequently required blood transfusions  Recipient of solid organ transplantation  Health care workers dealing with HBV patients  International travellers to endemic countries
  • 37. Contraindications  History of allergic reactions
  • 38. Storage  The vaccine should be stored at 2 – 8oc .  Freezing must be avoided.
  • 39. Tetanus Toxoid  2 types  1) Plain  2) Fluid (purified)  Fluid tetanus toxoid stimulates higher and longer immunity response than plain toxoid
  • 40. Dosage and Schedule  A primary course of immunisation consists of 2 doses given at interval of 1-2 months.  1st booster at 1 yr after the initial 2 doses.  2nd booster given 5 yrs after 3rd dose.  In pregnancy, 2 doses are given:  1st at 16-2o weeks  2nd at 20-24 weeks
  • 41. Administration  Intramuscular in upper arm into deltoid muscle.
  • 43. Storage  Tetanus Toxoid is stored at 4-10oc.  It is not allowed to freeze.
  • 44. Rabies Vaccine  Against the rabies virus.  Prevention by  1) post exposure prophylaxis 2) pre exposure prophylaxis  3) Post exposure treatment of persons who have been vaccinated previously.
  • 45. Dosage  Adult 0.5 ml or 1ml depending on type of vaccine
  • 46. Administration  Rabies vaccine is given intramuscular or intradermal
  • 47. Complications  Minor and transient erythema, pain and swelling at site of injection.  Fever, headache, dizziness, gastro intestinal symptoms.