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ADULT
IMMUNIZATION
 PRESENTER-DR.PRADEEP KATWAL
MODERATOR-DR. NAVEEN K. PANDEY
• Jenner was an
  English doctor, the
  pioneer of smallpox
  vaccination and the
  father of
  immunology….
Louis Pasteur
          A Vision to future of humanity

“When meditating over
a disease, I never
think of finding a
remedy for it, but,
instead, a means of
prevention.”



                                           3
Most successful medical
intervention ever developed for
prevention of infectious disease


  IMMUNIZATION
CONDITION         ANNUAL NO.        NO. OF CASES REDUCTION
                  OF                REPORTED IN (%) IN CASES
                  PREVACCINE        2010A        AFTER
                  CASES                          WIDESPREAD
                  (AVERAGE)                      VACCINATION
SMALLPOX          29,005            0                  100
DIPHTHERIA        21,053            0                  100
INVASIVE      16,069                4,167C             74
PNEUMOCOCC
AL INFECTION:
<5 YEARS OF
AGE
INVASIVE      63,067                44,000C            30
PNEUMOCOCC
AL INFECTION:
ALL AGES
c
 Data are from the CDC's Active Bacterial Core Surveillance Report;
www.cdc.gov/abcs/survreports/spneu08.pdf.
Source: Adapted from Roush et al., with permission.
• Immunization-
  – Immunization is the process whereby a
   person is made immune or resistant to an
   infectious disease, typically by the
   administration of a vaccine.

• Vaccine-
   A vaccine is any preparation intended to
  produce immunity to a disease by
  stimulating the production of antibodies..
Immunizing agents
1) Vaccines
• Live attenuated:
      Bacterial: BCG, Typhoid, plague
      Viral :   Oral polio , Yellow fever, Measles, Mumps,

                 Rubella, Influenza
• Inactivated or killed vaccines
     Bacterial: Typhoid, Cholera, Pertusis, Plague
     Viral :    Rabies, Salk (Polio), Influenza , Hepatitis B,

                Japanese encephalitis

2) Toxoids : Diphtheria, Tetanus
Physiological basis

ACQUIRED IMMUNITY
– HUMORAL IMMUNITY



– CELL-MEDIATED IMMUNITY
Antibody response after exposure
Central Role of Helper T Cells
ADJUVANTS




A vaccine adjuvant is a component that potentiates the
immune responses to an antigen and/or modulates it
towards the desired immune responses.
Aims of immunization
• Eradication
  – State where disease and its causal agent have been
    removed from natural environment
• Elimination
  – Reduction to zero cases or reduction in indegineous
    sustained transmission of infection in geographical
    region.
• Control
  – Reduction of illness outcomes and limitation of the
    disruptive impacts associated with outbreaks of
    disease in communities, schools, and institutions.
Why we need adult vaccines ?
Burden of Adult Vaccine-Preventable Disease

 Influenza:        10-20% of US population annually
                   200,000 hospitalizations
                   36,000 deaths (average)

 Pneumococcal:     2,000-5000 meningitis
                   40,000+ bloodstream infections
                   150,000-300,000 pneumonia

 Pertussis:         1 million
 Cervical cancer:   10,000
 Shingles:          1 million
 Death from vaccine-preventable diseases: 43,000
WHY ADULTS?
The burden

Vaccination gap

High risk group

Chronic medical conditions
Recommendation for adult
        immunization
• ACIP(advisory committee on immunization
  practices)
Influenza vaccine
• 2009,     update
 WHO
199 countries
officially reported
 over 482,300
 laboratory
 confirmed cases of
 the influenza H1N1
6,071 deaths
•   Annual vaccination
•   Age 6 months and older
•   Early autumn before influenza outbreak
•   Influenza A and influenza B
•   Influenza type/origin/isolate number/year
    of isolation/subtype
Live vaccine
•   Intranasal via spray
•   2-49 yrs of age
•   Non pregnant
•   Has currently
    – Circulating Strain of influenza A and b
    – Cold adapted attenuated master strain
• Protection >90% in young children
• Don’t give antiviral drugs for 2 weeks
Killed vaccine
• Inactivated vaccine

• 6 months or older

• Has influenza A and B
  – Previous year circulating strain

  – Anticipated strain circulating this year

• Immunocompromised

• Protection 50-80% is expected.**
Contraindication

 Egg allergy

 ?Pregnant women

 ?Gullian barre syndrome(if within 6 wks)
•    Vaccine was found to be 33% effective in preventing
    total respiratory illness (influenza-like illness and
    clinically diagnosed pneumonia). In prevention of
    pneumonia alone, vaccine was 43% effective. The
    estimate for prevention of pneumonia rose to 55% if the
    period under consideration was limited to the time of
    peak influenza activity. Given the number of eligible
    homes and the cohort methodology used, the results
    support continuation of current policy, encouraging use
    of vaccine in all nursing home residents.
NRS- 1011/-
influvac
A/california/7/2009(H1N1)
A/perth/16/2009(H3N2)
A/victoria/210/2009
B/brisbrane/60/2008

Per 0.5 ml
Pneumococcal vaccine
Polysaccharide-protein
 Polysaccharide vaccine    conjugate vaccine
       (PPV 23)            • The Difference



•CONFLIICTING RESULTS



 T Cell independent       • Infants and young
immunity                   • 7,10,13 serotype
Revaccinate after 5 yrs      – Invasive pneumococcal
                                vaccine
                              – Antibiotic resistant strain
Harrison figure




Changes in invasive pneumococcal disease (IPD) incidence, by serotype group,
among children <5 years old (first) and adults >65 years old (second), 1998–2007.
*7-Valent pneumococcal conjugate vaccine (PCV7) was introduced in the United
States for routine administration to infants and young children during the second half
of 2000. (Reprinted with permission from Pilishvili et al, 2010.)
Conclusion
The recent introduction of universal PCV vaccination in children has led
to a change in the epidemiology of IPD in adults. The incidence of IPD
associated with PCV serotypes is expected to decrease and that
associated with other serotypes is expected to increase in adults.
Despite a reduction in the incidence of IPD, vaccinating the elderly and
at-risk adults with PPV23 in Germany against IPD and NBPP remains a
cost-effective strategy because of its broad serotype coverage.
RS 1857/-
• Pneumo 23
Hepatitis B vaccination
BEHAVIOURAL
Sexually active person without long-term non-
monogamous relationship
Person with more than one sexual partner during six
months
Seeking STI evaluation
Current or recent IV drug user




OCCUPATIONAL

Healthcare professionals risk of exposure to
blood or potentially infectious body fluids
Pre-exposure prophylaxis

• Included in EPI schedule
• 3 IM injections (deltoid, not
  gluteal)
• 0,1,6 months
• Contains HBsAg (10 mcg)
   Post-exposure prophylaxis
• Administer both HBIG and HB vaccine
Hepatitis B vaccine

              RS 177 PER
              DOSE
Hepatitis A virus
• Behavioral:
  – Men who have sex with men
  – IV drugs users
• Occupational:
  – Persons working with HAV-infected primates or
    with HAV in a research laboratory setting.
• Medical:
  – Persons with chronic liver disease
  – persons who receive clotting factor concentrates.
• Other:
  – Persons traveling to or working in countries that
    have high or intermediate endemicity of hepatitis A
COMBINED HEPATITIS A
        HEPATITIS B VACCINE
• Approved by the FDA in United States for
  persons >18 years old
• Contains 720 EL.U. hepatitis A antigen and
   20 μg. HBsAg
• Vaccination schedule: 0,1,6 months
• Immunogenicity similar to single-antigen
  vaccines given separately
• Can be used in persons > 18 years old who
  need vaccination against both hepatitis A and
  B
• Formulation for children available in many
  other countries
Meningococcal Vaccine
Single dose is recommended -
•           Serogroups A,C,Y W135
    T cell independent

    Cannot be given in age less than 2 years of age

    Efficay C component >90% (children)

    Efficacy A component >95%(all age group)

    Duration of protection 2-5 yrs
Meseals Mumps Rubella
MMR
• All adults born in 1957 or later should
  have documentation of 1 or more MMR
  vaccine
• 2nd dose- 28 days after first dose
• Previous diagnosis of
  – Meseals
  – Mumps
  – Rubella
MESEALS MUMPS RUBELLA
OUTBREAK SETTING           OUTBREAK SETTING           CHILD BEARING AGE


Students of post-          Students of post           -If Non-pregnant
secondary school           secondary school
                                                      -IF immune status is
                                                      not known
Healthcare facility        Healthcare facility
workers                    workers                    Upon completion and
                                                      before discharge
International travellers   International travellers
Human papilloma virus
• Primary goal is to prevent cervical cancer
• All females 11-12 yrs
• Catchup vaccination 13-26 yrs
• Before sexual activity
• Schedule- [0-15days-6 months}
• Quadrivalent (HPV4) vaccine or bivalent
  vaccine (HPV2)
• May be administered to males aged 9
  through 26 years
• Four strains of human papillomavirus
  (HPV) -- HPV-6, 11, 16, and 18
Tetanus Diptheria pertusis
Tetanus,Diphtheria & acellular Pertusis
• Primary series : 3 dose
            1st & 2nd dose : at least 4 wks apart
            3rd dose: 6-12 months after the second.
    Tdap can substitute any one of the 3 doses of Td

• Booster dose : every 10 yrs
            Tdap or Td may be used.
• Tdap should replace single dose of Td in adult aged < 65
  yrs.
• Pregnancy:
         If last Td vaccine >10 yrs : Td at 2nd or 3rd trimester.
         If last Td vaccine <10 yrs : Td at immediate post partum
         period.
Varicella vaccination
• All adults without evidence of immunity
  2 doses of single-antigen varicella vaccine
  A second dose if received only 1 dose

Special consideration
1) close contact with persons at high risk for severe
  disease
2)Person with high risk for exposure or transmission.
Herpes zooster Vaccine
Herpes zooster
 • Single dose
 • Adults aged 60 years and older
 • Regardless of whether they report a
   previous episode of herpes zoster

                 Hib vaccine
1 dose of Hib vaccine should be considered for
persons who have sickle cell disease, leukemia, or HIV
infection, or who have had a splenectomy
Our senario
REFRENCES
• Harrison's Principles of Internal Medicine,
  18th Edition
• Guyton and Hall Textbook of Medical
  Physiology (12th Edn)
• http://www.cdc.gov/vaccines/default.htm
• http://www.fda.gov/BiologicsBloodVaccines
  /Vaccines/QuestionsaboutVaccines/ucm070
  418.htm
Adult vaccination

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Adult vaccination

  • 2. • Jenner was an English doctor, the pioneer of smallpox vaccination and the father of immunology….
  • 3. Louis Pasteur A Vision to future of humanity “When meditating over a disease, I never think of finding a remedy for it, but, instead, a means of prevention.” 3
  • 4. Most successful medical intervention ever developed for prevention of infectious disease IMMUNIZATION
  • 5. CONDITION ANNUAL NO. NO. OF CASES REDUCTION OF REPORTED IN (%) IN CASES PREVACCINE 2010A AFTER CASES WIDESPREAD (AVERAGE) VACCINATION SMALLPOX 29,005 0 100 DIPHTHERIA 21,053 0 100 INVASIVE 16,069 4,167C 74 PNEUMOCOCC AL INFECTION: <5 YEARS OF AGE INVASIVE 63,067 44,000C 30 PNEUMOCOCC AL INFECTION: ALL AGES c Data are from the CDC's Active Bacterial Core Surveillance Report; www.cdc.gov/abcs/survreports/spneu08.pdf. Source: Adapted from Roush et al., with permission.
  • 6. • Immunization- – Immunization is the process whereby a person is made immune or resistant to an infectious disease, typically by the administration of a vaccine. • Vaccine- A vaccine is any preparation intended to produce immunity to a disease by stimulating the production of antibodies..
  • 7. Immunizing agents 1) Vaccines • Live attenuated: Bacterial: BCG, Typhoid, plague Viral : Oral polio , Yellow fever, Measles, Mumps, Rubella, Influenza • Inactivated or killed vaccines Bacterial: Typhoid, Cholera, Pertusis, Plague Viral : Rabies, Salk (Polio), Influenza , Hepatitis B, Japanese encephalitis 2) Toxoids : Diphtheria, Tetanus
  • 8. Physiological basis ACQUIRED IMMUNITY – HUMORAL IMMUNITY – CELL-MEDIATED IMMUNITY
  • 10. Central Role of Helper T Cells
  • 11. ADJUVANTS A vaccine adjuvant is a component that potentiates the immune responses to an antigen and/or modulates it towards the desired immune responses.
  • 12. Aims of immunization • Eradication – State where disease and its causal agent have been removed from natural environment • Elimination – Reduction to zero cases or reduction in indegineous sustained transmission of infection in geographical region. • Control – Reduction of illness outcomes and limitation of the disruptive impacts associated with outbreaks of disease in communities, schools, and institutions.
  • 13. Why we need adult vaccines ? Burden of Adult Vaccine-Preventable Disease Influenza: 10-20% of US population annually 200,000 hospitalizations 36,000 deaths (average) Pneumococcal: 2,000-5000 meningitis 40,000+ bloodstream infections 150,000-300,000 pneumonia Pertussis: 1 million Cervical cancer: 10,000 Shingles: 1 million Death from vaccine-preventable diseases: 43,000
  • 14. WHY ADULTS? The burden Vaccination gap High risk group Chronic medical conditions
  • 15. Recommendation for adult immunization • ACIP(advisory committee on immunization practices)
  • 16.
  • 17.
  • 19. • 2009, update WHO 199 countries officially reported over 482,300 laboratory confirmed cases of the influenza H1N1 6,071 deaths
  • 20.
  • 21. Annual vaccination • Age 6 months and older • Early autumn before influenza outbreak • Influenza A and influenza B • Influenza type/origin/isolate number/year of isolation/subtype
  • 22. Live vaccine • Intranasal via spray • 2-49 yrs of age • Non pregnant • Has currently – Circulating Strain of influenza A and b – Cold adapted attenuated master strain • Protection >90% in young children • Don’t give antiviral drugs for 2 weeks
  • 23. Killed vaccine • Inactivated vaccine • 6 months or older • Has influenza A and B – Previous year circulating strain – Anticipated strain circulating this year • Immunocompromised • Protection 50-80% is expected.**
  • 24. Contraindication  Egg allergy  ?Pregnant women  ?Gullian barre syndrome(if within 6 wks)
  • 25. Vaccine was found to be 33% effective in preventing total respiratory illness (influenza-like illness and clinically diagnosed pneumonia). In prevention of pneumonia alone, vaccine was 43% effective. The estimate for prevention of pneumonia rose to 55% if the period under consideration was limited to the time of peak influenza activity. Given the number of eligible homes and the cohort methodology used, the results support continuation of current policy, encouraging use of vaccine in all nursing home residents.
  • 26.
  • 30. Polysaccharide-protein Polysaccharide vaccine conjugate vaccine (PPV 23) • The Difference •CONFLIICTING RESULTS  T Cell independent • Infants and young immunity • 7,10,13 serotype Revaccinate after 5 yrs – Invasive pneumococcal vaccine – Antibiotic resistant strain
  • 31. Harrison figure Changes in invasive pneumococcal disease (IPD) incidence, by serotype group, among children <5 years old (first) and adults >65 years old (second), 1998–2007. *7-Valent pneumococcal conjugate vaccine (PCV7) was introduced in the United States for routine administration to infants and young children during the second half of 2000. (Reprinted with permission from Pilishvili et al, 2010.)
  • 32. Conclusion The recent introduction of universal PCV vaccination in children has led to a change in the epidemiology of IPD in adults. The incidence of IPD associated with PCV serotypes is expected to decrease and that associated with other serotypes is expected to increase in adults. Despite a reduction in the incidence of IPD, vaccinating the elderly and at-risk adults with PPV23 in Germany against IPD and NBPP remains a cost-effective strategy because of its broad serotype coverage.
  • 35. BEHAVIOURAL Sexually active person without long-term non- monogamous relationship Person with more than one sexual partner during six months Seeking STI evaluation Current or recent IV drug user OCCUPATIONAL Healthcare professionals risk of exposure to blood or potentially infectious body fluids
  • 36. Pre-exposure prophylaxis • Included in EPI schedule • 3 IM injections (deltoid, not gluteal) • 0,1,6 months • Contains HBsAg (10 mcg) Post-exposure prophylaxis • Administer both HBIG and HB vaccine
  • 37. Hepatitis B vaccine RS 177 PER DOSE
  • 38. Hepatitis A virus • Behavioral: – Men who have sex with men – IV drugs users • Occupational: – Persons working with HAV-infected primates or with HAV in a research laboratory setting. • Medical: – Persons with chronic liver disease – persons who receive clotting factor concentrates. • Other: – Persons traveling to or working in countries that have high or intermediate endemicity of hepatitis A
  • 39. COMBINED HEPATITIS A HEPATITIS B VACCINE • Approved by the FDA in United States for persons >18 years old • Contains 720 EL.U. hepatitis A antigen and 20 μg. HBsAg • Vaccination schedule: 0,1,6 months • Immunogenicity similar to single-antigen vaccines given separately • Can be used in persons > 18 years old who need vaccination against both hepatitis A and B • Formulation for children available in many other countries
  • 41. Single dose is recommended -
  • 42. Serogroups A,C,Y W135 T cell independent Cannot be given in age less than 2 years of age Efficay C component >90% (children) Efficacy A component >95%(all age group) Duration of protection 2-5 yrs
  • 44. MMR • All adults born in 1957 or later should have documentation of 1 or more MMR vaccine • 2nd dose- 28 days after first dose • Previous diagnosis of – Meseals – Mumps – Rubella
  • 45. MESEALS MUMPS RUBELLA OUTBREAK SETTING OUTBREAK SETTING CHILD BEARING AGE Students of post- Students of post -If Non-pregnant secondary school secondary school -IF immune status is not known Healthcare facility Healthcare facility workers workers Upon completion and before discharge International travellers International travellers
  • 46. Human papilloma virus • Primary goal is to prevent cervical cancer • All females 11-12 yrs • Catchup vaccination 13-26 yrs • Before sexual activity • Schedule- [0-15days-6 months} • Quadrivalent (HPV4) vaccine or bivalent vaccine (HPV2) • May be administered to males aged 9 through 26 years
  • 47. • Four strains of human papillomavirus (HPV) -- HPV-6, 11, 16, and 18
  • 49. Tetanus,Diphtheria & acellular Pertusis • Primary series : 3 dose 1st & 2nd dose : at least 4 wks apart 3rd dose: 6-12 months after the second. Tdap can substitute any one of the 3 doses of Td • Booster dose : every 10 yrs Tdap or Td may be used. • Tdap should replace single dose of Td in adult aged < 65 yrs. • Pregnancy: If last Td vaccine >10 yrs : Td at 2nd or 3rd trimester. If last Td vaccine <10 yrs : Td at immediate post partum period.
  • 50. Varicella vaccination • All adults without evidence of immunity 2 doses of single-antigen varicella vaccine A second dose if received only 1 dose Special consideration 1) close contact with persons at high risk for severe disease 2)Person with high risk for exposure or transmission.
  • 52. Herpes zooster • Single dose • Adults aged 60 years and older • Regardless of whether they report a previous episode of herpes zoster Hib vaccine 1 dose of Hib vaccine should be considered for persons who have sickle cell disease, leukemia, or HIV infection, or who have had a splenectomy
  • 54. REFRENCES • Harrison's Principles of Internal Medicine, 18th Edition • Guyton and Hall Textbook of Medical Physiology (12th Edn) • http://www.cdc.gov/vaccines/default.htm • http://www.fda.gov/BiologicsBloodVaccines /Vaccines/QuestionsaboutVaccines/ucm070 418.htm

Notes de l'éditeur

  1. Twinrix ® is a combined hepatitis A and hepatitis B vaccine approved in 2001 by the Food and Drug Administration (FDA) for persons 18 years of age or older. Twinrix ® contains 720 EL.U. of hepatitis A antigen and 20 μg of hepatitis B surface antigen. Primary immunization consists of three doses, given on a 0-, 1-, and 6-month schedule, the same schedule as that used for single - antigen hepatitis B vaccine. Immunogenicity of the combined vaccine appears to be similar to that of the single - antigen vaccines when given separately. Twinrix ® can be used for immunization of persons 18 years of age or older who have indications for vaccination against both hepatitis A and hepatitis B, such as users of illicit injectable drugs, men who have sex with men, and persons with clotting factor disorders who receive therapeutic blood products. Formulation for children is available in many other countries. For international travel, hepatitis A vaccine is recommended for travelers to areas of high or intermediate hepatitis A endemicity (see slide 10). Hepatitis B vaccine is recommended for travelers to areas of high or intermediate hepatitis B endemicity who plan to live or work for at least 6 months in highly endemic countries (see slide 9 in hepatitis B slide set at http://www.cdc.gov/ncidod/diseases/hepatitis/slideset/hep_b/slide_9.htm).