Immunizations
June 5, 2015
Brenda Ormesher, MD Infectious Disease Peacehealth Medical Group Springfield, OR
Immunizations June 5, 2015 Brenda Ormesher, MD Infectious Disease - - PowerPoint PPT Presentation
Immunizations June 5, 2015 Brenda Ormesher, MD Infectious Disease Peacehealth Medical Group Springfield, OR Disclosures None Goals Understand basic public health impact of immunization Recognize types of vaccinations available
Brenda Ormesher, MD Infectious Disease Peacehealth Medical Group Springfield, OR
None
Understand basic public health impact of immunization Recognize types of vaccinations available Identify resources available for identifying CDC
recommended immunizations
Discuss differences and rationale for use of specific
vaccination formulations in practice
vac·cine/vakˈsēn/ (Noun) a substance used to stimulate the production of antibodies and provide immunity against one or several diseases, prepared from the causative agent
without inducing the disease.
One of the great public health achievements in human
history
Inoculation against smallpox was practiced 2000 years ago
but modern concept credited to Edward Jenner (1796)
Now 23 FDA approved vaccine-preventable diseases
http://www.immunize.org/catg.d/p4037.pdf
Antigens
component derived from disease- causing organism which trigger protective immune response
Stabilizers
Maintain effectiveness during storage
Factors affecting stability include temperature and pH
Include magnesium chloride (OPV), magnesium sulfate (RSV, measles), lactose-sorbitol and sorbitol- gelatin
Adjuvants
Added to vaccines to stimulate production of antibodies
Several hundred different types
Antibiotics
Trace amounts used in manufacturing to prevent bacterial contamination of tissue growth cells for viruses
Trace amounts (25 micrograms neomycin in MMR and IPV)
Preservatives
Multidose vaccines to prevent bacterial and fungal growth
Include thiomersal, formaldehyde (purification process removes almost all formaldehyde, <0.02% per dose)
http://vaccine-safety-training.org/adverse-events-causes.html
Live, attenuated Inactivated/ killed Toxoid (inactivated toxin) Subunit/ conjugate DNA vaccine Recombinant vector
pathogen) Examples:
MMR (measles, mumps, rubella) Varicella (chickenpox) Influenza nasal spray Rotavirus Zoster (shingles) Yellow fever Tuberculosis (BCG) Oral polio vaccine (OPV)
http://vaccine-safety-training.org/live-attenuated-vaccines.html
Produce inactivated vaccine by killing the microbe with chemicals,
heat, or radiation
More stable and safe than live vaccines (dead microbes cannot
mutate)
Stimulate a weaker immune system response than live vaccines Requires booster shots to maintain immunity Examples:
Polio (IPV) Hepatitis A Whole-cell pertussis (wP) Rabies
http://vaccine-safety-training.org/inactivated-whole-cell-vaccines.html
For bacteria that secrete toxins (toxin must be main cause of
illness)
Inactivate toxins by treating with formalin To increase immune response the toxoid is absorbed to
aluminum or calcium salts (serve as adjuvant)
Produces antibodies that lock onto & block the toxin Examples:
Diphtheria, tetanus (part of DTaP)
http://vaccine-safety-training.org/toxoid-vaccines.html
Use only part of a target pathogen (no live components) Protein or polysaccharide- Uses part of target pathogen to provoke a
response from the immune system Conjugate- Link antigens or toxins that immune system will recognize to the polysaccharide coating of bacteria
No guarantee that immunological memory will be formed in correct
manner
Examples:
Influenza (injection) Haemophilus influenza type b (Hib) Pertussis (part of DTaP) Pneumococcal Meningococcal Human papillomavirus (HPV)
Little or short-lived impact on
carriage of bacteria
Decreasing immune response
with time (needs boosters)
Limited ability to protect
children under 2 years
Enhances the immune
response and long term recognition
Protective immune response in
infants
Minimizes hyporesponsiveness Harder to design/ develop
http://www.nature.com/nri/journal/v9/n3/fig _tab/nri2494_F1.html
http://vaccine-safety-training.org/subunit-vaccines.html
CDC 2015 Adult Immunization Schedule
CDC 2015 Adult Immunization Schedule
iOS 5.0 or later or Google Play for Android 2.1
chedules/hcp/schedule- app.html#download
Adenovirus type 4 & 7
Anthrax
Chickenpox (Varicella)
Diphtheria
Hepatitis A
Hepatitis B
Hib (Haemophilis influenza type b)
HPV (Human Papillomavirus)
Influenza
Japanese encephalitis
Measles
Meningococcal
Mumps
Pertussis (Whooping cough)
Pneumococcal
Poliovirus
Rabies
Rotavirus
Shingles (Herpes zoster, varicella)
Tetanus
Tuberculosis
Typhoid fever
Yellow fever
http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/us-vaccines.pdf
That depends….
http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6332a3.htm#Tab
Cost $32/ dose
In pediatrics demonstrated superior efficacy in live
attenuated vaccine
reduction of 55% in culture confirmed influenza cases in ages 6
to 59 months
52% increased protection in children age 6 to 71 months)
http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6332a3.htm
Give Fluzone In a previously unvaccinated child (< 8 years old) give 2 doses
http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6332a3.htm
Pregnant? Immunosuppressed? Egg allergy? Children age 2 to 17 years receiving aspirin? Children age 2 to 4 years who have asthma with wheezing in past
12 months?
Influenza antiviral medications in past 48 hours? Care for severely immunosuppressed person who require a
protective environment?
http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6332a3.htm
Yes: do not give live attenuated vaccine (FluMist), give
inactivated influenza vaccine
No: give FluMist (cost $22 per dose)
http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6332a3.htm
Inactivated influenza vaccine high dose (60 mg of
hemagglutinin per strain) induced a significantly higher antibody response and provider better protection against lab-confirmed illness than standard inactivated influenza vaccine (15 mg of hemagglutinin per strain)
Cost of high dose influenza vaccine $30 vs $10 for standard
dose
DiazGranados, C. Et al. “Efficacy of High-Dose versus Standard-Dose Influenza Vaccine in Older Adults.” NEJM 2014; 371:635-645.
Vaccine effectiveness decline post-vaccination
By age: Vaccine effectiveness in < 65 years estimated at 44%,
vaccine effectiveness > 65 years estimated at 19%
By time: Vaccine effectiveness in first 100 days 61%, between
100 and 119 days was 42%, after 120 days was 0%
Castilla J, et al. “Decline in Vaccine Effectiveness with Time After Vaccination, Navarre, Spain, Season 2011/12.” Eurosurveillance, Volume 18, Issue 5, 31Jan2013.
Rationale for quadrivalent: historically influenza vaccines
contain only one strain of B virus although though there are two different lineages of B strains that circulate most seasons
Benefit: improved coverage of B strain which could account for
1-44% of influenza cases (based on data from preceding 10 years)
Negative: Cost ($15 for quad vs $10 for tri), supply
http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/us-vaccines.pdf
Pneumovax (PPSV23)- Pneumococcal polyvalent (polysaccharide) vaccine covering 23 serotypes, cost $85/ dose
Prevnar (PCV13)- Pneumococcal conjugate vaccine covering 13 serotypes, cost $150/ dose
Recommendation for adults 65 years
Recommendations for adults 19 years
disease, function or anatomic asplenia, congenital or acquired immunodeficiency, HIV infection, chronic renal failure, nephrotic syndrome, leukemia, Hodgkin disease, generalized malignancy, long-term immunosuppressive therapy, solid
Bonten M, Bolkenbaas M, Huijts S, et al. Community Acquired Pneumonia Immunization Trial in Adults (CAPiTA). Abstract no. 0541. Pneumonia 2014;3:95. https://pneumonia.org.au/public/journals/22/PublicFolder/ABSTRACTBOOKMASTERforwebupdated20-3-14.pdf .
http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/us-vaccines.pdf
http://www.meningitisinfo.com/Epidemiology_ssi.aspx
Menomune
Polysaccharide vaccine
Licensed for data on A & C strains (not enough date for W-135, Y)
Recommended for adults who require single dose only (travelers, military recruits)
Cost $125/ dose
Menactra
Polysaccharide conjugate vaccine
Licensed for A, C, Y, W-135
Asplenia, complement deficiencies, microbiologist, frequent international travelers to high endemic regions (African meningitis belt, Hajj)
Cost $100/ dose
Menveo
polysaccharide conjugate vaccine
Licensed for A, C, Y, W-135
Asplenia, complement deficiencies, microbiologist, frequent international travelers to high endemic regions (African meningitis belt, Hajj)
Cost $120/ dose
Trumenba
Composed of two recombinant lipidated factor H binding protein
(fHBP) variants from N. meningitidis serogroup B, one from fHBP subfamily A and one from subfamily B (A05 and B01, respectively)
Series of 3 shots at 0, 2 and 6 months Cost $120/ dose
Bexsero
Composed of 4 distinct antigens including factor H binding protein
(fHbp), Neisserial adhesin A (NadA), Neisserial heparin-binding antigen (NHBA), and PorA P1.4 immunodominant antigen of OMV NZ (strain NZ98/254)
Series of 2 shots at least 1 month apart Cost $160/does
Cervarix
Viral protein subunit vaccine
Covers serotype 16 and 18 (may provide cross protection for 31, 33, 45,52)
Contains novel adjuvant so may be responsible for great antibody response (unknown)
Series of 3 shots at 0, 1-2 and 6 months
Cost $130/ dose
Gardasil
Viral protein subunit vaccine
Covers serotype 6, 11, 16 and 18 (may provide cross protection for 31, 45)
Series of 3 shots at 0, 2 and 6 months
Cost $150/ dose
Gardasil 9
Viral protein subunit vaccine
Covers serotype 6, 11, 16, 18, 31, 33, 45, 52 and 58
Series of 3 shots at 0, 2 and 6 months
Cost $160/ dose
http://www.ganfyd.org/index.php?title=File:HPVCerv icalCancer.png