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    National Center for Immunization and Respiratory DiseasesCenters for Disease Control and Prevention

    Principles of Vaccination

    Epidemiology and Prevention of Vaccine-Preventable Diseases

    National Center for Immunization andRespiratory Diseases

    Centers for Disease Control and Prevention

    Revised March 2012

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    Principles of Vaccination

    Immunity

    Self vs. nonself

    Protection from infectious disease

    Usually indicated by the presence of antibody

    Very specific to a single organism

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    Principles of Vaccination

    Active Immunity

    Protection produced by the person's own

    immune system

    Usually permanent

    Passive Immunity

    Protection transferred from another person or animal

    Temporary protection that wanes with time

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    Principles of Vaccination

    Antigen

    A live or inactivated substance (e.g., protein,

    polysaccharide) capable of producing an

    immune response

    Antibody

    Protein molecules (immuno-globulin) produced by B

    lymphocytes to help eliminate an antigen

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    Passive Immunity

    Transfer of antibody produced by one human or

    other animal to another

    Temporary protection

    Transplacental most important source in infancy

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    Sources of Passive Immunity

    Almost all blood or blood products

    Homologous pooled human antibody (immune

    globulin)

    Homologous human hyperimmune globulin

    Heterologous hyperimmune serum (antitoxin)

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    Monoclonal Antibody

    Derived from a single type, or clone, of antibody-

    producing cells (B cells)

    Antibody is specific to a single antigen or closelyrelated group of antigens

    Used for diagnosis and therapy of certain cancers and

    autoimmune and infectious diseases

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    Antibody for Prevention of RSV

    Palivizumab (Synagis)

    monoclonal

    contains only RSV antibody

    will not interfere with the response to a live virus vaccine

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    Vaccination

    Active immunity produced by vaccine

    Immunity and immunologic memory similar tonatural infection but without risk of disease

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    Classification of Vaccines Live attenuated

    viral

    bacterial

    Inactivated

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    Inactivated Vaccines

    Whole

    viruses

    bacteria

    Fractional

    protein-based toxoid

    subunit polysaccharide-based

    pure

    conjugate

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    Principles of VaccinationGeneral Rule

    The more similar a vaccine is to the disease-causing

    form of the organism, the better the immune response

    to the vaccine

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    Live Attenuated Vaccines

    Attenuated (weakened) form of the "wild" virus or

    bacterium

    Must replicate to be effective

    Immune response similar to natural infection

    Usually produce immunity with one dose*

    *except those administered orally

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    Live Attenuated Vaccines

    Severe reactions possible

    Interference from circulating antibody

    Fragile must be stored and handled carefully

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    Live Attenuated Vaccines

    Viral measles, mumps,

    rubella, varicella, zoster,

    yellow fever, rotavirus,

    intranasal influenza,rotavirus, vaccinia

    Bacterial BCG*, oral typhoid

    *not available in the United States

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    Inactivated Vaccines

    Cannot replicate

    Generally not as effective as live vaccines

    Less interference from circulating antibody than

    live vaccines

    Generally require 3-5 doses

    Immune response mostly humoral

    Antibody titer may diminish with time

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    Inactivated VaccinesWhole-cell vaccines

    Viral polio, hepatitis A,

    rabies, influenza*

    Bacterial pertussis*, typhoid*

    cholera*, plague*

    *not available in the United States

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    Inactivated Vaccines

    Fractional vaccines

    Subunit hepatitis B, influenza,

    acellular pertussis,

    human papillomavirus,

    anthrax

    Toxoid diphtheria, tetanus

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    Polysaccharide Vaccines

    Pure polysaccharide

    pneumococcal

    meningococcal

    Salmonella Typhi (Vi)Conjugate polysaccharide

    Haemophi lus inf luenzae type b pneumococcal

    meningococcal

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    Pure Polysaccharide Vaccines

    Not consistently immunogenic in children younger

    than 2 years of age

    No booster response

    Antibody with less functional activity

    Immunogenicity improved by conjugation

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    National Center for Immunization and Respiratory DiseasesCenters for Disease Control and Prevention

    CDC Vaccines and ImmunizationContact Information

    Telephone 800.CDC.INFO

    Email [email protected]

    Website www.cdc.gov/vaccines