Title: Immunology the Basis of Vaccinology
1Immunology the Basis of Vaccinology
2Behavioral Objectives
- Differentiate between the functions of innate and
adaptive immune systems. - Discuss the roles of antigen presenting cells, T
cells and B cells in immunity - Classify the different types of vaccines.
- Discuss why infant immunization presents special
problems
3The immune system
- Innate immunity
- Adaptive immunity
4Purpose of the Immune System
- To prevent infectious diseases
- To cure infectious diseases
- (experiments in nature-boy in the bubble,
enhanced susceptibility of burn patients and
patients receiving chemotherapy to infection,
lack of immunity in naïve populations.)
5Characteristics of the IMMUNE SYSTEM
- Innate immunity
- -1st line of defense
- -provides initial defense against
- infection
- -relatively nonspecific
- -not enhanced by immunization
- -necessary for the establishment
- and enhancement of adaptive
- immunity
6The Role of the Innate Immune System in Adaptive
Immune Responses
- Antigen recognition by professional antigen
presenting cells dendritic cells,macrophages and
B cells via PAMPS and TOLL-like recptors - Antigen processing presentation by MHC class I
and MHC class II molecules. - Modulation of the adaptive immune response by
co-stimulation and cytokine secretion. - Effector functions induced by components of the
adaptive immune response
7- Adaptive immunity
- -develops slowly
- -broad activity
- -high degree of specificity
- -enhanced by immunization
- -activity heightened by cross talk with
- the Innate Immune system via cytokines
- ( chemical signals that change the
- behavior of other cell types)
-
-
8The adaptive immune system-the target of
vaccination
- Cells Effector function
- B lymphocytes Antibodies
- T lymphocytes Cytokines
- Cytoxicity
9Successful Immunization
- Requires the activation of T B lymphocytes
- T cells have receptors that specifically
recognize antigenic epitopes presented by MHC - B cells recognize proteins by receptors that
specifically bind epitopes in that protein - Clonal expansion (proliferation)
- Differentation to provide effector functions and
immunologic memory.
10- T cells
- CD4 cells provide help to
- other cells via cytokines
- CD8 cells are cytotoxic cells
- can also provide help
- B cells
- produce different isotypes of
- antibody which function
- differently depending on Fc
- region
11(No Transcript)
12Principles of Vaccination
Immunity
- Self vs. nonself
- Protection from infectious disease
- Usually indicated by the presence of antibody
- Very specific to a single organism
13Principles of Vaccination
Active Immunity
- Protection produced by the person's own immune
system - Usually permanent
- Protection transferred from another person or
animal - Temporary protection that wanes with time
Passive Immunity
14Principles of Vaccination
Antigen
- A live or inactivated substance (e.g., protein,
polysaccharide) capable of producing an immune
response - Protein molecules (immuno-globulin) produced by B
lymphocytes to help eliminate an antigen
Antibody
15Passive Immunity
- Transfer of antibody produced by one human or
other animal to another - Temporary protection
- Transplacental most important source in infancy
16Monoclonal Antibody
- Derived from a single type, or clone, of
antibody-producing cells (B cells) - Antibody is specific to a single antigen or
closely related group of antigens - Used for diagnosis and therapy of certain cancers
and autoimmune and infectious diseases
17Vaccination
- Active immunity produced by vaccine
- Immunity and immunologic memory similar to
natural infection but without risk of disease
18Classification of Vaccines
- Live attenuated
- viral
- bacterial
- Inactivated
19Inactivated Vaccines
Whole
- viruses
- bacteria
- protein-based
- toxoid
- subunit
- polysaccharide-based
- pure
- conjugate
Fractional
20- Principles of Vaccination
General Rule
The more similar a vaccine is to the
disease-causing form of the organism, the better
the immune response to the vaccine.
21Live Attenuated Vaccines
- Attenuated (weakened) form of the "wild" virus or
bacterium - Must replicate to be effective
- Immune response similar to natural infection
- Usually effective with one dose
except those administered orally
22Live Attenuated Vaccines
- Severe reactions possible
- Interference from circulating antibody
- Fragile must be stored and handled carefully
23Live Attenuated Vaccines
- Viral measles, mumps, rubella,
varicella/zoster, yellow fever, rotavirus,
intranasal influenza, rotavirus,
vaccinia - Bacterial BCG, oral typhoid
24Inactivated 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
25Inactivated Vaccines
Whole-cell vaccines
- Viral polio, hepatitis A, rabies,
influenza - Bacterial pertussis, typhoid cholera,
plague
not available in the United States
26Inactivated Vaccines
Fractional vaccines
- Subunit hepatitis B, influenza, acellular
pertussis, human papillomavirus, anthrax - Toxoid diphtheria, tetanus
27Pure 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
28Polysaccharide Vaccines
Pure polysaccharide
- pneumococcal
- meningococcal
- Salmonella Typhi (Vi)
- Haemophilus influenzae type b
- pneumococcal
- meningococcal
Conjugate polysaccharide
29Problems Associated with Infant Immunization
- Presence of maternal antibody
- complex with vaccine antigens to prevent
interaction with B cell receptors. - -Killing live vaccine organisms
- Immaturity of infant immune
- system.
30National Immunization ProgramContact Information
- Telephone 800.CDC.INFO
- Email nipinfo_at_cdc.gov
- Website www.cdc.gov/nip