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Vaccines H.Sidra Yasin (BIOT 412)

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H.Sidra Yasin (BIOT 412). Vaccines. What are the Methods to produce the vaccines How we can modify the Vaccines What are the Routs of administration of vaccines What are the Types of vaccines What is Reverse vaccinology and its purpose Summary of all topics with conclusion. - PowerPoint PPT Presentation

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Page 1: Vaccines

Vaccines

H.Sidra Yasin (BIOT 412)

Page 2: Vaccines

Learning objectivesLearning objectives

What are the Methods to produce the vaccines

How we can modify the VaccinesWhat are the Routs of administration of

vaccinesWhat are the Types of vaccines

What is Reverse vaccinology and its purpose

Summary of all topics with conclusion

Page 3: Vaccines

General Method to produce the General Method to produce the vaccinevaccine

Page 4: Vaccines

Immunisation Department, Centre for Infections

Vaccine compositionVaccine compositionFollowing are:

Component Purpose Example

Adjuvants enhance the immune response to a vaccine

aluminium salts

Preservatives prevent bacterial or fungal contamination of vaccine

thiomersal

Additives stabilise vaccines from adverse conditions such as freeze-drying or heat, thereby maintaining a vaccine’s potency

gelatine

Residuals from manufacturing process

Inactivating agents

Antibiotics - prevent bacterial contamination during manufacturing process

Egg proteins- some vaccine viruses are grown in chick embryo cells

Yeast proteins

formaldehyde

neomycin, streptomycin, polymyxin B

influenza, yellow fever

HepB vaccine

Page 5: Vaccines

Modifiers of vaccinesModifiers of vaccines

Page 6: Vaccines

Modifiers of vaccinesModifiers of vaccines

AdjuvantsBoosters

Page 7: Vaccines

AdjuvantsAdjuvants

Chemical substance that can be added to a vaccine in order to enhance the immune response to the vaccine.

Page 8: Vaccines

TypesTypes

1. Freund’s Adjuvant

2. Aluminum Hydroxide3. Aluminum Phosphate (Alum)

Page 9: Vaccines

BoostersBoosters

Periodic “booster” administration must be given in order to strengthen and lengthen the duration of immunity

Page 10: Vaccines

Routs of administrationRouts of administration

Page 11: Vaccines

RoutesRoutes Intradermal administration.

◦ Three types are; intravenous

intramuscular subcutaneous.

Oral administration.◦ Vaccine is usually given in

liquid form.◦ Foods

Intranasal administration.

Page 12: Vaccines

Types of vaccinesTypes of vaccines

Page 13: Vaccines

Types of vaccinesTypes of vaccines

Traditional Recombinant vaccines

1. TypesA. InactivatedB. Live C. Attenuated

2. Pathogens A. Bacteria B. Virus C. Parasites

1. Subunit Vaccines2. peptide vaccines3. Attenuated Vaccines4. Vector Vaccines5. Bacterial Antigen

Delivery Systems

Page 14: Vaccines

Traditional vaccinesTraditional vaccines

Page 15: Vaccines

Live, Attenuated VccinesLive, Attenuated Vccines

Act like natural infection Live, but weakened, viruses or bacteria Altered organisms, either genetically or

chemically but non pathogenic Example: Attenuated virus vaccine for yellow fever,

which utilizes the YF17D strain, a weakened form of the wild virus.

Page 16: Vaccines

Live, Attenuated vaccinesLive, Attenuated vaccines

Advantages Disadvantages

• Single dose sufficient to induce long-lasting immunity

• Strong immune response • Local and systemic immunity • Others…Polio and Adeno

• Potential to revert to virulence• Contraindicated in

immunosuppressed patients• Interference by viruses or

vaccines and passive antibody

• Poor stability• Potential for contamination

Page 17: Vaccines

Inactivated VaccinesInactivated VaccinesEither: Suspensions of whole intact killed

organisms ◦ e.g. whole cell Pertussis, Influenza, Rabies, HepA

Or: Acellular and sub-unit vaccines

◦ e.g. Acellular Pertussis vaccine contains between 2-5 components of the whole cell Pertussis bacteria

Page 18: Vaccines

Inactivated vaccinesInactivated vaccines

Page 19: Vaccines

1.whole 1.whole actual pathogen killed, either by a heat treatment or chemically Salk vaccine for polio, which utilizes whole

polioviruses that have been inactivated by formaldehyde.

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2.Fractional2.Fractional

Page 21: Vaccines

Protein based; ToxoidsProtein based; Toxoids Stimulates the antibody mediated response Exotoxins Toxoids are vaccines which consist of exotoxins Immunity against the toxins, but not necessarily the bacteria that produce

the toxins. Examples: Botulinum antitoxen Diphtheria antitoxen Pertusis Tetanus toxoids

Page 22: Vaccines

Protein based; SubunitProtein based; Subunit Pathogenic agent Use components of pathogenic organism instead of whole

organism Advantage: no extraneous pathogenic particles i.e DNA Disadvantage: Costly Exampleso HSVMethod of productiono Tuberculosiso Foot -and-Mouth Disease virus (FMDV)

Page 23: Vaccines

Polysaccharide based; purePolysaccharide based; pure

pure cell wall polysaccharide from bacteria

Page 24: Vaccines

Polysaccharide based; conjugatePolysaccharide based; conjugate

Polysaccharide linked to a carrier protein More potent lacks long term immunological memory

Protect against: o Hibo Pneumococcal diseaseso Tetanuso Diphtheria

Page 25: Vaccines

Inactivated vaccinesInactivated vaccines

Advantages Disadvantages

• Stable • Constituents clearly defined• Gives sufficient humoral

immunity if boosters given• No mutation or reversion• Can be used with immuno-

deficient patients

• Many vaccinees do not raise immunity

• Shorter lasting immunity • Boosters needed• Need several doses• Adjuvant needed• Failure in inactivation and

immunization with virulent viruses

• Others…

Page 26: Vaccines

Possible Limitations of Traditional Vaccine Possible Limitations of Traditional Vaccine ProductionProduction

Not all infectious agents can be grown in culture

Animal/human cell culture expensive if needed

Yield of viruses from cultures can be low

Safety precautions for culture of live agents

Insufficient killing/attenuation of agents

Reversion of attenuated agents

Traditional vaccines are less diverse

Page 27: Vaccines

New StrategiesNew Strategies

Delete virulence genes Use live nonpathogenic carriers for immunization

(unrelated pathogenic agent) Clone antigenic determinants into alternative host Address autoimmune system response/problems

Page 28: Vaccines

So!!!So!!!

Page 29: Vaccines

Recombinant vaccinesRecombinant vaccines

Page 30: Vaccines

TypesTypes

1. Subunit Vaccines2. Peptide vaccines3. DNA Vaccines4. Vector Vaccines

Page 31: Vaccines

Peptide vaccinesPeptide vaccines

Use discrete portion (domain) of a surface protein as Vaccine.

These domains are ‘epitopes’ antigenic determinants are recognized by antibodies

Use highly immunogenic carrier molecule

Page 32: Vaccines

With carrier proteinsWith carrier proteins

Page 33: Vaccines

DNA VaccinesDNA Vaccines DNA vaccines consist of plasmids that contains genes for

certain types of antigens. Once administered, the plasmid is taken up by the target

cell and the genes are expressed. The cell then either excretes the antigen or displays it on

an MHC-I molecule.

Page 34: Vaccines

Genetic ImmunizationGenetic ImmunizationDelivery of a gene for the antigen to a host organism

• Use vector containing cDNA from viral protein/eukaryotic promoter

• Inject into muscle

POTENTIAL• Eliminates purification of antigen• Protein is modified post-translationally

Page 35: Vaccines

Chimeric VaccinesChimeric Vaccines Consist of attenuated viruses have been engineered to

carry antigens from multiple types of pathogens. The yellow fever vaccine has been engineered to carry

antigens from HIV, different types of bacteria, malaria, even cancer.

immunity against several different diseases with one administration.

Page 36: Vaccines

Human Diseases for Which Recombinant Vaccines Are Human Diseases for Which Recombinant Vaccines Are Currently Being DevelopedCurrently Being Developed

Page 37: Vaccines

Vaccine Production methodsVaccine Production methods

Page 38: Vaccines

Vaccine Production MethodsVaccine Production Methods

Manufacturing strategies:◦In-vivo◦In-vitro◦Chemical Synthesis

Some vaccines can be produced using any one of the three methods while for other vaccines, only one method will work.

Page 39: Vaccines

In-VitroIn-Vitro Here, using recombinant

DNA technology, vaccines can be produced in yeast cultures, bacterial cultures, or cell cultures.

Recombinant vaccines, such as chimeric and Attenuated virus/bacteria vaccines, are produced in this manor.

Page 40: Vaccines

In-VivoIn-Vivo

Embryonated Chicken eggs are commonly used as in producing flu vaccines.

Vaccines, like anti-idiotype, can also be produced in lab animals, such as mice.

There are even some species of plant, such as bananas, that have been genetically engineered to produce a vaccine.

Page 41: Vaccines

Chemical SynthesisChemical Synthesis Produced in a lab.

Vaccines that utilize synthetic peptides as well as conjugated lipids and polysaccharides

Used in combination with either in-vivo or in-vitro production.

Page 42: Vaccines

Summary!!!Summary!!!

Page 43: Vaccines

Thank you!Thank you!

Page 44: Vaccines