critical factors in determining the antigenic composition of a vaccine
TRANSCRIPT
CRITICAL FACTORS IN DETERMINING THE ANTIGENIC COMPOSITIONOF A VACCINE
A. Its capacity to induce a protective response:-direct antibodies against externalAntigen-direct both B and T cell responseT cell important for intracellularparasites
B. Strain variations:
Single vs. multiple antigens – Flu would be multiple antigens, And changes with time
2. OTHER FACTORS TO CONSIDER WHEN GIVINGVACCINATIONS:
A. ROUTE-oral, intramuscular, intravenousEx. Salk vaccine – inactive, intra-Muscular. Confers protection to Brain, spinal cord, does not pro-Tect the intestines against polio Virus and does not therefore Prevent dissemination of virus.
Sabin vaccine – live attenuated,Oral – protects intestines as well As brain and spinal cord, and doesPrevent dissemination of virus
B. TIMING:-in advance of potential exposure autumn for flu prior to schooling for early childhood diseases
C. CONDITION OF THEPATIENT-age, genetic makeup, infection,-Pregnancy, immunosuppressive-StateEx. – if pregnant, no live agents
D. POTENTIAL RISKS-probability of exposureEx. – health care workers andHepatitis B, postal workers andanthrax
ACTIVE VS. PASSIVE VACCINATION
1. LIVE UNATTENUATED
• MEANS LIVE, BUT NOT WEAKENED
• CLOSELY RESEMBLES ACTUAL INFECTIONPROBLEM WITH FINDINGSUCH AN ORGANISM
EXAMPLES – HOGCHOLERA, SMALLPOX
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2. LIVE ATTENUATED
• MEANS LIVE BUT WEAKENED
• ATTENUATED THROUGH COLD-ADAPTATION, BY GROWING IN UNNATURAL HOST
EXAMPLES:MEASLES, MUMPS,RUBELLA, POLIO (SABIN), TUBERCULOSIS
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3. INACTIVATED
• A POLITE WORD FOR DEAD
• USING HEAT, FORMALDEHYDE, METHANOL, RADIATION
EXAMPLES:CHOLERA, PERTUSSIS, PLAGUE, INFLUENZA,POLIO (SALK)
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Which of the three vaccinesNeeds to be the mostConcentrated? Why?Live unattenuatedLive attenuatedInactivated
Which of the three vaccinesWould require booster(s)?Why?Live unattenuatedLive attenuatedInactivated
4. TOXOIDS
• PREPARED TO PROTECT AGAINST
BACTERIAL EXOTOXINS
PREPARED BY HEATING IN FORMALINPRECIPITATING WITHALUMALUM SERVES AS ANADJUVANT
EXAMPLES:DIPHTHERIATETANUS
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5. SUBUNIT
• MADE FROM A PIECE OR PART OF THE WHOLE
• THROUGH BIOCHEMICAL PURIFICATION OR GENETIC ENGINEERING
EXAMPLES:INFLUENZA, HEPATITIS B, H. INFLUENZAEPNEUMOCOCCUSMENINGOCOCCUS
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**GLYCOSOLATION
6. INFECTIOUS AGENTS AS CARRIERS OF GENES FOR
ANTIGEN PRODUCTION• GENES CODING FOR THE DESIRED
EPITOPE ARE INSERTED INTO A BENIGN CARRIER – A VIRUS, BACTERIA OR YEAST
EXAMPLES:HEPATITIS BMALARIA
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7. SYNTHETIC VACCINES
• PRODUCING SYNTHETIC POLYPEPTIDE VACCINES
• THROUGH GENETIC ENGINEERING
• IDENTIFY AMINO ACID SEQUENCE
• OFTEN PAIR PEPTIDES WITH LIPID
• THIS ELICITS A STRONGER IMMUNE REPSONSE
EXAMPLES:S. PYOGENESDIPHTHERIA ,H. INFLUENZAE IN CUBA
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