Vaccines 1 Flashcards

1
Q

Brief History

A

Smallpox epidemic in Europe in 16th and 17th century. Variolation - induced some protection, reducing symptoms but some still developed smallpox and died. 1798- noticed milkmaids who had cowpox didn’t get small pox, scratched material from cowpox lesions into skin. Rabies- 1880s. Mid-20th century - many vaccines including diphtheria, pertussis and typhoid.

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2
Q

Whats a vaccine

A

Biological product which safely induces an immune response. Must contain an antigen. Broadly classified as live or inactivated

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3
Q

Properties of a good vaccine - Antigen

A

Specific or cross reactive to protect against multiple pathogens/strains but not-cross reactive against host.

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4
Q

Properties of a good vaccine - Delivery System

A

Low side effects: non-toxic, no chance of pathogenic reversion. Induces a strong and long lasting memory response. No boosters needed for better compliance. Effective against the target pathogen inducing the right sort of immune response. Not injected. No refrigeration chain required. Cheap to manufacture and distribute. Easy to administer

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5
Q

What are critical antigens?

A

Induce protective antibodies to be made e.g surface proteins of influenza/ clostridium tetanii toxin.

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6
Q

What is herd immunity

A

Sufficient proportion of a population immune to an infectious disease providing indirect protection to those who are not immune. Infection cannot spread in population from vaccinated individuals protecting susceptible individuals.

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7
Q

Contraindications for vaccines

A

Acute illness side effect. Pregnancy ( no live vaccines, no vaccines in 1st trimester). Immunocompromised ( Due to drugs or irradiation/ chronic illness). Allergy

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8
Q

Principles of Vaccination - Passive Immunisation

A
  • Natural: Maternal antibodies passed to foetus or neonate.
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9
Q

Passive Immunisation - Artificial

A

Homologous pooled human antibody ( immune globulin) / globulins. Heterologous (equine) hyperimmune serum (antitoxin). Monoclonal antibodies e.g palivizumab for RSV.

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10
Q

Active Immunisation

A
  • Bodys immune system stimuatled to produce immune response against a specific pathogen/ antigen
  • Immune system

Exposed to antigen to induce production of antibodies and memory cells providing long-term protection against future exposure to the same pathogen to induce strong secondary immune response without causing illness from the primary challenge. Primary and secondary antigen challenges refer to different stages in this process.

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11
Q

Active Immunisation - Primary and secondary challenge

A

Primary antigen challenge involves vaccinated antigen exposure causing experience some symptoms of the disease if the antigen is a live or attenuated pathogen

Secondary immune response occurs when the

Immune system encounters the same antigen again at a different time naturally or via subsequent vaccinations. Much faster response, memory B cells quickly differentiate into plasma cells producing a large quantity of antibodies specific to the antigen. Memory T cells help to eliminate pathogen. may develop symptos but milder and of shorter duration.

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12
Q

Live attenuated vaccines adv and disadv

A

Live attenuated: Living but avirulent: Adapted to different host, genetically manipulated and grown in sub-optimal conditions. Adv: One booster. DisAdv: Reversion to virulence and poor stability

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13
Q

Vaccinations- Killed whole organism adv and disadv

A

Dead organism: Pathogen killed by chemical/ irradiations. Adv: Stable and long last lasting, safe, no reversion. DisAdv: Several doses, requires an adjuvant, inefficient.

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14
Q

Toxoid vaccines - adv and disAdv

A

Toxin causes the disease: toxin treated with formaldehyde. Adv: Stable and long lasting, safe. DisAdv: Not highly immunogenic requires an adjuvant

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15
Q

Subunit; Adv and DisAdv

A

Sub unit: Selection of antigens from the pathogen. Adv; Stable and long lasting, safe. DisAdv: Not highly immunogenic. requires an adjuvant

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16
Q

Virus-like particle vaccines

A

Outer coat of proteins produced recombinantly. Self assemble into virus particles. Adv: No viral genetic material, highly immunogenic, engineered to express additional antigens. DisAdv: Requires adjuvant

17
Q

Outer membrane vesicle vaccines

A

Outer membrane vesicle vaccines: Outer membrane gram-negative bacteria. Overexpression of desired antigens on surface Adv: non-infectious, no adjuvant, potential for cross-strain/ cross-species protection. DisAdv: Limited antigenic diveristy,lymphotic immune response due to bacterial components like LPS, variable immunogenicity, difficult/ time-consuming to produce

18
Q

Protein-polysaccharide conjugate vaccinations adv and DisAdv

A

Protein-polysaccharide conjugate vaccinations: Polysacccharides linked to carrier protein
Adv: Enhances immunogenicity, safe, produces protective levels of immunity in children. DisAd: Suppressive effect, can be expensive

19
Q

Viral Vectored vaccinations adv and DisAdv

A

Uses recombinant virus with genome altered to produce pathogen antigen. Adv: Mimic natural infection, no adjuvant. DisAdv: Pre-existing immunity to vector

20
Q

Nucleic acid vaccinations adv and disadv

A

DNA or RNA encoding target antigen. Potentially humoral and cell mediated immunity. Antigen expressed by cell after uptake. Adv: Highly versatile. DisAdv: Need to be delivered directly into cells, poor stability, need cold chain

21
Q

Adjuvant vaccinations DisAdv and Adv

A

Inactivated vaccines often given with an adjuvant. Enhances immune response: stabilising antigens, up regualtion of cytokines and chemokines, recruitment of immune cells at injection site, increased antigen uptake and presentation, activation and maturation of antigen presenting cells, activation of inflammasomes

22
Q

Common vaccine side effects

A

Injection site pain
▪ Redness
▪ Swelling
▪ Fever
▪ Malaise
▪ Headache

23
Q

Rare vaccine side effects

A
  • Anaphylaxis
24
Q

Very rare vaccine side effects

A
  • Narcolepsy (H1N1)
  • Idiopathic thrombocytopenic purpura (measles)