Vaccines (lecture 1) Flashcards

1
Q

10 Leading causes of death (Low-income countries)

A
  • Lower respiratory infections (11.30%)
  • Diarrhoea diseases (8.20%)
  • HIV/AIDS (7.80%)
    Ischaemic heart disease (6.10%)
  • Malaria (5.20%)
    Stroke/cerebrovascular disease (4.90%)
  • TB (4.30%)
    Prematurity low birth weight (3.20%)
    Birth aphyxia and birth trauma (2.90%)
    Neonatal infections (2.60%)
  • = communicable diseases
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2
Q

10 Leading causes of death (high income countries)

A
Ischaemic heart disease (12.80%)
Stroke/cerebrovascular disease (10.80%)
* Lower respiratory infections (6.10%)
Chronic obstructive pulmonary disease (5.80%)
* Diarrhoeal diseases (4.30%)
* HIV/AIDS (3.10%)
Trachea/bronchea/lung cancers (2.40%)
* TB (2.40%)
Diabetes mellitus (2.20%)
Road traffic accidents (2.10%)
  • = communicable disease
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3
Q

Solution to communicable diseases (infectious diseases)

A

Vaccines

  • Useful
  • Cost efficient
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4
Q

Give an overview to the immune system (4 types)

Organs
Complement
Phagocytes
Lymphocytes

A

Organs: Bone marrow, Thymus, Spleen, lymph nodes

Complement: Plasma proteins that interact with pathogens marking them for destruction by phagocytes

Phagocytes: Granulocytes, Macrophages and dendritic cells

Lymphocytes: T and B cells

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5
Q

What is systemic immunity and its role

A

A second line of defence past the skin, protection of internal environment

Defence within blood circulation via. Antibodies, cellular immunity

Does NOT induce mucosal immunity

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6
Q

What is mucosal immunity

A

The first line of defence i.e skin

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7
Q

How do most pathogens initiate infection?

Examples

A

By the mucosal surface (gastointestinal, urogenital, respiratory tracts)

E.g Influenza, tuberculosis , STD, Cholera and diphtheria

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8
Q

What is the components of the mucosal immune response and its affects on systemic immunity

A

IgA, T-cells.

Induction of mucosal immunity induces systemic immunity aswell.

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9
Q

What is humoral response?

A

The activation and proliferation of specific antibodies secreted by B-cells effectively combating infections.

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10
Q

Give an overview of humoral immune response

A

1) Activation - MACROPHAGE engulfing antigen by phagocytosis. the engulfed antigen is a phagosome. Antigens are usually marked by IgG
2) Lysosomes digest the phagosome, this is called ANTIGEN PROCESSING
3) Display (antigen presentation) - Class II MHC proteins combine and the MHC II displays the processed antigen
4) Helper T-cell : T cell combines to MHC II class protein and antigen. Macrophage will then release interleukin-1 which activates the helper T-cell
5) Activated T-cell will release its own cytokine which stimulate itself to proliferate with the same receptors specific for the antigen

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11
Q

What is the Humoral response effector phase?

Give an overview

A

part 2 of humoral immune response
Utilization of IgM receptors on B-cells.
This produces antibodies that bind and inactivate antigens.

Overview:

1) IgM binds to antigen and engulfed by endocytosis
2) Fuse lysosomes, digestions to fragments
3) MHC II attatchment and display
4) Helper T-cell binding with the same antigen specificity
5) T-cell release cytokine to stimulate B-cell to divide and produce clones
6) The clones produced can be plasma cells or memory cells

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12
Q

What are plasma cells

A

Cells that secrete antibodies, the same as the parent B-cell (originator). These antibodies bind and inactivate antigen.

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13
Q

What is cellular immune response
(Perforin)
Give an overview

A

A response system against infected cells by viruses or cancerous. This is done by cytotoxic T-cells what contains perforin. There is an activator phase and effector phase.

Overview:

1) Entry of virus, infection
2) Digestion, MHC I attatchment
3) Tc cell binds to cell and MHC I, antigen.
4) Tc proliferates with T-cell receptors specific for antigen
5) Infected cells present antigen via MHC I, this is marked for destruction.
6) Tc cells bind and secrete perforin, poking holes in the plasma membrane and causing cell to lyse.

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14
Q

What are the principles of vaccination

A

The more similar the vaccine is to the antigen, the better induced immune response.

Safe and must not cause undue harm

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15
Q

What is active immunity?

A

Protection produced by the persons own immune system, usually permanent.

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16
Q

What is passive immunity?

A

Usage of antibodies produced externally to induce immune response which is temporary and diminishes over time.

Transplacental is the most important source in infancy`

17
Q

What are the steps of vaccination?

A

Isolation > Inactivation > Injection

Not applicable for pathogens that cannot be grown in a lab.

18
Q

What is antigen variability?

Give examples

A

The change of the surface proteins in the antigen by mutation or different strains.

No change: 
Diphtheria
Tetanus
Polio
MMR
HBV
HAV
HIB

10 years:
Pneumococcus
Meningococcus

1 year:
Influenza

1 day:
HIV

19
Q

What type of induction (T, Ig) do the following require?

A
Antibodies:
Diphtheria
Tetanus
Polio (IPV)
HIB
HBV
Rabies
MMR
Influenza (killed/subunit)
Papillomavirus
Pneumococcus
Meningococcus

Antibodies/T-cells:
Polio (OPV)
Influenza (live)
Typhoid fever

T-cells exclusive:
TB
Cancer
HIV

20
Q

Give an overview of the classification of vaccines

A

Inactivated:
Whole inactivated viruses or killed bacterium (Polio,HepA,Rabies)

Live attenuated:
Viral and bacterial (not revert to virulent form) and replicate an immune response similar to original infectant (BCG,typhoid,rubella,measles)

Recombinant and subunits:
Protein or toxin sub-unit that cannot replicate (Tetanus, Diphtheria, anthrax)
Polysaccharides (meningococcal, pneumococcal)

DNA vaccines:
Antigen gene > expression > Introduction > induced immune response.

21
Q

How are inactivated vaccines made?

A

Heat / chemical

22
Q

How are live attenuated vaccines made?

A

Gene manipulation removing pathogenicity determinants

23
Q

How are subunit vaccines made?

A

identify proteins > clone genes > express

24
Q

How are reverse vaccines made?

A

High throughput analysis based on genome sequence

25
Q

What is genome based vaccinology?

A

Using the proteome and transcriptome to determine pathogenic elements. Followed genomics and pan genomics reverse vaccinology

26
Q

What is structural vaccinology?

A

Determining an antigens structure in 3D and studying their structural interactions

27
Q

How are new generation vaccines designed?

A

Genomics: Looking at genome for putative surface exposed proteins.
Proteomics: Identifying secreted or cell surface proteins
Transcriptomics: Using microarray to analyse gene regulation during host infection

28
Q

Give the full pathway of vaccine development

A
Genome sequence and analysis
Antigen selection
Protective immunity
Molecular epidemiology
Safety and protective immunity
Approval
Recommendation
Implementation