Prevention and treatment of viral disease COPY Flashcards

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1
Q

Define prophylaxis.

A

Preventing the diseases before the aetiological agent is acquired, by vaccination or giving the drug before infection

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2
Q

What are the four broad types of virus vaccines?

A
  • Live Attenuated
  • Inactivated
  • Purified Subunit
  • Cloning
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3
Q

Describe each of the types of virus vaccines.

A

Live Attenuated – live virus has its virulence reduced and then is administered to the patient
(mild infection)

Inactivated – the virus is taken and its genome is destroyed so that it is still stimulates a response but can no longer be infectious – given with adjuvant

Purified Subunits – the viral genome is taken and treated with proteases which chops it into small pieces. These subunits have antigens that can trigger an immune response.

Cloning – viral genome is cloned in a bacterium and the copies of the genome are either:
Injected into people
Put into virus-like particles
A new virus is made with a little segment of virulent material from the original virus

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4
Q

State what type of vaccine has been produced for each of these diseases:

A

Polio – inactivated + live attenuated

Smallpox – live attenuated

Rubella – live attenuated

Hepatitis B – cloned subunit

Influenza – inactivated + live attenuated

HPV – cloned subunit

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5
Q

How are Live Attenuated Vaccines made?

A

The virus is passed through the wrong type/wrong species of cells this makes the virus evolve and change its virulence

e.g. if a virus is passed through monkey cells then it will become a monkey virus and it will no longer be as virulent to humans

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6
Q

What are some differences between live attenuated vaccines and inactivated vaccines?

A
  • Live attenuated vaccines give rapid, broad, long-lived immunity, dose sparing
  • Inactivated vaccines often require boosters, high doses needed, safe
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7
Q

What types of vaccines exist for influenza?

A

Purified subunit vaccine

Live-attenuated (nasal spray)

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8
Q

What types of vaccines exist for polio?

A

SALK – inactivated

  • preparation of virus has been treated so it can no longer replicate
  • not a good vaccine because it needs a large dose

SABINE – live attenuated

  • this is much better
  • however if you give it to someone immunosuppressed they will have the persistent virus
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9
Q

How are recombinant attenuated virus vaccines made?

A
  • Pathogenic virus genome typically consists of receptor-binding gene, virulence gene and capsid protein genes
  • you can either mutate the virulence gene or delete the virulence gene
  • You then get a virus which is IMMUNOGENIC but NOT VIRULENT
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10
Q

What type of vaccine does rotavirus have?

A

Live attenuated reassortant

only given to babies as it can cause bowel blockage in older babies

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11
Q

Give two examples of subunit vaccines.

A

HPV

Hepatitis B Virus

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12
Q

What is the best available broad antiviral therapy and what are the limitations of it?

A

Interferons they switch on a natural antiviral response

– it activates inflammation and fever and can make the patient feel even more ill

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13
Q

What are the two strategies for inhibiting influenza?

A

Blocking the M2 channel

Neuraminidase inhibition

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14
Q

Describe inhibition of the M2 channel in influenza.

A
  • When endocytosed, influenza virus enters the endosome
  • The low pH of the endosome opens the M2 channel allowing protons to move into the endosome and break the bonds holding together the protein capsid of influenza
  • This allows influenza to uncoat and release its contents into the cytoplasm of the cell
  • Adamantes (rimantadine and amanatadine) can fit in the M2 channel and prevent protons from moving in, thus meaning that the influenza is locked in its protein shell
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15
Q

Describe neuraminidase inhibition in influenza.

A
  • Neuraminidase is usually produced by influenza to destroy sialic acid on the surface of the host cell thus meaning that the virus doesn’t bind to the same cell again
  • By blocking neuraminidase you can limit the spread of the virus to other cells because it just binds to the same cell again and again
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16
Q

Give two examples of neuraminidase inhibitors.

A

Oseltamivir (Tamiflu)

Zanamivir (Relenza)

17
Q

Give eight examples of HIV drugs.

A

NRTI (Nucleoside Reverse Transcriptase Inhibitor)

  • Zidovudine
  • Stavudine

NNRTI (Non-Nucleoside Reverse Transcriptase Inhibitor)

  • Efavirenz
  • Viramune

Integrase Inhibitor
- Reltagravir

Entry inhibitors
- Maraviroc

Protease Inhibitors
- Atazanavir

18
Q

State two treatments for Hepatitis C.

A

Interferons

Ribavirin

19
Q

what are examples of successful vaccine programs and why?

A
  • polio is successful
  • smallpox is successful
    this is because there is NO animal reservoir
  • easily identifiable
20
Q

what are examples of viruses for which both live and inactivated vaccines are available?

A
  • Influenza
  • Inactivated vaccine or the subunit vaccine consists only of the spike proteins
  • these are given to people who might be at risk
  • it does not give you flu
  • influenza vaccines must be updated regularly because influenza evolves fast
21
Q

what are the other best antivirals we have right now?

A
  • nuceloside analogues
  • when viruses replicate they add nucleotides
  • Nucleoside analogues look like normal bases but have a little bit missing
  • when the nucleoside analogue is integrated it means the chain is terminated.
22
Q

why is acyclovir a good antiviral?

A
  • specific to virus infected cells
  • it can only be phosphorylated by virus
    encoded enzyme - THYMIDINE KINASE
  • acyclovir has a higher affinity for Viral DNA polymerase than host
    DNA polymerase
23
Q

what is SVR?

A

not only are the patients feeling better, their viral load is going down