LESSON 3: ANT-IVIRAL agents Flashcards

1
Q

in humans and animals are preferably controlled by
immunization.

A

Viral infections

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2
Q

However, when a vaccine is not available, example for those major
viral diseases or emergence of a new virulent strain of virus,

A

antiviral chemotherapy

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2
Q

inhibit virus-specific events related to virus replication;
from preventing virus entry into host cells, interfering with uncoating, genome
replication or assembly to release of virus from host cells

A

Effective antiviral drugs

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3
Q

Classes of antiviral drugs:

A
  1. Immunomodulators:
  2. Ion-channel blocking compounds:
  3. Neuraminadase inhibitors:
  4. Antiviral drugs which inhibit viral genome replication
  5. Non-nucleoside polymerase inhibitors:
  6. Protease inhibitors:
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3
Q

In addition, the efficacy of antiviral chemotherapy is further complicated
by viral latency (ex:

A

(ex: herpesviruses)

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4
Q

produced by fibroblasts and other cell

A

ii. Interferon-β (IFN-β):

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4
Q

Type 1interferon : mediate the early immune responses to viral infections,
major examples

A

i.Interferon-α (IFN-α)
ii. Interferon-β (IFN-β

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4
Q

2 types of interferons:

A

a) Type 1interferons
b) Type 2interferon

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4
Q

enhance innate immune responses, indirect antiviral effects
by inducing cytokines prominently interferons

A
  1. Immunomodulators:
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5
Q

produced by mononuclear phagocytes

A

i. Interferon-α (IFN-α)

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6
Q

Neuraminidase
a) Example: (anti-influenza drugs

A

Oseltamivir and Zanamivir

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6
Q

Briefly, the presence of
amantadine interfere with the ion channel function of the —protein in the
nucleocapsid of the virus thus inhibits acid-mediated dissociation

A

M2 protein

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7
Q

prevents virus uncoating shortly after
endocytosis of virus by the host cell (

A
  1. Ion-channel blocking compounds:
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7
Q

Example of immunostimulating drugs to viral infections:

A

Imiquimod and
Inosine pranobex

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8
Q

or interferon-Ɣ (IFN-Ɣ) is produced by stimulated T cells
and NK cells.

A

b) Type 2interferon :

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9
Q

has antiviral activity against influenza A virus by
inhibiting an early step in the replication of the virus.

A

Amantadine

10
Q

interfere with release of virus from host cells

A

Neuraminadase inhibitors:

11
Q

is required to cleave sialic acid from the cell membrane of the
budding virions.

A

Neuraminidase

12
Q

a) Example: Nucleoside analogue drugs such as

A

i.Acyclovir: used against herpesvirus
ii. Famciclovir: has inhibitory activity against herpesviruses, poxviruses,
papillomaviruses and adenoviruses
iii. Penciclovir:used against herpesvirus

12
Q

Most of these drugs are
nucleoside analogues which inhibit viral polymerases, especially —-
by competing with natural substrates and incorporate into the growing DNA chain
where they often terminate elongation.

A

DNA polymerases,

13
Q

active against cytomegalovirus

A

Ganciclovir:

13
Q

anti-influenza drug

A

Ribavirin:

14
Q

Example: Thymidine analogue
Ophthalmic solutions containing idoxuridine are used for
treating herpesvirus keratitis in animals

A

Idoxuridine

14
Q

inhibit replication of viruses by binding
to the pyrophosphate binding site of the DNA polymerase to block binding of
nucleotides.

A

Non-nucleoside polymerase inhibitors

15
Q

ex. (against herpesvirus, HIV, hepatitis B virus)

A

Foscarnet

15
Q

: used against HIV proteases

A
  1. Protease inhibitors
16
Q
  1. Protease inhibitors: used against HIV proteases
    a) Examples:
A

Saquinavir, indinavir, ritonavir, nelfinavir, and amprenavi

17
Q

are highly selective and usually target a
specific viral protein, viruses can readily become resistant through point mutations in
the virus genome which often limits the usefulness of antiviral drugs.

A

antiviral compounds

18
Q

may involve the selection
and use of the antiviral compounds, drug concentration at the site of infection, initial
virus susceptibility to the treatment, inherent characteristics of the invading virus and
the immune status of the host.

A

Development of resistance, a “multifactorial process”