Pharmaceutical Agents Flashcards

1
Q

When were MABs discovered and how did it happen

A
  • 1975
  • fused mouse myeloma cells with antibody-producing B cells
  • created hybrid cells, known as a hybridomas
  • produce pure specific antibodies
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2
Q

What are monoclonal antibodies (MABs)

A
  • Designed antibodies that specifically target a certain antigen, such as one found on cancer cells
  • highly precise & targeted
  • used to treat many diseases
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3
Q

Before the discovery of MABs, what was there

A

Only polyclonal antibodies of varying speciality

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4
Q

What are the majority of MABs produced by

A

by Mammalian cell lines, but some produced by bacteria and yeasts

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5
Q

What is the first step in the process of creating MABs

A
  • Immunising an animal (mouse/rabbit) with desired antigen
  • The animal’s immune system produces a variety of antibodies in response
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6
Q

What happens after the first step in creating MABs

A

scientists isolate B-cells from immunised animal, and fuse them with immortal cancer cells, creating hybridomas

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7
Q

how does fusion of cancer cells and B cells occur

A

using electrofusion or chemical fusion techniques (such as polyethylene glycol)

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8
Q

what are antibodies

A

highly complex molecules, with extremely specific folding crucial to their function

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9
Q

what are the 4 types of MAB

A

murine
chimeric
humanised
fully human

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10
Q

murine MABs

A
  • fully derived from mice
  • hybridomas created by fusing mouse B cells with cancer cells
  • highly effective, but may induce an immune response in humans due to foreign origin
  • ‘omab’
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11
Q

what do the cancer cells that are fused with hybridomas provide

A

stable environment for hybridomas to produce desired MABs

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12
Q

chimeric MABs

A
  • lower chance of immune response
  • 50% human constant region, responsible for immune system activation
  • 50% mouse variable region, that recognises specific targets
  • ‘ximab’
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13
Q

humanised MABs

A
  • ~90% human, with complementary determining regions
  • smaller mice portion undergoes genetic modifications, making it more similar to human antibodies
  • decreased risk of immune response
  • ‘zumab’
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14
Q

fully human MABs

A
  • derived only from human sequences
  • can be generated using advanced techniques like phage display or transgenic animals
  • have lowest risk of immune response
  • typically very well tolerated in body
  • ‘umab’
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15
Q

what various factors does selection of MAB depend on

A
  • therapeutic purpose
  • efficacy
  • safety considerations
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16
Q

other types of MAB (specialised)

A
  • naked
  • bispecific
  • conjugated antibodies
17
Q

naked antibodies

A
  • unmodified
  • exert their therapeutic effect by binding and mediating immune response OR disrupt signalling pathways
18
Q

bispecific MABs

A
  • engineered to have 2 targets
  • therapeutic effect comes from bringing together their target (cancer/virus) cells and immune cells
19
Q

conjugated MABs

A
  • processed to be conjugated to another molecule, such as fluorescent dye or drug
  • conjugated antibody targets a specific molecule/cell in body/sample
  • when conjugated to drug, can deliver targeted therapy to specific cells such as cancer
20
Q

what is a magical bullet

A

a term used to describe a hypothetical, ideal drug/treatment that specifically targets and eliminates a disease, without harming healthy cells

21
Q

what is the significant role played by MABs in the development of magic bullets

A
  • they can be engineered to recognise & bind to specific molecules or cells
  • have potential to deliver targeted therapies to desired site, e.g. cancer cells
22
Q

why is the specificity of MABs so important

A
  • reduces risk of harmful side-effects
  • increases effectiveness of treatment