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Vocabulary flashcards covering the definitions, mechanisms, pharmacokinetics, and engineering of biologic targeted therapies from the lecture notes.
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Biologics
Genetically engineered proteins designed for the targeted modulation of protein targets.
ADCC
Antibody dependent cellular cytotoxicity, a mechanism triggered by antibody-based biologics to kill cancer cells.
CDC
Complement-dependant cytotoxicity, an immune response triggered by antibodies to destroy cancer cells.
Angiogenesis prevention
A mechanism of action for biologics that prevents the growth of cancer cells or tumours by cutting off blood supply.
IgG1 half life
A period of 14−21 days in serum achieved through recycling via the salvage neonate Fc receptor (FcRn).
Fc fusion protein half-life
A genetically engineered fusion of a peptide or protein with the IgG1 Fc region which results in an improved half life of 4−5 days.
PEGylation
The covalent coupling of protein to polyethylene glycol (macrogol) to increase molecular mass and hydrodynamic radius, thereby decreasing the rate of glomerular filtration by the kidney.
Hybridoma
A fusion of spleen beta cells from immunised mice with myeloma cells used to produce a single type of antibody (monoclonal antibody).
Chimeric antibodies
Antibodies developed using recombinant DNA technology that contain a mouse domain (Fab) and Human Fc IgG1.
Humanised antibodies
Antibodies containing human Fab and human Fc that retain only the mouse antibody binding site.
Adverse Effects of Biologics
Risks including serious infections (respiratory, active TB), opportunistic infections (latent TB, urinary tract), and a potential increase in the risk of non-melanoma skin cancer.