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what is the ending for mouse mAB
omab
what is ending for chimeric mAB
ximab
what is ending for humanized mAB
zumab
what is ending for human mAB
umab
what factor of a mAB makes it more likely to elicit anti-therapeutic immune response
the more component of a mAB that is non-human
adv of nanobodies as therapeutics compared to mammalian Ig
one protein binding domain = easier manu
more stable = more resistant to pH and chemistry changes
disadv of nanobodies as therapeutics compared to mammalian Ig
low bioavailability = need modifications for efficacy
small = hard to work with
purpose of Fc region
HUMAN fc regions illicit immune response for antibody dependent cytotoxicity and complement dependent cytotoxicity
this part of the mAB interacts with NK cell
which mAB can bind to two different proteins
bi specific mAB
what are the benefits of a fragmant as a therapeutic
better at distributing to dense and poorly vascularized tissues = tumors
what terms are for patient’s own cells
autologos, autogenic
what terms are for therapeutics from other people’s cells
allogenic, heterologous
what factors limit CAR T cell therapeutics
need a specific target
off-target effects =cytokine toxicity/storm
what type of gene therapy reduces expression of mutated gene
gene silencing
what type of gene therapy fixes the mutated gene
genome editing
what type of gene therapy adds in a good copy of the gene
ectopic expression
pros and cons of gene silencing
pro: gets rid of overactive gene, SAFE = no risk of of-target effects
con: temporary and requires continuous therapy
pros and cons of genome editing
pro: fixes any problem
con: can lead to off target mutations
pros and cons of ectopic expression
pro: long term and generally safe
con: use of viral vectors can be limiting for some populations
what are the types of viruses for gene therapy
HSV-1
lentivirus
adeno-associated
which viral vectors are episomal
HSV-1
adeno-associated (occasional integrating)
which viral vectors are integrating vectors
lentivirus
what is an episomal vector and pros?
virus does not integrate into host genome
pro: used short term, lower risk of mutations
what is a integrating vector and pros?
vector embeds into host genome
pro: good long term, risk of mutations (cancer)
what is the FDA approved oncolytic therapeutic
imlygic (talimogene laherparepvec)
imglytic is used for
melanoma
what type of vector is used for imglytic
HSV-1
what is target of imglytic
GM-CSF
what are the reasons for a placebo in vaccine trial
if there is an established treatment = unethical to use inactive placebo
what vaccine type needs target antigens
viral vector
mRNA
protein subunit
which vaccines do not need specitific target antigens
whole inactivated
live attenuated