Skip to main content
. 2022 Jan 12;12(1):70. doi: 10.3390/metabo12010070

Table 1.

Comparison of studies on PCSK9 editing in non-human primates.

First Author,
Journal
(Year of Publication) [Reference]
Wang,
Nature Biotechnology (2018/2021) [40,41]
Musunuru,
Nature (2021) [6]
Rothgangl,
Nature Biotechnology (2021) [44]
Non-human primate Rhesus macaques
(Macaca mulatta)
Cynomolgus macaques
(Macaca fascicularis)
Cynomolgus macaques
(Macaca fascicularis)
Delivery method Adeno-associated virus transducing genetic information for the meganuclease Lipid nanoparticle containing gRNA and base editor mRNA Lipid nanoparticle containing gRNA and base editor mRNA
Genome editing technology Meganuclease, induction of double strand breaks at specific site, random deletions/insertions after repair Adenine base editor, specific single-nucleotide exchange Adenine base editor, specific single-nucleotide exchange
Length of follow-up Up to 3 years 8 months 29 days
PCSK9 editing * Up to 46% 66% Max. 34%, mean 26%
Reduction PCSK9 Up to 84% 90% 32%
Reduction LDL-C Up to 60% 60% 14%
Off-target effects Up to 629 detected off-target DNA cleavages None detected None detected
Immune response T cell response None detected Humoral immune response against base editor

* The liver contains about 70% hepatocytes, which is why 70% editing means DNA editing in virtually all hepatocytes [6,40]. PCSK9: proprotein convertase subtilisin/kexin type 9; LDL-C: low-density lipoprotein cholesterol.