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. 2020 Sep 1;21(17):6336. doi: 10.3390/ijms21176336

Table 2.

Therapeutic approaches to recalibrate apoE functions by increasing lipidation.

Class Description Example References
ABCA1 agonist Antisense oligonucleotides miR-33
ARF6
[104]
[105]
Small peptides CS-6253
Ac-hE18A-NH2
4F
[73], [106,107]
[108]
[73], [109,110,111]
Nuclear Receptor agonist LXR agonist TO901317
GW3965
[112,113,114]
[112,113,114]
RXR agonist Bexarotene
LG100268
SPF1 and SPF2
[115,116,117,118,119]
[115,116,117]
[120,121]
Structure corrector Small molecule that corrects apoE4 structure PH002
GIND105 and GIND-25
[122]
[123,124,125]
Immunotherapy Targets non-lipidated apoE4 HAE-1 and HAE-4 [126,127]
Biologics AAV-directed therapy AAV-expressing human APOE2 gene [84], [128,129,130,131]