THERABEST Announces Upcoming Presentation of Pre-clinical Data on imNK Cells for Alzheimer’s Disease at AAIC
THERABEST Co., Ltd. plans to release its pre-clinical results of
immune-modulatory NK (imNK) cells on Alzheimer’s disease for the first time at an
international conference.
These research
findings on the therapeutic effect and mode of action of imNK cells will be
presented at the Alzheimer’s Accociation International Conference (AAIC), taking
place in San Diego, USA from July 31 to August 4.
The upcoming AAIC presentation will showcase the company’s aim to shift
the therapeutic paradigm to address Alzheimer’s disease with potential NK cell
therapy.
The human gene mutant transgenic Alzheimer’s disease animal model showed improvement in cognitive function and significant reduction of beta amyloid plaque aggregation. Spatial transcriptomic techniques, which allow the simultaneous examination of entire gene expression in individual brain regions and changes of a variety of brain cell types, was introduced to investigate the underlying mode of action analysis of Alzheimer’s disease treatment, revealing significant decrease in dysfunctional microglial cells inducing neuroinflammation in a certain brain region and increase in gene signatures associated with cellular respiration and immune metabolism.
Do Won Hwang, CTO of THERABEST, said “over the last three years, we’ve
witnessed that imNK cells, which secrete immunomodulatory cytokines and
neurotropic factors, can promote a decrease in pathological protein aggregate level
and recovery of cognitive function in various Alzheimer’s disease models. Thanks
to the joint research with Seoul National University, spatial transcriptome
analysis clearly elucidated a new mode of action of imNK cell therapy by observing
the recovery of inhibitory neurons in specialized brain region involved in
emotion control”.
THERABEST is planning for a clinical trial of EiNK, an “off-the-shelf”
iPSC-derived NK cell therapeutics allowing mass production with low cost, on
Alzheimer’s disease.