23andMe Investor Presentation Deck
Inhibition of CD200R1 has the potential to address resistance to anti-PD1
therapies
Blocking the CD200R1 pathway enhanced IFNy production from SEB-stimulated PBMCs compared to isotype control and anti-PD1 in
the majority of samples tested
Interferon-y
Fold Change Relative to Control
2
*L
Endometrial 1
Ovarian 1
Endometrial 2
Lung
Melanoma
Pancreatic
Endometrial 3
PBMCs from each respective patient were incubated with 100 nM of 23ME-00610, anti-PD-1, or isotype control. Cells were stimulated with SEB.
IFNy levels were determined by enzyme-linked immunosorbent assay. Mean biologic triplicates were normalized to isotype control. *P <0.05.
23ME '610
Isotype Control
anti-PD1
Prostate
Colorectal
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PBMC, peripheral blood
mononuclear cell; PD-1,
programmed death-1; SEB,
staphylococcal enterotoxin B.
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