23andMe Investor Presentation Deck
'610 Differentiation: Inhibition of CD200R1 Has the Potential to
Address Resistance to Anti-PD1 Therapies
IFNY
fold change relative to isotype
Y
Blocking the CD200R1 pathway enhanced IFNy production from SEB-stimulated
PBMCs compared to isotype control and anti-PD1 in the majority of samples tested
Colorectal
Endometrial 1
Endometrial 2
Endometrial 3
Lung
Ovarian
Melanoma
Prostate
Pancreatic
Isotype
23ME-00610
Anti-PD-1
PBMC, peripheral blood
mononuclear cell; PD-1,
programmed death-1; SEB,
staphylococcal enterotoxin B.
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-value<=0.05 compared to control
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