Basic Information
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Detection of m/hPD-1 protein expression by flow cytometry
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Strain specific PD-1 expression analysis in wild-type C57BL/6 mice and homozygous B-hPD-1/hPD-L1/hCCR8 mice by flow cytometry. Splenocytes were collected from wild-type C57BL/6 mice and homozygous B-hPD-1/hPD-L1/ hCCR8 mice stimulated with anti-CD3ε in vivo (7.5 μg/mice, stimulation for 24 hours, i.p.). Mouse PD-1 was only detectable in wild-type mice. Human PD-1 was only detectable in homozygous B-hPD-1/hPD-L1/ hCCR8 mice.
Strain specific PD-L1 expression analysis in wild-type C57BL/6 mice and homozygous B-hPD-1/hPD-L1/hCCR8 mice by flow cytometry. Splenocytes were collected from wild-type C57BL/6 mice and homozygous B-hPD-1/hPD-L1/ hCCR8 mice stimulated with anti-CD3ε in vivo (7.5 μg/mice, stimulation for 24 hours, i.p.). Mouse PD-L1 was only detectable in wild-type mice. Human PD-L1 was only detectable in homozygous B-hPD-1/hPD-L1/ hCCR8 mice.
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Protein expression analysis
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Strain specific analysis of CCR8 expression in B-hPD-1/hPD-L1/hCCR8 mice by FACS. MC38 cells were inoculated into wild-type C57BL/6 (+/+) and homozygous B-hPD-1/hPD-L1/hCCR8 mice (H/H). Tumors were harvested at approximately 500mm3, and the CCR8 were detect by flow cytometry. Mouse CCR8 was detectable on Treg cells of wild-type mice. Human CCR8 was detectable on Treg cells in homozygous B-hPD-1/hPD-L1/hCCR8 mice but not in wild-type mice.
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Combination therapy of anti-human PD-1 antibody and anti-human CCR8 antibody
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Antitumor activity of anti-human PD-1 antibody combined with anti-human CCR8 antibody in B-hPD-1/hPD-L1/hCCR8 mice. (A) Anti-human PD-1 antibody (in house) combined with anti-human CCR8 antibody (in house) inhibited MC38 tumor growth in B-hPD-1/hPD-L1/hCCR8 mice. Murine colon cancer B-hPD-L1 MC38 plus cells were subcutaneously implanted into homozygous B-hPD-1/hPD-L1/hCCR8 mice (male, 8 week-old, n=6). Mice were grouped when tumor volume reached approximately 100 mm3, at which time they were treated with human PD-1 and human CCR8 antibodies in panel B. (B) Body weight changes during treatment. As shown in panel A, Combination of hPD-1 and hCCR8 antibodies were more efficacious in controlling tumor growth in B-hPD-1/hPD-L1/hCCR8 mice. B-hPD-1/hPD-L1/hCCR8 mice provide a powerful preclinical model for in vivo evaluation of anti-human PD-1 and CCR8 antibodies. Values are expressed as mean ± SEM.
