Strain Name
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C57BL/6-Pdcd1tm1(PDCD1)Bcgen Tnfrsf4tm1(TNFRSF4)Bcgen/Bcgen
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Common Name
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B-hPD-1/hOX40 mice
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Background
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C57BL/6
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Catalog number
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120521
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Related Genes
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PD-1 (Programmed death-1) ;
TNFRSF4 (Tumor necrosis factor receptor superfamily, member 4, also known as OX40)
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NCBI Gene ID
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18566,22163
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Protein expression analysis
Strain specific OX40 and PD-1 expression analysis in homozygous B-hPD-1/hOX40 mice by flow cytometry. Splenocytes were collected from WT and homozygous B-hPD-1/hOX40 (H/H) mice stimulated with anti-CD3ε in vivo (7.5 μg/mice), and analyzed by flow cytometry with species-specific anti-OX40 antibody. Mouse OX40 and PD-1 were exclusively detected in WT mice. Human OX40 and PD-1 were exclusively detected in homozygous B-hPD-1/hOX40 but not WT mice.
Combination therapy of PD-1(pembrolizumab) Ab and OX40 Ab
Antitumor activity of anti-hOX40 antibody combined with anti-hPD-1 antibody pembrolizumab in B-hPD-1/hOX40 mice. (A) Anti-hOX40 antibody combined with anti-hPD-1 antibody pembrolizumab inhibited MC38 tumor growth in B-hPD-1/hOX40 mice. Murine colon cancer MC38 cells (5×105) were subcutaneously implanted into homozygous B-hPD-1/hOX40 mice (female, 6-7 week-old, n=6). Mice were grouped when tumor volume reached approximately 150±50 mm3, at which time they were treated with anti-hOX40 antibody combined with anti-hPD-1 antibody pembrolizumab with doses and schedules indicated in panel (B) Body weight changes during treatment. As shown in panel A, combination of anti-hOX40 and anti-hPD-1 antibody shows more inhibitory effects than individual groups, demonstrating that the B-hPD-1/hOX40 mice provide a powerful preclinical model for in vivo evaluating combination therapy efficacy of hOX40 antibodies and hPD-1 antibodies . Values are expressed as mean ± SEM.
Antitumor activity of anti-hOX40 antibody combined with anti-hPD-1 antibody pembrolizumab in B-hPD-1/hOX40 mice. (A) Anti-hOX40 antibody combined with anti-hPD-1 antibody pembrolizumab inhibited B16-F10-hPD-L1 cells tumor growth in B-hPD-1/hOX40 mice. Murine colon cancer B16-F10-hPD-L1 cells (1×105) were subcutaneously implanted into homozygous B-hPD-1/hOX40 mice (female, 7-8 week-old, n=5). Mice were grouped when tumor volume reached approximately 150±50 mm3, at which time they were treated with anti-hOX40 antibody combined with anti-hPD-1 antibody pembrolizumab with doses and schedules indicated in panel (B) Body weight changes during treatment. As shown in panel A, combination of anti-hOX40 and anti-hPD-1 antibody shows more inhibitory effects than individual groups, demonstrating that the B-hPD-1/hOX40 mice provide a powerful preclinical model for in vivo evaluating combination therapy efficacy of hOX40 antibodies and hPD-1 antibodies . Values are expressed as mean ± SEM.