B-hCTLA4/hOX40 mice

C57BL/6-Ctla4tm1(CTLA4)Bcgen Tnfrsf4tm1(TNFRSF4)Bcgen/Bcgen • 120531

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B-hCTLA4/hOX40 mice

Product nameB-hCTLA4/hOX40 mice
Catalog number120531
Strain nameC57BL/6-Ctla4tm1(CTLA4)Bcgen Tnfrsf4tm1(TNFRSF4)Bcgen/Bcgen
Strain backgroundC57BL/6
NCBI gene ID12477,22163
AliasesCtla4 (cytotoxic T-lymphocyte-associated protein 4)Tnfrsf4(Tumor necrosis factor receptor superfamily, member 4, also known as OX40)

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  • Description
  • Targeting strategy
  • Phenotypic analysis
  • Efficacy

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      Description

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      Tageting strategy

      Gene targeting strategy for B-hCTLA4/hOX40 mice. The exon 2 of the mouse Ctla4 gene that encodes the extracellular domain was replaced by human CTLA4 exon 3, and the exons 1-5 of the mouse Ox40 gene that encode the extracellular domain were replaced by human OX40 exons 1-5 in B-hCTLA4/hOX40 mice.

      Protein expression analysis

      Strain specific CTLA4 and OX40 expression analysis in homozygous B-hCTLA4/hOX40 mice by flow cytometry. Splenocytes were collected from WT and homozygous B-hCTLA4/hOX40 (H/H) mice stimulated with anti-CD3ε in vivo (7.5 μg/mice), and analyzed by flow cytometry with species-specific anti-CTLA4 antibody. Mouse CTLA4 and OX40 were exclusively detected in WT mice. Human CTLA4 CTLA4 and OX40 were exclusively detected in homozygous B-hCTLA4/hOX40 but not WT mice.

      Combination therapy of CTLA4 mAb (ipilimumab) and OX40 mAb

      Antitumor activity of anti-hOX40 antibody combined with anti-hCTLA4 antibody ipilimumab in B-hCTLA4/hOX40 mice. (A) Anti-hOX40 antibody combined with anti-hCTLA4 antibodies ipilimumab inhibited MC38 tumor growth in B-hCTLA4/hOX40 mice. Murine colon cancer MC38 cells (5×105) were subcutaneously implanted into homozygous B-hCTLA4/hOX40 mice (female, 5-8 week-old, n=8). Mice were grouped when tumor volume reached approximately 150±50 mm3, at which time they were treated with anti-hOX40 antibody combined with anti- hCTLA4 antibody ipilimumab with doses and schedules indicated in panel (B) Body weight changes during treatment. As shown in panel A, combination of anti-hOX40 and anti-hCTLA4 antibody shows more inhibitory effects than individual groups, demonstrating that the B-hCTLA4/hOX40 mice provide a powerful preclinical model for in vivo evaluating combination therapy efficacy of hOX40 antibodies and h B-hCTLA4 antibodies. Values are expressed as mean ± SEM.