A syngeneic tumor model to assess novel cancer vaccines

    • Model features: intact immune system, validated & robust immunization protocol
    • Tumor cell line:  Breast Cancer (4T1, EMT6), Colon Cancer (CT26, MC38), Gliobastoma (GL261), Lung Cancer (LLC1), Pancreatic cancer (Pan02), Renal Cancer (Renca), Sarcoma (MCA205)
    • Tumor implantation: subcutaneous or orthotopic
    • Protocol: co-administration of adjuvants poly(I:C) (TLR3 ligand) and agonistic anti-CD40 antibody
    • Readouts: body weight, tumor size, survival
syngeneic tumor models immunization cancer vaccine efficacy in vivo CRO services

TLR3 ligation/CD40 activation immunization in CT26 tumor model

Poly(I:C)/anti-CD40 antibody immunization delays tumor growth in CT26 tumor-bearing mice. Mice are challenged with CT26 tumor cells and exposed to Poly(I:C) and agonist anti-CD40 antibody, and tumor growth is monitored overtime. Poly(I:C)/anti-CD40 antibody treatment triggers an anti-tumor effect when compared to controls.

In vivo efficacy & mechanism of action studies for novel immunotherapies

in vivo efficacy study CRO breast cancer

Straightforward in vivo efficacy studies

  • N=10: Standard groups of 10 mice including groups exposed to test compound alone and in combination with reference therapy.
  • Weekly reports: monitoring tumor growth, body weight, and survival
in vivo cancer immunotherapy studies CRO services

Flexible sampling options

  • Monitoring response over time: satellite mice, serial bleeding, intra-tumoral biopsies
  • On-demand sample collection: blood, serum, plasma, tumor, organ samples
in vivo mechanism actin immunotherapy breast cancer

A flexible platform to quantify tumor-microenvironment & peripheral markers

  • Multiplex immunophenotyping by flow cytometry & digital pathology
  • Spatial transcriptomics & proteomics

Illustrative data: anti-tumor response in MC38 colorectal cancer model

TLR3 ligation/CD40 activation immunization in MC38 tumor model

Poly(I:C)/anti-CD40 antibody immunization triggers a slight anti-tumor effect in MC38 tumor-bearing mice. Mice are challenged with MC38 tumor cells and exposed to Poly(I:C) and anti-CD40 antibody, and tumor growth is monitored overtime. Poly(I:C)/anti-CD40 antibody treatment slows down tumor growth compared to controls, with a full tumor rejection in some immunized mice.

cancer vaccine in vivo study immuno-oncology CRO

Why working with Explicyte?

Experts
in Immuno-Oncology

  • 150+ in vivo campaigns conducted over the past 10 years
  • 20+ peer-reviewed publications in key immuno-oncology journals
  • Bespoke study designs based on client objectives and literature

Personalized
approach

  • A dedicated study director (PhD level) from experimental plan to final report
  • Weekly reports to provide regular updates & adapt experimental strategy
  • Comprehensive analytical platform to decipher anti-tumor response

Your contacts

explicyte team 2024

Talk to our team ! Your key contacts:

Study directors: Paul Marteau, PharmD (not on picture), Jean-Philippe Guégan, PhD Leadership: Imane Nafia, PhD (CSO), Alban Bessede, PhD (founder, CEO), Loic Cerf, MSc (COO)

Tell us about your project !

    Select department:

    In Vivo Immunization Tumor Models I Cancer Vaccines I CRO Services

    Because the low immunogenicity of tumor cells is one of the mechanisms that tumors use to escape from the immune surveillance, one of immunotherapeutic strategies aims at enhancing the presentation of tumor antigens to T cells. This makes therapeutic cancer vaccines an attractive alternative, in which adjuvants are necessary to facilitate the induction and achievement of the desired immune response to weak antigens. In this respect, Explicyte is offering an immunization model based on the co-administration of adjuvants poly(I:C) (TLR3 ligand) and agonistic anti-CD40 antibody into tumor-bearing mice, and adapted for the evaluation of drug candidate for their ability to boost the anti-tumor immunity.

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