Antagonist Development Service for Cancer Immunotherapy
Immuno-oncology Antagonist
Immunomodulators are a class of drugs that can regulate the function of the immune system, and are used for a series of immune-related diseases, such as autoimmune diseases, organ transplant rejection, etc., by suppressing or enhancing the activity of the immune system. Creative Biolabs offers a range of services related to immune antagonists, including synthesis and design, biomarker testing, in vitro and in vivo evaluation, and more to provide a solid theoretical basis for your cancer immunology research.
Glutamine and Arginine Metabolism Antagonist
Kynurenine Pathway Antagonist
ENPP1, TREX1and PARP7 Antagonist
Our Service
A great deal of research and design is required before an immune antagonist can be synthesized. The approximate synthetic route of the immune antagonist is shown in the figure below:
Fig.1 Synthesis of immune antagonists.
Assessing and regulating pathway-related biomarkers may predict response to tumor immunotherapy. Creative Biolabs offers assays for the following immuno-related markers of oncology:
Method
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Objective
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PD-L1 expression level, tumor mutational burden (TMB), microsatellite instability
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Screening for optimal immunotherapy outcomes
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Expression profiling of inflammatory genes in dendritic cells or tumor-infiltrating lymphocytes and T cells
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To predict response to immunotherapy drugs
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Correlation of peripheral blood with TME PD response
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To provide a suitable immunotherapy solution
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Tumor RNA gene expression evaluation
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For immune activation and cytokine assessment
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Tumor tissue DNA evaluation
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For the evaluation of TMB and tumor immunogenicity
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Expression of tumor PD-L1 on tumors and immune cells
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For comparison at baseline and in treatment
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In Vitro Evaluation
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Immune parameter assessment
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Molecular mechanistic assessment
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Safety assessment
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Tumor immune microenvironment analysis
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And so on
Choosing the right animal model is critical for preclinical trials, and Creative Biolabs can offer several common models:
Type
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Advantage
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Disadvantage
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Application
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isogenic mouse
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It can stably express luciferase groups and is easy to use.
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Tumors originate from mice and do not directly match human disease, so they are not a good predictor of clinical outcomes.
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Suitable for screening large numbers of drug candidates.
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Transgenic/Genetically Engineered Mouse Models (GEMMs)
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The disease progresses more naturally.
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Mutations in transgenic models limit neoantigen production and are less suitable for immuno-oncology studies
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Study the function of specific genes and disease mechanisms.
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Cell-derived xenograft model (CDX)
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In the construction of tumor cell lines, the tumorigenesis rate is high, the modeling time is short, the reproducibility is good, the cost is low, and fluorophores can be added.
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Tumors are cultured in vitro and lack a human-derived tumor growth environment. Immunodeficient mice need to be selected for construction, which is not fully suitable for studying the role of the immune system in tumor development.
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Conduct preclinical pharmacodynamics testing, PK/PD correlation and combination therapy studies.
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Patient-derived xenograft model (PDX)
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Heterogeneous tumors that follow the effects of human primary tumor resistance and TEM on drugs, preserving the genetic characteristics of patients.
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Some models are difficult to build and grow at a slower rate than CDX.
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Targeted reagent R&D and production, personalized therapy R&D.
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Humanized mouse/immune stand-in model
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Partial human immune system with human drug targets that allow the study of human cancer cell lines or primary patient-derived tumors in the context of autologous or xenoimmunology.
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The immune system is suboptimal, and human xenogeneic inhibitor versus host disease is common.
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To investigate the efficacy of murine homologous or alternative antibodies, as well as aspects of the human immune response in mouse models
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Tumor organoids
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Similar to the original tumor, it is a more clinically relevant model for preclinical research.
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Lack of key components in TME.
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Drug screening and prediction of efficacy to a certain extent; Avoid medication side effects.
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If you are interested in agonist development services for cancer immunotherapy, you can click here for more information!
For Research Use Only | Not For Clinical Use