- AminosalicylatesCorticosteroids for IBDCytokine-Targeted Therapies for IBDJanus Kinase Inhibitors for IBDDrugs Targeting Leukocyte Trafficking for IBDPPAR-γ Ligands for IBDAgents Targeting the TGF-β/Smad System in IBDMatrix Metalloproteinase Inhibitors for IBDImmunotherapies for IBDDrugs Targeting Toll-like Receptors in IBDS1P Receptor Modulators for IBD
- Antibiotic Therapies for IBDProbiotic Therapies for IBDFecal Microbiota Transplantation for IBDCell-based Therapies for IBD
- Drug Target Discovery for IBDLead Discovery for IBDLead Optimization for IBD
- In Vitro ADMEIn Vivo ADME TestingPharmacokinetic EvaluationBioanalysisMetabolite Profiling and IdentificationPreclinical Toxicology Studies for IBD DrugsIn Vitro Efficacy Testing for IBD Drugs
- Disease Activity Index AssessmentColon Length and Weight AssessmentColonoscopyHistology and Immunohistochemistry EvaluationInflammatory Marker AssessmentOxidative Stress Marker AssessmentIntestinal Permeability MeasurementImaging Services
- IBD Immunopathogenesis AnalysisGut Microbiota AnalysisGenetic Studies of IBDIntestinal Barrier Dysfunction in IBD
- Serum Biomarker Discovery for IBDSerological Biomarker Discovery for IBDInquiry
Immunotherapy R&D for IBD
Both UC and CD are forms of inflammatory bowel disease (IBD). As an autoimmune disease, the inflammation has been understood as being ignited in principle by the innate immune system and then perpetuated by the adaptive immune system, thereby facilitating progression of disease. A virtually exponential growth in the understanding of the role of the immune system in the pathophysiology of IBD has paved the way for a multitude of several (immune) targeted therapies, from the innate to the adaptive immune system and from the targets connecting both immune systems, including anti-leukocyte trafficking agents – integrins and adhesion molecules.
Fig. 1. New drugs in IBD targeting innate and adaptive immune system. (Holleran, et al., 2017)
Our Immunotherapy R&D Services
At Ace Therapeutics, we're the global leader in research into IBD. As a preclinical contract research provider for immune-regulating therapy R&D, we support competitive pharmaceutical and biotechnology companies seeking innovative breakthroughs leading to development of new therapeutics for IBD. Leading the frontiers of natural immune system biology, our research and development specialists provide immunology and gut biology, and drug discovery.
At Ace Therapeutics, we offer a comprehensive service for immunology research all the way to immunotherapy development for IBD.
Analysis of the Immune Mechanisms in the Pathogenesis of IBD
We support our clients in exploring the role of the innate and adaptive immune system in IBD pathogenesis. It is a central point in our understanding of the overlap in the interactions between the innate and adaptive immune systems that can guide us towards novel avenues of discovery on the immunological mechanisms of intestinal inflammation.
Analysis of the Innate Immune System in IBD
- Profiling of immune cells. We can assess the activity and functions of innate immune cells, including macrophages, dendritic and natural killer cells, and their role in intestinal inflammation.
- Cytokine and chemokine assay. For clients who would like to investigate the molecular mechanisms of upregulation of cytokines (e.g., IL-1β, TNF-α, IL-6) and chemokines in intestinal inflammation and the consequences to the immune response, we provide a quantification of several cytokines and chemokines.
- Intestinal barrier function. Our assessment helps clients evaluate changes in intestinal barrier function and the role of the immune system within intestinal epithelial cells in maintaining integrity.
Analysis of the Adaptive Immune System in IBD
- T-cell analysis. We examine the percentage and activity of particular T cells (such as Th1, Th2, Th17 and regulatory T-cells) in IBD.
- Assessment of the B cell response. B cells also function to create memory against infections. We can analyse B cell function in IBD.
- Analysis of the autoimmune response. Understanding the underlying mechanisms of immune responses to gut microbes generated by the adaptive immune system may also provide insights into their contribution to IBD.
Immunotherapy Development Services for IBD
Understanding the underlying molecular pathophysiology of immune based gastrointestinal inflammation in IBD guides us to our clients in identifying the innate and adaptive immune systems as potential targets for biologic therapies for IBD. We also explore and conduct preclinical proof of principle safety and efficacy tests for certain immunotherapies for IBD.
Types of Immunotherapies We Can Develop Details Targeting the adaptive immune system - Inhibitor of Th1/Th17-anti-aytokine-IL 12/23
- Anti-SMAD7
- JAK1/JAK3 inhibitors
- Anti-cytokine IL-13
Targeting pleiotropic factors between the adaptive and innate immune systems - Anti-TNF
- Sphingosine-1-phosphate receptor-1 (S1P1) agonists
- Anti-IL-6
Targeting the innate immune system - Anti-integrins (α4β7 and α4β1)
- Anti-adhesion molecules (MAdCAM-1, ICAM-1, and VCAM-1)
- TLR agonists and antagonists
- Targeting IL-33/ST2 axis
Cell therapies Using mesenchymal stem cells or engineered T regs Ace Therapeutics is committed to provide you all high-quality experimental data and analytical report to facilitate your immunotherapy development and accelerate the IBD drug development and short-in-time market. If you have any inquiry for our services, please feel free to contact us.
Reference
- Holleran, G., et al. (2017). The innate and adaptive immune system as targets for biologic therapies in inflammatory bowel disease. International journal of molecular sciences, 18(10), 2020.
! For research use only, not intended for any clinical use.Related ServicesAminosalicylate R&D for IBD Corticosteroid R&D for IBD Cytokine-Targeted Therapy R&D for IBD Development of Agents Targeting the TGF-β/Smad System in IBD Development of Cell-based Therapies for IBD Development of Drugs Targeting Leukocyte Trafficking for IBD Development of Drugs Targeting Toll-like Receptors in IBD Development of Gut Microbiome-based Therapeutics for IBD Janus Kinase Inhibitor R&D for IBD Matrix Metalloproteinase Inhibitor R&D for IBD PPAR-γ Ligand R&D for IBD S1P Receptor Modulator R&D for IBD
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