- 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
Cytokine-Targeted Therapy R&D for IBD
Although the etiology that triggers IBD is still unknown, enough progress has been made to allow us to characterize some of the cytokine-mediated signalling pathways assigned to the acute inflammatory process. Several cytokines were identified as main mediators of chronic IBD inflammation, and drugs that antagonize these molecules were designed as biological therapies in the treatment of IBD. Anti-TNF drugs clearly improved the activity and long-term results of IBD treatment compared with conventional therapies. Therefore, targeting these cytokines may provide new strategies for the treatment of IBD.
Fig. 1. Key roles of cytokines in gut homeostasis and inflammatory bowel disease. (Neurath, 2024)
Cytokine-Targeted Therapy R&D Services
Ace Therapeutics is committed to helping clients develop cytokine-based therapies for IBD. Our team of scientists consists of immunologists, molecular biologists and pharmacologists who have studied cytokines and their respective signaling pathways for many years. We have performed countless experiments and have vast experience on complex experimental design and testing.
Identification and Validation of Cytokines Involved in IBD Pathogenesis
Using high-throughput methods such as single-cell transcriptomics, proteomics, metagenomics and microbiome analyses and multimomics technologies, we further identify and verify IBD-pathogenic cytokines. Animal models of IBD are also essential to understand the pathogenetic mechanisms of cytokines. Using gene knockout and gene overexpression approaches, functional studies are also carried out.
Types of Cytokine-Targeted Therapies We Can Develop
Using spatially resolved, high-dimensional transcriptomic assessment of gene transcription by spatial transcriptomics, we can precisely localize mRNA molecules within the inflamed gut, as well as discern the position of mucosal cells prior to sequencing, which could facilitate monitoring of the trajectory of immune cell lineage, dissect disease endotypes and select appropriate anti-cytokine therapies for IBD.
We have extensive experience in the development of cytokine-targeted therapies, including:
Cytokine- and Chemokine-targeted Therapies Cytokines and Chemokines IL-1 family cytokines IL-1β, IL-18, IL-33, IL-36, IL-37, IL-38 IL-6 family cytokines IL-6, IL-11, Leukaemia inhibitory factor (LIF), and oncostatin M (OSM) TNF and the TNF superfamily TNF, TNF-like cytokine 1A (TL1A) The β-common chain cytokine family Granulocyte–macrophage colony-stimulating factor (GM-CSF), IL-3, IL-5 The γ-common chain cytokine family IL-2, IL-4, IL-7, IL-9, IL-21 The IL-12 cytokine family IL-12 and IL-23, IL-27, IL-35 The IL-17 cytokine family IL-17A and IL-17F The IL-10 cytokine family IL-10, IL-20, IL-22, IL-36, IL-37, IL-38 TGFβ - Interferon family IFNγ, IFNλ cytokine IL-28A Our Strategy for Improving Anti-cytokine Agents
We offer a variety of technologies to improve the target binding and pharmacokinetics or antibody-mediated cytotoxicity of monoclonal anti-cytokine antibodies in IBD.
- Modification of antibody formats. We assist our clients in developing bispecific antibody formats that target multiple cytokines to enhance drug concentration in the gut and improve the efficacy of treatments for IBD.
- We can design new target structures of antibodies that enable the blockade of several cytokines.
- Computational design of cytokines. We offer protein engineering methods such as directed evolution lead to cytokines with higher half-life through modifications such as Fc fusion protein design or PEGylation.
Ace Therapeutics helps our clients to develop cytokine-targeted therapies to IBD, including regulatory T cell transfer to restore the balance of cytokines, the blockade of pro-inflammatory cytokines or their receptors, as well as the inhibition of signalling kinases. If you have any needs, please feel free to contact us.
Reference
- Neurath, M. F. (2024). Strategies for targeting cytokines in inflammatory bowel disease. Nature Reviews Immunology, 1-18.
! For research use only, not intended for any clinical use.Related ServicesAminosalicylate R&D for IBD Corticosteroid 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 Immunotherapy R&D 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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