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Induction and Diverse Assessment Indicators of Experimental Autoimmune Encephalomyelitis
Published on: September 9, 2022
Emerging approaches for the therapy of autoimmune and chronic inflammatory disease
1The Kennedy Institute of Rheumatology Division, Faculty of Medicine, Imperial College London, 1 Aspenlea Road, Hammersmith, London W6 8LH, UK. andrew.cope@imperial.ac.uk
Abstract:
Progress in defining protein and gene signatures that characterize autoimmune-mediated inflammatory diseases has uncovered a large number of potential therapeutic targets. Preclinical data from rodent models can be generated rapidly, as can data from the genetic crosses of gene-deficient mice on autoimmune-susceptible backgrounds. But humans are not the same as mice, and however robust preclinical data might appear, therapeutic intervention in patients with autoimmune disease remains the definitive experiment. Several studies published in the past year have tested paradigms of autoimmune disease in clinical trials. Recent therapeutic approaches for targeting B-cell subsets and co-stimulatory pathways are described here in detail. It is our belief that the future of immunotherapy in the clinic will depend to some extent upon the availability of biomarkers for defining biological signatures of immune function in vivo.
Insights
Defining protein and gene signatures for autoimmune diseases reveals therapeutic targets. Clinical trials in humans, not just preclinical models, are essential for validating new immunotherapies and biomarkers.
Area of Science:
- Immunology
- Autoimmune Diseases
- Therapeutic Development
Background:
- Significant progress has been made in identifying protein and gene signatures for autoimmune-mediated inflammatory diseases.
- These signatures have uncovered numerous potential therapeutic targets for autoimmune conditions.
- Preclinical data from rodent models and genetic studies offer rapid insights but do not fully replicate human disease.
Purpose of the Study:
- To review recent therapeutic approaches targeting B-cell subsets and co-stimulatory pathways in autoimmune diseases.
- To emphasize the critical role of clinical trials in validating preclinical findings for human autoimmune disease treatment.
- To highlight the importance of biomarkers for assessing immune function in vivo for future immunotherapy.
Main Methods:
- Review of recent clinical trial data for autoimmune diseases.
- Detailed description of therapeutic strategies targeting B-cell subsets.
- Explanation of approaches targeting co-stimulatory pathways in immune responses.
Main Results:
- Several studies have tested autoimmune disease paradigms in clinical trials over the past year.
- Recent advances include targeted therapies for specific B-cell subsets.
- Progress has been made in modulating co-stimulatory pathways for therapeutic benefit.
Conclusions:
- Human clinical trials are the definitive test for therapeutic interventions in autoimmune diseases.
- Targeting B-cell subsets and co-stimulatory pathways represents a promising area of immunotherapy.
- Biomarkers for in vivo immune function are crucial for the future of clinical immunotherapy.
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