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Printable Handouts
Navigable Slide Index
- Introduction
- The NOD mouse model (1)
- Pancreatic byopsy from NOD mouse
- The NOD mouse model (2)
- Other NOD characteristics
- Immune cascade
- Type 1 diabetes: mice versus humans
- Diabetes prevention in the NOD mouse (1)
- Anti-CD3 therapy in NOD mice
- Diabetes prevention in the NOD mouse (2)
- Vitamin D effect on NOD mice
- Diabetes prevention in the NOD mouse (3)
- Diabetes prevention in humans (1)
- Anti-CD3 in new-onset type 1 diabetes mellitus
- C-peptide response in the anti-CD3 trial
- Immune response in the anti-CD3 trial
- Belgian-German anti-CD3 trial
- Belgian anti-CD3 trial
- Humanized anti-CD3 in T1D (1)
- Humanized anti-CD3 in T1D (2)
- Dosage differences in trials
- C-peptide positivity required in the Belgian trial
- HbA1c in anti-CD3 trial
- C-peptide/insulin dose in anti-CD3 trial (1)
- C-peptide/insulin dose in anti-CD3 trial (2)
- C-peptide/insulin dose in anti-CD3 trial (3)
- Conclusions of anti-CD3 trial
- Safety and immunological changes
- Flu-like syndrome during treatment
- Mononucleosis-like syndrome after treatment
- Anti-CD3 treatment results
- Diabetes prevention in humans (2)
- The ENDIT trial
- Diabetes prevention in NOD: Ag specific (1)
- Effect of insulin on diabetes in NOD
- Diabetes prevention in NOD: Ag specific (2)
- Diabetes prevention in humans: Ag specific (1)
- DPT-1 trial map
- DPT-1 intervention protocols
- DPT-1 staging scheme
- Parenteral antigen protocol
- DPT-1 screening results
- DPT-1 study: time to diabetes by treatment
- DPT-1 study: MMTT peak C-peptide by treatment
- Oral antigen protocol
- Diabetes prevention in humans: Ag specific (2)
- DiaPep277 trial
- Risk of shock in autoantigen vaccination
- Insulin peptide induction of anaphylaxis
- Anaphylaxis in NOD
- Incidence of HEL-induced shock: strain specific
- Diabetes prevention in humans: Ag specific (3)
- Trial to reduce IDDM in genetically at risk
- Pilot trial by the TRIGR group
- Vitamin D and type 1 diabetes in humans
- Epidemiological studies of vitamin D influence
- Experimental design
- Vitamin D and diabetes incidence
- Conclusions
- We can prevent type 1 diabetes in animals
Topics Covered
- Type 1 diabetes is an autoimmune disease characterized by an immune destruction of the insulin producing beta-cells in the islets of Langerhans of the pancreas
- As these cells are the only cells in the body that are able to synthesize and secrete insulin in a regulated manner, destruction of these cells renders the patient dependent on exogenous insulin administration for survival
- Interventions aimed at preventing the disease have not been successful until now, but lessons from the animal models open new perspectives
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Talk Citation
Mathieu, C. (2007, December 1). Can we prevent type I diabetes? [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved April 15, 2025, from https://doi.org/10.69645/NRVQ6038.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Chantal Mathieu has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.