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Updated: May 23, 2026

High-Efficiency Generation of Antigen-Specific Primary Mouse Cytotoxic T Cells for Functional Testing in an Autoimmune Diabetes Model
Published on: August 16, 2019
[Immunotherapy for type 1 diabetes mellitus (DM1)]
Cornelis R van der Torren1, Bart O Roep
1Leids Universitair Medisch Centrum, afd. Immunohaematologie & Bloedtransfusie, Leiden, the Netherlands.
Treatment of type 1 diabetes mellitus (DM1) has greatly improved but remains limited to combating the consequences of the disease. Target values for glucose regulation are achieved in only 20% of patients. Immunosuppression can slow disease progression, but does not cure DM1. Immunotherapy attempts to protect remaining insulin-producing β cells and β cell function. Promising results of immunotherapy in phase 2 studies in patients with DM1 could not be reproduced in phase 3 studies. These studies showed heterogeneity played a role in patient populations and between ethnic groups. In future studies better endpoints of efficacy, biomarkers of disease progression and response to therapy are essential. Vaccination with β-cell specific antigens to stimulate tolerance and vaccination combined with immunotherapy (biologicals) are options for future therapy. Discussion on the acceptability of the side effects of immunotherapy is desirable.
Treatment of type 1 diabetes mellitus (DM1) has greatly improved but remains limited to combating the consequences of the disease. Target values for glucose regulation are achieved in only 20% of patients. Immunosuppression can slow disease progression, but does not cure DM1. Immunotherapy attempts to protect remaining insulin-producing β cells and β cell function. Promising results of immunotherapy in phase 2 studies in patients with DM1 could not be reproduced in phase 3 studies. These studies showed heterogeneity played a role in patient populations and between ethnic groups. In future studies better endpoints of efficacy, biomarkers of disease progression and response to therapy are essential. Vaccination with β-cell specific antigens to stimulate tolerance and vaccination combined with immunotherapy (biologicals) are options for future therapy. Discussion on the acceptability of the side effects of immunotherapy is desirable.
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