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Early Assessment of Teplizumab Treatment Response Using Continuous Glucose Monitoring
Sari Krepel-Volsky1,2, Merav Gil-Margolis1,2, Keren Smuel-Zilberberg1,2
1The Jesse Z and Sara Lea Shafer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.
Insights
Continuous glucose monitoring (CGM) reveals varied responses to teplizumab in children with type 1 diabetes. Early CGM data may predict glycemic changes, offering insights into treatment effectiveness.
Area of Science:
- Immunology
- Endocrinology
- Pediatrics
Background:
- Type 1 diabetes (T1D) management requires continuous monitoring of glycemic control.
- Teplizumab is an immunomodulatory agent investigated for its potential impact on T1D progression.
- Understanding treatment effects in real-world settings is crucial for optimizing T1D care.
Purpose of the Study:
- To describe continuous glucose monitoring (CGM) trajectories in children with stage 2 T1D treated with teplizumab.
- To evaluate the utility of CGM metrics in assessing glycemic dynamics during immunomodulatory therapy.
- To explore early indicators of treatment response or disease progression.
Main Methods:
- Longitudinal follow-up of five children with stage 2 T1D receiving teplizumab.
- Utilized continuous glucose monitoring (CGM) to collect data on glycemic variability (GV) and time above 140 mg/dL.
- Analyzed CGM metrics over 8-19 months, correlating with T1D stage and glycated hemoglobin levels.
Main Results:
- Four of five participants maintained stage 2 T1D, showing stabilized or improved GV and reduced time above 140 mg/dL within 3-6 months.
- One participant progressed to stage 3 T1D within 4 months, exhibiting increasing glycemic variability and worsening excursions.
- CGM changes were detectable early and not mirrored by significant glycated hemoglobin shifts.
Conclusions:
- CGM may detect early glycemic dynamics following teplizumab therapy in T1D.
- CGM offers a practical approach for longitudinal monitoring of treatment effects.
- These hypothesis-generating findings require validation in larger pediatric cohorts.
Abstract:
We describe continuous glucose monitoring (CGM) trajectories in five children with stage 2 type 1 diabetes treated with teplizumab in a real-world setting. Participants were followed longitudinally using CGM metrics, including glycemic variability (GV) and time above 140 mg/dL. Over 8-19 months of follow-up, four participants remained in stage 2, while one progressed to stage 3 diabetes within 4 months of treatment. CGM-derived metrics demonstrated heterogeneous trajectories. Most participants showed stabilization or improvement in GV and time above 140 mg/dL within 3-6 months, whereas the progressor exhibited increasing variability and worsening glycemic excursions over time. These changes were detectable early and were not paralleled by substantial changes in glycated hemoglobin. These observations suggest that CGM may capture early directional changes in glycemic dynamics following immunomodulatory therapy and may provide a practical approach for longitudinal monitoring. Findings should be interpreted as hypothesis-generating and require validation in larger cohorts.
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