Publications by authors named "S Litwak"

Article Synopsis
  • A phase 2 trial investigated the effects of baricitinib, a JAK inhibitor, on β-cell function in patients with early-stage type 1 diabetes, comparing it to a placebo over 48 weeks.
  • Results showed that the baricitinib group had a significantly higher mean C-peptide level, indicating better β-cell function, and required a lower daily insulin dose compared to the placebo group.
  • While baricitinib improved certain measures of insulin production and glycemic control, the overall levels of glycated hemoglobin were similar between both groups, with no notable differences in adverse events reported.
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Article Synopsis
  • Immune checkpoint inhibitors can effectively treat cancer but are linked to immune-related side effects, including type 1 diabetes (T1D), prompting researchers to explore preventive treatments like JAK1/JAK2 inhibitors.* -
  • In experiments with nonobese diabetic mice, JAK1/JAK2 inhibitors successfully prevented and even reversed diabetes caused by PD-L1 blockade, inhibiting harmful immune cell activity in the pancreas.* -
  • The study demonstrates that JAK1/JAK2 inhibitors might be a viable option for managing diabetes resulting from cancer therapy, without compromising the anti-tumor effectiveness in other models.*
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Type 1 diabetes develops in childhood and adolescence, with peak incidence in the early teenage years. There is an urgent need for an accurate method to detect insulin-producing β-cells in patients that is not affected by alterations in β-cell function. As part of our research program to design specific probes to measure β-cell mass, we recently developed a novel insulin-binding peptide probe (IBPP) for the detection of β-cells in vivo.

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Most obese and insulin-resistant individuals do not develop diabetes. This is the result of the capacity of β-cells to adapt and produce enough insulin to cover the needs of the organism. The underlying mechanism of β-cell adaptation in obesity, however, remains unclear.

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Article Synopsis
  • Cytokines like IFN-γ and common γ chain cytokines play a harmful role in type 1 diabetes by promoting the destruction of insulin-producing β cells via CD8 T cells.
  • Research found that JAK1/JAK2 inhibitors can reverse autoimmune responses and reduce harmful signals in β cells related to these cytokines in non-obese diabetic mice.
  • The JAK1-selective inhibitor ABT 317 significantly reduced T cell proliferation and improved diabetes symptoms in treated mice, showing promise for future type 1 diabetes treatments.
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