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Article ; Online: Immune cells and their inflammatory mediators modify β cells and cause checkpoint inhibitor-induced diabetes.

Perdigoto, Ana Luisa / Deng, Songyan / Du, Katherine C / Kuchroo, Manik / Burkhardt, Daniel B / Tong, Alexander / Israel, Gary / Robert, Marie E / Weisberg, Stuart P / Kirkiles-Smith, Nancy / Stamatouli, Angeliki M / Kluger, Harriet M / Quandt, Zoe / Young, Arabella / Yang, Mei-Ling / Mamula, Mark J / Pober, Jordan S / Anderson, Mark S / Krishnaswamy, Smita /
Herold, Kevan C

JCI insight

2022  Volume 7, Issue 17

Abstract: Checkpoint inhibitors (CPIs) targeting programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) and cytotoxic T lymphocyte antigen 4 (CTLA-4) have revolutionized cancer treatment but can trigger autoimmune complications, including CPI-induced diabetes ...

Abstract Checkpoint inhibitors (CPIs) targeting programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) and cytotoxic T lymphocyte antigen 4 (CTLA-4) have revolutionized cancer treatment but can trigger autoimmune complications, including CPI-induced diabetes mellitus (CPI-DM), which occurs preferentially with PD-1 blockade. We found evidence of pancreatic inflammation in patients with CPI-DM with shrinkage of pancreases, increased pancreatic enzymes, and in a case from a patient who died with CPI-DM, peri-islet lymphocytic infiltration. In the NOD mouse model, anti-PD-L1 but not anti-CTLA-4 induced diabetes rapidly. RNA sequencing revealed that cytolytic IFN-γ+CD8+ T cells infiltrated islets with anti-PD-L1. Changes in β cells were predominantly driven by IFN-γ and TNF-α and included induction of a potentially novel β cell population with transcriptional changes suggesting dedifferentiation. IFN-γ increased checkpoint ligand expression and activated apoptosis pathways in human β cells in vitro. Treatment with anti-IFN-γ and anti-TNF-α prevented CPI-DM in anti-PD-L1-treated NOD mice. CPIs targeting the PD-1/PD-L1 pathway resulted in transcriptional changes in β cells and immune infiltrates that may lead to the development of diabetes. Inhibition of inflammatory cytokines can prevent CPI-DM, suggesting a strategy for clinical application to prevent this complication.
MeSH term(s) Animals ; Diabetes Mellitus ; Humans ; Inflammation Mediators ; Mice ; Mice, Inbred NOD ; Programmed Cell Death 1 Receptor ; Tumor Necrosis Factor Inhibitors
Chemical Substances Inflammation Mediators ; Programmed Cell Death 1 Receptor ; Tumor Necrosis Factor Inhibitors
Language English
Publishing date 2022-09-08
Publishing country United States
Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ISSN 2379-3708
ISSN (online) 2379-3708
DOI 10.1172/jci.insight.156330
Database MEDical Literature Analysis and Retrieval System OnLINE

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