Anakinra and Tocilizumab Enhance Survival and Function of Human Islets during Culture: Implications for Clinical Islet Transplantation

Author:

Sahraoui Afaf123,Kloster-Jensen Kristine123,Ueland Thor34,Korsgren Olle5,Foss Aksel123,Scholz Hanne123

Affiliation:

1. Institute for Surgical Research, Oslo University Hospital Rikshospitalet, Oslo, Norway

2. Section for Transplantation Surgery, Oslo University Hospital Rikshospitalet, Oslo, Norway

3. Institute of Clinical Medicine, University in Oslo, Oslo, Norway

4. Institute for Internal Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway

5. Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden

Abstract

Pretreatment culture before islet transplantation represents a window of opportunity to ameliorate the pro-inflammatory profile expressed by human β-cells in duress. Anakinra (IL-1 receptor antagonist) and tocilizumab (monoclonal IL-6 receptor antibody) are two known anti-inflammatory agents successfully used in the treatment of inflammatory states like rheumatoid arthritis. Both compounds have also been shown to reduce blood glucose and glycosylated hemoglobin in diabetic patients. We therefore sought to evaluate the impact of anakinra and tocilizumab on human β-cells. The islets were precultured with or without anakinra or tocilizumab and then transplanted in a marginal mass model using human islets in immunodeficient mice. Islet viability was evaluated in an in vitro model. The pretreatment culture led to a significantly improved engraftment in treated islets compared to the vehicle. Anakinra and tocilizumab are not toxic to human islets and significantly reduce markers of inflammation and cell death. These results strongly support a pretreatment culture with anakinra and tocilizumab prior to human islet transplantation.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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