Technique of Endoscopic Biopsy of Islet Allografts Transplanted into the Gastric Submucosal Space in Pigs

Author:

Fujita Minoru12,McGrath Kevin M.3,Bottino Rita14,Dons Eefje M.15,Long Cassandra1,Kumar Goutham1,Ekser Burcin6,Echeverri Gabriel J.7,Hata,‡‡ Jiro8,Haruma Ken2,Cooper David K. C.1,Hara Hidetaka1

Affiliation:

1. Thomas E. Starzl Transplantation Institute, University of Pittsburgh, Pittsburgh, PA, USA

2. Division of Gastroenterology, Department of Internal Medicine, Kawasaki Medical School, Kurashiki, Japan

3. Division of Gastroenterology, Hepatology and Nutrition, University of Pittsburgh, Pittsburgh, PA, USA

4. Division of Immunogenetics, Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA

5. Department of Surgery, Erasmus Medical Center Rotterdam, Rotterdam, The Netherlands

6. Department of Surgery, Transplantation and Advanced Technologies, Vascular Surgery and Organ Transplant Unit, University Hospital of Catania, Catania, Italy

7. Transplantation Unit, Fundacion Clinica Valle del Lili, ICESI University School of Medicine, Cali, Colombia

8. †Division of Endoscopy and Ultrasonography, Department of Clinical Pathology and Laboratory Medicine, Kawasaki Medical School, Kurashiki, Japan

Abstract

Currently, islet cells are transplanted into the liver via portal vein infusion. One disadvantage of this approach is that it is not possible to adequately biopsy the islets in the liver to assess for rejection. Islet transplantation (Tx) into the gastric submucosal space (GSMS) can be performed endoscopically and has the potential advantage of histological evaluation by endoscopic biopsy. The aim of this study was to determine whether a representative allograft sample could be obtained endoscopically. We performed islet Tx into the GSMS in nonimmunosup-pressed pigs using simple endoscopic submucosal injection. Islets were transplanted at four sites. Endoscopic ultrasonography and biopsy of the transplanted islets at two sites by modified endoscopic submucosal dissection were carried out successfully in all pigs 5 days after islet Tx. Tissue obtained at both biopsy and necropsy (including full-thickness sections of the gastric wall around the sites of the remaining islets and biopsies) were examined by histology and immunohistochemistry to confirm the presence of the islet grafts and any features of rejection. Representative allograft sampling was successfully obtained from all biopsy sites. All biopsies included islets with insulin-positive staining. There was significant CD3+ and CD68+ cell infiltration in the islet masses obtained at biopsy and from sections taken at necropsy, with similar histopathological features. Endoscopic biopsy of islet allografts in the GSMS is feasible, provides accurate histopathological data, and would provide a significant advance if translated into clinical practice.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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