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Analysis of peri-islet CD45-positive leucocytic infiltrates in long-standing type 1 diabetic patients.

Authors :
Reddy S
Zeng N
Al-Diery H
Jung D
Yeu C
Joret MO
Merrilees MJ
Wu F
Source :
Diabetologia [Diabetologia] 2015 May; Vol. 58 (5), pp. 1024-35. Date of Electronic Publication: 2015 Feb 17.
Publication Year :
2015

Abstract

Aims/hypothesis: The role of peri-islet CD45-positive leucocytes, as one component of insulitis, in beta cell death during human type 1 diabetes remains unclear. We undertook a case study, comparing and quantifying leucocytes in the peri- and intra-islet areas in insulin-positive and -negative islets, to assess whether peri-islet leucocytes are pathogenic to beta cells during type 1 diabetes.<br />Methods: Pancreatic sections from 12 diabetic patients (0.25-12 years of disease) and 13 non-diabetic individuals with and without autoantibodies were triple-immunostained for islet leucocytes, insulin and glucagon cells. Islets were graded for insulitis, enumerated and mapped for the spatial distribution of leucocytes in peri- and intra-islet areas in relation to insulin- and glucagon-immunopositive cells.<br />Results: In the non-diabetic autoantibody-negative group, the percentage of islets with insulitis was either absent or <1% in five out of eight cases and ranged from 1.3% to 19.4% in three cases. In the five non-diabetic autoantibody-positive cases, it varied from 1.5% to 16.9%. In the diabetic group, it was <1% in one case and 1.1-26.9% in 11 cases, with insulitis being absent in 68% of insulin-positive islets. Peri-islet leucocytes were more numerous than intra-islet leucocytes in islets with insulin positivity. Increasing numbers of exocrine leucocytes in non-diabetic autoantibody-positive and diabetic donors were also present.<br />Conclusions/interpretation: The prominence of peri-islet leucocytes in insulin-positive islets in most long-standing diabetic individuals suggests that they may be pathogenic to residual beta cells. Increasing numbers of leucocytes in the exocrine region may also participate in the pathogenesis of type 1 diabetes.

Details

Language :
English
ISSN :
1432-0428
Volume :
58
Issue :
5
Database :
MEDLINE
Journal :
Diabetologia
Publication Type :
Academic Journal
Accession number :
25687234
Full Text :
https://doi.org/10.1007/s00125-015-3519-6