Insulin autoantibodies (IAAs) occur in newly diagnosed human insulin-dependent diabetes mellitus (IDDM) patients, but their presence in BB rats is controversial, possibly due to assay differences or variability in the animals studied. To resolve this controversy, lAAs were measured in well-characterized inbred BB rats both in radioligand assays with 125I-labeled rat insulin I or II, respectively, and in an enzyme-linked immunosorbent assay (ELISA) with rat insulin as antigen. In prospective studies, a total of 57 serums from 16 diabetes-prone (DP) BB rats were obtained during an interval ranging from 15 wk to the last week before onset and at onset of diabetes. At comparable ages, 21 serums were obtained from 8 DP BB rats not developing diabetes, and 70 matched serums were obtained from 19 diabetes-resistant (DR) BB rats. Levels of antibody binding increased slightly with increasing age in DP and matched DR rats. Two rats were positive at onset of IDDM in all assays but not in earlier samples. Otherwise, only few isolated serums from both types of rats regardless of diabetes had increased binding in one of the assays. In a cross-sectional study, the insulin-binding levels in 150-day-old DP rats (n = 20) that had not yet developed diabetes did not correlate with insulitis present in 3 of 20 rats and did not differ from 150-day-old DR BB rats (n = 20). Diabetic BB rats (n = 20) killed at 150 days of age after treatment with protamine zinc insulin for 1–3 mo showed increased binding levels (P < 0.01–0.001) in all assays compared with the DR and DP rats. We conclude that 1) IAAs may be present at low frequency at onset of IDDM in BB rats, 2) different patterns of reactivity are found in the two radioligand assays and in the ELISA, and 3)IAAs are not a marker for later development of IDDM or insulitis in BB rats.
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Original Articles|
June 01 1990
Lack of Systematically Found Insulin Autoantibodies in Spontaneously Diabetic BB Rats
Helle Markholst;
Helle Markholst
Department of Medicine, University of Washington
Seattle, Washington; Hagedorn Research Laboratory, Gentofte, Denmark
Department of Pathology, Vrije Universiteit
Brussels
Department of Medicine, University of Massachusetts Medical School
Worcester, Massachusetts
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Leslie J Klaff;
Leslie J Klaff
Department of Medicine, University of Washington
Seattle, Washington; Hagedorn Research Laboratory, Gentofte, Denmark
Department of Pathology, Vrije Universiteit
Brussels
Department of Medicine, University of Massachusetts Medical School
Worcester, Massachusetts
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Günter Klöppel;
Günter Klöppel
Department of Medicine, University of Washington
Seattle, Washington; Hagedorn Research Laboratory, Gentofte, Denmark
Department of Pathology, Vrije Universiteit
Brussels
Department of Medicine, University of Massachusetts Medical School
Worcester, Massachusetts
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ÅKe Lernmark;
ÅKe Lernmark
Department of Medicine, University of Washington
Seattle, Washington; Hagedorn Research Laboratory, Gentofte, Denmark
Department of Pathology, Vrije Universiteit
Brussels
Department of Medicine, University of Massachusetts Medical School
Worcester, Massachusetts
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John P Mordes;
John P Mordes
Department of Medicine, University of Washington
Seattle, Washington; Hagedorn Research Laboratory, Gentofte, Denmark
Department of Pathology, Vrije Universiteit
Brussels
Department of Medicine, University of Massachusetts Medical School
Worcester, Massachusetts
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Jerry Palmer
Jerry Palmer
Department of Medicine, University of Washington
Seattle, Washington; Hagedorn Research Laboratory, Gentofte, Denmark
Department of Pathology, Vrije Universiteit
Brussels
Department of Medicine, University of Massachusetts Medical School
Worcester, Massachusetts
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Address correspondence and reprint requests to Helle Markholst, MD, Hagedorn Research Laboratory, Niels Steensensvej 6, DK-2820 Gentofte, Denmark.
Diabetes 1990;39(6):720–727
Article history
Received:
March 13 1989
Revision Received:
January 19 1990
Accepted:
January 19 1990
PubMed:
2189763
Citation
Helle Markholst, Leslie J Klaff, Günter Klöppel, ÅKe Lernmark, John P Mordes, Jerry Palmer; Lack of Systematically Found Insulin Autoantibodies in Spontaneously Diabetic BB Rats. Diabetes 1 June 1990; 39 (6): 720–727. https://doi.org/10.2337/diab.39.6.720
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