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Science 21 September 1990:
Vol. 249. no. 4975, pp. 1433 - 1436
DOI: 10.1126/science.2205920

Articles

Science, Vol 249, Issue 4975, 1433-1436
Copyright © 1990 by American Association for the Advancement of Science


articles

Acceleration of diabetes in young NOD mice with a CD4+ islet-specific T cell clone

K Haskins and M McDuffie

Barbara Davis Center for Childhood Diabetes, University of Colorado Health Sciences Center, Denver 80262.

Nonobese diabetic (NOD) mice develop an autoimmune form of diabetes, becoming hyperglycemic after 3 months of age. This process was accelerated by injecting young NOD mice with CD4+ islet-specific T cell clones derived from NOD mice. Overt diabetes developed in 10 of 19 experimental animals by 7 weeks of age, with the remaining mice showing marked signs of the disease in progress. Control mice did not become diabetic and had no significant pancreatic infiltration. This work demonstrates that a CD4 T cell clone is sufficient to initiate the disease process in the diabetes-prone NOD mouse.


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beta cell apoptosis in T cell-mediated autoimmune diabetes.
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T helper cell subsets in insulin-dependent diabetes.
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T cell receptor specificity and diabetes in nonobese diabetic mice.
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Science 262, 1583
   PDF »
Immunologic Aspects of Endocrine Diseases.
J. R. Baker Jr (1992)
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   Abstract »    PDF »
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F. Luhder, C. Chambers, J. P. Allison, C. Benoist, and D. Mathis (2000)
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