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Article has an altmetric score of 3

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Research Article Free access | 10.1172/JCI118006

In vivo activity and in vitro specificity of CD4+ Th1 and Th2 cells derived from the spleens of diabetic NOD mice.

D Healey, P Ozegbe, S Arden, P Chandler, J Hutton, and A Cooke

Department of Pathology, Cambridge University, United Kingdom.

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Department of Pathology, Cambridge University, United Kingdom.

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Department of Pathology, Cambridge University, United Kingdom.

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Department of Pathology, Cambridge University, United Kingdom.

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Department of Pathology, Cambridge University, United Kingdom.

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Department of Pathology, Cambridge University, United Kingdom.

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Published June 1, 1995 - More info

Published in Volume 95, Issue 6 on June 1, 1995
J Clin Invest. 1995;95(6):2979–2985. https://doi.org/10.1172/JCI118006.
© 1995 The American Society for Clinical Investigation
Published June 1, 1995 - Version history
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Abstract

CD4+ T cell lines were generated from the spleens of diabetic NOD mice against crude membrane preparations derived from a rat insulinoma. Adoptive transfer of these lines into neonatal mice confirms that overt diabetes is induced by gamma-IFN-secreting Th1 cells, whereas transfer of IL-4-secreting Th2 cells resulted in a nondestructive peri-islet insulitis. Analysis of the antigens recognized by individual T cell clones from the Th1 line included reactivity against an insulinoma membrane fraction enriched in proteins of approximately 38 kD. Immune responses to the same antigen preparation have been associated with T cell clones derived from human insulin-dependent diabetes mellitus. The specificity of Th2 cells includes reactivity to a fraction enriched in proteins of 30 kD. The data suggest that in insulin-dependent diabetes mellitus the balance between beta cell destruction, associated with intra-islet infiltration, and nondestructive (potential protective) peri-islet insulitis may depend on both the antigens recognized, and the prevailing cytokine environment.

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Referenced in 1 patents
17 readers on Mendeley
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