The Journal of Experimental Medicine
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© The Rockefeller University Press, 0022-1007/1997/12/2039/ $5.00
The Journal of Experimental Medicine, Volume 186, Number 12, December 15, 1997 2039-2043

Brief Definitive Reports

Determinant Spreading of T Helper Cell 2 (Th2) Responses to Pancreatic Islet Autoantigens

Jide Tian*, Paul V. Lehmann{ddagger}, and Daniel L. Kaufman*

From the * Department of Molecular and Medical Pharmacology, University of California, Los Angeles, California 90095-1735; and the {ddagger} Department of Pathology, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106

The nature (Th1 versus Th2) and dynamics of the autoimmune response during the development of insulin-dependent diabetes mellitus (IDDM) and after immunotherapy are unclear. Here, we show in nonobese diabetic (NOD) mice that the autoreactive T cell response starts and spreads as a pure Th1 type autoimmunity, suggesting that a spontaneous Th1 cascade underlies disease progression. Surprisingly, induction of antiinflammatory Th2 responses to a single β cell antigen (βCA) resulted in the spreading of Th2 cellular and humoral immunity to unrelated βCAs in an infectious manner and protection from IDDM. The data suggest that both Th1 and Th2 autoimmunity evolve in amplificatory cascades by generating site-specific, but not antigen-specific, positive feedback circuits. Determinant spreading of Th2 responses may be a fundamental mechanism underlying antigen-based immunotherapeutics, explaining observations of infectious tolerance and providing a new theoretical framework for therapeutic intervention.

Address correspondence to Dr. Daniel L. Kaufman, Department of Molecular and Medical Pharmacology, UCLA School of Medicine, Rm 23-167 CHS, University of California, Los Angeles, Los Angeles, CA 90095-1735. Phone: 310-794-9664; FAX: 310-825-6267; E-mail: dkaufman{at}pharm.medsch.ucla.edu


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