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Division of Immunology and the University of Rochester Cancer Center; and the Departments of Dental Research and Microbiology, School of Medicine and Dentistry, University of Rochester, Rochester, New York, 14642
Abstract
In previously published experiments we have distinguished two subpopulations of helper T cells (specific helper and nonspecific helper) in the spleens of antigen-primed mice. These subpopulations can be differentiated by their modes of action, and their activities and dose-response characteristics in mouse spleens primed with human
-globulin (HGG). In experiments designed to test whether the two subpopulations were derived from the same pool of precursors, or different pools, mice were injected with limiting doses of a tolerogenic form of HGG. They were subsequently challenged with an immunogenic dose of HGG and their spleens assayed for specific helper and nonspecific helper activities in response to HGG in vitro. Over the dose range of tolerogenic HGG studied, both the helper activities were found to be equally tolerized. The question of the possible involvement of suppressor T cells in the maintenance of the state of unresponsiveness was also addressed quantitatively by the use of this model system. No active suppression was demonstrable in the maintenance of tolerance in either T cell subpopulation. These results suggest that the two types of helper T cells are derived from a common precursor pool, or from different pools with identical susceptibilities to tolerogen. Suppressor cells do not appear to play a role in this form of tolerance.
Footnotes
1 Various segments of this work have been supported by United States Public Health Service Research Grants AI-11558 and CA-11198. and American Cancer Society Research Grant IM-49. J.T.H. is supported by United States Public Health Service Training Grant 5-T01-DE00003-18.
2 Portions of these data were presented before the 54th General Session of the International Association for Dental Research and Annual Session of the American Association for Dental Research, Miami Beach, Florida, March 25–28, 1976.
3 Address reprint requests to: Dr. J. T. Hoffeld, Department of Dental Research, University of Rochester Medical Center, Rochester, New York, 14642.
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