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From the Department of Biology, University of California at San Diego, La Jolla, California 92037
Abstract
We have found that sub-immunogenic doses of sheep red blood cells (SRBC) in vivo increase the plaque-forming cell (PFC) responses to trinitrophenyl and to SRBC when spleen cells are challenged in vitro using TNP-SRBC as antigen.
By mixing irradiated spleen cells from low dose-primed mice with normal spleen cells, the enhancing activity is shown to be radiation resistant. Treatment with anti-BA
abolishes the activity. We therefore infer that it resides in a thymus-derived helper-cell population.
While the enhancing activity is maximal for the carrier to which the mice were low dose primed, priming with SRBC gives a substantial enhancement of the response when burro RBC are used as carrier, but little enhancement when chicken RBC are used as carrier. There is little cross-reactivity between SRBC and burro RBC at the direct PFC level in this system, demonstrating that cross-reactivity at the T cell level need not parallel that at the B cell level.
Footnotes
1 Supported by United States Public Health Service Research Grant AI 08795-03 and American Cancer Society Grant E-395-D.
2 Supported by United States Public Health Service GM 00702-10 Genetics Training Grant.
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D. A. Rowley, F. W. Fitch, F. P. Stuart, H. Kohler, and H. Cosenza Specific Suppression of Immune Responses Science, September 21, 1973; 181(4105): 1133 - 1141. [Abstract] [PDF] |
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