An approach to the unification of suppressor T cell circuits: A simplified assay for the induction of suppression by T cell-derived, antigen-binding molecules (T-ABM)

Ben Chue, Thomas A. Ferguson, Kenneth D. Beaman, Stephen J. Rosenman, Robert E. Cone, Patrick M. Flood, Douglas R. Green

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

A system is presented in which the in vitro response to sheep red blood cells (SRBC) can be regulated using antigenic determinants coupled to SRBC and T cell-derived antigen-binding molecules (T-ABM) directed against the coupled determinants. T suppressor-inducer factors (TsiF's) are composed of two molecules, one of which is a T-ABM and one which bears I-J determinants (I-J+ molecule). Using two purified T-ABM which have not previously been shown to have in vitro activity, we produced antigen-specific TsiF's which were capable of inducing the suppression of the anti-SRBC response. Suppression was found to require both the T-ABM and the I-J+ molecule, SRBC conjugated with the antigen for which the T-ABM was specific, and a population of Ly-2+ T cells in the culture. Two monoclonal TsiF (or TsF1) were demonstrated to induce suppression of the anti-SRBC response in this system, provided the relevant antigen was coupled to the SRBC in culture. The results are discussed in terms of the general functions of T-ABM in the immune system. This model will be useful in direct, experimental comparisons of the function of T-ABM and suppressor T cell factors under study in different systems and laboratories.

Original languageEnglish
Pages (from-to)30-40
Number of pages11
JournalCellular Immunology
Volume118
Issue number1
DOIs
StatePublished - Jan 1989

Fingerprint

Dive into the research topics of 'An approach to the unification of suppressor T cell circuits: A simplified assay for the induction of suppression by T cell-derived, antigen-binding molecules (T-ABM)'. Together they form a unique fingerprint.

Cite this