Abstract
T3-associated disulphide linked heterodimers (Tin) comprised of clonally unique α-chains of molecular weight (MW) 49,000–54,000 and β chains of MW 43,000 have been identified as the antigen receptors on human cytotoxic effector and inducer T-lymphocytes1–3. Crosslinking of Ti molecules by either the appropriate nominal antigen/MHC specificity or anti-clonotypic monoclonal antibody results in clonal expansion of such cells via induction of IL-2 receptor expression, endogenous IL-2 release and IL-2-IL-2 receptor interaction4. To determine whether analogous antigen receptor molecules and autocrine growth mechanisms are utilized by suppressor T-cells5–7, we produced an anti-clonotypic monoclonal antibody against a non-cytotoxic T8+ suppressor T-cell, T8AC6, which defines a T3-associated disulphide-linked heterodimer of similar molecular weight to the above clonotypes. We find that T3-Ti triggering of suppressor clones (T8AC6, T8AC7 or T8RW) does not result in IL-2 production or T-cell proliferation and in contrast to inducer clones, also leads to a transient IL-2 unresponsive state. We suggest that such T3-Ti receptor mediated autoregulation of suppressor T-cell growth is necessary in the facilitation of initial inducer T-cell activation following antigenic perturbation.
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Bensussan, A., Acuto, O., Hussey, R. et al. T3-Ti receptor triggering of T8+ suppressor T cells leads to unresponsiveness to interleukin-2. Nature 311, 565–567 (1984). https://doi.org/10.1038/311565a0
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DOI: https://doi.org/10.1038/311565a0
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