Published in

National Academy of Sciences, Proceedings of the National Academy of Sciences, 17(93), p. 9102-9107, 1996

DOI: 10.1073/pnas.93.17.9102

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Expression of a second receptor rescues self-specific T cells from thymic deletion and allows activation of autoreactive effector function.

Journal article published in 1996 by T. Zal ORCID, S. Weiss, A. Mellor, B. Stockinger ORCID
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

Allelic exclusion at the T-cell receptor alpha chain locus is incomplete resulting in the generation of T cells that express two T-cell receptors. The potential involvement of such T cells in autoimmunity has been suggested [Padovan, E., Casorati, G., Dellabona, P., Meyer, S., Brockhaus, M. & Lanzavecchia, A. (1993) Science 262, 422-424; Heath, W. R. & Miller, J. F. A. P. (1993) J. Exp. Med. 178, 1807-1811]. Here we show that expression of a second T-cell receptor can rescue T cells with autospecific receptors from thymic deletion and allow their exit into the periphery. Dual receptor T cells, created by constitutive expression of two transgenic T-cell receptors on a Rag1-/- background, are tolerant to self by maintaining low levels of autospecific receptor, but selfreactive effector function (killing) can be induced through activation via the second receptor. This opens the possibility that T cells carrying two receptors in the periphery of normal individuals contain putatively autoreactive cells that could engage in autoimmune effector functions after recognition of an unrelated environmental antigen.