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An endogenous retrovirus mediating deletion of αβ T cells?

Abstract

A SPECIAL class of self-antigens (endogenous superantigens) is capable of deleting many murine T cells on the basis of their expression of particular T-cell receptor Vβ gene segments. In mice that endogenously express these antigens, tolerance is mediated in part by the clonal deletion of the relevant Vβ-bearing T cells1–17. The deletion of I–E-reactive Vβ 5.2-bearing T cells is dependent on the coexpression of an I–E tolerogenic coligand (Etc)14 and the gene for one of these coligands, Etc-1, maps to chromosome 12, near the mouse mammary tumour viral integrant, Mtv-9. Here we report a perfect genetic linkage between Etc-1 and Mtv-9 and show that Etc-1 is also involved in the I–E-dependent deletion of T cells bearing Vβ5.1 and Vβ11 domains. We also demonstrate that Mtv-9 transcripts are present in B cells expressing Etc-1 and suggest that the coligand recognized by roughly 15% of all T lymphocytes is encoded by the Mtv-9 genome.

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Woodland, D., Happ, M., Gollob, K. et al. An endogenous retrovirus mediating deletion of αβ T cells?. Nature 349, 529–530 (1991). https://doi.org/10.1038/349529a0

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