Negative selection, not receptor editing, is a physiological response of autoreactive thymocytes

Author:

Kreslavsky Taras1,Kim Hye-Jung1,Koralov Sergei B.1,Ghitza Dvora1,Buch Thorsten2,Cantor Harvey1,Rajewsky Klaus1,von Boehmer Harald1

Affiliation:

1. Department of Cancer Immunology and AIDS, Dana-Farber Cancer Institute; and Program in Cellular and Molecular Medicine, Children’s Hospital, and Immune Disease Institute, Harvard Medical School, Boston, MA 02115

2. Institute for Medical Microbiology, Immunology, and Hygiene, Technische Universität München, 81545 Munich, Germany

Abstract

Antigen receptor editing—a process of secondary rearrangements of antigen receptor genes in autoreactive lymphocytes—is a well-established tolerance mechanism in B cells, whereas its role in T cells remains controversial. Here, we investigated this issue using a novel Tcra knock-in locus, which ensured appropriate timing of TCRα expression and allowed secondary rearrangements. Under these conditions the only response to self-antigen that could be unambiguously identified was negative selection of CD4/CD8 double positive thymocytes. No evidence could be obtained for antigen-induced TCR editing, whereas replacement of the transgenic TCRα chain by ongoing gene rearrangement occurred in some cells irrespective of the presence or absence of self-antigen.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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