T cell help shapes B cell tolerance

Author:

Akama-Garren Elliot H.12ORCID,Yin Xihui3ORCID,Prestwood Tyler R.3,Ma Minghe1ORCID,Utz Paul J.3ORCID,Carroll Michael C.1ORCID

Affiliation:

1. Program in Cellular and Molecular Medicine, Boston Children’s Hospital, Harvard Medical School, Boston, MA 02115, USA.

2. Harvard-MIT Health Sciences and Technology, Harvard Medical School, Boston, MA 02115, USA.

3. Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.

Abstract

T cell help is a crucial component of the normal humoral immune response, yet whether it promotes or restrains autoreactive B cell responses remains unclear. Here, we observe that autoreactive germinal centers require T cell help for their formation and persistence. Using retrogenic chimeras transduced with candidate TCRs, we demonstrate that a follicular T cell repertoire restricted to a single autoreactive TCR, but not a foreign antigen–specific TCR, is sufficient to initiate autoreactive germinal centers. Follicular T cell specificity influences the breadth of epitope spreading by regulating wild-type B cell entry into autoreactive germinal centers. These results demonstrate that TCR-dependent T cell help can promote loss of B cell tolerance and that epitope spreading is determined by TCR specificity.

Publisher

American Association for the Advancement of Science (AAAS)

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