The TCR assigns naive T cells to a preferred lymph node

Author:

de Greef Peter C.1ORCID,Njeru Sospeter Ngoci2ORCID,Benz Claudia2,Fillatreau Simon345,Malissen Bernard6ORCID,Agenès Fabien78ORCID,de Boer Rob J.1ORCID,Kirberg Jörg2ORCID

Affiliation:

1. Theoretical Biology and Bioinformatics, Utrecht University, Utrecht, Netherlands.

2. Division of Immunology, Paul-Ehrlich-Institut, IMG53, Langen, Germany.

3. Université Paris Cité, CNRS, INSERM, Institut Necker Enfants Malades-INEM, F-75015 Paris, France.

4. Université Paris Cité, Faculté de Médecine, Paris, France.

5. AP-HP, Hôpital Necker-Enfants Malades, Paris, France.

6. Centre d’Immunologie de Marseille-Luminy, Aix Marseille Université, INSERM, CNRS, 13288 Marseille, France.

7. Univ. Grenoble Alpes, Inserm, U1216, Grenoble Institut Neurosciences, 38000 Grenoble, France.

8. Inserm, Délégation Régionale Auvergne Rhône Alpes, 69500 Bron, France.

Abstract

Naive T cells recirculate between the spleen and lymph nodes where they mount immune responses when meeting dendritic cells presenting foreign antigen. As this may happen anywhere, naive T cells ought to visit all lymph nodes. Here, deep sequencing almost-complete TCR repertoires led to a comparison of different lymph nodes within and between individual mice. We find strong evidence for a deterministic CD4/CD8 lineage choice and a consistent spatial structure. Specifically, some T cells show a preference for one or multiple lymph nodes, suggesting that their TCR interacts with locally presented (self-)peptides. These findings are mirrored in TCR-transgenic mice showing localized CD69 expression, retention, and cell division. Thus, naive T cells intermittently sense antigenically dissimilar niches, which is expected to affect their homeostatic competition.

Publisher

American Association for the Advancement of Science (AAAS)

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