Antigen-specific T-T interactions regulate CD4 T-cell expansion

Author:

Helft Julie12,Jacquet Alexandra12,Joncker Nathalie T.12,Grandjean Isabelle12,Dorothée Guillaume12,Kissenpfennig Adrien345,Malissen Bernard345,Matzinger Polly6,Lantz Olivier12

Affiliation:

1. Laboratoire d'Immunologie clinique,

2. Inserm U653, Institut Curie, Paris;

3. Centre d'Immunologie de Marseille-Luminy, Université de la Méditerrannée, Marseille;

4. Inserm U631, Marseille;

5. Centre National de la Recherche Scientifique (CNRS), UMR6102, Marseille, France; and

6. The Ghost Lab, Laboratory of Cellular and Molecular Immunology (LCMI), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD

Abstract

Abstract The regulation of CD4 T-cell numbers during an immune response should take account of the amount of antigen (Ag), the initial frequency of Ag-specific T cells, the mix of naive versus experienced cells, and (ideally) the diversity of the repertoire. Here we describe a novel mechanism of T-cell regulation that potentially deals with all of these parameters. We found that CD4 T cells establish a negative feedback loop by capturing their cognate major histocompatibility class (MHC)/peptide complexes from Ag-presenting cells and presenting them to Ag-experienced CD4 T cells, thereby inhibiting their recruitment into the response while allowing recruitment of naive T cells. The inhibition is Ag specific, begins at day 2 (long before Ag disappearance), and cannot be overcome by providing new Ag-loaded dendritic cells. In this way, CD4 T-cell proliferation is regulated in a functional relationship to the amount of Ag, while allowing naive T cells to generate repertoire variety.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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