RIPK1 and NF-κB signaling in dying cells determines cross-priming of CD8 + T cells

Author:

Yatim Nader123,Jusforgues-Saklani Hélène12,Orozco Susana4,Schulz Oliver5,Barreira da Silva Rosa12,Reis e Sousa Caetano5,Green Douglas R.6,Oberst Andrew4,Albert Matthew L.12

Affiliation:

1. Laboratory of Dendritic Cell Biology, Department of Immunology, Institut Pasteur, 25 Rue du Docteur Roux, 75015 Paris, France.

2. Institut National de la Santé et de la Recherche Médicale, U818, 25 Rue du Docteur Roux, 75015 Paris, France.

3. Frontières du Vivant Doctoral School, École Doctorale 474, Université Paris Diderot-Paris 7, Sorbonne Paris Cité, 8-10 Rue Charles V, 75004 Paris, France.

4. Department of Immunology, University of Washington, Campus Box 358059, 750 Republican Street, Seattle, WA 98109, USA.

5. Immunobiology Laboratory, The Francis Crick Institute, Lincoln’s Inn Fields Laboratory, 44 Lincoln's Inn Fields, London WC2A 3LY, UK.

6. Department of Immunology, St. Jude Children’s Research Hospital, 262 Danny Thomas Place, Memphis, TN 38105, USA.

Abstract

Dying to impress the immune system Besides reacting to microbes, T cells can also mount immune responses to fragments of dying cells, which they encounter displayed on dendritic cells. Not all dying cells activate T cells, however, so what differentiates the dying cells that do? Yatim et al. studied two forms of programmed cells death: apoptosis and necroptosis. Using mouse cells in culture and mouse models of inflammatory cell death and anti-tumor immunity, they found that programmed cell death initiated T cell immunity only when the dying cells signaled through the enzyme RIPK1 and the transcription factor NF-κB. Science , this issue p. 328

Funder

NIH

Francis Crick Institute

European Research Council

Cancer Research UK

Agence Nationale de Recherches sur le Sida et les Hepatitis

Agence Nationale de la Recherche

French National Cancer Institute (INCa)

Laboratories of Excellence Immuno-Onco

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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