Cross-reactivity between tumor MHC class I–restricted antigens and an enterococcal bacteriophage

Aurélie Fluckiger(Inserm), Romain Daillère(Inserm), Mohamed Sassi(Inserm), Barbara S. Sixt(Inserm), Peng Liu(Inserm), Friedemann Loos(Inserm), Corentin Richard(Université de Bourgogne), Catherine Rabu(Inserm), Maryam Tidjani Alou(Inserm), Anne‐Gaëlle Goubet(Inserm), Fabien Lemaître(Institut Gustave Roussy), Gladys Ferrere(Inserm), Lisa Derosa(Inserm), Connie P.M. Duong(Inserm), Meriem Messaoudene(Institut universitaire de cardiologie et de pneumologie de Québec), Andréanne Gagné(Institut universitaire de cardiologie et de pneumologie de Québec), Philippe Joubert(Institut universitaire de cardiologie et de pneumologie de Québec), Luisa De Sordi(Inserm), Laurent Debarbieux(Institut Pasteur), Sylvain Simon(Inserm), Clara‐Maria Scarlata(Université Toulouse III - Paul Sabatier), Maha Ayyoub(Université Toulouse III - Paul Sabatier), Belinda Palermo(Istituti di Ricovero e Cura a Carattere Scientifico), Francesco Facciolo(National Cancer Institute), Romain Boidot(Centre Georges François Leclerc), Richard Wheeler(Institut Pasteur), Ivo G. Boneca(Institut Pasteur), Zsófia Sztupinszki(Boston Children's Hospital), Krisztián Papp(Eötvös Loránd University), István Csabai(Eötvös Loránd University), Edoardo Pasolli(University of Naples Federico II), Nicola Segata(University of Trento), Carlos López-Otı́n(Inserm), Zoltán Szállási(Semmelweis University), Fabrice André(Inserm), Valerio Iebba(University of Trieste), Valentin Quiniou(Inserm), David Klatzmann(Inserm), Jacques Bou Khalil(Méditerranée Infection Foundation), S. Khelaifia(Méditerranée Infection Foundation), Didier Raoult(Méditerranée Infection Foundation), Laurence Albigès(Institut Gustave Roussy), Bernard Escudier(Inserm), Alexander Eggermont(Institut Gustave Roussy), Fathia Mami‐Chouaib(Université Paris-Sud), Paola Nisticò(National Cancer Institute), François Ghiringhelli(Centre Georges François Leclerc), Bertrand Routy(Institut universitaire de cardiologie et de pneumologie de Québec), Nathalie Labarrière(Inserm), Vincent Cattoir(Inserm), Guido Kroemer(Karolinska University Hospital), Laurence Zitvogel(Inserm)
Science
August 21, 2020
Cited by 380Open Access
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Abstract

Phages and cancer immunity Gut bacteria are involved in the education of T cell immune responses, and the intestinal ecosystem influences anticancer immunity. Fluckiger et al. report microbial antigens that might cross-react with antigens associated with tumor cells. They found that a type of intestinal bacteria called enterococci harbor a bacteriophage that modulates immune responses. In mouse models, administration of enterococci containing the bacteriophage boosted T cell responses after treatment with chemotherapy or programmed cell death protein 1 (PD-1) blockade. In humans, the presence of the bacteriophage was associated with improved survival after PD-1 immunotherapy. A fraction of human T cells specific for naturally processed melanoma epitopes appeared to be able to recognize microbial peptides. This “molecular mimicry” may represent cross-reactivity between tumors and microbial antigens. Science , this issue p. 936


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