CD80 expression promotes immune surveillance in Barrett’s metaplasia

Esophageal adenocarcinoma (EAC) is the final step of a pathway starting with esophageal reflux disease, Barrett’s metaplasia and Barrett’s dysplasia. Positive costimulatory ligands such as CD80 have been suggested to contribute to anti-tumor T-cell efficacy. Here we report for the first time the rol...

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Main Authors: Melania Scarpa, Matteo Fassan, Andromachi Kotsafti, Stefano Realdon, Luigi Dall’Olmo, Tiziana Morbin, Francesco Cavallin, Luca Saadeh, Matteo Cagol, Rita Alfieri, Carlo Castoro, Massimo Rugge, Ignazio Castagliuolo, Marco Scarpa
Format: Article
Language:English
Published: Taylor & Francis Group 2019-10-01
Series:OncoImmunology
Subjects:
Online Access:http://dx.doi.org/10.1080/2162402X.2019.1636618
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author Melania Scarpa
Matteo Fassan
Andromachi Kotsafti
Stefano Realdon
Luigi Dall’Olmo
Tiziana Morbin
Francesco Cavallin
Luca Saadeh
Matteo Cagol
Rita Alfieri
Carlo Castoro
Massimo Rugge
Ignazio Castagliuolo
Marco Scarpa
author_facet Melania Scarpa
Matteo Fassan
Andromachi Kotsafti
Stefano Realdon
Luigi Dall’Olmo
Tiziana Morbin
Francesco Cavallin
Luca Saadeh
Matteo Cagol
Rita Alfieri
Carlo Castoro
Massimo Rugge
Ignazio Castagliuolo
Marco Scarpa
author_sort Melania Scarpa
collection DOAJ
description Esophageal adenocarcinoma (EAC) is the final step of a pathway starting with esophageal reflux disease, Barrett’s metaplasia and Barrett’s dysplasia. Positive costimulatory ligands such as CD80 have been suggested to contribute to anti-tumor T-cell efficacy. Here we report for the first time the role of CD80 in the inflammatory esophageal carcinogenesis and characterize the immune environment of EAC. Mucosa samples from cancer were obtained during esophagectomy from patients affected by EAC. Fresh biopsies were obtained from patients who underwent endoscopy for screening or follow-up. A rodent model of reflux induced esophageal carcinogenesis was created with an esophago-gastro-jejunostomy. CD80 expression was increased in epithelial cells during metaplasia in the inflammatory esophageal carcinogenesis cascade. Cd80 null mice as well as WT mice that received antiCD80 antibodies showed a higher rate of dysplasia and KI-67+ cells. These results suggest that CD80 mediates an active immune surveillance process in early inflammation-driven esophageal carcinogenesis.
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spelling doaj.art-8df0e08859b741698002c7f43ea5d1e62022-12-22T00:45:00ZengTaylor & Francis GroupOncoImmunology2162-402X2019-10-0181010.1080/2162402X.2019.16366181636618CD80 expression promotes immune surveillance in Barrett’s metaplasiaMelania Scarpa0Matteo Fassan1Andromachi Kotsafti2Stefano Realdon3Luigi Dall’Olmo4Tiziana Morbin5Francesco Cavallin6Luca Saadeh7Matteo Cagol8Rita Alfieri9Carlo Castoro10Massimo Rugge11Ignazio Castagliuolo12Marco Scarpa13IRCCSUniversity of PaduaIRCCSHospital of VeniceHospital of VeniceHospital of VeniceIndependent StatisticianUniversity Hospital of PadovaHospital of VeniceHospital of VeniceHumanitas Research Hospital-Humanitas UniversityUniversity of PaduaUniversity of PaduaUniversity Hospital of PadovaEsophageal adenocarcinoma (EAC) is the final step of a pathway starting with esophageal reflux disease, Barrett’s metaplasia and Barrett’s dysplasia. Positive costimulatory ligands such as CD80 have been suggested to contribute to anti-tumor T-cell efficacy. Here we report for the first time the role of CD80 in the inflammatory esophageal carcinogenesis and characterize the immune environment of EAC. Mucosa samples from cancer were obtained during esophagectomy from patients affected by EAC. Fresh biopsies were obtained from patients who underwent endoscopy for screening or follow-up. A rodent model of reflux induced esophageal carcinogenesis was created with an esophago-gastro-jejunostomy. CD80 expression was increased in epithelial cells during metaplasia in the inflammatory esophageal carcinogenesis cascade. Cd80 null mice as well as WT mice that received antiCD80 antibodies showed a higher rate of dysplasia and KI-67+ cells. These results suggest that CD80 mediates an active immune surveillance process in early inflammation-driven esophageal carcinogenesis.http://dx.doi.org/10.1080/2162402X.2019.1636618barrett’s esophagusesophageal dysplasiaimmune surveillancecd80adenocarcinoma
spellingShingle Melania Scarpa
Matteo Fassan
Andromachi Kotsafti
Stefano Realdon
Luigi Dall’Olmo
Tiziana Morbin
Francesco Cavallin
Luca Saadeh
Matteo Cagol
Rita Alfieri
Carlo Castoro
Massimo Rugge
Ignazio Castagliuolo
Marco Scarpa
CD80 expression promotes immune surveillance in Barrett’s metaplasia
OncoImmunology
barrett’s esophagus
esophageal dysplasia
immune surveillance
cd80
adenocarcinoma
title CD80 expression promotes immune surveillance in Barrett’s metaplasia
title_full CD80 expression promotes immune surveillance in Barrett’s metaplasia
title_fullStr CD80 expression promotes immune surveillance in Barrett’s metaplasia
title_full_unstemmed CD80 expression promotes immune surveillance in Barrett’s metaplasia
title_short CD80 expression promotes immune surveillance in Barrett’s metaplasia
title_sort cd80 expression promotes immune surveillance in barrett s metaplasia
topic barrett’s esophagus
esophageal dysplasia
immune surveillance
cd80
adenocarcinoma
url http://dx.doi.org/10.1080/2162402X.2019.1636618
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