Early Hepatic Lesions Display Immature Tertiary Lymphoid Structures and Show Elevated Expression of Immune Inhibitory and Immunosuppressive Molecules

Author:

Meylan Maxime12ORCID,Petitprez Florent12ORCID,Lacroix Laetitia1,Di Tommaso Luca34,Roncalli Massimo34,Bougoüin Antoine1,Laurent Alexis5,Amaddeo Giuliana67,Sommacale Daniele57,Regnault Hélène6,Derman Jonathan8,Charpy Cécile8,Lafdil Fouad7,Pawlotsky Jean-Michel79,Sautès-Fridman Catherine1ORCID,Fridman Wolf H.1ORCID,Calderaro Julien178

Affiliation:

1. 1Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, USPC, Université de Paris, Inflammation, Complement and Cancer Team, Paris, France.

2. 2Programme Cartes d'Identité des Tumeurs, Ligue Nationale Contre le Cancer, Paris, France.

3. 3Department of Pathology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy.

4. 4Department of Biomedical Sciences, Humanitas University, Rozzano, Milan, Italy.

5. 5Service de Chirurgie Digestive et Hépatobiliaire, Assistance Publique Hôpitaux de Paris, Groupe Hospitalier Henri Mondor, Créteil, France; Université Paris-Est Créteil, Créteil France.

6. 6Assistance Publique–Hôpitaux de Paris, Service d'Hépatologie, Hôpital Henri Mondor, Paris, France.

7. 7Inserm U955, Equipe 18, Institut Mondor de Recherche Biomédicale, Créteil, France, Université Paris Est Créteil, Créteil, France.

8. 8Département de Pathologie, Assistance Publique Hôpitaux de Paris, Groupe Hospitalier Henri Mondor, Créteil, France; Université Paris-Est Créteil, Créteil France.

9. 9APHP, Groupe Hospitalier Henri Mondor, Service de Virologie, Bactériologie-Hygiène, Mycologie-Parasitologie et unité Transversale de Traitement des Infections, Créteil, France.

Abstract

AbstractPurpose:The impact of tertiary lymphoid structures (TLS) in hepatocellular carcinoma (HCC) progression is being extensively investigated. However, their presence during the early steps of human liver carcinogenesis remains unknown. We thus aimed to determine whether TLS are induced in preneoplastic/early hepatic lesions (EHL), and whether they are associated with a particular immune profile.Experimental Design:A series of 127 EHLs (low/high-grade dysplastic nodules, early HCC, and small and progressed HCC) was included in the study. TLSs were investigated by pathologic reviewing. Densities of immune cells were assessed using IHC. A subset of lesions was microdissected and gene expression profiling was performed with a custom NanoString panel.Results:Compared with surrounding cirrhotic nodules, EHL of all stages displayed increased densities of T cells, B cells, and dendritic cells. Immature TLSs were identified in 24% of EHL. Gene expression profiling identified a subset of EHL with elevated mRNA levels of various cytokines involved in immune cells' recruitment and TLS induction. This subgroup of EHL also showed overexpression of genes related to T- and B-cells' activation and antigen presentation, as well as those related to immunosuppression and immune exhaustion.Conclusions:Local immune activation occurs in the very early steps of liver carcinogenesis; however, it may not be fully efficient and paradoxically favor immune evasion and progression to full-blown HCC. These results have implications for the development of anti-HCC chemopreventive strategies in cirrhotic patients.

Funder

Cancer Research for Personalized Medecine

Labex Immuno-Oncology

Publisher

American Association for Cancer Research (AACR)

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