NKp46 is a diagnostic biomarker and may be a therapeutic target in gastrointestinal T-cell lymphoproliferative diseases: a CELAC study.
Antibodies, Monoclonal
/ immunology
Biomarkers
/ blood
Biopsy
/ methods
Celiac Disease
/ complications
Cells, Cultured
Enteropathy-Associated T-Cell Lymphoma
/ diagnosis
Female
France
Humans
Intestinal Mucosa
/ immunology
Intestine, Small
/ pathology
Killer Cells, Natural
/ immunology
Male
Middle Aged
Natural Cytotoxicity Triggering Receptor 1
/ immunology
Prognosis
antibody targeted therapy
coeliac disease
gastrointestinal lymphoma
tumour markers
Journal
Gut
ISSN: 1468-3288
Titre abrégé: Gut
Pays: England
ID NLM: 2985108R
Informations de publication
Date de publication:
08 2019
08 2019
Historique:
received:
10
08
2018
revised:
15
10
2018
accepted:
05
11
2018
pubmed:
19
11
2018
medline:
23
8
2019
entrez:
19
11
2018
Statut:
ppublish
Résumé
Primary GI T-cell lymphoproliferative diseases (T-LPD) are heterogeneous entities, which raise difficult diagnosis and therapeutic challenges. We have recently provided evidences that lymphomas complicating coeliac disease (CD) arise from innate-like lymphocytes, which may carry NK receptors (NKRs). NKRs expression was compared by flow cytometry in intraepithelial lymphocytes (IEL) from CD, type I or type II refractory CD (RCD). NKp46 was next assessed by immunohistochemistry in paraffin-embedded biopsies from 204 patients with CD, RCDI, RCDII or GI T-cell lymphomas and from a validation cohort of 61 patients. The cytotoxic properties of an anti-NKp46 monoclonal antibody conjugated to pyrrolobenzodiazepine (PBD) was tested NKp46 (but not CD94, NKG2A, NKG2C, NKG2D) was significantly more expressed by malignant RCDII IEL than by normal IEL in CD and RCDI. In paraffin biopsies, detection of >25 NKp46+ IEL per 100 epithelial cells discriminated RCDII from CD and RCDI. NKp46 was also detected in enteropathy-associated T-cell lymphomas (EATL, 24/29) and in monomorphic epitheliotropic intestinal T-cell lymphomas (MEITL, 4/4) but not in indolent T-LPD (0/15). Treatment with anti-NKp46-PBD could efficiently and selectively kill human NKp46+ primary IEL NKp46 is a novel biomarker useful for diagnosis and therapeutic stratification of GI T-LPD. Strong preclinical rationale identifies anti-NKp46-PBD as a promising therapy for RCDII, EATL and MEITL.
Identifiants
pubmed: 30448772
pii: gutjnl-2018-317371
doi: 10.1136/gutjnl-2018-317371
doi:
Substances chimiques
Antibodies, Monoclonal
0
Biomarkers
0
NCR1 protein, human
0
Natural Cytotoxicity Triggering Receptor 1
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Pagination
1396-1405Investigateurs
Yoram Bouhnik
(Y)
Charles-André Cuenod
(CA)
Sabine Brechignac
(S)
Matthieu Allez
(M)
Jacques Cosnes
(J)
Agnès Fourmestraux
(A)
Jean-Charles Delchier
(JC)
Jehan Dupuis
(J)
Corinne Haioun
(C)
Taoufik El Gnaoui
(TE)
Eric Lerebours
(E)
Guillaume Savoye
(G)
Herve Tilly
(H)
Bernard Flourie
(B)
Bertrand Coiffier
(B)
Xavier Hebuterne
(X)
Nadia Arab
(N)
Jérôme Filippi
(J)
Stéphane Schneider
(S)
Frank Zerbib
(F)
Noel Milpied
(N)
Krimo Bouabdallah
(K)
Reza Tabrizi
(R)
Stéphane Vigouroux
(S)
Arnaud Pigneux
(A)
Thibaut Leguay
(T)
Marie-Sarah Dilhuydy
(MS)
Charles Dauriac
(C)
Serge Bologna
(S)
Cyrille Hulin
(C)
Caroline Bonmati
(C)
Fréderic Magnin
(F)
Dana Ranta
(D)
Tamara Matysiakbudnik
(T)
Eric Deconinck
(E)
Philippe Pouderoux
(P)
Bruno Bonaz
(B)
Remy Gressin
(R)
Franck Carbonnel
(F)
Jean-Marc Gornet
(JM)
Julien Branche
(J)
Georgette Saint-Georges
(G)
Jean-Marie Reimund
(JM)
Stéphane Nancey
(S)
Maria Nachury
(M)
Stéphanie Viennot
(S)
Camille Zallot
(C)
Bettina Fabiani
(B)
Lysiane Marthey
(L)
Karine Juvin
(K)
Yann Le Baleur
(YL)
Sandy Kwiatek
(S)
Eric Saillard
(E)
Dominique Louvel
(D)
Xavier Roblin
(X)
Philippe Beau
(P)
Pierre Feugier
(P)
Laurent Peyrin-Biroulet
(L)
Hélène Zanaldi
(H)
Hedia Brixi-Benmansour
(H)
Guillaume Cadiot
(G)
Thierry Lecomte
(T)
Jean-Francois Bretagne
(JF)
Olivier Casasnovas
(O)
Denis Caillot
(D)
Laurent Bedenne
(L)
Jacques-Olivier Bay
(JO)
Corinne Bouteloup
(C)
Bernard Duclos
(B)
Carine Foucaud
(C)
Informations de copyright
© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: FL and CB are senior directors and have ownership interest (including patents) in Innate Pharma. MC, JB and OH received research grants from Innate Pharma.