Localization of TNF alpha in ileocolonic biopsies of patients with inflammatory bowel disease.


Journal

Annals of diagnostic pathology
ISSN: 1532-8198
Titre abrégé: Ann Diagn Pathol
Pays: United States
ID NLM: 9800503

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 04 06 2018
revised: 08 10 2018
accepted: 25 10 2018
pubmed: 6 11 2018
medline: 14 6 2019
entrez: 3 11 2018
Statut: ppublish

Résumé

Although antitumor necrosis factor alfa (TNFα) agents are widely used to treat patients with inflammatory bowel diseases (IBD) - both Crohn's disease (CD) and ulcerative colitis (UC) - there is still some uncertainty in the cell type expressing TNFα in human ileo-colonic segments. We investigated the immunohistochemical (IHC) expression of TNFα in the ileo-colonic segments of patients with both active CD and UC, to establish its anatomic and cellular localization in the inflamed sites. Our aim was to identify patients potentially resistant to anti TNFα agents. Ileo-colonic slides of complete histological mapping of patients with CD and UC before any treatment was started were obtained, and serial sections assessed for TNFα expression, together with IHC markers for lymphocytes, macrophages, and plasma cells. TNFα was expressed in almost all inflamed segments of IBD patients, albeit with different strength, and was present, in addition to lymphocytes and, to a lesser extent, to macrophages, in plasma cells, where it had a strong positivity, as also demonstrated by colocalization of specific IHC staining. The expression of TNFα was mostly focal in CD patients and more diffuse in UC patients, likely due to the different patterns of inflammation (transmural and mucosal) of the two entities. In IBD, TNFα is strongly expressed also in plasma cells, and it is easily evidenced by conventional IHC techniques. It remains to be established whether this observation might be useful in future to establish in routine biopsy samples whether patients may be responsive to treatments toward this cytokine.

Sections du résumé

BACKGROUND BACKGROUND
Although antitumor necrosis factor alfa (TNFα) agents are widely used to treat patients with inflammatory bowel diseases (IBD) - both Crohn's disease (CD) and ulcerative colitis (UC) - there is still some uncertainty in the cell type expressing TNFα in human ileo-colonic segments.
AIMS OBJECTIVE
We investigated the immunohistochemical (IHC) expression of TNFα in the ileo-colonic segments of patients with both active CD and UC, to establish its anatomic and cellular localization in the inflamed sites. Our aim was to identify patients potentially resistant to anti TNFα agents.
PATIENTS AND METHODS METHODS
Ileo-colonic slides of complete histological mapping of patients with CD and UC before any treatment was started were obtained, and serial sections assessed for TNFα expression, together with IHC markers for lymphocytes, macrophages, and plasma cells.
RESULTS RESULTS
TNFα was expressed in almost all inflamed segments of IBD patients, albeit with different strength, and was present, in addition to lymphocytes and, to a lesser extent, to macrophages, in plasma cells, where it had a strong positivity, as also demonstrated by colocalization of specific IHC staining. The expression of TNFα was mostly focal in CD patients and more diffuse in UC patients, likely due to the different patterns of inflammation (transmural and mucosal) of the two entities.
CONCLUSIONS CONCLUSIONS
In IBD, TNFα is strongly expressed also in plasma cells, and it is easily evidenced by conventional IHC techniques. It remains to be established whether this observation might be useful in future to establish in routine biopsy samples whether patients may be responsive to treatments toward this cytokine.

Identifiants

pubmed: 30388432
pii: S1092-9134(18)30183-7
doi: 10.1016/j.anndiagpath.2018.10.011
pii:
doi:

Substances chimiques

Tumor Necrosis Factor-alpha 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

20-25

Informations de copyright

Copyright © 2018. Published by Elsevier Inc.

Auteurs

Vincenzo Villanacci (V)

Pathology Section, Department of Molecular and Translational Medicine, Spedali Civili and University of Brescia, Italy. Electronic address: villanac@alice.it.

Moris Cadei (M)

Pathology Section, Department of Molecular and Translational Medicine, Spedali Civili and University of Brescia, Italy.

Francesco Lanzarotto (F)

Gastroenterology Section, 1st Medical Clinic, Spedali Civili and University of Brescia, Italy.

Chiara Ricci (C)

Gastroenterology Section, 1st Medical Clinic, Spedali Civili and University of Brescia, Italy.

Elisabetta Antonelli (E)

Gastroenterology Unit, Perugia General Hospital, Italy.

Rosanna Cannatelli (R)

Gastroenterology Section, 1st Medical Clinic, Spedali Civili and University of Brescia, Italy.

Tiziana Gulotta (T)

Pathology Section, Department of Molecular and Translational Medicine, Spedali Civili and University of Brescia, Italy.

Lucia Fontana (L)

Pathology Section, Department of Molecular and Translational Medicine, Spedali Civili and University of Brescia, Italy.

Valentina Pasquali (V)

Pathology Section, Department of Molecular and Translational Medicine, Spedali Civili and University of Brescia, Italy.

Sandra Sigala (S)

Pharmacology Section, University of Brescia, Italy.

Tiziana Salviato (T)

Department of Pathology, University of Trieste School of Medicine, Trieste, Italy.

Riccardo Nascimbeni (R)

Department of Surgery, University of Brescia, Italy.

Gabrio Bassotti (G)

Gastroenterology and Hepatology Section, Department of Medicine, University of Perugia School of Medicine, Perugia, Italy.

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