Paradoxical gastrointestinal reactions in patients taking tumor necrosis factor inhibitors: a rare event that broadens the histologic spectrum of medication-associated injury.


Journal

Human pathology
ISSN: 1532-8392
Titre abrégé: Hum Pathol
Pays: United States
ID NLM: 9421547

Informations de publication

Date de publication:
03 2019
Historique:
received: 01 10 2018
revised: 01 11 2018
accepted: 04 11 2018
pubmed: 20 11 2018
medline: 26 11 2019
entrez: 20 11 2018
Statut: ppublish

Résumé

Tumor necrosis factor (TNF) inhibitors are widely used in the therapy of certain autoimmune disorders. Paradoxical immunologic reactions manifesting as new-onset autoimmune disease or exacerbation of the underlying condition have been reported in association with these drugs. In this study, we reviewed gastrointestinal biopsies and clinical findings in patients with rheumatologic disease on TNF inhibitor therapy and compared to patients with rheumatologic disease not on TNF inhibitors. Eighteen biopsies from 9 patients treated with TNF inhibitor therapy and 249 biopsies from 120 control patients not treated with TNF inhibitors were included. Among patients taking a TNF inhibitor, 55.6% were female, and the median age was 47 (range, 30-67 years). Four (44.4%) patients were taking etanercept, 4 (44.4%) adalimumab, and 1 (11.1%) certolizumab pegol. Of the 120 control patients, 75 (62.5%) were female and the median age was 62 (range, 26-85 years). Paradoxical reactions were observed in 3 (33.3%) of 9 patients on TNF inhibitors, including 2 (22.2%) with inflammatory bowel disease-like changes and 1 (11.1%) with sarcoid-like granulomas. All 3 patients showed symptomatic and histologic improvement or resolution after discontinuation of therapy. These reactions were not observed in any of the control patients (P = .0002). Our results indicate that among patients with rheumatologic disease, paradoxical reactions of the gastrointestinal tract are associated with TNF inhibitor therapy. Knowledge of this association is important because symptoms and histologic features may improve following medication switch.

Identifiants

pubmed: 30452927
pii: S0046-8177(18)30432-5
doi: 10.1016/j.humpath.2018.11.003
pii:
doi:

Substances chimiques

Antirheumatic Agents 0
Tumor Necrosis Factor-alpha 0
Adalimumab FYS6T7F842
Etanercept OP401G7OJC
Certolizumab Pegol UMD07X179E

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

202-209

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Danielle Hutchings (D)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21287. Electronic address: dhutch15@jhmi.edu.

James A Miller (JA)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21287.

Lysandra Voltaggio (L)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21287.

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Classifications MeSH