Crosstalk between tumor necrosis factor-alpha signaling and aryl hydrocarbon receptor signaling in nuclear factor -kappa B activation: A possible molecular mechanism underlying the reduced efficacy of TNF-inhibitors in rheumatoid arthritis by smoking.
Aged
Antirheumatic Agents
/ therapeutic use
Arthritis, Rheumatoid
/ drug therapy
Cells, Cultured
Cigarette Smoking
/ adverse effects
Drug Resistance
Humans
Infliximab
/ therapeutic use
Japan
/ epidemiology
Lymphocyte Activation
Male
Middle Aged
NF-kappa B
/ genetics
Protein Kinase Inhibitors
/ therapeutic use
Receptor Cross-Talk
Receptors, Aryl Hydrocarbon
/ metabolism
Registries
Signal Transduction
T-Lymphocytes
/ immunology
Transcriptional Activation
Treatment Outcome
Tumor Necrosis Factor-alpha
/ metabolism
Withholding Treatment
/ statistics & numerical data
AhR
NF-κB
Rheumatoid arthritis
Smoking
TNF-inhibitor
TNFα
Journal
Journal of autoimmunity
ISSN: 1095-9157
Titre abrégé: J Autoimmun
Pays: England
ID NLM: 8812164
Informations de publication
Date de publication:
03 2019
03 2019
Historique:
received:
13
11
2018
revised:
14
12
2018
accepted:
16
12
2018
pubmed:
29
12
2018
medline:
27
6
2020
entrez:
29
12
2018
Statut:
ppublish
Résumé
To examine the influence of smoking on biologics treatment against different therapeutic targets, such as TNFα, IL-6, and T cell, in rheumatoid arthritis (RA) and elucidate the underlying molecular mechanism. The association between drug-discontinuation due to poor therapeutic response and smoking status was analyzed individually in biologics against different therapeutic targets by a multivariable logistic regression analysis using the "NinJa" Registry, one of the largest cohorts of Japanese RA patients. In vitro enhancement of TNFα-induced NF-κB activation and subsequent proinflammatory cytokine production by cigarette chemical components was examined by RT-PCR, qPCR, ELISA, and western blotting using an immortalized rheumatoid synovial cell line, MH7A. The rate of drug-discontinuation due to poor therapeutic response was higher in the current smoking group than in the never- or ever-smoking groups (the odds ratio of current/never smoking: 2.189, 95%CI; 1.305-3.672,P = 0.003; current/ever: 1.580, 95%CI; 0.879-2.839,P = 0.126) in the TNF inhibitor (TNFi) treatment group. However, this tendency was not observed in either the IL-6 or T cell inhibitor treatment groups. Cigarette smoke chemical components, such as benzo[α]pyrene, known as aryl hydrocarbon receptor (AhR) ligands, themselves activated NF-κB and induced proinflammatory cytokines, IL-1β and IL-6. Furthermore, they also significantly enhanced TNFα-induced NF-κB activation and proinflammatory cytokine production. This enhancement was dominantly inhibited by Bay 11-7082, an NF-κB inhibitor. These results suggest a crosstalk between TNFα signaling and AhR signaling in NF-κB activation which may constitute one of the molecular mechanisms underlying the higher incidence of drug-discontinuation in RA patients undergoing TNFi treatment with smoking habits.
Identifiants
pubmed: 30591403
pii: S0896-8411(18)30662-0
doi: 10.1016/j.jaut.2018.12.004
pii:
doi:
Substances chimiques
Antirheumatic Agents
0
NF-kappa B
0
Protein Kinase Inhibitors
0
Receptors, Aryl Hydrocarbon
0
Tumor Necrosis Factor-alpha
0
Infliximab
B72HH48FLU
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
95-102Informations de copyright
Copyright © 2018. Published by Elsevier Ltd.